Login| Sign Up| Help| Contact|

Patent Searching and Data


Title:
ERWINIA ISOLATES AND USES THEREOF
Document Type and Number:
WIPO Patent Application WO/2020/263734
Kind Code:
A1
Abstract:
The present disclosure provides fungicidal Erwinia and Pseudomonas strains useful for protecting plants and enhancing crop yield, as well as cultures and inoculant compositions comprising the isolated strains, cellular extracts derived from the isolated strains, and cell-free filtrates derived from cultures of the isolated strains.

Inventors:
YOUNG HUGH (US)
YOSHIDA SHIGENOBU (JP)
Application Number:
PCT/US2020/038926
Publication Date:
December 30, 2020
Filing Date:
June 22, 2020
Export Citation:
Click for automatic bibliography generation   Help
Assignee:
NOVOZYMES BIOAG AS (DK)
NAT AGRICULTURE & FOOD RES ORG (JP)
YOUNG HUGH (US)
International Classes:
A01N63/20; A01N63/27; C12R1/18; C12R1/38
Domestic Patent References:
WO2018128985A12018-07-12
WO2017044473A12017-03-16
WO2017044545A12017-03-16
WO2017116837A12017-07-06
WO2017116846A12017-07-06
WO2017210163A12017-12-07
WO2017210166A12017-12-07
WO2018118740A12018-06-28
WO2018175681A12018-09-27
WO2018183491A12018-10-04
WO2018218008A12018-11-29
WO2018218016A12018-11-29
WO2018218035A12018-11-29
WO2010049751A12010-05-06
WO2005063784A12005-07-14
WO2007117500A22007-10-18
WO2008071674A22008-06-19
WO2003000051A22003-01-03
WO2009015266A22009-01-29
WO2010037228A12010-04-08
WO2011140051A12011-11-10
WO2012135704A12012-10-04
WO2013090884A12013-06-20
WO2014078647A12014-05-22
WO2015069708A12015-05-14
WO2017027821A12017-02-16
WO2017077104A12017-05-11
WO2017083623A12017-05-18
WO2017131971A12017-08-03
WO2017205258A12017-11-30
WO2018129016A12018-07-12
WO2018129018A12018-07-12
WO2018175677A12018-09-27
Foreign References:
EP3254565A12017-12-13
US5484464A1996-01-16
US5586411A1996-12-24
US5695541A1997-12-09
US5804208A1998-09-08
US5916029A1999-06-29
US6569425B22003-05-27
US6808917B12004-10-26
US6824772B22004-11-30
US7429477B22008-09-30
US8148138B22012-04-03
US8278247B22012-10-02
US8445256B22013-05-21
US8883679B22014-11-11
US8921089B22014-12-30
US8999698B22015-04-07
US9017442B22015-04-28
US9101088B22015-08-11
US9234251B22016-01-12
US9340464B22016-05-17
US7989393B22011-08-02
US5549718A1996-08-27
US5175149A1992-12-29
US5321011A1994-06-14
US5545718A1996-08-13
US4536207A1985-08-20
US5965545A1999-10-12
US5702752A1997-12-30
US5990291A1999-11-23
US6146668A2000-11-14
US7576213B22009-08-18
US20060258534A12006-11-16
US20110230345A12011-09-22
US20180201549A12018-07-19
USPP62296798P
USPP62271857P
USPP62347773P
USPP62343217P
USPP62296784P
USPP62271873P
USPP62347785P
USPP62347794P
USPP62347805P
Other References:
WORLD DATA CENTRE FOR MICROORGANISMS. CULTURE COLLECTIONS INFORMATION WORLDWIDE: "NARO, GENEBANK MICROORGANISM SECTION", 25 July 2002 (2002-07-25), XP002800449, Retrieved from the Internet [retrieved on 20200923]
MESANZA NEBAI ET AL: "Native rhizobacteria as biocontrol agents ofHeterobasidion annosums.s. andArmillaria melleainfection ofPinus radiata", BIOLOGICAL CONTROL, SAN DIEGO, CA, US, vol. 101, 15 June 2016 (2016-06-15), pages 8 - 16, XP029694837, ISSN: 1049-9644, DOI: 10.1016/J.BIOCONTROL.2016.06.003
EUGENIA ITURRITXA ET AL: "Biocontrol of Fusarium circinatum Infection of Young Pinus radiata Trees", FORESTS, vol. 8, no. 2, 1 January 2017 (2017-01-01), pages 32, XP055733440, ISSN: 1999-4907, DOI: 10.3390/f8020032
CUNNINGHAM ET AL., CAN. J. BOT., vol. 68, 1990, pages 2270
FRIESEN ET AL., APPL. MICROBIOL. BIOTECH., vol. 68, 2005, pages 397
DENARIE ET AL., ANN. REV. BIOCHEM., vol. 65, 1996, pages 503
BURGES: "FORMULATION OF MICROBIAL BIOPESTICIDES: BENEFICIAL MICROORGANISMS, NEMATODES AND SEED TREATMENTS", 2012, SPRINGER SCIENCE & BUSINESS MEDIA
INOUEHORIKOSHI, J., FERMENTATION BIOENG., vol. 71, no. 3, 1991, pages 194
POUCI ET AL., AM. J. AGRIC. BIOL. SCI, vol. 3, no. 1, 2008, pages 299
STEFFEYGRAY: "ILLINOIS AGRONOMY HANDBOOK", 2008, article "Managing Insect Pests,"
LOUX ET AL.: "WEED CONTROL GUIDE FOR OHIO", 2015, INDIANA AND ILLINOIS
HANEL ET AL., PLANTA, vol. 232, 2010, pages 787
PROME ET AL., PURE & APPL. CHEM., vol. 70, no. 1, 1998, pages 55
SAMAIN ET AL., CARBOHYDRATE RES., vol. 302, 1997, pages 35
COTTAZ ET AL., METH. ENG., vol. 7, no. 4, 2005, pages 311
SAMAIN ET AL., J. BIOTECHNOL., vol. 72, 1999, pages 33
D'HAEZE ET AL., GLYCOBIOL., vol. 12, no. 6, 2002, pages 79R
DEMONT-CAULET ET AL., PLANT PHYSIOL., vol. 120, no. 1, 1999, pages 83
MULLER ET AL., PLANT PHYSIOL., vol. 124, 2000, pages 733
ROBINA ET AL., TETRAHEDRON, vol. 58, 2002, pages 521 - 530
ROUGE ET AL.: "THE MOLECULAR IMMUNOLOGY OF COMPLEX CARBOHYDRATES-3", 2011, SPRINGER SCIENCE, article "Docking of Chitin Oligomers and Nod Factors on Lectin Domains of the LysM-RLK Receptors in the Medicago-Rhizobium Symbiosis,"
VAN DER HOIST ET AL., CURR. OPIN. STRUC. BIOL., vol. 11, 2001, pages 608
; WAN ET AL., PLANT CELL, vol. 21, 2009, pages 1053
AAM ET AL., MAR. DRUGS, vol. 8, 2010, pages 1482
LIMPANAVECH ET AL., SCIENTIA HORTICULTURAE, vol. 116, 2008, pages 65
LODHI ET AL., BIOMED RES. INTL., vol. 2014, no. 654913, March 2014 (2014-03-01)
MOURYA ET AL., POLYMER SCI, vol. 53, no. 7, 2011, pages 583
ROUGE ET AL.: "ADVANCES IN EXPERIMENTAL MEDICINE AND BIOLOGY", 2011, SPRINGER SCIENCE, article "The Molecular Immunology of Complex Carbohydrates,"
XIA ET AL., FOOD HYDROCOLLOIDS, vol. 25, 2011, pages 170
POCHANAVANICH ET AL., LETT. APPL. MICROBIOL., vol. 35, 2002, pages 17
JAIN ET AL., PLANT BIOCHEM. & BIOTECHNOL., vol. 11, 2002, pages 1
SHAW ET AL., ENVIRON. MICROBIOL., vol. 11, 2006, pages 1867
RALSTON ET AL., PLANT PHYSIOL., vol. 137, 2005, pages 1375
MABOOD ET AL., PLANT PHYSIOL. BIOCHEM., vol. 44, no. 11, 2006, pages 759
MABOOD ET AL., AGR. J., vol. 98, no. 2, 2006, pages 289
MABOOD ET AL., FIELD CROPS RES., vol. 95, no. 2-3, 2006, pages 412
MABOODSMITH: "Linoleic and linolenic acid induce the expression of nod genes in Bradyrhizobium japonicum USDA 3,", PLANT BIOL., 2001
HALFORD: "Smoke Signals,", CHEM. ENG. NEWS, 12 April 2010 (2010-04-12)
MCCARTY: "WETTING AGENTS", 2001, CLEMSON UNIVERSITY COOPERATIVE EXTENSION SERVICE PUBLICATION
Attorney, Agent or Firm:
RUCKER, Adam L. et al. (US)
Download PDF:
Claims:
THAT WHICH IS CLAIMED:

1. An isolated microbial strain selected from the group consisting of:

the isolated Erwinia strain deposited as accession number NRRL B-67766 (E. billingiae NRRL B-67766);

the isolated Pseudomonas gessardii strain having the deposit accession number NRRL B-67767 (P. gessardii NRRL B-67767); and

the isolated Pseudomonas libanesis strain having the deposit accession number NRRL B-67769 (P. libanesis NRRL B-67769).

2. A biologically pure culture selected from the group consisting of:

a biologically pure culture of E. billingiae NRRL B-67766;

a biologically pure culture of P. gessardii NRRL B-67767; and

a biologically pure culture of P. libanesis NRRL B-67769.

3. A cell-free filtrate derived from a bacterial culture comprising E. billingiae NRRL B-67766 and/or P. gessardii NRRL B-67767 and/or P. libanesis NRRL B-67769 and/or one or more close relatives of one of the foregoing strains.

4. A cellular extract derived from E. billingiae NRRL B-67766, P. gessardii NRRL B-67767 and/or P. libanesis NRRL B-67769 and/or from one or more close relatives of one of the foregoing strains.

5. A non-naturally occurring composition comprising E. billingiae NRRL B-67766 or a close relative thereof, a cell-free filtrate derived from a culture comprising E. billingiae NRRL B-67766 or a close relative thereof, a cellular extract derived from E. billingiae NRRL B-67766 or a close relative thereof, P. gessardii NRRL B-67767 or a close relative thereof, a cell-free filtrate derived from a culture comprising P. gessardii NRRL B-67767 or a close relative thereof, a cellular extract derived from P. gessardii NRRL B-67767 or a close relative thereof, P. libanesis NRRL B-67769 or a close relative thereof, a cell-free filtrate derived from a culture comprising P. libanesis NRRL B-67769 or a close relative thereof, and/or a cellular extract derived from P. libanesis NRRL B-67769 or a close relative thereof.

6. A non-naturally occurring seed composition comprising a plant propagation material, optionally a seed, and a coating that covers at least a portion of an outer surface of said seed, said coating comprising the isolated strain of claim 1, the biologically pure culture of claim 2, the cell-free filtrate of claim 3 and/or the cellular extract of claim 4.

7. Use of E. billingiae NRRL B-67766 or a close relative thereof, a cell-free filtrate derived from a culture comprising E. billingiae NRRL B-67766 or a close relative thereof, a cellular extract derived from E. billingiae NRRL B-67766 or a close relative thereof, P. gessardii NRRL B-67767 or a close relative thereof, a cell-free filtrate derived from a culture comprising P. gessardii NRRL B-67767 or a close relative thereof, a cellular extract derived from P. gessardii NRRL B-67767 or a close relative thereof, P. libanesis NRRL B-67769 or a close relative thereof, a cell-free filtrate derived from a culture comprising P. libanesis NRRL B-67769 or a close relative thereof, and/or a cellular extract derived from P. libanesis NRRL B-67769 or a close relative thereof for treating a plant or plant part.

8. Use of E. billingiae NRRL B-67766 or a close relative thereof, a cell-free filtrate derived from a culture comprising E. billingiae NRRL B-67766 or a close relative thereof, a cellular extract derived from E. billingiae NRRL B-67766 or a close relative thereof, P. gessardii NRRL B-67767 or a close relative thereof, a cell-free filtrate derived from a culture comprising P. gessardii NRRL B-67767 or a close relative thereof, a cellular extract derived from P. gessardii NRRL B-67767 or a close relative thereof, P. libanesis NRRL B-67769 or a close relative thereof, a cell-free filtrate derived from a culture comprising P. libanesis NRRL B-67769 or a close relative thereof, and/or a cellular extract derived from P. libanesis NRRL B-67769 or a close relative thereof for killing, inhibiting the growth of and/or inhibiting the reproduction/proliferation of a fungal plant pest.

9. Use of E. billingiae NRRL B-67766 or a close relative thereof, a cell-free filtrate derived from a culture comprising E. billingiae NRRL B-67766 or a close relative thereof, a cellular extract derived from E. billingiae NRRL B-67766 or a close relative thereof, P. gessardii NRRL B-67767 or a close relative thereof, a cell-free filtrate derived from a culture comprising P. gessardii NRRL B-67767 or a close relative thereof, a cellular extract derived from P. gessardii NRRL B-67767 or a close relative thereof, P. libanesis NRRL B-67769 or a close relative thereof, a cell-free filtrate derived from a culture comprising P. libanesis NRRL B-67769 or a close relative thereof, and/or a cellular extract derived from P. libanesis NRRL B-67769 or a close relative thereof for reducing fungal disease severity in a plant or plant part.

10. Use of E. billingiae NRRL B-67766 or a close relative thereof, a cell-free filtrate derived from a culture comprising E. billingiae NRRL B-67766 or a close relative thereof, a cellular extract derived from E. billingiae NRRL B-67766 or a close relative thereof, P. gessardii NRRL B-67767 or a close relative thereof, a cell-free filtrate derived from a culture comprising P. gessardii NRRL B-67767 or a close relative thereof, a cellular extract derived from P. gessardii NRRL B-67767 or a close relative thereof, P. libanesis NRRL B-67769 or a close relative thereof, a cell-free filtrate derived from a culture comprising P. libanesis NRRL B-67769 or a close relative thereof, and/or a cellular extract derived from P. libanesis NRRL B-67769 or a close relative thereof for enhancing growth and/or yield in a plant or plant part.

11. A method comprising introducing E. billingiae NRRL B-67766 or a close relative thereof, a cell-free filtrate derived from a culture comprising E. billingiae NRRL B-67766 or a close relative thereof, a cellular extract derived from E. billingiae NRRL B-67766 or a close relative thereof, P.

gessardii NRRL B-67767 or a close relative thereof, a cell-free filtrate derived from a culture comprising P. gessardii NRRL B-67767 or a close relative thereof, a cellular extract derived from P. gessardii NRRL B-67767 or a close relative thereof, P. libanesis NRRL B-67769 or a close relative thereof, a cell-free filtrate derived from a culture comprising P. libanesis NRRL B-67769 or a close relative thereof, and/or a cellular extract derived from P. libanesis NRRL B-67769 or a close relative thereof into a plant growth medium.

12. A method comprising applying E. billingiae NRRL B-67766 or a close relative thereof, a cell- free filtrate derived from a culture comprising E. billingiae NRRL B-67766 or a close relative thereof, a cellular extract derived from E. billingiae NRRL B-67766 or a close relative thereof, P. gessardii NRRL B-67767 or a close relative thereof, a cell-free filtrate derived from a culture comprising P. gessardii NRRL B-67767 or a close relative thereof, a cellular extract derived from P. gessardii NRRL B-67767 or a close relative thereof, P. libanesis NRRL B-67769 or a close relative thereof, a cell-free filtrate derived from a culture comprising P. libanesis NRRL B-67769 or a close relative thereof, and/or a cellular extract derived from P. libanesis NRRL B-67769 or a close relative thereof to a plant propagation material, optionally a seed.

13. A method comprising applying E. billingiae NRRL B-67766 or a close relative thereof, a cell- free filtrate derived from a culture comprising E. billingiae NRRL B-67766 or a close relative thereof, a cellular extract derived from E. billingiae NRRL B-67766 or a close relative thereof, P. gessardii NRRL B-67767 or a close relative thereof, a cell-free filtrate derived from a culture comprising P. gessardii NRRL B-67767 or a close relative thereof, a cellular extract derived from P. gessardii NRRL B-67767 or a close relative thereof, P. libanesis NRRL B-67769 or a close relative thereof, a cell-free filtrate derived from a culture comprising P. libanesis NRRL B-67769 or a close relative thereof, and/or a cellular extract derived from P. libanesis NRRL B-67769 or a close relative thereof to a plant.

14. A method comprising:

applying the non-naturally occurring composition of claim 5 to a plant or plant part; and/or introducing the non-naturally occurring composition of claim 5 into a plant growth medium. 15. A method comprising introducing the non-naturally occurring seed composition of claim 6 into a plant growth medium.

Description:
ERWINIA ISOLATES AND USES THEREOF REFERENCE TO A SEQUENCE LISTING

This application contains a Sequence Listing in computer readable form, which is incorporated herein by reference. REFERENCE TO DEPOSIT OF BIOLOGICAL MATERIALS

The present disclosure contains references to biological materials deposited under the terms of the Budapest Treaty on the International Recognition of the Deposit of Microorganisms for the Purposes of Patent Procedure at the Agricultural Research Service Culture Collection, 1815 North University Street, Peoria, Illinois 61604, U.S.A. BACKGROUND

Inoculant compositions comprising agriculturally beneficial microorganisms are well known in the art. See, e.g., U.S Patent Nos.5,484,464; 5,586,411; 5,695,541; 5,804,208; 5,916,029; 6,569,425; 6,808,917; 6,824,772; 7,429,477; 8,148,138; 8,278,247; 8,445,256; 8,883,679; 8,921,089; 8,999,698; 9,017,442; 9,101,088; 9,234,251; 9,340,464.

Nevertheless, because of burgeoning populations and increasing demands for more efficient and productive farms, there remains a need for new compositions and methods for preventing and treating pest infections/infestations and enhancing crop yield. SUMMARY OF THE CLAIMED INVENTION

The present disclosure provides isolated microbial strains useful for treating plants and plant parts, as well as compositions comprising the isolated strains and methods of using the isolated strains.

A first aspect of the present disclosure is an isolated Erwinia strain deposited as accession number NRRL B-67766 (E. billingiae NRRL B-67766).

A second aspect of the present disclosure is a biologically pure culture of E. billingiae NRRL B- 67766.

A third aspect of the present disclosure is a cell-free filtrate derived from a E. billingiae NRRL B- 67766 culture.

A fourth aspect of the present disclosure is a cellular extract derived from E. billingiae NRRL B- 67766.

A fifth aspect of the present disclosure is a non-naturally occurring composition comprising E. billingiae NRRL B-67766 or a close relative thereof, a cell-free filtrate derived from a culture comprising E. billingiae NRRL B-67766 or a close relative thereof, and/or a cellular extract derived from E. billingiae NRRL B-67766 or a close relative thereof.

A sixth aspect of the present disclosure is a non-naturally occurring seed composition comprising a plant propagation material, optionally a seed, and a coating that covers at least a portion of an outer surface of said seed, said coating comprising E. billingiae NRRL B-67766, a biologically pure culture of E. billingiae NRRL B-67766, a cell-free filtrate derived from a E. billingiae NRRL B-67766 culture and/or a cellular extract derived from E. billingiae NRRL B-67766.

A seventh aspect of the present disclosure is use of E. billingiae NRRL B-67766 or a close relative thereof, a cell-free filtrate derived from a culture comprising E. billingiae NRRL B-67766 or a close relative thereof, and/or a cellular extract derived from E. billingiae NRRL B-67766 or a close relative thereof for treating a plant or plant part.

An eighth aspect of the present disclosure is Use of E. billingiae NRRL B-67766 or a close relative thereof, a cell-free filtrate derived from a culture comprising E. billingiae NRRL B-67766 or a close relative thereof, and/or a cellular extract derived from E. billingiae NRRL B-67766 or a close relative thereof for killing, inhibiting the growth of and/or inhibiting the reproduction/proliferation of a fungal plant pest.

A ninth aspect of the present disclosure is use of E. billingiae NRRL B-67766 or a close relative thereof, a cell-free filtrate derived from a culture comprising E. billingiae NRRL B-67766 or a close relative thereof, and/or a cellular extract derived from E. billingiae NRRL B-67766 or a close relative thereof for reducing disease severity in a plant or plant part.

A tenth aspect of the present disclosure is use of E. billingiae NRRL B-67766 or a close relative thereof, a cell-free filtrate derived from a culture comprising E. billingiae NRRL B-67766 or a close relative thereof, and/or a cellular extract derived from E. billingiae NRRL B-67766 or a close relative thereof for enhancing growth and/or yield in a plant or plant part.

An eleventh aspect of the present disclosure is a method comprising introducing E. billingiae NRRL B-67766 or a close relative thereof, a cell-free filtrate derived from a culture comprising E.

billingiae NRRL B-67766 or a close relative thereof, and/or a cellular extract derived from E. billingiae NRRL B-67766 or a close relative thereof into a plant growth medium.

A twelfth aspect of the present disclosure is a method comprising applying E. billingiae NRRL B- 67766 or a close relative thereof, a cell-free filtrate derived from a culture comprising E. billingiae NRRL B-67766 or a close relative thereof, and/or a cellular extract derived from E. billingiae NRRL B-67766 or a close relative thereof to a plant propagation material, optionally a seed.

A thirteenth aspect of the present disclosure is a method comprising applying E. billingiae NRRL B-67766 or a close relative thereof, a cell-free filtrate derived from a culture comprising E. billingiae NRRL B-67766 or a close relative thereof, and/or a cellular extract derived from E. billingiae NRRL B- 67766 or a close relative thereof to a plant.

A fourteenth aspect of the present disclosure is a method comprising introducing a non-naturally occurring composition comprising E. billingiae NRRL B-67766 or a close relative thereof, a cell-free filtrate derived from a culture comprising E. billingiae NRRL B-67766 or a close relative thereof, and/or a cellular extract derived from E. billingiae NRRL B-67766 or a close relative thereof into a plant growth medium.

A fifteenth aspect of the present disclosure is a method comprising introducing a non-naturally occurring seed composition comprising a plant propagation material, optionally a seed, and a coating that covers at least a portion of an outer surface of said seed, said coating comprising E. billingiae NRRL B- 67766, a biologically pure culture of E. billingiae NRRL B-67766, a cell-free filtrate derived from a E. billingiae NRRL B-67766 culture and/or a cellular extract derived from E. billingiae NRRL B-67766 into a plant growth medium DETAILED DESCRIPTION

This description is not intended to be a detailed catalog of all the different ways in which the invention may be implemented or of all the features that may be added to the instant invention. For example, features illustrated with respect to one embodiment may be incorporated into other embodiments and features illustrated with respect to a particular embodiment may be deleted from that embodiment. In addition, numerous variations and additions to the various embodiments suggested herein, which do not depart from the instant invention, will be apparent to those skilled in the art in light of the instant disclosure. Hence, the following description is intended to illustrate some particular embodiments of the invention and not to exhaustively specify all permutations, combinations and variations thereof.

The terminology used herein is for the purpose of describing particular embodiments only and is not intended to be limiting of the invention.

Unless otherwise defined, all terms (including technical and scientific terms) used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs. It will be further understood that terms, such as those defined in commonly used dictionaries, should be interpreted as having a meaning that is consistent with their meaning in the context of the specification and relevant art and should not be interpreted in an idealized or overly formal sense unless expressly so defined herein. For the sake of brevity and/or clarity, well-known functions or constructions may not be described in detail.

As used herein, the singular forms "a," "an," and "the" are intended to include the plural forms as well, unless the context clearly indicates otherwise.

As used herein, the terms "acaricide" and "acaricidal" refer to an agent or combination of agents the application of which is toxic to an acarid (i.e., kills an acarid, inhibits the growth of an acarid and/or inhibits the reproduction/proliferation of an acarid).

As used herein, the term "agriculturally beneficial agent" refers to any agent (e.g., chemical or biological agent) or combination of agents the application of which causes or provides a beneficial and/or useful effect in agriculture including, but not limited to, agriculturally beneficial microorganisms, biostimulants, nutrients, pesticides (e.g., acaricides, fungicides, herbicides, insecticides, and nematicides) and plant signal molecules.

As used herein, the term "agriculturally beneficial microorganism" refers to a microorganism having at least one agriculturally beneficial property (e.g., the ability to fix nitrogen, the ability to solubilize phosphate, and/or the ability to produce an agriculturally beneficial agent, such as a plant signal molecule or pesticidal agent).

As used herein, the term "agriculturally acceptable carrier" refers to a substance or composition that can be used to deliver an agriculturally beneficial agent to a plant, plant part or plant growth medium (e.g., soil) without causing/having an unduly adverse effect on plant growth and/or yield. As used herein, the term "foliar-compatible carrier" refers to a material that can be foliarly applied to a plant or plant part without causing/having an unduly adverse effect on the plant, plant part, plant growth, plant health, or the like. As used herein, the term "seed-compatible carrier" refers to a material that can be applied to a seed without causing/having an unduly adverse effect on the seed, the plant that grows from the seed, seed germination, or the like. As used herein, the term "soil-compatible carrier" refers to a material that can be added to a soil without causing/having an unduly adverse effect on plant growth, soil structure, soil drainage, or the like.

As used herein, the term "and/or" is intended to include any and all combinations of one or more of the associated listed items, as well as the lack of combinations when interpreted in the alternative ("or"). Thus, the phrase "A, B and/or C" is to be interpreted as "A, A and B, A and B and C, A and C, B, B and C, or C."

As used herein, the terms "associated with," in association with" and "associated therewith," when used in reference to a relationship between a microbial strain or inoculant composition of the present disclosure and a plant or plant part, refer to at least a juxtaposition or close proximity of the microbial strain or inoculant composition and the plant or plant part. Such a juxtaposition or close proximity may be achieved by contacting or applying the microbial strain or inoculant composition directly to the plant or plant part and/or by applying the microbial strain or inoculant composition to the plant growth medium (e.g., soil) in which the plant or plant part will be grown (or is currently being grown). According to some embodiments, the microbial strain or inoculant composition is applied as a coating to the outer surface of the plant or plant part. According to some embodiments, the microbial strain or inoculant composition is applied to soil at, near or surrounding the site in which the plant or plant part will be grown (or is currently being grown).

As used herein, the term "aqueous" refers to a composition that contains more than a trace amount of water (i.e., more than 0.5% water by weight, based upon the total weight of the composition).

As used herein, the term "biologically pure culture" refers to a microbial culture that is free or essentially free of biological contamination and that has genetic uniformity such that different subculutres taken therefrom will exhibit identicial or substantially identical genotyopes and phenotypes. In some embodiments, the biologically pure culture is 100% pure (i.e., all subcultures taken therefrom exhibit identical genotypes and phenotypes). In some embodiments, the biologically pure culture is at least 90, 91, 92, 93, 94, 95, 96, 97, 98, 99, 99.5, 99.6, 99.7, 99.8, or 99.9% pure (i.e., at least 90, 91, 92, 93, 94, 95, 96, 97, 98, 99, 99.5, 99.6, 99.7, 99.8, or 99.9% of the subcultures taken therefrom exhibit identical genotypes and phenotypes).

As used herein, the term "biostimulant" refers to an agent or combination of agents the application of which enhances one or more metabolic and/or physiological processes of a plant or plant part (e.g., carbohydrate biosynthesis, ion uptake, nucleic acid uptake, nutrient delivery, photosynthesis and/or respiration).

As used herein, the term "BRADY" is to be interpreted as a shorthand substitute for the phrase "Bradyrhizobium spp.8A57, Bradyrhizobium elkanii SEMIA 501, Bradyrhizobium elkanii SEMIA 587, Bradyrhizobium elkanii SEMIA 5019, Bradyrhizobium japonicum 61A227, Bradyrhizobium japonicum 61A228, Bradyrhizobium japonicum 61A273, Bradyrhizobium japonicum E-109, Bradyrhizobium japonicum NRRL B-50586 (also deposited as NRRL B-59565), Bradyrhizobium japonicum NRRL B- 50587 (also deposited as NRRL B-59566), Bradyrhizobium japonicum NRRL B-50588 (also deposited as NRRL B-59567), Bradyrhizobium japonicum NRRL B-50589 (also deposited as NRRL B-59568), Bradyrhizobium japonicum NRRL B-50590 (also deposited as NRRL B-59569), Bradyrhizobium japonicum NRRL B-50591 (also deposited as NRRL B-59570), Bradyrhizobium japonicum NRRL B- 50592 (also deposited as NRRL B-59571), Bradyrhizobium japonicum NRRL B-50593 (also deposited as NRRL B-59572), Bradyrhizobium japonicum NRRL B-50594 (also deposited as NRRL B-50493), Bradyrhizobium japonicum NRRL B-50608, Bradyrhizobium japonicum NRRL B-50609,

Bradyrhizobium japonicum NRRL B-50610, Bradyrhizobium japonicum NRRL B-50611,

Bradyrhizobium japonicum NRRL B-50612, Bradyrhizobium japonicum NRRL B-50726,

Bradyrhizobium japonicum NRRL B-50727, Bradyrhizobium japonicum NRRL B-50728,

Bradyrhizobium japonicum NRRL B-50729, Bradyrhizobium japonicum NRRL B-50730,

Bradyrhizobium japonicum SEMIA 566, Bradyrhizobium japonicum SEMIA 5079, Bradyrhizobium japonicum SEMIA 5080, Bradyrhizobium japonicum USDA 6, Bradyrhizobium japonicum USDA 110, Bradyrhizobium japonicum USDA 122, Bradyrhizobium japonicum USDA 123, Bradyrhizobium japonicum USDA 127, Bradyrhizobium japonicum USDA 129 and/or Bradyrhizobium japonicum USDA 532C."

As used herein, the term "cell-free filtrate" refers to a filtrate of a bacterial culture that is devoid or substantially devoid of living bacterial cells.

As used herein, the term "celluar extract" refers to a substance or combination of substances isolated from a bacterial cell.

As used herein, the terms "colony forming unit" and "cfu" refer to a microbial cell/spore capable of propagating on or in a suitable growth medium or substrate (e.g., a soil) when conditions (e.g., temperature, moisture, nutrient availability, pH, etc.) are favorable for germination and/or microbial growth.

As used herein, the term "consists essentially of,", when used in reference to inoculant compositions and methods of the present disclosure, means that the compositions/methods may contain additional components/steps so long as the additional components/steps do not materially alter the composition/method. The term "materially alter," as applied to a composition/method of the present disclosure, refers to an increase or decrease in the effectiveness of the composition/method of at least 20%. For example, a component added to an inoculant composition of the present disclosure may be deemed to "materially alter" the composition if it increases or decreases the composition's ability to reduce one or more aspects of disease severity by at least 20%.

As used herein, the term "diazotroph" refers to an organism capable of converting atmospheric nitrogen (N 2 ) into a form that may be utilized by a plant or plant part (e.g., ammonia (NH 3 ), ammonium (NH 4 +), etc.).

As used herein, the term "dispersant" refers to an agent or combination of agents the application of which reduces the cohesiveness of like particles, the surface tension of a liquid, the interfacial tension between two liquids and/or the interfacial tension between or a liquid and a solid. As used herein, the terms "effective amount," "effective concentration" and "effective amount/concentration" refer to an amount or concentration sufficient to cause a desired effect (e.g. ¸ reduced disease severity and/or enhanced crop yield). The absolute value of the amount/concentration that is sufficient to cause the desired effect may be affected by factors such as the type and magnitude of effect desired, the type, size and volume of material to which the inoculant compositon will be applied, the type(s) of microorganisms in the composition, the number of microorganisms in the composition, the stability of the microorganism(s) in the inoculant composition and the storage conditions (e.g., temperature, relative humidity, duration). Those skilled in the art will understand how to select an effective amount/concentration using routine dose-response experiments.

As used herein, the term "endogenous gene" refers to a gene consisting of an endogenous polynucleotide.

As used herein, the term "endogenous polynucleotide" refers to a polynucleotide that is native to the referenced host cell.

As used herein, the term "enhanced dispersion" refers to an improvement in one or more characteristics of microbial dispersion as compared to one or more controls (e.g., a control composition that is identical to an inoculant composition of the present disclosure except that it lacks one or more of the components found in the inoculant composition of the present disclosure). Exemplary microbial dispersion characteristics include, but are not limited to, the percentage of microbes that exist as single cells/spores when the inoculant composition is diluted in water. An inoculant composition that improves one or more microbial dispersion characteristics of the microorganism(s) contained therein as compared to a control composition (e.g., a control composition that is identical to the inoculant composition except that it lacks one or more of the components found in the inoculant composition) provides enhanced dispersion and can be referred to as a "readily dispersable inoculant composition."

As used herein, the terms "enhanced growth" and "enhanced plant growth" refer to an

improvement in one or more characteristics of plant growth and/or development as compared to one or more control plants (e.g., a plant germinated from an untreated seed or an untreated plant). Exemplary plant growth/development characteristics include, but are not limited to, biomass, carbohydrate biosynthesis, chlorophyll content, cold tolerance, drought tolerance, height, leaf canopy, leaf length, leaf mass, leaf number, leaf surface area, leaf volume, lodging resistance, nutrient uptake and/or accumulation (e.g., ammonium, boron, calcium, copper, iron, magnesium, manganese, nitrate, nitrogen, phosphate, phosphorous, potassium, sodium, sulfur and/or zinc uptake/accumulation), rate(s) of photosynthesis, root area, root diameter, root length, root mass, root nodulation (e.g., nodule mass, nodule number, nodule volume), root number, root surface area, root volume, salt tolerance, seed germination, seedling emergence, shoot diameter, shoot length, shoot mass, shoot number, shoot surface area, shoot volume, spread, stand, stomatal conductance and survival rate. Unless otherwise indicated, references to enhanced plant growth are to be interpreted as meaning that microbial strains, inoculant compositions and methods of the present disclosure enhance plant growth by enhancing nutrient availability, improving soil characteristics, etc. and are not to be interpreted as suggesting that microbial strains, inoculant compositions and methods of the present disclosure act as plant growth regulators. As used herein, the terms "enhanced stability" and "enhanced microbial stability" refer to an improvement in one or more characteristics of microbial stability as compared to one or more controls (e.g., a control composition that is identical to an inoculant composition of the present disclosure except that it lacks one or more of the components found in the inoculant composition of the present disclosure). Exemplary microbial stability characteristics include, but are not limited to, the ability to germinate and/or propagate after being coated on a seed and/or stored for a defined period of time and the ability to cause a desired effect (e.g., enhanced plant yield and/or increased pesticidal activity) after being coated on a seed and/or stored for a defined period of time. A microorganism that exhibits improvement in one or more microbial stability characteristics as compared to a control microorganism when each is subjected to the same conditions (e.g., seed coating and storage conditions) displays enhanced stability and can be referred to as a "stable microorganism." An inoculant composition that improves one or more microbial stability characteristics of the microorganism(s) contained therein as compared to a control composition (e.g., a control composition that is identical to the inoculant composition except that it lacks one or more of the components found in the inoculant composition) provides enhanced stability and can be referred to as a "stable inoculant composition."

As used herein, the terms "enhanced survival" and "enhanced microbial survival" refer to an improvement in the survival rate of one or more microorganisms in an inoculant composition as compared to one or more microorganisms in a control composition (e.g., a control composition that is identical to an inoculant composition of the present disclosure except that it lacks one or more of the components found in the inoculant composition of the present disclosure). An inoculant composition that improves the survival rate of one or more of the microorganisms contained therein as compared to a control composition (e.g., a control composition that is identical to the inoculant composition except that it lacks one or more of the components found in the inoculant composition) provides enhanced survival and can be referred to as a stable inoculant composition.

As used herein, the terms "enhanced yield" and "enhanced plant yield" refer to an improvement in one or more characteristics of plant yield as compared to one or more control plants (e.g., a control plant germinated from an untreated seed). Exemplary plant yield characteristics include, but are not limited to, biomass; bushels per acre; grain weight per plot (GWTPP); nutritional content; percentage of plants in a given area (e.g., plot) that fail to produce grain; yield at standard moisture percentage (YSMP), such as grain yield at standard moisture percentage (GYSMP); yield per plot (YPP), such as grain weight per plot (GWTPP); and yield reduction (YRED). Unless otherwise indicated, references to enhanced plant yield are to be interpreted as meaning that microbial strains, inoculant compositions and methods of the present disclosure enhance plant yield by enhancing nutrient availability, improving soil characteristics, etc. and are not to be interpreted as suggesting that microbial strains, inoculant compositions and methods of the present disclosure act as plant growth regulators.

As used herein, the term "expression" includes any step involved in the production of the polypeptide including, but not limited to, transcription, post-transcriptional modification, translation, post- translational modification, and secretion. Expression can be measured—for example, to detect increased expression—by techniques known in the art, such as measuring levels of mRNA and/or translated polypeptide.

As used herein, the term "foliage" refers to those portions of a plant that normally grow above the ground, including, but not limited to, leaves, stalks, stems, flowers, fruiting bodies and fruits.

As used herein, the terms "foliar application" and "foliarly applied" refer to the application of one or more active ingredients to the foliage of a plant (e.g., to the leaves of the plant). Application may be effected by any suitable means, including, but not limited to, spraying the plant with a composition comprising the active ingredient(s). In some embodiments, the active ingredient(s) is/are applied to the leaves, stems and/or stalk of the plant and not to the flowers, fruiting bodies or fruits of the plant.

As used herein, the terms "fungicide" and "fungicidal" refer to an agent or combination of agents the application of which is toxic to a fungus (i.e., kills a fungus, inhibits the growth of a fungus and/or inhibits the reproduction/proliferation of a fungus).

As used herein, the term "fulvic acid" encompasses pure fulvic acids and fulvic acid salts (fulvates). Non-limiting examples of fulvic acids include ammonium fulvate, boron fulvate, potassium fulvate, sodium fulvate, etc. In some embodiments, the fulvic acid comprises, consists essentially of or consists MDL Number MFCD09838488 (CAS Number 479-66-3).

As used herein, the terms "herbicide" and "herbicidal" refer to an agent or combination of agents the application of which is toxic to a weed (i.e., kills a weed, inhibits the growth of a weed and/or inhibits the reproduction/proliferation of a weed).

As used herein, the term "heterologous gene" refers to a gene comprising a heterologous polypeptide.

As used herein, the term "heterologous polynucleotide" refers to a polynucleotide that is not native to the referenced host cell. For the purposes of the present disclosure, extraneous copies of polynucleotides that are otherwise native to the referenced host cell are deemed heterologous polynucleotides.

As used herein, the term "humic acid" encompasses pure humic acids and humic acid salts (humates). Non-limiting examples of humic acids include ammonium humate, boron humate, potassium humate, sodium humate, etc. In some embodiments, the humic acid comprises, consists essentially of or consists of one or more of MDL Number MFCD00147177 (CAS Number 1415-93-6), MDL Number MFCD00135560 (CAS Number 68131-04-4), MDL Number MFCS22495372 (CAS Number 68514-28- 3), CAS Number 93924-35-7 and CAS Number 308067-45-0.

As used herein, the terms "inoculant composition" and "inoculum" refer to a composition comprising microbial cells and/or spores, said cells/spores being capable of propagating/germinating on or in a suitable growth medium or substrate (e.g., a soil) when conditions (e.g., temperature, moisture, nutrient availability, pH, etc.) are favorable for germination and/or microbial growth.

As used herein, the terms "insecticide" and "insecticidal" refer to an agent or combination of agents the application of which is toxic to an insect (i.e., kills an insect, inhibits the growth of an insect and/or inhibits the reproduction/proliferation of an insect).

As used herein, the term "isolated microbial strain" refers to a microbe that has been removed from the environment in which it is normally found.

As used herein, the term "isomer" includes all stereoisomers of the compounds and/or molecules to which it refers, including enantiomers and diastereomers, as well as all conformers, roatmers and tautomers, unless otherwise indicated. Compounds and/or molecules disclosed herein include all enantiomers in either substantially pure levorotatory or dextrorotatory form, or in a racemic mixture, or in any ratio of enantiomers. Where embodiments disclose a (D)-enantiomer, that embodiment also includes the (L)-enantiomer; where embodiments disclose a (L)-enantiomer, that embodiment also includes the (D)-enantiomer. Where embodiments disclose a (+)-enantiomer, that embodiment also includes the (-)- enantiomer; where embodiments disclose a (-)-enantiomer, that embodiment also includes the (+)- enantiomer. Where embodiments disclose a (S)-enantiomer, that embodiment also includes the (R)- enantiomer; where embodiments disclose a (R)-enantiomer, that embodiment also includes the (S)- enantiomer. Embodiments are intended to include any diastereomers of the compounds and/or molecules referred to herein in diastereomerically pure form and in the form of mixtures in all ratios. Unless stereochemistry is explicitly indicated in a chemical structure or chemical name, the chemical structure or chemical name is intended to embrace all possible stereoisomers, conformers, rotamers and tautomers of compounds and/or molecules depicted.

As used herein, the term "modified microbial strain" refers to a microbial strain that is modified from a strain isolated from nature. Modified microbial strains may be produced by any suitable method(s), including, but not limited to, chemical or other form of induced mutation to a polynucleotide within any genome within the strain; the insertion or deletion of one or more nucleotides within any genome within the strain, or combinations thereof; an inversion of at least one segment of DNA within any genome within the strain; a rearrangement of any genome within the strain; generalized or specific transduction of homozygous or heterozygous polynucleotide segments into any genome within the strain; introduction of one or more phage into any genome of the strain; transformation of any strain resulting in the introduction into the strain of stably replicating autonomous extrachromosomal DNA; any change to any genome or to the total DNA composition within the strain isolated from nature as a result of conjugation with any different microbial strain; and any combination of the foregoing. The term modified microbial strains includes a strain with (a) one of more heterologous nucleotide sequences, (b) one or more non-naturally occurring copies of a nucleotide sequence isolated from nature (i.e., additional copies of a gene that naturally occurs in the microbial strain from which the modified microbial strain was derived), (c) a lack of one or more nucleotide sequences that would otherwise be present in the natural reference strain by for example deleting nucleotide sequence, and (d) added extrachromosomal DNA. In some embodiments, modified microbial strains comprise a combination of two or more nucleotide sequences (e.g., two or more naturally occurring genes that do not naturally occur in the same microbial strain) or comprise a nucleotide sequence isolated from nature at a locus that is different from the natural locus.

As used herein, the terms "nematicide" and "nematicidal" refer to an agent or combination of agents the application of which is toxic to a nematode (i.e., kills a nematode, inhibits the growth of a nematode and/or inhibits the reproduction/proliferation of a nematode).

As used herein, the term "nitrogen fixing organism" refers to an organism capable of converting atmospheric nitrogen (N 2 ) into a form that may be utilized by a plant or plant part (e.g., ammonia (NH 3 ), ammonium (NH +

4 ), etc.). As used herein, the term "non-aqueous" refers to a composition that comprises no more than a trace amount of water (i.e., no more than 0.5% water by weight, based upon the total weight of the composition).

As used herein, the term "nutrient" refers to a compound or element useful for nourishing a plant (e.g., vitamins, macrominerals, micronutrients, trace minerals, organic acids, etc. that are necessary for plant growth and/or development).

As used herein, the term "PENI" is to be interpreted as a shorthand substitute for the phrase "Penicillium bilaiae ATCC 18309, Penicillium bilaiae ATCC 20851, Penicillium bilaiae ATCC 22348, Penicillium bilaiae NRRL 50162, Penicillium bilaiae NRRL 50169, Penicillium bilaiae NRRL 50776, Penicillium bilaiae NRRL 50777, Penicillium bilaiae NRRL 50778, Penicillium bilaiae NRRL 50777, Penicillium bilaiae NRRL 50778, Penicillium bilaiae NRRL 50779, Penicillium bilaiae NRRL 50780, Penicillium bilaiae NRRL 50781, Penicillium bilaiae NRRL 50782, Penicillium bilaiae NRRL 50783, Penicillium bilaiae NRRL 50784, Penicillium bilaiae NRRL 50785, Penicillium bilaiae NRRL 50786, Penicillium bilaiae NRRL 50787, Penicillium bilaiae NRRL 50788, Penicillium bilaiae NRRL 67154, Penicillium bilaiae NRRL 67155, Penicillium bilaiae NRRL 67156, Penicillium bilaiae NRRL 67157, Penicillium bilaiae NRRL 67158, Penicillium bilaiae NRRL 67159, Penicillium bilaiae RS7B-SD1, Penicillium brevicompactum AgRF18, Penicillium canescens ATCC 10419, Penicillium expansum ATCC 24692, Penicillium expansum YT02, Penicillium fellatanum ATCC 48694, Penicillium gaestrivorus NRRL 50170 , Penicillium glabrum DAOM 239074, Penicillium glabrum CBS 229.28, Penicillium janthinellum ATCC 10455, Penicillium lanosocoeruleum ATCC 48919, Penicillium radicum ATCC 201836, Penicillium radicum FRR 4717, Penicillium radicum FRR 4719, Penicillium radicum N93/47267 and/or Penicillium raistrickii ATCC 10490."

As used herein, the term "Penicillium bilaiae" is intended to include all iterations of the species name, such as "Penicillium bilaji" and "Penicillium bilaii."

As used herein, the terms "percent identity," "% identity" and "percent identical" refer to the relatedness of two or more nucleotide or amino acid sequences, which may be calculated by (i) comparing two optimally aligned sequences over a window of comparison, (ii) determining the number of positions at which the identical nucleic acid base (for nucleotide sequences) or amino acid residue (for proteins) occurs in both sequences to yield the number of matched positions, (iii) dividing the number of matched positions by the total number of positions in the window of comparison, and then (iv) multiplying this quotient by 100% to yield the percent identity. If the "percent identity" is being calculated in relation to a reference sequence without a particular comparison window being specified, then the percent identity is determined by dividing the number of matched positions over the region of alignment by the total length of the reference sequence. Accordingly, for purposes of the present invention, when two sequences (query and subject) are optimally aligned (with allowance for gaps in their alignment), the "percent identity" for the query sequence is equal to the number of identical positions between the two sequences divided by the total number of positions in the query sequence over its length (or a comparison window), which is then multiplied by 100%.

As used herein, the term "pest" includes any organism or virus that negatively affects a plant, including, but not limited to, organisms and viruses that spread disease, damage host plants and/or compete for soil nutrients. The term "pest" encompasses organisms and viruses that are known to associate with plants and to cause a detrimental effect on the plant's health and/or vigor. Plant pests include, but are not limited to, arachnids (e.g., mites, ticks, spiders, etc.), bacteria, fungi, gastropods (e.g., slugs, snails, etc.), invasive plants (e.g., weeds), insects (e.g., white flies, thrips, weevils, etc.), nematodes (e.g., root-knot nematode, soybean cyst nematode, etc.), rodents and viruses (e.g., tobacco mosaic virus (TMV), tomato spotted wilt virus (TSWV), cauliflower mosaic virus (CaMV), etc.).

As used herein, the terms "pesticide" and "pesticidal" refer to agents or combinations of agents the application of which is toxic to a pest (i.e., kills a pest, inhibits the growth of a pest and/or inhibits the reproduction/proliferation of a pest). Non-limiting examples of pesticides include acaricides, fungicides, herbicides, insecticides, and nematicides, etc.

As used herein, the term "phosphate-solubilizing microorganism" refers to a microorganism capable of converting insoluble phosphate into a soluble form of phosphate.

As used herein, the term "plant" includes all plant populations, including, but not limited to, agricultural, horticultural and silvicultural plants. The term "plant" encompasses plants obtained by conventional plant breeding and optimization methods (e.g., marker-assisted selection) and plants obtained by genetic engineering, including cultivars protectable and not protectable by plant breeders' rights.

As used herein, the term "plant cell" refers to a cell of an intact plant, a cell taken from a plant, or a cell derived from a cell taken from a plant. Thus, the term "plant cell" includes cells within seeds, suspension cultures, embryos, meristematic regions, callus tissue, leaves, shoots, gametophytes, sporophytes, pollen and microspores.

As used herein, the term "plant growth regulator" refers to an agent or combination of agents the application of which accelerates or retards the growth/maturation rate of a plant through direct physiological action on the plant or which otherwise alters the behavior of a plant through direct physiological action on the plant. "Plant growth regulator" shall not be interpreted to include any agent or combination of agents excluded from the definition of "plant regulator" that is set forth section 2(v) of the Federal Insecticide, Fungicide, and Rodenticide Act (7 U.S.C. § 136(v)). Thus, "plant growth regulator" does not encompass microorganisms applied to a plant, plant part or plant growth medium for the purpose of enhancing the availability and/or uptake of nutrients, nutrients necessary to normal plant growth, soil amendments applied for the purpose of improving soil characteristics favorable for plant growth or vitamin hormone products as defined by 40 C.F.R. § 152.6(f).

As used herein, the term "plant part" refers to any part of a plant, including cells and tissues derived from plants. Thus, the term "plant part" may refer to any of plant components or organs (e.g., leaves, stems, roots, etc.), plant tissues, plant cells and seeds. Examples of plant parts, include, but are not limited to, anthers, embryos, flowers, fruits, fruiting bodies, leaves, ovules, pollen, rhizomes, roots, seeds, shoots, stems and tubers, as well as scions, rootstocks, protoplasts, calli and the like.

As used herein, the term "plant propagation material" refers to a plant part from which a whole plant can be generated. Examples of plant propagation materials include, but are not limited to, cuttings (e.g., leaves, stems), rhizomes, seeds, tubers and cells/tissues that can be cultured into a whole plant. As used herein, the term "progeny" encompasses both immediate offspring and any decendants thereof. Progeny may be produced using any suitable method(s), including, but not limited to, protoplast fusion, traditional breeding programs and combinations thereof.

As used herein, the terms "reduced disease severity" refers to a reduction in one or more characteristics of disease severity as compared to one or more control plants (e.g., a control plant germinated from an untreated seed, an untreated control plant, etc.). Exemplary disease severity characteristics include, but are not limited to, disease incidence (i.e., percentage of infected/infested plants within a given area/location), diseased area (e.g., surface area exhibiting lesions), pathogen load (i.e., amount/concentration of pest(s) per plant, acre, etc.), rate of infection/infestation, symptom severity (e.g., yellowing, necrosis, etc.) and toxin load (e.g., amount/concentration of pest toxin(s) per plant, acre, etc.). Unless otherwise indicated, references to reduced disease severity are to be interpreted as meaning that microbial strains, cultures, cell-free filtrates, cellular extracts, inoculant compositions and methods of the present disclosure reduce disease severity by killing pests, inhibiting the growth of pests, inhibiting the reproduction/proliferation of pests, etc. and are not to be interpreted as suggesting that microbial strains, cultures, cell-free filtrates, cellular extracts, inoculant compositions and methods of the present disclosure act as plant growth regulators.

As used herein, the terms "spore" and "microbial spore" refer to a microorganism in its dormant, protected state.

As used herein, the term "stabilizing compound" refers to an agent or combination of agents the application of which enhances the survival and/or stability of a microorganism in an inoculant composition.

As used herein with respect to inoculant compositions, the term "stable" refers to an inoculant composition in which microorganisms exhibit enhanced stability and/or enhanced survival. In general, an inoculant composition may be labeled "stable" if it improves the survival rate and/or at least one microbial stability characteristic of at least one microorganism contained therein.

As used herein with respect to microbial strains, the term "survival rate" refers to the percentage of microbial cell/spore that are viable (i.e., capable of propagating on or in a suitable growth medium or substrate (e.g., a soil) when conditions (e.g., temperature, moisture, nutrient availability, pH, etc.) are favorable for germination and/or microbial growth) at a given period of time.

As used herein, the term "toxin" refers to an extractable, pesticidal component of a

microorganism.

As used herein, the term "whole broth culture" refers to a population of microorganisms together with the liquid media in which the population was grown/propagated.

While certain aspects of the present disclosure will hereinafter be described with reference to embodiments thereof, it will be understood by those of ordinary skill in the art that various changes in form and details may be made therein without departing from the spirit and scope of the present disclosure as defined by the claims.

All publications, patent applications, patents and other references mentioned herein are incorporated by reference in their entirety, except insofar as they contradict any disclosure expressly set forth herein.

The present disclosure provides strains, cultures, cell-free filtrates, cellular extracts (e.g., toxins) and inoculant compositions useful for preventing and/or treating myriad plant infections/infestations.

In some embodiments, the strain is a pesticidal Erwinia strain, optionally a pesticidal Erwinia billingiae strain, such as the isolated Erwinia billingiae strain having the deposit accession number NRRL B-67766 (E. billingiae NRRL B-67766).

In some embodiments, the strain is a progeny of E. billingiae NRRL B-67766, a modified microlbial strain derived from E. billingiae NRRL B-67766, or a modified microbial strain derived from progeny of E. billingiae NRRL B-67766.

In some embodiments, the strain comprises a 16S sequence that is about/at least 95, 95.05, 95.1, 95.15, 95.2, 95.25, 95.3, 95.35, 95.4, 95.45, 95.5, 95.55, 95.6, 95.65, 95.7, 95.75, 95.8, 95.85, 95.9, 95.95, 96, 96.05, 96.1, 96.15, 96.2, 96.25, 96.3, 96.35, 96.4, 96.45, 96.5, 96.55, 96.6, 96.65, 96.7, 96.75, 96.8, 96.85, 96.9, 96.95, 97, 97.5, 97.55, 97.6, 97.65, 97.7, 97.75, 97.8, 97.85, 97.9, 97.95, 98, 98.05, 98.1, 98.15, 98.2, 98.25, 98.3, 98.35, 98.4, 98.45, 98.5, 98.55, 98.6, 98.65, 98.7, 98.75, 98.8, 98.85, 98.9, 98.95, 99, 99.05, 99.1, 99.15, 99.2, 99.25, 99.3, 99.35, 99.4, 99.45, 99.5, 99.55, 99.6, 99.65, 99.7, 99.75, 99.8, 99.85, 99.9, 99.91, 99.92, 99.93, 99.94, 99.95, 99.96, 99.97, 99.98, 99.99 or 100% identical to SEQ ID NO: 1.

In some embodiments, the strain comprises a whole genome sequence that is about/at least 95, 95.5, 95.55, 95.6, 95.65, 95.7, 95.75, 95.8, 95.85, 95.9, 95.95, 96, 96.05, 96.1, 96.15, 96.2, 96.25, 96.3, 96.35, 96.4, 96.45, 96.5, 96.55, 96.6, 96.65, 96.7, 96.75, 96.8, 96.85, 96.9, 96.95, 97, 97.5, 97.55, 97.6, 97.65, 97.7, 97.75, 97.8, 97.85, 97.9, 97.95, 98, 98.05, 98.1, 98.15, 98.2, 98.25, 98.3, 98.35, 98.4, 98.45, 98.5, 98.55, 98.6, 98.65, 98.7, 98.75, 98.8, 98.85, 98.9, 98.95, 99, 99.05, 99.1, 99.15, 99.2, 99.25, 99.3, 99.35, 99.4, 99.45, 99.5, 99.55, 99.6, 99.65, 99.7, 99.75, 99.8, 99.85, 99.9, 99.91, 99.92, 99.93, 99.94, 99.95, 99.96, 99.97, 99.98, 99.99 or 100% identical to that of E. billingiae NRRL B-67766.

The present disclosure encompasses close relatives of E. billingiae NRRL B-67766 that exhibit pesticidal activity, including, but not limited to, closely related progeny of E. billingiae NRRL B-67766 (e.g., progeny having a 16S sequence that is about/at least 95, 95.5, 95.55, 95.6, 95.65, 95.7, 95.75, 95.8, 95.85, 95.9, 95.95, 96, 96.05, 96.1, 96.15, 96.2, 96.25, 96.3, 96.35, 96.4, 96.45, 96.5, 96.55, 96.6, 96.65, 96.7, 96.75, 96.8, 96.85, 96.9, 96.95, 97, 97.5, 97.55, 97.6, 97.65, 97.7, 97.75, 97.8, 97.85, 97.9, 97.95, 98, 98.05, 98.1, 98.15, 98.2, 98.25, 98.3, 98.35, 98.4, 98.45, 98.5, 98.55, 98.6, 98.65, 98.7, 98.75, 98.8, 98.85, 98.9, 98.95, 99, 99.05, 99.1, 99.15, 99.2, 99.25, 99.3, 99.35, 99.4, 99.45, 99.5, 99.55, 99.6, 99.65, 99.7, 99.75, 99.8, 99.85, 99.9, 99.91, 99.92, 99.93, 99.94, 99.95, 99.96, 99.97, 99.98, 99.99 or 100% identical to SEQ ID NO: 1 and/or a whole genome sequence that is about/at least 95, 95.5, 95.55, 95.6, 95.65, 95.7, 95.75, 95.8, 95.85, 95.9, 95.95, 96, 96.05, 96.1, 96.15, 96.2, 96.25, 96.3, 96.35, 96.4, 96.45, 96.5, 96.55, 96.6, 96.65, 96.7, 96.75, 96.8, 96.85, 96.9, 96.95, 97, 97.5, 97.55, 97.6, 97.65, 97.7, 97.75, 97.8, 97.85, 97.9, 97.95, 98, 98.05, 98.1, 98.15, 98.2, 98.25, 98.3, 98.35, 98.4, 98.45, 98.5, 98.55, 98.6, 98.65, 98.7, 98.75, 98.8, 98.85, 98.9, 98.95, 99, 99.05, 99.1, 99.15, 99.2, 99.25, 99.3, 99.35, 99.4, 99.45, 99.5, 99.55, 99.6, 99.65, 99.7, 99.75, 99.8, 99.85, 99.9 or 99.95% identical to the whole genome sequence of E. billingiae NRRL B-67766), closely related modified microbial strains derived from E. billingiae NRRL B-67766 (e.g., modified microbial strains derived from E. billingiae NRRL B-67766 and having a 16S sequence that is about/at least 95, 95.5, 95.55, 95.6, 95.65, 95.7, 95.75, 95.8, 95.85, 95.9, 95.95, 96, 96.05, 96.1, 96.15, 96.2, 96.25, 96.3, 96.35, 96.4, 96.45, 96.5, 96.55, 96.6, 96.65, 96.7, 96.75, 96.8, 96.85, 96.9, 96.95, 97, 97.5, 97.55, 97.6, 97.65, 97.7, 97.75, 97.8, 97.85, 97.9, 97.95, 98, 98.05, 98.1, 98.15, 98.2, 98.25, 98.3, 98.35, 98.4, 98.45, 98.5, 98.55, 98.6, 98.65, 98.7, 98.75, 98.8, 98.85, 98.9, 98.95, 99, 99.05, 99.1, 99.15, 99.2, 99.25, 99.3, 99.35, 99.4, 99.45, 99.5, 99.55, 99.6, 99.65, 99.7, 99.75, 99.8, 99.85, 99.9, 99.91, 99.92, 99.93, 99.94, 99.95, 99.96, 99.97, 99.98, 99.99 or 100% identical to SEQ ID NO: 1 and/or a whole genome sequence that is about/at least 95, 95.5, 95.55, 95.6, 95.65, 95.7, 95.75, 95.8, 95.85, 95.9, 95.95, 96, 96.05, 96.1, 96.15, 96.2, 96.25, 96.3, 96.35, 96.4, 96.45, 96.5, 96.55, 96.6, 96.65, 96.7, 96.75, 96.8, 96.85, 96.9, 96.95, 97, 97.5, 97.55, 97.6, 97.65, 97.7, 97.75, 97.8, 97.85, 97.9, 97.95, 98, 98.05, 98.1, 98.15, 98.2, 98.25, 98.3, 98.35, 98.4, 98.45, 98.5, 98.55, 98.6, 98.65, 98.7, 98.75, 98.8, 98.85, 98.9, 98.95, 99, 99.05, 99.1, 99.15, 99.2, 99.25, 99.3, 99.35, 99.4, 99.45, 99.5, 99.55, 99.6, 99.65, 99.7, 99.75, 99.8, 99.85, 99.9 or 99.95% identical to the whole genome sequence of E. billingiae NRRL B-67766), closely related modified microbial strains derived from progeny of E. billingiae NRRL B-67766 (e.g., modified microbial strains derived from one or more progeny of E. billingiae NRRL B-67766 and having a 16S sequence that is about/at least 95, 95.5, 95.55, 95.6, 95.65, 95.7, 95.75, 95.8, 95.85, 95.9, 95.95, 96, 96.05, 96.1, 96.15, 96.2, 96.25, 96.3, 96.35, 96.4, 96.45, 96.5, 96.55, 96.6, 96.65, 96.7, 96.75, 96.8, 96.85, 96.9, 96.95, 97, 97.5, 97.55, 97.6, 97.65, 97.7, 97.75, 97.8, 97.85, 97.9, 97.95, 98, 98.05, 98.1, 98.15, 98.2, 98.25, 98.3, 98.35, 98.4, 98.45, 98.5, 98.55, 98.6, 98.65, 98.7, 98.75, 98.8, 98.85, 98.9, 98.95, 99, 99.05, 99.1, 99.15, 99.2, 99.25, 99.3, 99.35, 99.4, 99.45, 99.5, 99.55, 99.6, 99.65, 99.7, 99.75, 99.8, 99.85, 99.9, 99.91, 99.92, 99.93, 99.94, 99.95, 99.96, 99.97, 99.98, 99.99 or 100% identical to SEQ ID NO: 1 and/or a whole genome sequence that is about/at least 95, 95.5, 95.55, 95.6, 95.65, 95.7, 95.75, 95.8, 95.85, 95.9, 95.95, 96, 96.05, 96.1, 96.15, 96.2, 96.25, 96.3, 96.35, 96.4, 96.45, 96.5, 96.55, 96.6, 96.65, 96.7, 96.75, 96.8, 96.85, 96.9, 96.95, 97, 97.5, 97.55, 97.6, 97.65, 97.7, 97.75, 97.8, 97.85, 97.9, 97.95, 98, 98.05, 98.1, 98.15, 98.2, 98.25, 98.3, 98.35, 98.4, 98.45, 98.5, 98.55, 98.6, 98.65, 98.7, 98.75, 98.8, 98.85, 98.9, 98.95, 99, 99.05, 99.1, 99.15, 99.2, 99.25, 99.3, 99.35, 99.4, 99.45, 99.5, 99.55, 99.6, 99.65, 99.7, 99.75, 99.8, 99.85, 99.9 or 99.95% identical to the whole genome sequence of E. billingiae NRRL B-67766), and other closely related strains (e.g., pesticidal Erwinia strains having a 16S sequence that is about/at least 95, 95.5, 95.55, 95.6, 95.65, 95.7, 95.75, 95.8, 95.85, 95.9, 95.95, 96, 96.05, 96.1, 96.15, 96.2, 96.25, 96.3, 96.35, 96.4, 96.45, 96.5, 96.55, 96.6, 96.65, 96.7, 96.75, 96.8, 96.85, 96.9, 96.95, 97, 97.5, 97.55, 97.6, 97.65, 97.7, 97.75, 97.8, 97.85, 97.9, 97.95, 98, 98.05, 98.1, 98.15, 98.2, 98.25, 98.3, 98.35, 98.4, 98.45, 98.5, 98.55, 98.6, 98.65, 98.7, 98.75, 98.8, 98.85, 98.9, 98.95, 99, 99.05, 99.1, 99.15, 99.2, 99.25, 99.3, 99.35, 99.4, 99.45, 99.5, 99.55, 99.6, 99.65, 99.7, 99.75, 99.8, 99.85, 99.9, 99.91, 99.92, 99.93, 99.94, 99.95, 99.96, 99.97, 99.98, 99.99 or 100% identical to SEQ ID NO: 1 and/or a whole genome sequence that is about/at least 95, 95.5, 95.55, 95.6, 95.65, 95.7, 95.75, 95.8, 95.85, 95.9, 95.95, 96, 96.05, 96.1, 96.15, 96.2, 96.25, 96.3, 96.35, 96.4, 96.45, 96.5, 96.55, 96.6, 96.65, 96.7, 96.75, 96.8, 96.85, 96.9, 96.95, 97, 97.5, 97.55, 97.6, 97.65, 97.7, 97.75, 97.8, 97.85, 97.9, 97.95, 98, 98.05, 98.1, 98.15, 98.2, 98.25, 98.3, 98.35, 98.4, 98.45, 98.5, 98.55, 98.6, 98.65, 98.7, 98.75, 98.8, 98.85, 98.9, 98.95, 99, 99.05, 99.1, 99.15, 99.2, 99.25, 99.3, 99.35, 99.4, 99.45, 99.5, 99.55, 99.6, 99.65, 99.7, 99.75, 99.8, 99.85, 99.9 or 99.95% identical to the whole genome sequence of E. billingiae NRRL B-67766). In some embodiments, the strain is a pesticidal Pseudomonas strain, optionally a pesticidal Pseudomonas gessardii, such as the isolated Pseudomonas gessardii strain having the deposit accession number NRRL B-67767 (P. gessardii NRRL B-67767), or a pesticidal Pseudomonas libanesis, such as the isolated Pseudomonas libanesis strain having the deposit accession number NRRL B-67769 (P.

libanesis NRRL B-67769).

In some embodiments, the strain is a progeny of P. gessardii NRRL B-67767, a modified microlbial strain derived from P. gessardii NRRL B-67767, or a modified microbial strain derived from progeny of P. gessardii NRRL B-67767.

In some embodiments, the strain comprises a 16S sequence that is about/at least 95, 95.05, 95.1, 95.15, 95.2, 95.25, 95.3, 95.35, 95.4, 95.45, 95.5, 95.55, 95.6, 95.65, 95.7, 95.75, 95.8, 95.85, 95.9, 95.95, 96, 96.05, 96.1, 96.15, 96.2, 96.25, 96.3, 96.35, 96.4, 96.45, 96.5, 96.55, 96.6, 96.65, 96.7, 96.75, 96.8, 96.85, 96.9, 96.95, 97, 97.5, 97.55, 97.6, 97.65, 97.7, 97.75, 97.8, 97.85, 97.9, 97.95, 98, 98.05, 98.1, 98.15, 98.2, 98.25, 98.3, 98.35, 98.4, 98.45, 98.5, 98.55, 98.6, 98.65, 98.7, 98.75, 98.8, 98.85, 98.9, 98.95, 99, 99.05, 99.1, 99.15, 99.2, 99.25, 99.3, 99.35, 99.4, 99.45, 99.5, 99.55, 99.6, 99.65, 99.7, 99.75, 99.8, 99.85, 99.9, 99.91, 99.92, 99.93, 99.94, 99.95, 99.96, 99.97, 99.98, 99.99 or 100% identical to one or more of SEQ ID NO: 2.

In some embodiments, the strain comprises a whole genome sequence that is about/at least 95, 95.5, 95.55, 95.6, 95.65, 95.7, 95.75, 95.8, 95.85, 95.9, 95.95, 96, 96.05, 96.1, 96.15, 96.2, 96.25, 96.3, 96.35, 96.4, 96.45, 96.5, 96.55, 96.6, 96.65, 96.7, 96.75, 96.8, 96.85, 96.9, 96.95, 97, 97.5, 97.55, 97.6, 97.65, 97.7, 97.75, 97.8, 97.85, 97.9, 97.95, 98, 98.05, 98.1, 98.15, 98.2, 98.25, 98.3, 98.35, 98.4, 98.45, 98.5, 98.55, 98.6, 98.65, 98.7, 98.75, 98.8, 98.85, 98.9, 98.95, 99, 99.05, 99.1, 99.15, 99.2, 99.25, 99.3, 99.35, 99.4, 99.45, 99.5, 99.55, 99.6, 99.65, 99.7, 99.75, 99.8, 99.85, 99.9, 99.91, 99.92, 99.93, 99.94, 99.95, 99.96, 99.97, 99.98, 99.99 or 100% identical to that of P. gessardii NRRL B-67767.

The present disclosure encompasses close relatives of P. gessardii NRRL B-67767 that exhibit pesticidal activity, including, but not limited to, closely related progeny of P. gessardii NRRL B-67767 (e.g., progeny having a 16S sequence that is about/at least 95, 95.5, 95.55, 95.6, 95.65, 95.7, 95.75, 95.8, 95.85, 95.9, 95.95, 96, 96.05, 96.1, 96.15, 96.2, 96.25, 96.3, 96.35, 96.4, 96.45, 96.5, 96.55, 96.6, 96.65, 96.7, 96.75, 96.8, 96.85, 96.9, 96.95, 97, 97.5, 97.55, 97.6, 97.65, 97.7, 97.75, 97.8, 97.85, 97.9, 97.95, 98, 98.05, 98.1, 98.15, 98.2, 98.25, 98.3, 98.35, 98.4, 98.45, 98.5, 98.55, 98.6, 98.65, 98.7, 98.75, 98.8, 98.85, 98.9, 98.95, 99, 99.05, 99.1, 99.15, 99.2, 99.25, 99.3, 99.35, 99.4, 99.45, 99.5, 99.55, 99.6, 99.65, 99.7, 99.75, 99.8, 99.85, 99.9, 99.91, 99.92, 99.93, 99.94, 99.95, 99.96, 99.97, 99.98, 99.99 or 100% identical to SEQ ID NO: 2 and/or a whole genome sequence that is about/at least 95, 95.5, 95.55, 95.6, 95.65, 95.7, 95.75, 95.8, 95.85, 95.9, 95.95, 96, 96.05, 96.1, 96.15, 96.2, 96.25, 96.3, 96.35, 96.4, 96.45, 96.5, 96.55, 96.6, 96.65, 96.7, 96.75, 96.8, 96.85, 96.9, 96.95, 97, 97.5, 97.55, 97.6, 97.65, 97.7, 97.75, 97.8, 97.85, 97.9, 97.95, 98, 98.05, 98.1, 98.15, 98.2, 98.25, 98.3, 98.35, 98.4, 98.45, 98.5, 98.55, 98.6, 98.65, 98.7, 98.75, 98.8, 98.85, 98.9, 98.95, 99, 99.05, 99.1, 99.15, 99.2, 99.25, 99.3, 99.35, 99.4, 99.45, 99.5, 99.55, 99.6, 99.65, 99.7, 99.75, 99.8, 99.85, 99.9 or 99.95% identical to the whole genome sequence of P. gessardii NRRL B-67767), closely related modified microbial strains derived from P. gessardii NRRL B-67767 (e.g., modified microbial strains derived from P. gessardii NRRL B-67767 and having a 16S sequence that is about/at least 95, 95.5, 95.55, 95.6, 95.65, 95.7, 95.75, 95.8, 95.85, 95.9, 95.95, 96, 96.05, 96.1, 96.15, 96.2, 96.25, 96.3, 96.35, 96.4, 96.45, 96.5, 96.55, 96.6, 96.65, 96.7, 96.75, 96.8, 96.85, 96.9, 96.95, 97, 97.5, 97.55, 97.6, 97.65, 97.7, 97.75, 97.8, 97.85, 97.9, 97.95, 98, 98.05, 98.1, 98.15, 98.2, 98.25, 98.3, 98.35, 98.4, 98.45, 98.5, 98.55, 98.6, 98.65, 98.7, 98.75, 98.8, 98.85, 98.9, 98.95, 99, 99.05, 99.1, 99.15, 99.2, 99.25, 99.3, 99.35, 99.4, 99.45, 99.5, 99.55, 99.6, 99.65, 99.7, 99.75, 99.8, 99.85, 99.9, 99.91, 99.92, 99.93, 99.94, 99.95, 99.96, 99.97, 99.98, 99.99 or 100% identical to SEQ ID NO: 2 and/or a whole genome sequence that is about/at least 95, 95.5, 95.55, 95.6, 95.65, 95.7, 95.75, 95.8, 95.85, 95.9, 95.95, 96, 96.05, 96.1, 96.15, 96.2, 96.25, 96.3, 96.35, 96.4, 96.45, 96.5, 96.55, 96.6, 96.65, 96.7, 96.75, 96.8, 96.85, 96.9, 96.95, 97, 97.5, 97.55, 97.6, 97.65, 97.7, 97.75, 97.8, 97.85, 97.9, 97.95, 98, 98.05, 98.1, 98.15, 98.2, 98.25, 98.3, 98.35, 98.4, 98.45, 98.5, 98.55, 98.6, 98.65, 98.7, 98.75, 98.8, 98.85, 98.9, 98.95, 99, 99.05, 99.1, 99.15, 99.2, 99.25, 99.3, 99.35, 99.4, 99.45, 99.5, 99.55, 99.6, 99.65, 99.7, 99.75, 99.8, 99.85, 99.9 or 99.95% identical to the whole genome sequence of P. gessardii NRRL B-67767), closely related modified microbial strains derived from progeny of P. gessardii NRRL B-67767 (e.g., modified microbial strains derived from one or more progeny of P. gessardii NRRL B-67767 and having a 16S sequence that is about/at least 95, 95.5, 95.55, 95.6, 95.65, 95.7, 95.75, 95.8, 95.85, 95.9, 95.95, 96, 96.05, 96.1, 96.15, 96.2, 96.25, 96.3, 96.35, 96.4, 96.45, 96.5, 96.55, 96.6, 96.65, 96.7, 96.75, 96.8, 96.85, 96.9, 96.95, 97, 97.5, 97.55, 97.6, 97.65, 97.7, 97.75, 97.8, 97.85, 97.9, 97.95, 98, 98.05, 98.1, 98.15, 98.2, 98.25, 98.3, 98.35, 98.4, 98.45, 98.5, 98.55, 98.6, 98.65, 98.7, 98.75, 98.8, 98.85, 98.9, 98.95, 99, 99.05, 99.1, 99.15, 99.2, 99.25, 99.3, 99.35, 99.4, 99.45, 99.5, 99.55, 99.6, 99.65, 99.7, 99.75, 99.8, 99.85, 99.9, 99.91, 99.92, 99.93, 99.94, 99.95, 99.96, 99.97, 99.98, 99.99 or 100% identical to SEQ ID NO: 2 and/or a whole genome sequence that is about/at least 95, 95.5, 95.55, 95.6, 95.65, 95.7, 95.75, 95.8, 95.85, 95.9, 95.95, 96, 96.05, 96.1, 96.15, 96.2, 96.25, 96.3, 96.35, 96.4, 96.45, 96.5, 96.55, 96.6, 96.65, 96.7, 96.75, 96.8, 96.85, 96.9, 96.95, 97, 97.5, 97.55, 97.6, 97.65, 97.7, 97.75, 97.8, 97.85, 97.9, 97.95, 98, 98.05, 98.1, 98.15, 98.2, 98.25, 98.3, 98.35, 98.4, 98.45, 98.5, 98.55, 98.6, 98.65, 98.7, 98.75, 98.8, 98.85, 98.9, 98.95, 99, 99.05, 99.1, 99.15, 99.2, 99.25, 99.3, 99.35, 99.4, 99.45, 99.5, 99.55, 99.6, 99.65, 99.7, 99.75, 99.8, 99.85, 99.9 or 99.95% identical to the whole genome sequence of P. gessardii NRRL B-67767), and other closely related strains (e.g., pesticidal Pseudomonas strains having a 16S sequence that is about/at least 95, 95.5, 95.55, 95.6, 95.65, 95.7, 95.75, 95.8, 95.85, 95.9, 95.95, 96, 96.05, 96.1, 96.15, 96.2, 96.25, 96.3, 96.35, 96.4, 96.45, 96.5, 96.55, 96.6, 96.65, 96.7, 96.75, 96.8, 96.85, 96.9, 96.95, 97, 97.5, 97.55, 97.6, 97.65, 97.7, 97.75, 97.8, 97.85, 97.9, 97.95, 98, 98.05, 98.1, 98.15, 98.2, 98.25, 98.3, 98.35, 98.4, 98.45, 98.5, 98.55, 98.6, 98.65, 98.7, 98.75, 98.8, 98.85, 98.9, 98.95, 99, 99.05, 99.1, 99.15, 99.2, 99.25, 99.3, 99.35, 99.4, 99.45, 99.5, 99.55, 99.6, 99.65, 99.7, 99.75, 99.8, 99.85, 99.9, 99.91, 99.92, 99.93, 99.94, 99.95, 99.96, 99.97, 99.98, 99.99 or 100% identical to SEQ ID NO: 2 and/or a whole genome sequence that is about/at least 95, 95.5, 95.55, 95.6, 95.65, 95.7, 95.75, 95.8, 95.85, 95.9, 95.95, 96, 96.05, 96.1, 96.15, 96.2, 96.25, 96.3, 96.35, 96.4, 96.45, 96.5, 96.55, 96.6, 96.65, 96.7, 96.75, 96.8, 96.85, 96.9, 96.95, 97, 97.5, 97.55, 97.6, 97.65, 97.7, 97.75, 97.8, 97.85, 97.9, 97.95, 98, 98.05, 98.1, 98.15, 98.2, 98.25, 98.3, 98.35, 98.4, 98.45, 98.5, 98.55, 98.6, 98.65, 98.7, 98.75, 98.8, 98.85, 98.9, 98.95, 99, 99.05, 99.1, 99.15, 99.2, 99.25, 99.3, 99.35, 99.4, 99.45, 99.5, 99.55, 99.6, 99.65, 99.7, 99.75, 99.8, 99.85, 99.9 or 99.95% identical to the whole genome sequence of P. gessardii NRRL B-67767). In some embodiments, the strain is a progeny of P. libanesis NRRL B-67769, a modified microlbial strain derived from P. libanesis NRRL B-67769, or a modified microbial strain derived from progeny of P. libanesis NRRL B-67769.

In some embodiments, the strain comprises a 16S sequence that is about/at least 95, 95.05, 95.1, 95.15, 95.2, 95.25, 95.3, 95.35, 95.4, 95.45, 95.5, 95.55, 95.6, 95.65, 95.7, 95.75, 95.8, 95.85, 95.9, 95.95, 96, 96.05, 96.1, 96.15, 96.2, 96.25, 96.3, 96.35, 96.4, 96.45, 96.5, 96.55, 96.6, 96.65, 96.7, 96.75, 96.8, 96.85, 96.9, 96.95, 97, 97.5, 97.55, 97.6, 97.65, 97.7, 97.75, 97.8, 97.85, 97.9, 97.95, 98, 98.05, 98.1, 98.15, 98.2, 98.25, 98.3, 98.35, 98.4, 98.45, 98.5, 98.55, 98.6, 98.65, 98.7, 98.75, 98.8, 98.85, 98.9, 98.95, 99, 99.05, 99.1, 99.15, 99.2, 99.25, 99.3, 99.35, 99.4, 99.45, 99.5, 99.55, 99.6, 99.65, 99.7, 99.75, 99.8, 99.85, 99.9, 99.91, 99.92, 99.93, 99.94, 99.95, 99.96, 99.97, 99.98, 99.99 or 100% identical to one or more of SEQ ID NO: 3.

In some embodiments, the strain comprises a whole genome sequence that is about/at least 95, 95.5, 95.55, 95.6, 95.65, 95.7, 95.75, 95.8, 95.85, 95.9, 95.95, 96, 96.05, 96.1, 96.15, 96.2, 96.25, 96.3, 96.35, 96.4, 96.45, 96.5, 96.55, 96.6, 96.65, 96.7, 96.75, 96.8, 96.85, 96.9, 96.95, 97, 97.5, 97.55, 97.6, 97.65, 97.7, 97.75, 97.8, 97.85, 97.9, 97.95, 98, 98.05, 98.1, 98.15, 98.2, 98.25, 98.3, 98.35, 98.4, 98.45, 98.5, 98.55, 98.6, 98.65, 98.7, 98.75, 98.8, 98.85, 98.9, 98.95, 99, 99.05, 99.1, 99.15, 99.2, 99.25, 99.3, 99.35, 99.4, 99.45, 99.5, 99.55, 99.6, 99.65, 99.7, 99.75, 99.8, 99.85, 99.9, 99.91, 99.92, 99.93, 99.94, 99.95, 99.96, 99.97, 99.98, 99.99 or 100% identical to that of P. libanesis NRRL B-67769.

The present disclosure encompasses close relatives of P. libanesis NRRL B-67769 that exhibit pesticidal activity, including, but not limited to, closely related progeny of P. libanesis NRRL B-67769 (e.g., progeny having a 16S sequence that is about/at least 95, 95.5, 95.55, 95.6, 95.65, 95.7, 95.75, 95.8, 95.85, 95.9, 95.95, 96, 96.05, 96.1, 96.15, 96.2, 96.25, 96.3, 96.35, 96.4, 96.45, 96.5, 96.55, 96.6, 96.65, 96.7, 96.75, 96.8, 96.85, 96.9, 96.95, 97, 97.5, 97.55, 97.6, 97.65, 97.7, 97.75, 97.8, 97.85, 97.9, 97.95, 98, 98.05, 98.1, 98.15, 98.2, 98.25, 98.3, 98.35, 98.4, 98.45, 98.5, 98.55, 98.6, 98.65, 98.7, 98.75, 98.8, 98.85, 98.9, 98.95, 99, 99.05, 99.1, 99.15, 99.2, 99.25, 99.3, 99.35, 99.4, 99.45, 99.5, 99.55, 99.6, 99.65, 99.7, 99.75, 99.8, 99.85, 99.9, 99.91, 99.92, 99.93, 99.94, 99.95, 99.96, 99.97, 99.98, 99.99 or 100% identical to SEQ ID NO: 3 and/or a whole genome sequence that is about/at least 95, 95.5, 95.55, 95.6, 95.65, 95.7, 95.75, 95.8, 95.85, 95.9, 95.95, 96, 96.05, 96.1, 96.15, 96.2, 96.25, 96.3, 96.35, 96.4, 96.45, 96.5, 96.55, 96.6, 96.65, 96.7, 96.75, 96.8, 96.85, 96.9, 96.95, 97, 97.5, 97.55, 97.6, 97.65, 97.7, 97.75, 97.8, 97.85, 97.9, 97.95, 98, 98.05, 98.1, 98.15, 98.2, 98.25, 98.3, 98.35, 98.4, 98.45, 98.5, 98.55, 98.6, 98.65, 98.7, 98.75, 98.8, 98.85, 98.9, 98.95, 99, 99.05, 99.1, 99.15, 99.2, 99.25, 99.3, 99.35, 99.4, 99.45, 99.5, 99.55, 99.6, 99.65, 99.7, 99.75, 99.8, 99.85, 99.9 or 99.95% identical to the whole genome sequence of P. libanesis NRRL B-67769), closely related modified microbial strains derived from P. libanesis NRRL B-67769 (e.g., modified microbial strains derived from P. libanesis NRRL B-67769 and having a 16S sequence that is about/at least 95, 95.5, 95.55, 95.6, 95.65, 95.7, 95.75, 95.8, 95.85, 95.9, 95.95, 96, 96.05, 96.1, 96.15, 96.2, 96.25, 96.3, 96.35, 96.4, 96.45, 96.5, 96.55, 96.6, 96.65, 96.7, 96.75, 96.8, 96.85, 96.9, 96.95, 97, 97.5, 97.55, 97.6, 97.65, 97.7, 97.75, 97.8, 97.85, 97.9, 97.95, 98, 98.05, 98.1, 98.15, 98.2, 98.25, 98.3, 98.35, 98.4, 98.45, 98.5, 98.55, 98.6, 98.65, 98.7, 98.75, 98.8, 98.85, 98.9, 98.95, 99, 99.05, 99.1, 99.15, 99.2, 99.25, 99.3, 99.35, 99.4, 99.45, 99.5, 99.55, 99.6, 99.65, 99.7, 99.75, 99.8, 99.85, 99.9, 99.91, 99.92, 99.93, 99.94, 99.95, 99.96, 99.97, 99.98, 99.99 or 100% identical to SEQ ID NO: 3 and/or a whole genome sequence that is about/at least 95, 95.5, 95.55, 95.6, 95.65, 95.7, 95.75, 95.8, 95.85, 95.9, 95.95, 96, 96.05, 96.1, 96.15, 96.2, 96.25, 96.3, 96.35, 96.4, 96.45, 96.5, 96.55, 96.6, 96.65, 96.7, 96.75, 96.8, 96.85, 96.9, 96.95, 97, 97.5, 97.55, 97.6, 97.65, 97.7, 97.75, 97.8, 97.85, 97.9, 97.95, 98, 98.05, 98.1, 98.15, 98.2, 98.25, 98.3, 98.35, 98.4, 98.45, 98.5, 98.55, 98.6, 98.65, 98.7, 98.75, 98.8, 98.85, 98.9, 98.95, 99, 99.05, 99.1, 99.15, 99.2, 99.25, 99.3, 99.35, 99.4, 99.45, 99.5, 99.55, 99.6, 99.65, 99.7, 99.75, 99.8, 99.85, 99.9 or 99.95% identical to the whole genome sequence of P. libanesis NRRL B-67769), closely related modified microbial strains derived from progeny of P. libanesis NRRL B-67769 (e.g., modified microbial strains derived from one or more progeny of P. libanesis NRRL B-67769 and having a 16S sequence that is about/at least 95, 95.5, 95.55, 95.6, 95.65, 95.7, 95.75, 95.8, 95.85, 95.9, 95.95, 96, 96.05, 96.1, 96.15, 96.2, 96.25, 96.3, 96.35, 96.4, 96.45, 96.5, 96.55, 96.6, 96.65, 96.7, 96.75, 96.8, 96.85, 96.9, 96.95, 97, 97.5, 97.55, 97.6, 97.65, 97.7, 97.75, 97.8, 97.85, 97.9, 97.95, 98, 98.05, 98.1, 98.15, 98.2, 98.25, 98.3, 98.35, 98.4, 98.45, 98.5, 98.55, 98.6, 98.65, 98.7, 98.75, 98.8, 98.85, 98.9, 98.95, 99, 99.05, 99.1, 99.15, 99.2, 99.25, 99.3, 99.35, 99.4, 99.45, 99.5, 99.55, 99.6, 99.65, 99.7, 99.75, 99.8, 99.85, 99.9, 99.91, 99.92, 99.93, 99.94, 99.95, 99.96, 99.97, 99.98, 99.99 or 100% identical to SEQ ID NO: 3 and/or a whole genome sequence that is about/at least 95, 95.5, 95.55, 95.6, 95.65, 95.7, 95.75, 95.8, 95.85, 95.9, 95.95, 96, 96.05, 96.1, 96.15, 96.2, 96.25, 96.3, 96.35, 96.4, 96.45, 96.5, 96.55, 96.6, 96.65, 96.7, 96.75, 96.8, 96.85, 96.9, 96.95, 97, 97.5, 97.55, 97.6, 97.65, 97.7, 97.75, 97.8, 97.85, 97.9, 97.95, 98, 98.05, 98.1, 98.15, 98.2, 98.25, 98.3, 98.35, 98.4, 98.45, 98.5, 98.55, 98.6, 98.65, 98.7, 98.75, 98.8, 98.85, 98.9, 98.95, 99, 99.05, 99.1, 99.15, 99.2, 99.25, 99.3, 99.35, 99.4, 99.45, 99.5, 99.55, 99.6, 99.65, 99.7, 99.75, 99.8, 99.85, 99.9 or 99.95% identical to the whole genome sequence of P. libanesis NRRL B-67769), and other closely related strains (e.g., pesticidal Pseudomonas strains having a 16S sequence that is about/at least 95, 95.5, 95.55, 95.6, 95.65, 95.7, 95.75, 95.8, 95.85, 95.9, 95.95, 96, 96.05, 96.1, 96.15, 96.2, 96.25, 96.3, 96.35, 96.4, 96.45, 96.5, 96.55, 96.6, 96.65, 96.7, 96.75, 96.8, 96.85, 96.9, 96.95, 97, 97.5, 97.55, 97.6, 97.65, 97.7, 97.75, 97.8, 97.85, 97.9, 97.95, 98, 98.05, 98.1, 98.15, 98.2, 98.25, 98.3, 98.35, 98.4, 98.45, 98.5, 98.55, 98.6, 98.65, 98.7, 98.75, 98.8, 98.85, 98.9, 98.95, 99, 99.05, 99.1, 99.15, 99.2, 99.25, 99.3, 99.35, 99.4, 99.45, 99.5, 99.55, 99.6, 99.65, 99.7, 99.75, 99.8, 99.85, 99.9, 99.91, 99.92, 99.93, 99.94, 99.95, 99.96, 99.97, 99.98, 99.99 or 100% identical to SEQ ID NO: 3 and/or a whole genome sequence that is about/at least 95, 95.5, 95.55, 95.6, 95.65, 95.7, 95.75, 95.8, 95.85, 95.9, 95.95, 96, 96.05, 96.1, 96.15, 96.2, 96.25, 96.3, 96.35, 96.4, 96.45, 96.5, 96.55, 96.6, 96.65, 96.7, 96.75, 96.8, 96.85, 96.9, 96.95, 97, 97.5, 97.55, 97.6, 97.65, 97.7, 97.75, 97.8, 97.85, 97.9, 97.95, 98, 98.05, 98.1, 98.15, 98.2, 98.25, 98.3, 98.35, 98.4, 98.45, 98.5, 98.55, 98.6, 98.65, 98.7, 98.75, 98.8, 98.85, 98.9, 98.95, 99, 99.05, 99.1, 99.15, 99.2, 99.25, 99.3, 99.35, 99.4, 99.45, 99.5, 99.55, 99.6, 99.65, 99.7, 99.75, 99.8, 99.85, 99.9 or 99.95% identical to the whole genome sequence of P. libanesis NRRL B-67769).

Strains of the present disclosure may be cultured using any suitable method(s), including, but not limited to, liquid-state fermentation and solid-state fermentation. See, generally, Cunningham et al., CAN. J. BOT.68:2270 (1990); Friesen et al., APPL. MICROBIOL. BIOTECH.68:397 (2005).

Strains of the present disclosure may be harvested during any suitable growth phase. In some embodiments, strains of the present disclosure are allowed to reach the stationary growth phase and then harvested.

Strains of the present disclosure may be harvested and/or concentrated using any suitable method(s), including, but not limited to, centrifugation (e.g., density gradient centrifugation, disc stack centrifugation, tubular bowl centrifugation), coagulation, decanting, felt bed collection, filtration (e.g., drum filtration, sieving, ultrafiltration), flocculation, impaction and trapping (e.g., cyclone spore trapping, liquid impingement).

The present disclosure extends to cultures (e.g., whole broth cultures) comprising, consisting essentially of or consisting of one or more strains of the present disclosure. In some embodiments, at least 95, 95.5, 95.55, 95.6, 95.65, 95.7, 95.75, 95.8, 95.85, 95.9, 95.95, 96, 96.05, 96.1, 96.15, 96.2, 96.25, 96.3, 96.35, 96.4, 96.45, 96.5, 96.55, 96.6, 96.65, 96.7, 96.75, 96.8, 96.85, 96.9, 96.95, 97, 97.5, 97.55, 97.6, 97.65, 97.7, 97.75, 97.8, 97.85, 97.9, 97.95, 98, 98.05, 98.1, 98.15, 98.2, 98.25, 98.3, 98.35, 98.4, 98.45, 98.5, 98.55, 98.6, 98.65, 98.7, 98.75, 98.8, 98.85, 98.9, 98.95, 99, 99.05, 99.1, 99.15, 99.2, 99.25, 99.3, 99.35, 99.4, 99.45, 99.5, 99.55, 99.6, 99.65, 99.7, 99.75, 99.8, 99.85, 99.9, 99.91, 99.92, 99.93, 99.94, 99.95, 99.96, 99.97, 99.98, 99.99 or 100% of subcultures taken from the culture exhibit a genotype that is at least 95, 95.5, 95.55, 95.6, 95.65, 95.7, 95.75, 95.8, 95.85, 95.9, 95.95, 96, 96.05, 96.1, 96.15, 96.2, 96.25, 96.3, 96.35, 96.4, 96.45, 96.5, 96.55, 96.6, 96.65, 96.7, 96.75, 96.8, 96.85, 96.9, 96.95, 97, 97.5, 97.55, 97.6, 97.65, 97.7, 97.75, 97.8, 97.85, 97.9, 97.95, 98, 98.05, 98.1, 98.15, 98.2, 98.25, 98.3, 98.35, 98.4, 98.45, 98.5, 98.55, 98.6, 98.65, 98.7, 98.75, 98.8, 98.85, 98.9, 98.95, 99, 99.05, 99.1, 99.15, 99.2, 99.25, 99.3, 99.35, 99.4, 99.45, 99.5, 99.55, 99.6, 99.65, 99.7, 99.75, 99.8, 99.85, 99.9, 99.91, 99.92, 99.93, 99.94, 99.95, 99.96, 99.97, 99.98, 99.99 or 100% identical to that of E. billingiae NRRL B-67766, P. gessardii NRRL B-67767 or P. libanesis NRRL B-67769. In some embodiments, the culture is a biologically pure culture of E. billingiae NRRL B-67766, P. gessardii NRRL B-67767 or P. libanesis NRRL B-67769.

The present disclosure also extends to cell-free filtrates derived from cultures of the present disclosure and to cellular extracts derived from strains of the present disclosure. Cell-free filtrates and cellular extracts may be produced by any suitable means known it the art, including, but not limited to, enzyme-mediated lysis, osmotic lysis, milling and sonication. See, e.g., PROTEIN PURIFICATION

PROTOCOLS, Doonan (ed.), Humana Press (1996).

Strains, cultures, cell-free filtrates and cellular extracts of the present disclosure may be formulated into any suitable type of composition, including, but not limited to, foliar treatments, seed coatings and soil treatments.

In some embodiments, the present disclosure provides inoculant compositions comprising one or more strains of the present disclosure (e.g., one or more pesticidal Erwinia strains and/or one or more pesticidal Pseudomonas strains).

Strains of the present disclosure may be incorporated into inoculant compositions in any suitable amount/concentration. The absolute value of the amount/concentration that is/are sufficient to cause the desired effect(s) may be affected by factors such as the type, size and volume of material to which the compositon will be applied and storage conditions (e.g., temperature, relative humidity, duration). Those skilled in the art will understand how to select an effective amount/concentration using routine dose- response experiments.

In some embodiments, inoculant compositions of the present disclosure comprise one or more strains of the present disclosure in an amount ranging from about 1 x 10 1 to about 1 x 10 15 colony-forming units (cfu) per gram and/or milliliter of inoculant composition. For example, inoculant compositions of the present disclosure may comprise about 1 x 10 1 , 1 x 10 2 , 1 x 10 3 , 1 x 10 4 , 1 x 10 5 , 1 x 10 6 , 1 x 10 7 , 1 x 10 8 , 1 x 10 9 , 1 x 10 10 , 1 x 10 11 , 1 x 10 12 or more cfu of pesticidal Erwinia (e.g., E. billingiae NRRL B-67766) and/or pesticidal Pseudomonas (e.g., P. gessardii NRRL B-67767 and/or P. libanesis NRRL B-67769) per gram and/or milliliter of inoculant composition. In some embodiments, inoculant compositions of the present disclosure comprise at least 1 x 10 4 , 1 x 10 5 , 1 x 10 6 , 1 x 10 7 , 1 x 10 8 , 1 x 10 9 , 1 x 10 10 , 1 x 10 11 , 1 x 10 12 cfu of pesticidal Erwinia (e.g., E. billingiae NRRL B-67766) and/or pesticidal Pseudomonas (e.g., P. gessardii NRRL B-67767 and/or P. libanesis NRRL B-67769) per gram and/or milliliter of inoculant composition.

In some embodiments, strains of the present disclosure comprise about 0.1 to about 95% (by weight) of the inoculant composition. For example, inoculant compositions of the present disclosure may comprise about 0.1, 0.2, 0.3, 0.4, 0.5, 0.6, 0.7, 0.8, 0.9, 1, 1.25, 1.5, 1.75, 2, 2.25, 2.5, 2.75, 3, 3.25, 3.5, 3.75, 4, 4.25, 4.5, 4.75, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95% or more (by weight) pesticidal Erwinia (e.g., E. billingiae NRRL B-67766) and/or pesticidal Pseudomonas (e.g., P. gessardii NRRL B-67767 and/or P. libanesis NRRL B-67769). In some embodiments, pesticidal Erwinia (e.g., E. billingiae NRRL B-67766) and/or pesticidal Pseudomonas (e.g., P. gessardii NRRL B-67767 and/or P. libanesis NRRL B-67769) comprise(s) about 1 to about 25%, about 5 to about 20%, about 5 to about 15%, about 5 to about 10% or about 8 to about 12% (by weight) of the inoculant composition.

In some embodiments, inoculant compositions of the present disclosure comprise one or more strains of the present disclosure in an effective amount/concentration for preventing and/or treating one or more pest infections/infestations when the inoculant composition is introduced into a plant growth medium (e.g., a soil). For example, inoculant compositions of the present disclosure may comprise E. billingiae NRRL B-67766, P. gessardii NRRL B-67767 and/or P. libanesis NRRL B-67769 in an amount/concentration effective to kill one or more pests (e.g., one or more fungal pests), to inhibit the growth of one or more pests (e.g., one or more fungal pests), and/or to inhibit the

reproduction/proliferation of one or more pests (e.g., one or more fungal pests) when the compositon is introduced into a field.

In some embodiments, inoculant compositions of the present disclosure comprise one or more strains of the present disclosure in an effective amount/concentration for preventing and/or treating one or more pest infections/infestations when the inoculant composition is applied to a plant or plant part. For example, inoculant compositions of the present disclosure may comprise E. billingiae NRRL B-67766, P. gessardii NRRL B-67767 and/or P. libanesis NRRL B-67769 in an amount/concentration effective to kill one or more pests (e.g., one or more fungal pests), to inhibit the growth of one or more pests (e.g., one or more fungal pests), and/or to inhibit the reproduction/proliferation of one or more pests (e.g., one or more fungal pests) when the compositon is coated onto a seed or sprayed onto a plant. In some embodiments, inoculant compositions of the present disclosure comprise one or more strains of the present disclosure in an effective amount/concentration for enhancing plant growth/yield when the inoculant composition is introduced into a plant growth medium (e.g., a soil). For example, inoculant compositions of the present disclosure may comprise E. billingiae NRRL B-67766, P. gessardii NRRL B-67767 and/or P. libanesis NRRL B-67769 in an amount/concentration effective to improve the growth and/or yield of plants (e.g., wheat) grown in a field treated with the composition, as compared to plants grown in an untreated control field, for example.

In some embodiments, inoculant compositions of the present disclosure comprise one or more strains of the present disclosure in an effective amount/concentration for enhancing plant growth/yield when the inoculant composition is applied to a plant or plant part. For example, inoculant compositions of the present disclosure may comprise E. billingiae NRRL B-67766, P. gessardii NRRL B-67767 and/or P. libanesis NRRL B-67769 in an amount/concentration effective to improve the growth and/or yield of plants (e.g., wheat) grown from seeds that were treated with the composition and/or plants (e.g., wheat) that were directly treated with the composition.

In some embodiments, one or more cell-free filtrates of the present disclosure comprises about 0.1 to about 95% (by weight) of the composition. For example, compositions of the present disclosure may comprise about 0.1, 0.2, 0.3, 0.4, 0.5, 0.6, 0.7, 0.8, 0.9, 1, 1.25, 1.5, 1.75, 2, 2.25, 2.5, 2.75, 3, 3.25, 3.5, 3.75, 4, 4.25, 4.5, 4.75, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95% or more (by weight) of a cell-free filtrate derived from a culture comprising E. billingiae NRRL B-67766, P. gessardii NRRL B-67767 and/or P. libanesis NRRL B-67769. In some embodiments, a cell-free filtrate of one or more pesticidal Erwinia strains and/or one or more pesticidal Pseudomonas strains comprise(s) about 1 to about 25%, about 5 to about 20%, about 5 to about 15%, about 5 to about 10% or about 8 to about 12% (by weight) of the composition.

In some embodiments, compositions of the present disclosure comprise one or more cell-free filtrates in an effective amount/concentration for preventing and/or treating one or more pest

infections/infestations when the composition is introduced into a plant growth medium (e.g., a soil). For example, compositions of the present disclosure may comprise a cell-free filtrate of E. billingiae NRRL B-67766, P. gessardii NRRL B-67767 and/or P. libanesis NRRL B-67769 in an amount/concentration effective to kill one or more pests (e.g., one or more fungal pests), to inhibit the growth of one or more pests (e.g., one or more fungal pests), and/or to inhibit the reproduction/proliferation of one or more pests (e.g., one or more fungal pests) when the compositon is introduced into a field.

In some embodiments, compositions of the present disclosure comprise one or more cell-free filtrates in an effective amount/concentration for preventing and/or treating one or more pest

infections/infestations when the composition is applied to a plant or plant part. For example, inoculant compositions of the present disclosure may comprise a cell-free filtrate of E. billingiae NRRL B-67766, P. gessardii NRRL B-67767 and/or P. libanesis NRRL B-67769 in an amount/concentration effective to kill one or more pests (e.g., one or more fungal pests), to inhibit the growth of one or more pests (e.g., one or more fungal pests), and/or to inhibit the reproduction/proliferation of one or more pests (e.g., one or more fungal pests) when the compositon is coated onto a seed or sprayed onto a plant.

In some embodiments, compositions of the present disclosure comprise one or more cell-free filtrates in an effective amount/concentration for enhancing plant growth/yield when the inoculant composition is introduced into a plant growth medium (e.g., a soil). For example, inoculant compositions of the present disclosure may comprise a cell-free filtrate of E. billingiae NRRL B-67766, P. gessardii NRRL B-67767 and/or P. libanesis NRRL B-67769 in an amount/concentration effective to improve the growth and/or yield of plants (e.g., wheat) grown in a field treated with the composition, as compared to plants grown in an untreated control field, for example.

In some embodiments, compositions of the present disclosure comprise one or more cell-free filtrates in an effective amount/concentration for enhancing plant growth/yield when the inoculant composition is applied to a plant or plant part. For example, inoculant compositions of the present disclosure may comprise a cell-free filtrate of E. billingiae NRRL B-67766, P. gessardii NRRL B-67767 and/or P. libanesis NRRL B-67769 in an amount/concentration effective to improve the growth and/or yield of plants (e.g., wheat) grown from seeds that were treated with the composition and/or plants (e.g., wheat) that were directly treated with the composition.

In some embodiments, one or more cellular extracts of the present disclosure comprises about 0.1 to about 95% (by weight) of the composition. For example, compositions of the present disclosure may comprise about 0.1, 0.2, 0.3, 0.4, 0.5, 0.6, 0.7, 0.8, 0.9, 1, 1.25, 1.5, 1.75, 2, 2.25, 2.5, 2.75, 3, 3.25, 3.5, 3.75, 4, 4.25, 4.5, 4.75, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95% or more (by weight) of a cellular extract derived from E. billingiae NRRL B-67766, P. gessardii NRRL B-67767 and/or P. libanesis NRRL B- 67769. In some embodiments, a cellular extract of one or more pesticidal Erwinia strains and/or one or more pesticidal Pseudomonas strains comprise(s) about 1 to about 25%, about 5 to about 20%, about 5 to about 15%, about 5 to about 10% or about 8 to about 12% (by weight) of the composition.

In some embodiments, compositions of the present disclosure comprise one or more cellular extracts in an effective amount/concentration for preventing and/or treating one or more pest

infections/infestations when the composition is introduced into a plant growth medium (e.g., a soil). For example, compositions of the present disclosure may comprise a cellular extract derived from E. billingiae NRRL B-67766, P. gessardii NRRL B-67767 and/or P. libanesis NRRL B-67769 in an

amount/concentration effective to kill one or more pests (e.g., one or more fungal pests), to inhibit the growth of one or more pests (e.g., one or more fungal pests), and/or to inhibit the

reproduction/proliferation of one or more pests (e.g., one or more fungal pests) when the compositon is introduced into a field.

In some embodiments, compositions of the present disclosure comprise one or more cellular extracts in an effective amount/concentration for preventing and/or treating one or more pest

infections/infestations when the composition is applied to a plant or plant part. For example, inoculant compositions of the present disclosure may comprise a cellular extract derived from E. billingiae NRRL B-67766, P. gessardii NRRL B-67767 and/or P. libanesis NRRL B-67769 in an amount/concentration effective to kill one or more pests (e.g., one or more fungal pests), to inhibit the growth of one or more pests (e.g., one or more fungal pests), and/or to inhibit the reproduction/proliferation of one or more pests (e.g., one or more fungal pests) when the compositon is coated onto a seed or sprayed onto a plant.

In some embodiments, compositions of the present disclosure comprise one or more cellular extracts in an effective amount/concentration for enhancing plant growth/yield when the inoculant composition is introduced into a plant growth medium (e.g., a soil). For example, inoculant compositions of the present disclosure may comprise a cellular extract derived from E. billingiae NRRL B-67766, P. gessardii NRRL B-67767 and/or P. libanesis NRRL B-67769 in an amount/concentration effective to improve the growth and/or yield of plants (e.g., wheat) grown in a field treated with the composition, as compared to plants grown in an untreated control field, for example.

In some embodiments, compositions of the present disclosure comprise one or more cellular extracts in an effective amount/concentration for enhancing plant growth/yield when the inoculant composition is applied to a plant or plant part. For example, inoculant compositions of the present disclosure may comprise a cellular extract derived from E. billingiae NRRL B-67766, P. gessardii NRRL B-67767 and/or P. libanesis NRRL B-67769 in an amount/concentration effective to improve the growth and/or yield of plants (e.g., wheat) grown from seeds that were treated with the composition and/or plants (e.g., wheat) that were directly treated with the composition.

Compositions of the present disclosure may comprise any suitable carrier(s), including, but not limited to, foliar-compatible carriers, seed-compatible carriers and soil-compatible carriers. Selection of appropriate carrier materials will depend on the intended application(s) and the microorganism(s), culture(s), cell-free filtrate(s) and/or cellular extract(s) present in the composition. In some embodiments, the carrier material(s) will be selected to provide an composition in the form of a liquid, gel, slurry, or solid. In some embodiments, the carrier will consist essentially of or consist of one or more stabilizing compounds.

In some embodiments, the composition comprises one or more solid carriers. According to some embodiments, the composition comprises one or more powders (e.g., wettable powders) and/or granules. Non-limiting examples of solid carriers include clays (e.g., attapulgite clays, montmorillonite clay, etc.), peat-based powders and granules, freeze-dried powders, spray-dried powders, spray-freeze-dried powders and combinations thereof.

In some embodiments, the composition comprises one or more liquid and/or gel carriers.

According to some embodiments, the composition comprises one or more non-aqueous solvents.

According to some embodiments, the composition comprises one or more aqueous solvents (e.g., water). According to some embodiments, an aqueous solvent, such as water, may be combined with a co-solvent, such as ethyl lactate, methyl soyate/ethyl lactate co-solvent blends (e.g., STEPOSOL™, Stepan), isopropanol, acetone, 1,2-propanediol, n-alkylpyrrolidones (e.g., AGSOLEX™ wetting agents; Ashland, Inc., Covington, KY ), petroleum based-oils (e.g., AROMATIC™ and SOLVESSO™ fluids; ExxonMobil Chemical Company, Spring, TX), isoparrafinic hyydrocarbons (e.g., ISOPAR™ fluids; ExxonMobil Chemical Company, Spring, TX), cycloparaffinic hydrocarbons (e.g., NAPPAR™ 6; ExxonMobil Chemical Company, Spring, TX), mineral spirits (e.g., VARSOL™; ExxonMobil Chemical Company, Spring, TX), and mineral oils (e.g., paraffin oil). According to some embodiments, the composition comprises one or more inorganic solvents, such as decane, dodecane, hexylether and nonane. According to some embodiments, the composition comprises one or more organic solvents, such as acetone, dichloromethane, ethanol, hexane, methanol, propan-2-ol and trichloroethylene. Non-limiting examples of liquid/gel carriers include oils (e.g., mineral oil, olive oil, peanut oil, soybean oil, sunflower oil), polyethylene glycols (e.g., PEG 200, PEG 300, PEG 400, etc.), propylene glycols (e.g., PPG-9, PPG-10, PPG-17, PPG-20, PPG-26, etc.), ethoxylated alcohols (e.g., TOMADOL® (Air Products and Chemicals, Inc., Allentown, PA), TERGITOL™ 15-S surfactants such as TERGITOL™15-S-9 (The Dow Chemical Company, Midland, MI), etc.), isoparrafinic hyydrocarbons (e.g., ISOPAR™, ISOPAR™ L, ISOPAR™ M, ISOPAR™ V; ExxonMobil Chemical Company, Spring, TX), pentadecane, polysorbates (e.g.

polysorbate 20, polysorbate 40, polysorbate 60, polysorbate 80, etc.), silicones (siloxanes, trisiloxanes, etc.) and combinations thereof. In some embodiments, the carrier comprises, consists essentially of or consists of dodecane. In some embodiments, the carrier comprises, consists essentially of or consists of methyl soyate. In some embodiments, the carrier comprises, consists essentially of or consists of one or more paraffin oils and/or waxes.

Additional examples of carriers may be found in BURGES, FORMULATION OF MICROBIAL BIOPESTICIDES: BENEFICIAL MICROORGANISMS, NEMATODES and SEED TREATMENTS (Springer Science & Business Media) (2012); Inoue & Horikoshi, J. FERMENTATION

BIOENG.71(3):194 (1991).

Compositions of the present disclosure may comprise any suitable stabilizing compound(s), including, but not limited to, maltodextrins, monosaccharides, disaccharides, oligosaccharides, sugar alcohols, humic acids, fulvic acids, malt extracts, peat extracts, betaines, prolines, sarcosines, peptones, skim milks, oxidation control components, hygroscopic polymers and UV protectants.

In some embodiments, the composition comprises one or more maltodextrins (e.g., one or more maltodextrins having a dextrose equivalent value (DEV) of about 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, or 25). According to some embodiments, the composition comprises one or more maltodextrins having a DEV of about 5 to about 6, 7, 8, 9, 10, 11, 12, 14, 15, 16, 17, 18, 19 or 20, about 10 to about 11, 12, 14, 15, 16, 17, 18, 19 or 20, or about 15 to about 16, 17, 18, 19 or 20. According to some embodiments, the composition comprises a combination of maltodextrins having a DEV of about 5 to about 6, 7, 8, 9, 10, 11, 12, 14, 15, 16, 17, 18, 19 or 20, about 10 to about 11, 12, 14, 15, 16, 17, 18, 19 or 20, or about 15 to about 16, 17, 18, 19 or 20. Non-limiting examples of maltodextrins include MALTRIN® M040 (DEV = 5; molecular weight = 3600; Grain Processing Corporation, Muscatine, IA), MALTRIN® M100 (DEV = 10; molecular weight = 1800; Grain Processing Corporation, Muscatine, IA), MALTRIN® M150 (DEV = 15; molecular weight = 1200; Grain Processing Corporation, Muscatine, IA), MALTRIN® M180 (DEV = 18; molecular weight = 1050; Grain Processing Corporation, Muscatine, IA), MALTRIN® M200 (DEV = 20; molecular weight = 900; Grain Processing Corporation, Muscatine, IA), MALTRIN® M250 (DEV = 25; molecular weight = 720; Grain Processing Corporation, Muscatine, IA); MALTRIN QD® M580 (DEV = 16.5–19.9; Grain Processing Corporation, Muscatine, IA); MALTRIN QD® M585 (DEV = 15.0–19.9; Grain Processing Corporation, Muscatine, IA); MALTRIN QD® M600 (DEV = 20.0–23.0; Grain Processing Corporation, Muscatine, IA); GLOBE® Plus 15 DE (Ingredion Inc., Westchester, IL); and combinations thereof.

In some embodiments, the composition comprises one or more monosaccharides (e.g., allose, altrose, arabinose, fructose, galactose, glucose, gulose, iodose, lyxose, mannose, ribose, talose, threose and/or xylose). According to some embodiments, the composition comprises gluscose. According to some embodiments, the composition does not comprise glucose.

In some embodiments, the composition comprises one or more disaccharides (e.g., cellobiose, chitobiose, gentiobiose, gentiobiulose, isomaltose, kojibiose, lactose, lactulose, laminaribiose, maltose (e.g., maltose monohydrate, anhydrous maltose), maltulose, mannobiose, melibiose, melibiulose, nigerose, palatinose, rutinose, rutinulose, sophorose, sucrose, trehalose, turanose and/or xylobiose).

According to some embodiments, the composition comprises maltose. According to some embodiments, the composition does not comprise maltose. According to some embodiments, the composition comprises trehalose. According to some embodiments, the composition does not comprise trehalose.

In some embodiments, the composition comprises one or more oligosaccharides (e.g., fructo- oligosaccharides, galacto-oligosaccharides, mannon-oligosaccharides and/or raffinose).

In some embodiments, the composition comprises one or more sugar alcohols (e.g., arabitol, erythritol, fucitol, galactitol, glycerol, iditol, inositol, isomalt, lactitol, maltitol, maltotetraitol, maltotriitol, mannitol, polyglycitol, ribitol, sorbitol, threitol, volemitol and/or xylitol).

In some embodiments, the composition comprises one or more humic acids (e.g., one or more leonardite humic acids, lignite humic acids, peat humic acids and water-extracted humic acids). In some embodiments, the composition comprises ammonium humate, boron humate, potassium humate and/or sodium humate. In some embodiments, one or more of ammonium humate, boron humate, potassium humate and sodium humate is/are excluded from the composition. Nonlimiting examples of humic acids that may be useful in embodiments of the present disclosure include MDL Number MFCD00147177 (CAS Number 1415-93-6), MDL Number MFCD00135560 (CAS Number 68131-04-4), MDL Number MFCS22495372 (CAS Number 68514-28-3), CAS Number 93924-35-7, and CAS Number 308067-45-0.

In some embodiments, the composition comprises one or more fulvic acids (e.g., one or more leonardite fulvic acids, lignite fulvic acids, peat fulvic acids and/or water-extracted fulvic acids). In some embodiments, the composition comprises ammonium fulvate, boron fulvate, potassium fulvate and/or sodium fulvate. In some embodiments, one or more of ammonium fulvate, boron fulvate, potassium fulvate and sodium fulvate is/are excluded from compositions of the present disclosure. Nonlimiting examples of fulvic acids that may be useful in embodiments of the present disclosure include MDL Number MFCD09838488 (CAS Number 479-66-3).

In some embodiments, the composition comprises one or more betaines (e.g., trimethylglycine). In some embodiments, the composition comprises one or more peptones (e.g., bacterial peptones, meat peptones, milk peptones, vegetable peptones and yeast peptones).

In some embodiments, the composition comprises one or more oxidation control components (e.g., one or more antioxidants and/or oxygen scavengers). According to some embodiments, the composition comprises one or more oxygen scavengers, such as ascrobic acid, ascorbate salts, catechol and/or sodium hydrogen carbonate. According to some embodiments, the composition comprises one or more antioxidants, such as ascorbic acid, ascorbyl palmitate, ascorbyl stearate, calcium ascorbate, carotenoids, lipoic acid, phenolic compounds (e.g., flavonoids, flavones, flavonols), potassium ascorbate, sodium ascorbate, thiols (e.g., glutathione, lipoic acid, N-acetyl cysteine), tocopherols, tocotrienols, ubiquinone and/or uric acid. Non-limiting examples of antioxidants include those that are soluble in the cell membrane (e.g., alpha tocopherol (vitamin E), ascorbyl palmitate) and those that are soluble in water (e.g., ascorbic acid and isomers or ascorbic acid, sodium or potassium salts of ascorbic acid or isomers or ascorbic acid, glutathione, sodium or potassium salts of glutathione). In some embodiments, use of a membrane-soluble antioxidant necessitates the addition of one or more surfactants to adequately disperse the antioxidant within the composition. According to some embodiments, the composition is/comprises ascorbic acid and/or glutathione.

In some embodiments, the composition comprises one or more hygroscopic polymers (e.g., hygroscopic agars, albumins, alginates, carrageenans, celluloses, gums (e.g., cellulose gum, guar gum, gum arabic, gum combretum, xantham gum), methyl celluloses, nylons, pectins, polyacrylic acids, polycaprolactones, polycarbonates, polyethylene glycols (PEG), polyethylenimines (PEI), polylactides, polymethylacrylates (PMA), polyurethanes, polyvinyl alcohols (PVA), polyvinylpyrrolidones (PVP), propylene glycols, sodium carboxymethyl celluloses and/or starches). Non-limiting examples of polymers include AGRIMER™ polymers (e.g., 30, AL-10 LC, AL-22, AT/ATF, VA 3E, VA 3l, VA 5E, VA 5l, VA 6, VA 6E, VA 7E, VA 7l, VEMA AN-216, VEMA AN-990, VEMA AN-1200, VEMA AN-1980, VEMA H-815MS; Ashland Specialty Ingredients, Wilmington, DE), EASYSPERSE™ polymers (Ashland Specialty Ingredients, Wilmington, DE); DISCO™ AG polymers (e.g., L-250, L-280, L-285, L-286, L- 320, L-323, L-517, L-519, L-520, L800; Incotec Inc., Salinas, CA), KELZAN® polymers (Bri-Chem Supply Ltd., Calgary, Alberta, CA), SEEDWORX™ polymers (e.g., Bio 200; Aginnovation, LLC, Walnut Groove, CA), TICAXAN® xanthan powders, such as PRE-HYDRATED® TICAXAN® Rapid-3 Powder (TIC Gums, White Marsh, MD) and combinations thereof. Additional examples of polymers may be found in Pouci, et al. AM. J. AGRIC. BIOL. SCI.3(1):299 (2008).

In some embodiments, the composition comprises one or more UV protectants (e.g., one or more aromatic amino acids (e.g., tryptophan, tyrosine), carotenoids, cinnamates, lignosulfonates (e.g., calcium lignosulfonate, sodium lignosulfonate), melanins, mycosporines, polyphenols and/or salicylates). Non- limiting examples of UV protectants include Borregaard LignoTech™ lignosulfonates (e.g., Borresperse 3A, Borresperse CA, Borresperse NA, Marasperse AG, Norlig A, Norlig 11D, Ufoxane 3A, Ultrazine NA, Vanisperse CB; Borregaard Lignotech, Sarpsborg, Norway) and combinations thereof. Additional examples of UV protectants may be found in BURGES, FORMULATION OF MICROBIAL BIOPESTICIDES: BENEFICIAL MICROORGANISMS, NEMATODES AND SEED TREATMENTS (Springer Science & Business Media) (2012).

Additional examples of stabilizing compounds, and of combinations of carriers and stabilizing compounds, may be found in International Patent Publication Nos. WO2017/044473, WO2017/044545, WO2017/116837, WO2017/116846, WO2017/210163, WO2017/210166, WO2018/118740,

WO2018/175681, WO2018/183491, WO2018/218008, WO2018/218016 and WO2018/218035.

Compositions of the present disclosure may comprise any suitable biostimulant(s), including, but not limited to, seaweed extracts (e.g., Ascophyllum nodosum extracts, such as alginate, Ecklonia maxima extracts, etc.), myo-inositol, glycine and combinations thereof.

Compositions of the present disclosure may comprise any suitable microbial extract(s), including, but not limited to, bacterial extracts, fungal extracts and combinations thereof. In some embodiments, compositions of the present disclosure comprise one or more extracts of media comprising one or more diazotrophs, phosphate-solubilizing microorganisms and/or biopesticides. In some embodiments, compositions of the present disclosure comprise an extract of media comprising one or more of the microbial strains included in Appendix A.

Compositions of the present disclosure may comprise any suitable nutrient(s), including, but not limited to, organic acids (e.g., acetic acid, citric acid, lactic acid, malic acid, taurine, etc.), macrominerals (e.g., phosphorous, calcium, magnesium, potassium, sodium, iron, etc.), trace minerals (e.g., boron, cobalt, chloride, chromium, copper, fluoride, iodine, manganese, molybdenum, selenium, zinc, etc.), vitamins, (e.g., vitamin A, vitamin B complex (i.e., vitamin B 1 , vitamin B 2 , vitamin B 3 , vitamin B 5 , vitamin B 6 , vitamin B 7 , vitamin B 8 , vitamin B 9 , vitamin B 12 , choline) vitamin C, vitamin D, vitamin E, vitamin K, carotenoids (a-carotene, b-carotene, cryptoxanthin, lutein, lycopene, zeaxanthin, etc.) and combinations thereof. In some embodiments, compositions of the present disclosure comprise phosphorous, boron, chlorine, copper, iron, manganese, molybdenum and/or zinc.

Compositions of the present disclosure may comprise any suitable pest attractant(s) and/or feeding stimulant(s), including, but not limited to, brevicomin, ceralure, codlelure, cue-lure, disparlure, dominicalure, eugenol, frontalin, gossyplure, grandlure, hexalure, ipsdienol, ipsenol, japonilure, latitlure, lineatin, litlure, looplure, medlure, megatomic acid, methyl eugenol, moguchun, a-multistriatin, muscalure, orfalure, oryctalure, ostramone, rescalure, siglure, sulcatol, trimedlure and/or trunc-call.

Compositions of the present disclosure may comprise any suitable pesticide(s), including, but not limited to, acaricides, fungicides, herbicides, insecticides and nematicides.

Fungicides may be selected to provide effective control against a broad spectrum of

phytopathogenic fungi (and fungus-like organisms), including, but not limited to, soil-borne fungi from the classes Ascomycetes, Basidiomycetes, Chytridiomycetes, Deuteromycetes (syn. Fungi imperfecti), Peronosporomycetes (syn. Oomycetes), Plasmodiophoromycetes and Zygomycetes. According to some embodiments, the composition comprises a fungicide (or combination of fungicides) that is toxic to one or more strains of Albugo (e.g., A. candida), Alternaria (e.g. ¸A. alternata), Aspergillus (e.g., A. candidus, A. clavatus, A. flavus, A. fumigatus, A. parasiticus, A. restrictus, A. sojae, A. solani), Blumeria (e.g., B. graminis), Botrytis (e.g., B. cinerea), Cladosporum (e.g., C. cladosporioides), Colletotrichum (e.g., C. acutatum, C. boninense, C. capsici, C. caudatum, C. coccodes, C. crassipes, C. dematium, C.

destructivum, C. fragariae, C. gloeosporioides, C. graminicola, C. kehawee, C. lindemuthianum, C. musae, C. orbiculare, C. spinaceae, C. sublineolum, C. trifolii, C. truncatum), Fusarium (e.g., F.

graminearum, F. moniliforme, F. oxysporum, F. roseum, F. tricinctum), Helminthosporium, Magnaporthe (e.g., M. grisea, M. oryzae), Melamspora (e.g., M. lini), Mycosphaerella (e.g., M. graminicola),

Nematospora, Penicillium (e.g., P. rugulosum, P. verrucosum), Phakopsora (e.g., P. pachyrhizi), Phomopsis, Phytophthora (e.g., P. infestans), Puccinia (e.g., P. graminis, P. striiformis, P. tritici, P. triticina), Pucivinia (e.g., P. graministice), Pythium, Pytophthora, Rhizoctonia (e.g., R. solani),

Scopulariopsis, Selerotinia, Thielaviopsis and/or Ustilago (e.g.¸U. maydis). Additional examples of fungi may be found in Bradley, Managing Diseases, in ILLINOIS AGRONOMY HANDBOOK (2008).

Herbicides may be selected to provide effective control against a broad spectrum of plants, including, but not limited to, plants from the families Asteraceae, Caryophyllaceae, Poaceae and

Polygonaceae. According to some embodiments, the composition comprises an herbicide (or combination of herbicides) that is toxic to one or more strains of Echinochloa (e.g., E. brevipedicellata, E. callopus, E. chacoensis, E. colona, E. crus-galli, E. crus-pavonis, E. elliptica, E. esculenta, E. frumentacea, E.

glabrescens, E. haploclada, E. helodes, E. holciformis, E. inundata, E. jaliscana, E. Jubata, E.

kimberleyensis, E. lacunaria, E. macrandra, E. muricata, E. obtusiflora, E. oplismenoides, E. orzyoides, E. paludigena, E. picta, E. pithopus, E. polystachya, E. praestans, E. pyramidalis, E. rotundiflora, E. stagnina, E. telmatophila, E. turneriana, E. ugandensis, E. walteri), Fallopia (e.g., F. baldschuanica, F. japonica, F. sachalinensis), Stellaria (e.g., S. media) and/or Taraxacum (e.g., T. albidum, T. aphrogenes, T. brevicorniculatum, T. californicum, T. centrasiatum, T. ceratophorum, T. erythrospermum, T.

farinosum, T. holmboei, T. japonicum, T. kok-saghyz, T. laevigatum T. officinale, T. platycarpum).

Additional species of plants that may be targeted by compositions of the present disclosure may be found in Hager, Weed Management, in ILLINOIS AGRONOMY HANDBOOK (2008) and LOUX ET AL., WEED CONTROL GUIDE FOR OHIO, INDIANA AND ILLINOIS (2015).

Insecticides may be selected to provide effective control against a broad spectrum of insects, including, but not limited to, insects from the orders Coleoptera, Dermaptera, Diptera, Hemiptera, Homoptera, Hymenoptera, Lepidoptera, Orthoptera and Thysanoptera. For example, compositions of the present disclosure may comprise one or more insecticides toxic to insects from the families Acrididae, Aleytodidae, Anobiidae, Anthomyiidae, Aphididae, Bostrichidae, Bruchidae, Cecidomyiidae,

Cerambycidae, Cercopidae, Chrysomelidae, Cicadellidae, Coccinellidae, Cryllotalpidae, Cucujidae, Curculionidae, Dermestidae, Elateridae, Gelechiidae, Lygaeidae, Meloidae, Membracidae, Miridae, Noctuidae, Pentatomidae, Pyralidae, Scarabaeidae, Silvanidae, Spingidae, Tenebrionidae and/or

Thripidae. According to some embodiments, the composition comprises an insecticide (or combination of insecticides) that is toxic to one or more species of Acalymma, Acanthaoscelides (e.g., A. obtectus, ), Anasa (e.g., A. tristis), Anastrepha (e.g., A. ludens), Anoplophora (e.g., A. glabripennis), Anthonomus (e.g., A. eugenii), Acyrthosiphon (e.g., A. pisum), Bactrocera (e.g. B¸ . dosalis), Bemisia (e.g., B.

argentifolii, B. tabaci), Brevicoryne (e.g., B. brassicae), Bruchidius (e.g., B. atrolineatus), Bruchus (e.g., B. atomarius, B. dentipes, B. lentis, B. pisorum and/or B. rufipes), Callosobruchus (e.g., C. chinensis, C. maculatus, C. rhodesianus, C. subinnotatus, C. theobromae), Caryedon (e.g., C. serratus), Cassadinae, Ceratitis (e.g., C. capitata), Chrysomelinae, Circulifer (e.g., C. tenellus), Criocerinae, Cryptocephalinae, Cryptolestes (e.g., C. ferrugineus, C. pusillis, C. pussilloides), Cylas (e.g., C. formicarius), Delia (e.g., D. antiqua), Diabrotica, Diaphania (e.g., D. nitidalis), Diaphorina (e.g., D. citri), Donaciinae, Ephestia (e.g, E. cautella, E. elutella, E., keuhniella), Epilachna (e.g., E. varivestris), Epiphyas (e.g., E. postvittana), Eumolpinae, Galerucinae, Helicoverpa (e.g., H. zea), Heteroligus (e.g., H. meles), Iobesia (e.g., I.

botrana), Lamprosomatinae, Lasioderma (e.g., L. serricorne), Leptinotarsa (e.g., L. decemlineata), Leptoglossus, Liriomyza (e.g., L. trifolii), Manducca, Melittia (e.g., M. cucurbitae), Myzus (e.g., M. persicae), Nezara (e.g., N. viridula), Orzaephilus (e.g., O. merator, O. surinamensis), Ostrinia (e.g., O. nubilalis), Phthorimaea (e.g., P. operculella), Pieris (e.g., P. rapae), Plodia (e.g., P. interpunctella), Plutella (e.g., P. xylostella), Popillia (e.g., P. japonica), Prostephanus (e.g., P. truncates), Psila, Rhizopertha (e.g., R. dominica), Rhopalosiphum (e.g., R. maidis), Sagrinae, Solenopsis (e.g., S. Invicta), Spilopyrinae, Sitophilus (e.g., S. granaries, S. oryzae and/or S. zeamais), Sitotroga (e.g., S. cerealella), Spodoptera (e.g., S. frugiperda), Stegobium (e.g., S. paniceum), Synetinae, Tenebrio (e.g., T. malens and/or T. molitor), Thrips (e.g., T. tabaci), Trialeurodes (e.g., T. vaporariorum), Tribolium (e.g., T. castaneum and/or T. confusum), Trichoplusia (e.g., T. ni), Trogoderma (e.g., T. granarium) and

Trogossitidae (e.g., T. mauritanicus). Additional species of insects that may be targeted by compositions of the present disclosure may be found in CAPINERA, HANDBOOK OF VEGETABLE PESTS (2001) and Steffey and Gray, Managing Insect Pests, in ILLINOIS AGRONOMY HANDBOOK (2008).

Nematicides may be selected to provide effective control against a broad spectrum of nematodes, including, but not limited to, phytoparasitic nematodes from the classes Chromadorea and Enoplea. According to some embodiments, the composition comprises a nematicide (or combination of nematicides) that is toxic to one or more strains of Anguina, Aphelenchoides, Belonolaimus,

Bursaphelenchus, Ditylenchus, Globodera, Helicotylenchus, Heterodera, Hirschmanniella, Meloidogyne, Naccobus, Pratylenchus, Radopholus, Rotylenshulus, Trichodorus, Tylenchulus and/or Xiphinema.

Additional species that may be targeted by compositions of the present disclosure may be found in CAPINERA, HANDBOOK OF VEGETABLE PESTS (2001) and Niblack, Nematodes, in ILLINOIS AGRONOMY HANDBOOK (2008).

In some embodiments, compositions of the present disclosure comprise one or more chemical fungicides. Non-limiting examples of chemical fungicides include strobilurins, such as azoxystrobin, coumethoxystrobin, coumoxystrobin, dimoxystrobin, enestroburin, fluoxastrobin, kresoxim-methyl, metominostrobin, orysastrobin, picoxystrobin, pyraclostrobin, pyrametostrobin, pyraoxystrobin, pyribencarb, trifloxystrobin, 2-[2-(2,5-dimethyl-phenoxymethyl)-phenyl]-3-methoxy-acrylic acid methyl ester and 2-(2-(3-(2,6-dichlorophenyl)-1-methyl-allylideneaminooxymeth yl)-phenyl)-2-methoxyimino-N- methyl-acetamide; carboxamides, such as carboxanilides (e.g., benalaxyl, benalaxyl-M, benodanil, bixafen, boscalid, carboxin, fenfuram, fenhexamid, flutolanil, fluxapyroxad, furametpyr, isopyrazam, isotianil, kiralaxyl, mepronil, metalaxyl, metalaxyl-M (mefenoxam), ofurace, oxadixyl, oxycarboxin, penflufen, penthiopyrad, sedaxane, tecloftalam, thifluzamide, tiadinil, 2-amino-4-methyl-thiazole-5- carboxanilide, N-(4'-trifluoromethylthiobiphenyl-2-yl)-3-difluoromethyl-1-m ethyl-1H-pyra- zole-4- carboxamide, N-(2-(1,3,3-trimethylbutyl)-phenyl)-1,3-dimethyl-5-fluoro-1H -pyrazole-4-carboxamide), carboxylic morpholides (e.g., dimethomorph, flumorph, pyrimorph), benzoic acid amides (e.g., flumetover, fluopicolide, fluopyram, zoxamide), carpropamid, dicyclomet, fenehexamid, mandiproamid, oxytetracyclin, silthiofam, spiroxamine, and N-(6-methoxy-pyridin-3-yl) cyclopropanecarboxylic acid amide; azoles, such as triazoles (e.g., azaconazole, bitertanol, bromuconazole, cyproconazole, difenoconazole, diniconazole, diniconazole-M, epoxiconazole, fenbuconazole, fluquinconazole, flusilazole, flutriafol, hexaconazole, imibenconazole, ipconazole, metconazole, myclobutanil, oxpoconazole, paclobutrazole, penconazole, propiconazole, prothioconazole, simeconazole, tebuconazole, tetraconazole, triadimefon, triadimenol, triticonazole, uniconazole) and imidazoles (e.g., cyazofamid, imazalil, pefurazoate, prochloraz, triflumizol); heterocyclic compounds, such as pyridines (e.g., fluazinam, pyrifenox (cf.D1b), 3-[5-(4-chloro-phenyl)-2,3-dimethyl-isoxazolidin-3-yl]-pyrid ine, 3-[5-(4- methyl-phenyl)-2,3-dimethyl-isoxazolidin-3-yl]-pyridine), pyrimidines (e.g., bupirimate, cyprodinil, diflumetorim, fenarimol, ferimzone, mepanipyrim, nitrapyrin, nuarimol, pyrimethanil), piperazines (e.g., triforine), pirroles (e.g., fenpiclonil, fludioxonil), morpholines (e.g., aldimorph, dodemorph, dodemorph- acetate, fenpropimorph, tridemorph), piperidines (e.g., fenpropidin), dicarboximides (e.g., fluoroimid, iprodione, procymidone, vinclozolin), non-aromatic 5-membered heterocycles (e.g., famoxadone, fenamidone, flutianil, octhilinone, probenazole, 5-amino-2-isopropyl-3-oxo-4-ortho-tolyl-2,3-dihydro- pyrazole-1-carbothioic acid S-allyl ester), acibenzolar-S-methyl, ametoctradin, amisulbrom, anilazin, blasticidin-S, captafol, captan, chinomethionat, dazomet, debacarb, diclomezine, difenzoquat, difenzoquat-methylsulfate, fenoxanil, Folpet, oxolinic acid, piperalin, proquinazid, pyroquilon, quinoxyfen, triazoxide, tricyclazole, 2-butoxy-6-iodo-3-propylchromen-4-one, 5-chloro-1-(4,6- dimethoxy-pyrimidin-2-yl)-2-methyl-1H-benzoimidazole and 5-chloro-7-(4-methylpiperidin-1-yl)-6- (2,4,6-trifluorophenyl)-[1,2,4]triazolo-[1,5-a]pyrimidine; benzimidazoles, such as carbendazim; and other active substances, such as guanidines (e.g., guanidine, dodine, dodine free base, guazatine, guazatine- acetate, iminoctadine), iminoctadine-triacetate and iminoctadine-tris(albesilate); antibiotics (e.g., kasugamycin, kasugamycin hydrochloride-hydrate, streptomycin, polyoxine and validamycin A);

nitrophenyl derivates (e.g., binapacryl, dicloran, dinobuton, dinocap, nitrothal-isopropyl, tecnazen);

organometal compounds (e.g., fentin salts, such as fentin-acetate, fentin chloride, fentin hydroxide);

sulfur-containing heterocyclyl compounds (e.g., dithianon, isoprothiolane); organophosphorus compounds (e.g., edifenphos, fosetyl, fosetyl-aluminum, iprobenfos, phosphorus acid and its salts, pyrazophos, tolclofos-methyl); organochlorine compounds (e.g., chlorothalonil, dichlofluanid, dichlorophen, flusulfamide, hexachlorobenzene, pencycuron, pentachlorphenole and its salts, phthalide, quintozene, thiophanate-methyl, thiophanate, tolylfluanid, N-(4-chloro-2-nitro-phenyl)-N-ethyl-4-methyl- benzenesulfonamide) and inorganic active substances (e.g., Bordeaux mixture, copper acetate, copper hydroxide, copper oxychloride, basic copper sulfate, sulfur) and combinations thereof. In some embodiments, compositions of the present disclosure comprise acibenzolar-S-methyl, azoxystrobin, benalaxyl, bixafen, boscalid, carbendazim, cyproconazole, dimethomorph, epoxiconazole, fludioxonil, fluopyram, fluoxastrobin, flutianil, flutolanil, fluxapyroxad, fosetyl-Al, ipconazole, isopyrazam, kresoxim-methyl, mefenoxam, metalaxyl, metconazole, myclobutanil, orysastrobin, penflufen, penthiopyrad, picoxystrobin, propiconazole, prothioconazole, pyraclostrobin, sedaxane, silthiofam, tebuconazole, thiabendazole, thifluzamide, thiophanate, tolclofos-methyl, trifloxystrobin and triticonazole. In some embodiments, compositions of the present disclosure comprise azoxystrobin, pyraclostrobin, fluoxastrobin, trifloxystrobin, ipconazole, prothioconazole, sedaxane, fludioxonil, metalaxyl, mefenoxam, thiabendazole, fluxapyroxad and/or fluopyram. In some embodiments, compositions of the present disclosure comprise one or more aromatic hydrocarbons, benzimidazoles, benzthiadiazole, carboxamides, carboxylic acid amides, morpholines, phenylamides, phosphonates, quinone outside inhibitors (e.g. strobilurins), thiazolidines, thiophanates, thiophene carboxamides and/or triazoles.

In some embodiments, compositions of the present disclosure comprise one or more chemical herbicides. Non-limiting examples of chemical herbicides include 2,4-dichlorophenoxyacetic acid (2,4- D), 2,4,5-trichlorophenoxyacetic acid (2,4,5-T), ametryn, amicarbazone, aminocyclopyrachlor, acetochlor, acifluorfen, alachlor, atrazine, azafenidin, bentazon, benzofenap, bifenox, bromacil, bromoxynil, butachlor, butafenacil, butroxydim, carfentrazone-ethyl, chlorimuron, chlorotoluro, clethodim, clodinafop, clomazone, cyanazine, cycloxydim, cyhalofop, desmedipham, desmetryn, dicamba, diclofop, diflufenican, dimefuron, diuron, dithiopyr, ethofumesate, fenoxaprop, fluazifop, fluazifop-P, flufenacet, fluometuron, flufenpyr-ethyl, flumiclorac-pentyl, flumioxazin, fluoroglycofen, fluthiacet- methyl, fomesafe, fomesafen, foramsulfuron, glyphosate, glufosinate, haloxyfop, hexazinone, imazamox, imazaquin, imazethapyr, indaziflam, iodosulfuron, ioxynil, isoproturon, isoxaflutole, lactofen, linuron, mecoprop, mecoprop-P, mesosulfuron, mesotrion, metamitron, metazochlor, methibenzuron , metolachlor (and S-metolachlor ), metoxuron, metribuzin, monolinuron, oxadiargyl, oxadiazon, oxaziclomefone, oxyfluorfen,

phenmedipham, pretilachlor, profoxydim, prometon, prometry, propachlor, propanil , propaquizafop, propisochlor, propoxycarbazone, pyraflufen-ethyl, pyrazon, pyrazolynate, pyrazoxyfen, pyridate, quizalofop, quizalofop-P (e.g., quizalofop-ethyl, quizalofop-P-ethyl, clodinafop-propargyl, cyhalofop- butyl, diclofop- methyl, fenoxaprop-P-ethyl, fluazifop-P-butyl, haloxyfop-methyl, haloxyfop-R-methyl), saflufenacil, sethoxydim, siduron, simazine, simetryn, sulcotrione, sulfentrazone, tebuthiuron, tembotrione, tepraloxydim, terbacil, terbumeton, terbuthylazine, thaxtomin (e.g., the thaxtomins described in US Patent No.: 7,989,393), thenylchlor, thiencarbazone-methyl, tralkoxydim, triclopyr, trietazine, tropramezone, salts and esters thereof; racemic mixtures and resolved isomers thereof and combinations thereof. In some embodiments, compositions of the present disclosure comprise acetochlor, clethodim, dicamba, flumioxazin, fomesafen, glyphosate, glufosinate, mesotrione, quizalofop, saflufenacil, sulcotrione, S-3100 and/or 2,4-D. In some embodiments, compositions of the present disclosure comprise glyphosate, glufosinate, dicamba, 2,4-D, acetochlor, metolachlor, pyroxasulfone, flumioxazin, fomesafen, lactofen, metribuzin, mesotrione, and/or ethyl 2-((3-(2-chloro-4-fluoro-5-(3-methyl-2,6-dioxo-4- (trifluoromethyl)-2,3-dihydropyrimidin-1(6H)-yl)phenoxy)pyri din-2-yl)oxy)acetate. In some

embodiments, compositions of the present disclosure comprise one or more acetyl CoA carboxylase (ACCase) inhibitors, acetolactate synthase (ALS) inhibitors, acetohydroxy acid synthase (AHAS) inhibitors, photosystem II inhibitors, photosystem I inhibitors, protoporphyrinogen oxidase (PPO or Protox) inhibitors, carotenoid biosynthesis inhibitors, enolpyruvyl shikimate-3-phosphate (EPSP) synthase inhibitor, glutamine synthetase inhibitor, dihydropteroate synthetase inhibitor, mitosis inhibitors, 4- hydroxyphenyl-pyruvate-dioxygenase (4-HPPD) inhibitors, synthetic auxins, auxin herbicide salts, auxin transport inhibitors, nucleic acid inhibitors and/or one or more salts, esters, racemic mixtures and/or resolved isomers thereof.

In some embodiments, compositions of the present disclosure comprise one or more chemical insecticides and/or nematicides. Non-limiting examples of chemical insecticides and nematicides include abamectin, acrinathrin, aldicarb, aldoxycarb, alpha-cypermethrin, betacyfluthrin, bifenthrin, cyhalothrin, cypermethrin, deltamethrin, esfenvalerate, etofenprox, fenpropathrin, fenvalerate, flucythrinate, fosthiazate, lambda-cyhalothrin, gamma-cyhalothrin, permethrin, tau-fluvalinate, transfluthrin, zeta- cypermethrin, cyfluthrin, bifenthrin, tefluthrin, eflusilanat, fubfenprox, pyrethrin, resmethrin,

imidacloprid, acetamiprid, thiamethoxam, nitenpyram, thiacloprid, dinotefuran, clothianidin,

chlorfluazuron, diflubenzuron, lufenuron, teflubenzuron, triflumuron, novaluron, flufenoxuron, hexaflumuron, bistrifluoron, noviflumuron, buprofezin, cyromazine, methoxyfenozide, tebufenozide, halofenozide, chromafenozide, endosulfan, fipronil, ethiprole, pyrafluprole, pyriprole, flubendiamide, chlorantraniliprole, cyazypyr, emamectin, emamectin benzoate, abamectin, ivermectin, milbemectin, lepimectin, tebufenpyrad, fenpyroximate, pyridaben, fenazaquin, pyrimidifen, tolfenpyrad, dicofol, cyenopyrafen, cyflumetofen, acequinocyl, fluacrypyrin, bifenazate, diafenthiuron, etoxazole, clofentezine, spinosad, triarathen, tetradifon, propargite, hexythiazox, bromopropylate, chinomethionat, amitraz, pyrifluquinazon, pymetrozine, flonicamid, pyriproxyfen, diofenolan, chlorfenapyr, metaflumizone, indoxacarb, chlorpyrifos, spirodiclofen, spiromesifen, spirotetramat, pyridalyl, spinctoram, acephate, triazophos, profenofos, oxamyl, spinetoram, fenamiphos, fenamipclothiahos, 4-{[(6-chloropyrid-3- yl)methyl](2,2-difluoroethyl)amino}furan-2(5H)-one, 3,5-disubstituted-1,2,4-oxadiazole compounds, 3- phenyl-5-(thien-2-yl)-1,2,4-oxadiazole, cadusaphos, carbaryl, carbofuran, ethoprophos, thiodicarb, aldicarb, aldoxycarb, metamidophos, methiocarb, sulfoxaflor, methamidophos, cyantraniliprole and tioxazofen and combinations thereof. In some embodiments, compositions of the present disclosure comprise abamectin, aldicarb, aldoxycarb, bifenthrin, carbofuran, chlorantraniliporle, chlothianidin, cyfluthrin, cyhalothrin, cypermethrin, cyantraniliprole, deltamethrin, dinotefuran, emamectin, ethiprole, fenamiphos, fipronil, flubendiamide, fosthiazate, imidacloprid, ivermectin, lambda-cyhalothrin, milbemectin, nitenpyram, oxamyl, permethrin, spinetoram, spinosad, spirodichlofen, spirotetramat, tefluthrin, thiacloprid, thiamethoxam, tioxazofen and/or thiodicarb. In some embodiments, compositions of the present disclosure comprise one or more carbamates, diamides, macrocyclic lactones,

neonicotinoids, organophosphates, phenylpyrazoles, pyrethrins, spinosyns, synthetic pyrethroids, tetronic acids and/or tetramic acids. In some embodiments, compositions of the present disclosure comprise an insecticide selected from the group consisting of clothianidin, thiamethoxam, imidacloprid,

cyantraniliprole, chlorantraniliprole, fluopyram and tioxazafen.

In some embodiments, compositions of the present disclosure comprise one or more biopesticides (e.g., one or more biofungicides, bioinsecticides and/or bionematicides). Examples of microbial strains that exhibit biopesticidal activity are included in Appendix A, along with strains that exhibit nitrogen- fixing activity, phosphate-solubilizing activity, etc. Additional examples of pesticides may be found in Bradley, Managing Diseases, in ILLINOIS AGRONOMY HANDBOOK (2008); Hager, Weed Management, in ILLINOIS AGRONOMY HANDBOOK (2008); LOUX ET AL., WEED CONTROL GUIDE FOR OHIO, INDIANA AND ILLINOIS (2015); Niblack, Nematodes, in ILLINOIS AGRONOMY HANDBOOK (2008); and Steffey and Gray, Managing Insect Pests, in ILLINOIS AGRONOMY HANDBOOK (2008).

Compositions of the present disclosure may comprise any suitable plant signal molecule(s), including, but not limited to, lipo-chitooligosaccharides (LCOs), chitin oligomers, chitosan oligomers, chitinous compounds, flavonoids, non-flavonoid nod-gene inducers, jasmonic acid or derivatives thereof, linoleic acid or derivatives thereof, linolenic acid or derivatives thereof and karrikins. Compositions of the present disclosure may comprise any suitable LCO(s). LCOs, sometimes referred to as symbiotic nodulation (Nod) signals or Nod factors, consist of an oligosaccharide backbone of b-l,4-linked N-acetyl-D-glucosamine ("GIcNAc") residues with an N-linked fatty acyl chain condensed at the non-reducing end. LCOs differ in the number of GIcNAc residues in the backbone, in the length and degree of saturation of the fatty acyl chain and in the substitutions of reducing and non-reducing sugar residues. See, e.g., Denarie, et al., ANN. REV. BIOCHEM. 65:503 (1996); Hamel, et al., PLANTA 232:787 (2010); Prome, et al., PURE & APPL. CHEM.70(1):55 (1998).

In some embodiments, inoculant compositions of the present disclosure comprise one or more LCOs represented by formula I:

in which G is a hexosamine which can be substituted, for example, by an acetyl group on the nitrogen, a sulfate group, an acetyl group and/or an ether group on an oxygen; R 1 , R 2 , R 3 , R 5 , R 6 and R 7 , which may be identical or different, represent H, CH 3 CO--, C x H y CO-- where x is an integer between 0 and 17 and y is an integer between 1 and 35, or any other acyl group such as, for example, a carbamoyl; R 4 represents a saturated or mono-, di- or tri-unsaturated aliphatic chain containing at least 12 carbon atoms; and n is an integer between 1 and 4.

In some embodiments, inoculant compositions of the present disclosure comprise one or more LCOs represented by formula II:

in which R represents H or CH 3 CO-- and n is equal to 2 or 3. See, e.g., U.S. Patent No.5,549,718. A number of Bradyrhizobium japonicum-derived LCOs have also been described, including BjNod-V (C 18:1 ), BjNod-V (A C , C 18:1 ), BjNod-V (C 16:1 ) and BjNod-V (A C , C 16:0 ) (with "V" indicating the presence of five N-acetylglucosamines, "Ac" an acetylation, the number following the "C" indicating the number of carbons in the fatty acid side chain and the number following the ":" indicating the number of double bonds). See, e.g., U.S. Patent Nos.5,175,149 and 5,321,011. Additional LCOs obtained from bacterial strains include NodRM, NodRM-1, NodRM-3. When acetylated (the R=CH 3 CO--), they become AcNodRM-1 and AcNodRM-3, respectively (U.S. Patent No.5,545,718).

In some embodiments, inoculant compositions of the present disclosure comprise one or more LCOs represented by formula III:

in which n = 1 or 2; R 1 represents C16, C16:0, C16:1, C16:2, C18:0, C18:1D9Z or C18:1D11Z; and R 2 represents hydrogen or SO 3 H.

In some embodiments, inoculant compositions of the present disclosure comprise one or more LCOs represented by formula IV:

in which R 1 represents C14:0, 3OH-C14:0, iso-C15:0, C16:0, 3-OH-C16:0, iso-C15:0, C16:1, C16:2, C16:3, iso-C17:0, iso-C17:1, C18:0, 3OH-C18:0, C18:0/3-OH, C18:1, OH-C18:1, C18:2, C18:3, C18:4, C19:1 carbamoyl, C20:0, C20:1, 3-OH-C20:1, C20:1/3-OH, C20:2, C20:3, C22:1 and C18-26(w-1)-OH (which according to D'Haeze, et al., Glycobiology 12:79R-105R (2002), includes C18, C20, C22, C24 and C26 hydroxylated species and C16:1D9, C16:2 (D2,9) and C16:3 (D2,4,9)); R 2 represents hydrogen or methyl; R 3 represents hydrogen, acetyl or carbamoyl; R 4 represents hydrogen, acetyl or carbamoyl; R 5 represents hydrogen, acetyl or carbamoyl; R 6 represents hydrogen, arabinosyl, fucosyl, acetyl, SO 3 H, sulfate ester, 3-0-S-2-0-MeFuc, 2-0-MeFuc and 4-0-AcFuc; R 7 represents hydrogen, mannosyl or glycerol; R 8 represents hydrogen, methyl, or–CH 2 OH; R 9 represents hydrogen, arabinosyl, or fucosyl; R 10 represents hydrogen, acetyl or fucosyl; and n represents 0, 1, 2 or 3. Naturally occurring LCOs embraced by this structure are described in D'Haeze, et al., supra.

Further examples of LCOs (and derivatives thereof) that may be useful in compositions and methods of the present disclosure are provided below as structures V–XXXIII:

LCOs may be obtained from any suitable source. In some embodiments, the LCO is obtained (i.e., isolated and/or purified) from a bacterial strain. For example, in some embodiments, compositions of the present disclosure comprise one or more LCOs obtained from a of Azorhizobium, Bradyrhizobium (e.g., B. japonicum), Mesorhizobium, Rhizobium (e.g., R. leguminosarum), or Sinorhizobium (e.g., S. meliloti). In some embodiments, the LCO is obtained (i.e., isolated and/or purified) from a mycorrhizal fungus. For example, in some embodiments, compositions of the present disclosure comprise one or more LCOs obtained from a strain of Glomerocycota (e.g., Glomus intraradicus). See, e.g., WO 2010/049751 (in which the LCOs are referred to as "Myc factors"). In some embodiments, the LCO is synthetic. For example, in some embodiments, compositions of the present disclosure comprise one or more of the synthetic LCOs described in WO 2005/063784, WO 2007/117500 and/or WO 2008/071674. In some embodiments, the synthetic LCO contains one or more modifications or substitutions, such as those described in Spaink, CRIT. REV. PLANT SCI. 54:257 (2000) and D'Haeze, supra. LCOs and precursors for the construction of LCOs (e.g., chitin oligomers, which are themselves useful as plant signal molecules) may be synthesized by genetically engineered organisms. See, e.g., Samain et al., CARBOHYDRATE RES.302:35 (1997); Cottaz, et al., METH. ENG.7(4):311 (2005); and Samain, et al., J. BIOTECHNOL.72:33 (1999).

It is to be understood that compositions and methods of the present disclosure may comprise analogues, derivatives, hydrates, isomers, salts and/or solvates of LCOs. Thus, in some embodiments, compositions of the present disclosure comprise one, two, three, four, five, six, seven, eight, nine, ten, or more LCOs represented by one or more of formulas I–IV and/or structures V–XXXIII and/or one, two, three, four, five, six, seven, eight, nine, ten, or more analogues, derivatives, hydrates, isomers, salts and/or solvates of LCOs represented by one or more of formulas I–IV and/or structures V–XXXIII.

LCOs (and derivatives thereof) may be utilized in various forms of purity and may be used alone or in the form of a culture of LCO-producing bacteria or fungi. In some embodiments, the LCO(s) included in compositions of the present disclosure is/are at least 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, 99.5% or more pure.

Compositions of the present disclosure may comprise any suitable chitin oligomer(s) and/or chitosan oligomer(s). See, e.g., D'Haeze et al., GLYCOBIOL.12(6):79R (2002); Demont-Caulet et al., PLANT PHYSIOL.120(1):83 (1999); Hanel et al., PLANTA 232:787 (2010); Muller et al., PLANT PHYSIOL.124:733 (2000); Robina et al., TETRAHEDRON 58:521-530 (2002); Rouge et al., Docking of Chitin Oligomers and Nod Factors on Lectin Domains of the LysM-RLK Receptors in the Medicago-Rhizobium Symbiosis, in THE MOLECULAR IMMUNOLOGY OF COMPLEX CARBOHYDRATES-3 (Springer Science, 2011); Van der Holst et al., CURR. OPIN. STRUC. BIOL. 11:608 (2001); Wan et al., PLANT CELL 21:1053 (2009); and PCT/F100/00803 (2000).

In some embodiments, inoculant compositions of the present disclosure comprise one or more chitin oligosaccharides represented by formula XXXIV:

in which R 1 represents hydrogen or methyl; R 2 represents hydrogen or methyl; R 3 represents hydrogen, acetyl or carbamoyl; R 4 represents hydrogen, acetyl or carbamoyl; R 5 represents hydrogen, acetyl or carbamoyl; R 6 represents hydrogen, arabinosyl, fucosyl, acetyl, sulfate ester, 3-0-S-2-0-MeFuc, 2-0- MeFuc and 4-0-AcFuc; R 7 represents hydrogen, mannosyl or glycerol; R 8 represents hydrogen, methyl, or –CH 2 OH; R 9 represents hydrogen, arabinosyl, or fucosyl; R 10 represents hydrogen, acetyl or fucosyl; and n represents 0, 1, 2 or 3.

In some embodiments, inoculant compositions of the present disclosure comprise one or more chitin oligosaccharides represented by formula XXXV:

in which n = 1 or 2; R 1 represents hydrogen or methyl; and R 2 represents hydrogen or SO 3 H.

Further examples of oligosaccharides (and derivatives thereof) that may be useful in compositions and methods of the present disclosure are provided below as structures XXXVI–LXXXIII:

In some embodiments, inoculant compositions of the present disclosure comprise one or more of the oligosaccharides set forth above as structures XXXVI–LXXXIII in a deacetylated form (e.g., an oligosaccharide corresponding to structure XXXVI above except that one or more of the acetyl groups has been removed, optionally replaced by a hydrogen or methyl group).

Chitin oligosaccharides and chitosan oligosaccharides may be obtained from any suitable source. Chitin oligosaccharides and chitosan oligosaccharides may be harvested from chitin/chitosan (see, e.g., Aam et al., MAR. DRUGS 8:1482 (2010); D'Haeze et al., GLYCOBIOL.12(6):79R (2002); Demont-Caulet et al., PLANT PHYSIOL.120(1):83 (1999); Hanel et al., PLANTA 232:787 (2010); Limpanavech et al., SCIENTIA HORTICULTURAE 116:65 (2008); Lodhi et al., BIOMED RES. INTL. Vol. 2014 Art. 654913 (March 2014); Mourya et al., POLYMER SCI.53(7):583 (2011); Muller et al., PLANT PHYSIOL.124:733 (2000); Robina et al., TETRAHEDRON 58:521 (2002); Rouge et al., The Molecular Immunology of Complex Carbohydrates, in ADVANCES IN EXPERIMENTAL MEDICINE AND BIOLOGY (Springer Science, 2011); Van der Holst et al., CURR. OPIN. STRUC. BIOL. 11:608 (2001); Wan et al., PLANT CELL 21:1053 (2009); Xia et al., FOOD HYDROCOLLOIDS 25:170 (2011); PCT/F100/00803 (2000)). They may also be synthetically generated (see, e.g., Cottaz et al., METH. ENG.7(4):311 (2005); Samain et al., CARBOHYDRATE RES.302:35 (1997); Samain et al., J. BIOTECHNOL. 72:33 (1999)). In some embodiments, they are derived from a naturally occurring LCO. For example, in some embodiments, compositions of the present disclosure comprise one or more chitin/chitosan oligosaccharides derived from an LCO obtained (i.e., isolated and/or purified) from a strain of Azorhizobium, Bradyrhizobium (e.g., B. japonicum), Mesorhizobium, Rhizobium (e.g., R. leguminosarum), Sinorhizobium (e.g., S. meliloti), or mycorhizzal fungus (e.g., Glomus intraradicus). In some embodiments, compositions of the present disclosure comprise one or more chitin oligosaccharides and/or chitosan oligosaccharides derived from an LCO obtained (i.e., isolated and/or purified) from a strain of Azorhizobium, Bradyrhizobium (e.g., B. japonicum), Mesorhizobium, Rhizobium (e.g., R. leguminosarum), Sinorhizobium (e.g., S. meliloti), or mycorhizzal fungus (e.g., Glomus intraradicus). In some embodiments, the chitin oligosaccharide(s) and/or chitosan oligosaccharide(s) is/are derived from an LCO represented by one or more of formulas I–IV and/or structures V–XXXIII. Thus, in some embodiments, compositions of the present disclosure may comprise one or more chitin oligosaccharides represented by one or more of formulas I–IV and/or structures V–XXXIII except that the pendant fatty acid is replaced with a hydrogen or methyl group.

It is to be understood that compositions of the present disclosure may comprise analogues, derivatives, hydrates, isomers, salts and/or solvates of chitin oligosaccharides and/or chitosan oligosaccharides. Thus, in some embodiments, compositions of the present disclosure comprise one, two, three, four, five, six, seven, eight, nine, ten, or more chitin oligosaccharides represented by one or more of formulas XXXIV–XXXV and/or structures XXXVI–LXXXIII and/or one, two, three, four, five, six, seven, eight, nine, ten, or more analogues, derivatives, hydrates, isomers, salts and/or solvates of chitin oligosaccharides represented by one or more of formulas XXXIV–XXXV and/or structures XXXVI– LXXXIII.

Chitin oligosaccharides and chitosan oligosaccharides (and analogues, derivatives, hydrates, isomers, salts and/or solvates thereof) may be utilized in various forms of purity and may be used alone or in the form of a culture of CO-producing bacteria or fungi. In some embodiments, the chitin oligosaccharides and/or chitosan oligosaccharides included in compositions of the present disclosure is/are at least 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, 99.5% or more pure.

compositions of the present disclosure may comprise any suitable chitinous compound(s), including, but not limited to, chitin (IUPAC: N-[5-[[3-acetylamino-4,5-dihydroxy-6- (hydroxymethyl)oxan-2yl]methoxymethyl]-2-[[5-acetylamino-4,6 -dihydroxy-2-(hydroxymethyl)oxan-3- yI]methoxymethyl]-4-hydroxy-6-(hydroxymethyl)oxan-3-ys]ethan amide), chitosan(IUPAC: 5-amino-6- [5-amino-6-[5-amino-4,6-dihydroxy-2(hydroxymethyl)oxan-3-yl] oxy-4-hydroxy-2-(hydroxymethyl)oxan- 3-yl]oxy-2(hydroxymethyl)oxane-3,4-diol) and isomers, salts and solvates thereof.

Chitins and chitosans, which are major components of the cell walls of fungi and the exoskeletons of insects and crustaceans, are composed of GIcNAc residues.

Chitins and chitosans may be obtained commercially or prepared from insects, crustacean shells, or fungal cell walls. Methods for the preparation of chitin and chitosan are known in the art. See, e.g., U.S. Patent Nos.4,536,207 (preparation from crustacean shells) and 5,965,545 (preparation from crab shells and hydrolysis of commercial chitosan); Pochanavanich, et al., LETT. APPL. MICROBIOL.35:17 (2002) (preparation from fungal cell walls).

Deacetylated chitins and chitosans may be obtained that range from less than 35% to greater than 90% deacetylation and cover a broad spectrum of molecular weights, e.g., low molecular weight chitosan oligomers of less than 15kD and chitin oligomers of 0.5 to 2kD; "practical grade" chitosan with a molecular weight of about 15kD; and high molecular weight chitosan of up to 70kD. Chitin and chitosan compositions formulated for seed treatment are commercially available. Commercial products include, for example, ELEXA® (Plant Defense Boosters, Inc.) and BEYOND™ (Agrihouse, Inc.).

compositions of the present disclosure may comprise any suitable flavonoid(s), including, but not limited to, anthocyanidins, anthoxanthins, chalcones, coumarins, flavanones, flavanonols, flavans and isoflavonoids, as well as analogues, derivatives, hydrates, isomers, polymers, salts and solvates thereof.

Flavonoids are phenolic compounds having the general structure of two aromatic rings connected by a three-carbon bridge. Classes of flavonoids include are known in the art. See, e.g., Jain et al., J. PLANT BIOCHEM. & BIOTECHNOL.11:1 (2002); Shaw et al., ENVIRON. MICROBIOL.11:1867 (2006). Flavonoid compounds are commercially available, e.g., from Novozymes BioAg, Saskatoon, Canada; Natland International Corp., Research Triangle Park, NC; MP Biomedicals, Irvine, CA; LC Laboratories, Woburn MA. Flavonoid compounds may be isolated from plants or seeds, e.g., as described in U.S. Patents 5,702,752; 5,990,291; and 6,146,668. Flavonoid compounds may also be produced by genetically engineered organisms, such as yeast, as described in Ralston et al., PLANT PHYSIOL.137:1375 (2005).

In some embodiments, compositions of the present disclosure comprise one or more

anthocyanidins. According to some embodiments, the composition comprises cyanidin, delphinidin, malvidin, pelargonidin, peonidin and/or petunidin.

In some embodiments, compositions of the present disclosure comprise one or more

anthoxanthins. According to some embodiments, the composition comprises one or more flavones (e.g., apigenin, baicalein, chrysin, 7,8-dihydroxyflavone, diosmin, flavoxate, 6—hydroxyflavone, luteolin, scutellarein, tangeritin and/or wogonin) and/or flavonols (e.g., amurensin, astragalin, azaleatin, azalein, fisetin, furanoflavonols galangin, gossypetin, 3-hydroxyflavone, hyperoside, icariin, isoquercetin, kaempferide, kaempferitrin, kaempferol, isorhamnetin, morin, myricetin, myricitrin, natsudaidain, pachypodol, pyranoflavonols quercetin, quericitin, rhamnazin, rhamnetin, robinin, rutin, spiraeoside, troxerutin and/or zanthorhamnin).

In some embodiments, compositions of the present disclosure comprise one or more flavanones. According to some embodiments, the composition comprises butin, eriodictyol, hesperetin, hesperidin, homoeriodictyol, isosakuranetin, naringenin, naringin, pinocembrin, poncirin, sakuranetin, sakuranin and/or sterubin.

In some embodiments, compositions of the present disclosure comprise one or more flavanonols. According to some embodiments, the composition comprises dihydrokaempferol and/or taxifolin.

In some embodiments, compositions of the present disclosure comprise one or more flavans. According to some embodiments, the composition comprises one or more flavan-3-ols (e.g., catechin (C), catechin 3-gallate (Cg), epicatechins (EC), epigallocatechin (EGC) epicatechin 3-gallate (ECg), epigallcatechin 3-gallate (EGCg), epiafzelechin, fisetinidol, gallocatechin (GC), gallcatechin 3-gallate (GCg), guibourtinidol, mesquitol, robinetinidol, theaflavin-3-gallate, theaflavin-3'-gallate, theflavin-3,3'- digallate, thearubigin), flavan-4-ols (e.g., apiforol and/or luteoforol) and/or flavan-3,4-diols (e.g., leucocyanidin, leucodelphinidin, leucofisetinidin, leucomalvidin, luecopelargonidin, leucopeonidin, leucorobinetinidin, melacacidin and/or teracacidin) and/or dimers, trimers, oligomers and/or polymers thereof (e.g., one or more proanthocyanidins).

In some embodiments, compositions of the present disclosure comprise one or more

isoflavonoids. According to some embodiments, the composition comprises one or more isoflavones (e.g, biochanin A, daidzein, formononetin, genistein and/or glycitein), isoflavanes (e.g., equol, ionchocarpane and/or laxifloorane), isoflavandiols, isoflavenes (e.g., glabrene, haginin D and/or 2-methoxyjudaicin), coumestans (e.g., coumestrol, plicadin and/or wedelolactone), pterocarpans and/or roetonoids.

compositions of the present disclosure may comprise any suitable flavonoid derivative, including, but not limited to, neoflavonoids (e.g, calophyllolide, coutareagenin, dalbergichromene, dalbergin, nivetin) and pterocarpans (e.g., bitucarpin A, bitucarpin B, erybraedin A, erybraedin B, erythrabyssin II, erthyrabissin-1, erycristagallin, glycinol, glyceollidins, glyceollins, glycyrrhizol, maackiain, medicarpin, morisianine, orientanol, phaseolin, pisatin, striatine, trifolirhizin).

Flavonoids and derivatives thereof may be incorporated into compositions of the present disclosure in any suitable form, including, but not limited to, polymorphic and crystalline forms.

compositions of the present disclosure may comprise any suitable non-flavonoid nod-gene inducer(s), including, but not limited to, jasmonic acid ([1R-[1a,2b(Z)]]-3-oxo-2- (pentenyl)cyclopentaneacetic acid; JA), linoleic acid ((Z,Z)-9,12-Octadecadienoic acid) and linolenic acid ((Z,Z,Z)-9,12,15-octadecatrienoic acid), as well as analogues, derivatives, hydrates, isomers, polymers, salts and solvates thereof.

Jasmonic acid and its methyl ester, methyl jasmonate (MeJA), collectively known as jasmonates, are octadecanoid-based compounds that occur naturally in some plants (e.g., wheat), fungi (e.g.,

Botryodiplodia theobromae, Gibbrella fujikuroi), yeast (e.g., Saccharomyces cerevisiae) and bacteria (e.g., Escherichia coli). Linoleic acid and linolenic acid may be produced in the course of the biosynthesis of jasmonic acid. Jasmonates, linoleic acid and linolenic acid (and their derivatives) are reported to be inducers of nod gene expression or LCO production by rhizobacteria. See, e.g., Mabood, et al. PLANT PHYSIOL. BIOCHEM.44(11):759 (2006); Mabood et al., AGR. J.98(2):289 (2006); Mabood, et al., FIELD CROPS RES.95(2-3):412 (2006); Mabood & Smith, Linoleic and linolenic acid induce the expression of nod genes in Bradyrhizobium japonicum USDA 3, PLANT BIOL. (2001). Non-limiting examples of derivatives of jasmonic acid, linoleic acid, linolenic acid include esters, amides, glycosides and salts. Representative esters are compounds in which the carboxyl group of linoleic acid, linolenic acid, or jasmonic acid has been replaced with a --COR group, where R is an --OR 1 group, in which R 1 is: an alkyl group, such as a C 1 -C 8 unbranched or branched alkyl group, e.g., a methyl, ethyl or propyl group; an alkenyl group, such as a C 2 -C 8 unbranched or branched alkenyl group; an alkynyl group, such as a C 2 -C 8 unbranched or branched alkynyl group; an aryl group having, for example, 6 to 10 carbon atoms; or a heteroaryl group having, for example, 4 to 9 carbon atoms, wherein the heteroatoms in the heteroaryl group can be, for example, N, O, P, or S. Representative amides are compounds in which the carboxyl group of linoleic acid, linolenic acid, or jasmonic acid has been replaced with a --COR group, where R is an NR 2 R 3 group, in which R 2 and R 3 are independently: hydrogen; an alkyl group, such as a C 1 -C 8 unbranched or branched alkyl group, e.g., a methyl, ethyl or propyl group; an alkenyl group, such as a C 2 -C 8 unbranched or branched alkenyl group; an alkynyl group, such as a C 2 -C 8 unbranched or branched alkynyl group; an aryl group having, for example, 6 to 10 carbon atoms; or a heteroaryl group having, for example, 4 to 9 carbon atoms, wherein the heteroatoms in the heteroaryl group can be, for example, N, O, P, or S. Esters may be prepared by known methods, such as acid-catalyzed nucleophilic addition, wherein the carboxylic acid is reacted with an alcohol in the presence of a catalytic amount of a mineral acid. Amides may also be prepared by known methods, such as by reacting the carboxylic acid with the appropriate amine in the presence of a coupling agent such as dicyclohexyl carbodiimide (DCC), under neutral conditions. Suitable salts of linoleic acid, linolenic acid and jasmonic acid include e.g., base addition salts. The bases that may be used as reagents to prepare metabolically acceptable base salts of these compounds include those derived from cations such as alkali metal cations (e.g., potassium and sodium) and alkaline earth metal cations (e.g., calcium and magnesium). These salts may be readily prepared by mixing together a solution of linoleic acid, linolenic acid, or jasmonic acid with a solution of the base. The salts may be precipitated from solution and be collected by filtration or may be recovered by other means such as by evaporation of the solvent.

compositions of the present disclosure may comprise any suitable karrakin(s), including, but not limited to, 2H-furo[2,3-c]pyran-2-ones, as well as analogues, derivatives, hydrates, isomers, polymers, salts and solvates thereof.

In some embodiments, the inoculant composition comprises one or more karrakins represented by formula LXXXIV:

in which Z is O, S or NR 5 ; R 1 , R 2 , R 3 and R 4 are each independently H, alkyl, alkenyl, alkynyl, phenyl, benzyl, hydroxy, hydroxyalkyl, alkoxy, phenyloxy, benzyloxy, CN, COR 6 , COOR=, halogen, NR 6 R 7 , or NO 2 ; and R 5 , R 6 and R 7 are each independently H, alkyl or alkenyl, or a biologically acceptable salt thereof.

Examples of biologically acceptable salts of karrakins include acid addition salts formed with biologically acceptable acids, examples of which include hydrochloride, hydrobromide, sulphate or bisulphate, phosphate or hydrogen phosphate, acetate, benzoate, succinate, fumarate, maleate, lactate, citrate, tartrate, gluconate; methanesulphonate, benzenesulphonate and p-toluenesulphonic acid.

Additional biologically acceptable metal salts may include alkali metal salts, with bases, examples of which include the sodium and potassium salts. Examples of compounds embraced by formula XXXX and which may be suitable for use in the present disclosure include 3-methyl-2H-furo[2,3-c]pyran-2-one (where R 1 =CH 3 , R 2 , R 3 , R 4 =H), 2H-furo[2,3-c]pyran-2-one (where R 1 , R 2 , R 3 , R4=H), 7-methyl-2H- furo[2,3-c]pyran-2-one (where R 1 , R 2 , R 4 =H, R 3 =CH 3 ), 5-methyl-2H-furo[2,3-c]pyran-2-one (where R 1 , R 2 , R 3 =H, R 4 =CH 3 ), 3,7-dimethyl-2H-furo[2,3-c]pyran-2-one (where R 1 , R 3 =CH 3 , R 2 , R 4 =H), 3,5- dimethyl-2H-furo[2,3-c]pyran-2-one (where R 1 , R 4 =CH 3 , R 2 , R 3 =H), 3,5,7-trimethyl-2H-furo[2,3-c]pyran- 2-one (where R 1 , R 3 , R 4 =CH 3 , R 2 =H), 5-methoxymethyl-3-methyl-2H-furo[2,3-c]pyran-2-one (where R 1 =CH 3 , R 2 , R 3 =H, R 4 =CH 2 OCH 3 ), 4-bromo-3,7-dimethyl-2H-furo[2,3-c]pyran-2-one (where R 1 , R 3 =CH 3 , R 2 =Br, R 4 =H), 3-methylfuro[2,3-c]pyridin-2(3H)-one (where Z=NH, R 1 =CH 3 , R 2 , R 3 , R 4 =H) and 3,6-dimethylfuro[2,3-c]pyridin-2(6H)-one (where Z=N--CH 3 , R 1 =CH 3 , R 2 , R 3 , R 4 =H). See, e.g., U.S. Patent No.7,576,213; Halford, Smoke Signals, in CHEM. ENG. NEWS (April 12, 2010) (reporting that karrikins or butenolides contained in smoke act as growth stimulants and spur seed germination after a forest fire and can invigorate seeds such as corn, tomatoes, lettuce and onions that had been stored).

compositions of the present disclosure may comprise gluconolactone and/or one or more analogues, derivatives, hydrates, isomers, polymers, salts and/or solvates thereof.

compositions of the present disclosure may comprise any suitable excipient(s), including, but not limited to, dispersants, drying agents, anti-freezing agents, seed flowability agents, safeners, anti-settlign agents, pH buffers and adhesives.

compositions of the present disclosure may comprise any suitable agriculturally acceptable dispersant(s), including, but not limited to, surfactants and wetting agents. Selection of appropriate dispersants will depend on the intended application(s) and the microorganism(s) present in the composition. In general, the dispersant(s) will have low toxicity for the microorganism(s) in the composition and for the plant part(s) to which the composition is to be applied. In some embodiments, the dispersant(s) will be selected to wet and/or emulsify one or more soils. Non-limiting examples of dispersants include Atlox™ (e.g., 4916, 4991; Croda International PLC, Edison, NJ), Atlox

METASPERSE™ (Croda International PLC, Edison, NJ), BIO-SOFT® (e.g., N series, such as N1-3, N1- 7, N1-5, N1-9, N23-3, N2.3-6.5, N25-3, N25-7, N25-9, N91-2.5, N91-6, N91-8; Stepan Company, Northfield, IL), MAKON® nonionic surfactants (e.g., DA-4, DA-6 and DA-9; Stepan Company, Northfield, IL), MORWET® powders (Akzo Nobel Surface Chemistry LLC, Chicago, IL),

MULTIWET™ surfactants (e.g., MO-85P-PW-(AP); Croda International PLC, Edison, NJ), SILWET® L-77 (Helena Chemical Company, Collierville, TN), SPAN™ surfactants (e.g., 20, 40, 60, 65, 80 and 85; Croda Inc., Edison NJ), TAMOL™ dispersants (The Dow Chemical Company, Midland, MI ),

TERGITOL™ surfactants (e.g., TMN-6 and TMN-100X; The Dow Chemical Company, Midland, MI), TERSPERSE surfactants (e.g., 2001, 2020, 2100, 2105, 2158, 2700, 4894 and 4896; Hunstman Corp., The Woodlands, TX), TRITON™ surfactants (e.g., X-100; The Dow Chemical Company, Midland, MI), TWEEN® surfactants (e.g., TWEEN® 20, 21, 22, 23, 28, 40, 60, 61, 65, 80, 81 and 85; Croda

International PLC, Edison, NJ) and combinations thereof. Additional examples of dispersants may be found in BAIRD & ZUBLENA.1993. SOIL FACTS: USING WETTING AGENTS (NONIONIC SURFACTANTS) ON SOIL (North Carolina Cooperative Extension Service Publication AG-439-25) (1993); BURGES,

FORMULATION OF MICROBIAL BIOPESTICIDES: BENEFICIAL MICROORGANISMS, NEMATODES AND SEED TREATMENTS (Springer Science & Business Media) (2012); MCCARTY, WETTING AGENTS (Clemson University Cooperative Extension Service Publication) (2001). In some embodiments, compositions of the present disclosure comprise one or more anionic surfactants. According to some embodiments, the composition comprises one or more water-soluble anionic surfactants and/or one or more water-insoluble anionic surfactants, optionally one or more anionic surfactants selected from the group consisting of alkyl carboxylates (e.g., sodium stearate), alkyl sulfates (e.g., alkyl lauryl sulfate, sodium lauryl sulfate), alkyl ether sulfates, alkyl amido ether sulfates, alkyl aryl polyether sulfates, alkyl aryl sulfates, alkyl aryl sulfonates, alkyl sulfonates, alkyl amide sulfonates, alkyl aryl sulfonates, alkyl benzene sulfonates, alkyl diphenyloxide sulfonate, alpha-olefin sulfonates, alkyl naphthalene sulfonates, paraffin sulfonates, alkyl sulfosuccinates, alkyl ether sulfosuccinates, alkylamide sulfosuccinates, alkyl sulfosuccinamates, alkyl sulfoacetates, alkyl phosphates, alkyl ether phosphates, acyl sarconsinates, acyl isethionates, N-acyl taurates, N-acyl-N-alkyltaurates, benzene sulfonates, cumene sulfonates, dioctyl sodium sulfosuccinate, ethoxylated sulfosuccinates, lignin sulfonates, linear alkylbenzene sulfonates, monoglyceride sulfates, perfluorobutanesulfonate, perfluorooctanesulfonate, phosphate ester, styrene acrylic polymers, toluene sulfonates and xylene sulfonates.

In some embodiments, compositions of the present disclosure comprise one or more cationic surfactants. According to some embodiments, the composition comprises one or more pH-dependent amines and/or one or more quaternary ammonium cations, optionally one or more cationic surfactants selected from the group consisting of alkyltrimethylammonium salts (e.g., cetyl trimethylammonium bromide, cetyl trimethylammonium chloride), cetylpyridinium chloride, benzalkonium chloride, benzethonium chloride, 5-Bromo-5-nitro-1,3-dioxane, dimethyldioctadecylammonium chloride, cetrimonium bromide, dioctadecyldimethylammonium bromide and/or octenidine dihydrochloride.

In some embodiments, compositions of the present disclosure comprise one or more nonionic surfactants. According to some embodiments, the composition comprises one or more water-soluble nonionic surfactants and/or one or more water-insoluble nonionic surfactants, optionally one or more nonionic surfactants selected from the group consisting of alcohol ethoxylates (e.g., TERGITOL™ 15-S surfactants, such as TERGITOL™15-S-9 (The Dow Chemical Company, Midland, MI)), alkanolamides, alkanolamine condensates, carboxylic acid esters, cetostearyl alcohol, cetyl alcohol, cocamide DEA, dodecyldimethylamine oxides, ethanolamides, ethoxylates of glycerol ester and glycol esters, ethylene oxide polymers, ethylene oxide-propylene oxide copolymers, glucoside alkyl ethers, glycerol alkyl ethers, glycerol esters, glycol alkyl ethers (e.g., polyoxyethylene glycol alkyl ethers, polyoxypropylene glycol alkyl ethers), glycol alkylphenol ethers (e.g., polyoxyethylene glycol alkylphenol ethers,), glycol esters, monolaurin, pentaethylene glycol monododecyl ethers, poloxamer, polyamines, polyglycerol

polyricinoleate, polysorbate, polyoxyethylenated fatty acids, polyoxyethylenated mercaptans, polyoxyethylenated polyoxyproylene glycols, polyoxyethylene glycol sorbitan alkyl esters, polyethylene glycol-polypropylene glycol copolymers, polyoxyethylene glycol octylphenol ethers, polyvinyl pynolidones, sugar-based alkyl polyglycosides, sulfoanylamides, sorbitan fatty acid alcohol ethoxylates, sorbitan fatty acid ester ethoxylates, sorbitan fatty acid ester and/or tertiary acetylenic glycols.

In some embodiments, compositions of the present disclosure comprise at least one nonionic surfactant. According to some embodiments, the composition comprises at least one water insoluble nonionic surfactant and at least one water soluble nonionic surfactant. In some embodiments, compositions of the present disclosure comprise a combination of nonionic surfactants having hydrocarbon chains of substantially the same length.

In some embodiments, compositions of the present disclosure comprise one or more zwitterionic surfactants. According to some embodiments, the composition comprises one or more betaines and/or one or more sultaines, optionally one or more zwitterionic surfactants selected from the group consisting of 3- [(3-Cholamidopropyl)dimethylammonio]-1-propanesulfonate, cocamidopropyl betaine, cocamidopropyl hydroxysultaine, phosphatidylserine, phosphatidylethanolamine, phosphatidylcholine and/or one or more sphingomyelins.

In some embodiments, compositions of the present disclosure comprise one or more soaps and/or organosilicone surfactants. According to some embodiments, the composition comprises one or more alkali metal salts of fatty acids.

In some embodiments, compositions of the present disclosure comprise one or more wetting agents. According to some embodiments, the composition comprises one or more naphthalene sulfonates, optionally one or more alkyl naphthalene sulfonates (e.g., sodium alkyl naphthalene sulfonate), one or more isopropyl naphthalene sulfonates (e.g., sodium isopropyl naphthalene sulfonate) and/or one or more butyl naphthalene sulfonates (e.g., sodium n-butyl naphthalene sulfonate).

Compositions of the present disclosure may comprise any suitable drying agent(s), including, but not limited to, drying powders. Non-limiting examples of drying agents include AEROSIL® hydrophobic fumed silica powders (Evonik Corporation, Parsippany, NJ), BENTOLITE® powders (BYK-Chemie GmbH, Wesel, Germany), INCOTEC® powders (INCOTEC Inc., Salinas, CA), SIPERNAT® silica powders (Evonik Corporation, Parsippany, NJ) and combinations thereof. Additional examples of drying agents may be found in BURGES, FORMULATION OF MICROBIAL BIOPESTICIDES: BENEFICIAL

MICROORGANISMS, NEMATODES AND SEED TREATMENTS (Springer Science & Business Media) (2012). In some embodiments, compositions of the present disclosure comprise calcium stearate, clay (e.g., attapulgite clay, montmorillonite clay), graphite, magnesium stearate, magnesium sulfate, powdered milk, silica (e.g., fumed silica, hydrophobically-coated silica, precipitated silica), soy lecithin and/or talc.

compositions of the present disclosure may comprise any suitable anti-freezing agent(s), including, but not limited to, ethylene glycol, glycerin, propylene glycol and urea.

compositions of the present disclosure may comprise any seed flowability agent to improve the lubricity of the treated seeds. The flowability agent may comprise one or more liquid lubricants, solid lubricants, liquid emulsions, or suspensions of solid lubricants. Non-limiting examples of flowability agents include, for example, lubricants such as fats and oils, natural and synthetic waxes, graphite, talc, fluoropolymers (e.g., polytetrafluoroethylene), and solid lubricants such as molybdenum disulfide and tungsten disulfide. In some instances, the flowability agent comprises a wax material. Non-limiting examples of wax materials that can be incorporated into the liquid seed treatment composition include plant and animal-derived waxes such as carnauba wax, candelilla wax, ouricury wax, beeswax, spermaceti, and petroleum derived waxes, such as paraffin wax. For example, in some instances, the flowability agent comprises carnauba wax. In some instances, the flowability agent comprises an oil. For example, the flowability agent may comprise soybean oil. Non-limiting examples of commercially available wax materials suitable for use as flowability agents include AQUAKLEAN 418 supplied by Micro Powders, Inc. (an anionic aqueous emulsion comprising extra light carnauba wax at 35% solids content).

compositions of the present disclosure may comprise any suitable safener(s), including, but not limited to, napthalic anhydride.

compositions of the present disclosure may comprise any suitable pH buffer(s), including, but not limited to, potassium phosphate monobasic and potassium phosphate dibasic. In some embodiments, the composition comprises one or more pH buffers selected to provide a composition having a pH of less than 10, typically from about 4.5 to about 9.5, from about 6 to about 8, or about 7.

compositions of the present disclosure may comprise any suitable anti-settling agent(s), including, but not limited to, polyvinyl acetate, polyvinyl alcohols with different degrees of hydrolysis,

polyvinylpyrrolidones, polyacrylates, acrylate-, polyol- or polyester-based paint system binders which are soluble or dispersible in water, moreover copolymers of two or more monomers such as acrylic acid, methacrylic acid, itaconic acid, maleic acid, fumaric acid, maleic anhydride, vinylpyrrolidone, ethylenically unsaturated monomers such as ethylene, butadiene, isoprene, chloroprene, styrene, divinylbenzene, ot-methylstyrene or p-methylstyrene, further vinyl halides such as vinyl chloride and vinylidene chloride, additionally vinyl esters such as vinyl acetate, vinyl propionate or vinyl stearate, moreover vinyl methyl ketone or esters of acrylic acid or methacrylic acid with monohydric alcohols or polyols such as methyl acrylate, methyl methacrylate, ethyl acrylate, ethylene methacrylate, lauryl acrylate, lauryl methacrylate, decyl acrylate, N,N-dimethylamino-ethyl methacrylate, 2-hydroxyethyl methacrylate, 2-hydroxypropyl methacrylate or glycidyl methacrylate, furthermore diethyl esters or monoesters of unsaturated dicarboxylic acids, furthermore (meth)acrylamido-N-methylol methyl ether, amides or nitriles such as acrylamide, methacrylamide, N-methylol(meth)acrylamide, acrylonitrile, methacrylonitrile, and also N-substituted maleiraides and ethers such as vinyl butyl ether, vinyl isobutyl ether or vinyl phenyl ether, and combinations thereof.

compositions of the present disclosure may comprise any suitable adhesive(s), including, but not limited to, adhesive compositions comprising, consisting essentially of or consisting of one or more disaccharides (e.g. maltose), gums (e.g., cellulose gum, guar gum, gum arabic, gum combretum, xantham gum), maltodextrins (e.g., one or more maltodextrins (each and/or collectively) having a DEV of about 10 to about 20), monosaccharides, oils (e.g., mineral oil, olive oil, peanut oil, soybean oil and/or sunflower oil) and/or oligosaccharides.

compositions of the present disclosure may comprise any suitable effect pigment(s). Effect pigments, which are sometimes also referred to in the art as "pearl pigments," are a class of materials that provide reflectivity, shine, and/or a pearlescent effect when applied as a coating. In some instances, the effect pigment is in the form of a powder comprising a substrate material and a metal oxide coating. For example, the effect pigment may comprise a substrate material including but not limited to talc, silicate materials (e.g., mica), clay minerals, calcium carbonate, kaolin, phlogopite, alumina, and similar substances. In some instances, the substrate material comprises a hydrophilic material. The substrate material may be coated with a semi-transparent layer of a metal oxide, including but not limited to titanium dioxide, iron oxide, chromium oxide, or zirconium oxide. Alternatively, in some instances, the effect pigment comprises metal powder or metal flakes. The metal powder or metal flakes may comprise a metal including, but not limited to aluminum, copper, silver, or bronze. In some instances, the effect pigment comprises a silicate based substrate. Non-limiting examples of particulate silicates that can be incorporated into the dry powder coating include mica coated with titanium dioxide (e.g., SUNMICA FINE WHITE 2800102, which is commercially available from Sun Chemical Corp.). Other non-limiting examples of commercially available effect pigments that can be incorporated into the dry powder include MAGNA PEARL, LUMINA and MEARLIN pigments from BASF Corporation; PHIBRO PEARL from PhibroChem; and IRIDESIUM 120 from Aakash Chemicals. In some instances, the dry powder has a mean particle size of from about 1 to about 25 microns.

compositions of the present disclosure may comprise any suitable growth medium suitable for culturing one or more of the microorganisms in the composition. For example, in some embodiments, compositions of the present disclosure comprise Czapek-Dox medium, glycerol yeast extract, mannitol yeast extract, potato dextrose broth and/or YEM media.

Carriers, stabilizing compounds, biostimulants, microbial extracts, nutrients, pest attractants and/or feeding stimulants, pesticides, plant signal molecules, dispersants, drying agents, safeners, flowability agents, anti-settling agents, buffers, adhesives, etc. may be incorporated into compositions of the present disclosure in any suitable amount(s)/concentration(s). The absolute value of the

amount/concentration that is/are sufficient to cause the desired effect(s) may be affected by factors such as the type, size and volume of material to which the compositon will be applied, the type(s) of

microorganisms in the composition, the number of microorganisms in the composition, the stability of the microorganisms in the composition and storage conditions (e.g., temperature, relative humidity, duration). Those skilled in the art will understand how to select effective amounts/concentrations/combinations using routine dose-response experiments. Guidance for the selection of appropriate

amounts/concentrations/combinations can be found, for example, in International Patent Publication Nos. WO2017/044473, WO2017/044545, WO2017/116837, WO2017/116846, WO2017/210163,

WO2017/210166, WO2018/118740, WO2018/175681, WO2018/183491, WO2018/218008,

WO2018/218016 and WO2018/218035.

In some embodiments, compositions of the present disclosure comprise one or more carriers in an amount/concentration of about 1 to about 99% or more (by weight, based upon the total weight of the composition). For example, compositions of the present disclosure may comprsise about 1, 2, 3, 4, 5, 6, 7, 8, 9,10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 91, 92, 93, 94, 95, 96, 97, 98 or 99% (by weight) of one or more non-aqueous carriers.

In some embodiments, compositions of the present disclosure comprise one or more stabilizing compounds in an amount/concentration of about 0.0001 to about 95% or more (by weight, based upon the total of the composition). For example, compositions of the present disclosure may comprise about 0.0001 to about 0.001, about 0.001 to about 1%, about 0.25 to about 5%, about 1 to about 10%, about 5 to about 25%, about 10% to about 30%, about 20% to about 40%, about 25% to about 50%, about 30 to about 60%, about 50 to about 75%, or about 75 to about 95% (by weight), optionally about 0.0005, 0.001, 0.002, 0.003, 0.004, 0.005, 0.0075, 0.01, 0.02, 0.03, 0.04, 0.05.0.06, 0.07, 0.08, 0.09, 0.1, 0.2, 0.3, 0.4, 0.5, 1, 1.5, 2, 2.5, 3, 3.5, 4, 4.5, 5, 5.5, 6, 6.5, 7, 7.5, 8, 8.5, 9, 9.5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95%, of one or more maltodextrins, monosaccharides, disaccharides, sugar alcohols, humic acids, betaines, prolines, sarcosines, peptones, oxidation control components, hygroscopic polymers and/or UV protectants.

In some embodiments, compositions of the present disclosure comprise one or more stabilizing compounds at a concentration of about 1 x 10 -20 M to about 1 x 10 -1 M. For example, compositions of the present disclosure may comprise about 1 x 10 -15 M to about 1 x 10 -10 M, about 1 x 10 -14 M to about 1 x 10- 8 M, about 1 x 10 -14 M to about 1 x 10 -6 M, about 1 x 10 -12 M to about 1 x 10 -8 M, about 1 x 10 -12 M to about 1 x 10 -6 M, about 1 x 10 -10 M to about 1 x 10 -6 M, or about 1 x 10 -8 M to about 1 x 10 -2 M, optionally about 1 x 10 -20 M, 1 x 10 -19 M, 1 x 10 -18 M, 1 x 10 -17 M, 1 x 10 -16 M, 1 x 10 -15 M, 1 x 10 -14 M, 1 x 10 -13 M, 1 x 10 -12 M, 1 x 10 -11 M, 1 x 10 -10 M, 1 x 10 -9 M, 1 x 10 -8 M, 1 x 10 -7 M, 1 x 10 -6 M, 1 x 10 -5 M, 1 x 10 -4 M, 1 x 10 -3 M, 1 x 10 -2 M, 1 x 10 -1 M or more, of one or more maltodextrins, monosaccharides, disaccharides, sugar alcohols, humic acids, betaines, prolines, sarcosines, peptones, oxidation control components, hygroscopic polymers and/or UV protectants.

In some embodiments, compositions of the present disclosure comprise one or more

monosaccharides in an amount/concentration of about 0.005 to about 50% (by weight) of the composition. For example, compositions of the present disclosure may comprise about/at least/less than 0.01, 0.02, 0.03, 0.04, 0.05, 0.06, 0.07, 0.08, 0.09, 0.1, 0.15, 0.2, 0.25, 0.3, 0.35, 0.4, 0.45, 0.5, 0.75, 1, 1.25, 1.5, 2, 2.5, 3, 3.5, 4, 4.5, 5, 5.5, 6, 6.5, 7, 7.5, 8, 8.5, 9, 10, 15, 20, 25% (by weight) of one or more

monosaccharides (e.g., arabinose, fructose and/or glucose). In some embodiments, one or more monosaccharides is/are present in a concentration ranging from about 1 x 10 -20 M to about 1 x 10 -1 M. For example, one or more monosaccharides may be included at a concentration of about/at least/less than1 x 10 -20 M, 1 x 10 -19 M, 1 x 10 -18 M, 1 x 10 -17 M, 1 x 10 -16 M, 1 x 10 -15 M, 1 x 10 -14 M, 1 x 10 -13 M, 1 x 10 -12 M, 1 x 10 -11 M, 1 x 10 -10 M.

In some embodiments, compositions of the present disclosure comprise one or more disaccharides in an amount/concentration of about 0.005 to about 50% (by weight) of the composition. For example, compositions of the present disclosure may comprise about/at least/less than 0.01, 0.02, 0.03, 0.04, 0.05, 0.06, 0.07, 0.08, 0.09, 0.1, 0.15, 0.2, 0.25, 0.3, 0.35, 0.4, 0.45, 0.5, 0.75, 1, 1.25, 1.5, 2, 2.5, 3, 3.5, 4, 4.5, 5, 5.5, 6, 6.5, 7, 7.5, 8, 8.5, 9, 10, 15, 20, 25% (by weight) of one or more disaccharides (e.g., maltose, sucrose and/or trehalose). In some embodiments, one or more disaccharides is/are present in a concentration ranging from about 1 x 10 -20 M to about 1 x 10 -1 M. For example, one or more disaccharides may be included at a concentration of about/at least/less than 1 x 10 -20 M, 1 x 10 -19 M, 1 x 10 -18 M, 1 x 10- 17 M, 1 x 10 -16 M, 1 x 10 -15 M, 1 x 10 -14 M, 1 x 10 -13 M, 1 x 10 -12 M, 1 x 10 -11 M, 1 x 10 -10 M.

In some embodiments, compositions of the present disclosure comprise one or more

maltodextrins in an amount/concentration of about 0.001 to about 95% or more (by weight) of the composition. In some embodiments, the maltodextrin(s) comprise(s) about 0.001 to about 1%, about 0.25 to about 5%, about 1 to about 10%, about 5 to about 25%, about 10% to about 30%, about 20% to about 40%, about 25% to about 50%, about 50 to about 75%, or about 75 to about 95% (by weight) of the composition. For example, compositions of the present disclosure may comprise about/at least/less than 0.01, 0.02, 0.03, 0.04, 0.05.0.06, 0.07, 0.08, 0.09, 0.1, 0.2, 0.3, 0.4, 0.5, 1, 1.5, 2, 2.5, 3, 3.5, 4, 4.5, 5, 5.5, 6, 6.5, 7, 7.5, 8, 8.5, 9, 9.5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95% or more (by weight) of one or more maltodextrins (e.g., one or more maltodextrins (each and/or collectively) having a DEV value of about 15 to about 20).

In some embodiments, compositions of the present disclosure comprise one or more sugar alcohols in an amount/concentration of about 0.001 to about 95% or more (by weight) of the composition. In some embodiments, the sugar alcohol(s) (e.g., arabitol, mannitol, sorbitol and/or xylitol) comprise(s) about 0.001 to about 1%, about 0.25 to about 5%, about 1 to about 10%, about 5 to about 25%, about 10% to about 30%, about 20% to about 40%, about 25% to about 50%, about 50 to about 75%, or about 75 to about 95% (by weight) of the composition. For example, compositions of the present disclosure may comprise about/at least/less than 0.01, 0.02, 0.03, 0.04, 0.05.0.06, 0.07, 0.08, 0.09, 0.1, 0.2, 0.3, 0.4, 0.5, 1, 1.5, 2, 2.5, 3, 3.5, 4, 4.5, 5, 5.5, 6, 6.5, 7, 7.5, 8, 8.5, 9, 9.5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95% or more (by weight) of one or more sugar alcohols (e.g., arabitol, mannitol, sorbitol and/or xylitol).

In some embodiments, compositions of the present disclosure comprise one or more humic acids in an amount/concentration of about 0.001 to about 95% or more (by weight) of the composition. In some embodiments, the humic acid(s) (e.g., potassium humate) comprise(s) about 0.001 to about 1%, about 0.25 to about 5%, about 1 to about 10%, about 5 to about 25%, about 10% to about 30%, about 20% to about 40%, about 25% to about 50%, about 50 to about 75%, or about 75 to about 95% (by weight) of the composition. For example, compositions of the present disclosure may comprise about/at least/less than 0.01, 0.02, 0.03, 0.04, 0.05.0.06, 0.07, 0.08, 0.09, 0.1, 0.2, 0.3, 0.4, 0.5, 1, 1.5, 2, 2.5, 3, 3.5, 4, 4.5, 5, 5.5, 6, 6.5, 7, 7.5, 8, 8.5, 9, 9.5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95% or more (by weight) of one or more humic acids (e.g., potassium humate and/or sodium humate).

In some embodiments, compositions of the present disclosure comprise one or more UV protectants in an amount/concentration of about 0.0001 to about 5% or more (by weight) of the composition. In some embodiments, the UV protectant(s) (e.g., calcium lignosulfate and/or sodium lignosulfate) comprise(s) about 0.0001 to about 0.001, about 0.001 to about 1%, about 0.25 to about 5%, (by weight) of the composition. For example, compositions of the present disclosure may comprise about/at least/less than 0.0005, 0.001, 0.002, 0.003, 0.004, 0.005, 0.0075, 0.01, 0.02, 0.03, 0.04, 0.05, 0.06, 0.07, 0.08, 0.09, 0.1, 0.15, 0.2, 0.25, 0.3, 0.35, 0.4, 0.45, 0.5, 0.75, 1, 1.25, 1.5, 2, 2.5, 3, 3.5, 4, 4.5, 5% or more (by weight) of one or more UV protectants (e.g., calcium lignosulfate and/or sodium lignosulfate).

In some embodiments, compositions of the present disclosure comprise one or more oxidation control components in an amount/concentration of about 0.0001 to about 5% or more (by weight) of the composition. For example, compositions of the present disclosure may comprise about/at least/less than 0.0005, 0.001, 0.002, 0.003, 0.004, 0.005, 0.0075, 0.01, 0.02, 0.03, 0.04, 0.05, 0.06, 0.07, 0.08, 0.09, 0.1, 0.15, 0.2, 0.25, 0.3, 0.35, 0.4, 0.45, 0.5, 0.75, 1, 1.25, 1.5, 2, 2.5, 3, 3.5, 4, 4.5, 5% of one or more oxidation control components. In some embodiments, the amount/concentration of oxidation control components is about 0.005 to about 2% (by weight) of the composition. In some embodiments, the oxidation control component(s) is/are present in a concentration ranging from about 1 x 10 -20 M to about 1 x 10 -1 M. For example, one or more oxidation control components may be added at a concentration of about/at least/less than 1 x 10 -20 M, 1 x 10 -19 M, 1 x 10 -18 M, 1 x 10 -17 M, 1 x 10 -16 M, 1 x 10 -15 M, 1 x 10 -14 M, 1 x 10 -13 M, 1 x 10 -12 M, 1 x 10 -11 M, 1 x 10 -10 M. In some embodiments, compositions of the present disclosure comprise one or more commercial antioxidants used in accordance with the manufacturer's recommended amounts/concentrations. In some embodiments, compositions of the present disclosure comprise one or more commercial oxygen scavengers used in accordance with the manufacturer's recommended amounts/concentrations.

In some embodiments, compositions of the present disclosure comprise one or more stabilizing compounds in an amount/concentration sufficient to ensure Strains of the present disclosureremain viable following storage at 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39 and/or 40°C and 0, 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95% or more relative humidity for a period of 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 28, 32, 36, 40, 44, 48, 52, 56, 60, 64, 68, 72, 76, 80, 84, 88, 92, 96, 100, 104 weeks or more; desiccation by about 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95% or more; desiccation by about 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95% or more and storage at 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39 and/or 40°C and 0, 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95% or more relative humidity for a period of 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 28, 32, 36, 40, 44, 48, 52, 56, 60, 64, 68, 72, 76, 80, 84, 88, 92, 96, 100, 104 weeks or more; cryopreservation at or below -80°C for a period of 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 28, 32, 36, 40, 44, 48, 52, 56, 60, 64, 68, 72, 76, 80, 84, 88, 92, 96, 100, 104 weeks or more; application to plant propagation material (optionally, seed); application to plant propagation material and desiccation by about 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95% or more; application to a plant propagation material and storage at 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39 and/or 40°C and 0, 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95% or more relative humidity for a period of 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 28, 32, 36, 40, 44, 48, 52, 56, 60, 64, 68, 72, 76, 80, 84, 88, 92, 96, 100, 104 weeks or more; foliar application; foliar application and desiccation by about 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95% or more; and/or foliar application and exposure to temperatures of 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39 and/or 40°C and relative humidities of 0, 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95% or more for a period of 0.1, 0.2, 0.25, 0.5, 0.75, 1, 1.5, 2, 2.5, 3, 3.5, 4, 4.5, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21 days or more.

In some embodiments, compositions of the present disclosure comprise one or more stabilizing compounds in an amount/concentration sufficient to ensure at least 0.01, 0.05, 0.1, 0.5, 1, 2, 3, 4, 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95% of Strains of the present disclosureremain viable following storage at 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39 and/or 40°C and 0, 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95% or more relative humidity for a period of 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 28, 32, 36, 40, 44, 48, 52, 56, 60, 64, 68, 72, 76, 80, 84, 88, 92, 96, 100, 104 weeks or more; desiccation by about 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95% or more; desiccation by about 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95% or more and storage at 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39 and/or 40°C and 0, 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95% or more relative humidity for a period of 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 28, 32, 36, 40, 44, 48, 52, 56, 60, 64, 68, 72, 76, 80, 84, 88, 92, 96, 100, 104 weeks or more;

cryopreservation at or below -80°C for a period of 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 28, 32, 36, 40, 44, 48, 52, 56, 60, 64, 68, 72, 76, 80, 84, 88, 92, 96, 100, 104 weeks or more; application to plant propagation material (optionally, seed); application to plant propagation material and desiccation by about 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95% or more; application to a plant propagation material and storage at 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39 and/or 40°C and 0, 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95% or more relative humidity for a period of 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 28, 32, 36, 40, 44, 48, 52, 56, 60, 64, 68, 72, 76, 80, 84, 88, 92, 96, 100, 104 weeks or more; foliar application; foliar application and desiccation by about 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95% or more; and/or foliar application and exposure to temperatures of 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39 and/or 40°C and relative humidities of 0, 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95% or more for a period of 0.1, 0.2, 0.25, 0.5, 0.75, 1, 1.5, 2, 2.5, 3, 3.5, 4, 4.5, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21 days or more.

In some embodiments, compositions of the present disclosure comprise one or more stabilizing compounds in an amount/concentration sufficient to ensure at least 1 x 10 1 , 1 x 10 2 , 1 x 10 3 , 1 x 10 4 , 1 x 10 5 , 1 x 10 6 , 1 x 10 7 , 1 x 10 8 , 1 x 10 9 , 1 x 10 10 or more colony-forming units of Strains of the present disclosureremain viable per gram and/or milliliter of composition following storage at 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39 and/or 40°C and 0, 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95% or more relative humidity for a period of 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 28, 32, 36, 40, 44, 48, 52, 56, 60, 64, 68, 72, 76, 80, 84, 88, 92, 96, 100, 104 weeks or more; desiccation by about 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95% or more; desiccation by about 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95% or more and storage at 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39 and/or 40°C and 0, 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95% or more relative humidity for a period of 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 28, 32, 36, 40, 44, 48, 52, 56, 60, 64, 68, 72, 76, 80, 84, 88, 92, 96, 100, 104 weeks or more; cryopreservation at or below -80°C for a period of 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 28, 32, 36, 40, 44, 48, 52, 56, 60, 64, 68, 72, 76, 80, 84, 88, 92, 96, 100, 104 weeks or more; application to plant propagation material (optionally, seed);

application to plant propagation material and desiccation by about 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95% or more; application to a plant propagation material and storage at 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39 and/or 40°C and 0, 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95% or more relative humidity for a period of 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 28, 32, 36, 40, 44, 48, 52, 56, 60, 64, 68, 72, 76, 80, 84, 88, 92, 96, 100, 104 weeks or more; foliar application; foliar application and desiccation by about 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95% or more; and/or foliar application and exposure to temperatures of 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39 and/or 40°C and relative humidities of 0, 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95% or more for a period of 0.1, 0.2, 0.25, 0.5, 0.75, 1, 1.5, 2, 2.5, 3, 3.5, 4, 4.5, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21 days or more.

In some embodiments, compositions of the present disclosure comprise one or more stabilizing compounds in an amount/concentration sufficient to ensure the deliquescence relative humidity (DRH) of the composition is less than 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85 or 90 at the temperature(s) at which the composition is to be stored (e.g., 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39 and/or 40°C).

In some embodiments, compositions of the present disclosure comprise two or more stabilizing compounds that synergistically enhance the stability and/or survival of Strains of the present

disclosureremain.

Stablizing compounds may be incorporated into compositions of the present disclosure in any suitable ratio(s).

In some embodiments, compositions of the present disclosure comprise one or more

maltodextrins and one or more monosaccharides, disaccharides, sugar alcohols and/or humic acids in a maltodextrin:(monosaccharide, disaccharide, sugar alcohol and/or humic acid) ratio of about 5:95, 10:90, 15:85, 20:80, 25:75, 30:70, 35:65, 40:60, 45:55, 50:50, 55:45, 60:40, 65:35, 70:30, 75:25, 80:20, 85:15, 90:10, 95:5. For example, compositions of the present disclosure may comprise one or more maltodextrins (e.g., one or more maltodextrins (each and/or collectively) having a DEV of about 15 to about 20) and one or more sugar alcohols (e.g., sorbitol and/or xylitol) and/or humic acids (e.g., potassium humate) in a maltodextrin:(sugar alcohol/humic acid) ratio of about 5:95, about 15:85, about 25:75 or about 50:50.

In some embodiments, compositions of the present disclosure comprise one or more biostimulants in an amount/concentration of about 0.0001 to about 5% or more (by weight) of the composition. In some embodiments, the biostimulant(s) (e.g., glycine and/or seaweed extract) comprise(s) about about 0.0001, 0.0002, 0.0003, 0.0004, 0.0005, 0.0006, 0.0007, 0.0008, 0.0009, 0.001, 0.0015, 0.002, 0.0025, 0.003, 0.0035, 0.004, 0.0045, 0.005, 0.0055, 0.006, 0.0065, 0.007, 0.0075, 0.008, 0.0085, 0.009, 0.0095, 0.01, 0.015, 0.02, 0.025, 0.03, 0.035, 0.04, 0.045, 0.05, 0.06, 0.07, 0.08, 0.09, 0.1, 0.02, 0.3, 0.4, 0.5, 0.6, 0.7, 0.8, 0.9, 1 to about 1, 1.1, 1.2, 1.3, 1.4, 1.5, 1.6, 1.7, 1.8, 1.9, 2, 2.1, 2.2, 2.3, 2.4, 2.5, 2.6, 2.7, 2.8, 2.9, 3, 3.1, 3.2, 3.3, 3.4, 3.5, 3.6, 3.7, 3.8, 3.9, 4, 4.1, 4.2, 4.3, 4.4., 4.5, 4.6, 4.7, 4.8, 4.9, 5% (by weight) of the composition. For example, compositions of the present disclosure may comprise about 0.0005, 0.00075, 0.001, 0.002, 0.003, 0.004, 0.005, 0.006, 0.007, 0.008, 0.009, 0.01, 0.02, 0.03, 0.04, 0.05, 0.06, 0.07, 0.08, 0.09, 0.1, 0.15, 0.2, 0.25, 0.3, 0.35, 0.4, 0.45, 0.5, 0.55, 0.6, 0.65, 0.7, 0.75, 0.8, 0.85, 0.9, 0.95, 1, 1.1, 1.2, 1.3, 1.4, 1.5, 1.6, 1.7, 1.8, 1.9, 2, 2.1, 2.2, 2.3, 2.4, 2.5, 2.6, 2.7, 2.8, 2.9, 3, 3.1, 3.2, 3.3, 3.4, 3.5, 3.6, 3.7, 3.8, 3.9, 4, 4.1, 4.2, 4.3, 4.4., 4.5, 4.6, 4.7, 4.8, 4.9, 5% or more (by weight) of one or more biostimulants (e.g., glycine and/or seaweed extract).

In some embodiments, compositions of the present disclosure comprise one or more microbial extracts in an amount/concentration of about 0.0001 to about 5% or more (by weight) of the composition. In some embodiments, the microbial extract(s) comprise(s) about 0.0001, 0.0002, 0.0003, 0.0004, 0.0005, 0.0006, 0.0007, 0.0008, 0.0009, 0.001, 0.0015, 0.002, 0.0025, 0.003, 0.0035, 0.004, 0.0045, 0.005, 0.0055, 0.006, 0.0065, 0.007, 0.0075, 0.008, 0.0085, 0.009, 0.0095, 0.01, 0.015, 0.02, 0.025, 0.03, 0.035, 0.04, 0.045, 0.05, 0.06, 0.07, 0.08, 0.09, 0.1, 0.02, 0.3, 0.4, 0.5, 0.6, 0.7, 0.8, 0.9, 1 to about 1, 1.1, 1.2, 1.3, 1.4, 1.5, 1.6, 1.7, 1.8, 1.9, 2, 2.1, 2.2, 2.3, 2.4, 2.5, 2.6, 2.7, 2.8, 2.9, 3, 3.1, 3.2, 3.3, 3.4, 3.5, 3.6, 3.7, 3.8, 3.9, 4, 4.1, 4.2, 4.3, 4.4., 4.5, 4.6, 4.7, 4.8, 4.9, 5% (by weight) of the composition. For example, compositions of the present disclosure may comprise about 0.0005, 0.00075, 0.001, 0.002, 0.003, 0.004, 0.005, 0.006, 0.007, 0.008, 0.009, 0.01, 0.02, 0.03, 0.04, 0.05, 0.06, 0.07, 0.08, 0.09, 0.1, 0.15, 0.2, 0.25, 0.3, 0.35, 0.4, 0.45, 0.5, 0.55, 0.6, 0.65, 0.7, 0.75, 0.8, 0.85, 0.9, 0.95, 1, 1.1, 1.2, 1.3, 1.4, 1.5, 1.6, 1.7, 1.8, 1.9, 2, 2.1, 2.2, 2.3, 2.4, 2.5, 2.6, 2.7, 2.8, 2.9, 3, 3.1, 3.2, 3.3, 3.4, 3.5, 3.6, 3.7, 3.8, 3.9, 4, 4.1, 4.2, 4.3, 4.4., 4.5, 4.6, 4.7, 4.8, 4.9, 5% or more (by weight) of one or more microbial extracts.

In some embodiments, compositions of the present disclosure comprise one or more nutrients in an amount/concentration of about 0.0001 to about 5% or more (by weight) of the composition. In some embodiments, the nutrient(s) (e.g., phosphorous, boron, chlorine, copper, iron, manganese, molybdenum and/or zinc) comprise(s) about 0.0001, 0.0002, 0.0003, 0.0004, 0.0005, 0.0006, 0.0007, 0.0008, 0.0009, 0.001, 0.0015, 0.002, 0.0025, 0.003, 0.0035, 0.004, 0.0045, 0.005, 0.0055, 0.006, 0.0065, 0.007, 0.0075, 0.008, 0.0085, 0.009, 0.0095, 0.01, 0.015, 0.02, 0.025, 0.03, 0.035, 0.04, 0.045, 0.05, 0.06, 0.07, 0.08, 0.09, 0.1, 0.02, 0.3, 0.4, 0.5, 0.6, 0.7, 0.8, 0.9, 1 to about 1, 1.1, 1.2, 1.3, 1.4, 1.5, 1.6, 1.7, 1.8, 1.9, 2, 2.1, 2.2, 2.3, 2.4, 2.5, 2.6, 2.7, 2.8, 2.9, 3, 3.1, 3.2, 3.3, 3.4, 3.5, 3.6, 3.7, 3.8, 3.9, 4, 4.1, 4.2, 4.3, 4.4., 4.5, 4.6, 4.7, 4.8, 4.9, 5% (by weight) of the composition. For example, compositions of the present disclosure may comprise about 0.0005, 0.00075, 0.001, 0.002, 0.003, 0.004, 0.005, 0.006, 0.007, 0.008, 0.009, 0.01, 0.02, 0.03, 0.04, 0.05, 0.06, 0.07, 0.08, 0.09, 0.1, 0.15, 0.2, 0.25, 0.3, 0.35, 0.4, 0.45, 0.5, 0.55, 0.6, 0.65, 0.7, 0.75, 0.8, 0.85, 0.9, 0.95, 1, 1.1, 1.2, 1.3, 1.4, 1.5, 1.6, 1.7, 1.8, 1.9, 2, 2.1, 2.2, 2.3, 2.4, 2.5, 2.6, 2.7, 2.8, 2.9, 3, 3.1, 3.2, 3.3, 3.4, 3.5, 3.6, 3.7, 3.8, 3.9, 4, 4.1, 4.2, 4.3, 4.4., 4.5, 4.6, 4.7, 4.8, 4.9, 5% or more (by weight) of one or more the nutrients (e.g., phosphorous, boron, chlorine, copper, iron, manganese, molybdenum and/or zinc). In some embodiments, compositions of the present disclosure comprise one or more pest attractant(s) and/or feeding stimulant(s) in an amount/concentration of about 0.0001 to about 5% or more (by weight) of the composition. In some embodiments, the pest attractant(s) and/or feeding stimulant(s) comprise(s) about 0.0001, 0.0002, 0.0003, 0.0004, 0.0005, 0.0006, 0.0007, 0.0008, 0.0009, 0.001, 0.0015, 0.002, 0.0025, 0.003, 0.0035, 0.004, 0.0045, 0.005, 0.0055, 0.006, 0.0065, 0.007, 0.0075, 0.008, 0.0085, 0.009, 0.0095, 0.01, 0.015, 0.02, 0.025, 0.03, 0.035, 0.04, 0.045, 0.05, 0.06, 0.07, 0.08, 0.09, 0.1, 0.02, 0.3, 0.4, 0.5, 0.6, 0.7, 0.8, 0.9, 1 to about 1, 1.1, 1.2, 1.3, 1.4, 1.5, 1.6, 1.7, 1.8, 1.9, 2, 2.1, 2.2, 2.3, 2.4, 2.5, 2.6, 2.7, 2.8, 2.9, 3, 3.1, 3.2, 3.3, 3.4, 3.5, 3.6, 3.7, 3.8, 3.9, 4, 4.1, 4.2, 4.3, 4.4., 4.5, 4.6, 4.7, 4.8, 4.9, 5% (by weight) of the composition. For example, compositions of the present disclosure may comprise about 0.0005, 0.00075, 0.001, 0.002, 0.003, 0.004, 0.005, 0.006, 0.007, 0.008, 0.009, 0.01, 0.02, 0.03, 0.04, 0.05, 0.06, 0.07, 0.08, 0.09, 0.1, 0.15, 0.2, 0.25, 0.3, 0.35, 0.4, 0.45, 0.5, 0.55, 0.6, 0.65, 0.7, 0.75, 0.8, 0.85, 0.9, 0.95, 1, 1.1, 1.2, 1.3, 1.4, 1.5, 1.6, 1.7, 1.8, 1.9, 2, 2.1, 2.2, 2.3, 2.4, 2.5, 2.6, 2.7, 2.8, 2.9, 3, 3.1, 3.2, 3.3, 3.4, 3.5, 3.6, 3.7, 3.8, 3.9, 4, 4.1, 4.2, 4.3, 4.4., 4.5, 4.6, 4.7, 4.8, 4.9, 5% or more (by weight) of one or more pest attractants and/or feeding stimulants.

In some embodiments, compositions of the present disclosure comprise one or more LCOs at a concentration of about 1 x 10 -15 M to about 1 x 10 -10 M, about 1 x 10 -14 M to about 1 x 10 -8 M, about 1 x 10 -14 M to about 1 x 10 -6 M, about 1 x 10 -12 M to about 1 x 10 -8 M, about 1 x 10 -12 M to about 1 x 10 -6 M, about 1 x 10 -10 M to about 1 x 10 -6 M, or about 1 x 10 -8 M to about 1 x 10 -2 M. For example, compositions of the present disclosure may comprise about 1 x 10 -20 M, 1 x 10 -19 M, 1 x 10 -18 M, 1 x 10 -17 M, 1 x 10 -16 M, 1 x 10 -15 M, 1 x 10 -14 M, 1 x 10 -13 M, 1 x 10 -12 M, 1 x 10 -11 M, 1 x 10 -10 M, 1 x 10 -9 M, 1 x 10 -8 M, 1 x 10 -7 M, 1 x 10 -6 M, 1 x 10 -5 M, 1 x 10 -4 M, 1 x 10 -3 M, 1 x 10 -2 M, 1 x 10 -1 M or more of one or more LCOs (e.g., one, two, three, four or more of the LCOs set forth as structures V–XXXIII.

In some embodiments, compositions of the present disclosure comprise one or more chitin oligomers at a concentration of about 1 x 10 -15 M to about 1 x 10 -10 M, about 1 x 10 -14 M to about 1 x 10 -8 M, about 1 x 10 -14 M to about 1 x 10 -6 M, about 1 x 10 -12 M to about 1 x 10 -8 M, about 1 x 10 -12 M to about 1 x 10 -6 M, about 1 x 10 -10 M to about 1 x 10 -6 M, or about 1 x 10 -8 M to about 1 x 10 -2 M. For example, compositions of the present disclosure may comprise about 1 x 10 -20 M, 1 x 10 -19 M, 1 x 10 -18 M, 1 x 10 -17 M, 1 x 10 -16 M, 1 x 10 -15 M, 1 x 10 -14 M, 1 x 10 -13 M, 1 x 10 -12 M, 1 x 10 -11 M, 1 x 10 -10 M, 1 x 10 -9 M, 1 x 10 -8 M, 1 x 10 -7 M, 1 x 10 -6 M, 1 x 10 -5 M, 1 x 10 -4 M, 1 x 10 -3 M, 1 x 10 -2 M, 1 x 10 -1 M or more of one or more chitin oligomers (e.g., one, two, three, four or more of the chitin oligomers set forth as structures XXXVI–LXXXIII.

In some embodiments, compositions of the present disclosure comprise one or more chitosan oligomers at a concentration of about 1 x 10 -15 M to about 1 x 10 -10 M, about 1 x 10 -14 M to about 1 x 10 -8 M, about 1 x 10 -14 M to about 1 x 10 -6 M, about 1 x 10 -12 M to about 1 x 10 -8 M, about 1 x 10 -12 M to about 1 x 10 -6 M, about 1 x 10 -10 M to about 1 x 10 -6 M, or about 1 x 10 -8 M to about 1 x 10 -2 M. For example, compositions of the present disclosure may comprise about 1 x 10 -20 M, 1 x 10 -19 M, 1 x 10 -18 M, 1 x 10 -17 M, 1 x 10 -16 M, 1 x 10 -15 M, 1 x 10 -14 M, 1 x 10 -13 M, 1 x 10 -12 M, 1 x 10 -11 M, 1 x 10 -10 M, 1 x 10 -9 M, 1 x 10 -8 M, 1 x 10 -7 M, 1 x 10 -6 M, 1 x 10 -5 M, 1 x 10 -4 M, 1 x 10 -3 M, 1 x 10 -2 M, 1 x 10 -1 M or more of one or more chitosan oligomers (e.g., one, two, three, four or more of the oligosaccharides in a deacetylated form).

In some embodiments, compositions of the present disclosure comprise one or more chitins at a concentration of about 1 x 10 -15 M to about 1 x 10 -10 M, about 1 x 10 -14 M to about 1 x 10 -8 M, about 1 x 10 -14 M to about 1 x 10 -6 M, about 1 x 10 -12 M to about 1 x 10 -8 M, about 1 x 10 -12 M to about 1 x 10 -6 M, about 1 x 10 -10 M to about 1 x 10 -6 M, or about 1 x 10 -8 M to about 1 x 10 -2 M. For example, compositions of the present disclosure may comprise about 1 x 10 -20 M, 1 x 10 -19 M, 1 x 10 -18 M, 1 x 10 -17 M, 1 x 10 -16 M, 1 x 10 -15 M, 1 x 10 -14 M, 1 x 10 -13 M, 1 x 10 -12 M, 1 x 10 -11 M, 1 x 10 -10 M, 1 x 10 -9 M, 1 x 10 -8 M, 1 x 10 -7 M, 1 x 10 -6 M, 1 x 10 -5 M, 1 x 10 -4 M, 1 x 10 -3 M, 1 x 10 -2 M, 1 x 10 -1 M or more of one or more chitins.

In some embodiments, compositions of the present disclosure comprise one or more chitosans at a concentration of about 1 x 10 -15 M to about 1 x 10 -10 M, about 1 x 10 -14 M to about 1 x 10 -8 M, about 1 x 10 -14 M to about 1 x 10 -6 M, about 1 x 10 -12 M to about 1 x 10 -8 M, about 1 x 10 -12 M to about 1 x 10 -6 M, about 1 x 10 -10 M to about 1 x 10 -6 M, or about 1 x 10 -8 M to about 1 x 10 -2 M. For example, compositions of the present disclosure may comprise about 1 x 10 -20 M, 1 x 10 -19 M, 1 x 10 -18 M, 1 x 10 -17 M, 1 x 10 -16 M, 1 x 10 -15 M, 1 x 10 -14 M, 1 x 10 -13 M, 1 x 10 -12 M, 1 x 10 -11 M, 1 x 10 -10 M, 1 x 10 -9 M, 1 x 10 -8 M, 1 x 10 -7 M, 1 x 10 -6 M, 1 x 10 -5 M, 1 x 10 -4 M, 1 x 10 -3 M, 1 x 10 -2 M, 1 x 10 -1 M or more of one or more chitosans.

In some embodiments, compositions of the present disclosure comprise one or more dispersants in an amount/concentration of about 0.001 to about 25% or more (by weight) of the composition. In some embodiments, the dispersant(s) comprise(s) 0.001, 0.0015, 0.002, 0.0025, 0.003, 0.0035, 0.004, 0.0045, 0.005, 0.0055, 0.006, 0.0065, 0.007, 0.0075, 0.008, 0.0085, 0.009, 0.0095, 0.01, 0.015, 0.02, 0.025, 0.03, 0.035, 0.04, 0.045, 0.05, 0.06, 0.07, 0.08, 0.09, 0.1, 0.02, 0.3, 0.4, 0.5, 0.6, 0.7, 0.8, 0.9, 1, 1.1, 1.2, 1.3, 1.4, 1.5, 1.6, 1.7, 1.8, 1.9, 2, 2.1, 2.2, 2.3, 2.4, 2.5, 2.6, 2.7, 2.8, 2.9, 3, 3.1, 3.2, 3.3, 3.4, 3.5, 3.6, 3.7, 3.8, 3.9, 4, 4.1, 4.2, 4.3, 4.4., 4.5, 4.6, 4.7, 4.8, 4.9, 5, 6, 7, 8, 9 or 10 to about 1, 1.5, 2, 2.5, 3, 3.5, 4, 4.5, 5, 5.5, 6, 6.5, 7, 7.5, 8, 8.5, 9, 9.5, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19 or 20% (by weight) of the composition. For example, compositions of the present disclosure may comprise about 0.01, 0.02, 0.03, 0.04, 0.05.0.06, 0.07, 0.08, 0.09, 0.1, 0.2, 0.3, 0.4, 0.5, 1, 1.5, 2, 2.5, 3, 3.5, 4, 4.5, 5, 5.5, 6, 6.5, 7, 7.5, 8, 8.5, 9, 9.5, 10, 15, 20% or more (by weight) of one or more dispersants (e.g., one or more surfactants and/or wetting agents).

In some embodiments, compositions of the present disclosure comprise one or more drying agents in an amount/concentration of about 0.001 to about 95% or more (by weight) of the composition. In some embodiments, the drying agent(s) comprise(s) about ) 0.001, 0.0015, 0.002, 0.0025, 0.003, 0.0035, 0.004, 0.0045, 0.005, 0.0055, 0.006, 0.0065, 0.007, 0.0075, 0.008, 0.0085, 0.009, 0.0095, 0.01, 0.015, 0.02, 0.025, 0.03, 0.035, 0.04, 0.045, 0.05, 0.06, 0.07, 0.08, 0.09, 0.1, 0.02, 0.3, 0.4, 0.5, 0.6, 0.7, 0.8, 0.9, 1, 1.1, 1.2, 1.3, 1.4, 1.5, 1.6, 1.7, 1.8, 1.9, 2, 2.1, 2.2, 2.3, 2.4, 2.5, 2.6, 2.7, 2.8, 2.9, 3, 3.1, 3.2, 3.3, 3.4, 3.5, 3.6, 3.7, 3.8, 3.9, 4, 4.1, 4.2, 4.3, 4.4., 4.5, 4.6, 4.7, 4.8, 4.9, 5, 6, 7, 8, 9 or 10 to about 1, 1.5, 2, 2.5, 3, 3.5, 4, 4.5, 5, 5.5, 6, 6.5, 7, 7.5, 8, 8.5, 9, 9.5, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19 or 20% (by weight) of the composition. For example, compositions of the present disclosure may comprise about 0.01, 0.02, 0.03, 0.04, 0.05.0.06, 0.07, 0.08, 0.09, 0.1, 0.2, 0.3, 0.4, 0.5, 1, 1.5, 2, 2.5, 3, 3.5, 4, 4.5, 5, 5.5, 6, 6.5, 7, 7.5, 8, 8.5, 9, 9.5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95% or more (by weight) of one or more drying agents (e.g., lecithin and/or talc).

In some embodiments, the compositions of the present disclosure comprise about 0.5 to about 10 grams of drying powder per liter of composition. For example, compositions of the present disclosure may comprise about 0.5, 1, 1.25, 1.5, 1.75, 2, 2.25, 2.5, 2.75, 3, 3.25, 3.5, 3.75, 4, 4.25, 4.5, 4.75, 5, 5.5, 6, 6.5, 7, 7.5, 8, 8.5, 9, 9.5, 10 grams or more of drying powder per liter of composition.

In some embodiments, compositions of the present disclosure comprise one or more buffers in an amount/concentration of about 0.0001 to about 5% or more (by weight) of the composition. In some embodiments, the buffer(s) comprise(s) about 0.0001, 0.0002, 0.0003, 0.0004, 0.0005, 0.0006, 0.0007, 0.0008, 0.0009, 0.001, 0.0015, 0.002, 0.0025, 0.003, 0.0035, 0.004, 0.0045, 0.005, 0.0055, 0.006, 0.0065, 0.007, 0.0075, 0.008, 0.0085, 0.009, 0.0095, 0.01, 0.015, 0.02, 0.025, 0.03, 0.035, 0.04, 0.045, 0.05, 0.06, 0.07, 0.08, 0.09, 0.1, 0.02, 0.3, 0.4, 0.5, 0.6, 0.7, 0.8, 0.9, 1 to about 1, 1.1, 1.2, 1.3, 1.4, 1.5, 1.6, 1.7, 1.8, 1.9, 2, 2.1, 2.2, 2.3, 2.4, 2.5, 2.6, 2.7, 2.8, 2.9, 3, 3.1, 3.2, 3.3, 3.4, 3.5, 3.6, 3.7, 3.8, 3.9, 4, 4.1, 4.2, 4.3, 4.4., 4.5, 4.6, 4.7, 4.8, 4.9, 5% (by weight) of the composition. For example, compositions of the present disclosure may comprise about 0.0005, 0.00075, 0.001, 0.002, 0.003, 0.004, 0.005, 0.006, 0.007, 0.008, 0.009, 0.01, 0.02, 0.03, 0.04, 0.05, 0.06, 0.07, 0.08, 0.09, 0.1, 0.15, 0.2, 0.25, 0.3, 0.35, 0.4, 0.45, 0.5, 0.55, 0.6, 0.65, 0.7, 0.75, 0.8, 0.85, 0.9, 0.95, 1, 1.1, 1.2, 1.3, 1.4, 1.5, 1.6, 1.7, 1.8, 1.9, 2, 2.1, 2.2, 2.3, 2.4, 2.5, 2.6, 2.7, 2.8, 2.9, 3, 3.1, 3.2, 3.3, 3.4, 3.5, 3.6, 3.7, 3.8, 3.9, 4, 4.1, 4.2, 4.3, 4.4., 4.5, 4.6, 4.7, 4.8, 4.9, 5% or more (by weight) of one or more buffers (e.g., potassium phosphate monobasic and/or potassium phosphate dibasic).

In some embodiments, compositions of the present disclosure comprise one or more commercial carriers, antioxidants, oxygen scavengers, hygroscopic polymers, UV protectants, biostimulants, microbial extracts, nutrients, pest attractants and/or feeding stimulants, pesticides, plant signal molecules, disperants, drying agents, anti-freezing agents, buffers and/or adhesives used in accordance with the manufacturer's recommended amounts/concentrations.

In some embodiments, Strains of the present disclosure are the only microbial strains in compositions of the present disclosure.

In some embodiments, compositions of the present disclosure comprise one or more

microorganisms in addition to strains of the present disclosure. Any suitable microorganism(s) may be added, including, but not limited to, agriculturally beneficial microorganisms such as diazotrophs (e.g., symbiotic diazotrophs), phosphate-solubilizing microorganisms, mycorrhizal fungi and biopesticides. In some embodiments, compositions of the present disclosure comprise one or more microorganisms selected from the genera and species listed in Appendix A. Selection of additional microbes (if any) will depend on the intended application(s).

Non-limiting examples of bacteria that may be included in compositions of the present disclosure include Azospirillum brasilense INTA Az-39, Bacillus amyloliquefaciens D747, Bacillus

amyloliquefaciens NRRL B 50349, Bacillus amyloliquefaciens TJ1000, Bacillus amyloliquefaciens FZB24, Bacillus amyloliquefaciens FZB42, Bacillus amyloliquefaciens IN937a, Bacillus

amyloliquefaciens IT-45, Bacillus amyloliquefaciens TJ1000, Bacillus amyloliquefaciens MBI600, Bacillus amyloliquefaciens BS27 (deposited as NRRL B-5015), Bacillus amyloliquefaciens BS2084 (deposited as NRRL B-50013), Bacillus amyloliquefaciens 15AP4 (deposited as ATCC PTA-6507), Bacillus amyloliquefaciens 3AP4 (deposited as ATCC PTA-6506), Bacillus amyloliquefaciens LSSA01 (deposited as NRRL B-50104), Bacillus amyloliquefaciens ABP278 (deposited as NRRL B-50634), Bacillus amyloliquefaciens 1013 (deposited as NRRL B-50509), Bacillus amyloliquefaciens 918

(deposited as NRRL B-50508), Bacillus amyloliquefaciens 22CP1 (deposited as ATCC PTA-6508) and Bacillus amyloliquefaciens BS18 (deposited as NRRL B-50633), Bacillus cereus I-1562, Bacillus firmus I-1582, Bacillus lichenformis BA842 (deposited as NRRL B-50516), Bacillus lichenformis BL21 (deposited as NRRL B-50134), Bacillus mycoides NRRL B-21664, Bacillus pumilus NRRL B 21662, Bacillus pumilus NRRL B-30087, Bacillus pumilus ATCC 55608, Bacillus pumilus ATCC 55609, Bacillus pumilus GB34, Bacillus pumilus KFP9F, Bacillus pumilus QST 2808, Bacillus subtilis ATCC 55078, Bacillus subtilis ATCC 55079, Bacillus subtilis MBI 600, Bacillus subtilis NRRL B-21661, Bacillus subtilis NRRL B-21665, Bacillus subtilis CX-9060, Bacillus subtilis GB03, Bacillus subtilis GB07, Bacillus subtilis QST-713, Bacillus subtilis FZB24, Bacillus subtilis D747, Bacillus subtilis 3BP5 (deposited as NRRL B-50510), Bacillus thuringiensis ATCC 13367, Bacillus thuringiensis GC-91, Bacillus thuringiensis NRRL B-21619, Bacillus thuringiensis ABTS-1857, Bacillus thuringiensis SAN 401 I, Bacillus thuringiensis ABG-6305, Bacillus thuringiensis ABG-6346, Bacillus thuringiensis AM65- 52, Bacillus thuringiensis SA-12, Bacillus thuringiensis SB4, Bacillus thuringiensis ABTS-351, Bacillus thuringiensis HD-1, Bacillus thuringiensis EG 2348, Bacillus thuringiensis EG 7826, Bacillus thuringiensis EG 7841, Bacillus thuringiensis DSM 2803, Bacillus thuringiensis NB-125, Bacillus thuringiensis NB-176, BRADY, Mesorhizobium huakii LL32, Pseudomonas jessenii PS06, Rhizobium leguminosarum 162BB1, Rhizobium leguminosarum 162P17, Rhizobium leguminosarum 175G10b, Rhizobium leguminosarum D36, Rhizobium leguminosarum SO12A-2 (IDAC 080305-01), Rhizobium loti 95C11, Rhizobium loti 95C14, Sinorhizobium fredii CCBAU114, Sinorhizobium fredii USDA 205, Sinorhizobium meliloti 102F34a, Sinorhizobium meliloti 102F51a, Sinorhizobium meliloti 102F77b, Sinorhizobium meliloti B401, Yersinia entomophaga O82KB8 and combinations thereof, as well as microorganisms having at least at least 75, 80, 85, 90, 95, 96, 97, 97.5.98, 98.5, 99, 99.5, 99.6, 99.7, 99.8, 99.9% or more identical to any of the aforementioned strains on the basis of 16S rDNA sequence identity.

Non-limiting examples of fungi that may be included in compositions of the present disclosure include Gliocladium virens ATCC 52045, Gliocladium virens GL-21, Glomus intraradices RTI-801, Metarhizium anisopliae F52, PENI, Trichoderma asperellum SKT-1, Trichoderma asperellum ICC 012, Trichoderma atroviride LC52, Trichoderma atroviride CNCM 1-1237, Trichoderma fertile JM41R, Trichoderma gamsii ICC 080, Trichoderma hamatum ATCC 52198, Trichoderma harzianum ATCC 52445, Trichoderma harzianum KRL-AG2, Trichoderma harzianum T-22, Trichoderma harzianum TH- 35, Trichoderma harzianum T-39, Trichoderma harzianum ICC012, Trichoderma reesi ATCC 28217, Trichoderma virens ATCC 58678, Trichoderma virens Gl-3, Trichoderma virens GL-21, Trichoderma virens G-41, Trichoderma viridae ATCC 52440, Trichoderma viridae ICC080, Trichoderma viridae TV1 and combinations thereof, as well as microorganisms having at least at least 75, 80, 85, 90, 95, 96, 97, 97.5.98, 98.5, 99, 99.5, 99.6, 99.7, 99.8, 99.9% or more identical to any of the aforementioned strains on the basis of internal transcribed spacer (ITS) and/or cytochrome c oxidase (CO1) sequence identity. Non-limiting examples of mycorrhizal fungi that may be included in compositions of the present disclosure include mycorrhizal strains such as Gigaspora margarita, Glomus aggregatum, Glomus brasilianum, Glomus clarum, Glomus deserticola, Glomus etunicatum, Glomus intraradices, Glomus monosporum, Glomus mosseae, Laccaria bicolor, Laccaria laccata, Paraglomus brazilianum, Pisolithus tinctorius, Rhizopogon amylopogon, Rhizopogon fulvigleba, Rhizopogon luteolus, Rhizopogon villosuli, Scleroderma cepa and Scleroderma citrinum and combinations thereof.

Additional examples of microorganisms that may be added to compositions of the present disclosure can be found in Appendix A.

Additional microorganisms may be incorporated into compositions of the present disclosure in any suitable amount(s)/concentration(s). The absolute value of the amount/concentration that is/are sufficient to cause the desired effect(s) may be affected by factors such as the type, size and volume of material to which the compositon will be applied, the microorganisms in the composition, the number of microorganisms in the composition, the stability of the microorganisms in the composition and storage conditions (e.g., temperature, relative humidity, duration). Those skilled in the art will understand how to select an effective amount/concentration using routine dose-response experiments. Guidance for the selection of appropriate amounts/concentrations can be found, for example, in International Patent Publication Nos. WO2003/000051, WO2009/015266, WO2010/037228, WO2011/140051,

WO2012/135704, WO2013/090884, WO2014/078647, WO2015/069708, WO2017/027821,

WO2017/044473, WO2017/044545, WO2017/077104, WO2017/083623, WO2017/116837,

WO2017/116846, WO2017/131971, WO2017/205258, WO2017/210163, WO2017/210166,

WO2018/118740, WO2018/129016, WO2018/129018, WO2018/175677, WO2018/175681,

WO2018/183491, WO2018/218008, WO2018/218016 and WO2018/218035, and in U.S. Patent Publication Nos.2006/258534, 2011/230345 and 2018/201549.

In some embodiments, one or more additional microorganisms is/are present in an effective amount/concentration for fixing atmospheric nitrogen, solubilizing phosphate, controlling one or more phytopathogenic pests, enhancing stress tolerance and/or enhancing plant growth/yield when the composition is introduced into a plant growth medium (e.g., a soil).

In some embodiments, one or more additional microorganisms is/are present in an effective amount/concentration for fixing atmospheric nitrogen, solubilizing phosphate, controlling one or more phytopathogenic pests, enhancing stress tolerance and/or enhancing plant growth/yield when the composition is applied to a plant or plant part.

In some embodiments, one or more additional microorganisms is/are present in an amount ranging from about 1 x 10 1 to about 1 x 10 12 colony-forming units (cfu) per gram and/or millilitre of composition. According to some embodiments, the composition comprises about 1 x 10 1 , 1 x 10 2 , 1 x 10 3 , 1 x 10 4 , 1 x 10 5 , 1 x 10 6 , 1 x 10 7 , 1 x 10 8 , 1 x 10 9 , 1 x 10 10 , 1 x 10 11 , 1 x 10 12 or more cfu of one or more additional microorganisms per gram and/or milliliter of composition (e.g., about 1 x 10 4 to about 1 xo 10 9 cfu/g of Bacillus amyloliquefaciens TJ1000 (also known as 1BE, isolate ATCC BAA-390), BRADY, Metarhizium anisopliae F52, PENI, Trichoderma virens Gl-3, and/or Yersinia entomophaga O82KB8). In some embodiments, compositions of the present disclosure comprise at least 1 x 10 4 , 1 x 10 5 , 1 x 10 6 , 1 x 10 7 , 1 x 10 8 , 1 x 10 9 , 1 x 10 10 , 1 x 10 11 , 1 x 10 12 cfu of one or more additional microorganisms per gram and/or millilitre of composition.

In some embodiments, spores from one or more additional microorganims comprise about 0.1 to about 90% (by weight) of the composition. According to some embodiments, the composition comprises about 0.1, 0.2, 0.3, 0.4, 0.5, 0.6, 0.7, 0.8, 0.9, 1, 1.25, 1.5, 1.75, 2, 2.25, 2.5, 2.75, 3, 3.25, 3.5, 3.75, 4, 4.25, 4.5, 4.75, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95% or more (by weight) of microbial spores from one or more additional microorganisms (e.g., about 10% Bacillus amyloliquefaciens TJ1000, Metarhizium anisopliae F52, Penicillium bilaiae ATCC 20851, Penicillium bilaiae RS7B-SD1 and/or Trichoderma virens Gl-3 spores). In some embodiments, the amount/concentration of microbial spores from one or more additional microorganisms is about 1 to about 25%, about 5 to about 20%, about 5 to about 15%, about 5 to about 10% or about 8 to about 12% (by weight) of the composition.

It is to be understood that additional microorganisms in compositions of the present disclosure may comprise vegetative cells and/or dormant spores. According to some embodiments, at least 1, 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 96, 97, 98, 99% or more additional microorganims are present in compositons of the present disclosure as vegetative cells. According to some embodiments, at least 1, 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 96, 97, 98, 99% or more additional microorganims are present in compositons of the present disclosure as spores. compositions of the present disclosure may be formulated as any suitable type of composition, including, but not limited to, foliar inoculants, seed coatings and soil inoculants.

In some embodiments, compositions of the present disclosure are formulated as amorphous solids. In some embodiments, compositions of the present disclosure are formulated as amorphous liquids.

In some embodiments, compositions of the present disclosure are formulated as wettable powders. In some embodiments, compositions of the present disclosure are formulated as liquid compositions that are subsequently dried to produce a powder or granuale. For example, in some embodiments, liquid compositions of the present disclosure are drum dried, evaporation dried, fluidized bed dried, freeze dried, spray dried, spray-freeze dried, tray dried and/or vacuum dried to produce powders/granuales. Such powders/granuales may be further processed using any suitable method(s), including, but not limited to, flocculation, granulation and milling, to achieve a desired particle size or physical format. The precise method(s) and parameters of processing dried powders/granuales that are appropriate in a given situation may be affected by factors such as the desired particle size(s), the type, size and volume of material to which the compositon will be applied, the type(s) of microorganisms in the composition, the number of microorganisms in the composition, the stability of the microorganisms in the composition and the storage conditions (e.g., temperature, relative humidity, duration). Those skilled in the art will understand how to select appropriate methods and parameters using routine experiments.

In some embodiments, compositions of the present disclosure are frozen for cryopreservation. For example, in some embodiments, liquid compositions of the present disclosure are flash-frozen and stored in a cryopreservation storage unit/facility. The precise method(s) and parameters of freezing and preserving compositions of the present disclosure that are appropriate in a given situation may be affected by factors such as the type(s) of microorganisms in the composition, the number of microorganisms in the composition, the stability of the microorganisms in the composition and the storage conditions (e.g., temperature, relative humidity, duration). Those skilled in the art will understand how to select appropriate methods and parameters using routine experiments.

compositions of the present disclosure may be formulated as aqueous or non-aqueous compositions. In some embodiments, compositions of the present disclosure comprise no water. In some embodiments, compositions of the present disclosure comprise a trace amount of water. In some embodiments, compositions of the present disclosure comprise less than 0.01, 0.02, 0.03, 0.04, 0.05, 0.06, 0.07, 0.08, 0.09, 0.1, 0.15, 0.2, 0.25, 0.3, 0.35, 0.4, 0.45, 0.5, 0.55, 0.6, 0.65, 0.7, 0.750.8, 0.85, 0.9, 0.95, 1, 1.25, 1.5, 1.75, 2, 2.25, 2.5, 2.75, 3, 3.25, 3.5, 3.75, 4, 4.25, 4.5, 4.75 or 5% water by weight, based upon the total weight of the composition.

In some embodiments, compositions of the present disclosure are formulated to have a pH of about 4.5 to about 9.5. In some embodiments, compositions of the present disclosure have a pH of about 6 to about 7.5. In some embodiments, compositions of the present disclosure have a pH of about 5, 5.5, 6, 6.5, 7, 7.5, 8 or 8.5.

As noted above, compositions of the present disclosure may contain a variety of carriers, stabilizers, nutrients, pesticides, plant signal molcules, dispersants, etc. It is to be understood that the components to be included in the composition and the order in which components are incorporated into the composition may be chosen or designed to maintain or enhance the dispersion, stability and/or survival of the Strains of the present disclosureduring storage, distribution, and/or application of the composition.

It is to be understood that compositions of the present disclosure are non-naturally occurring compositions. According to some embodiments, the composition comprises one or more non-naturally occurring components. According to some embodiments, the composition comprises a non-naturally occurring combination of naturally occurring components.

The present disclosure extends to kits comprising, consisting essentially of, or consisting of two or more containers, each comprising one or more components of an compositon of the present disclosure. For example, one or more strains of the present disclosure and the agriculturally acceptable carrier may be housed in separate containers for long-term storage, then combined prior to applying the composition to a plant or plant propagation material. Optional constituents, such as stabilizing compounds, pesticides and plant signaling molecules, may be added to either of the two containers or housed in one or more separate containers for long-term storage. In some embodiments, the kit further comprises one or more oxygen scavengers, such as activated carbon, ascorbic acid, iron powder, mixtures of ferrous carbonate and metal halide catalysts, sodium chloride and/or sodium hydrogen carbonate.

The containers may comprise any suitable material(s), including, but not limited to, materials that reduce the amount of light, moisture and/or oxygen that contact the coated plant propagation material when the container is sealed. In some embodiments, the containers comprise, consist essentially of, or consist of a material having light permeability of less than about 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70 or 75%. In some embodiments, the containers comprise, consist essentially of, or consist of a material having an oxygen transmission rate of less than about 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 60, 70, 80, 90, 100, 125, 150, 175, 200, 225, 250, 275, 300, 325, 350, 375, 400, 425, 450, 475, or 500 cm 3 /m 2 ·day (as measured in accordance with ASTM D3985).

In some embodiments, the containers reduce the amount of ambient light that reaches said coated plant propagation material by about 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95 or 100% when sealed.

In some embodiments, the containers reduce the amount of ambient moisture that reaches said plant propagation material by about 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95 or 100% when sealed.

In some embodiments, the containers reduce the amount of ambient oxygen that reaches said plant propagation material by about 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95 or 100% when sealed.

Strains, cultures, cell-free filtrates, cellular extracts and inoculant compositions of the present disclosure may be applied to any plant type, including, but not limited to, row crops and vegetables. In some embodiments, strains, cultures, cell-free filtrates, cellular extracts and inoculant compositions of the present disclosure are formulated for the treatment of one or more plants selected from the families Amaranthaceae (e.g., chard, spinach, sugar beet, quinoa), Asteraceae (e.g., artichoke, asters, chamomile, chicory, chrysanthemums, dahlias, daisies, echinacea, goldenrod, guayule, lettuce, marigolds, safflower, sunflowers, zinnias), Brassicaceae (e.g., arugula, broccoli, bok choy, Brussels sprouts, cabbage, cauliflower, canola, collard greens, daikon, garden cress, horseradish, kale, mustard, radish, rapeseed, rutabaga, turnip, wasabi, watercress, Arabidopsis thaliana), Cucurbitaceae (e.g., cantaloupe, cucumber, honeydew, melon, pumpkin, squash (e.g., acorn squash, butternut squash, summer squash), watermelon, zucchini), Fabaceae (e.g., alfalfa, beans, carob, clover, guar, lentils, mesquite, peas, peanuts, soybeans, tamarind, tragacanth, vetch), Malvaceae (e.g., cacao, cotton, durian, hibiscus, kenaf, kola, okra), Poaceae (e.g., bamboo, barley, corn, fonio, lawn grass (e.g., Bahia grass, Bermudagrass, bluegrass, Buffalograss, Centipede grass, Fescue, or Zoysia), millet, oats, ornamental grasses, rice, rye, sorghum, sugar cane, triticale, wheat and other cereal crops, Polygonaceae (e.g., buckwheat), Rosaceae (e.g., almonds, apples, apricots, blackberry, blueberry, cherries, peaches, plums, quinces, raspberries, roses, strawberries), Solanaceae (e.g., bell peppers, chili peppers, eggplant, petunia, potato, tobacco, tomato) and Vitaceae (e.g., grape). In some embodiments, strains, cultures, cell-free filtrates, celluar extracts and inoculant compositions of the present disclosure are formulated for the treatment of one or more plants with which the strain(s) is/are not naturally associated (e.g., one or more plants that does not naturally exist in the geographical location(s) from which the strain(s) was/were isolated). In some embodiments, strains, cultures, cell-free filtrates, celluar extracts and inoculant compositions of the present disclosure are formulated for the treatment of one or more acaricide-, fungicide-, gastropodicide-, herbicide-, insecticide- , nematicide-, rodenticide- and/or virucide-resistant plants (e.g., one or more plants resistant to acetolactate synthase inhibitors (e.g., imidazolinone, pryimidinyoxy(thio)benzoates, sulfonylaminocarbonyltriazolinone, sulfonylurea, triazolopyrimidines), bialaphos, glufosinate, glyphosate, hydroxyphenylpyruvatedioxygenase inhibitors and/or phosphinothricin). Non-limiting examples of plants that may be treated with strains, cultures, cell-free filtrates, celluar extracts and inoculant compositions of the present disclosure include plants sold under the BOLLGARD II®, DROUGHTGARD®,

GENUITY®, RIB COMPLETE®, ROUNDUP READY®, ROUNDUP READY 2 YIELD®, ROUNDUP READY 2 EXTEND™, SMARTSTAX®, VT DOUBLE PRO®, VT TRIPLE PRO®, YIELDGARD®, YIELDGARD VT ROOTWORM/RR2®, YIELDGARD VT TRIPLE® and/or XTENDFLEX™ tradenames.

Strains, cultures, cell-free filtrates, celluar extracts and inoculant compositions of the present disclosure may be beneficially incorporated into ACCELERON®, ACTINOVATE®, CELL-TECH®, JUMPSTART®, MET52®, NEMASTRIKE™, NITRAGIN®, OPTIMIZE®, QUICKROOTS®, TAGTEAM® and/or TORQUE® products. Strains of the present disclosure may also be beneificially incorporated into AVAIL®, BAR MAX NORTE, BAR MAX SUR, BIOBOOST®, BIOPOWER, BIOSINC®, COMO PLATINUM, CROP+®, DEFENDR™, DIAMONBRAND®, DYNA-START™, EXCALIBRE-SA™, EXCEED®, EXCELLORATE™, FIRST UP®, FLEXCONNECT™, FORZA™, FUNGI-PHITE®, GRAPH-EX®, GRAPH-EX SA®, GUARD·N®, HEADSUP®, ILEVO®,

INTRACEPT™, LAUNCHER™, LEGACY™, MARAUDER®, MASTERFIX L PREMIER,

MAXIMIZE™, MEGAPACK™, MICROAZ-IF LIQUID™, MICROAZ-ST DRY™, MICROSTAR®, MICROSYNC™, MORE THAN MANURE®, NATURALL™, N-CHARGE®, N-DURE™, N-FORCE, N-TAKE™, NODULATOR®, NUE CHARGE G™, NUTRI-GROW®, NUTRIPACTION®, NUTRI- PHITE®, NUTRISPHERE-N®, OBVIUS®, PBX™, PONCHO®, PREMAX®, PREMAXR®, PRE- VAIL™, PRESIDE CL®, PRESIDE ULTRA®, PRIMACY ALPHA®, PRIMO, PROSURGE™, PULSERHIZO®, RECOVER®, SABREX®, RILEGUM®, RIZOFOS®, RIZOLIQ®, SAFE ZONE™, SEED+™, SIGNUM®, SIMBIOSE®, SOYRHIZO®, SOYSUPERB®, STAMINA®, STATUS®, STERICS®, STIMUCONTROL®, SYSTIVA®, TAKE OFF®, TAKE OFF ST®, TERRAMAX DRY™, TERRAMAX LIQUID-IF, TRIDENT™, TUXEDO®, VAULT®, VERTEX-IF, VIGOR®, VIGOR SEED, VOTIVO®, WUXAL TERIOS and XITEBIO® YIELD+ products.

Strains, cultures, cell-free filtrates, cellular extracts and inoculant compositions of the present disclosure may be applied to any part/portion of a plant. In some embodiments, one or more strains of the present disclosure (or an inoculant composition of the present disclosure) is applied to plant propagation materials (e.g., cuttings, rhizomes, seeds and tubers). In some embodiments, one or more strains, cultures, cell-free filtrates, celluar extracts and/or inoculant compositions of the present disclosure is applied to the roots of a plant. In some embodiments, one or more strains, cultures, cell-free filtrates, celluar extracts and/or inoculant compositions of the present disclosure is applied to the foliage of a plant. In some embodiments, one or more strains, cultures, cell-free filtrates, celluar extracts and/or inoculant compositions of the present disclosure is applied to both the roots and the foliage of a plant. In some embodiments, one or more strains, cultures, cell-free filtrates, celluar extracts and/or inoculant compositions of the present disclosure is applied to plant propagation materials and to the plants that grow from said plant propagation materials. Strains, cultures, cell-free filtrates, cellular extracts and inoculant compositions of the present disclosure may be applied to any plant growth medium, including, but not limited to, soil.

Strains, cultures, cell-free filtrates, cellular extracts and inoculant compositions of the present disclosure may be applied to plants, plant parts and/or plant growth media in any suitable manner, including, but not limited to, on-seed application, in-furrow application and foliar application.

Strains, cultures, cell-free filtrates, cellular extracts and inoculant compositions of the present disclosure may be applied using any suitable method(s), including, but not limited to, coating, dripping, dusting, encapsulating, immersing, spraying and soaking. Batch systems, in which predetermined batch sizes of material and inoculant composition are delivered into a mixer, may be employed. Continuous treatment systems, which are calibrated to apply inoculant composition at a predefined rate in proportion to a continuous flow of material, may also be employed.

In some embodiments, one or more strains, cultures, cell-free filtrates, celluar extracts and/or inoculant compositions of the present disclosure is applied directly to plant propagation material (e.g., seeds). According to some embodiments, plant propagation materials are soaked in a composition comprising one or more strains, cultures, cell-free filtrates and/or celluar extracts of the present disclosure for at least 0.1, 0.2, 0.3, 0.4, 0.5, 0.6, 0.7, 0.8, 0.9, 1, 1.25, 1.5, 1.75, 2, 3, 4, 5, 6, 9, 12, 15, 18, 21, 24, 36, 48 hours. According to some embodiments, plant propagation materials are coated with one or more strains, cultures, cell-free filtrates, celluar extracts and/or inoculant compositions of the present disclosure. Plant propagation materials may be coated with one or more additional layers (e.g., one or more protective layers that serves to enhance the stability and/or survival of strains of the present disclosure and/or one or more sequestration layers comprising substances that may reduce the stability and/or survival of strains of the present disclosure if included in same layer. In some embodiments, the coating comprises, consists essentially of, or consists of an inoculant composition of the present disclosure and a drying powder.

In some embodiments, one or more strains, cultures, cell-free filtrates, celluar extracts and/or inoculant compositions of the present disclosure is applied directly to a plant growth medium (e.g., a soil). According to some embodiments, one or more strains, cultures, cell-free filtrates, celluar extracts and/or inoculant compositions of the present disclosure is applied in the vicinity of a plant propagation material (e.g., a seed). According to some embodiments, one or more strains, cultures, cell-free filtrates, celluar extracts and/or inoculant compositions of the present disclosure is applied to the root zone of a plant. According to some embodiments, one or more strains, cultures, cell-free filtrates, celluar extracts and/or inoculant compositions of the present disclosure is applied using a drip irrigation system.

In some embodiments, one or more strains, cultures, cell-free filtrates, celluar extracts and/or inoculant compositions of the present disclosure is applied directly to plants. According to some embodiments, one or more strains, cultures, cell-free filtrates, celluar extracts and/or inoculant compositions of the present disclosure is sprayed and/or sprinkled on the plant(s) to be treated.

In some embodiments, one or more strains, cultures, cell-free filtrates, celluar extracts and/or inoculant compositions of the present disclosure is freeze- spray- or spray-freeze-dried and then applied to plants/plant parts. For examples, in some embodiments, an inoculant composition comprising one or more strains of the present disclosure and one or more stabilizing components (e.g., one or more maltodextrins having a DEV of about 15 to about 20) is freeze- spray- or spray-freeze-dried, mixed with a drying powder (e.g., a drying powder comprising calcium stearate, attapulgite clay, montmorillonite clay, graphite, magnesium stearate, silica (e.g., fumed silica, hydrophobically-coated silica and/or precipitated silica) and/or talc), then coated on seed that was been pre-treated with one or more adhesives (e.g., an adhesive composition comprising one or more maltodextrins, one or more mono-, di- or oligosaccharides, one or more peptones, etc.), one or more pesticides and/or one or more plant signal molecules (e.g., one or more LCOs).

Strains, cultures, cell-free filtrates, cellular extracts and inoculant compositions of the present disclosure may be applied to plants, plant parts and/or plant growth media in any suitable

amount(s)/concentration(s).

In some embodiments, one or more strains of the present disclosure is applied at a rate of about 1 x 10 1 to about 1 x 10 20 cfu per kilogram of plant propagation material. According to some embodiments, one or more strains of the present disclosure is applied in an amount sufficient to ensure the plant propagation materials are coated with about/at least 1 x 10 4 , 1 x 10 5 , 1 x 10 6 , 1 x 10 7 , 1 x 10 8 , 1 x 10 9 , 1 x 10 10 , 1 x 10 11 , 1 x 10 12 , 1 x 10 13 , 1 x 10 14 , 1 x 10 15 cfu per kilogram of plant propagation material.

According to some embodiments, one or more strains of the present disclosure is applied in an amount sufficient to ensure that an average of about/at least 1 x 10 3 , 1 x 10 4 , 1 x 10 5 , 1 x 10 6 , 1 x 10 7 , 1 x 10 8 , 1 x 10 9 , 1 x 10 10 , 1 x 10 11 , 1 x 10 12 , 1 x 10 13 , 1 x 10 14 , 1 x 10 15 cfu is applied to each seed.

In some embodiments, one or more strains of the present disclosure is applied at a rate of about 1 x 10 1 to about 1 x 10 20 cfu per plant. According to some embodiments, one or more strains of the present disclosure is applied in an amount sufficient to ensure each plant is treated with about/at least 1 x 10 4 , 1 x 10 5 , 1 x 10 6 , 1 x 10 7 , 1 x 10 8 , 1 x 10 9 , 1 x 10 10 , 1 x 10 11 , 1 x 10 12 , 1 x 10 13 , 1 x 10 14 , 1 x 10 15 cfu. According to some embodiments, one or more strains of the present disclosure is applied in an amount sufficient to ensure that an average of about/at least 1 x 10 3 , 1 x 10 4 , 1 x 10 5 , 1 x 10 6 , 1 x 10 7 , 1 x 10 8 , 1 x 10 9 , 1 x 10 10 , 1 x 10 11 , 1 x 10 12 , 1 x 10 13 , 1 x 10 14 , 1 x 10 15 cfu is applied to each plant.

In some embodiments one or more strains of the present disclosure is applied at a rate of about 1 x 10 1 to about 1 x 10 20 cfu per acre of treated crops. According to some embodiments, one or more strains of the present disclosure is applied in an amount sufficient to ensure each acre of treated crops is treated with about/at least 1 x 10 4 , 1 x 10 5 , 1 x 10 6 , 1 x 10 7 , 1 x 10 8 , 1 x 10 9 , 1 x 10 10 , 1 x 10 11 , 1 x 10 12 , 1 x 10 13 , 1 x 10 14 , 1 x 10 15 cfu. According to some embodiments, one or more strains of the present disclosure is applied in an amount sufficient to ensure that an average of about/at least 1 x 10 3 , 1 x 10 4 , 1 x 10 5 , 1 x 10 6 , 1 x 10 7 , 1 x 10 8 , 1 x 10 9 , 1 x 10 10 , 1 x 10 11 , 1 x 10 12 , 1 x 10 13 , 1 x 10 14 , 1 x 10 15 cfu is applied to each acre of treated crops.

In some embodiments, one or more strains of the present disclosure is applied at a rate of about 1 x 10 1 to about 1 x 10 20 cfu per acre of plant growth media. According to some embodiments, one or more strains of the present disclosure is applied in an amount sufficient to ensure each acre of plant growth media is treated with about/at least 1 x 10 4 , 1 x 10 5 , 1 x 10 6 , 1 x 10 7 , 1 x 10 8 , 1 x 10 9 , 1 x 10 10 , 1 x 10 11 , 1 x 10 12 , 1 x 10 13 , 1 x 10 14 , 1 x 10 15 cfu. According to some embodiments, one or more strains of the present disclosure is applied in an amount sufficient to ensure that an average of about/at least 1 x 10 3 , 1 x 10 4 , 1 x 10 5 , 1 x 10 6 , 1 x 10 7 , 1 x 10 8 , 1 x 10 9 , 1 x 10 10 , 1 x 10 11 , 1 x 10 12 , 1 x 10 13 , 1 x 10 14 , 1 x 10 15 cfu is applied to each acre of plant growth media.

In some embodiments, cultures, cell-free filtrates, cellular extracts and inoculant compositions of the present diclosure are applied at a rate of about 0.05 to about 100 milliliters and/or grams thereof per kilogram of plant propagation material. According to some embodiments, one or more cultures, cell-free filtrates, cellular extracts or inoculant compositions of the present diclosure is/are applied in an amount sufficient to ensure the plant propagation materials are coated with about/at least 0.05, 0.1, 0.125, 0.15, 0.175, 0.2, 0.225, 0.2.5, 0.275, 0.3, 0.325, 0.35, 0.375, 0.4, 0.425, 0.45, 0.475, 0.5, 0.55, 0.6, 0.65, 0.7, 0.75, 0.8, 0.85, 0.9, 0.95, 1, 1.25, 1.5, 1.75, 2, 2.25, 2.5, 2.75, 3, 3.25, 3.5, 3.75, 4, 4.25, 4.5, 4.75, 5, 5.5, 6, 6.5, 7, 7.5, 8, 8.5, 9, 9.5, 10, 20, 30, 40, 50, 60, 70, 80, 90 or 100 milliliters and/or grams thereof per kilogram of plant propagation material. According to some embodiments, one or more cultures, cell-free filtrates, cellular extracts or inoculant compositions of the present diclosure is/are applied in an amount sufficient to ensure that an average of about/at least 0.05, 0.1, 0.125, 0.15, 0.175, 0.2, 0.225, 0.2.5, 0.275, 0.3, 0.325, 0.35, 0.375, 0.4, 0.425, 0.45, 0.475, 0.5, 0.55, 0.6, 0.65, 0.7, 0.75, 0.8, 0.85, 0.9, 0.95, 1, 1.25, 1.5, 1.75, 2, 2.25, 2.5, 2.75, 3, 3.25, 3.5, 3.75, 4, 4.25, 4.5, 4.75 or 5 milliliters and/or grams thereof is applied to each seed.

In some embodiments, cultures, cell-free filtrates, cellular extracts and inoculant compositions of the present diclosure are applied at a rate of about 0.5 to about 100 milliliters and/or grams thereof per plant. According to some embodiments, one or more cultures, cell-free filtrates, cellular extracts or inoculant compositions of the present diclosure is/are applied in an amount sufficient to ensure each plant is treated with about/at least 0.05, 0.1, 0.125, 0.15, 0.175, 0.2, 0.225, 0.2.5, 0.275, 0.3, 0.325, 0.35, 0.375, 0.4, 0.425, 0.45, 0.475, 0.5, 0.55, 0.6, 0.65, 0.7, 0.75, 0.8, 0.85, 0.9, 0.95, 1, 1.25, 1.5, 1.75, 2, 2.25, 2.5, 2.75, 3, 3.25, 3.5, 3.75, 4, 4.25, 4.5, 4.75, 5, 5.5, 6, 6.5, 7, 7.5, 8, 8.5, 9, 9.5, 10, 20, 30, 40, 50, 60, 70, 80, 90 or 100 milliliters and/or grams thereof. According to some embodiments, one or more cultures, cell- free filtrates, cellular extracts or inoculant compositions of the present diclosure is/are applied in an amount sufficient to ensure that an average of about/at least 0.05, 0.1, 0.125, 0.15, 0.175, 0.2, 0.225, 0.2.5, 0.275, 0.3, 0.325, 0.35, 0.375, 0.4, 0.425, 0.45, 0.475, 0.5, 0.55, 0.6, 0.65, 0.7, 0.75, 0.8, 0.85, 0.9, 0.95, 1, 1.25, 1.5, 1.75, 2, 2.25, 2.5, 2.75, 3, 3.25, 3.5, 3.75, 4, 4.25, 4.5, 4.75 or 5 milliliters and/or grams thereof is applied to each plant.

In some embodiments, cultures, cell-free filtrates, cellular extracts and inoculant compositions of the present diclosure are applied at a rate of about 0.5 to about 100 milliliters and/or grams thereof per acre of treated crops. According to some embodiments, one or more cultures, cell-free filtrates, cellular extracts or inoculant compositions of the present diclosure is/are applied in an amount sufficient to ensure each acre of treated crops is treated with about/at least 0.05, 0.1, 0.125, 0.15, 0.175, 0.2, 0.225, 0.2.5, 0.275, 0.3, 0.325, 0.35, 0.375, 0.4, 0.425, 0.45, 0.475, 0.5, 0.55, 0.6, 0.65, 0.7, 0.75, 0.8, 0.85, 0.9, 0.95, 1, 1.25, 1.5, 1.75, 2, 2.25, 2.5, 2.75, 3, 3.25, 3.5, 3.75, 4, 4.25, 4.5, 4.75, 5, 5.5, 6, 6.5, 7, 7.5, 8, 8.5, 9, 9.5, 10, 20, 30, 40, 50, 60, 70, 80, 90 or 100 milliliters and/or grams thereof. According to some embodiments, one or more cultures, cell-free filtrates, cellular extracts or inoculant compositions of the present diclosure is/are applied in an amount sufficient to ensure that an average of about/at least 0.05, 0.1, 0.125, 0.15, 0.175, 0.2, 0.225, 0.2.5, 0.275, 0.3, 0.325, 0.35, 0.375, 0.4, 0.425, 0.45, 0.475, 0.5, 0.55, 0.6, 0.65, 0.7, 0.75, 0.8, 0.85, 0.9, 0.95, 1, 1.25, 1.5, 1.75, 2, 2.25, 2.5, 2.75, 3, 3.25, 3.5, 3.75, 4, 4.25, 4.5, 4.75 or 5 milliliters and/or grams thereof is applied to each acre of treated crops.

In some embodiments, cultures, cell-free filtrates, cellular extracts and inoculant compositions of the present diclosure are applied at a rate of about 0.5 to about 100 milliliters and/or grams thereof per acre of plant growth media. According to some embodiments, one or more cultures, cell-free filtrates, cellular extracts or inoculant compositions of the present diclosure is/are applied in an amount sufficient to ensure each acre of plant growth media is treated with about/at least 0.05, 0.1, 0.125, 0.15, 0.175, 0.2, 0.225, 0.2.5, 0.275, 0.3, 0.325, 0.35, 0.375, 0.4, 0.425, 0.45, 0.475, 0.5, 0.55, 0.6, 0.65, 0.7, 0.75, 0.8, 0.85, 0.9, 0.95, 1, 1.25, 1.5, 1.75, 2, 2.25, 2.5, 2.75, 3, 3.25, 3.5, 3.75, 4, 4.25, 4.5, 4.75, 5, 5.5, 6, 6.5, 7, 7.5, 8, 8.5, 9, 9.5, 10, 20, 30, 40, 50, 60, 70, 80, 90 or 100 milliliters and/or grams thereof. According to some embodiments, one or more cultures, cell-free filtrates, cellular extracts or inoculant compositions of the present diclosure is/are applied in an amount sufficient to ensure that an average of about/at least 0.05, 0.1, 0.125, 0.15, 0.175, 0.2, 0.225, 0.2.5, 0.275, 0.3, 0.325, 0.35, 0.375, 0.4, 0.425, 0.45, 0.475, 0.5, 0.55, 0.6, 0.65, 0.7, 0.75, 0.8, 0.85, 0.9, 0.95, 1, 1.25, 1.5, 1.75, 2, 2.25, 2.5, 2.75, 3, 3.25, 3.5, 3.75, 4, 4.25, 4.5, 4.75 or 5 milliliters and/or grams thereof is applied to each acre of plant growth media.

In some embodiments, cultures/inoculant compositions of the present diclosure are applied in an amount sufficient to ensure the plant propagation materials are coated with about/at least 1 x 104 , 1 x 10 5 , 1 x 10 6 , 1 x 10 7 , 1 x 10 8 , 1 x 10 9 , 1 x 10 10 , 1 x 10 11 , 1 x 10 12 , 1 x 10 13 , 1 x 10 14 , 1 x 10 15 cfu of Erwinia (e.g., E. billingiae NRRL B-67766) per kilogram of plant propagation material. According to some embodiments, one or more cultures/inoculant compositions of the present diclosure is/are applied in an amount sufficient to ensure that an average of about/at least 1 x 10 3 , 1 x 10 4 , 1 x 10 5 , 1 x 10 6 , 1 x 10 7 , 1 x 10 8 , 1 x 10 9 , 1 x 10 10 , 1 x 10 11 , 1 x 10 12 , 1 x 10 13 , 1 x 10 14 , 1 x 10 15 cfu of Erwinia (e.g., E. billingiae NRRL B-67766) is applied to each seed.

In some embodiments, cultures/inoculant compositions of the present diclosure are applied in an amount sufficient to ensure each plant is treated with about/at least 1 x 10 4 , 1 x 10 5 , 1 x 10 6 , 1 x 10 7 , 1 x 10 8 , 1 x 10 9 , 1 x 10 10 , 1 x 10 11 , 1 x 10 12 , 1 x 10 13 , 1 x 10 14 , 1 x 10 15 cfu of Erwinia (e.g., E. billingiae NRRL B-67766). According to some embodiments, one or more cultures/inoculant compositions of the present diclosure is/are applied in an amount sufficient to ensure that an average of about/at least 1 x 10 3 , 1 x 10 4 , 1 x 10 5 , 1 x 10 6 , 1 x 10 7 , 1 x 10 8 , 1 x 10 9 , 1 x 10 10 , 1 x 10 11 , 1 x 10 12 , 1 x 10 13 , 1 x 10 14 , 1 x 10 15 cfu of Erwinia (e.g., E. billingiae NRRL B-67766) is applied to each plant.

In some embodiments, cultures/inoculant compositions of the present diclosure are applied in an amount sufficient to ensure each acre of treated crops is treated with about/at least 1 x 10 4 , 1 x 10 5 , 1 x 10 6 , 1 x 10 7 , 1 x 10 8 , 1 x 10 9 , 1 x 10 10 , 1 x 10 11 , 1 x 10 12 , 1 x 10 13 , 1 x 10 14 , 1 x 10 15 cfu of Erwinia (e.g., E. billingiae NRRL B-67766). According to some embodiments, one or more cultures/inoculant

compositions of the present diclosure is/are applied in an amount sufficient to ensure that an average of about/at least 1 x 10 3 , 1 x 10 4 , 1 x 10 5 , 1 x 10 6 , 1 x 10 7 , 1 x 10 8 , 1 x 10 9 , 1 x 10 10 , 1 x 10 11 , 1 x 10 12 , 1 x 10 13 , 1 x 10 14 , 1 x 10 15 cfu of Erwinia (e.g., E. billingiae NRRL B-67766) is applied to each acre of treated crops. In some embodiments, cultures/inoculant compositions of the present diclosure are applied in an amount sufficient to ensure each acre of plant growth media is treated with about/at least 1 x 10 4 , 1 x 10 5 , 1 x 10 6 , 1 x 10 7 , 1 x 10 8 , 1 x 10 9 , 1 x 10 10 , 1 x 10 11 , 1 x 10 12 , 1 x 10 13 , 1 x 10 14 , 1 x 10 15 cfu of Erwinia (e.g., E. billingiae NRRL B-67766). According to some embodiments, one or more cultures/inoculant compositions of the present diclosure is/are applied in an amount sufficient to ensure that an average of about/at least 1 x 10 3 , 1 x 10 4 , 1 x 10 5 , 1 x 10 6 , 1 x 10 7 , 1 x 10 8 , 1 x 10 9 , 1 x 10 10 , 1 x 10 11 , 1 x 10 12 , 1 x 10 13 , 1 x 10 14 , 1 x 10 15 cfu of Erwinia (e.g., E. billingiae NRRL B-67766) is applied to each acre of plant growth media.

In some embodiments, cultures/inoculant compositions of the present diclosure are applied in an amount sufficient to ensure the plant propagation materials are coated with about/at least 1 x 10 4 , 1 x 10 5 , 1 x 10 6 , 1 x 10 7 , 1 x 10 8 , 1 x 10 9 , 1 x 10 10 , 1 x 10 11 , 1 x 10 12 , 1 x 10 13 , 1 x 10 14 , 1 x 10 15 cfu of

Pseudomonas (e.g., P. gessardii NRRL B-67767 and/or P. libanesis NRRL B-67769) per kilogram of plant propagation material. According to some embodiments, one or more cultures/inoculant compositions of the present diclosure is/are applied in an amount sufficient to ensure that an average of about/at least 1 x 10 3 , 1 x 10 4 , 1 x 10 5 , 1 x 10 6 , 1 x 10 7 , 1 x 10 8 , 1 x 10 9 , 1 x 10 10 , 1 x 10 11 , 1 x 10 12 , 1 x 10 13 , 1 x 10 14 , 1 x 10 15 cfu of Pseudomonas (e.g., P. gessardii NRRL B-67767 and/or P. libanesis NRRL B-67769) is applied to each seed.

In some embodiments, cultures/inoculant compositions of the present diclosure are applied in an amount sufficient to ensure each plant is treated with about/at least 1 x 10 4 , 1 x 10 5 , 1 x 10 6 , 1 x 10 7 , 1 x 10 8 , 1 x 10 9 , 1 x 10 10 , 1 x 10 11 , 1 x 10 12 , 1 x 10 13 , 1 x 10 14 , 1 x 10 15 cfu of Pseudomonas (e.g., P. gessardii NRRL B-67767 and/or P. libanesis NRRL B-67769). According to some embodiments, one or more cultures/inoculant compositions of the present diclosure is/are applied in an amount sufficient to ensure that an average of about/at least 1 x 10 3 , 1 x 10 4 , 1 x 10 5 , 1 x 10 6 , 1 x 10 7 , 1 x 10 8 , 1 x 10 9 , 1 x 10 10 , 1 x 10 11 , 1 x 10 12 , 1 x 10 13 , 1 x 10 14 , 1 x 10 15 cfu of Pseudomonas (e.g., P. gessardii NRRL B-67767 and/or P. libanesis NRRL B-67769) is applied to each plant.

In some embodiments, cultures/inoculant compositions of the present diclosure are applied in an amount sufficient to ensure each acre of treated crops is treated with about/at least 1 x 10 4 , 1 x 10 5 , 1 x 10 6 , 1 x 10 7 , 1 x 10 8 , 1 x 10 9 , 1 x 10 10 , 1 x 10 11 , 1 x 10 12 , 1 x 10 13 , 1 x 10 14 , 1 x 10 15 cfu of Pseudomonas (e.g., P. gessardii NRRL B-67767 and/or P. libanesis NRRL B-67769). According to some embodiments, one or more cultures/inoculant compositions of the present diclosure is/are applied in an amount sufficient to ensure that an average of about/at least 1 x 10 3 , 1 x 10 4 , 1 x 10 5 , 1 x 10 6 , 1 x 10 7 , 1 x 10 8 , 1 x 10 9 , 1 x 10 10 , 1 x 10 11 , 1 x 10 12 , 1 x 10 13 , 1 x 10 14 , 1 x 10 15 cfu of Pseudomonas (e.g., P. gessardii NRRL B-67767 and/or P. libanesis NRRL B-67769) is applied to each acre of treated crops.

In some embodiments, cultures/inoculant compositions of the present diclosure are applied in an amount sufficient to ensure each acre of plant growth media is treated with about/at least 1 x 10 4 , 1 x 10 5 , 1 x 10 6 , 1 x 10 7 , 1 x 10 8 , 1 x 10 9 , 1 x 10 10 , 1 x 10 11 , 1 x 10 12 , 1 x 10 13 , 1 x 10 14 , 1 x 10 15 cfu of

Pseudomonas (e.g., P. gessardii NRRL B-67767 and/or P. libanesis NRRL B-67769). According to some embodiments, one or more cultures/inoculant compositions of the present diclosure is/are applied in an amount sufficient to ensure that an average of about/at least 1 x 10 3 , 1 x 10 4 , 1 x 10 5 , 1 x 10 6 , 1 x 10 7 , 1 x 10 8 , 1 x 10 9 , 1 x 10 10 , 1 x 10 11 , 1 x 10 12 , 1 x 10 13 , 1 x 10 14 , 1 x 10 15 cfu of Pseudomonas (e.g., P. gessardii NRRL B-67767 and/or P. libanesis NRRL B-67769) is applied to each acre of plant growth media.

Strains, cultures, cell-free filtrates, cellular extracts and inoculant compositions of the present disclosure may be applied to plants, plant parts and/or plant growth media at any time, including, but not limited to, prior to planting, at the time of planting, after planting, prior to germination, at the time of germination, after germination, prior to seedling emergence, at the time of seedling emergence, after seedling emergence, prior to the vegetative stage, during the vegetative stage, after the vegetative stage, prior to the reproductive stage, during the reproductive stage, after the reproductive stage, prior to flowering, at the time of flowering, after flowering, prior to fruiting, at the time of fruiting, after fruiting, prior to ripening, at the time of ripening, and after ripening.

In some embodiments, one or more strains, cultures, cell-free filtrates, celluar extracts and/or inoculant compositions of the present disclosure is applied to plant propagation materials (e.g., seeds) about/at least 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 28, 32, 36, 40, 44, 48, 52, 56, 60, 64, 68, 72, 76, 80, 84, 88, 92, 96, 100, 104 weeks prior to planting.

In some embodiments, one or more strains, cultures, cell-free filtrates, celluar extracts and/or inoculant compositions of the present disclosure is applied to plant propagation materials (e.g., seeds) at the time of planting.

In some embodiments, one or more strains, cultures, cell-free filtrates, celluar extracts and/or inoculant compositions of the present disclosure is applied to plant propagation materials (e.g., seeds) after planting but before germination.

In some embodiments, one or more strains, cultures, cell-free filtrates, celluar extracts and/or inoculant compositions of the present disclosure is applied to plants following emergence.

In some embodiments, one or more strains, cultures, cell-free filtrates, celluar extracts and/or inoculant compositions is applied to a plant or plant part post-harvest (e.g., to prevent pest damage during a post-harvest storage period)

The present disclosure extends to plants and plant parts (e.g., coated plant propagation materials) that have been treated with one or more strains, cultures, cell-free filtrates, celluar extracts and/or inoculant compositions of the present disclosure, to plants that grow from plant parts (e.g., coated plant propagation materials) that have been treated with one or more strains, cultures, cell-free filtrates, celluar extracts and/or inoculant compositions of the present disclosure, to plant parts harvested from plants that have been treated with one or more strains, cultures, cell-free filtrates, celluar extracts and/or inoculant compositions of the present disclosure, to plant parts harvested from plants that grow from plant parts (e.g., coated plant propagation materials) that have been treated with one or more strains, cultures, cell- free filtrates, celluar extracts and/or inoculant compositions of the present disclosure, to processed products derived from plants that have been treated with one or more strains, cultures, cell-free filtrates, celluar extracts and/or inoculant compositions of the present disclosure, to processed products derived from plants that grow from plant parts (e.g., coated plant propagation materials) that have been treated with one or more strains, cultures, cell-free filtrates, celluar extracts and/or inoculant compositions of the present disclosure, to crops comprising a plurality of plants that have been treated with ne or more strains, cultures, cell-free filtrates, celluar extracts and/or inoculant compositions of the present disclosure, and to crops comprising a plurality of plants that grow from plant parts (e.g., coated plant propagation materials) that have been treated with one or more strains, cultures, cell-free filtrates, celluar extracts and/or inoculant compositions of the present disclosure.

In some embodiments, the present disclosure provides coated plant propagation materials comprising, consisting essentially of, or consisting of a plant propagation material and a coating that covers at least a portion of the outer surface of the plant propagation material, said coating comprising, consisting essentially of, or consisting of one or more strains, cultures, cell-free filtrates, celluar extracts and/or inoculant compositions of the present disclosure.

In some embodiments, the coating comprises two, three, four, five or more layers. According to some embodiments, the coating comprises an inner layer that contains one or more strains, cultures, cell- free filtrates and/or cellular extracts of the present disclosure and one or more outer layers free or substantially free of strains, cultures, cell-free filtrates and/or cellular extracts. In some embodiments, the coating comprises an inner layer that is an inoculant composition of the present disclosure and an outer layer that is equivalent to an inoculant composition of the present disclosure except that it does not contain the strains, cultures, cell-free filtrates and/or cellular extracts.

In some embodiments, the coating comprises, consists essentially of, or consists of a

culture/inoculant composition of the present disclosure and a drying powder. Drying powders may be applied in any suitable amount(s)/concentration(s). The absolute value of the amount/concentration that is/are sufficient to cause the desired effect(s) may be affected by factors such as the type, size and volume of material to which the compositon will be applied, the type(s) of microorganisms in the composition, the number of microorganisms in the composition, the stability of the microorganisms in the composition and storage conditions (e.g., temperature, relative humidity, duration). Those skilled in the art will understand how to select an effective amount/concentration using routine dose-response experiments. Guidance for the selection of appropriate amounts/concentrations can be found, for example, in International Patent Publication Nos. WO2017/044473, WO2017/044545, WO2017/116837, WO2017/116846,

WO2017/210163 and WO2017/210166 and in U.S. Provisional Patent Application Nos.62/296,798; 62/271,857; 62/347,773; 62/343,217; 62/296,784; 62/271,873; 62/347,785; 62/347,794; and 62/347,805. In some embodiments, the drying powder is applied in an amount ranging from about 0.5 to about 10 grams of drying powder per kilogram of plant propagation material. For example, in some embodiments, about 0.5, 1, 1.25, 1.5, 1.75, 2, 2.25, 2.5, 2.75, 3, 3.25, 3.5, 3.75, 4, 4.25, 4.5, 4.75, 5, 5.5, 6, 6.5, 7, 7.5, 8, 8.5, 9, 9.5, 10 grams or more of drying powder (e.g., drying powder comprising magnesium stearate, magnesium sulfate, powdered milk, silica, soy lecithin and/or talc) is applied per kilogram of seed. In some embodiments, a drying powder comprising calcium stearate, attapulgite clay, montmorillonite clay, graphite, magnesium stearate, silica (e.g., fumed silica, hydrophobically-coated silica and/or precipitated silica) and/or talc is applied to seeds coated with an inoculant composition of the present disclosure at a rate of about 1, 1.25, 1.5, 1.75, 2, 2.25, 2.5, 2.75, or 3 grams per kilogram of seed.

In some embodiments, the coating completely covers the outer surface of the plant propagation material. In some embodiments, the average thickness of the coating is at least 1.5, 1.6, 1.7, 1.8, 1.9, 2.0, 2.1, 2.2, 2.3, 2.4, 2.5, 2.6, 2.7, 2.8, 2.9, 3.0, 3.1, 3.2, 3.3, 3.4, 3.5, 4, 4.5, 5 µm or more. In some embodiments, the average thickness of the coating is about 1.5 to about 3.0 µm.

The present disclosure extends to kits comprising, consisting essentially of, or consisting of one or more plants and/or plant parts (e.g., coated plant propagation materials) that have been treated with one or more strains, cultures, cell-free filtrates, celluar extracts and/or inoculant compositions of the present disclosure and a container housing the treated plant(s) and/or plant part(s). In some embodiments, the kit further comprises one or more oxygen scavengers, such as activated carbon, ascorbic acid, iron powder, mixtures of ferrous carbonate and metal halide catalysts, sodium chloride and/or sodium hydrogen carbonate.

The container may comprise any suitable material(s), including, but not limited to, materials that reduce the amount of light, moisture and/or oxygen that contact the coated plant propagation material when the container is sealed. In some embodiments, the container comprises, consists essentially of, or consists of a material having light permeability of less than about 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70 or 75%. In some embodiments, the container comprises, consists essentially of, or consists of a material having an oxygen transmission rate of less than about 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 60, 70, 80, 90, 100, 125, 150, 175, 200, 225, 250, 275, 300, 325, 350, 375, 400, 425, 450, 475, or 500 cm3 /m 2 ·day (as measured in accordance with ASTM D3985).

In some embodiments, the container reduces the amount of ambient light that reaches said coated plant propagation material by about 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95 or 100% when sealed.

In some embodiments, the container reduces the amount of ambient moisture that reaches said plant propagation material by about 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95 or 100% when sealed.

In some embodiments, the container reduces the amount of ambient oxygen that reaches said plant propagation material by about 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95 or 100% when sealed.

In some embodiments, kits of the present disclosure comprise 1, 2, 3, 4, 5 or more additional containers. The additional containers may comprise any suitable component(s) or composition(s), including, but not limited to, agriculturally beneficial microorganisms, biostimulants, drying agents, nutrients, oxidation control components and pesticides. Examples of agriculturally beneficial

microorganisms, biostimulants, drying agents, nutrients, oxidation control components and pesticides that may be included in the additional containers are described above.

The present disclosure also extends to animal feed compositions comprising, consisting essentially of or consisting of a food component and a microbial component, said microbial component comprising, consisting essentially of, or consisting of one or more strains, cultures, cell-free filtrates, celluar extracts and/or inoculant compositions of the present disclosure.

Animal feed compositions of the present disclosure may comprise any suitable food component, including, but not limited to, fodder (e.g., grains, hay, legumes, silage and/or straw) and forage (e.g., grass).

Animal feed compositions of the present disclosure may be fed to any suitable animal, including, but not limited to, farm animals, zoo animals, laboratory animals and/or companion animals. In some embodiments, the animal feed composition is formulated to meet the dietary needs of birds (e.g., chickens, ducks, quails and/or turkeys), bovids (e.g., antelopes, bison, cattle, gazelles, goats, impala, oxen, sheep and/or wildebeests), canines, cervids (e.g., caribou, deer, elk and/or moose), equines (e.g., donkeys, horses and/or zebras), felines, fish, pigs, rabbits, rodents (e.g., guinea pigs, hamsters, mice and/or rats) and the like.

The present disclosure extends to methods and uses for strains, cultures, cell-free filtrates, celluar extracts and/or inoculant compositions of the present disclosure.

In some embodiments, methods and uses of the present disclosure comprise, consist essentially of or consist of applying one or more strains, cultures, cell-free filtrates, celluar extracts and/or inoculant compositions of the present disclosure to a plant or plant part (e.g., plant propagation material). Strains, cultures, cell-free filtrates, celluar extracts and inoculant compositions of the present disclosure may be applied to any type of plant, to any part/portion of a plant, in any suitable manner, in any suitable amount(s)/concentration(s) and at any suitable time(s).

In some embodiments, methods and uses of the present disclosure comprise, consist essentially of or consist of applying one or more strains, cultures, cell-free filtrates, celluar extracts and/or inoculant compositions of the present disclosure to a plant growth medium. Strains, cultures, cell-free filtrates, celluar extracts and inoculant compositions of the present disclosure may be applied to any plant growth medium, in any suitable manner, in any suitable amount(s)/concentration(s) and at any suitable time(s).

In some embodiments, methods and uses of the present disclosure comprise, consist essentially of or consist of introducing a plant or plant part (e.g., plant propagation material) that has been treated with one or more strains, cultures, cell-free filtrates, celluar extracts and/or inoculant compositions of the present disclosure into a plant growth medium (e.g., a soil). Such methods may further comprise introducing one or more nutrients (e.g., nitrogen and/or phosphorous) into the plant growth medium. Any suitable nutrient(s) may be added to the growth medium, including, but not limited to, rock phosphate, monoammonium phosphate, diammonium phosphate, monocalcium phosphate, super phosphate, triple super phosphate, ammonium polyphosphate, fertilizers comprising one or more phosphorus sources, and combinations thereof.

In some embodiments, methods and uses of the present disclosure comprise, consist essentially of or consist of growing a plant from a plant propagation material that has been treated with one or more strains, cultures, cell-free filtrates, celluar extracts and/or inoculant compositions of the present disclosure.

Strains, cultures, cell-free filtrates, celluar extracts and inoculant compositions of the present disclosure may be used to protect and enhance the growth and/or yield of various plants, including, but not limited to, cereals and pseudocereals, such as barley, buckwheat, corn, millet, oats, quinoa, rice, rye, sorghum and wheat, and legumes, such as alfalfa, beans, carob, clover, guar, lentils, mesquite, peas, peanuts, soybeans, tamarind, tragacanth and vetch.

Strains, cultures, cell-free filtrates, celluar extracts and inoculant compositions of the present disclosure may be used to prevent and/or treat infections/infestations by myriad plant pests, including, but not limited to, fungi and fungus-like organisms (e.g., soil-borne fungi from the classes Ascomycetes, Basidiomycetes, Chytridiomycetes, Deuteromycetes, Peronosporomycetes (syn. Oomycetes),

Plasmodiophoromycetes and Zygomycetes). In some embodiments, strains, cultures, cell-free filtrates, celluar extracts and inoculant compositions of the present disclosure are effective to kill, inhibit the growth of and/or inhibit the reproduction/proliferation of one or more strains of Albugo (e.g., A. candida), Alternaria (e.g. ¸A. alternata, A. solani), Aphanomyces, Armillaria, Ascomycota, Aspergillus (e.g., A. candidus, A. clavatus, A. flavus, A. fumigatus, A. parasiticus, A. restrictus, A. sojae, A. solani),

Bipolaris, Blumeria (e.g., B. graminis), Boeremia, Botrytis (e.g., B. cinerea), Calonectria, Ceratocystis, Cercospora (e.g., C. sojina, C. zeae-maydis), Chaetomium, Cladosporum (e.g., C. cladosporioides), Claviceps (e.g., C. purpurea), Colletotrichum (e.g., C. acutatum, C. boninense, C. capsici, C. caudatum, C. coccodes, C. crassipes, C. dematium, C. destructivum, C. fragariae, C. gloeosporioides, C.

graminicola, C. kehawee, C. lindemuthianum, C. musae, C. orbiculare, C. spinaceae, C. sublineolum, C. trifolii, C. truncatum), Coniella, Coniophora, Cryphonectria, Curvularia, Diplocarpon, Exserohilum (e.g., E. turcicum), Fibroporia, Fusarium (e.g., F. graminearum, F. moniliforme, F. oxysporum, F. roseum, F. tricinctum, F. virguliforme), Gaummannomuces, Gloeosporium, Guignardia, Helminthosporium, Magnaporthe (e.g., M. grisea, M. oryzae), Melamspora (e.g., M. lini), Microdochium (e.g. M. nivale), Monilinia, Mycosphaerella (e.g., M. graminicola), Nematospora,

Neofabraea, Neofusicoccum, Penicillium (e.g., P. rugulosum, P. verrucosum), Peronosporaceae, Phakopsora (e.g., P. pachyrhizi), Phoma, Phomopsis, Physoderma, Phytophthora (e.g., P. infestans), Phytomyxea, Phytoplasma, Pilidium, Plasmodiophora, Plasmospora (e.g., P. vitcola),

Pleiochaeta, Plenodomus, Poria, Protostegia, Pseudopersonospora (e.g., P. cubensis),

Pseudopyricularia, Puccinia (e.g., P. graminis, P. striiformis, P. tritici, P. triticina), Pucivinia (e.g., P. graministice), Pyrenophora, Pythium, Rhizoctonia (e.g., R. solani), Rhizopus, Saccharata, Sclerotinia (e.g., S. sclerotiorum), Sclerotium, Scopulariopsis, Septoria (e.g., S. tritici), Selerotinia, Serpula,

Setosphaeria (e.g., S. turcicum), Spiroplasma, Spongospora, Stenocarpella, Synchytrium, Taphrina, Thielaviopsis, Thyrostroma, Ustilago (e.g. U¸ . maydis), Venturia, Verticillium, Wilsonomyces or

Zymoseptoria. Additional examples of fungi and fungus-like organisms that may be treated with strains, cultures, cell-free filtrates, extracts and inoculant compositions of the present disclosure may be found in Bradley, Managing Diseases, in ILLINOIS AGRONOMY HANDBOOK (2008).

Non-limiting examples of plant conditions/diseases against which strains, cultures, cell-free filtrates, cellular extracts and inoculant compositions of the present disclosure may be used prevent and/or treat include anthracnose, apple scab, bacterial canker, black knot, blight (e.g., chestnut blight, early blight, fire blight, late blight, potato blight, wheat blight), blossom end rot, bottom rot, black root rot, black spot, blotch, brown patch, brown rot, canker rot, club root, cottony rot, damping off, decay, dollar spot, dutch elm disease, gall, leaf blot, leaf curl, leaf spot (e.g., frog eye leaf spot, gray leaf spot), mildew (e.g., downy mildew, powdery mildew), mold (e.g., white mold), mosaic virus, pink root, wilting (e.g., clematis wilt, Fusarium wilt, Verticillium wilt), powdery scab, red thread, Rhixoctonia disease, rice blast, root rot, rust (e.g., Asian soy rust), scab, soft rot, sclerotium rot, smut, stalk rot, sudden death syndrome, warts (e.g., crown wart, potato wart), wet rot, white rot, white ear rot, and yellow spots.

Strains, cultures, cell-free filtrates, celluar extracts and inoculant compositions of the present disclosure may be used to protect and enhance the growth and/or yield of plants under various growth conditions, including, but not limited to, nutritional deficits (e.g., calcium, iron, manganese, magnesium, nitrogen, phosphorous, potassium and/or sulfur deficiencies), humidity extremes, pH extremes, temperature extremes, (e.g., average daytime temperatures below 60, 61, 62, 63, 64, 65, 66, 67, 68, 69, 70, 71, 72, 7374 or 75°C, average daytime temperatures above 85, 86, 87, 88, 89, 90, 91, 92, 93, 94, 95, 96, 97, 98, 99, 100°C or more, average nighttime temperatures below 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63, 64, 65, 66, 67, 68, 69 or 70°C, average nighttime temperatures above 70, 71, 72, 73, 74, 75, 76, 77, 78, 79, 80, 81, 82, 83, 84, 85°C or more, etc.) and drought conditions (e.g., less than 5, 6, 7, 8, 9, 10, 11, 12, 13, 14 or 15 inches of rainfall during the growing season). It is to be understood that any determination of what constitutes a nutritional deficit, temperature extreme, drought condition, etc. must account for the plant species/variety being grown, as different species/varieties may have different preferences and requirements.

Strains, cultures, cell-free filtrates, celluar extracts and inoculant compositions of the present disclosure may be used to protect and enhance the growth and/or yield of plants in various geographical regions, including, but not limited to, agricultural regions in Afghanistan, Argentina, Australia,

Bangladesh, Bolivia, Brazil, Canada, Chile, China, Columbia, Ecuador, Egypt, Ethiopia, Europe (e.g., agricultural regions in Austria, Belgium, Bulgaria, Czech Republic, Denmark, France, Germany,

Hungary, Ireland, Italy, Lithuania, the Netherlands, Poland, Romania, Spain, Sweden and/or the United Kingdom), India, Indonesia, Iran, Iraq, Japan, Kazakhstan, Kenya, Malawi, Mexico, Morocco, Nigeria, Pakistan, Paraguay, Peru, the Philippines, Russia, South Africa, Taiwan, Tanzania, Thailand, Turkey, Ukraine, the United States (e.g., agricultural regions in Arkansas, Colorado, Idaho, Illinois, Indiana, Iowa, Kansas, Kentucky, Michigan, Minnesota, Mississippi, Missouri, Montana, Nebraska, North Dakota, Ohio, Oklahoma, South Dakota, Texas and/or Wisconsin), Uzbekistan, Venezuela, Vietnam, Zambia and/or Zimbabwe. In some embodiments, one or more strains of the present disclosure (or an inoculant composition of the present disclosure) is used to enhance plant growth and/or yield in a geographical region that encompasses multiple agricultural regions (e.g., agricultural regions in Illinois, Iowa, southern Minnesota and eastern Nebraska). Examples of such geographical regions include, but are not limited to, a northern corn region encompassing agricultural regions in Iowa (e.g., northern Iowa), Michigan,

Minnesota, North Dakota, South Dakota and/or Wisconsin; a central corn region encompassing agricultural regions in Illinois (e.g., northern and/or central Illinois), Indiana (e.g., northern Indiana), Iowa (e.g., southern Iowa), Kansas (e.g., northern Kansas), Missouri (e.g,, northern Missouri), Nebraska (e.g., northern and/or southern Nebraska) and/or Ohio; a southern corn region encompassing agricultural regions in Alabama (e.g., northern and/or southern Alabama), Arkansas, Georgia (e.g., northern and/or southern Georgia), Illinois (e.g., southern Illinois), Indiana (e.g., southern Indiana), Kansas, Kentucky, Louisiana, Maryland, Missouri (e.g., central and/or southern Missouri), Mississippi (e.g., northern and/or southern Mississippi), Nebraska (e.g., southern Nebraska), North Carolina, Oklahoma, South Carolina, Tennessee, Texas and/or Virginia; a northern wheat region encompassing agricultural regions in Minnesota, Montana (e.g., eastern Montana), Nebraska, North Dakota, South Dakota and/or Wyoming (e.g., eastern Wyoming); a northern wheat region encompassing agricultural regions in Idaho, Oregon and/or Washington; a central wheat region encompassing agricultural regions in Colorado, Nebraska, South Dakota and/or Wyoming (e.g., eastern Wyoming); a central wheat region encompassing agricultural regions in Illinois, Indiana, Iowa, Missouri and/or Ohio; a central wheat region encompassing agricultural regions in Kansas, Oklahoma and/or Texas; and a southern wheat region encompassing agricultural regions in Oklahoma and/or Texas.

Strains, cultures, cell-free filtrates, celluar extracts and inoculant compositions of the present disclosure may be used to kill, inhibit the growth of and/or inhibit the reproduction/proliferation of myriad plant pests. In some embodiments, application of one or more strains, cultures, cell-free filtrates, celluar extracts and/or inoculant compositions of the present disclosure to a plant or plant part (e.g., plant propagation material) or to a plant growth medium (e.g., a soil) is effective to kill about/at least 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95% or more of one or more pests present on/in said plant, plant part or plant growth medium. For example, in some embodiments, application of E. billingiae NRRL B-67766, P. gessardii NRRL B-67767 and/or P. libanesis NRRL B-67769 (or a cell-free filtrate or celluar extract derived therefrom) to a plant (e.g, a cereal or pseudocereal, such as barley, buckwheat, corn, millet, oats, quinoa, rice, rye, sorghum or wheat) is effective to kill about/at least 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95% or more of phytopathogenic fungi (e.g.,

phytopathogenic Zymoseptoria) on the surface of said plant.

In some embodiments, application of one or more strains, cultures, cell-free filtrates, celluar extracts and/or inoculant compositions of the present disclosure to a plant or plant part (e.g., plant propagation material) or to a plant growth medium (e.g., a soil) is effective to inhibit the growth of one or more pests present on/in said plant, plant part or plant growth medium by about/at least 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95% or more as compared to the growth of said pest(s) on a control plant, plant part or plant growth medium (e.g., untreated control plants and/or plants treated with an alternative microbial strain). For example, in some embodiments, application of E. billingiae NRRL B-67766, P. gessardii NRRL B-67767 and/or P. libanesis NRRL B-67769 (or a cell-free filtrate or celluar extract derived therefrom) to a plant (e.g, a cereal or pseudocereal, such as barley, buckwheat, corn, millet, oats, quinoa, rice, rye, sorghum or wheat) is effective to inhibit the growth of one or more phytopathogenic fungi (e.g., phytopathogenic Zymoseptoria) by about/at least 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95% or more.

In some embodiments, application of one or more strains, cultures, cell-free filtrates, celluar extracts and/or inoculant compositions of the present disclosure to a plant or plant part (e.g., plant propagation material) or to a plant growth medium (e.g., a soil) is effective to inhibit the

reproduction/proliferation of one or more pests present on/in said plant, plant part or plant growth medium by about/at least 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95% or more as compared to the reproduction/proliferation of said pest(s) on a control plant, plant part or plant growth medium (e.g., untreated control plants and/or plants treated with an alternative microbial strain). For example, in some embodiments, application of E. billingiae NRRL B-67766, P. gessardii NRRL B-67767 and/or P. libanesis NRRL B-67769 (or a cell-free filtrate or celluar extract derived therefrom) to a plant (e.g, a cereal or pseudocereal, such as barley, buckwheat, corn, millet, oats, quinoa, rice, rye, sorghum or wheat) is effective to inhibit the reproduction/proliferation of one or more phytopathogenic fungi (e.g., phytopathogenic Zymoseptoria) by about/at least 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95% or more.

Accordingly, in some embodiments, methods and uses of the present disclosure comprise, consist essentially of or consist of applying one or more strains, cultures, cell-free filtrates, celluar extracts and/or inoculant compositions of the present disclosure to seed, to the plant growth medium in which said seed is being or will be grown, and/or to the plant(s) that grow(s) from said seed in an amount/concentration effective to kill, inhibit the growth of and/or inhibit the reproduction/proliferation of one or more plant pests.

Strains, cultures, cell-free filtrates, celluar extracts and inoculant compositions of the present disclosure may be used to reduce numerous aspects of disease severity, including, but not limited to, disease incidence, diseased area, pathogen load, rate of infection/infestation, symptom severity and/or toxin load, . In some embodiments, application of one or more strains, cultures, cell-free filtrates, celluar extracts and/or inoculant compositions of the present disclosure to a plant or plant part (e.g., plant propagation material) or to a plant growth medium (e.g., a soil) reduces one or more aspects of disease severity (e.g., disease incidence, diseased area, pathogen load, rate of infection/infestation, symptom severity and/or toxin load) by about/at least 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95% or more. For example, in some embodiments, application of E. billingiae NRRL B-67766, P. gessardii NRRL B-67767 and/or P. libanesis NRRL B-67769 (or a cell-free filtrate or celluar extract derived therefrom) to a plant (e.g, a cereal or pseudocereal, such as barley, buckwheat, corn, millet, oats, quinoa, rice, rye, sorghum or wheat) reduces the disease incidence, diseased area, pathogen load, rate of infection/infestation, symptom severity and/or toxin load of a fungal infection (e.g., an infection mediated by Zymoseptoria) by about/at least 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95% or more as compared to that of a corresponding fungal infection in untreated control plants and/or plants treated with an alternative microbial strain.

Accordingly, in some embodiments, methods and uses of the present disclosure comprise, consist essentially of or consist of applying one or more strains, cultures, cell-free filtrates, celluar extracts and/or inoculant compositions of the present disclosure to seed, to the plant growth medium in which said seed is being or will be grown, and/or to the plant(s) that grow(s) from said seed in an amount/concentration effective to reduce one or more characteristics of disease severity.

In some embodiments, one or more strains, cultures, cell-free filtrates, celluar extracts and/or inoculant compositions of the present disclosure is applied to seed in an amount/concentration effective to reduce 1, 2, 3, 4, 5 or more characteristics of disease severity (e.g., disease incidence, diseased area, pathogen load, rate of infection/infestation, symptom severity and/or toxin load) of the plant that grows from said seed by at least about 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95% or more as compared to one or more control plants (e.g., plants grown from untreated seed and/or plants grown from seed treated with a control composition that is identical to the inoculant composition of the present disclosure except that it lacks at least one of the strains of the present disclosure found in the inoculant composition).

In some embodiments, one or more strains, cultures, cell-free filtrates, celluar extracts and/or inoculant compositions of the present disclosure is applied to plants (e.g., to the foliage of plants) in an amount/concentration effective to reduce 1, 2, 3, 4, 5 or more characteristics of disease severity (e.g., disease incidence, diseased area, pathogen load, rate of infection/infestation, symptom severity and/or toxin load) of the plant that grows from said seed by at least about 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95% or more as compared to one or more control plants (e.g., untreated plants and/or plants treated with a control composition that is identical to the inoculant composition of the present disclosure except that it lacks at least one of the strains of the present disclosure found in the inoculant composition).

In some embodiments, one or more strains, cultures, cell-free filtrates, celluar extracts and/or inoculant compositions of the present disclosure is introduced into a plant growth medium (e.g., soil) in an amount/concentration effective to reduce 1, 2, 3, 4, 5 or more characteristics of disease severity (e.g., disease incidence, diseased area, pathogen load, rate of infection/infestation, symptom severity and/or toxin load) of plants grown therein by at least about 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 100, 105, 110, 115, 120, 125, 150, 175, 200, 225, 250% or more as compared to one or more controls (e.g., plants grown in untreated soil and/or plants grown in soil treated with an alternative microbial strain).

In some embodiments, application of one or more strains, cultures, cell-free filtrates, celluar extracts and/or inoculant compositions of the present disclosure enhances 1, 2, 3, 4, 5 or more growth characteristics and/or 1, 2, 3, 4, 5 or more yield characteristics by about/at least 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 100, 105, 110, 115, 120, 125, 150, 175, 200, 225, 250% or more as compared to one or more controls (e.g., untreated control plants and/or plants treated with an alternative microbial strain). For example, in some embodiments, application of E. billingiae NRRL B- 67766, P. gessardii NRRL B-67767 and/or P. libanesis NRRL B-67769 (or a cell-free filtrate or celluar extract derived therefrom) enhance(s) cereal or pseudocereal yield by about/at least 0.25, 0.5, 0.75, 1, 1.1, 1.2, 1.3, 1.4, 1.5, 1.6, 1.7, 1.8, 1.9, 2.0, 2.1, 2.2, 2.3, 2.4, 2.5, 2.6, 2.7, 2.8, 2.9, 3.0, 3.1, 3.2, 3.3, 3.4, 3.5, 3.6, 3.7, 3.8, 3.9, 4, 4.1, 4.2, 4.3, 4.4, 4.5 or 4.6 bushels per acre as compared to the yield of untreated control plants and/or plants treated with an alternative microbial strain. Similarly, in some embodiments, application of E. billingiae NRRL B-67766, P. gessardii NRRL B-67767 and/or P. libanesis NRRL B- 67769 (or a cell-free filtrate or celluar extract derived therefrom) enhance(s) legume yield by about/at least 0.25, 0.5, 0.75, 1, 1.1, 1.2, 1.3, 1.4, 1.5, 1.6, 1.7, 1.8, 1.9 or 2.0 bushels per acre as compared to the yield of untreated control plants and/or plants treated with an alternative microbial strain.

Accordingly, in some embodiments, methods and uses of the present disclosure comprise, consist essentially of or consist of applying one or more strains, cultures, cell-free filtrates, celluar extracts and/or inoculant compositions of the present disclosure to cereal, pseudocereal or legume seed, to the plant growth medium in which said cereal, pseudocereal or legume seed is being or will be grown, and/or to the plant(s) that grow(s) from said cereal, pseudocereal or legume seed in an amount/concentration effective to enhance one or more plant growth characteristics and/or one or more plant yield characteristics.

In some embodiments, one or more strains, cultures, cell-free filtrates, celluar extracts and/or inoculant compositions of the present disclosure is applied to seed in an amount/concentration effective to enhance 1, 2, 3, 4, 5 or more plant growth characteristics (e.g., biomass) and/or 1, 2, 3, 4, 5 or more plant yield characteristics (e.g., bushels per acre) of the plant that grows from said seed by at least about 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 100, 105, 110, 115, 120, 125, 150, 175, 200, 225, 250% or more as compared to one or more control plants (e.g., plants grown from untreated seed and/or plants grown from seed treated with a control composition that is identical to the inoculant composition of the present disclosure except that it lacks at least one of the strains of the present disclosure found in the inoculant composition). According to some embodiments, one or more strains, cultures, cell-free filtrates, celluar extracts and/or inoculant compositions of the present disclosure is applied to cereal or psuedocereal seed in an amount effective to enhance yield by about/at least 0.25, 0.5, 0.75, 1, 1.1, 1.2, 1.3, 1.4, 1.5, 1.6, 1.7, 1.8, 1.9, 2, 2.1, 2.2, 2.3, 2.4, 2.5, 2.6, 2.7, 2.8, 2.9, 3, 3.1, 3.2, 3.3, 3.4, 3.5, 3.6, 3.7, 3.8, 3.9, 4, 4.1, 4.2, 4.3, 4.4, 4.54.6, 4.7, 4.8, 4.9, 5 or more bushels per acre. According to some embodiments, one or more strains, cultures, cell-free filtrates, celluar extracts and/or inoculant compositions of the present disclosure is applied to legume seed in an amount effective to enhance yield by about/at least 0.25, 0.5, 0.75, 1, 1.1, 1.2, 1.3, 1.4, 1.5, 1.6, 1.7, 1.8, 1.9, 2, 2.1, 2.2, 2.3, 2.4, 2.5, 2.6, 2.7, 2.8, 2.9, 3 or more bushels per acre.

In some embodiments, one or more strains, cultures, cell-free filtrates, celluar extracts and/or inoculant compositions of the present disclosure is applied to plants in an amount/concentration effective to enhance 1, 2, 3, 4, 5 or more plant growth characteristics (e.g., biomass) and/or 1, 2, 3, 4, 5 or more plant yield characteristics (e.g., bushels per acre) of the plant that grows from said seed by at least about 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 100, 105, 110, 115, 120, 125, 150, 175, 200, 225, 250% or more as compared to one or more control plants (e.g., untreated plants and/or plants treated with a control composition that is identical to the inoculant composition of the present disclosure except that it lacks at least one of the strains of the present disclosure found in the inoculant composition). According to some embodiments, one or more strains, cultures, cell-free filtrates, celluar extracts and/or inoculant compositions of the present disclosure is applied to cereal or psuedocereal plants in an amount effective to enhance yield by about/at least 0.25, 0.5, 0.75, 1, 1.1, 1.2, 1.3, 1.4, 1.5, 1.6, 1.7, 1.8, 1.9, 2, 2.1, 2.2, 2.3, 2.4, 2.5, 2.6, 2.7, 2.8, 2.9, 3, 3.1, 3.2, 3.3, 3.4, 3.5, 3.6, 3.7, 3.8, 3.9, 4, 4.1, 4.2, 4.3, 4.4, 4.54.6, 4.7, 4.8, 4.9, 5 or more bushels per acre. According to some embodiments, one or more strains, cultures, cell-free filtrates, celluar extracts and/or inoculant compositions of the present disclosure is applied to leguminous plants in an amount effective to enhance yield by about/at least 0.25, 0.5, 0.75, 1, 1.1, 1.2, 1.3, 1.4, 1.5, 1.6, 1.7, 1.8, 1.9, 2, 2.1, 2.2, 2.3, 2.4, 2.5, 2.6, 2.7, 2.8, 2.9, 3 or more bushels per acre.

In some embodiments, one or more strains, cultures, cell-free filtrates, celluar extracts and/or inoculant compositions of the present disclosure is introduced into a plant growth medium (e.g., soil) in an amount/concentration effective to enhance 1, 2, 3, 4, 5 or more plant growth characteristics (e.g., biomass) and/or 1, 2, 3, 4, 5 or more plant yield characteristics (e.g., bushels per acre) of plants grown therein by at least about 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 100, 105, 110, 115, 120, 125, 150, 175, 200, 225, 250% or more as compared to one or more controls (e.g., plants grown in untreated soil and/or plants grown in soil treated with an alternative microbial strain). According to some embodiments, one or more strains, cultures, cell-free filtrates, celluar extracts and/or inoculant compositions of the present disclosure is introduced into the plant growth medium in an amount effective to enhance cereal or psuedocereal yield by about/at least 0.25, 0.5, 0.75, 1, 1.1, 1.2, 1.3, 1.4, 1.5, 1.6, 1.7, 1.8, 1.9, 2, 2.1, 2.2, 2.3, 2.4, 2.5, 2.6, 2.7, 2.8, 2.9, 3, 3.1, 3.2, 3.3, 3.4, 3.5, 3.6, 3.7, 3.8, 3.9, 4, 4.1, 4.2, 4.3, 4.4, 4.54.6, 4.7, 4.8, 4.9, 5 or more bushels per acre. According to some embodiments, one or more strains, cultures, cell-free filtrates, celluar extracts and/or inoculant compositions of the present disclosure is introduced into the plant growth medium in an amount effective to enhance legume yield by about/at least 0.25, 0.5, 0.75, 1, 1.1, 1.2, 1.3, 1.4, 1.5, 1.6, 1.7, 1.8, 1.9, 2, 2.1, 2.2, 2.3, 2.4, 2.5, 2.6, 2.7, 2.8, 2.9, 3 or more bushels per acre.

Particular embodiments of the present disclosure are described in the following numbered paragraphs:

1. An isolated strain of the present disclosure, optionally E. billingiae NRRL B-67766 or a close relative thereof (e.g., a closely related progeny of E. billingiae NRRL B-67766 or a closely related modified microbial strain derived from E. billingiae NRRL B-67766), P. gessardii NRRL B-67767 or a close relative thereof (e.g., a closely related progeny of P. gessardii NRRL B-67767or a closely related modified microbial strain derived from P. gessardii NRRL B-67767), or P. libanesis NRRL B-67769 or a close relative threeof (e.g., a closely related progeny of P. libanesis NRRL B-67769 or a closely related modified microbial strain derived from P. libanesis NRRL B-67769).

2. A biologically pure culture of E. billingiae NRRL B-67766 or a close relative thereof (e.g., a closely related progeny of E. billingiae NRRL B-67766 or a closely related modified microbial strain derived from E. billingiae NRRL B-67766).

3. A biologically pure culture of P. gessardii NRRL B-67767 or a close relative thereof (e.g., a closely related progeny of P. gessardii NRRL B-67767or a closely related modified microbial strain derived from P. gessardii NRRL B-67767).

4. A biologically pure culture of P. libanesis NRRL B-67769 or a close relative thereof (e.g., a closely related progeny of P. libanesis NRRL B-67769 or a closely related modified microbial strain derived from P. libanesis NRRL B-67769).

5. A whole broth culture comprising one or more strains of the present disclosure, optionally E. billingiae NRRL B-67766 or a close relative thereof (e.g., a closely related progeny of E. billingiae NRRL B-67766 or a closely related modified microbial strain derived from E. billingiae NRRL B-67766), P. gessardii NRRL B-67767 or a close relative thereof (e.g., a closely related progeny of P. gessardii NRRL B-67767or a closely related modified microbial strain derived from P. gessardii NRRL B-67767), and/or P. libanesis NRRL B-67769 or a close relative threeof (e.g., a closely related progeny of P. libanesis NRRL B-67769 or a closely related modified microbial strain derived from P. libanesis NRRL B-67769).

6. A cell-free filtrate derived from a culture comprising one or more strains of the present disclosure, optionally E. billingiae NRRL B-67766 or a close relative thereof (e.g., a closely related progeny of E. billingiae NRRL B-67766 or a closely related modified microbial strain derived from E. billingiae NRRL B-67766), P. gessardii NRRL B-67767 or a close relative thereof (e.g., a closely related progeny of P. gessardii NRRL B-67767or a closely related modified microbial strain derived from P. gessardii NRRL B-67767), and/or P. libanesis NRRL B-67769 or a close relative threeof (e.g., a closely related progeny of P. libanesis NRRL B-67769 or a closely related modified microbial strain derived from P. libanesis NRRL B-67769).

7. A cellular extract derived from a strain of the present disclosure, optionally E. billingiae NRRL B-67766 or a close relative thereof (e.g., a closely related progeny of E. billingiae NRRL B-67766 or a closely related modified microbial strain derived from E. billingiae NRRL B-67766), P. gessardii NRRL B-67767 or a close relative thereof (e.g., a closely related progeny of P. gessardii NRRL B- 67767or a closely related modified microbial strain derived from P. gessardii NRRL B-67767), or P. libanesis NRRL B-67769 or a close relative threeof (e.g., a closely related progeny of P. libanesis NRRL B-67769 or a closely related modified microbial strain derived from P. libanesis NRRL B-67769).

8. An inoculant compositon comprising, consisting essentially of or consisting of one or more strains of the present disclosure, optionally E. billingiae NRRL B-67766 or a close relative thereof (e.g., a closely related progeny of E. billingiae NRRL B-67766 or a closely related modified microbial strain derived from E. billingiae NRRL B-67766), P. gessardii NRRL B-67767 or a close relative thereof (e.g., a closely related progeny of P. gessardii NRRL B-67767or a closely related modified microbial strain derived from P. gessardii NRRL B-67767), and/or P. libanesis NRRL B-67769 or a close relative threeof (e.g., a closely related progeny of P. libanesis NRRL B-67769 or a closely related modified microbial strain derived from P. libanesis NRRL B-67769), and an agriculturally acceptable carrier.

9. The inoculant composition of paragraph 8, said composition comprising about 1 x 10 3 to about 1 x 10 12 colony-forming units (cfu) of (each of) said one or more strains of the present disclosure per gram and/or milliliter of inoculant composition, optionally about/at least 1 x 10 3 , 1 x 10 4 , 1 x 10 5 , 1 x 10 6 , 1 x 10 7 , 1 x 10 8 , 1 x 10 9 , 1 x 10 10 , 1 x 10 11 , or 1 x 10 12 cfu per gram and/or milliliter of inoculant composition.

10. The inoculant composition of any one of paragraphs 8–9, said composition further comprising one or more stabilizing compounds.

11. The inoculant composition of paragraph 10, said one or more stabilizing compounds comprising, consisting essentially of or consisting of:

one or more monosaccharides, optionally arabinose, fructose and/or glucose;

one or more disaccharides, optionally maltose, sucrose and/or trehalose;

one or more maltodextrins, optionally one or more maltodextrins (e.g., one or more maltodextrins (each and/or collectively) having a DEV value of about 15 to about 20;

one or more sugar alcohols, optionally arabitol, mannitol, sorbitol and/or xylitol;

one or more humic acids, optionally potassium humate and/or sodium humate;

one or more fulvic acids, optionally potassium fulvate and/or sodium fulvate;

one or more hygroscopic polymers, optionally one or more albumins, alginates, celluloses, gums (e.g., cellulose gum, guar gum, gum arabic, gum combretum, xantham gum), methyl celluloses, nylons, pectins, polyacrylic acids, polycarbonates, polyethylene glycols (PEG), polyethylenimines (PEI), polylactides, polymethylacrylates (PMA), polyurethanes, polyvinyl alcohols (PVA),

polyvinylpyrrolidones (PVP), propylene glycols, sodium carboxymethyl celluloses and/or starches;

one or more oxidation control components, optionally one or more antioxidants (e.g., ascorbic acid, ascorbyl palmitate, ascorbyl stearate, calcium ascorbate, one or more carotenoids, lipoic acid, one or more phenolic compounds (e.g., one or more flavonoids, flavones and/or flavonols), potassium ascorbate, sodium ascorbate, one or more thiols (e.g., glutathione, lipoic acid and/or N-acetyl cysteine), one or more tocopherols, one or more tocotrienols, ubiquinone and/or uric acid) and/or one or more oxygen scavengers, optionally ascorbic acid and/or sodium hydrogen carbonate; and/or

one or more UV protectants, optionally one or more lignosulfites.

12. The inoculant composition of any one of paragraphs 10–11, said one or more stabilizing compounds comprising about 0.0001 to about 10% (by weight) of said composition, optionally about 2 to about 6% (by weight) of said composition, optionally about 0.0005, 0.001, 0.002, 0.003, 0.004, 0.005, 0.0075, 0.01, 0.02, 0.03, 0.04, 0.05, 0.06, 0.07, 0.08, 0.09, 0.1, 0.15, 0.2, 0.25, 0.3, 0.35, 0.4, 0.45, 0.5, 1, 1.5, 2, 2.5, 3, 3.5, 4, 4.5, 5, 5.5, 6, 7, 7.5, 8, 8.5, 9, 9.5 or 10% (by weight) of said composition.

13. The inoculant composition of any one of paragraphs 10–12, wherein said one or more stabilizing compounds is/are present in an amount/concentration sufficient to ensure said one or more strains of the present disclosure remain(s) viable in inoculant compositions of the present disclosure following:

storage at 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39 and/or 40°C and 0, 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95% or more relative humidity for a period of 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 28, 32, 36, 40, 44, 48, 52, 56, 60, 64, 68, 72, 76, 80, 84, 88, 92, 96, 100, 104 weeks or more;

desiccation by about 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95% or more;

desiccation by about 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95% or more and storage at 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39 and/or 40°C and 0, 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95% or more relative humidity for a period of 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 28, 32, 36, 40, 44, 48, 52, 56, 60, 64, 68, 72, 76, 80, 84, 88, 92, 96, 100, 104 weeks or more;

cryopreservation at or below -80°C for a period of 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 28, 32, 36, 40, 44, 48, 52, 56, 60, 64, 68, 72, 76, 80, 84, 88, 92, 96, 100, 104 weeks or more;

application to plant propagation material (optionally, seed);

application to plant propagation material and desiccation by about 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95% or more;

application to a plant propagation material and storage at 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39 and/or 40°C and 0, 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95% or more relative humidity for a period of 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 28, 32, 36, 40, 44, 48, 52, 56, 60, 64, 68, 72, 76, 80, 84, 88, 92, 96, 100, 104 weeks or more;

foliar application;

foliar application and desiccation by about 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95% or more; and/or

foliar application and exposure to temperatures of 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39 and/or 40°C and relative humidities of 0, 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95% or more for a period of 0.1, 0.2, 0.25, 0.5, 0.75, 1, 1.5, 2, 2.5, 3, 3.5, 4, 4.5, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21 days or more.

14. The inoculant composition of any one of paragraphs 10–12, wherein said one or more stabilizing compounds is/are present in an amount/concentration sufficient to ensure at least 0.01, 0.05, 0.1, 0.5, 1, 2, 3, 4, 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95% of said one or more strains of the present disclosure remains viable following:

storage at 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39 and/or 40°C and 0, 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95% or more relative humidity for a period of 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 28, 32, 36, 40, 44, 48, 52, 56, 60, 64, 68, 72, 76, 80, 84, 88, 92, 96, 100, 104 weeks or more;

desiccation by about 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95% or more;

desiccation by about 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95% or more and storage at 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39 and/or 40°C and 0, 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95% or more relative humidity for a period of 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 28, 32, 36, 40, 44, 48, 52, 56, 60, 64, 68, 72, 76, 80, 84, 88, 92, 96, 100, 104 weeks or more;

cryopreservation at or below -80°C for a period of 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 28, 32, 36, 40, 44, 48, 52, 56, 60, 64, 68, 72, 76, 80, 84, 88, 92, 96, 100, 104 weeks or more;

application to plant propagation material (optionally, seed);

application to plant propagation material and desiccation by about 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95% or more;

application to a plant propagation material and storage at 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39 and/or 40°C and 0, 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95% or more relative humidity for a period of 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 28, 32, 36, 40, 44, 48, 52, 56, 60, 64, 68, 72, 76, 80, 84, 88, 92, 96, 100, 104 weeks or more; foliar application;

foliar application and desiccation by about 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95% or more; and/or

foliar application and exposure to temperatures of 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39 and/or 40°C and relative humidities of 0, 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95% or more for a period of 0.1, 0.2, 0.25, 0.5, 0.75, 1, 1.5, 2, 2.5, 3, 3.5, 4, 4.5, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21 days or more.

15. The inoculant composition of any one of paragraphs 10–12, wherein said one or more stabilizing compounds is/are present in an amount/concentration sufficient to ensure at least 1 x 10 1 , 1 x 10 2 , 1 x 10 3 , 1 x 10 4 , 1 x 10 5 , 1 x 10 6 , 1 x 10 7 , 1 x 10 8 , 1 x 10 9 , 1 x 10 10 or more colony-forming units of said one or more strains of the present disclosure per gram and/or milliliter of inoculant composition remain viable following:

storage at 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39 and/or 40°C and 0, 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95% or more relative humidity for a period of 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 28, 32, 36, 40, 44, 48, 52, 56, 60, 64, 68, 72, 76, 80, 84, 88, 92, 96, 100, 104 weeks or more;

desiccation by about 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95% or more;

desiccation by about 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95% or more and storage at 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39 and/or 40°C and 0, 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95% or more relative humidity for a period of 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 28, 32, 36, 40, 44, 48, 52, 56, 60, 64, 68, 72, 76, 80, 84, 88, 92, 96, 100, 104 weeks or more;

cryopreservation at or below -80°C for a period of 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 28, 32, 36, 40, 44, 48, 52, 56, 60, 64, 68, 72, 76, 80, 84, 88, 92, 96, 100, 104 weeks or more;

application to plant propagation material (optionally, seed);

application to plant propagation material and desiccation by about 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95% or more;

application to a plant propagation material and storage at 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39 and/or 40°C and 0, 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95% or more relative humidity for a period of 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 28, 32, 36, 40, 44, 48, 52, 56, 60, 64, 68, 72, 76, 80, 84, 88, 92, 96, 100, 104 weeks or more;

foliar application; foliar application and desiccation by about 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95% or more; and/or

foliar application and exposure to temperatures of 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39 and/or 40°C and relative humidities of 0, 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95% or more for a period of 0.1, 0.2, 0.25, 0.5, 0.75, 1, 1.5, 2, 2.5, 3, 3.5, 4, 4.5, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21 days or more.

16. The inoculant composition of any one of paragraphs 8–15, said composition further comprising one or more biostimulants, optionally one or more seaweed extracts, myo-inositol and/or glycine.

17. The inoculant composition of any one of paragraphs 8–16, said composition further comprising one or more microbial extracts, optionally one or more of the microbial extracts expressly disclosed above.

18. The inoculant composition of any one of paragraphs 8–17, said composition further comprising one or more nutrients, optionally one or more vitamins (e.g., vitamin A, vitamin B complex (i.e., vitamin B 1 , vitamin B 2 , vitamin B 3 , vitamin B 5 , vitamin B 6 , vitamin B 7 , vitamin B 8 , vitamin B 9 , vitamin B 12 and/or choline) vitamin C, vitamin D, vitamin E and/or vitamin K), carotenoids (a-carotene, b-carotene, cryptoxanthin, lutein, lycopene and/or zeaxanthin), macrominerals (e.g., calcium, iron, magnesium, phosphorous, potassium and/or sodium), trace minerals (e.g., boron, cobalt, chloride, chromium, copper, fluoride, iodine, iron, manganese, molybdenum, selenium and/or zinc) and/or organic acids (e.g., acetic acid, citric acid, lactic acid, malic aclid and/or taurine).

19. The inoculant composition of any one of paragraphs 8–18, said composition further comprising one or more pest attractant and/or feeding stimulants, optionally brevicomin, ceralure, codlelure, cue-lure, disparlure, dominicalure, eugenol, frontalin, gossyplure, grandlure, hexalure, ipsdienol, ipsenol, japonilure, latitlure, lineatin, litlure, looplure, medlure, megatomic acid, methyl eugenol, moguchun, a-multistriatin, muscalure, orfalure, oryctalure, ostramone, rescalure, siglure, sulcatol, trimedlure and/or trunc-call.

20. The inoculant composition of any one of paragraphs 8–19, said composition further comprising one or more pesticides, optionally:

one or more fungicides, optionally one or more of the fungicides expressly disclosed above; one or more herbicides, optionally one or more of the herbicides expressly disclosed above; one or more insecticides, optionally one or more of the insecticides expressly disclosed above; and/or

one or more nematicides, optionally one or more of the nematicides expressly disclosed on above. 21. The inoculant composition of any one of paragraphs 8–20, said composition further comprising one or more lipo-chitooligosaccharides, optionally one or more of the lipo- chitooligosaccharides represented by formulas I–IV.

22. The inoculant composition of any one of paragraphs 8–20, said composition further comprising one or more of the lipo-chitooligosaccharides represented by structures V–XXXIII. 23. The inoculant composition of any one of paragraphs 8–22, said composition further comprising one or more chitooligosaccharides, optionally one or more of the chitin oligosaccharides represented by formulas XXXIV–XXXV.

24. The inoculant composition of any one of paragraphs 8–22, said composition further comprising one or more of the chitin oligosaccharides represented by structures XXXVI–LXXXIII.

25. The inoculant composition of any one of paragraphs 8–24, said composition further comprising one or more chitinous compounds, optionally one or more chitins and/or one or more chitosans.

26. The inoculant composition of any one of paragraphs 8–25, said composition further comprising one or more flavonoids, optionally one or more anthocyanidins, such as cyanidin, delphinidin, malvidin, pelargonidin, peonidin and/or petunidin; anthoxanthins, such as flavones (e.g., apigenin, baicalein, chrysin, 7,8-dihydroxyflavone, diosmin, flavoxate, 6—hydroxyflavone, luteolin, scutellarein, tangeritin and/or wogonin) and/or flavonols (e.g., amurensin, astragalin, azaleatin, azalein, fisetin, furanoflavonols galangin, gossypetin, 3-hydroxyflavone, hyperoside,icariin, isoquercetin, kaempferide, kaempferitrin, kaempferol, isorhamnetin, morin, myricetin, myricitrin, natsudaidain, pachypodol, pyranoflavonols quercetin, quericitin, rhamnazin, rhamnetin, robinin, rutin, spiraeoside, troxerutin and/or zanthorhamnin); flavanones, such as butin, eriodictyol, hesperetin, hesperidin, homoeriodictyol, isosakuranetin, naringenin, naringin, pinocembrin, poncirin, sakuranetin, sakuranin and/or sterubin; flavanonols, such as dihydrokaempferol and/or taxifolin; flavans, such as flavan-3-ols (e.g., catechin (C), catechin 3-gallate (Cg), epicatechins (EC), epigallocatechin (EGC) epicatechin 3-gallate (ECg), epigallcatechin 3-gallate (EGCg), epiafzelechin, fisetinidol, gallocatechin (GC), gallcatechin 3-gallate (GCg), guibourtinidol, mesquitol, robinetinidol, theaflavin-3-gallate, theaflavin-3'-gallate, theflavin-3,3'- digallate, thearubigin), flavan-4-ols (e.g., apiforol and/or luteoforol) and/or flavan-3,4-diols (e.g., leucocyanidin, leucodelphinidin, leucofisetinidin, leucomalvidin, luecopelargonidin, leucopeonidin, leucorobinetinidin, melacacidin and/or teracacidin); and/or isoflavonoids, such as isoflavones (e.g, biochanin A, daidzein, formononetin, genistein and/or glycitein), isoflavanes (e.g., equol, ionchocarpane and/or laxifloorane), isoflavandiols, isoflavenes (e.g., glabrene, haginin D and/or 2-methoxyjudaicin), coumestans (e.g., coumestrol, plicadin and/or wedelolactone), pterocarpans and/or roetonoids; and/or one oor more analogues, derivatives, hydrates, isomers, polymers, salts and solvates thereof, such as neoflavonoids (e.g, calophyllolide, coutareagenin, dalbergichromene, dalbergin and/or nivetin) and/or pterocarpans (e.g., bitucarpin A, bitucarpin B, erybraedin A, erybraedin B, erythrabyssin II, erthyrabissin- 1, erycristagallin, glycinol, glyceollidins, glyceollins, glycyrrhizol, maackiain, medicarpin, morisianine, orientanol, phaseolin, pisatin, striatine and/or trifolirhizin).

27. The inoculant composition of any one of paragraphs 8–26, said composition further comprising jasmonic acid and/or one or more derivatives thereof.

28. The inoculant composition of any one of paragraphs 8–27, said composition further comprising linoleic acid and/or one or more derivatives thereof.

29. The inoculant composition of any one of paragraphs 8–28, said composition further comprising linolenic acid and/or one or more derivatives thereof. 30. The inoculant composition of any one of paragraphs 8–29, said composition further comprising one or more karrakins, optionally one or more karrakins represented by formula LXXXIV.

31. The inoculant composition of any one of paragraphs 8–30, said composition further comprising gluconolactone.

32. The inoculant composition of any one of paragraphs 8–31, said composition further comprising one or more additional microorganisms.

33. The inoculant composition of paragraph 32, said one or more additional microorganisms comprising, consisting essentially of or consisting of one or more microorganisms that improve the availability of a soil nutrient, optionally one or more diazotrophs and/or phosphate-solubilixing microorganisms.

34. The inoculant composition of paragraph 32, said one or more additional microorganisms comprising, consisting essentially of or consisting of Azospirillum brasilense INTA Az-39, Azospirillum brasilense AZ39, Azospirillum brasilense XOH, Azospirillum brasilense BR 11002, Azospirillum brasilense BR 11005, Azospirillum brasilense Ab-V5, Azospirillum brasilense Ab-V6, Bacillus amyloliquefaciens D747, Bacillus amyloliquefaciens NRRL B-50349, Bacillus amyloliquefaciens TJ1000, Bacillus amyloliquefaciens FZB24, Bacillus amyloliquefaciens FZB42, Bacillus amyloliquefaciens IN937a, Bacillus amyloliquefaciens IT-45, Bacillus amyloliquefaciens MBI600, Bacillus

amyloliquefaciens BS27 (deposited as NRRL B-5015), Bacillus amyloliquefaciens BS2084 (deposited as NRRL B-50013), Bacillus amyloliquefaciens 15AP4 (deposited as ATCC PTA-6507), Bacillus amyloliquefaciens 3AP4 (deposited as ATCC PTA-6506), Bacillus amyloliquefaciens LSSA01 (deposited as NRRL B-50104), Bacillus amyloliquefaciens ABP278 (deposited as NRRL B-50634), Bacillus amyloliquefaciens 1013 (deposited as NRRL B-50509), Bacillus amyloliquefaciens 918 (deposited as NRRL B-50508), Bacillus amyloliquefaciens 22CP1 (deposited as ATCC PTA-6508) and Bacillus amyloliquefaciens BS18 (deposited as NRRL B-50633), Bacillus cereus I-1562, Bacillus firmus I-1582, Bacillus lichenformis BA842 (deposited as NRRL B-50516), Bacillus lichenformis BL21 (deposited as NRRL B-50134), Bacillus megaterium O62UKE (deposited as NRRL B-67352), Bacillus megaterium O723G4 (deposited as NRRL B-67357), Bacillus megaterium O132FX (deposited as NRRL B-67521), Bacillus megaterium O14VDF (deposited as NRRL B-67522), Bacillus megaterium O249FV (deposited as NRRL B-67523), Bacillus megaterium O33Y38 (deposited as NRRL B-67524), Bacillus megaterium O62RUA (deposited as NRRL B-67525), Bacillus megaterium O62RV8 (deposited as NRRL B-67526), Bacillus megaterium O62STA (deposited as NRRL B-67527), Bacillus megaterium O7237E (deposited as NRRL B-67528), Bacillus megaterium O72NWX (deposited as NRRL B-67529), Bacillus megaterium O72T97 (deposited as NRRL B-67530), Bacillus megaterium NRRL B-67533, Bacillus megaterium NRRL B-67534, Bacillus mycoides NRRL B-21664, Bacillus pumilus NRRL B-21662, Bacillus pumilus NRRL B-30087, Bacillus pumilus ATCC 55608, Bacillus pumilus ATCC 55609, Bacillus pumilus GB34, Bacillus pumilus KFP9F, Bacillus pumilus QST 2808, Bacillus subtilis ATCC 55078, Bacillus subtilis ATCC 55079, Bacillus subtilis MBI 600, Bacillus subtilis NRRL B-21661, Bacillus subtilis NRRL B- 21665, Bacillus subtilis CX-9060, Bacillus subtilis GB03, Bacillus subtilis GB07, Bacillus subtilis QST- 713, Bacillus subtilis FZB24, Bacillus subtilis D747, Bacillus subtilis 3BP5 (deposited as NRRL B- 50510), Bacillus thuringiensis ATCC 13367, Bacillus thuringiensis GC-91, Bacillus thuringiensis NRRL B-21619, Bacillus thuringiensis ABTS-1857, Bacillus thuringiensis SAN 401 I, Bacillus thuringiensis ABG-6305, Bacillus thuringiensis ABG-6346, Bacillus thuringiensis AM65-52, Bacillus thuringiensis SA-12, Bacillus thuringiensis SB4, Bacillus thuringiensis ABTS-351, Bacillus thuringiensis HD-1, Bacillus thuringiensis EG 2348, Bacillus thuringiensis EG 7826, Bacillus thuringiensis EG 7841, Bacillus thuringiensis DSM 2803, Bacillus thuringiensis NB-125, Bacillus thuringiensis NB-176, BRADY, Lysinibacillus sphaericus O62Q8F (deposited as NRRL B-67350), Lysinibacillus sphaericus O62S63 (deposited as NRRL B-67351), Lysinibacillus sphaericus O62QG9 (deposited as NRRL B-67486), Mesorhizobium huakii LL32, Pseudomonas jessenii PS06, Rhizobium leguminosarum 162BB1,

Rhizobium leguminosarum 162P17, Rhizobium leguminosarum 175G10b, Rhizobium leguminosarum D36, Rhizobium leguminosarum SO12A-2 (IDAC 080305-01), Rhizobium loti 95C11, Rhizobium loti 95C14, Sinorhizobium fredii CCBAU114, Sinorhizobium fredii USDA 205, Sinorhizobium meliloti 102F34a, Sinorhizobium meliloti 102F51a, Sinorhizobium meliloti 102F77b, Sinorhizobium meliloti B401, Sinorhizobium meliloti MSDJ0848, Streptomyces NRRL B-30145, Streptomyces M1064, Streptomyces WYE 53 (deposited as ATCC 55750), Streptomyces lydicus WYEC 108 (deposited as ATCC 55445), Yersinia entomophaga MH96 (also known as O43NEW) (deposited as DSM 18238, DSM 22339, ATCC BAA-1678 and NRRL B-67598), Yersinia entomophaga O82KB8, Yersinia entomophaga O24G3R (deposited as NRRL B-67599), Yersinia entomophaga O24KEK (deposited as NRRL B-67600), Yersinia entomophaga O333A4 (deposited as NRRL B-67601), Yersinia entomophaga O23ZMJ, Yersinia entomophaga O348UX and/or Yersinia entomophaga O33ZDX.

35. The inoculant composition of paragraph 32, said one or more additional microorganisms comprising, consisting essentially of or consisting of Gliocladium virens ATCC 52045, Gliocladium virens GL-21, Glomus intraradices RTI-801, Metarhizium anisopliae F52, PENI, Trichoderma asperellum SKT-1, Trichoderma asperellum ICC 012, Trichoderma atroviride LC52, Trichoderma atroviride CNCM 1-1237, Trichoderma fertile JM41R, Trichoderma gamsii ICC 080, Trichoderma hamatum ATCC 52198, Trichoderma harzianum ATCC 52445, Trichoderma harzianum KRL-AG2, Trichoderma harzianum T-22, Trichoderma harzianum TH-35, Trichoderma harzianum T-39,

Trichoderma harzianum ICC012, Trichoderma reesi ATCC 28217, Trichoderma virens ATCC 58678, Trichoderma virens Gl-3, Trichoderma virens GL-21, Trichoderma virens G-41, Trichoderma viridae ATCC 52440, Trichoderma viridae ICC080, and/or Trichoderma viridae TV1.

36. The inoculant composition of paragraph 32, said one or more additional microorganisms comprising, consisting essentially of or consisting of one or more biopesticides, optionally one or more acaricidal, insecticidal and/or nematicidal microorganisms and one or more fungicidal microorganisms.

37. The inoculant composition of any one of claims 32–36, said composition comprising about 1 x 10 3 to about 1 x 10 12 colony-forming units (cfu) of said one or more additional microorganisms per gram and/or milliliter of inoculant composition, optionally about/at least 1 x 10 3 , 1 x 10 4 , 1 x 10 5 , 1 x 10 6 , 1 x 10 7 , 1 x 10 8 , 1 x 10 9 , 1 x 10 10 , 1 x 10 11 , or 1 x 10 12 cfu of said one or more additional microorganisms per gram and/or milliliter of inoculant composition.

38. The inoculant composition of any one of paragraphs 8–37, wherein said composition is non- aqueous.

39. The inoculant composition of any one of paragraphs 8–37, wherein said composition is aqueous.

40. The inoculant composition of any one of paragraphs 8–37, wherein said composition comprises less than 0.01, 0.02, 0.03, 0.04, 0.05, 0.06, 0.07, 0.08, 0.09, 0.1, 0.15, 0.2, 0.25, 0.3, 0.35, 0.4, 0.45, 0.5, 0.55, 0.6, 0.65, 0.7, 0.75, 0.8, 0.85, 0.9, 0.95, 1, 1.25, 1.5, 1.75, 2, 2.25, 2.5, 2.75, 3, 3.25, 3.5, 3.75, 4, 4.25, 4.5, 4.75 or 5% water (by weight, based upon the total weight of the composition).

41. The inoculant composition of any one of paragraphs 8–40, wherein said composition is an amorphous liquid.

42. The inoculant composition of any one of paragraphs 8–40, wherein said composition is an amorphous solid.

43. The inoculant composition of any one of paragraphs 8–40, wherein said composition is a freeze-, spray- or spray-freeze-dried composition, optionally a freeze-, spray- or spray-freeze-dried powder.

44. A non-naturally occurring composition, comprising the isolated strain of paragraph 1 and a plant or plant part to which the isolated strain of paragraph 1 has been applied.

45. A non-naturally occurring composition, comprising the biologically pure culture of any one of paragraphs 2–4 and a plant or plant part to which the biologically pure culture of any one of paragraphs 2– 4 has been applied.

46. A non-naturally occurring composition, comprising the whole broth culture of paragraph 5 and a plant or plant part to which the whole broth culture of paragraph 5 has been applied.

47. A non-naturally occurring composition, comprising the cell-free filtrate of paragraph 6 and a plant or plant part to which the cell-free filtrate of paragraph 6 has been applied.

48. A non-naturally occurring composition, comprising the cellular extract of paragraph 7 and a plant or plant part to which the cellular extract of paragraph 7 has been applied.

49. A non-naturally occurring composition, comprising the inoculant composition of any one of paragraphs 8–43 and a plant or plant part to which the inoculant composition of any one of paragraphs 8– 43 has been applied.

50. The non-naturally occurring composition of any one of paragraphs 44–49, comprising, consisting essentially of, or consisting of: a plant propagation material, optionally a seed; and a coating that covers at least a portion of the outer surface of said plant propagation material, said coating comprising, consisting essentially of, or consisting of comprising the isolated strain of paragraph 1, the biologically pure culture of any one of paragraphs 2–4, the whole broth culture of paragraph 5, the cell- free filtrate of paragraph 6, the cellular extract of paragraph 7, or the inoculation composition of any one of paragraphs 8–43.

51. The non-naturally occurring composition of paragraph 50, said coating comprising, consisting essentially of, or consisting of an inner coating layer that comprises one or more strains of the present disclosure, optionally E. billingiae NRRL B-67766 or a close relative thereof (e.g., a closely related progeny of E. billingiae NRRL B-67766 or a closely related modified microbial strain derived from E. billingiae NRRL B-67766), P. gessardii NRRL B-67767 or a close relative thereof (e.g., a closely related progeny of P. gessardii NRRL B-67767or a closely related modified microbial strain derived from P. gessardii NRRL B-67767), and/or P. libanesis NRRL B-67769 or a close relative threeof (e.g., a closely related progeny of P. libanesis NRRL B-67769 or a closely related modified microbial strain derived from P. libanesis NRRL B-67769), and an outer coating layer that is devoid (or essentially devoid) of said one or more strains of the present disclosure.

52. The non-naturally occurring composition of any one of paragraphs 50–51, wherein said coating comprises about 1 x 10 1 to about 1 x 10 15 colony-forming units of (each of) one or more strains of the present disclosure, optionally E. billingiae NRRL B-67766 or a close relative thereof (e.g., a closely related progeny of E. billingiae NRRL B-67766 or a closely related modified microbial strain derived from E. billingiae NRRL B-67766), P. gessardii NRRL B-67767 or a close relative thereof (e.g., a closely related progeny of P. gessardii NRRL B-67767or a closely related modified microbial strain derived from P. gessardii NRRL B-67767), and/or P. libanesis NRRL B-67769 or a close relative threeof (e.g., a closely related progeny of P. libanesis NRRL B-67769 or a closely related modified microbial strain derived from P. libanesis NRRL B-67769), optionally 1 x 10 4 , 1 x 10 5 , 1 x 10 6 , 1 x 10 7 or more colony- forming units.

53. A plant germinated from the plant part of any one of paragraphs 44–52.

54. A plant part harvested from the plant of any one of paragraphs 44–53.

55. A processed product produced from the plant part of paragraph 54.

56. A crop comprising, consisting essentially of, or consisting of a plurality of the plant of any one of paragraphs 44–53.

57. A kit, comprising: the plant or plant part of any one of paragraphs 44–54; and a container housing said plant or plant part.

58. The kit of claim 57, said container reducing the amount of ambient light that reaches said coated plant propagation material by about 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95 or 100% when sealed.

59. The kit of any one of paragraphs 57–58, said container reducing the amount of ambient oxygen that reaches said plant propagation material by about 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95 or 100% when sealed.

60. The kit of any one of paragraphs 57–59, said container comprising, consisting essentially of, or consisting of a material having light permeability of less than about 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70 or 75%.

61. The kit of any one of paragraphs 57–60, said container comprising, consisting essentially of, or consisting of a material having an oxygen transmission rate of less than about 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 60, 70, 80, 90, 100, 125, 150, 175, 200, 225, 250, 275, 300, 325, 350, 375, 400, 425, 450, 475, or 500 cm 3 /m 2 ·day (as measured in accordance with ASTM D3985).

62. The kit of any one of paragraphs 57–61, said kit furthering comprising one or more oxygen- absorbing compound, optionally activated carbon, iron powder, sodium chloride, ferrous carbonate, one or more metal halide catalysts and/or sodium hydrogen carbonate. 63. A method, comprising, consisting essentially of or consisting of: applying the isolated strain of paragraph 1, the biologically pure culture of any one of paragraphs 2–4, the whole broth culture of claim 5, the cell-free filtrate of claim 6, the cellular extract of claim 7, or the inoculant compositon of any one of paragraphs 8–43 to a plant or plant part, optionally a seed.

64. The method of paragraph 63, in which said isolated strain, biologically pure culture, whole broth culture, cell-free filtrate, cellular extract, or inoculant composition is applied to the plant or plant part in an effective amount/concentration for killing one or more fungal pests, inhibiting the growth of one or more fungal pests, inhibiting the reproduction/proliferation of one or more fungal pests and/or reducing the severity of one or more fungal diseases in/on/of said palnt or plant part.

65. The method of paragraph 63, in which said isolated strain, biologically pure culture, whole broth culture, cell-free filtrate, cellular extract, or inoculant composition is applied to the plant or plant part in an effective amount/concentration for enhancing the growth and/or yield of said plant or plant part.

66. A method, comprising, consisting essentially of or consisting of: applying the isolated strain of paragraph 1, the biologically pure culture of any one of paragraphs 2–4, the whole broth culture of claim 5, the cell-free filtrate of claim 6, the cellular extract of claim 7, or the inoculant compositon of any one of paragraphs 8–43 to a plant propagation material, optionally a seed, at the time of planting said plant propagation material in a plant growth medium, optionally a soil.

67. A method, comprising, consisting essentially of or consisting of: applying the isolated strain of paragraph 1, the biologically pure culture of any one of paragraphs 2–4, the whole broth culture of claim 5, the cell-free filtrate of claim 6, the cellular extract of claim 7, or the inoculant compositon of any one of paragraphs 8–43 to a plant propagation material, optionally a seed, about/at least 1, 2, 3, 4, 5, 6, 7, 8, 9, 10,11, 12, 15, 18, 21, 24, 27, 30, 33, 36, 39, 42, 45, 48 hours or more prior to planting said plant propagation material in a plant growth medium, optionally a soil.

68. A method, comprising, consisting essentially of or consisting of: applying the isolated strain of paragraph 1, the biologically pure culture of any one of paragraphs 2–4, the whole broth culture of claim 5, the cell-free filtrate of claim 6, the cellular extract of claim 7, or the inoculant compositon of any one of paragraphs 8–43 to a plant propagation material, optionally a seed, about/at least 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 28, 32, 36, 40, 44, 48, 52, 56, 60, 64, 68, 72, 76, 80, 84, 88, 92, 96, 100, 104 weeks or more prior to planting said plant propagation material in a plant growth medium, optionally a soil.

69. A method, comprising, consisting essentially of or consisting of: applying the isolated strain of paragraph 1, the biologically pure culture of any one of paragraphs 2–4, the whole broth culture of claim 5, the cell-free filtrate of claim 6, the cellular extract of claim 7, or the inoculant compositon of any one of paragraphs 8–43 to a plant propagation material, optionally a seed, about/at least 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36 months or more prior to planting said plant propagation material in a plant growth medium, optionally a soil.

70. The method of any one of paragraphs 66–69, in which said isolated strain, biologically pure culture, whole broth culture, cell-free filtrate, cellular extract, or inoculant compositon is applied to the plant propagation material in an effective amount/concentration for killing one or more fungal pests, inhibiting the growth of one or more fungal pests, inhibiting the reproduction/proliferation of one or more fungal pests and/or reducing the severity of one or more fungal diseases in/on/of the plant propagation material and/or a plant that grows from said plant propagation material.

71. The method of any one of paragraphs 66–69, in which said isolated strain, biologically pure culture, whole broth culture, cell-free filtrate, cellular extract, or inoculant compositon is applied to the plant propagation material in an effective amount/concentration for enhancing the growth and/or yield of a plant that grows from said plant propagation material.

72. A method, comprising, consisting essentially of or consisting of: introducing the isolated strain of paragraph 1, the biologically pure culture of any one of paragraphs 2–4, the whole broth culture of claim 5, the cell-free filtrate of claim 6, the cellular extract of claim 7, or the inoculant compositon of any one of paragraphs 8–43 into a plant growth medium, optionally a soil.

73. The method of paragraph 63, in which said isolated strain, biologically pure culture, whole broth culture, cell-free filtrate, cellular extract, or inoculant compositon is introduced into said plant growth medium about/at least 1, 2, 3, 4, 5, 6, 7, 8, 9, 10,11, 12, 15, 18, 21, 24, 27, 30, 33, 36, 39, 42, 45, 48 hours or more prior to planting a plant propagation material, optionally a seed, in said plant growth medium.

74. The method of paragraph 63, in which said isolated strain, biologically pure culture, whole broth culture, cell-free filtrate, cellular extract, or inoculant compositon is introduced into said plant growth medium about/at least 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 28, 32, 36, 40, 44, 48, 52, 56, 60, 64, 68, 72, 76, 80, 84, 88, 92, 96, 100, 104 weeks or more prior to planting a plant propagation material, optionally a seed, in said plant growth medium.

75. The method of paragraph 63, in which said isolated strain, biologically pure culture, whole broth culture, cell-free filtrate, cellular extract, or inoculant compositon is introduced into said plant growth medium about/at least 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36 months or more prior to planting a plant propagation material, optionally a seed, in said plant growth medium.

76. The method of paragaph 63, in which said isolated strain, biologically pure culture, whole broth culture, cell-free filtrate, cellular extract, or inoculant compositon is introduced into said plant growth medium at the time of planting a plant propagation material, optionally a seed, in said plant growth medium.

77. The method of paragaph 63, in which said isolated strain, biologically pure culture, whole broth culture, cell-free filtrate, cellular extract, or inoculant compositon is introduced into said plant growth medium after planting a plant propagation material, optionally a seed, in said plant growth medium.

78. The method of any one of paragraphs 72–77, in which said isolated strain, biologically pure culture, whole broth culture, cell-free filtrate, cellular extract, or inoculant compositon is introduced into the plant growth medium in an effective amount/concentration for for killing one or more fungal pests, inhibiting the growth of one or more fungal pests, inhibiting the reproduction/proliferation of one or more fungal pests and/or reducing the severity of one or more fungal diseases in/on/of the plant growth medium and/or a plant or plant part grown therein.

79. The method of any one of paragraphs 72–77, in which said isolated strain, biologically pure culture, whole broth culture, cell-free filtrate, cellular extract, or inoculant compositon is introduced into the plant growth medium in an effective amount/concentration for enhancing the growth and/or yield of a plant or plant part grown therein.

80. A method, comprising, consisting essentially of or consisting of: introducing the non- naturally occurring composition of any one of paragraphs 44–52 into a plant growth medium, optionally a soil.

81. Use of an isolated strain of the present disclosure, optionally E. billingiae NRRL B-67766 or a close relative thereof (e.g., a closely related progeny of E. billingiae NRRL B-67766 or a closely related modified microbial strain derived from E. billingiae NRRL B-67766), P. gessardii NRRL B-67767 or a close relative thereof (e.g., a closely related progeny of P. gessardii NRRL B-67767or a closely related modified microbial strain derived from P. gessardii NRRL B-67767), or P. libanesis NRRL B-67769 or a close relative threeof (e.g., a closely related progeny of P. libanesis NRRL B-67769 or a closely related modified microbial strain derived from P. libanesis NRRL B-67769), for treating a plant or plant part.

82. Use of an isolated strain of the present disclosure, optionally E. billingiae NRRL B-67766 or a close relative thereof (e.g., a closely related progeny of E. billingiae NRRL B-67766 or a closely related modified microbial strain derived from E. billingiae NRRL B-67766), P. gessardii NRRL B-67767 or a close relative thereof (e.g., a closely related progeny of P. gessardii NRRL B-67767or a closely related modified microbial strain derived from P. gessardii NRRL B-67767), or P. libanesis NRRL B-67769 or a close relative threeof (e.g., a closely related progeny of P. libanesis NRRL B-67769 or a closely related modified microbial strain derived from P. libanesis NRRL B-67769), for treating a plant growth medium, optionally a soil.

83. Use of an isolated strain of the present disclosure, optionally E. billingiae NRRL B-67766 or a close relative thereof (e.g., a closely related progeny of E. billingiae NRRL B-67766 or a closely related modified microbial strain derived from E. billingiae NRRL B-67766), P. gessardii NRRL B-67767 or a close relative thereof (e.g., a closely related progeny of P. gessardii NRRL B-67767or a closely related modified microbial strain derived from P. gessardii NRRL B-67767), or P. libanesis NRRL B-67769 or a close relative threeof (e.g., a closely related progeny of P. libanesis NRRL B-67769 or a closely related modified microbial strain derived from P. libanesis NRRL B-67769), for for killing one or more fungal pests, inhibiting the growth of one or more fungal pests, inhibiting the reproduction/proliferation of one or more fungal pests and/or reducing the severity of one or more fungal diseases.

84. Use of an isolated strain of the present disclosure, optionally E. billingiae NRRL B-67766 or a close relative thereof (e.g., a closely related progeny of E. billingiae NRRL B-67766 or a closely related modified microbial strain derived from E. billingiae NRRL B-67766), P. gessardii NRRL B-67767 or a close relative thereof (e.g., a closely related progeny of P. gessardii NRRL B-67767or a closely related modified microbial strain derived from P. gessardii NRRL B-67767), or P. libanesis NRRL B-67769 or a close relative threeof (e.g., a closely related progeny of P. libanesis NRRL B-67769 or a closely related modified microbial strain derived from P. libanesis NRRL B-67769), for enhancing plant growth, optionally root area, root biomass, root length, root surface area, root volume, shoot diameter, shoot length, shoot girth:length ratio, shoot biomass, shoot surface area and/or shoot volume, and/or yield, optionally average pod count per plant, average pod weight per plant and/or bushels per acre.

85. Use of a biologically pure culture of E. billingiae NRRL B-67766 or a close relative thereof (e.g., a closely related progeny of E. billingiae NRRL B-67766 or a closely related modified microbial strain derived from E. billingiae NRRL B-67766) for treating a plant or plant part.

86. Use of a biologically pure culture of E. billingiae NRRL B-67766 or a close relative thereof (e.g., a closely related progeny of E. billingiae NRRL B-67766 or a closely related modified microbial strain derived from E. billingiae NRRL B-67766) for treating a plant growth medium, optionally a soil.

87. Use of a biologically pure culture of E. billingiae NRRL B-67766 or a close relative thereof (e.g., a closely related progeny of E. billingiae NRRL B-67766 or a closely related modified microbial strain derived from E. billingiae NRRL B-67766) for killing one or more fungal pests, inhibiting the growth of one or more fungal pests, inhibiting the reproduction/proliferation of one or more fungal pests and/or reducing the severity of one or more fungal diseases.

88. Use of a biologically pure culture of E. billingiae NRRL B-67766 or a close relative thereof (e.g., a closely related progeny of E. billingiae NRRL B-67766 or a closely related modified microbial strain derived from E. billingiae NRRL B-67766) for enhancing plant growth, optionally root area, root biomass, root length, root surface area, root volume, shoot diameter, shoot length, shoot girth:length ratio, shoot biomass, shoot surface area and/or shoot volume, and/or yield, optionally average pod count per plant, average pod weight per plant and/or bushels per acre.

89. Use of a biologically pure culture of P. gessardii NRRL B-67767 or a close relative thereof (e.g., a closely related progeny of P. gessardii NRRL B-67767or a closely related modified microbial strain derived from P. gessardii NRRL B-67767) for treating a plant or plant part.

90. Use of a biologically pure culture of P. gessardii NRRL B-67767 or a close relative thereof (e.g., a closely related progeny of P. gessardii NRRL B-67767or a closely related modified microbial strain derived from P. gessardii NRRL B-67767) for treating a plant growth medium, optionally a soil.

91. Use of a biologically pure culture of P. gessardii NRRL B-67767 or a close relative thereof (e.g., a closely related progeny of P. gessardii NRRL B-67767or a closely related modified microbial strain derived from P. gessardii NRRL B-67767) for killing one or more fungal pests, inhibiting the growth of one or more fungal pests, inhibiting the reproduction/proliferation of one or more fungal pests and/or reducing the severity of one or more fungal diseases.

92. Use of a a biologically pure culture of P. gessardii NRRL B-67767 or a close relative thereof (e.g., a closely related progeny of P. gessardii NRRL B-67767or a closely related modified microbial strain derived from P. gessardii NRRL B-67767) for enhancing plant growth, optionally root area, root biomass, root length, root surface area, root volume, shoot diameter, shoot length, shoot girth:length ratio, shoot biomass, shoot surface area and/or shoot volume, and/or yield, optionally average pod count per plant, average pod weight per plant and/or bushels per acre.

93. Use of a biologically pure culture of P. libanesis NRRL B-67769 or a close relative thereof (e.g., a closely related progeny of P. libanesis NRRL B-67769 or a closely related modified microbial strain derived from P. libanesis NRRL B-67769) for treating a plant or plant part.

94. Use of a biologically pure culture of P. libanesis NRRL B-67769 or a close relative thereof (e.g., a closely related progeny of P. libanesis NRRL B-67769 or a closely related modified microbial strain derived from P. libanesis NRRL B-67769) for treating a plant growth medium, optionally a soil.

95. Use of a biologically pure culture of P. libanesis NRRL B-67769 or a close relative thereof (e.g., a closely related progeny of P. libanesis NRRL B-67769 or a closely related modified microbial strain derived from P. libanesis NRRL B-67769) for killing one or more fungal pests, inhibiting the growth of one or more fungal pests, inhibiting the reproduction/proliferation of one or more fungal pests and/or reducing the severity of one or more fungal diseases.

96. Use of a a biologically pure culture of P. libanesis NRRL B-67769 or a close relative thereof (e.g., a closely related progeny of P. libanesis NRRL B-67769 or a closely related modified microbial strain derived from P. libanesis NRRL B-67769) for enhancing plant growth, optionally root area, root biomass, root length, root surface area, root volume, shoot diameter, shoot length, shoot girth:length ratio, shoot biomass, shoot surface area and/or shoot volume, and/or yield, optionally average pod count per plant, average pod weight per plant and/or bushels per acre.

97. Use of a whole broth culture comprising one or more strains of the present disclosure, optionally E. billingiae NRRL B-67766 or a close relative thereof (e.g., a closely related progeny of E. billingiae NRRL B-67766 or a closely related modified microbial strain derived from E. billingiae NRRL B-67766), P. gessardii NRRL B-67767 or a close relative thereof (e.g., a closely related progeny of P. gessardii NRRL B-67767or a closely related modified microbial strain derived from P. gessardii NRRL B-67767), and/or P. libanesis NRRL B-67769 or a close relative threeof (e.g., a closely related progeny of P. libanesis NRRL B-67769 or a closely related modified microbial strain derived from P. libanesis NRRL B-67769), for treating a plant or plant part.

98. Use of a whole broth culture comprising one or more strains of the present disclosure, optionally E. billingiae NRRL B-67766 or a close relative thereof (e.g., a closely related progeny of E. billingiae NRRL B-67766 or a closely related modified microbial strain derived from E. billingiae NRRL B-67766), P. gessardii NRRL B-67767 or a close relative thereof (e.g., a closely related progeny of P. gessardii NRRL B-67767or a closely related modified microbial strain derived from P. gessardii NRRL B-67767), and/or P. libanesis NRRL B-67769 or a close relative threeof (e.g., a closely related progeny of P. libanesis NRRL B-67769 or a closely related modified microbial strain derived from P. libanesis NRRL B-67769), for treating a plant growth medium, optionally a soil.

99. Use of a whole broth culture comprising one or more strains of the present disclosure, optionally E. billingiae NRRL B-67766 or a close relative thereof (e.g., a closely related progeny of E. billingiae NRRL B-67766 or a closely related modified microbial strain derived from E. billingiae NRRL B-67766), P. gessardii NRRL B-67767 or a close relative thereof (e.g., a closely related progeny of P. gessardii NRRL B-67767or a closely related modified microbial strain derived from P. gessardii NRRL B-67767), and/or P. libanesis NRRL B-67769 or a close relative threeof (e.g., a closely related progeny of P. libanesis NRRL B-67769 or a closely related modified microbial strain derived from P. libanesis NRRL B-67769), for killing one or more fungal pests, inhibiting the growth of one or more fungal pests, inhibiting the reproduction/proliferation of one or more fungal pests and/or reducing the severity of one or more fungal diseases.

100. Use of a whole broth culture comprising one or more strains of the present disclosure, optionally E. billingiae NRRL B-67766 or a close relative thereof (e.g., a closely related progeny of E. billingiae NRRL B-67766 or a closely related modified microbial strain derived from E. billingiae NRRL B-67766), P. gessardii NRRL B-67767 or a close relative thereof (e.g., a closely related progeny of P. gessardii NRRL B-67767or a closely related modified microbial strain derived from P. gessardii NRRL B-67767), and/or P. libanesis NRRL B-67769 or a close relative threeof (e.g., a closely related progeny of P. libanesis NRRL B-67769 or a closely related modified microbial strain derived from P. libanesis NRRL B-67769), for enhancing plant growth, optionally root area, root biomass, root length, root surface area, root volume, shoot diameter, shoot length, shoot girth:length ratio, shoot biomass, shoot surface area and/or shoot volume, and/or yield, optionally average pod count per plant, average pod weight per plant and/or bushels per acre.

101. Use of a cell-free filtrate derived from a culture comprising one or more strains of the present disclosure, optionally E. billingiae NRRL B-67766 or a close relative thereof (e.g., a closely related progeny of E. billingiae NRRL B-67766 or a closely related modified microbial strain derived from E. billingiae NRRL B-67766), P. gessardii NRRL B-67767 or a close relative thereof (e.g., a closely related progeny of P. gessardii NRRL B-67767or a closely related modified microbial strain derived from P. gessardii NRRL B-67767), and/or P. libanesis NRRL B-67769 or a close relative threeof (e.g., a closely related progeny of P. libanesis NRRL B-67769 or a closely related modified microbial strain derived from P. libanesis NRRL B-67769), for treating a plant or plant part.

102. Use of a cell-free filtrate derived from a culture comprising one or more strains of the present disclosure, optionally E. billingiae NRRL B-67766 or a close relative thereof (e.g., a closely related progeny of E. billingiae NRRL B-67766 or a closely related modified microbial strain derived from E. billingiae NRRL B-67766), P. gessardii NRRL B-67767 or a close relative thereof (e.g., a closely related progeny of P. gessardii NRRL B-67767or a closely related modified microbial strain derived from P. gessardii NRRL B-67767), and/or P. libanesis NRRL B-67769 or a close relative threeof (e.g., a closely related progeny of P. libanesis NRRL B-67769 or a closely related modified microbial strain derived from P. libanesis NRRL B-67769), for treating a plant growth medium, optionally a soil.

103. Use of a cell-free filtrate derived from a culture comprising one or more strains of the present disclosure, optionally E. billingiae NRRL B-67766 or a close relative thereof (e.g., a closely related progeny of E. billingiae NRRL B-67766 or a closely related modified microbial strain derived from E. billingiae NRRL B-67766), P. gessardii NRRL B-67767 or a close relative thereof (e.g., a closely related progeny of P. gessardii NRRL B-67767or a closely related modified microbial strain derived from P. gessardii NRRL B-67767), and/or P. libanesis NRRL B-67769 or a close relative threeof (e.g., a closely related progeny of P. libanesis NRRL B-67769 or a closely related modified microbial strain derived from P. libanesis NRRL B-67769), for killing one or more fungal pests, inhibiting the growth of one or more fungal pests, inhibiting the reproduction/proliferation of one or more fungal pests and/or reducing the severity of one or more fungal diseases.

104. Use of a cell-free filtrate derived from a culture comprising one or more strains of the present disclosure, optionally E. billingiae NRRL B-67766 or a close relative thereof (e.g., a closely related progeny of E. billingiae NRRL B-67766 or a closely related modified microbial strain derived from E. billingiae NRRL B-67766), P. gessardii NRRL B-67767 or a close relative thereof (e.g., a closely related progeny of P. gessardii NRRL B-67767or a closely related modified microbial strain derived from P. gessardii NRRL B-67767), and/or P. libanesis NRRL B-67769 or a close relative threeof (e.g., a closely related progeny of P. libanesis NRRL B-67769 or a closely related modified microbial strain derived from P. libanesis NRRL B-67769), for enhancing plant growth, optionally root area, root biomass, root length, root surface area, root volume, shoot diameter, shoot length, shoot girth:length ratio, shoot biomass, shoot surface area and/or shoot volume, and/or yield, optionally average pod count per plant, average pod weight per plant and/or bushels per acre.

105. Use of a cellular extract derived from a strain of the present disclosure, optionally E.

billingiae NRRL B-67766 or a close relative thereof (e.g., a closely related progeny of E. billingiae NRRL B-67766 or a closely related modified microbial strain derived from E. billingiae NRRL B-67766), P. gessardii NRRL B-67767 or a close relative thereof (e.g., a closely related progeny of P. gessardii NRRL B-67767or a closely related modified microbial strain derived from P. gessardii NRRL B-67767), or P. libanesis NRRL B-67769 or a close relative threeof (e.g., a closely related progeny of P. libanesis NRRL B-67769 or a closely related modified microbial strain derived from P. libanesis NRRL B-67769), for treating a plant or plant part.

106. Use of a cellular extract derived from a strain of the present disclosure, optionally E.

billingiae NRRL B-67766 or a close relative thereof (e.g., a closely related progeny of E. billingiae NRRL B-67766 or a closely related modified microbial strain derived from E. billingiae NRRL B-67766), P. gessardii NRRL B-67767 or a close relative thereof (e.g., a closely related progeny of P. gessardii NRRL B-67767or a closely related modified microbial strain derived from P. gessardii NRRL B-67767), or P. libanesis NRRL B-67769 or a close relative threeof (e.g., a closely related progeny of P. libanesis NRRL B-67769 or a closely related modified microbial strain derived from P. libanesis NRRL B-67769), for treating a plant growth medium, optionally a soil.

107. Use of a cellular extract derived from a strain of the present disclosure, optionally E.

billingiae NRRL B-67766 or a close relative thereof (e.g., a closely related progeny of E. billingiae NRRL B-67766 or a closely related modified microbial strain derived from E. billingiae NRRL B-67766), P. gessardii NRRL B-67767 or a close relative thereof (e.g., a closely related progeny of P. gessardii NRRL B-67767or a closely related modified microbial strain derived from P. gessardii NRRL B-67767), or P. libanesis NRRL B-67769 or a close relative threeof (e.g., a closely related progeny of P. libanesis NRRL B-67769 or a closely related modified microbial strain derived from P. libanesis NRRL B-67769), for killing one or more fungal pests, inhibiting the growth of one or more fungal pests, inhibiting the reproduction/proliferation of one or more fungal pests and/or reducing the severity of one or more fungal diseases.

108. Use of a cellular extract derived from a strain of the present disclosure, optionally E. billingiae NRRL B-67766 or a close relative thereof (e.g., a closely related progeny of E. billingiae NRRL B-67766 or a closely related modified microbial strain derived from E. billingiae NRRL B-67766), P. gessardii NRRL B-67767 or a close relative thereof (e.g., a closely related progeny of P. gessardii NRRL B-67767or a closely related modified microbial strain derived from P. gessardii NRRL B-67767), or P. libanesis NRRL B-67769 or a close relative threeof (e.g., a closely related progeny of P. libanesis NRRL B-67769 or a closely related modified microbial strain derived from P. libanesis NRRL B-67769), for enhancing plant growth, optionally root area, root biomass, root length, root surface area, root volume, shoot diameter, shoot length, shoot girth:length ratio, shoot biomass, shoot surface area and/or shoot volume, and/or yield, optionally average pod count per plant, average pod weight per plant and/or bushels per acre.

109. Use of an inoculant compositon comprising, consisting essentially of or consisting of one or more strains of the present disclosure, optionally E. billingiae NRRL B-67766 or a close relative thereof (e.g., a closely related progeny of E. billingiae NRRL B-67766 or a closely related modified microbial strain derived from E. billingiae NRRL B-67766), P. gessardii NRRL B-67767 or a close relative thereof (e.g., a closely related progeny of P. gessardii NRRL B-67767or a closely related modified microbial strain derived from P. gessardii NRRL B-67767), and/or P. libanesis NRRL B-67769 or a close relative threeof (e.g., a closely related progeny of P. libanesis NRRL B-67769 or a closely related modified microbial strain derived from P. libanesis NRRL B-67769), for treating a plant or plant part.

110. Use of an inoculant compositon comprising, consisting essentially of or consisting of one or more strains of the present disclosure, optionally E. billingiae NRRL B-67766 or a close relative thereof (e.g., a closely related progeny of E. billingiae NRRL B-67766 or a closely related modified microbial strain derived from E. billingiae NRRL B-67766), P. gessardii NRRL B-67767 or a close relative thereof (e.g., a closely related progeny of P. gessardii NRRL B-67767or a closely related modified microbial strain derived from P. gessardii NRRL B-67767), and/or P. libanesis NRRL B-67769 or a close relative threeof (e.g., a closely related progeny of P. libanesis NRRL B-67769 or a closely related modified microbial strain derived from P. libanesis NRRL B-67769), for treating a plant growth medium, optionally a soil.

111. Use of an inoculant compositon comprising, consisting essentially of or consisting of one or more strains of the present disclosure, optionally E. billingiae NRRL B-67766 or a close relative thereof (e.g., a closely related progeny of E. billingiae NRRL B-67766 or a closely related modified microbial strain derived from E. billingiae NRRL B-67766), P. gessardii NRRL B-67767 or a close relative thereof (e.g., a closely related progeny of P. gessardii NRRL B-67767or a closely related modified microbial strain derived from P. gessardii NRRL B-67767), and/or P. libanesis NRRL B-67769 or a close relative threeof (e.g., a closely related progeny of P. libanesis NRRL B-67769 or a closely related modified microbial strain derived from P. libanesis NRRL B-67769), for killing one or more fungal pests, inhibiting the growth of one or more fungal pests, inhibiting the reproduction/proliferation of one or more fungal pests and/or reducing the severity of one or more fungal diseases.

112. Use of an inoculant compositon comprising, consisting essentially of or consisting of one or more strains of the present disclosure, optionally E. billingiae NRRL B-67766 or a close relative thereof (e.g., a closely related progeny of E. billingiae NRRL B-67766 or a closely related modified microbial strain derived from E. billingiae NRRL B-67766), P. gessardii NRRL B-67767 or a close relative thereof (e.g., a closely related progeny of P. gessardii NRRL B-67767or a closely related modified microbial strain derived from P. gessardii NRRL B-67767), and/or P. libanesis NRRL B-67769 or a close relative threeof (e.g., a closely related progeny of P. libanesis NRRL B-67769 or a closely related modified microbial strain derived from P. libanesis NRRL B-67769), for enhancing plant growth, optionally root area, root biomass, root length, root surface area, root volume, shoot diameter, shoot length, shoot girth:length ratio, shoot biomass, shoot surface area and/or shoot volume, and/or yield, optionally average pod count per plant, average pod weight per plant and/or bushels per acre.

113. The non-naturally occurring composition of any one of claims 44–52, plant of paragraph 53, plant part of paragraph 54, processed product of paragraph 55, crop of paragraph 56, kit of any one of paragraphs 57–62, method of any one of claims 63– 80, or use of any one of claims 81–104 in which said plant or plant part is a monocot.

114. The non-naturally occurring composition of any one of claims 44–52, plant of paragraph 53, plant part of paragraph 54, processed product of paragraph 55, crop of paragraph 56, kit of any one of paragraphs 57–62, method of any one of claims 63– 80, or use of any one of claims 81–104 in which said plant or plant part is a dicot.

115. The non-naturally occurring composition of any one of claims 44–52, plant of paragraph 53, plant part of paragraph 54, processed product of paragraph 55, crop of paragraph 56, kit of any one of paragraphs 57–62, method of any one of claims 63– 80, or use of any one of claims 81–104 in which said plant or plant part is leguminous.

116. The non-naturally occurring composition of any one of claims 44–52, plant of paragraph 53, plant part of paragraph 54, processed product of paragraph 55, crop of paragraph 56, kit of any one of paragraphs 57–62, method of any one of claims 63– 80, or use of any one of claims 81–104 in which said plant or plant part is non-leguminous.

117. The non-naturally occurring composition of any one of claims 44–52, plant of paragraph 53, plant part of paragraph 54, processed product of paragraph 55, crop of paragraph 56, kit of any one of paragraphs 57–62, method of any one of claims 63– 80, or use of any one of claims 81–104 in which said plant or plant part is of the family Amaranthaceae, optionally chard, spinach, sugar beet, or quinoa; of the family Asteraceae, optionally artichoke, asters, chamomile, chicory, chrysanthemums, dahlias, daisies, echinacea, goldenrod, guayule, lettuce, marigolds, safflower, sunflowers, or zinnias;of the family

Brassicaceae, optionally arugula, broccoli, bok choy, Brussels sprouts, cabbage, cauliflower, canola, collard greens, daikon, garden cress, horseradish, kale, mustard, radish, rapeseed, rutabaga, turnip, wasabi, watercress, or Arabidopsis thaliana; of the family Cucurbitaceae, optionally cantaloupe, cucumber, honeydew, melon, pumpkin, squash (e.g., acorn squash, butternut squash, summer squash), watermelon, or zucchini; of the family Fabaceae, optionally alfalfa, beans, carob, clover, guar, lentils, mesquite, peas, peanuts, soybeans, tamarind, tragacanth, or vetch; of the family Malvaceae, optionally cacao, cotton, durian, hibiscus, kenaf, kola, or okra; of the family Poaceae, optionally bamboo, barley, corn, fonio, lawn grass (e.g., Bahia grass, Bermudagrass, bluegrass, Buffalograss, Centipede grass, Fescue, or Zoysia), millet, oats, ornamental grasses, rice, rye, sorghum, sugar cane, triticale, or wheat; of the family

Polygonaceae, optionally buckwheat; of the family Rosaceae, optionally almonds, apples, apricots, blackberry, blueberry, cherries, peaches, plums, quinces, raspberries, roses, or strawberries; of the family Solanaceae, optionally bell peppers, chili peppers, eggplant, petunia, potato, tobacco, or tomato; or of the family Vitaceae, optionally grape.

118. A method of making a seed treatment, comprising, consisting essentially of or consisting of: inoculating a culture medium with the isolated strain of paragraph 1 or the biologically pure culture of any one of paragraphs 2–4, incubating the inoculated culture medium at a temperature of about 4 to about 37°C until the microbial density therein is about 1 x 10 3 to about 1 x 10 12 colony-forming units (cfu) per milligram and/or milliliter of inoculated culture medium, optionally about/at least 1 x 10 3 , 1 x 10 4 , 1 x 10 5 , 1 x 10 6 , 1 x 10 7 , 1 x 10 8 , 1 x 10 9 , 1 x 10 10 , 1 x 10 11 , or 1 x 10 12 colony forming units per

milligram/milliliter, and collecting microorganisms from the inoculated culture medium under conditions suitable for producing a seed treatment.

119. A synthetic microbial consortium, comprising, consisting essentially of or consisting of the isolated strain of paragraph 1 and one or more additional microorganisms. DEPOSIT OF BIOLOGICAL MATERIALS

E. billingiae NRRL B-67766 and P. gessardii NRRL B-67767 were deposited on April 11, 2019, under the terms of the Budapest Treaty on the International Recognition of the Deposit of Microorganisms for the Purposes of Patent Procedure at the Agricultural Research Service Culture Collection, 1815 North University Street, Peoria, Illinois 61604, U.S.A.

P. libanesis NRRL B-67769 was deposited on May 10, 2019, under the terms of the Budapest Treaty on the International Recognition of the Deposit of Microorganisms for the Purposes of Patent Procedure at the Agricultural Research Service Culture Collection, 1815 North University Street, Peoria, Illinois 61604, U.S.A.

E. billingiae NRRL B-67766, P. gessardii NRRL B-67767 and P. libanesis NRRL B-67769 were each deposited under conditions that assure access to the culture will be available during the pendency of this patent application to one determined by the Commissioner of Patents and Trademarks to be entitled thereto under 37 C.F.R. §1.14 and 35 U.S.C. §122. Each deposit represents a pure culture of the deposited strain. Each deposit is available as required by foreign patent laws in countries wherein counterparts of the subject application or its progeny are filed. However, it should be understood that the availability of a deposit does not constitute a license to practice the subject invention in derogation of patent rights granted by governmental action. EXAMPLES

The following examples are not intended to be a detailed catalogue of all the different ways in which the present disclosure may be implemented or of all the features that may be added to the present disclosure. Subjects skilled in the art will appreciate that numerous variations and additions to the various embodiments may be made without departing from the present disclosure. Hence, the following descriptions are intended to illustrate some particular embodiments of the invention and not to exhaustively specify all permutations, combinations and variations thereof. Example 1

Bacterial Strain Library

The National Agriculture and Food Research Organization (NARO) in Tsukuba, Japan possesses a collection of more than 20,000 bacterial strains isolated from the leaves of plants, such as barley, rice, tomato and wheat. Tsushima, SCIENCE & TECHNONEWS TSUKUBA 79:18 (2006).

A total of 503 bacterial strains were selected randomly from this collection and screened for fungicidal activity against Fusarium graminearum, a causative agent of head blight in wheat and barley. Example 2

Primary Screening of Bacterial Strains

Fifteen wheat seeds (cv. Ayahikari) were sown per plastic nursery box (15 x 6 x 10 cm) in culture soil, then grown in a greenhouse for 50-60 days under fluorescent light to promote heading.

Bacteria were cultured in PPG liquid medium (200 g potato, 5 g peptone, 5 g glucose, 3 g Na 2 HPO 4 ·12H 2 O, 0.5 g KH 2 PO 4 , 3 g NaCl, per 1,000 ml) at 25°C. Bacteria were harvested from the medium by low speed centrifugation, then resuspended in water at a concentration of OD 610 = 0.13-0.26 (approximately 10 8 CFU/ml). Tween 20 was added to the diluted bacteria at a concentration of 0.1% (v/v).

Approximately 5 ml of each bacterial cell suspension was sprayed onto approximately 10 wheat heads, using an atomizer. Negative controls were wheat heads onto which no bacteria were sprayed. As positive control, a 4000-fold dilution of a chemical fungicide, iminoctadine tris(abesilate) was sprayed onto wheat heads. The sprayed plants were placed into the greenhouse for 1 day.

Conidia of Fusarium graminearum strain H3 were prepared by culturing the organism on half- strength oatmeal agar plates under a BLB lamp (12 h light intervals) for 2-3 weeks. Conidia were harvested from the agar plates, washed once using low speed centrifugation and then suspended in water at a concentration of 10 5 conidia per ml. Tween 20 was added to the diluted bacteria at a concentration of 0.1% (v/v). Four to five ml of this conidial suspension was sprayed per wheat box after 1 day of bacteria treatment of the wheat heads. These wheat heads were placed into an incubation chamber (20℃, nearly 100% humidity) for 48 hours.

After the 48-hour incubation period, the plants were placed into a greenhouse. After 5-7 days in the greenhouse, severity of disease was evaluated based on the proportion of diseased spikelets among total spikelets of each wheat head. Bacteria strains were scored as having activity when total disease spikelets in presence of the bacteria were significantly lower than untreated controls (p<0.05). Example 3

Secondary Screening of Bacterial Strains

Bacterial strains which were scored as having activity in the experiments described above were tested further. These experiments were similar to those described in Example 2 above, but included a commericiallly available biopesticide as an additional positive control: BOTOKILLER® (Idemitsu Kosan Co., Ltd, Tokyo, Japan). Top-performing strains exhibited fungicidal activity similar to that of iminoctadine tris(abesilate) and superior to that of the commercially available biopesticide. E. billingiae NRRL B-67766, P. gessardii NRRL B-67767 and P. libanesis NRRL B-67769 are three of those top- performing strains. Example 4

Identification and Sequencing of Certain Top-Performing Strains The isolated strains deposited as NRRL B-67766, NRRL B-67767 and NRRL B-67769 were identified as Erwinia billingiae, Pseudomonas gessardii and Pseudomonas libanesis, respectively, by MALDI Biotyper and 16S sequencing. MALDI Biotyping was performed using a Bruker MALDI-TOF (Matrix Assisted Laser Desorption Ionization-Time of Flight) Mass Spectrometer. NRRL B-67766, NRRL B-67767 and NRRL B-67769 were each applied to targets using the direct application method and the resulting protein spectrums were compared against the Bruker BDAL library and an internal Novozymes library of named microbial strains.16S ribosomal DNA sequences were determined by colony PCR and Sanger sequencing with degenerate primers targeting the 16S ribosomal gene sequences. The 16S rDNA sequences for E. billingiae NRRL B-67766, P. gessardii NRRL B-67767 and P. libanesis NRRL B-67769 are provided as SEQ ID NOs: 1–3. SEQ ID NO: 1 (E. billingiae NRRL B-6776616S rDNA sequence)

SEQ ID NO: 2 (P. gessardii NRRL B-6776716S rDNA sequence)

SEQ ID NO: 3 (P. libanesis NRRL B-6776916S rDNA sequence)

Example 5

E. billingiae NRRL B-67766 Protected Plants Against Blotch, Rust and Powdery Mildew

These studies were designed to test the ability of E. billingiae NRRL B-67766 to control fungal pathogens that cause leaf blotch, rust and powdery mildew.

E. billingiae NRRL B-67766 was cultured in PPG liquid medium (200 g potato, 5 g peptone, 5 g glucose, 3 g Na 2 HPO 4 ·12H 2 O, 0.5 g KH 2 PO 4 , 3 g NaCl, per 1,000 ml) at 25°C. Bacteria were harvested from the medium by low speed centrifugation, then resuspended in water at a concentration of OD 610 = 0.13-0.26 (approximately 10 8 CFU/ml). Tween 20 was added to the diluted bacteria at a concentration of 0.1% (v/v).

Winter wheat cultivars were sown in 1 liter pots (15 seeds per pot) and cultivated under greenhouse conditions. Six pots were used for each experimental condition. After approximately 1 month, seedling plants were treated with bacterial suspensions that had a concentration of approximately 106 cfu/ml. The bacterial suspensions were sprayed onto the plants until the leaves were saturated (rate of approximately 4 L/ha). Commerically available fungicides, prothioconazole (PROLINE® EC 250; Bayer Crop Science, St. Louis, MO, USA) and SERENADE® (Bayer Crop Science, St. Louis, MO, USA), were applied at a rate of 0.8 L/ha in accordance with the manufacturer's instructions as positive controls.

Negative controls were untreated plants and plants sprayed with water.

One day after application of E. billingiae NRRL B-67766, the plants were inoculated with pathogens.

For leaf blotch, a mixture of 5 isolates of Septoria tritici (also known as Zymoseptoria tritici) were prepared as a suspension containing 2 x 10 6 spores/ml of solution. Two ml of suspension was sprayed onto the plants in each pot. The pathogen-inoculated plants were kept in the dark for 1 day following pathogen inoculation to facilitate infection. Plants were then kept in the greenhouse under high- humidity (>90%) conditions at a temperature of 15°C. After 3 weeks, initial symptoms were observed. Disease assessments were carried out 19, 26 and 30 days following pathogen inoculation. Percent leaf area attacked by pathogen were observed and standard European Meditarranean Plant Protection

Organization (EPPO) scales were used. E. billingiae NRRL B-67766 exhibited fungicidal activity similar to that of prothioconazole, reducing fungal lesions by 40-60% relative to the untreated control or commercially available biopesticide. The efficacy of E. billingiae NRRL B-67766 against Septoria was consistent across multiple trials.

For rust, plants were inoculated with spores of Puccinia striiformis using spreader plants. The plants were kept in a dark incubator for 20 h following inoculation. Subsequently, the plants were kept in the greenhouse under conditions of approximately 75% relative humidity and 20°C. After 1 week, initial symptoms were observed. Disease assessments were carried out at 7, 9 and 14 days following pathogen inoculation. General attack per pot as well as number of rust lesions per pot were assessed. E. billingiae NRRL B-67766 reduced fungal lesions by 50-70% relative to the untreated control or commercially available biopesticide.

For powdery mildew, Blumeria graminis infections occurred from natural inoculum that existed in the environment when plants were treated during the rust trial. E. billingiae NRRL B-67766 and P. gessardii NRRL B-67767 reduced fungal lesions by approximately 30% relative to untreated control or commercially available biopesticide. Example 6

E. billingiae NRRL B-67766 Protected Plants Against Head Blight This study was designed to test the ability of E. billingiae NRRL B-67766 to control fungal pathogens that cause head blight.

E. billingiae NRRL B-67766 was cultured in PPG liquid medium (200 g potato, 5 g peptone, 5 g glucose, 3 g Na 2 HPO 4 ·12H 2 O, 0.5 g KH 2 PO 4 , 3 g NaCl, per 1,000 ml) at 25°C. Bacteria were harvested from the medium by low speed centrifugation, then resuspended in water at a concentration of OD 610 = 0.13-0.26 (approximately 10 8 CFU/ml). Tween 20 was added to the diluted bacteria at a concentration of 0.1% (v/v).

Spring wheat was grown in the ground in a permeable tent under natural weather conditions. Plants were grown until anthesis and then sprayed with the E. billingiae NRRL B-67766 suspension at GS 65 using a portable sprayer at a rate similar to 200l/ha (roughly 10 mL of biocontrol per plot). Twenty- four hours (24 h) after treatment sprays, plants were inoculated with a mixture of Fusarium culmorum and Fusarium graminearum spore suspension. Negative controls were untreated plants and plants sprayed with water. Disease assessments were made 15, 22, and 26 days following pathogen inoculation by counting the incidence and severity of infected wheat heads. E. billingiae NRRL B-67766 reduced fungal lesions by approximately 40% relative to untreated controls. Example 7

E. billingiae NRRL B-67766 Protected Plants Against Blotch

This study was designed to test the ability of E. billingiae NRRL B-67766 to control fungal pathogens that cause leaf blotch.

E. billingiae NRRL B-67766 was cultured in PPG liquid medium (200 g potato, 5 g peptone, 5 g glucose, 3 g Na 2 HPO 4 ·12H 2 O, 0.5 g KH 2 PO 4 , 3 g NaCl, per 1,000 ml) at 25°C. Bacteria were harvested from the medium by low speed centrifugation, then resuspended in water at a concentration of OD 610 = 0.13-0.26 (approximately 10 8 CFU/ml). Tween 20 was added to the diluted bacteria at a concentration of 0.1% (v/v).

A microplot field trial was conducted under natural weather conditions using wheat plants grown in a 22 m 2 plot. Moderate to severe Septoria pathogen infestation resulted from naturally occurring inoculum in the field environment. Treated plants were sprayed with a commercial fungicide or E.

billingiae NRRL B-67766 at 3 main plant growth stages from GS 32, GS 37-39 and GS 51-53. Negative controls were untreated plants and plants sprayed with water. Disease assessments were made at multiple growth stages and on multiple leaves following biocontrol treatments. E. billingiae NRRL B-67766 reduced fungal lesions by greater than 40% relative to untreated controls. Example 8

E. billingiae NRRL B-67766

Exhibited Antifungal Activity Against Zymoseptoria with Differing Chemical Resistance Profiles This study was designed to test the ability of E. billingiae NRRL B-67766 to control fungal pathogens having different chemical resistance profiles.

Three strains of Zymoseptoria tritici were challenged with two commercially available fungicides, a triazolinthione thought to interfere with the synthesis of ergosterol (prothioconazole) and a pyrazole carboxamide thought to inhibit succinate dehydrogenase (fluxapyroxad). Table 1 Table 1. Susceptibility of Zymoseptoria tritici strains to chemical fungicides

Each of the Z. tritici strains was grown on PDA plates in the presence of E. billingiae NRRL B- 67766. Antifungal activity was measured by the appearance of clearing zones around the E. billingiae colonies. E. billingiae NRRL B-67766 exhibited antagonistic effects against all three strains of Z. tritici, suggesting E. billingiae NRRL B-67766 can protect plants from fungal pests having myriad chemical resistance profiles and may act through multiple modes of action. Example 9

E. billingiae NRRL B-67766 Taxonomically Distinguished from Pathogenic Strains of E. amylovora A pipeline was developed for the identification of unique genomic regions within a population of strains of a prokaryotic species. This pipeline was used to compare E. billingiae NRRL B-67766 with other Erwinia strains of various species by creating a high-resolution strain-level taxonomy assessment using variable sites within the core-genome alignment. Whole genome phylogeny derived from 7906 high-quality SNPs from the core-genome alignment led to a clear separation of the clade comprising E. billingiae NRRL B-67766 from the clade comprising pathogenic E. amylovora strains. Example 10

Extracts of E. billingiae NRRL B-67766 Cultures

Exhibited Activity Against Zymoseptoria and Fusarium

This study was designed to test the ability of cell-free filtrates and cellular extracts derived from cultures of E. billingiae NRRL B-67766 to control fungal pathogens that cause leaf blotch and head blight.

E. billingiae NRRL B-67766 was cultured at 25°C in four distinct media: proprietary media 1, proprietary media 2, potato dextrose broth (P6685; Sigma-Alrdich, Inc., St. Louis, MO, USA) and PPG (200 g potato, 5 g peptone, 5 g glucose, 3 g Na 2 HPO 4 ·12H 2 O, 0.5 g KH 2 PO 4 , 3 g NaCl, per 1,000 ml).

Extracts of the E. billingiae NRRL B-67766 cultures were were prepared by lysing the cells, centrifugation to remove cellular debris, and evaporative-concentration of the resultant supernatant.

Each of the extracts was screened for activity against Zymoseptoria tritici CBS 115943 and Fusarium graminearum BRFM 1982. Proprietary media 1 extract reduced the viability of Fusarium graminearum BRFM 1982 and Zymoseptoria tritici CBS 115943 by approximately 40% and 50–75%, respectively, relative to an extract of the uninoculated media control. Proprietary media 2 and PDB extracts reduced the viability of Zymoseptoria tritici CBS 115943 by 50–75% relative to the uninoculated control extracts. Example 11

E. billingiae NRRL B-67766 Protects Plants from Fungal Diseases This study is designed to test the ability of E. billingiae NRRL B-67766 to protect plants from fungal pathogens in an open field.

E. billingiae NRRL B-67766 is cultured in PPG liquid medium (200 g potato, 5 g peptone, 5 g glucose, 3 g Na 2 HPO 4 ·12H 2 O, 0.5 g KH 2 PO 4 , 3 g NaCl, per 1,000 ml) at 25°C. Bacteria are harvested from the medium by low speed centrifugation, then resuspended in water at a concentration of OD 610 = 0.13-0.26 (approximately 10 8 CFU/ml). Tween 20 is added to the diluted bacteria at a concentration of 0.1% (v/v).

Winter wheat cultivars (Bergamo, Bermude, Cellule, Hereford, Informer, RGT Volupto and Torp) are sown in seven distinct field locations in Europe (four in France and three in Denmark). Plants are sprayed with one of two commercially available chemical fungicides (prothioconazole; PROLINE® EC 250; Bayer Crop Science, St. Louis, MO, USA; metconazole, JUVENTUS®, BASF Crop Protection, Ludwugshafen, Germany), one of two commercially available biofungicides (SERENADE® (Bayer Crop Science, St. Louis, MO, USA; HELIOSOUFRE S®, Action Pin, Castets, France), or E. billingiae NRRL B-67766 suspension at three time points (BBCH31-33; BBCH35-37; BBCH39). Disease severity is assessed following each treatment and again 20, 30 and 40 days after the final treatment.

Plants treated with E. billingiae NRRL B-67766 exhibit reduced fungal disease severity and increased yield as compared to both untreated control plants and plants treated with the commercially available biopesticide. Example 12

P. gessardii NRRL B-67767 Protected Plants Against Blotch and Powdery Mildew

These studies were designed to test the ability of P. gessardii NRRL B-67767 to control fungal pathogens that cause leaf blotch and powdery mildew.

E. billingiae NRRL B-67766 was cultured in PPG liquid medium (200 g potato, 5 g peptone, 5 g glucose, 3 g Na 2 HPO 4 ·12H 2 O, 0.5 g KH 2 PO 4 , 3 g NaCl, per 1,000 ml) at 25°C. Bacteria were harvested from the medium by low speed centrifugation, then resuspended in water at a concentration of OD 610 = 0.13-0.26 (approximately 10 8 CFU/ml). Tween 20 was added to the diluted bacteria at a concentration of 0.1% (v/v).

Winter wheat cultivars were sown in 1 liter pots (15 seeds per pot) and cultivated under greenhouse conditions. Six pots were used for each experimental condition. After approximately 1 month, seedling plants were treated with bacterial suspensions that had a concentration of approximately 10 6 cfu/ml. The bacterial suspensions were sprayed onto the plants until the leaves were saturated (rate of approximately 4 L/ha). Commerically available fungicides, prothioconazole (PROLINE® EC 250; Bayer Crop Science, St. Louis, MO, USA) and SERENADE® (Bayer Crop Science, St. Louis, MO, USA), were applied at a rate of 0.8 L/ha in accordance with the manufacturer's instructions as positive controls.

Negative controls were untreated plants and plants sprayed with water.

One day after application of the bacteria, the plants were inoculated with pathogens.

For leaf blotch, a mixture of 5 isolates of Septoria tritici (also known as Zymoseptoria tritici) were prepared as a suspension containing 2 x 10 6 spores/ml of solution. Two ml of suspension was sprayed onto the plants in each pot. The pathogen-inoculated plants were kept in the dark for 1 day following pathogen inoculation to facilitate infection. Plants were then kept in the greenhouse under high- humidity (>90%) conditions at a temperature of 15°C. After 3 weeks, initial symptoms were observed. Disease assessments were carried out 19, 26 and 30 days following pathogen inoculation. Percent leaf area attacked by pathogen were observed and standard European Meditarranean Plant Protection

Organization (EPPO) scales were used. P. gessardii NRRL B-67767 exhibited fungicidal activity similar to that of prothioconazole, reducing fungal lesions by 40-60% relative to the untreated control or commercially available biopesticide. For powdery mildew, Blumeria graminis infections occurred from natural inoculum that existed in the environment when plants were treated during the rust trial. P. gessardii NRRL B-67767 reduced fungal lesions by approximately 30% relative to untreated control or commercially available biopesticide. Example 13

Extracts of P. gessardii NRRL B-67767 Cultures

Exhibited Activity Against Zymoseptoria and Fusarium

This study was designed to test the ability of cell-free filtrates and cellular extracts derived from cultures of P. gessardii NRRL B-67767 to control fungal pathogens that cause leaf blotch and head blight.

P. gessardii NRRL B-67767 was cultured at 25°C in four distinct media: proprietary media 1, proprietary media 2, potato dextrose broth (P6685; Sigma-Alrdich, Inc., St. Louis, MO, USA) and PPG (200 g potato, 5 g peptone, 5 g glucose, 3 g Na 2 HPO 4 ·12H 2 O, 0.5 g KH 2 PO 4 , 3 g NaCl, per 1,000 ml).

Extracts of the P. gessardii NRRL B-67767 cultures were were prepared by lysing the cells, centrifugation to remove cellular debris, and evaporative-concentration of the resultant supernatant.

Each of the extracts was screened for activity against Zymoseptoria tritici CBS 115943 and Fusarium graminearum BRFM 1982.

Proprietary media 1 extract reduced the viability of Fusarium graminearum BRFM 1982 by 30– 45% relative to an extract of the uninoculated media control. Proprietary media 2 and PDB extracts reduced the viability of Zymoseptoria tritici CBS 115943 by 65–80% relative to the uninoculated control extracts. Example 14

E. billingiae NRRL B-67766 and P. gessardii NRRL B-67767 Persisted on Wheat Leaves

This study was designed to test the ability of E. billingiae NRRL B-67766 and P. gessardii NRRL B-67767 to colonize and persist on the foliar surface of wheat plants.

Wheat plants were sprayed as described in Example 2 on the leaves of wheat plants at about 10 6 CFU/mL. Following spray application, leaves were harvested at 24-hour intervals for 5 days, and genomic DNA was extracted from leaf samples. In order to determine the survival of E. billingiae NRRL B-67766 and P. gessardii NRRL B-67767 on leaves, a qPCR-based method was developed. Strain-specific primers were utilized to track and monitor persistence of E. billingiae NRRL B-67766 and P. gessardii NRRL B- 67767 on wheat leaves.

E. billingiae NRRL B-67766 and P. gessardii NRRL B-67767 persisted on the leaves of the wheat plants throughout the duration of the study. Example 15

P. libanesis NRRL B-67769 Protected Plants Against Blotch

This study was designed to test the ability of P. libanesis NRRL B-67769 to control fungal pathogens that cause leaf blotch.

P. libanesis NRRL B-67769 was cultured in PPG liquid medium (200 g potato, 5 g peptone, 5 g glucose, 3 g Na 2 HPO 4 ·12H 2 O, 0.5 g KH 2 PO 4 , 3 g NaCl, per 1,000 ml) at 25°C. Bacteria were harvested from the medium by low speed centrifugation, then resuspended in water at a concentration of OD 610 = 0.13-0.26 (approximately 10 8 CFU/ml). Tween 20 was added to the diluted bacteria at a concentration of 0.1% (v/v).

Winter wheat was sown in 1 liter pots (15 seeds per pot) and cultivated under greenhouse conditions. Six pots were used for each experimental condition. After approximately 1 month, seedling plants were treated with bacterial suspensions that had a concentration of approximately 10 6 cfu/ml. The bacterial suspensions were sprayed onto the plants until the leaves were saturated (rate of approximately 4 L/ha). Commerically available fungicides, prothioconazole (PROLINE® EC 250; Bayer Crop Science, St. Louis, MO, USA) and SERENADE® (Bayer Crop Science, St. Louis, MO, USA), were applied at a rate of 0.8 L/ha in accordance with the manufacturer's instructions as positive controls. Negative controls were untreated plants and plants sprayed with water.

One day after application of the bacteria, the plants were inoculated with pathogens.

A mixture of 5 isolates of Septoria tritici (also known as Zymoseptoria tritici) were prepared as a suspension containing 2 x 10 6 spores/ml of solution. Two ml of suspension was sprayed onto the plants in each pot. The pathogen-inoculated plants were kept in the dark for 1 day following pathogen inoculation to facilitate infection. Plants were then kept in the greenhouse under high-humidity (>90%) conditions at a temperature of 15°C. After 3 weeks, initial symptoms were observed. Disease assessments were carried out 19, 26 and 30 days following pathogen inoculation. Percent leaf area attacked by pathogen were observed and standard European Meditarranean Plant Protection Organization (EPPO) scales were used. P. libanesis NRRL B-67769 reduced fungal lesions as compared to both the untreated control and the commercially available biopesticides.

Appendix A

Acinetobacter, Actinomycetes, Aegerita, Agrobacterium (e.g., A. radiobacter strains such as K1026 and K84), Akanthomyces, Alcaligenes, Alternaria, Aminobacter (e.g., A. aganoensis, A.

aminovorans, A. anthyllidis, A. ciceronei, A. lissarensis, A. niigataensis), Ampelomyces (e.g., A.

quisqualis strains such as M-10), Anabaena (e.g., A. aequalis, A. affinis, A. angstumalis angstumalis, A. angstumalis marchita, A. aphanizomendoides, A. azollae, A. bornetiana, A. catenula, A. cedrorum, A. circinalis, A. confervoides, A. constricta, A. cyanobacterium, A. cycadeae, A. cylindrica, A. echinispora, A. felisii, A. flos-aquae flos-aquae, A. flos-aquae minor, A. flos-aquae treleasei, A. helicoidea, A.

inaequalis, A. lapponica, A. laxa, A. lemmermannii, A. levanderi, A. limnetica, A. macrospora macrospora, A. macrospora robusta, A. monticulosa, A. nostoc, A. ascillarioides, A. planctonica, A. raciborski, A. scheremetievi, A. sphaerica, A. spiroides crassa, A. spiroides sprroides, A. subcylindrica, A. torulosa, A. unispora, A. variabilis, A. verrucosa, A. viguieri, A. wisconsinense, A. zierlingii),

Arthrobacter, Arthrobotrys (e.g., A. aggregata, A. alaskana, A. ameropora, A. anomala, A. apscheronica, A. arthrobotryoides, A. azerbaijanica, A. bakunika, A. botryospora, A. brochopaga, A. chazarica, A. chilensis, A. cladodes, A. calvispora, A. compacta, A. conoides, A. constringens, A. cylindrospora, A. dactyloides, A. deflectans, A. dendroides, A. doliiformis, A. drechsleri, A. elegans, A. ellipsospora, A. entomopaga, A. ferox, A. foliicola, A. fruticulosa, A. globospora, A. hatospora, A. hertziana, A. indica, A. irregularis, A. javanica, A. kirghizica, A. longa, A. longiphora, A. longiramulifera, A. longispora, A. mangrovispora, A. megaspora, A. microscaphoides, A. microspora, A. multisecundaria, A. musiformis, A. nematopaga, A. nonseptata, A. oligospora, A. oudemansii, A. oviformis, A. perpasta, A. polycephala, A. pseudoclavata, A. pyriformis, A. recta, A. robusta, A. rosea, A. scaphoides, A. sclerohypha, A. shahriari, A. shizishanna, A. sinensis, A. soprunovii, A. stilbacea, A. straminicola, A. superba, A. tabrizica, A.

venusta, A. vermicola, A. yunnanensis), Aschersonia, Ascophaera, Aspergillus (e.g., A. flavus strains such as NRRL 21882, A. parasiticus), Aulosira (e.g., A. aenigmatica, A. africana, A. bohemensis, A.

bombayensis, A. confluens, A. fertilissima, A. fertilissma var. tenius, A. fritschii, A. godoyana, A. implexa, A. laxa, A. plantonica, A. prolifica, A. pseuodoramosa, A. schauinslandii, A. striata, A. terrestris, A. thermalis), Aureobacterium, Aureobasidium (e.g., A. pullulans strains such as DSM 14940 and DSM 14941), Azobacter, Azorhizobium (e.g., A. caulinodans, A. doebereinerae, A. oxalatiphilum), Azospirillum (e.g. , A. amazonense strains such as BR 11140 (SpY2T), A. brasilense strains such as INTA Az-39, AZ39, XOH, BR 11002, BR 11005, Ab-V5 and Ab-V6, A. canadense, A. doebereinerae, A. formosense, A. halopraeferans, A. irakense, A. largimobile, A. lipoferum strains such as BR 11646, A. melinis, A. oryzae, A. picis, A. rugosum, A. thiophilum, A. zeae), Azotobacter (e.g., A. agilis, A. armeniacus, A. sp. AR, A. beijerinckii, A. chroococcum, A. DCU26, A. FA8, A. nigricans, A. paspali, A. salinestris, A.

tropicalis, A. vinelandii), Bacillus (e.g., B. amyloliquefaciens strains such as D747, NRRL B-50349, TJ1000 (also known as 1BE, isolate ATCC BAA-390), FZB24, FZB42, IN937a, IT-45, TJ1000, MBI600, BS27 (deposited as NRRL B-5015), BS2084 (deposited as NRRL B-50013), 15AP4 (deposited as ATCC PTA-6507), 3AP4 (deposited as ATCC PTA-6506), LSSA01 (deposited as NRRL B-50104), ABP278 (deposited as NRRL B-50634), 1013 (deposited as NRRL B-50509), 918 (deposited as NRRL B-50508), 22CP1 (deposited as ATCC PTA-6508) and BS18 (deposited as NRRL B-50633), B. cereus strains such as I-1562, B. firmus strains such as I-1582, B. laevolacticus, B. lichenformis strains such as BA842 (deposited as NRRL B-50516) and BL21 (deposited as NRRL B-50134), B. macerns, B. megaterium strains such as O62UKE (deposited as NRRL B-67352), O723G4 (deposited as NRRL B-67357), O132FX (deposited as NRRL B-67521), O14VDF (deposited as NRRL B-67522), O249FV (deposited as NRRL B-67523), O33Y38 (deposited as NRRL B-67524), O62RUA (deposited as NRRL B-67525), O62RV8 (deposited as NRRL B-67526), O62STA (deposited as NRRL B-67527), O7237E (deposited as NRRL B-67528), O72NWX (deposited as NRRL B-67529), O72T97 (deposited as NRRL B-67530), NRRL B-67533 and NRRL B-67534, B. mycoides strains such as NRRL B-21664, B. pasteurii, B.

pumilus strains such as NRRL B-21662, NRRL B-30087, ATCC 55608, ATCC 55609, GB34, KFP9F and QST 2808, B. sphaericus, B. subtilis strains such as ATCC 55078, ATCC 55079, MBI 600, NRRL B- 21661, NRRL B-21665, CX-9060, GB03, GB07, QST 713, FZB24, D747 and 3BP5 (deposited as NRRL B-50510), B. thuringiensis strains such as ATCC 13367, GC-91, NRRL B-21619, ABTS-1857, SAN 401 I, ABG-6305, ABG-6346, AM65-52, SA-12, SB4, ABTS-351, HD-1, EG 2348, EG 7826, EG 7841, DSM 2803, NB-125 and NB-176), Beijerinckia, Beauveria (e.g., B. bassiana strains such as ATCC 26851, ATCC 48023, ATCC 48585, ATCC 74040, ATCC-74250, DSM 12256 and PPRI 5339), Beijerinckia, Blastodendrion, Bosea (e.g., B. eneae, B. lathyri, B. lupini, B. massiliensis, B. minatitlanensis, B.

robiniae, B. thiooxidans, B. vestrisii), Bradyrhizobium (e.g., B. arachidis, B. bete, B. canariense, B. cytisi, B. daqingense, B. denitrificans, B. diazoefficiens, B. elkanii strains such as SEMIA 501, SEMIA 587 and SEMIA 5019, B. ganzhouense, B. huanghuauhaiense, B.icense, B. ingae, B. iriomotense, B. japonicum strains such as 61A227, 61A228, 61A273, E-109 NRRL B-50586 (also deposited as NRRL B-59565), NRRL B-50587 (also deposited as NRRL B-59566), NRRL B-50588 (also deposited as NRRL B-59567), NRRL B-50589 (also deposited as NRRL B-59568), NRRL B-50590 (also deposited as NRRL B-59569), NRRL B-50591 (also deposited as NRRL B-59570), NRRL B-50592 (also deposited as NRRL B-59571), NRRL B-50593 (also deposited as NRRL B-59572), NRRL B-50594 (also deposited as NRRL B-50493), NRRL B-50608, NRRL B-50609, NRRL B-50610, NRRL B-50611, NRRL B-50612, NRRL B-50726, NRRL B-50727, NRRL B-50728, NRRL B-50729, NRRL B-50730, SEMIA 566, SEMIA 5079, SEMIA 5080, USDA 6, USDA 110, USDA 122, USDA 123, USDA 127, USDA 129 and USDA 532C, B.

jicamae, B. lablabi, B. liaoningense, B. manausense, B. neotropicale, B. oligotrophicum, B. ottawaense, B. pachyrhizi, B. paxllaeri, B. retamae, B. rifense, B. valentinum, B. yuanmingense), Burkholderia (e.g., B. acidipaludis, B. ambifaria, B. andropogonis, B. anthina, B. arboris, B. bannensis, B. bryophila, B. caledonica, B. caribensis, B. caryophylli, B. cenocepacua, B. choica, B. cocovenenans, B. contaminans, B. denitrificans, B. diazotrophica, B. diffusa, B. dilworthii, B. dolosa, B. eburnea, B. endofungorum, B. ferrariae, B. fungorum, B. ginsengisoli, B. gladioli, B. glathei, B. glumae, B. graminis, B. grimmiae, B. heleia, B. hospital, B. humi, B. kururiensis, B. lata, B. latens, B. mallei, B. megapolitana, B. metallica, B. mimosarum, B. multivorans, B. nodosa, B. norimbergensis, B. oklahomensis, B. phenazinium, B.

phenoliruptrix, B. phymatum, B. phytofirmans, B. pickettii, B. plantarii, B. pseudomallei, B.

pseudomultivorans, B. pyrrocinia, B. rhizoxinica, B. rhynchosiae, B. sabiae, B. sacchari, B. sartisoli, B. sediminicola, B. seminalis, B. silvatlantica, B. singaporensis, B. soli, B. sordidcola, B. sp. strains such as A396, B. sprentiae, B. stabilis, B. symbiotica, B. telluris, B. terrae, B. terrestris, B. terricola, B. thailandensis, B. tropica, B. tuberum, B.ubonensis, B.udeis, B.unamae, B.vandii, B.vietnamiensis, B.xenovorans, B.zhejiangensis), Brevibacillus, Burkholderia (e.g., B. sp. A396 nov. rinojensis NRRL B- 50319), Calonectria, Candida (e.g., C. oleophila such I-182, C. saitoana), Candidatus (e.g., C.

Burkholderia calva, C. Burkholderia crenata, C. Burkholderia hispidae, C. Burkholderia kirkii, C.

Burkholderia mamillata, C. Burkholderia nigropunctata, C. Burkholderia rigidae, C. Burkholderia schumannianae, C. Burkholderia verschuerenii, C. Burkholderia virens, C. Phytoplasma allocasuarinae, C. Phytoplasma americanum, C. Phytoplasma asteris, C. Phytoplasma aurantifolia, C. Phytoplasma australiense, C. Phytoplasma balanitae, C. Phytoplasma brasiliense, C. Phytoplasma caricae, C.

Phytoplasma castaneae, C. Phytoplasma cocosnigeriae, C. Phytoplasma cocostanzaniae, C. Phytoplasma convolvuli, C. Phytoplasma costaricanum, C. Phytoplasma cynodontis, C. Phytoplasma fragariae, C. Phytoplasma fraxini, C. Phytoplasma graminis, C. Phytoplasma japonicum, C. Phytoplasma luffae, C. Phytoplasma lycopersici, C. Phytoplasma malasianum, C. Phytoplasma mali, C. Phytoplasma omanense, C. Phytoplasma oryzae, C. Phytoplasma palmae, C. Phytoplasma palmicola, C. Phytoplasma phoenicium, C. Phytoplasma pini, C. Phytoplasma pruni, C. Phytoplasma prunorum, C. Phytoplasma pyri, C.

Phytoplasma rhamni, C. Phytoplasma rubi, C. Phytoplasma solani, C. Phytoplasma spartii, C.

Phytoplasma sudamericanum, C. Phytoplasma tamaricis, C. Phytoplasma trifolii, C. Phytoplasma ulmi, C. Phytoplasma vitis, C. Phytoplasma ziziphi), Chromobacterium (e.g., C. subtsugae NRRL B-30655 and PRAA4-1, C. vaccinia strains such as NRRL B-50880, C. violaceum), Chryseomonas, Clavibacter, Clonostachys (e.g., C. rosea f. catenulata (also referred to as Gliocladium catenulatum) strains such as J1446), Clostridium, Coelemomyces, Coelomycidium, Colletotrichum (e.g., C. gloeosporioides strains such as ATCC 52634), Comomonas, Conidiobolus, Coniothyrium (e.g., C. minitans strains such as CON/M/91-08), Cordyceps, Corynebacterium, Couchia, Cryphonectria (e.g., C. parasitica),

Cryptococcus (e.g., C. albidus), Cryptophlebia (e.g., C. leucotreta), Culicinomyces, Cupriavidus (e.g., C. alkaliphilus, C. basilensis, C. campinensis, C. gilardii, C. laharis, C. metallidurans, C. numazuensis, C. oxalaticus, C. pampae, C. pauculus, C. pinatubonensis, C. respiraculi, C. taiwanensis), Curtobacterium, Cydia (e.g., C. pomonella strains such as V03 and V22), Dactylaria (e.g., D. candida), Delftia (e.g., D. acidovorans strains such as RAY209), Desulforibtio, Desulfovibrio, Devosia (e.g., D. neptuniae), Dilophosphora (e.g., D. alopecuri), Engyodontium, Enterobacter, Entomophaga, Entomophthora, Erwinia (e.g., E. billingiae such as O63B38 (deposited as NRRL B-67766), Erynia, Escherichia (e.g., E. intermedia), Eupenicillium, Exiguobacaterium, Filariomyces, Filobasidiella, Flavobacterium (e.g., F. H492 NRRL B-50584), Frankia (e.g., F. alni), Fusarium (e.g., F. laterium, F. oxysporum , F. solani), Gibellula, Gigaspora (e.g.¸G. margarita), Gliocladium (e.g., G.virens strains such as ATCC 52045 and GL-21), Glomus (e.g. ¸G. aggregatum¸G. brasilianum¸G. clarum¸G. deserticola¸G. etunicatum¸G.

fasciculatum¸G. intraradices strains such as RTI-801 G¸ . monosporum G¸ . mosseae), Gluconobacter, Halospirulina, Harposporium (e.g., H. anguillulae), Hesperomyces, Hirsutella (e.g., H. minnesotensis, H. rhossiliensis, H. thomsonii strains such as ATCC 24874), Hydrogenophage, Hymenoscyphous (e.g., H. ericae), Hymenostilbe, Hypocrella, Isaria (e.g., I. fumosorosea strains such as Apopka-97 (deposited as ATCC 20874)), Klebsiella (e.g., K. pneumoniae, K. oxytoca), Kluyvera, Laccaria (e.g., L. bicolor, L. laccata), Lactobacillus, Lagenidium, Lecanicillium (e.g., L. lecanii strains such as KV01, L. longisporum strains such as KV42 and KV71), Leptolegnia, Lysinibacillus (e.g., L. sphaericus strains such as O62Q8F (deposited as NRRL B-67350), O62S63 (deposited as NRRL B-67351) and O62QG9 (deposited as NRRL B-67486), Lysobacter (e.g., L. antibioticus strains such as 13-1 and HS124, L. enzymogenes strains such as 3.1T8), Massospora, Meristacrum (e.g., M. asterospermum), Mesorhizobium (e.g., M. abyssinicae, M. albiziae, M. alhagi, M. amorphae, M. australicum, M. camelthorni, M. caraganae, M. chacoense, M. ciceri, M. gobiense, M. hawassense, M. huakuii strains such as LL32, M. loti, M. mediterraneum, M. metallidurans, M. muleiense, M. opportunistum, M. plurifarium, M. qingshengii, M. robiniae, M. sangaii, M. septentrionale, M. shangrilense, M. shonense, M. silamurunense, M. tamadayense, M. tarimense, M. temperatum, M. thiogangeticum, M. tianshanense), Metarhizium (e.g., M. anisopliae (also referred to as M. brunneum, Metarrhizium anisopliae, and green muscadine) strains such as IMI 330189, FI-985, FI- 1045, F52 (deposited as DSM 3884, DSM 3885, ATCC 90448, SD 170 and ARSEF 7711) and ICIPE 69), M. flavoviride strains such as ATCC 32969), Methylobacterium (e.g., M. adhaesivum, M. aerolatum, M. aminovorans, M. aquaticum, M. brachiatum, M. brachythecii, M. bullatum, M. cerastii, M.

chloromethanicum, M. dankookense, M. dichloromethanicum, M. extorquens, M. fujisawaense, M.

gnaphalii, M. goesingense, M. gossipiicola, M. gregans, M. haplocladii, M. hispanicum, M. iners, M. isbiliense, M. jeotgali, M. komagatae, M. longum, M. lusitanum, M. marchantiae, M. mesophilicum, M. nodulans, M. organophilum, M. oryzae, M. oxalidis, M. persicinum, M. phyllosphaerae, M. platani, M. podarium, M. populi, M. radiotolerans, M. rhodesianum, M. rhodinum, M. salsuginis, M. soli, M.

suomiense, M. tardum, M. tarhaniae, M. thiocyanatum, M. thurigiense, M. trifolii, M. variabile,

M.zatmanii), Metschnikowia (e.g., M. fructicola), Microbacterium (e.g., M. laevaniformans, M.

trichothecenolyticum strains such as O34A7Y (deposited as NRRL B-67602) and O34A8B (deposited as NRRL B-67822)), Microdochium (e.g., M. dimerum), Microsphaeropsis (e.g., M. ochracea P130A), Microvirga (e.g., M. aerilata, M. aerophila, M. flocculans, M. guangxiensis, M. lotononidis, M. lupini, M. subterranea, M. vignae, M. zambiensis), Monacrosporium (e.g., M. cionopagum), Mucor, Muscodor (e.g., M. albus such NRRL 30547, QST 20799 and SA-13, M. roseus strains such as NRRL 30548),

Mycoderma, Myiophagus, Myriangium, Myrothecium (e.g., M. verrucaria), Nectria, Nematoctonus (e.g., N. geogenius, N. leiosporus), Neozygites, Nomuraea (e.g., N. rileyi strains such as SA86101, GU87401, SR86151, CG128 and VA9101), Nostoc (e.g., N. azollae, N. caeruleum, N. carneum, N. comminutum, N. commune, N. ellipsosporum, N. flagelliforme, N. linckia, N. longstaffi, N. microscopicum, N. muscorum, N. paludosum, N. pruniforme, N. punctifrome, N. sphaericum, N. sphaeroides, N. spongiaeforme, N. verrucosum), Ochrobactrum (e.g., O. anthropi, O. cicero, O. cytisi, O. daejeonense, O. gallinifaecis, O. grigonense, O. guangzhouense, O. haematophilum, O. intermedium, O. lupini, O. oryzae, O. pectoris, O. pituitosum, O. pseudointermedium, O. pseudogrignonense, O. rhizosphaerae, O. thiophenivorans,O. tritici), Oidiodendron, Paecilomyces (e.g., P. fumosoroseus strains such as FE991 and FE 9901, P.

lilacinus strains such as 251, DSM 15169 and BCP2), Paenibacillus (e.g., P. alvei strains such as NAS6G6, P. azotofixans, P. peoriae strains such as NRRL B-67884 and NRRL B-67885, P. polymyxa strains such as ABP166 (deposited as NRRL B-50211)), Pandora, Pantoea (e.g., P. agglomerans strains such as NRRL B-21856, P. vagans strains such as C9-1), Paraglomus (e.g., P. brazilianum), Paraisaria, Pasteuria, Pasteuria (e.g., P. nishizawae strains such as Pn1, P. penetrans, P. ramose, P. sp. strains such as ATCC PTA-9643 and ATCC SD-5832, P. thornea, P. usage), Penicillium (e.g., P. albidum, P.

aurantiogriseum, P. bilaiae (formerly known as P. bilaii and P. bilaji) strains such as ATCC 18309, ATCC 20851, ATCC 22348, NRRL 50162, NRRL 50169, NRRL 50776, NRRL 50777, NRRL 50778, NRRL 50777, NRRL 50778, NRRL 50779, NRRL 50780, NRRL 50781, NRRL 50782, NRRL 50783, NRRL 50784, NRRL 50785, NRRL 50786, NRRL 50787, NRRL 50788, NRRL 67154, NRRL 67155, NRRL 67156, NRRL 67157, NRRL 67158, NRRL 67159 and RS7B-SD1, P. brevicompactum strains such as AgRF18, P. canescens strains such as ATCC 10419, P. chyrsogenum, P. citreonigrum, P.

citrinum, P. digitatum, P. expansum strains such as ATCC 24692 and YT02, P. fellatanum strains such as ATCC 48694, P. frequentas, P. fuscum, P. fussiporus, P. gaestrivorus strains such as NRRL 50170, P. glabrum strains such as DAOM 239074 and CBS 229.28, P. glaucum, P. griseofulvum, P. implicatum, P. janthinellum strains such as ATCC 10455, P. lanosocoeruleum strains such as ATCC 48919, P. lilacinum, P. minioluteum, P. montanense, P.nigricans, P. oxalicum, P. pinetorum, P. pinophilum, P. purpurogenum, P. radicum strains such as ATCC 201836, FRR 4717, FRR 4719 and N93/47267, P. raistrickii strains such as ATCC 10490, P. rugulosum, P. simplicissimum, P. solitum, P. variabile, P. velutinum, P.

viridicatum), Phingobacterium, Phlebiopsis (e.g., P. gigantea), Photorhabdus, Phyllobacterium (e.g., P. bourgognense, P. brassicacearum, P. catacumbae, P. endophyticum, P. ifriqiyense, P. leguminum, P. loti, P. myrsinacearum, P. sophorae, P. trifolii), Pichia (e.g., P. anomala strains such as WRL-076), Pisolithus (e.g., P. tinctorius), Planktothricoides, Plectonema, Pleurodesmospora, Pochonia (e.g., P.

chlamydopora), Podonectria, Polycephalomyces, Prochlorocoous (e.g., P. marinus), Prochloron (e.g., P. didemni), Prochlorothrix, Pseudogibellula, Pseudomonas (e.g., P. agarici, P. antartica, P. aurantiaca, P. aureofaciens, P. azotifigens, P. azotoformans, P. balearica, P. blatchfordae, P. brassicacearum, P.

brenneri, P. cannabina, P. cedrina, P. cepacia, P. chlororaphis strains such as MA 342, P. congelans, P. corrugata, P. costantinii, P. denitrificans, P. entomophila, P. fluorescens strains such as ATCC 27663, CL 145A and A506, P. fragii, P. fuscovaginae, P. fulva, P. gessardii such as O63B39 (deposited as NRRL B-67767), P. jessenii strains such as PS06, P. kilonensis, P. koreensis strains such as O82GYH (deposited as NRRL B-67883), P. libanensis such as O63B3D (deposited as NRRL B-67769), P. lili, P. lundensis, P. lutea, P. luteola, P. mandelii, P. marginalis, P. meditrranea, P. meridana, P. migulae, P. moraviensis, P. mucidolens, P. orientalis, P. oryzihabitans, P. palleroniana, P. panacis, P. parafulva, P. peli, P. pertucinogena, P. plecoglossicida, P. protogens, P. proteolytica, P. putida, P. pyrocina strains such as ATCC 15958, P. rhodesiae, P. sp. strains such as DSM 13134, P. striata, P. stutzeri, P. syringae, P. synxantha, P. taetrolens, P. thisvervalensis, P. tolaasii, P. veronii), Pseudozyma (e.g., P. flocculosa strains such as PF-A22 UL), Pythium (e.g., P. oligandrum strains such as DV 74), Rhizobium (e.g., R. aggregatum, R. alamii, R. alkalisoli, P. alvei, P. azibense, P. borbori, R. calliandrae, R.cauense, R.

cellulosilyticum, R. daejeonense, R. endolithicum, R. endophyticum, R. etli, R. fabae, R. flavum, R. fredii, R. freirei, R. galegae, R. gallicum, R. giardinii, R. grahamii, R. hainanense, R. halophytocola, R.

halotolerans, R. helanshanense, R. herbae, R. huautlense, R. indigoferae, R. jaguaris, R. kunmingense, R. laguerreae, R. larrymoorei, R. leguminosarum strains such as 162BB1, 162P17, 175G10b, D36 and SO12A-2 (IDAC 080305-01), R. lemnae, R. leucaenae, R. loessense, R. loti strains such as 95C11 and 95C14, R. lupini, R. lusitanum, R. mayense, R. mesoamericanum, R. mesosinicum, R. miluonense, R. mongolense, R. multihospitium, R. naphthalenivorans, R. nepotum,, R. oryzae, R. pakistanensis, R.

paknamense, R. paranaense, R. petrolearium, R. phaseoli, R. phenanthrenilyticum, R. pisi, R. pongamiae, R. populi, R. pseudoryzae, R. pusense, R. qilianshanese, r. radiobacter, R. rhizogenes, R. rhizoryzae, R. rozettiformans, R. rubi, R. selenitireeducens, R. skierneiwicense, R. smilacinae, R. soli, R. sophorae, R. sophoriradicis, R. sphaerophysae, R. straminoryzae, R. subbaraonis, R. sullae, R. taibaishanense, R. tarimense, R. tibeticum, R. trifolii strains such as RP113-7, R. tropici strains such as SEMIA 4080, R. tubonense, R. undicola, R. vallis, R. viciae strains such as P1NP3Cst, SU303 and WSM 1455, R. vignae, R. vitis, R. yanglingense, R. yantingense), Rhizoctonia, Rhizopogon (e.g., R. amylopogon, R. fulvigleba, R. luteolus, R. villosuli), Rhodococcus, Saccharopolyspora (e.g., S. spinosa), Scleroderma (e.g., S. cepa S. citrinum), Septobasidium, Serratia, Shinella (e.g., S. kummerowiae), Sinorhizoium (e.g., S. abri, S.

adhaerens, S. americanum, S. arboris, S. chiapanecum, S. fredii strains such as CCBAU114 and USDA 205, S. garamanticus, S. indiaense, S. kostiense, S. kummerowiae, S. medicae, S. meliloti strains such as 102F34a, 102F51a, 102F77b, B401 and MSDJ0848, S. mexicanus, S. numidicus, S. psoraleae, S. saheli, S. sesbaniae, S. sojae, S. terangae, S. xinjiangense), Sorosporella, Sphaerodes (e.g., S. mycoparasitica strains such as IDAC 301008-01), Spodoptera (e.g., S. littoralis), Sporodiniella, Steinernema (e.g., S. carpocapsae, S. feltiae, S. kraussei strains such as L137), Stenotrophomonas, Streptomyces (e.g., S.

NRRL B-30145, S. M1064, S. WYE 53 (deposited as ATCC 55750), S. cacaoi strains such as ATCC 19093, S. galbus strains such as NRRL 30232, S. griseoviridis strains such as K61, S. lydicus strains such as WYEC 108 (deposited as ATCC 55445), S. violaceusniger strains such as YCED-9 (deposited as ATCC 55660)), Streptosporangium, Stillbella, Swaminathania, Talaromyces (e.g., T. aculeatus, T. flavus strains such as V117b), Tetranacrium, Thiobacillus, Tilachlidium, Tolypocladium, Tolypothrix,

Torrubiella, Torulospora, Trenomyces, Trichoderma (e.g. T. asperellum strains such as SKT-1, T.

atroviride strains such as LC52 and CNCM 1-1237, T. fertile strains such as JM41R, T. gamsii strains such as ICC 080, T. hamatum strains such as ATCC 52198, T. harzianum strains such as ATCC 52445, KRL-AG2, T-22, TH-35, T-39 and ICC012, T. polysporum, T. reesi strains such as ATCC 28217 T.

stromaticum, T. virens strains such as ATCC 58678, GL-3, GL-21 and G-41, T. viridae strains such as ATCC 52440, ICC080 and TV1), Typhula, Ulocladium (e.g., U. oudemansii strains such as HRU3), Uredinella, Variovorax, Verticillium (e.g., V. chlamydosporum , V. lecanii strains such as ATCC 46578), Vibrio, Xanthobacter, Xanthomonas. Xenorhadbus, Yersinia (e.g., Y. entomophaga strains such as MH96 (also known as O43NEW) (deposited as DSM 18238, DSM 22339, ATCC BAA-1678 and NRRL B- 67598), O82KB8, O24G3R (deposited as NRRL B-67599), O24KEK (deposited as NRRL B-67600), O333A4 (deposited as NRRL B-67601), O23ZMJ, O348UX and O33ZDX), Zoophthora