CROSS REFERENCE TO RELATED APPLICATIONS

[0001] The present Application is a PCT International Patent Application claiming the benefit of priority to U.S. Provisional Patent Application No. 62/113,792, filed on July 25, 2015, whic is hereby incorporated by reference in its entirety for all purposes. The following applications are generally related to the instant disclosure, U.S. Provisional Patent Application No. 62/113,792, filed on February 09, 2015, and U.S. Provisional Patent Application No. 62/165,620, filed on May 22, 2015, and U.S. Provisional Patent Application No. 62/280,503, filed on January 19, 2016, each of which is hereby incorporated by reference in its entirety for all purposes.

DESCRIPTION OF THE TEXT FILE SUBMITTED ELECTRONICALLY

[0002] The contents of the text file submitted electronically herewith are incorporated herein by reference in their entirety: A computer readable format copy of the Sequence Listing (filename: BICO_005_02WO_SeqList_ST25.txt, date recorded July 22, 2016, file size 477 kilobytes).

FIELD

[0003] The present disclosure relates to isolated and biologically pure microorganisms that have application, inter alia, in agriculture. The disclosed microorganisms can be utilized in their isolated and biologically pure states, as well as being formulated into agriculturally acceptable compositions. Further, the disclosure provides agriculturally beneficial microbial consortia, containing at least two members of the disclosed microorganisms, as well as methods of utilizing said consortia in agricultural applications.

BACKGROUND

[0004] According to the United Nations World Food Program, there are close to 900 million malnourished people in the world. The malnourishment epidemic is particularly striking in the developing nations of the world, where one in six children is underweight. The paucity of available food can be attributed to many socioeconomic factors; however, regardless of ultimate cause, the fact remains that there is a shortage of food available to feed a growing world population, which is expected to reach 9 billion people by 2.050. The United Nations estimates that agricultural yields must, increase by 70-100% to feed the projected global population in 2050.

[0005] These startling world population and malnutrition figures highlight the importance of agricultural efficiency and productivity, in sustaining the world's growing population. The technological advancements achieved by modern row crop agriculture, which has led to never before seen crop yields, are impressive. However, despite the advancements made by technological innovations such as genetically engineered crops and new novel pesticidal and herbicidal compounds, there is a need for improved crop performance, in order to meet the demands of an exponentially increasing global population.

[0006] Scientists have estimated that if the global agricultural "yield gap" (which is the difference between the best observed yield and results elsewhere) could be closed, then worldwide crop production w ould rise by 45-70%. That is, if all farmers, regardless of worldwide location, could achieve the highest attainable yield expected for their respective regions, then a great majority of the deficiencies in worldwide food production could be addressed. However, solving the problem of how to achieve higher yields across a heterogenous worldwide landscape are difficult.

[0007] Often, yield gaps can be explained by inadequate water, substandard farming practices, inadequate fertilizers, and the non-availability of herbicides and pesticides. However, to vastly increase the worldwide use of water, fertilizers, herbicides, and pesticides, would not only be economically infeasible for most of the world, but would have negative environmental consequences .

[0008] Thus, meeting global agricultural yield expectations, by simply scaling up current high-input agricultural systems— utilized in most of the developed world— is simply not feasible.

[0009] There is therefore an urgent need in the art for improved methods of increasing crop performance and imparting beneficial traits to desired plant species. SUMMARY OF THE DISCLOSURE

[0010] The present disclosure addresses this important issue of how to improve crop performance, thereby closing the worldwide yield gap, along with providing ways of imparting other beneficial traits to plant species.

[0011] The solution to increasing crop performance and increasing yield proffered by the present disclosure is not detrimental to the earth's resources, as it does not rely upon increased water consumption or increased input of synthetic chemicals into a system. Rather, the present disclosure utilizes microbes to impart beneficial properties, including increased yields, to desirable plants.

[0012] The disclosure therefore offers an environmentally sustainable solution that allows farmers to increase yields of important crops, which is not reliant upon increased utilization of synthetic herbicides and pesticides.

[0013] In embodiments, the disclosure provides for an efficient and broadly applicable agricultural platform utilizing microbes and microbial consortia that promote one or more desirable plant properties.

[0014] In some embodiments, a single microbe is utilized. In some aspects, the single microbe is isolated and purified. In some aspects, the single microbe is a taxonomic species of bacteria. In some aspects, the single microbe is an identifiable strain of a taxonomic species of bacteri a. In some aspects, the single microbe is a novel, newly discovered strain of a taxonomic species of bacteria,

[0015] In some embodiments, a single microbe from Table 1 is utilized. In other embodiments, a single microbe from Table 2 is utilized. In yet other embodiments, a single microbe from Table 3 is utilized. In additional embodiments, a single microbe from Table 4 is utilized.

[0016] In some embodiments, a microbe from the genus Bosea is utilized.

[0017] In some aspects, the single microbe— whether a taxonomically identifiable species or strain— is combined with one or more other microbes of a different species or strain. In certain aspects, the combination of two or more microbes fonns a consortia or consortium. The terms consortia and consortium are utilized interchangeably. [0018] In certain aspects, the disclosure provides for the development of highly functional microbial consortia that help promote the development and expression of a desired phenotypic or genotypic plant trait. In some embodiments, the consortia of the present disclosure possess functional attributes that are not found in nature, when the individual microbes are living alone. That is, in various embodiments, the combination of particular microbial species into consortia, leads to the microbial combination possessing functional attributes that are not possessed by any one individual member of the consortia when considered alone.

[0019] In some embodiments, this functional attribute possessed by the microbial consortia is the ability to impart one or more beneficial properties to a plant species, for example: increased growth, increased yield, increased nitrogen utilization efficiency, increased stress tolerance, increased drought tolerance, increased photosynthetic rate, enhanced water use efficiency, increased pathogen resistance, modifications to plant architecture that don't necessarily impact plant yield, but rather address plant functionality, etc.

[0020] The ability to impart these beneficial properties upon a plant is not possessed, in some embodiments, by the individual microbes as they would occur in nature. Rather, in some embodiments, it is by the hand of man combining these microbes into consortia that a functional composition is developed, said functional composition possessing attributes and functional properties that do not exist in nature.

[0021] However, in other embodiments, the disclosure provides for individual isolated and biologically pure microbes that are able to impart beneficial properties upon a desired plant species, without the need to combine said microbes into consortia.

[0022] In embodiments, the microbial consortia can be any combination of individual microbes from Table 1. In other embodiments, the microbial consortia can be any combination of individual microbes from Table 2, In yet other embodiments, the microbial consortia can be any combination of individual microbes from Table 3. In additional embodiments, the microbial consortia can be any combination of individual microbes from Table 4. In yet other embodiments, the microbial consortia can be any combination of individual microbes from any of Tables 1-4. In certain embodiments, the microbial consortia comprise two microbes, or three microbes, or four microbes, or five microbes, or six microbes, or seven microbes, or eight microbes, or nine microbes, or 10 microbes, or more than 10 microbes. [0023] Another object of the disclosure relates to the use of the isolated microbes and microbial consortia as plant growth promoters. In other aspects, the isolated microbes and microbial consortia function as growth modifiers, which can, e.g. subvert normal senescence that leads to increased biomass.

[0024] Yet another object of the disclosure relates to the use of the isolated microbes and microbial consortia as soil health enhancers and plant health enhancers.

[0025] Another object of the disclosure is to design a microbial consortium, which is able to perform multidimensional activities in common. In certain aspects, the microbes comprising the consortium act svnergistically. In aspects, the effect that the microbial consortium has on a certain plant characteristic is greater than the effect that would be observed had any one individual microbial member of the consortium been utilized singularly. That is, in some aspects, the consortium exhibit a greater than additive effect upon a desired plant characteristic, as compared to the effect that would be found if any individual member of the consortium had been utilized by itself.

[0026] In some aspects, the consortia lead to the establishment of other plant-microbe interactions, e.g. by acting as primary colonizers or founding populations that set the trajectory for the future microbiome development.

[0027] In embodiments, the disclosure is directed to synergistic combinations (or mixtures) of microbial isolates.

[0028] In some aspects, the consortia taught herein provide a wide range of agricultural applications, including: improvements in yield of grain, fruit, and flowers; improvements in growth of plant parts; improved resistance to disease; improved sun'ivabiiity in extreme climate: and improvements in other desired plant phenotypic characteristics. Significantly, these benefits to plants can be obtained without any hazardous side effects to the environment.

[0029] In some aspects, the individual microbes of the disclosure, or consortia comprising same, can be combined into an agriculturally acceptable composition.

[0030] In some embodiments, the agricultural compositions of the present disclosure include, but are not limited to: wetters, compatibilizing agents, antifoam agents, cleaning agents, sequestering agents, drift reduction agents, neutralizing agents, buffers, corrosion inhibitors, dyes, odorants, spreading agents, penetration aids, sticking agents, binders , dispersing agents, thickening agents, stabilizers, ernulsifiers, freezing point depressants, antimicrobial agents, fertilizers, pesticides, herbicides, inert carriers, polymers, and the like.

[0031 ] In one embodiment of the present disclosure, the microbes (including isolated single species, or strains, or consortia), are supplied in the form of seed coatings or other applications to the seed. In embodiments, the seed coating may be applied to a naked and untreated seed. In other embodiments, the seed coating may be applied as a seed overcoat to a previously treated seed.

[0032] In some embodiments, the applied microbes may become endophytic and consequently will be present in the growing plant that was treated and its subsequent offspring. In other embodiments the microbes might be applied at the same time as a co- treatment with seed treatments.

[0033] In one embodiment of the present disclosure, the microbes are supplied in the form of granules, or plug, or soil drench that is applied to the plant growth media. In other embodiments, the microbes are supplied in the form of a foliar application, such as a foliar spray or liquid composition. The foliar spray or liquid application may be applied to a growing plant or to a growth media, e.g. soil.

[0034] In embodiments, the agricultural compositions of the disclosure can be formulated as: (1 ) solutions; (2) wettable powders; (3) dusting powders; (4) soluble powders; (5) emulsions or suspension concentrates; (6) seed dressings, (7) tablets; (8) water-dispersible granules; (9) water soluble granules (slow or fast release); (10) microencapsulated granules or suspensions; and (11 ) as irrigation components, among others. In certain aspects, the compositions may be diluted in an aqueous medium prior to conventional spray application. The compositions of the present disclosure can be applied to the soil, plant, seed, rhizosphere, rhizosheath, or other area to which it would be beneficial to apply the microbial compositions.

[0035] Still another object of the disclosure relates to the agricultural compositions being formulated to provide a high colony forming units (CFU) bacterial population or consortia. In some aspects, the agricultural compositions have adjuvants that provide for a pertinent shelf life. In embodiments, the CFU concentration of the taught agricultural compositions is higher than the concentration at which the microbes would exist naturally, outside of the disclosed methods. In another embodiment, the agricultural composition contains the microbial cells in a concentration of 10 ³ -10 CFU per gram of the carrier or 10 ⁵ - 10 CFU per gram of the carrier. In an aspect the microbial cells are applied as a seed coat directly to a seed at a concentration of Ιθ θ ⁹ CFU. In other aspects, the microbial cells are applied as a seed overcoat on top of another seed coat at a concentration of 10 ³ -10 ⁹ CFU. In other aspects, the microbial cells are applied as a co-treatment together with nother seed treatment at a rate of 10 ⁵ -1G ⁹ CFU.

[0036] In aspects, the disclosure is directed to agricultural microbial formulations that promote plant growth. In aspects, the disclosure provides for the taught isolated microbes, and consortia comprising same, to be formulated as an agricultural bioinoculant. The taught bioinoculants can be applied to plants, seeds, or soil. Suitable examples of formulating bioinoculants comprising isolated microbes can be found in U.S. Pat. No. 7,097,830, which is herein incorporated by reference.

[0037] The disclosed polymicrobial formulations can: lower the need for nitrogen containing fertilizers, solubiiize minerals, protect plants against pathogens, and make available to the plant valuable nutrients, such as phosphate, thus reducing and eliminating the need for using chemical pesticides and chemical fertilizers.

[0038] In some embodiments, the isolated and biologically pure microbes of the present disclosure can be utilized, in a method of imparting one or more beneficial properties or traits to a desired plant species.

[0039] In some embodiments, the agriculturally acceptable composition containing isolated and biologically pure microbes of the present disclosure can be utilized, in a method of imparting one or more beneficial properties or traits to a desired plant species.

[0040] In some embodiments, the consortia of the present disclosure can be utilized, in a method of imparting one or more beneficial properties or traits to a desired plant species.

[0041] In some embodiments, the agriculturally acceptable composition containing consortia of the present disclosure can be utilized, in a method of imparting one or more beneficial properties or traits to a desired plant species.

[0042] In some aspects, the isolated and biologically pure microbes of the present disclosure, and/or the consortia of the present disclosure, are derived from an accelerated microbiai selection process ("AMS" process). The AMS process utilized in some aspects of the present disclosure is described, for example, in: (1) International Patent Application No. PCT/NZ2012/000041 , published on September 20, 2012, as International Publication No. WO 2012125050 Al, and (2) International Patent Application No. PCT/NZ2013/000171, published on March 27, 2014, as International Publication No. WO 2014046553 Al, each of these PCT Applications is herein incorporated by reference in their entirety for all purposes. The AMS process is described in the present disclosure, for example, in FIGS. 1-4.

[0043] However, in other embodiments, the microbes of the present disclosure are not derived from an accelerated microbial selection process. In some aspects, the microbes utilized in embodiments of the disclosure are chosen from amongst members of microbes present in a database. In particular aspects, the microbes utilized in embodiments of the disclosure are chosen from microbes present in a database based upon particular characteristics of said microbes.

[0044] The present disclosure provides that a plant element or plant part can be effectively augmented, by coating said plant element or plant past with an isolated microbe or microbial consortia, in an amount that is not normally found on the plant element or plant part

[0045] Some embodiments described herein are methods for preparing an agricultural seed composition, or seed coating, comprising: contacting the surface of a seed with a formulation comprising a purified microbial population that comprises at least one isolated microbe that is heterologous to, or rarely present on the seed. Further embodiments entail preparing an agricultural plant composition, comprising: contacting the surface of a plant with a formulation comprising a purified microbial population that comprises at least one isolated microbe that is heterologous to the plant.

[0046] In some aspects, applying an isolated microbe, microbial consortia, and/or agricultural composition of the disclosure to a seed or plant modulates a trait of agronomic importance. The trait of agronomic importance can be, e.g., disease resistance, drought tolerance, heat tolerance, cold tolerance, salinity tolerance, metal tolerance, herbicide tolerance, chemical tolerance, improved water use efficiency, improved nitrogen utilization, improved resistance to nitrogen stress, improved nitrogen fixation, pest resistance, herbivore resistance, pathogen resistance, increased yield, increased yield under water limited conditions, health enhancement, vigor improvement, growth improvement, photosynthetic capability- improvement, nutrition enhancement, altered protein content, altered oil content, increased biomass, increased shoot lengtli, increased root lengtli, improved root architecture, increased seed weight, faster seed germination, altered seed carbohydrate composition, altered seed oil composition, number of pods, delayed senescence, stay-green, and altered seed protein composition. In some aspects, at least 2, 3, 4, or more traits of agronomic importance are modulated. In some aspects, the modulation is a positive effect on one of the aforementioned agronomic traits.

[0047] In some aspects, the isolated microbes, consortia, and/or agricultural compositions of the disclosure can be applied to a plant, in order to modulate or alter a plant characteristic such as altered oil content, altered protein content, altered seed carbohydrate composition, altered seed oil composition, altered seed protein composition, chemical tolerance, cold tolerance, delayed senescence, disease resistance, drought tolerance, ear weight, growth improvement, health enhancement, heat tolerance, herbicide tolerance, herbivore resistance, improved nitrogen fixation, improved nitrogen utilization, improved root architecture, improved water use efficiency, increased biomass, decreased biomass, increased root length, decreased root length, increased seed weight, increased shoot length, decreased shoot length, increased yield, increased yield under water-limited conditions, kernel mass, kernel moisture content, metal tolerance, number of ears, number of kernels per ear, number of pods, nutrition enhancement, pathogen resistance, pest resistance, photosynthetic capability improvement, salinity tolerance, stay-green, vigor improvement, increased dry weight of mature seeds, increased fresh weight of mature seeds, increased number of mature seeds per plant, increased chlorophyll content, increased number of pods per plant, increased length of pods per plant, reduced number of wilted leaves per plant, reduced number of severely wilted leaves per plant, and increased number of non-wilted leaves per plant, a detectable modulation in the level of a metabolite, a detectable modulation in the level of a transcript, and a detectable modulation in the proteome relative to a reference plant.

[0048] In some embodiments, the agricultural formulations taught herein comprise at least one member selected from the group consisting of an agriculturally compatible carrier, a tackifier, a microbial stabilizer, a fungicide, an antibacterial agent, an herbicide, a nematicide, an insecticide, a plant growth regulator, a rodenticide, and a nutrient

[0049] The methods described herein can include contacting a seed or plant with at least 100 CFU or spores, at least 300 CFU or spores, at least 1,000 CFU or spores, at least 3,000 CFU or spores, at least 10,000 CFU or spores, at least 30,000 CFU or spores, at least 100,000 CFU or spores, at least 300,000 CFU or spores, at least 1,000,000 CFU or spores or more, of the microbes taught herein. [0050] In some embodiments of the methods described herein, an isolated microbe of the disclosure is present in a formulation in an amount effective to be detectable within and/or on a target tissue of an agricultural plant. For example, the microbe is detected in an amount of at least 100 CFU or spores, at least 300 CFU or spores, at least 1,000 CFU or spores, at least 3,000 CFU or spores, at least 10,000 CFU or spores, at least 30,000 CFU or spores, at least 100,000 CFU or spores, at least 300,000 CFU or spores, at least 1,000,000 CFU or spores, or more, in and/or on a target tissue of a plant. Alternatively or in addition, the microbes of the disclosure may be present in a formulation in an amount effective to increase the biomass and/or yield of a plant that has had such a formulation applied thereto, by at least 1%, at least 2%, at least 3%, at least 5%, at least 10%, at least 15%, at least 20%, at least 30%, at least 40%, at least 50%, at least 60%, at least 70%, at least 80%, at least 90%, at least 100%, or more, when compared with a reference agricultural plant thai has not had the formulations of the disclosure applied. Alternatively or in addition, the microbes of the disclosure may be present in a formulation in an amount effective to detectably modulate an agronomic trait of interest of a plant that has had such a formulation applied thereto, by at least 1 %, at least 2%, at least 3%, at least 5%, at least 10%, at least 15%, at least 20%, at least 30%, at least 40%, at least 50%, at least 60%, at least 70%, at least 80%, at least 90%, at least 100%, or more, when compared with a reference agricultural plant that has not had the formulations of the disclosure applied.

[0051] In some embodiments, the agricultural compositions taught herein are shelf-stable. In some aspects, the microbes taught herein are freeze dried. Also described herein are a plurality of isolated microbes confined within an object selected from the group consisting of: bottle, jar, ampule, package, vessel, bag, box, bin, envelope, carton, container, silo, shipping container, truck bed, and case.

[0052] In some aspects, combining a selected plant species with a disclosed microbe— operational taxonomic unit (OTU), strain, or composition comprising any of the aforementioned— leads to improved yield from crops and generation of products thereof. Therefore, in one aspect, the present disclosure provides a synthetic combination of a seed of a first plant and a preparation of a microbe(s) that is coated onto the surface of the seed of the first plant, such that the microbe is present at a higher level on the surface of the seed, than is present on the surface of an uncoated reference seed. In another aspect, the present disclosure provides a synthetic combination of a part of a first plant and a preparation of a microbe(s) that is coated onto the surface of the part of the first plant, such that the microbe is present at a higher level on the surface of the part of the first plant, than is present on the surface of an uncoated reference plant part. The aforementioned methods can be used alone, or in parallel with plant breeding and transgenic technologies.

[0053] In some embodiments, an isolated bacterial strain may be selected from the group consisting of Chryseobacteriiim daecheongen.se deposited as NRRL Accession Deposit No. NRRL B-67291 : Chryseobacteriiim rhizosphaerae deposited as NRRL. Accession Deposit No. NRRL B-67288; Chryseobacteriiim rhizosphaerae deposited as NRRL, Accession Deposit No. NRRL B-67287; Frigidibacter albus deposited as NRRL Accession Deposit No. NRRL B-67285; Frigidibacter albus deposited as NRRL Accession Deposit No. NRRL B- 67283: Frigidibacter albus deposited as NRRL Accession Deposit No. NRRL B-67284; Arthrobacter nicotmovorans deposited as NRRL Accession Deposit No. NRRL B-67289; Arthrohacter nicotmovorans deposited as NRRL Accession Deposit No. NRRL, B-67209; Pseudotnonas helmanticensis deposited as NRRL Accession Deposit No. NRRL B-67295; Pseudotnonas helmanticensis deposited as NRRL, Accession Deposit No. NRRL B-97296; Pseudotnonas helmanticensis deposited as NRRL Accession Deposit No. NRRL B-67297; Agrobacterium fabrum deposited as NRRL Accession Deposit No. NRRL B-67286; Exiguobacterium sibiricurn deposited as NRRL, Accession Deposit No. NRRL B-67294; Exiguobacterium antarcticum deposited as NRRL Accession Deposit No. NRRL B-67292; Exiguobacterium antarcticum deposited as NRRL Accession Deposit No. NRRL B-67293; Leifsonia lichenia deposited as NRRL Accession Deposit No. NRRL B-67298; Leifsonia lichenia deposited as NRRL Accession Deposit No. NRRL B-67299; Turnebacillus permanentifrigoris deposited as NRRL Accession Deposit No. NRRL B-67302; Turnebacillus permanentifrigoris deposited as NRRL Accession Deposit No. NRRL B- 67300: Turnebacillus permanentifrigoris deposited as NRRL Accession Deposit No. NRRL B-67303; and Turnebacillus permanentifrigoris deposited as NRRL Accession Deposit No. NRRL B-67301.

[0054] In some embodiments, the isolated bacterial strain has substantially similar morphological and physiological characteristics as an isolated bacterial strain of the present disclosure. In some embodiments, the isolated bacterial strain has substantially similar genetic characteristics as an isolated bacterial strain of the present disclosure. In some embodiments, an isolated bacterial strain of the present disclosure is in substantially pure culture. [0055] In some embodiments, progeny and/or mutants of an isolated bacterial strain of the present disclosure are contemplated. In some embodiments, an isolated bacterial strain of the present disclosure comprises a polynucleotide sequence sharing at least 97% sequence identity with any one of SEQ ID Nos: 1 -307, In other embodiments, an isolate bacteria] strain of the present disclosure comprises a polynucleotide sequence sharing at least 97% sequence identity with any one of SEQ ID NOs: 2-13, 14, 17-19, 22-27, 29, 31, 33, and 34.

[0056] In some embodiments, a cell-free or inactivated preparation of an isolated bacterial strain of the present disclosure is contemplated, or a mutant of said isolated bacterial strain. In some embodiments, a metabolite produced by an isolated bacterial strain of the present disclosure is contemplated, or a mutant of said isolated bacterial strain.

[0057] In some embodiments, an agricultural composition comprises an isolated bacterial strain and an agriculturally acceptable carrier. The isolated bacterial strain may be present in the composition at 1 ^χ 10 ^J to I ^χ I0 ^{! 2} bacterial ceils per gram. The agricultural composition may be formulated as a seed coating.

[0058] In some embodiments, a method of imparting at least one beneficial train upon a plant species comprises applying an isolated bacterial strain to the plant or to a growth medium in which said plant is located. In some embodiments, a method of imparting at least one beneficial trait upon a plant species comprises applying an agricultural composition of the present disclosure to the plant or to a growth medium in which the plant is located.

[0059] In some embodiments a microbial consortium comprises at least two microbes selected from the groups consisting of: A) Stenotrophomonas maltophilia, Rhodococcus erythropolis, Pantoea vagans, Pseudomonas oryzihabitans, Rahnella aquatilis, Duganella radicis, Exiguobacterium acetylicum, Arthrobacter pascens, Pseudomonas putida, Bacillus megatarium, Bacillus aryabhattai, Bacillus cereus, Novosphingobium sediminicoia, Rhizobium etli, Ensifer adhaerens, Chitinophaga terrae, Variovorax ginsengisoli, Pedobacter terrae, Massilia albidiflava, Dyadobacter soli, Bosea robiniae, Microbacterium rnaritypicum, Microbacterium azadirachtae, Sphingopyxis aiaskensis, Arthrobacter pascens, Chryseobacteriuni rhizosphaerae, Variovorax paradoxus, Hydrogenophaga atypica, and Microbacterium oleivorans; and/or B) Chryseobacteriuni daecheongense, Chryseobacterium rhizosphaerae, Frigidibacter albus, Arthrobacter nicotinovorans, Pseudomonas helmanticensis, Agrobacterium fabrum, Achromobacter pulmonis, Exiguobacterium sibiricum, Exiguobacterium antarcticun , Leifsonia lichenia, Tumebacillus permanentifrigoris, Novosphingobium lindaniclasticum, and Massilia kyonggiensis; and combinations thereof, and wherein at least one microbe from B) is selected.

[0060] In some embodiments, the microbial consortium, has substantially similar morphological and physiological characteristics as a microbial consortium of the present disclosure. In some embodiments, the microbial consortium has substantially similar genetic characteristics as a microbial consortium of the present disclosure. In some embodiments, the microbial consortium is in substantially pure culture. In some embodiments, a subsequent generation of any microbe of the microbial consortium is contemplated. In some embodiments, a mutant of any microbe of microbial consortium is contemplated. In some embodiments, a cell-free or inactivated preparation of the microbial consortium, or a mutant of any microbe in the microbial consortium, is contemplated. In some embodiments, a metabolite produced by the microbial consortium, or a mutant of any microbe in the microbial consortium, is contemplated.

[0061] In some embodiments, an agricultural composition comprises a microbial consortium and an agriculturally acceptable carrier. The microbial consortium of the agricultural composition may be present in the composition at 1 ^χ 10 ³ to 1 ^x 10 ¹² bacterial cells per gram. In some embodiments, the agricultural composition is formulated as a seed coating. In some embodiments, a method of imparting at least one beneficial train upon a plant species comprises applying a microbial consortium to said plant, or to a growtli medium in which said plant is located. In some embodiments, a method of imparting at least one beneficial trait upon a plant species, comprising applying the agricultural composition to the plant, or to a growth medium in which said plant is located.

[0062] In some embodiments, a microbial consortium comprises at least two microbes selected from the group consisting of Chryseohacterium daecheongense deposited as NRJ 1, Accession Deposit No. NRRL B-67291 ; Chryseohacterium rhizosphaerae deposited as NRRL Accession Deposit No. NRRL. B-67288; Chryseohacterium rhizosphaerae deposited as NRRL Accession Deposit No. NRRL B-67287; Frigidihacter albus deposited as NRRL Accession Deposit No. NRRL B-67285; Frigidihacter albus deposited as NRRL Accession Deposit No. NRRL B-67283; Frigidihacter albus deposited as NRRL Accession Deposit No. NRRL B-67284; Arthrohacter nicotinovorans deposited as NRRL. Accession Deposit No. NRRL B-67289; Arthrohacter nicotinovorans deposited as NRRL Accession Deposit No. NRRL B-67290; Pseudomonas helmanticensis deposited as NRRL Accession Deposit No. NRRL B-67295; Pseudomonas helmanticensis deposited as NRRL Accession Deposit No. NRRL B-67296; Pseudornonas helmanticensis deposited as NRRL Accession Deposit No. NRRL B-67297; Agrobacterium fabrum deposited as NRRL, Accession Deposit No. NRRL, B-67286; Exiguohacterium sibiricum deposited as NRRL Accession Deposit No. NRRL B- 67294; Exiguohacterium antarcticiim deposited as NRRL Accession Deposit No. NRRL B- 67292: Exiguobacterium antarcticiim deposited as NRRL Accession Deposit No. NRRL B- 67293: Leifsonia lichenia deposited as NRRL Accession Deposit No. NRRL B-67298; Leifsonia lichenia deposited as NRRL Accession Deposit No. NRRL B-67299; Tumebacilras permanentifrigoris deposited as NRRL Accession Deposit No. NRRL B-673Q2; Tumebacillus permanentifrigoris deposited as NRRL Accession Deposit No. NRRL B- 67300; Tumebacillus permanentifrigoris deposited as NRRL Accession Deposit No. NRRL B-67303; Tumebacillus permanentifrigoris deposited as NRRL Accession Deposit No. NRRL B-67301; and combinations thereof.

[0063] In one embodiment, the microbial consortium comprises Leifsonia lichenia deposited as NRRL Accession Deposit No. NRRL B-67298, Tumebacillus permanentifrigoris deposited as NRRL Accession Deposit No. NRRL B-67301 , Chryseobacterium rhizosphaerae deposited as NRRL Accession Deposit No. NRRL B-67288, and Frigidibacter albus deposited as NRRL Accession Deposit No. NRRL B-67285. In another embodiment, the microbial consortium comprises Exiguobacterium sibiricum deposited as NRRL Accession Deposit No. NRRL B-67294, and Massilia kyonggiensis deposited as NRRL Accession Deposit No. NRRL B-67198. In another embodiment, the microbial consortium comprises Chryseobacterium. rhizosphaerae deposited as NRRL Accession Deposit No. NRRL B-67288, Frigidibacter albus deposited as NRRL Accession Deposit No. NRRL B- 67285, and Arthrobacter nicotinovorans deposited as NRRL Accession Deposit No. NRRL B-67289.

[0064] In some embodiments, a method of imparting at least one beneficial train upon a plant species comprises applying at least one isolated bacterial species to the plant, or to a growth medium in which the plant is located, wherein the at least one isolated bacterial species is selected from the group consisting of: Agrobacterium fabrum, Novosphingobium lindaniclasticum, Pedobacter terrae, Chryseobacterium daecheongense, Chryseobacterium rhizosphaerae, Frigidibacter albus, Arthrobacter nicotinovorans, Pseudornonas helmanticensis, Agrobacterium fabrum. Achromobacter pulmonis, Exiguobacterium sibiricum, Exiguobacterium antarcticiim, Pedobacter terrae, Leifsonia lichenia, Massilia kyongiensis, Tumebacillus permanentifrigoris, and combinations thereof. In a further embodiment, the at least one isolated bacterial species is a strain selected from the group consisting of: Chryseobacterium daecheongense deposited as NRRL Accession Deposit No. NRRL B-67291; Chryseobacterium rhizosphaerae deposited as NRRL Accession Deposit No. NRRL B-67288; Chryseobacterium rhizosphaerae deposited as NRRL Accession Deposit No. NRRL B-67287; Frigidibacter aibiis deposited as NRRL Accession Deposit No. NRRL B-67285; Frigidibacter aibus deposited as NRRL Accession Deposit No. NRRL B- 67283: Frigidibacter albus deposited as NRRL- Accession Deposit No. NRRL B-67284; Arihrohacter riicotiriovorans deposited as NRRL Accession Deposit No. NRRL B-67289; Arthrobacier mcotinovorans deposited as NRRL, Accession Deposit No. NRRL, B-67290; Pseudomonas helmanticens s deposited as NRRL Accession Deposit No. NRRL B-67295; Pseudomonas helmanticensis deposited as NRRL Accession Deposit No. NRRL B-67296; Pseudomonas helmanticensis deposited as NRRL Accession Deposit No. NRRL B-67297; Agrobacterium fabriim deposited as NRRL Accession Deposit No. NRRL B-67286; Exiguobactermm sibiricum deposited as NRRL Accession Deposit No. NRRL B-67294; Exiguobacterium antarcticum deposited as NRRL Accession Deposit No. NRRL B-67292; Exiguobacterium antarcticu deposited as NRRL Accession Deposit No. NRRL B-67293; Leifsonia lichenia deposited as NRRL Accession Deposit No. NRRL B-67298; Leifsonia lichenia deposited as NRRL Accession Deposit No. NRRL- B-67299; Tumebacillus permanentifrigoris deposited as NRRL, Accession Deposit No. N RRL B-67302; Tumebacillus permanentifrigoris deposited as NRRL Accession Deposit No. NRRL B- 67300: Tumebacillus permanentifrigoris deposited as NRRL Accession Deposit No. NRRL B-67303; and Tumebacillus permanentifrigoris deposited as NRRL, Accession Deposit No. NRRL B-67301.

[0065] In some embodiments, an isolated bacterial strain is selected from. Table 4. In some embodiments, an isolated bacterial strain is contemplated having substantially similar morphological and physiological characteristics as an isolated bacterial strain selected from Table 4. In some embodiments, an isolated bacterial strain is contemplated having substantially similar genetic characteristics as an isolated bacterial strain from Table 4. In some embodiments, a substantially pure culture is contemplated of an isolated bacterial strain from Table 4. In some embodiments, a progeny or a mutant of an isolated bacterial strain from Table 4 is contemplated. In some embodiments, a cell-free or inactivated preparation is contemplated from an isolated bacterial strain, or a mutant thereof, from Table 4. In some embodiments, a metabolite produced by an isolated bacterial strain, or a mutant thereof, from Table 4.

[0066] In some embodiments, an agricultural composition comprises an isolated bacterial strain from Table 4 and an agriculturally acceptable carrier. In some embodiments, the isolated bacterial strain is present in the agricultural composition at l x l0 ³ to 1 ^χ 10" bacterial ceils per gram. In some embodiments, the agricultural composition is formulated as a seed coating. In some embodiments, a method of imparting at least one beneficial train upon a plant species comprises applying an isolated bacterial strain from Table 4 to the plant, or to a growth medium in which said plant is located. In some embodiments, a method of imparting at least one beneficial trait upon a plant species comprises applying an agricultural composition of the present disclosure to the plant, or to a growth medium in which said plant is located.

[0067] In some embodiments, a microbial consortium comprises at least two microbes selected from those listed in Table 4. In some embodiments, a microbial consortium, is selected from the consortia listed in Table 5, wherein the consortium comprises at least one microbe listed in Table 4. In some embodiments, a microbial consortium is selected from the consortia listed in Table 6, wherein the consortium comprises at least one microbe listed in Table 4. In some embodiments, a microbial consortium is selected from the consortia listed in Table 7, wherein the consortium comprises at least one microbe listed in Table 4. In some embodiments, a microbial consortium is selected from the consortia listed in Table 8, wherein the consortium comprises at least one microbe listed in Table 4. In some embodiments, a microbial consortium is selected from the consortia listed in Table 9, wherein the consortium comprises at least one microbe listed in Table 4. In some embodiments, a microbial consortium is selected from, the consortia listed in Table 10, wherein the consortium comprises at least one microbe listed in Table 4, In some embodiments, a microbial consortium is selected from the consortia listed in Table 11, wherein the consortium comprises at least one microbe listed in Table 4.

[0068] In some embodiments, a plant seed enhanced with a microbial seed coating comprises a plant seed and a seed coating applied onto said plant seed, wherein the seed coating comprises at least two microbes as listed in Tables 1-4, and wherein at least one microbe is selected from Table 4. In a further embodiment, the seed coating comprises a consortium of microbes as listed in Tables 5-11. In a further embodiment, the seed coating comprises at least one microbe as listed in Table 4 at a concentration of ! h i' io 1 χ 10 ⁹ bacterial cells per seed. In sorne embodiments, a microbe selected from Table 4 is used in agriculture. In some embodiments, a synthetic combination of a plant and microbe comprises at least one plant and at least one microbe selected from Table 4.

[0069] In some embodiments, a method of increasing or promoting a desirable phenotypic trait of a plant species comprises applying at least one bacteria selected from Table 4 to said plant, or to a growth medium in which said plant is located. In a further embodiment, the method of applying the at least one bacteria occurs by coating a plant seed with said bacteria, coating a plant part with said bacteria, spraying said bacteria onto a plant part, spraying said bacteria into a furrow into which a plant or seed will be placed, drenching said bacteria onto a plant part or into an area into which a plant will be placed, spreading said bacteria onto a plant part or into an area into which a plant will be placed, broadcasting said bacteria onto a plant part or into an area into which a plant will be placed, and combinations thereof.

[0070] In any of the methods, the microbe can include a 16S nucleic acid sequence having at least 97% sequence identity to a 16S nucleic acid sequence of a bacteria selected from a genus provided in Table 4.

BRIEF DESCRIPTION OF THE FIGURES

[0071 ] FIG. 1 shows a generalized process schematic of a disclosed method of accelerated microbial selection (AMS), also referred to herein as directed microbial selection. When the process is viewed in the context of a microbial consortium, the schematic is illustrative of a process of directed evolution of a microbial consortium. The process is one method, by which the beneficial microbes of the present disclosure were obtained.

[0072] FIG. 2 shows a generalized process flow chart of an embodiment, by which the beneficial microbes of the present disclosure were obtained.

[0073] FIG. 3 shows a graphic representation and associated flow chart of an embodiment, by which the beneficial microbes of the present disclosure were obtained.

[0074] FIG. 4 shows a graphic representation and associated flow chart of an embodiment, by which the beneficial microbes of the present disclosure were obtained.

[0075] FIG. 5 shows a graphic representation of the average total biomass of wheat, in grams of fresh weight, at seven days post inoculation with individual microbial strains (BC1). [0076] FIG. 6A and FIG. 6B shows a graphic representation of the average wheat shoot (A) and root (B) biomass, in grams of fresh weight, at six days post inoculation (DPI) with individual microbial strains. Seeds were inoculated, placed on wet germination paper and rolled. Rolls were incubated at 25°C in sealed plastic bins. Each individual strain was tested in triplicates of 30 seeds each. The horizontal red line represents the water control.

[0077] FIG. 7 A and FIG. 7B shows a graphic representation of average corn shoot biomass, in grams of fresh weight, at six days post inoculation (DPI) with individual microbial strains. Seeds were inoculated, placed on wet germination paper and rolled. Rolls were incubated at 25°C in sealed plastic bins. Each individual strain was tested in triplicates of 30 seeds each. Due to the amount of samples tested, rolls were placed in two independent bins with a respective water control, represented individually in Figure 7 by graphs A and B. The horizontal red line represents the water control.

[0078] FIG. 8A and FIG. 8B shows a graphic representation of average com root biomass, in grams of fresh weight, at six days post inoculation (DPI) with individual microbial strains. Seeds were inoculated, placed on wet germination paper and rolled. Rolls were incubated at 25°C in sealed plastic bins. Each individual strain was tested in triplicates of 30 seeds each. Due to the amount of samples tested, rolls were placed in two independent bins with a respective water control, represented individually in Figure 8 by graphs A and B. The horizontal red line represents the water control.

[0079] FIG. 9 shows a graphic representation of the average shoot length, in millimeters, of maize at 4 days post treatment with individual microbial strains. Maize seeds were inoculated with individual microbial strains (BDNZ numbers) and subjected to a germination test. Seeds were inoculated, placed on wet paper towels and rolled. Rolls were incubated in sealed plastic bags at 25°C. Each individual strain was tested in duplicates of 30 seeds each. Shoot length was measured at 4 days post inoculation (DPI). Standard error bars are shown . Results show- that while germination rates were good for all strains tested, some strains caused a relative increase in shoot length at 4 days post inoculation (DPI) compared to the water control in vivo.

[0080] FIG. 10 shows a graphic representation of the average root length, in millimeters, of maize at 4 days post treatment with individual microbial strains. Maize seeds were inoculated with individual microbial strains (BDNZ numbers) and subjected to a germination test. Seeds were inoculated, placed on wet paper towels and rolled. Rolls were incubated in sealed plastic bags at 25°C. Each individual strain was tested in duplicates of 30 seeds each. Root length was measured at 4 days post inoculation (DPI). Standard error bars are shown. Results show that while germination rates were good for all strains tested, some strains caused a relative increase in root length at 4 days post inoculation (DPI) compared to the water control in vivo.

[0081] FIG. 11 shows a graphic representation of the average shoot length, in millimeters, of wheat at 4 days post treatment with individual microbial strains.Wheat seeds were inoculated with individual microbial strains (BDNZ numbers) and subjected to a germination test. Seed were inoculated, placed on wet paper towels and roiled. Rolls were incubated in sealed plastic bags at 25°C. Each individual strain was tested in duplicates of 30 seeds each. Shoot length was measured at 4 days post treatment. Results show that germination rates were good for all strains tested (>90 %) and some strains caused a relative increase in shoot length at 4 days post inoculation (DPI) compared to the water control in vitro.

[0082] FIG. 12 shows a graphic representation of the average root length, in millimeters, of wheat at 4 days post treatment with individual microbial strains. Wheat seeds were inoculated with individual microbial strains (BDNZ numbers) and subjected to a germination test. Seed were inoculated, placed on wet paper towels and rolled. Rolls were incubated in sealed plastic bags at 25°C. Each individual strain was tested in duplicates of 30 seeds each. Root length was measured at 4 days post treatment. Results show that germination rates were good for all strains tested (>90%) and some strains caused a relative increase in root length at 4 days post inoculation (DPI) compared to the water control in vitro.

[0083] FIG. 13 shows a graphic representation of the average shoot length, in millimeters, of tomato at 4 days post treatment with individual microbial strains. Tomato seeds were inoculated with individual microbial strains (BDNZ numbers) and subjected to a germination test. Seeds were inoculated, placed on wet paper towels and rolled. Rolls were incubated in sealed plastic bags at 25°C. Each individual strain was tested in duplicates of 50 seeds each. Shoot length was measured at 4 days post treatment. Hie mean length of shoots of the water control seed can be seen in the far right bar labelled "H20". Results show that germination rates were good for all strains tested and some strains caused a relative increase in shoot length at 4 days post inoculation (DPI) compared to the water control in vitro.

[0084] FIG. 14 shows a graphic representation of the average root length, in millimeters, of tomato at 4 days post treatment with individual microbial strains. Tomato seeds were inoculated with individual microbial strains (BDNZ numbers) and subjected to a germination test. Seeds were inoculated, placed on wet paper towels and rolled. Rolls were incubated in sealed plastic bags at 25°C. Each individual strain was tested in duplicates of 50 seeds each. Root length was measured at 4 days post treatment. The mean length of roots of the water control seed can he seen in the far right bar labelled "H20". Results show that germination rates were good for all strains tested and some strains caused a relative increase in root length at 4 days post inoculation (DPI) compared to the water control in vitro.

[0085] FIG, ISA and FIG. 15B shows a graphic representation of average com shoot length, in millimeters, at six days post inoculation (DPI) with individual microbial strains. Seeds were inoculated, placed on wet germination paper and rolled. Rolls were incubated at 25°C in sealed plastic bins. Each individual strain was tested in triplicates of 30 seeds each. Due to the amount of samples tested, rolls were placed in two independent bins with a respective water control, represented individually in Figure 15 by graphs A and B. The horizontal red line represents the water control .

[0086] FIG. 16A and FIG, 16 B shows a graphic representation of average com root length, in millimeters, at six days post inoculation (DPI) with individual microbial strains. Seeds were inoculated, placed on wet germination paper and rolled. Rolls were incubated at 25°C in sealed plastic bins. Each individual strain was tested in triplicates of 30 seeds each. Due to the amount of samples tested, rolls were placed in two independent bins with a respective water control, represented individually in Figure 16 by graphs A and B. The horizontal red line represents the water control .

BUDAPEST TREATY ON THE INTERNATIONAL RECOGNITION OF THE DEPOSIT OF MICROORGANISMS FOR THE PURPOSE OF PATENT PROCEDURES

[0087] The microorganisms described in this Application were deposited with the Agricultural Research Service Culture Collection (NRRL), which is an International Depositary Authority, located at 1815 North University Street Peoria, IL 61604, USA.

[0088] The deposits were made under the terms of the Budapest Treaty on the International Recognition of the Deposit of Microorganisms for the Purposes of Patent Procedure. [0089] The deposits were made in accordance with, and to satisfy, the criteria set forth in 37 C.F.R. §§ 1.801-1.809 and the Manual of Patent Examining Procedure §§ 2402-2411.05.

[009Θ] The NRRL accession numbers, dates of deposit, and descriptions for the aforementioned Budapest Treaty deposits are provided in Tables 1-4.

Budapest Treaty Representative SEQ 1D International Deposited No. Depositary Species

Microbial Species Strains Origin

Authority Available to

Accession No. & the Public

Bate of Deposit

DSM-2286*

1. Azotobacter chroococcum

BDNZ 57597 NZ 289

BDNZ 54499 278

2. Panloea agglomerans

(recently reassigned to NRRL B-67224

BDNZ 55529 NZ 289

Pantoea vagans) Januar ' 29, 2016

BDNZ 57547 288

BCI 1208 DSM-23078* 62

3. Pantoea agglomerans

(recently reassigned to

BCI 1274 US 68 Pantoea vagans)

BCI 1355 90

BDNZ 54480 DSM-50090* 276

4. Pseudomonas fluoresceins

BDNZ 56530 NZ 285 BDNZ 56249 284

DSM-50090*

5. Pseudomonas fluorescens

BCI 1352 US 88

6. P eudomonas oryzihabitans NRRL B-67225

BDNZ 55530 NZ 283

January 29, 2016 BCI 1184 DSM-6835* 58

7. Pseudomonas oryzihabitans

BCI 1195 US 59

BCI 1 Ϊ 99 60

DSM-29I *

8. Pseudomonas putida

BDNZ 60303 NZ 294

BCI 159 DSM-291 * 100

BCI 178 104

BCI 234 109

BCI 235 1 10

BCI 244 112

BCI 357 124

BCI 360 126

BCI 363 127

9. Pseudomonas putida

US

BCI 365 128 BCI 367 129 BCI 368 130 BCI 369 131 BCI 370 132 BCI 372 134 BCI 375 135 BCI 458 144 BCI 459 BCI 460 BCI 461 BCI 462 BCI 467 BCI 469 BCI 470 BCI 571 BCI 593 BCI 731 BCI 791 BCI 802 BCI 805 BCI 806 BCI 809 BCI 1312 BCI 1314 BCI 1315 BCI 1319 BCI 1330 BCI 1333 84

BCI 1351 87

BCI 1353 89

BCI 1356 91

BCI 1358 93

BCI 1363 96

NRRL B-67228

BDNZ 56532 Januar ' 29, 2016 286 Rahnella aquatilis

BDNZ 57157 NZ 287 BDNZ 58013 NRRL B-67229 293

Januaty 29, 2016

BCI 29 NRRL B-67165 118 Rahnella aquatilis

US December 18,

BCI 1158 2015 54

DSM-11541*

Rhizobium etli

BDNZ 60473 NZ 295

BDNZ 54093 NRRL B-67227 274 Rhodococcus erytnropoiis

NZ January 29, 2016

BDNZ 54299 275

DSM-43066*

Rhodococcus erythropolis

BCI 1182 US 57 Stenolrophomonas NRRL B-67226

maltophilia BDNZ 54073 NZ January 29, 2016 273

BCI 7 194 Stenolrophomonas DSM-50170* maltophilia US

BCI 64 183 BCI 77 BCI 1 5 BCI 120 BCI 164 BCI 171 BCI 181 BCI 271 BCI 343 BCI 344 BCI 380 BCI 539 BCI 545 BCI 551 BCI 574 BCI 588 BCI 590 BCI 601 BCI 602 BCI 606 BCI 607 BCI 610 BCI 617 BCI 618 BCI 619 BCI 620 BCI 623 BCI 665 BCI 693 BCI 787 BCI 790 BCI 793 BCI 795 BCI 808 BCI 903 BCI 908 BCI 970 BCI 996 BCI 997 BCI 1032 BCI 1092 BCI 1096 46 BCI 1116 50 BCI 1224 64 BCI 1279 69 BCI 13 16 BCI 1320 BCI 1322 80 BCI 1325 81 BCI 1331 83 BCI 1344 85 BCI 1350 86 BCI 1357 92 BCI 1362 95

*Denotes a microbial species that has been deposited and is available to the public, but said species is not a deposit of the exact BCI or BDNZ strain.

TABLE 2

Budapest Representative SEQ ID Treaty Deposited No.

International Species

Depositary Available to

Microbial Species Strain Origin

Authority the Piiblic

Accession No.

& Date of

Deposit

291

DSM-1838*

I. Azospirillum lipoferiim BDNZ57661

NZ

300 BDNZ66460

2. Bacillus megaterium DSM-32*

BDNZ55076 NZ 279

BCI 251 DSM-32* 113 BCI 255 114

3. Bacillus megaterium

US BCI 262 115 BCT 264 116

4. Bacillus BDNZ 66 18 DSM-13778* 303 psychrosaccharolyticus NZ

BDNZ 66544 306

5. Duganella zoogloeoides DSM-16928*

BDNZ 66500 NZ 302

6. Herbaspirillum huttiense DSM-10281*

BDNZ 54487 NZ 277

7. Herbaspirillum huttiense DSM-10281 *

BCI 9 US 217

8. PaenibacUlus DSM-5051*

chondroitinus BDNZ 57634 NZ 290

BDNZ 55146 DSM-36* 280

9. PaenibacUlus polyinyxa

NZ BDNZ 66545 304

10. PaenibacUlus polymyxa DSM-36*

BCI 1118 US 51

^♦ Denotes a microbial species that lias been deposited and is available to the public, but said species is not a deposit of the exact BCI or BDNZ strain.

TABLE 3

Accession No.

& Bate of

Deposit

DSM-19728*

Flavohacterium glaciei

BDNZ 66487 NZ 301

BDNZ 55184 NZ NRRL B-67235

February 8, 281 2016

assiiia niastensis

BCI 1217 US NRRL B-67199

December 29, 63 2015

DSM-17472*

Massiiia kyonggiensis

(Massiiia alhidiflava) BCI 36 us 125

DSM-7462*

Sphingobium yanoikuyae

BDNZ 57662 NZ 292

DSM-1088*

Bacillus subtilis

BDNZ 66347 NZ 263

DSM-1088*

BCI 395

138 Bacillus subtilis

BCI 989 U S 225

43 BCI 1089

Bosea mi nali Iianensis DSM-13099*

BDNZ 66354 NZ 264 Bosea thiooxidans DSM-9653*

BDNZ 54522 NZ 240

BCI 703 NRRL B-67187 196 Bosea thiooxidans

US December 29,

2015 BCI 985 36 BC1 1111 49

BCI 1.041

38 Bosea robinae

BCT 689 US NRRL B-67186 190

December 29,

2015 200

BCI 765

NRRL B-67185

Bosea eneae

BCI 1267 US December 29, 67

2015

Caulobacter henrici DSM-4730*

BDNZ 66341 NZ 262

DSM-15887*

Pseudodiiganella

violaceimgra BDNZ 66361 NZ 265 Luteibacter yeojuensis DSM-17673*

BDNZ 57549 NZ 235 Mucilaginibacter gossypii

BDNZ66321 NZ 297

BCI 142 99 Mucilaginibacter gossypii

BCI 1156 US 53 BCI 1307 71 Paenibacillus amylolyticus DSM-1 1730*

BDNZ 66316 NZ 296

BDNZ 66373 NZ NRRL B-67231

DSM-14656* 266

February 8,

Polaromonas ginsengiso!i

2016

270 BDNZ 66821 NZ NRRL B-67234 February 8,

2016

DSM-14656*

Ramlibacter henchirensis

BDNZ 66331 NZ 261

NRRL B-67208

Ramlibacter henchirensis

BCI 739 US December 29, 199

20 5

Lei fsonia sninshuensis DSM-15165*

(previously Rhizobium

BDNZ 61433 NZ 250 leguminosarum bv. trifolii)

DSM-30132*

Rhizobium pisi

BDNZ 66326 NZ 260 Rhodoferax ferrireducens DSM-15236*

BDNZ 66374 NZ 267

DSM-24952*

Sphingobium

ch!orophenoliciim BDNZ 61473 NZ 251

Sphingobium DSM-24952* qiiisquiliarum BDNZ 66576 NZ 269

DSM-131.28*

Herbaspiril!um frisingense

BDNZ 50525 NZ 234 Caulibacter henrici DSM-4730*

BDNZ 66341 NZ 262

DSM-3695*

Chitinophaga arvensicola

BDNZ 56343 NZ 246

DSM-15887*

BDNZ 66361 NZ NRRL B-67232 265 Duganella violaceinigra Febraary 8,

20 6

248 BDNZ 58291 NZ NRRL B-67233

February 8,

2016

DSM-6220*

BDNZ 52707 (Frateuria 238 aurantia)

Frateuria sp.

NZ

DSM-26515*

BDNZ 60517 (Frateuria 249 terrea)

BDNZ 54456 239 Janthinobactermm sp.

NZ BDNZ 63491 252

DSM-16549*

Luteibacter rhizovicinus

BDNZ 65069 NZ 255

DSM-2898*

Lysinibacillus fusiformis

BDNZ 63466 NZ 254

BDNZ 65589 DSM-7285* 258 Novosphingobium rosa

NZ BDNZ 65619 259 Rhizobi'um miluonense

BDNZ 65070 NZ 256

DSM-21508*

Stenotrophomonas

cheiatiphaga BDNZ 54952 NZ 243

DSM-21508*

Stenotrophomonas

cheiatiphaga BDNZ 47207 NZ 232

DSM-21508*

Stenotrophomonas

cheiatiphaga BDNZ 64212 NZ 253

DSM-21508*

Stenotrophomonas

cheiatiphaga UN IV 64208 NZ 305 DSM-21508*

Stenotropnomonas

chelatiphaga BDNZ 58264 NZ 247

DSM-14405*

Stenotropnomonas

rhizophila BDNZ 50839 NZ 236

DSM-14405*

Stenotrophomonas

rhizophila BDNZ 48183 NZ 233

DSM-14405*

Stenotrophomonas

rhizophila BDNZ 45125 NZ 228

DSM-14405*

Stenotrophomonas

rhizophila BDNZ 46120 NZ 230

DSM-14405*

Stenotrophomonas

rhizophila BDNZ 46012 NZ 229

DSM-14405*

Stenotrophomonas

rhizophila BDNZ 51718 NZ 237

DSM-14405*

Stenotrophomonas

rhizophila BDNZ 56181 NZ 245

DSM-14405*

Stenotrophomonas

rhizophila BDNZ 54999 NZ 244

DSM-14405*

Stenotrophomonas

rhizophila BDNZ 54850 NZ 242

DSM-14405*

Stenotrophomonas

rhizophila BDNZ 54841 NZ 241

DSM-14405*

Stenotrophomonas BDNZ 66478 NZ 268 rhizophila

DSM-14405*

Stenotropnomonas

rhizophila. BDNZ 46856 NZ 231

DSM-14405*

Stenotropnomonas

rhizophila BDNZ 65303 NZ 257 Sienotrophomonas terrae DSM-15236*

BDNZ 68599 NZ 27 !

DSM-18941*

Sienotrophomonas terrae

BDNZ 68741 NZ 272

DSM-23806*

Achromobacter spanius

BCi 385 U S 137 Acidovorax soli NRRL B-67182

BCI 690 US 19 ]

Dec. 29, 2015 Arthrobacter cupressi NRRL B-67183

BCI 59 US 166

Dec. 29. 2015

DSM-12798*

Arthrobacter mysorens

BCI 700 US 195

DSM-20545*

Arthrobacter pascens

BCI 682 us 187

DSM-9356*

Bacillus oleronhis

BCI 1071 us 42

DSM-2046*

Bacillus cereus or Bacillus

ihuringiensis (In

BCI 715 us [97 Taxonomic Flux)

NRRL B-67I 88

Chitinophaga terrae

BCI 79 us December 29, 203

2015 NRRL B-67190

64. Delfiia laciistris

BCI 124 US December 29, 65

2015

NRRL B-67192

65. Duganella radicis

BCI 105 U S December 29, 3

2015

66. Duganella radicis

BCI 57 US 161

NRRL B-67166

67. Duganella radici

BCI 31 us January 13, 21

2016

NRRL B-67194

68. Dyadobacier soli

BCI 68 us December 29, 186

2015

DSM-20416*

69. Exiguobacterium

acetylicum BCI 23 us 108

DSM-20416*

70. Exiguobacterium

ace ty !i cum BCI 83 us 216

DSM-20416*

71. Exiguobacterium

acetylicum BCI 125 us 66

72. Exiguobacterium NRRL B-67175

aurantiacum BCI 50 us December 18, 155

2015

DSM-27935*

73. Exiguobacterium sp. (In

Taxonomic Flux) BCI 81 us 214

74. Exiguobacterium NRRL B-67167

sibiricum BCI 116 us December 18, 16

2016

DSM-17796*

75. Herbaspiril!um BCI 58 us NRRL B-67236 164 chlorophenoliciim February 8,

2016

DSM-16656*

76. Kosakonia radicincitans

BCI 107 US 41

77. Massilia kyonggiensis NRRL B-67198

(M si Ha alb idifi ava) BCI 97 U S December 29, 32

2015

78. Microbacterium sp.

BCI 688 us DSM-16050*

189

79. Microbacterium' NRRL B-67170

oleivorans BCI 132 us December 18, 78

2015

80. Miicilaginibacter gossypii

BCI 142 us 98

81. Novosphigobium NRRL B-67201

lindaniclasticiiW! BCI 684 us December 29, 188

2015

82. Novosphingobium NRRL B-67202

resinovoriim BCI 557 us December 29, 160

2015

DSM-27057*

83. Novosphingobium

sediminicola BCI 136 us 94

DSM-27057*

84. No vosphingob turn

sediminicola BCI 82 us 215

85. No vosphingobi urn NRRL B-67168

sediminicola BCI 130 us December 18, 28

2015

86. Paembaci iis NRRL B-67204

glycani!yticus BCI 418 us December 29, 141

2015 87. Pedobacter rhizosphaerae NRRL B-67205

(Pedobacter soli) BCI 598 US December 29, 169

2015

NRRL B-67206

88. Pedobacter terrae

BCI 91 U S December 29, 220

2015

NRRL B-67207

89. Pseudomonas jinjuensis

BCI 804 us December 29, 209

2015

90. Rhizobium grahamii

BCI 691 us 192

91. Rhizobium lemnae

(taxonomic name changed NRRL B-672I0

December 2015 to BCI 34 us December 29, 121 Rhizobium rhizoryzae) 2015

DSM-22668*

92. Agrobacterium fabrum or

NRRL B-67212

Rhizobium pusense (In

BCI 106 us December 29, 40 Taxonomic Flux)

2015

DSM-22668*

93. Agrobacterium fabrum or

Rhizobium pusense (in

BCI 11 us 47 Taxonomic Flux)

DSM-22668*

94. Agrobacterium fabrum or

Rhizobium pusense (In

BCI 609 us 175 Taxonomic Flux)

NRRL B-67169

95. Ensifer adhaerens

BCI 131 us December 18, 72

2015

DSM-13593*

96. Sphingopyxis alaskensis NRRL B-67215

BCI 914 us 221

December 29, 2015

NRRL B-67216

97. Variovorax ginsengisoli

BCI 137 US December 29, 97

2015

DSM-2923*

NRRL B-67230

98. Bacillus niacini

BC1 4718 US February 8, 153

2016

99. Exiguobacterium NRRL B -67167

sibiricum BCI 116 US December 18, 16

2015

100. Chryseobacterium NRRL B-67172

daecheongense BCI 45 US December 18, 1

2015

101. Achromobacter NRRL B-67174

pulmonis BCI 49 December 18, 15

2015

NRRL B-67181

102. 4 cidovorax soli

BCI 648 December 29, 184

2015

NRRL B-67184

103. Arthrobacter cupressi

BCI 62 December 29, 180

2015

NRRL B-67189

104. Chininophaga terrae

BCI 109 December 29, 44

2015

NRRL B-67191

105, Delftia lacustris

BCI 2350 December 29, 11 1

2015

NRRL B-67193

106. Duganella violaceinigra

BCI 2204 December 29, 107

2015 NRRL B-67195

107. Dyadobacter soli

BCI 96 December 29, 222

2015

NRRL B-67196

108, Flavobactermm glacei

BCI 4005 December 29, 139

2015

109. F!erbaspir ilium NRRL B-67197

chloropheno!icum BCI 162 December 29, 101

2015

110. Novosphingobium NRRL B-67200

lindaniclasticum BCI 608 30

December 29,

2015

111. Nocosphingobium NRRL B-67203

resinovorum BCI 3709 December 29, 133

2015

NRRL 15-6 ^" 209

112. Ramlibacter

henchirensis BCI 1959 106

December 29,

2015

NRRL B-6721 1

1 13. Rhizobium rhizoryzae

BCI 661 December 29, 35

2015

114. Sinorhizobium

NRRL B-67213

chiapanecum (Ensifer

BCI 111 December 29, 48 adhaerens)

2015

NRRL B-67214

1 15. Sphingopyxis alaskensis

BCI 412 December 29, 140

2015

NRRL B-67217

116. Variovorax ginsengisoli

BCI 3078 December 29, 1 19

2015 NRRL B-67171

i 17. Kosakonia radicincitans

BCI 44 December 18, 142

2015

NRRL B-67176 DSM17933*

1 18, Pedobacter terrae

BCI 53 December 18, 20

2015

1 19. Agrohacterium fab rum

or Rhizobium pusense (In

NRRL B-67173

Taxonomic Flux)

BCI 46 December 18, 146 (previously Rhizobium

2015

sp.)

^♦ Denotes a microbial species that l as been deposited and is available to the public, but said species is not a deposit of the exact BCI or BDNZ strain.

TABLE 4 NRRL B-67285

BCI 712 US 5

July 14, 2016

Frigidibacter aibus or

Delfulviimonas dentrijicans BCI 402 us NRRL B-67283 6

(In Taxonomic Flux) July 14, 2016

BC1 745 US 7

NRRL B-67284

July 14, 2016 B-67289

BCT 717 us NRRL

8

July 14, 2016

Arthrobacter mcotinovorans

DSM420*

BCI 3189 us NRRL B-67290 9

July 14, 2016

NRRL B-67295

BCI 616 us 10

July 14, 2016 Psetidomonas helmanticensis BCI 2945 us NRRL B-67296 1 1

DSM28442*

July 14, 2016

BCI 800 us NRRL B-67297 12

July 14, 2016

Agrobacteriumfabrum or

Rhizobium pusense (In

BCI 958 us NRRL B-67286 14 Taxonomic Flux) ('previously DSM22668*

July 14, 2016

Rhizobiu sp.) Exiguobacterium sibiricum BCI 718 us NRRL B-67294 17

DSM17290*

July 14, 2016

BCI 63 us NRRL B-67292

18 Exiguobacterium July 14, 2016

antarctic m DSM14480*

BCI 225 us NRRL B-67293 19

July 14, 2016 NRRL B-67298

BDNZ 72243 NZ 22

July 21 , 2016

9. Leifsonia lichenia

BDNZ 72289 NZ NRRL B-67299 23

July 21, 2016

BDNZ 72229 NZ NRRL B-67302 24

July 22, 20 6

BDNZ 74542 NZ NRRL B-67300 25

10. Tumebacillus July 21 , 2016

permanentifrigoris DSM118773*

NRRL B-67303

BDNZ 72366 NZ 26

July 22, 20 6

NRRL B-67301

BDNZ 72287 NZ 307

July 21, 2016

1 1. Bacillus asahii BCI 928 US 27

12. No vosphingob rum

BDNZ 71628 NZ 29 sediminicola DSM27057*

13. No vosphingob rum

BDNZ 71222 NZ 31 lindaniclasticiiW! DSM25409*

BCI 94 US 33

14. Massilia kyonggiensis

DSM101532*

BDNZ 73021 NZ 34

^♦ Denotes a microbial species that has been deposited and is available to the public, but said species is not a deposit of the exact BCI or BDNZ strain.

[0091] While the following terms are believed to be well understood by one of ordinary skill in the art, the following definitions are set forth to facilitate explanation of the presently disclosed subject matter.

[0092] The term "a" or "an" refers to one or more of that entity, i.e. can refer to a plural referents. As such, the terms "a" or "an", "one or more" and "at least one" are used interchangeably herein, in addition, reference to "an element" by the indefinite article "a" or "an" does not exclude the possibility that more than one of the elements is present, unless the context clearly requires that there is one and only one of the elements.

[0093] As used herein the terms "microorganism" or "microbe" should be taken broadly. These terms are used interchangeably and include, but are not limited to, the two prokaryotic domains, Bacteria and Archaea, as well as eukaryotic fungi and protists. In some embodiments, the disclosure refers to the "microbes" of Tables 1-4, or the "microbes" of various other tables present in the disclosure. This characterization can refer to not only the identified taxonomic bacterial genera of the tables, but also the identified taxonomic species, as well as the various novel and newly identified bacterial strains of said tables.

[0094] The term "microbial consortia" or "microbial consortium" refers to a subset of a microbial community of individual microbial species, or strains of a species, which can be described as carrying out a common function, or can be described as participating in, or leading to, or correlating with, a recognizable parameter or plant phenotypic trait. The community may comprise two or more species, or strains of a species, of microbes. In some instances, the microbes coexist within the community symbiotically.

[0095] The term "microbial community" means a group of microbes comprising two or more species or strains. Unlike microbial consortia, a microbial community does not have to be carrying out a common function, or does not have to be participating in, or leading to, or correlating with, a recognizable parameter or plant phenotypic trait.

[0096] The term "accelerated microbial selection" or "AMS" is used interchangeably with the term "directed microbial selection" or "DMS" and refers to the iterative selection methodology that was utilized, in some embodiments of the disclosure, to derive the claimed microbial species or consortia of said species.

[0097] As used herein, "isolate," "isolated," "isolated microbe," and like terms, are intended to mean that the one or more microorganisms has been separated from at least one of the materials with which it is associated in a particular environment (for example soil, water, plant tissue).

[0098] Thus, an "isolated microbe" does not exist in its naturally occurring environment; rather, it is through the various techniques described herein that the microbe has been removed from its natural setting and placed into a non-naturally occurring state of existence. Thus, the isolated strain may exist as, for example, a biologically pure culture, or as spores (or other forms of the strain) in association with an agricultural carrier.

[0099] In certain aspects of the disclosure, the isolated microbes exist as isolated and biologically pure cultures. It will be appreciated by one of skill in the art, that an isolated and biologically pure culture of a particular microbe, denotes that said culture is substantially free (within scientific reason) of other living organisms and contains only the individual microbe in question. The culture can contain varying concentrations of said microbe. The present disclosure notes that isolated and biologically pure microbes often "necessarily differ from less pure or impure materials." See, e.g. In re Bergstrom, 427 F.2d 1394, (CCPA 1970)(discussing purified prostaglandins), see also, In re Bergy, 596 F.2d 952 (CCPA 1979)(discussing purified microbes), see also, Parke-Davis & Co. v. H.K. Midford & Co., 189 F. 95 (S.D.N.Y. 1911) (Learned Hand discussing purified adrenaline), aff'd in pari, rev 'd in part, 196 F. 496 (2d Cir. 1912), each of which are incorporated herein by reference. Furthermore, in some aspects, the disclosure provides for certain quantitative measures of the concentration, or purity limitations, that must be found within an isolated and biologically pure microbial culture. The presence of these purity values, in certain embodiments, is a further attribute that distinguishes the presently disclosed microbes from those microbes existing in a natural state. See, e.g., Merck & Co. v. Olin Mathiesort Chemical Corp., 253 F.2d 156 (4th Cir. 1958) (discussing purity limitations for vitamin B 12 produced by microbes), incorporated herein by reference.

[00100] As used herein, "individual isolates" should be taken to mean a composition, or culture, comprising a predominance of a single genera, species, or strain, of microorganism, following separation from one or more other microorganisms. The phrase should not be taken to indicate the extent to which the microorganism, has been isolated or purified. However, "individual isolates" can comprise substantially only one genus, species, or strain, of microorganism. [00101] The term "growth medium" as used herein, is any medium which is suitable to support growth of a plant. By way of example, the media may be natural or artificial including, but not limited to: soil, potting mixes, bark, vermiculite, hydroponic solutions alone and applied to solid plant support systems, and tissue culture gels. It should be appreciated thai the media may be used alone or in combination with one or more other media. It may also be used with or without the addition of exogenous nutrients and physical support systems for roots and foliage.

[00102] In one embodiment, the growth medium is a naturally occurring medium such as soil, sand, mud, clay, humus, regolith, rock, or water. In another embodiment, the growth medium is artificial . Such an artificial growth medium may be constructed to mimic the conditions of a naturally occurring medium; however, this is not necessary. Artificial growth media can be made from one or more of any number and combination of materials including sand, minerals, glass, rock, water, metals, salts, nutrients, water. In one embodiment, the growth medium is sterile. In another embodiment, the growth medium is not sterile.

[00103] The medium may be amended or enriched with additional compounds or components, for example, a component which may assist in the interaction and/or selection of specific groups of microorganisms with the plant and each other. For example, antibiotics (such as penicillin) or sterilants (for example, quaternary ammonium salts and oxidizing agents) could be present and/or the physical conditions (such as salinity, plant nutrients (for example organic and inorganic minerals (such as phosphorus, nitrogenous salts, ammonia, potassium and micronutrients such as cobalt and magnesium), pH, and/or temperature) could be amended.

[00104] As used herein, the term "plant" includes the whole plant or any parts or derivatives thereof, such as plant ceils, plant protoplasts, plant ceil tissue cultures from w ^r hich plants can be regenerated, plant calli, embryos, pollen, ovules, fruit, flowers, leaves, seeds, roots, root tips and the like.

[00105] As used herein, the term "cuitivar" refers to a variety, strain, or race, of plant that has been produced by horticultural or agronomic techniques and is not normally found in wild populations.

[00106] As used herein, the terms "dicotyledon," "dicot" and "dicotyledonous" refer to a flowering plant having an embryo containing two cotyledons. As used herein, the terms "monocotyledon," "monocot" and "monocotyledonous" refer to a flowering plant having an embryo containing only one cotyledon. There are of course other known differences between these groups, which would be readily recognized by one of skill in the art.

[00107] As used herein, "improved" should be taken broadly to encompass improvement of a characteristic of a plant, as compared to a control plant, or as compared to a known average quantity associated with the characteristic in question. For example, "improved" plant biomass associated with application of a beneficial microbe, or consortia, of the disclosure can be demonstrated by comparing the biomass of a plant treated by the microbes taught herein to the biomass of a control plant not treated. Alternatively, one could compare the biomass of a plant treated by the microbes taught herein to the average biomass normally- attained by the given plant, as represented in scientific or agricultural publications known to those of skill in the art. In the present disclosure, "improved" does not necessarily demand that the data be statistically significant (i.e. p < 0.05); rather, any quantifiable difference demonstrating that one value (e.g. the average treatment value) is different from another (e.g. the average control value) can rise to the level of "improved."

[001.08] As used herein, "inhibiting and suppressing" and like terms should not be construed to require complete inhibition or suppression, although this may be desired in some embodiments.

[00109] As used herein, the term "genotype" refers to the genetic makeup of an individual cell, cell culture, tissue, organism (e.g., a plant), or group of organisms.

[00110] As used herein, the term "allele(s)" means any of one or more alternative forms of a gene, all of which alleles relate to at least one trait or characteristic. n a diploid cell, the two alleles of a given gene occupy corresponding loci on a pair of homologous chromosomes. Since the present disclosure, in embodiments, relates to QTLs, i.e. genomic regions that may comprise one or more genes or regulatory sequences, it is in some instances more accurate to refer to "haplotype" (i.e. an allele of a chromosomal segment) instead of "allele", however, in those instances, the term "allele" should be understood to comprise the term "haplotype". Alleles are considered identical when they express a similar phenotype. Differences in sequence are possible but not important as long as they do not influence phenotype.

[00111] As used herein, the term "locus" (loci plural) means a specific place or places or a site on a chromosome where for example a gene or genetic marker is found. [00112] As used herein, the term "genetically linked" refers to two or more traits that are co- inherited at a high rate during breeding such that they are difficult to separate through crossing.

[00113] A "recombination" or "recombination event" as used herein refers to a chromosomal crossing over or independent assortment. The term "recombinant" refers to a plant having a new genetic makeup arising as a result of a recombination event.

[00114] As used herein, the term "molecular marker" or "genetic marker" refers to an indicator that is used in methods for visualizing differences in characteristics of nucleic acid sequences. Examples of such indicators are restriction fragment length polymorphism (RFLP) markers, amplified fragment length polymorphism (AFLP) markers, single nucleotide polymorphisms (SNPs), insertion mutations, nucrosateliite markers (SSRs), sequence-characterized amplified regions (SCARs), cleaved amplified polymorphic sequence (CAPS) markers or isozyme markers or combinations of the markers described herein which defines a specific genetic and chromosomal location. Mapping of molecular markers in the vicinity of an allele is a procedure which can be performed by the average person skilled in molecular-biological techniques.

[00115] As used herein, the term "trait" refers to a characteristic or phenotype. For example, in the context of some embodiments of the present disclosure, yield of a crop relates to the amount of marketable biomass produced by a plant (e.g. , fruit, fiber, grain). Desirable traits may also include other plant characteristics, including but not limited to: water use efficiency, nutrient use efficiency, production, mechanical harvestability, fruit maturity, shelf life, pest/disease resistance, early plant maturity, tolerance to stresses, etc. A trait may be inherited in a dominant or recessive manner, or in a partial or incomplete-dominant manner. A trait may be monogenic (i. e. determined by a single locus) or polygenic (i.e. determined by more than one locus) or may also result from the interaction of one or more genes with the environment.

[00116] A dominant trait results in a complete phenotypic manifestation at heterozygous or homozygous state; a recessive trait manifests itself only when present at homozygous state.

[00117] In the context of this disclosure, traits may also result from the interaction of one or more plant genes and one or more microorganism genes. [00118] As used herein, the term "homozygous" means a genetic condition existing when two identical alleles reside at a specific locus, but are positioned individually on corresponding pairs of homologous chromosomes in the cell of a diploid organism. Conversely, as used herein, the term "heterozygous" means a genetic condition existing when two different alleles reside at a specific locus, but are positioned individually on corresponding pairs of homologous chromosomes in the ceil of a diploid organism.

[00119] As used herein, the term "phenotype" refers to the observable characteristics of an individual cell, cell culture, organism (e.g., a plant), or group of organisms which results from the interaction between that individual's genetic makeup (i.e., genotype) and the environment.

[00120] As used herein, the term "chimeric" or "recombinant" when describing a nucleic acid sequence or a protein sequence refers to a nucleic acid, or a protein sequence, that links at least two heterologous polynucleotides, or two heterologous polypeptides, into a single macromoiecuie, or that re-arranges one or more elements of at least one natural nucleic acid or protein sequence. For example, the term "recombinant" can refer to an artificial combination of two otherwise separated segments of sequence, e.g. , by chemical synthesis or by the manipulation of isolated segments of nucleic acids by genetic engineering techniques.

[00121] As used herein, a "synthetic nucleotide sequence" or "synthetic polynucleotide sequence" is a nucleotide sequence that is not known to occur in nature or that is not naturally occurring. Generally, such a synthetic nucleotide sequence will comprise at least one nucleotide difference when compared to any other naturally occurring nucleotide sequence.

[00122] As used herein, the term "nucleic acid" refers to a polymeric form of nucleotides of any length, either ribonucleotides or deoxyribonucleotides, or analogs thereof. This term refers to the primary structure of the molecule, and thus includes double- and single-stranded DNA, as well as double- and single-stranded RNA. It also includes modified nucleic acids such as methylated and/or capped nucleic acids, nucleic acids containing modified bases, backbone modifications, and the like. The terms "nucleic acid" and "nucleotide sequence" are used interchangeably.

[00123] As used herein, the term "gene" refers to any segment of DNA associated with a biological function. Thus, genes include, but are not limited to, coding sequences and/or the regulatory sequences required for their expression. Genes can also include non-expressed DNA segments that, for example, form recognition sequences for other proteins. Genes can be obtained from a variety of sources, including cloning from a source of interest or synthesizing from known or predicted sequence information, and may include sequences designed to have desired parameters,

[00124] As used herein, the term "homologous ^" ' or "homologue" or "ortholog" is known in the art and refers to related sequences that share a common ancestor or family member and are determined based on the degree of sequence identity. The terms "homology," "homologous," "substantially similar" and "corresponding substantially" are used interchangeably herein. They refer to nucleic acid fragments wherein changes in one or more nucleotide bases do not affect the ability of the nucleic acid fragment to mediate gene expression or produce a certain phenotype. These terms also refer to modifications of the nucleic acid fragments of the instant disclosure such as deletion or insertion of one or more nucleotides that do not substantially alter the functional properties of the resulting nucleic acid fragment relative to the initial, unmodified fragment. It is therefore understood, as those skilled in the art will appreciate, that the disclosure encompasses more than the specific exemplary sequences. These terms describe the relationship between a gene found in one species, subspecies, variety, cultivar or strain and the corresponding or equivalent gene in another species, subspecies, variety, cultivar or strain. For purposes of this disclosure homologous sequences are compared. "Homologous sequences" or "homoiogues" or "orthologs" are thought, believed, or known to be functionally related. A functional relationship may be indicated in any one of a number of ways, including, but not limited to: (a) degree of sequence identity and/or (b) the same or similar biological function. Preferably, both (a) and (b) are indicated. Homology can be determined using software programs readily available in the art, such as those discussed in Current Protocols in Molecular Biology (F.M, Ausubel et al., eds., 1987) Supplement 30, section 7.718, Table 7.71. Some alignment programs are MacVector (Oxford Molecular Ltd, Oxford, U.K.), ALIGN Pius (Scientific and Educational Software, Pennsylvania) and AlignX (Vector NTL Invstrogen, Carlsbad, CA). Another alignment program is Sequencher (Gene Codes, Ann Arbor, Michigan), using default parameters.

[00125] As used herein, the term "nucleotide change" refers to, e.g. , nucleotide substitution, deletion, and/or insertion, as is well understood in the art. For example, mutations contain alterations that produce silent substitutions, additions, or deletions, but do not alter the properties or activities of the encoded protein or how the proteins are made.

[00126] As used herein, the term "protein modification" refers to, e.g., amino acid substitution, amino acid modification, deletion, and/or insertion, as is well understood in the art.

[00127] As used herein, the term "at least a portion" or "fragment" of a nucleic acid or polypeptide means a portion having the minimal size characteristics of such sequences, or any larger fragment of the full length molecule, up to and including the full length molecule. A fragment of a polynucleotide of the disclosure may encode a biologically active portion of a genetic regulatory element. A biologically active portion of a genetic regulatory element can be prepared by isolating a portion of one of the polynucleotides of the disclosure that comprises the genetic regulatory element and assessing activity as described herein. Similarly, a portion of a polypeptide may be 4 amino acids, 5 amino acids, 6 amino acids, 7 amino acids, and so on, going up to the full length polypeptide. The length of the portion to be used will depend on the particular application. A portion of a nucleic acid useful as a hybridization probe may be as short as 12 nucleotides; in some embodiments, it is 20 nucleotides. A portion of a polypeptide useful as an epitope may be as short as 4 amino acids. A portion of a polypeptide that performs the function of the full-length polypeptide would generally be longer than 4 amino acids.

[00128] Variant polynucleotides also encompass sequences derived from a mutagenic and recombinogenic procedure such as DNA shuffling. Strategies for such DNA shuffling are known in the art. See, for example, Stemmer (1994) PNAS 91 : 10747-10751; Stemmer (1994) Nature 370:389-391; Crameri el a/. (1997) Nature Biotech. 15:436-438; Moore el a/. (1997) J. Mol. Biol. 272:336-347; Zhang et at (1997) PNAS 94:4504-4509; Crameri el al (1998) Nature 391 :288-291 ; and U.S. Patent Nos. 5,605,793 and 5,837,458. For PGR amplifications of the polynucleotides disclosed herein, oligonucleotide primers can be designed for use in PGR reactions to amplify corresponding DNA sequences from cDNA or genomic DNA extracted from any plant of interest. Methods for designing PGR primers and PGR cloning are generally known in the art and are disclosed in Sambrook et /. (1989) Molecular Cloning: A Laboratory Manual (2nd ed., Cold Spring Harbor Laboratory Press, Plainview, New Y ork). See also Innis et al, eds. (1990) PGR Protocols: A Guide to Methods and Applications (Academic Press, New York); Innis and Gelfand, eds. (1995) PCR Strategies (Academic Press, New York); and Innis and Gelfand, eds. (1999) PCR Methods Manual (Academic Press, New York). Known methods of PCR include, but are not limited to, methods using paired primers, nested primers, single specific primers, degenerate primers, gene-specific primers, vector-specific primers, partially -mismatched primers, and the like.

[00129] The term "primer ^" ' as used herein refers to an oligonucleotide which is capable of annealing to the amplification target allowing a DNA polymerase to attach, thereby serving as a point of initiation of DNA synthesis when placed under conditions in which synthesis of primer extension product is induced, i.e., in the presence of nucleotides and an agent for polymerization such as DNA polymerase and at a suitable temperature and pH. The (amplification) primer is preferably single stranded for maximum efficiency in amplification. Preferably, the primer is an oligodeoxyribonucleotide. The primer must be sufficiently long to prime the synthesis of extension products in the presence of the agent for polymerization. The exact lengths of the primers will depend on many factors, including temperature and composition (A/T vs. G/C content) of primer. A pair of bi-directional primers consists of one forward and one reverse primer as commonly used in the art of DNA amplification such as in PCR amplification.

[00130] The terms "stringency" or "stringent hybridization conditions" refer to hybridization conditions that affect the stability of hybrids, e.g. , temperature, salt concentration, pH, formamide concentration and the like. These conditions are empirically optimized to maximize specific binding and minimize non-specific binding of primer or probe to its target nucleic acid sequence. The terms as used include reference to conditions under which a probe or primer will hybridize to its target sequence, to a detectably greater degree than other sequences (e.g. at least 2-fold over background). Stringent conditions are sequence dependent and will be different in different circumstances. Longer sequences hybridize specifically at higher temperatures. Generally, stringent conditions are selected to be about 5° C lower than the thermal melting point (Tm) for the specific sequence at a defined ionic strength and pH. The Tm is the temperature (under defined ionic strength and pH) at which 50% of a complementary target sequence hybridizes to a perfectly matched probe or primer. Typically, stringent conditions will be those in which the salt concentration is less than about 1.0 M Na+ ion, typically about 0.01 to 1.0 M Na + ion concentration (or other salts) at pH 7.0 to 8.3 and the temperature is at least about 30° C for short probes or primers (e.g. 10 to 50 nucleotides) and at least about 60° C for long probes or primers (e.g. greater than 50 nucleotides). Stringent conditions may also be achieved with the addition of destabilizing agents such as formamide. Exemplary low stnngent conditions or "conditions of reduced stringency" include hybridization with a buffer solution of 30% formamide, 1 M NaCl, 1% SDS at 37° C and a wash in 2xSSC at 40° C. Exemplary high stringency conditions include hybridization in 50% formamide, 1M NaCl, 1% SDS at 37° C, and a wash in O.l xSSC at 60° C. Hybridization procedures are well known in the art and are described by e.g. Ausubel et ciL, 1998 and Sambrook et al , 2001 , In some embodiments, stringent conditions are hybridization in 0.25 M Na2HP04 buffer (pH 7.2) containing 1 mM Na2EDTA, 0.5-20% sodium dodecyl sulfate at 45°C, such as 0.5%, 1%, 2%, 3%, 4%, 5%, 6%, 7%, 8%, 9%, 10%, 11%, 12%, 13%, 14%, 15%, 16%, 17%, 18%, 19% or 20%, followed by a wash in 5 SSC. containing 0, 1 % (w/v) sodium dodecyl sulfate, at 55°C to 65°C.

[00131] As used herein, ' ^" promoter" refers to a DNA sequence capable of controlling the expression of a coding sequence or functional RNA. The promoter sequence consists of proximal and more distal upstream elements, the latter elements often referred to as enhancers. Accordingly, an "enhancer" is a DNA sequence that can stimulate promoter activ ity, and may be an innate element of the promoter or a heterologous element inserted to enhance the level or tissue specificity of a promoter. Promoters may be derived in their entirety from a native gene, or be composed of different elements derived from different promoters found in nature, or even comprise synthetic DNA segments. It is understood by those skilled in the art that different promoters may direct the expression of a gene in different tissues or cell types, or at different stages of development, or in response to different environmental conditions. It is further recognized that since in most cases the exact boundaries of regulatory sequences have not been completely defined, DNA fragments of some variation may have identical promoter activity.

[00132] As used herein, a "plant promoter" is a promoter capable of initiating transcription in plant cells whether or not its origin is a plant cell, e.g. it is well known that Agrobacterium promoters are functional in plant cells. Thus, plant promoters include promoter DNA obtained from plants, plant viruses and bacteria such as Agrobacterium and Brady rhizobium bacteria. A plant promoter can be a constitutive promoter or a non-constitutive promoter.

[00133] As used herein, a "constitutive promoter" is a promoter which is active under most conditions and/or during most development stages. There are several advantages to using constitutive promoters in expression vectors used in plant biotechnology, such as: high level of production of proteins used to select transgenic cells or plants: high level of expression of reporter proteins or scorable markers, allowing easy detection and quantification; high level of production of a transcription factor that is part of a regulatory transcription system; production of compounds that requires ubiquitous activit ' in the plant; and production of compounds that are required during all stages of plant development. Non-limiting exemplary- constitutive promoters include, CaMV 35S promoter, opine promoters, ubiquitin promoter, alcohol dehydrogenase promoter, etc.

[00134] As used herein, a "non-constitutive promoter" is a promoter which is active under certain conditions, in certain types of cells, and/or during certain development stages. For example, tissue specific, tissue preferred, cell type specific, cell type preferred, inducible promoters, and promoters under development control are non-constitutive promoters. Examples of promoters under developmental control include promoters that preferentially initiate transcription in certain tissues, such as stems, leaves, roots, or seeds.

[00135] As used herein, "inducible" or "repressibie" promoter is a promoter which is under chemical or environmental factors control. Examples of environmental conditions that may- effect transcription by inducible promoters include anaerobic conditions, or certain chemicals, or the presence of light.

[00136] As used herein, a "tissue specific" promoter is a promoter that initiates transcription only in certain tissues. Unlike constitutive expression of genes, tissue-specific expression is the result of several interacting levels of gene regulation. As such, in the art sometimes it is preferable to use promoters from homologous or closely related plant species to achieve efficient and reliable expression of transgenes in particular tissues. This is one of the main reasons for the large amount of tissue-specific promoters isolated from particular plants and tissues found in both scientific and patent literature.

[00137] As used herein, the term "operably linked" refers to the association of nucleic acid sequences on a single nucleic acid fragment so that the function of one is regulated by the other. For example, a promoter is operably linked with a coding sequence when it is capable of regulating the expression of that coding sequence (i .e., that the coding sequence is under the transcriptional control of the promoter). Coding sequences can be operably linked to regulatory sequences in a sense or antisense orientation. In another example, the complementary RNA regions of the disclosure can be operably linked, either directly or indirectly, 5' to the target mRNA, or 3' to the target mRNA, or within the target mRNA, or a first complementary region is 5' ^' and its complement is 3' ^' to the target mRNA.

[00138] As used herein, the phrases "recombinant construct", "expression construct", "chimeric construct", "construct", and "recombinant DNA construct" are used interchangeably herein. A recombinant construct comprises an artificial combination of nucleic acid fragments, e.g., regulatory and coding sequences that are not found together in nature. For example, a chimeric construct may comprise regulatory sequences and coding sequences that are derived from different sources, or regulatory sequences and coding sequences derived from the same source, but arranged in a manner different than that found in nature. Such construct may be used by itself or may be used in conjunction with a vector. If a vector is used then the choice of vector is dependent upon the method that will be used to transform host cells as is well known to those skilled in the art. For example, a piasmid vector can be used. The skilled artisan is well aware of the genetic elements that must be present on the vector in order to successfully transform, select and propagate host cells comprising any of the isolated nucleic acid fragments of the disclosure. The skilled artisan will also recognize that different independent transformation events will result in different levels and patterns of expression (Jones et al , (1985) EMBO J. 4:241 1 -2418; De Almeida et al , (1989) Mol. Gen. Genetics 218:78-86), and thus that multiple events must be screened in order to obtain lines displaying the desired expression level and pattern. Such screening may be accomplished by Southern analysis of DNA, Northern analysis of mRNA expression, immunoblotting analysis of protein expression, or phenotypic analysis, among others. Vectors can be plasmids, viruses, bacteriophages, pro-viruses, phagemids, transposons, artificial chromosomes, and the like, that replicate autonomously or can integrate into a chromosome of a host cell. A vector can also be a naked RNA polynucleotide, a naked DNA polynucleotide, a polynucleotide composed of both DNA and RNA within the same strand, a poly-iysine-conjugated DNA or RNA, a peptide-conjugated DNA or RNA, a liposome- conjugated DN A, or the like, that is not autonomously replicating. As used herein, the term "expression" refers to the production of a functional end-product e.g. , an mRNA or a protein (precursor or mature).

[00139] In some embodiments, the cell or organism has at least one heterologous trait. As used herein, the term "heterologous trait" refers to a phenotype imparted to a transformed host cell or transgenic organism by an exogenous DNA segment, heterologous polynucleotide or heterologous nucleic acid. Various changes in phenotype are of interest to the present disclosure, including but not limited to modifying the fatty acid composition in a plant, altering the amino acid content of a plant, altering a plant's pathogen defense mechanism, increasing a plant's yield of an economically important trait {e.g., grain yield, forage yield, etc.) and the like. These results can be achieved by providing expression of heterologous products or increased expression of endogenous products in plants using the methods and compositions of the present disclosure

[00140] A ^" 'syntiietic combination" can include a combination of a plant and a microbe of the disclosure. The combination may be achieved, for example, by coating the surface of a seed of a plant, such as an agricultural plant, or host plant tissue (root, stem, leaf, etc.), with a microbe of the disclosure. Further, a "synthetic combination" can include a combination of microbes of various strains or species. Syntiietic combinations have at lest one variable that distinguishes the combination from any combination that occurs in nature. That variable may be, inter alia, a concentration of microbe on a seed or plant tissue that does not occur naturally, or a combination of microbe and plant that does not naturally occur, or a combination of microbes or strains that do not occur naturally together. In each of these instances, the synthetic combination demonstrates the hand of man and possesses structural and/or functional attributes that are not present when die individual elements of the combination are considered in isolation.

[00141] In some embodiments, a microbe can be '"endogenous" to a seed or plant. As used herein, a microbe is considered "endogenous" to a plant or seed, if the microbe is derived from the plant specimen from which it is sourced. That is, if the microbe is naturally found associated with said plant. In embodiments in which an endogenous microbe is applied to a plant, then the endogenous microbe is applied in an amount that differs from the levels found on the plant in nature. Thus, a microbe that is endogenous to a given plant can still form a synthetic combination with the plant, if the microbe is present on said plant at a level that does not occur naturally.

[00142] In some embodiments, a microbe can be "exogenous" (also termed "heterologous") to a seed or plant. As used herein, a microbe is considered "exogenous" to a plant or seed, if the microbe is not derived from the plant specimen from which it is sourced. That is, if the microbe is not naturally found associated with said plant. For example, a microbe that is normally associated with leaf tissue of a maize plant is considered exogenous to a leaf tissue of another rnaize plant that naturally lacks said microbe. In another example, a microbe that is normally associated with a maize plant is considered exogenous to a wheat plant that naturally lacks said microbe.

[00143] Microbes can also be "exogenously disposed" on a given plant tissue. This means that the microbe is placed upon a plant tissue that it is not naturally found upon. For instance, if a given microbe only naturally occurs on the roots of a given plant, then that microbe could be exogenously applied to the above-ground tissue of a plant and would thereby be "exogenously disposed" upon said plant tissue. As such, a microbe is deemed exogenous!}' disposed, when applied on a plant that does not naturally have the microbe present or does not naturally have the microbe present in the number that is being applied

[00144] The compositions and methods herein may provide for an improved "agronomic trait" or 'trait of agronomic importance" to a host plant, which may include, but not be limited to, the following: altered oil content, altered protein content, altered seed carbohydrate composition, altered seed oil composition, and altered seed protein composition, chemical tolerance, cold tolerance, delayed senescence, disease resistance, drought tolerance, ear weight, growth improvement, health enhancement, heat tolerance, herbicide tolerance, herbivore resistance, improved nitrogen fixation, improved nitrogen utilization, improved root architecture, improved water use efficiency, increased biomass, increased root length, increased seed weight, increased shoot length, increased yield, increased yield under water-limited conditions, kernel mass, kernel moisture content, metal tolerance, number of ears, number of kernels per ear, number of pods, nutrition enhancement, pathogen resistance, pest resistance, photosynthetic capability improvement, salinity tolerance, stay-green, vigor improvement, increased dry weight of mature seeds, increased fresh weight of mature seeds, increased number of mature seeds per plant, increased chlorophyll content, increased number of pods per plant, increased length of pods per plant, reduced number of wilted leaves per plant, reduced number of severely wilted leaves per plant, and increased number of non-wilted leaves per plant, a detectable modulation in the level of a metabolite, a detectable modulation in the level of a transcript, and a detectable modulation in the proteome, compared to an isoline plant grown from a seed without said seed treatment formulation. Ability to Impart Beneficial Traits Upon a Given Plant Species by Microbes and Consortia of the Disclosure

[00145] The present disclosure utilizes microbes to impart beneficial properties (or beneficial traits) to desirable plant species, such as agronomic species of interest. In the current disclosure, the terminology "beneficial property" or "beneficial trait" is used interchangeably and denotes that a desirable plant phenotypic or genetic property of interest is modulated, by the application of a microbe or microbial consortia as described herein. As aforementioned, in some aspects, it may very well be that a metabolite produced by a given microbe is ultimately responsible for modulating or imparting a beneficial trait to a given plant.

[00146] 1 here are a vast number of beneficial traits that can be modulated by the application of microbes of the disclosure. For instance, the microbes may have the ability to impart one or more beneficial properties to a plant species, for example: increased growth, increased yield, increased nitrogen utilization efficiency, increased stress tolerance, increased drought tolerance, increased photosynthetic rate, enhanced water use efficiency, increased pathogen resistance, modifications to plant architecture that don't necessarily impact plant yield, but rattier address plant functionality, causing the plant to increase production of a metabolite of interest, etc.

[00147] In aspects, the microbes taught herein provide a wide range of agricultural applications, including: improvements in yield of grain, fruit, and flowers, improvements in growth of plant parts, improved resistance to disease, improved survivability in extreme climate, and improvements in other desired plant phenotypic characteristics.

[00148] In some aspects, the isolated microbes, consortia, and/or agricultural compositions of the disclosure can be applied to a plant, in order to modulate or alter a plant characteristic such as altered oil content, altered protein content, altered seed carbohydrate composition, altered seed oil composition, altered seed protein composition, chemical tolerance, cold tolerance, delayed senescence, disease resistance, drought tolerance, ear weight, growth improvement, health enhancement, heat tolerance, herbicide tolerance, herbivore resistance, improved nitrogen fixation, improved nitrogen utilization, improved root architecture, improved water use efficiency, increased biomass, increased root length, increased seed weight, increased shoot length, increased yield, increased yield under water-limited conditions, kernel mass, kernel moisture content, metal tolerance, number of ears, number of kernels per ear, number of pods, nutrition enhancement, pathogen resistance, pest resistance, photosynthetic capability improvement, salinity tolerance, stay-green, vigor improvement, increased dry weight of mature seeds, increased fresh weight of mature seeds, increased number of mature seeds per plant, increased chlorophyll content, increased number of pods per plant, increased length of pods per plant, reduced number of wilted leaves per plant, reduced number of severely wilted leaves per plant, and increased number of non -wilted leaves per plant, a detectable modulation in the level of a metabolite, a detectable modulation in the le vel of a transcript, and a detectable modulation in the proteome relative to a reference plant,

[00149] In some aspects, the isolated microbes, consortia, and/or agricultural compositions of the disclosure can be applied to a plant, in order to modulate in a negati ve w ay, a particular plant characteristic. For example, in some aspects, the microbes of the disclosure are able to decrease a phenotypic trait of interest, as this functionality can be desirable in some applications. For instance, the microbes of the disclosure may possess the ability to decrease root growth or decrease root length. Or the microbes may possess the ability to decrease shoot growth or decrease the speed at which a plant grows, as these modulations of a plant trait could be desirable in certain applications.

Isolated Microbes - Tables 1-4

[00150] In aspects, the present disclosure provides isolated microbes, including novel strains of identified microbial species, presented in Tables 1-4.

[00151] in other aspects, the present disclosure provides isolated whole microbial cultures of the species and strains identified in Tables 1-4. These cultures may comprise microbes at various concentrations.

[00152] In aspects, the disclosure provides for utilizing a microbe selected from Tables 1-4 in agriculture.

[0153] In some embodiments, the disclosure provides isolated microbial species belonging to genera of: Achromobacter, Agrobacterium, Arthrobacter, Azotobacter, Azospirillum, Bacillus, Bosea, Caulobacter, Chryseobacterium, Delfulviimonas, Duganella, Exiguobacterium, Flavobacterium, Frigidibacter, Herbaspirillum, Leifsonia, Luteibacter, Massiiia, Mucilaginibacter, Novosphingobium, Pantoeo, Paenibacillus, Pedobacter, Poiaromonas, Pseudoduganella, Pseudomonas, Rahneiia, Ramlibacter, Rhizobium, Rhodococcus, Rhodoferax, Sphingobium, Stenotrophomonas and Tumebacillus. [0154] n some embodiments, the disclosure provides isolated microbial species belonging to genera of: Achromobacter, Agrobacterium, Aithrobacter, Chryseobacterium, Delfuiviimonas, Exiguobacterium, Frigidibacter, Leifsonia, Massilia, Novosphingobium, Pedobacter, Pseudomonas, and Turnebacillus.

[0155] In some embodiments, a microbe from the genus Bosea is utilized in agriculture to impart one or more beneficial properties to a plant species.

[0156] In some embodiments, the disclosure provides isolated microbial species, selected from the group consisting of: Achromobacter pulmonis, Agrobacterium fabrum (previously Rhizobium pusense), Arthrobacter nicotinovorans, Azotobacter chroococcum, Chryseobacterium daecheongense, Chryseobacterium rhizosphaerae, Duganella radicis, Exiguobacterium antarcticum, Exiguobacterium sibiricurn, Frigidibacter albus (previously Delfuiviimonas dentrificans) Leifsonia lichenia, Pantoea agglomerans (recently reassigned to Pantoea vagans), Pedobacter terrae, Pseudomonas fluorescens, Pseudomonas helmanticensis, Pseudomonas oryzihabitans, Pseudomonas putida, Rahnella aquatilis, Rhizobium etli, Rhodococcus erythropolis, Stenotrophomonas maltophilia and Turnebacillus permanentifrigoris .

[0157] In some embodiments, the disclosure provides isolated microbial species, selected from the group consisting of: Achromobacter pulmonis, Agrobacterium fabrum (previously Rhizobium pusense), Arthrobacter nicotinovorans, Chryseobacterium daecheongense, Chryseobacterium rhizosphaerae, Exiguobacterium antarcticum, Exiguobacterium sibiricurn, Frigidibacter albus (previously Delfuiviimonas dentrificans) Leifsonia lichenia, Massilia kyonggiensis, Novosphingobium lindaniclasticum, Novosphingobium sediminicoia, Pedobacter terrae, Pseudomonas helmanticensis, and Turnebacillus permanentifrigoris.

[0158] In some embodiments, the disclosure provides novel isolated microbial strains of species, selected from the group consisting of: Achromobacter, Agrobacterium, Arthrobacter, Azotobacter, Azospirillum, Bacillus, Bosea, Caulobacler, Chryseobacterium, Delfuiviimonas, Duganella, Exiguobacterium, Flavobacterium, Frigidibacter, Herbaspmllum, Leifsonia, Luteibacter, Massilia, Mucilaginibacter, Novosphingobium, Pantoea, Paenibacillus, Pedobacter, Polaromonas, Pseudoduganella, Pseudomonas, Rahnella, Ramiibacter, Rhizobium, Rhodococcus, Rhodoferax, Sphingobium, Stenotrophomonas and Turnebacillus, Particular novel strains of these aforementioned species can be found in Tables 1-4. [0159] Furthermore, the disclosure relates to microbes having characteristics substantially similar to that of a microbe identified in Tables 1-4.

[0160] The isolated microbial species, and novel strains of said species, identified in the present disclosure, are able to impart beneficial properties or traits to target plant species.

[0161] For instance, the isolated microbes described in Tables 1-4, or consortia of said microbes, are able to improve plant health and vitality. The improved plant health and vitality can be quantitatively measured, for example, by measuring the effect that said microbial application has upon a plant phenotypic or genotypic trait.

Microbial Consortia - Tables 1-4

[0162] In aspects, the disclosure provides microbial consortia compri sing a combination of at least any two microbes selected from amongst the microbes identified in Table 1.

[0163] In other aspects, the disclosure provides microbial consortia comprising a combination of at least any two microbes selected from amongst the microbes identified in Table 2.

[0164] In yet other aspects, the disclosure provides microbial consortia comprising a combination of at least any two microbes selected from amongst the microbes identified in Table 3.

[0165] In additional aspects, the disclosure provides microbial consortia comprising a combination of at least any two microbes selected from amongst the microbes identified in Table 4.

[0166] Also, the disclosure provides microbial consortia comprising a combination of at least any two microbes selected from amongst the microbes identified in Tables 1-4.

[0167] In certain embodiments, the consortia of the present disclosure comprise two microbes, or three microbes, or four microbes, or five microbes, or six microbes, or seven microbes, or eight microbes, or nine microbes, or ten or more microbes. Said microbes of the consortia are different microbial species, or different strains of a microbial species.

[0168] In some embodiments, the disclosure provides consortia, comprising: at least two isolated microbial species belonging to genera of: Achromobacter, Agrobacterium, Arthrobacter, Azotobacter, Azospirillum, Bacillus, Bosea, Caulobacter, Chr seobacterium, Delfulviimonas, Duganella, Exigiiobacterium, Flavobacterium, Frigidibacter, Herbaspirillum, Leifionia, Luteibacter, Massilia, Mucilaginibacter, Novosphingobium, Pantoeo, Paenibacillus, Pedobacter, Polaromonas, Pseudoduganella, Pse domonas, Rahnella, Ramlibacter, Rkizobium, Rkodococcus, Rhodoferax, Sphingobium, Stenotrophomonas and TumebaciHus.

[0169] In some embodiments, the disclosure provides consortia, comprising: at least two isolated microbial species, selected from the group consisting of: Ackromohacter pulmonis, Agrobacterium fabnirn (previously Rkizobium pusense), Artkrohacter nicotiriovorans, Azotobacter ckroococcum, Chryseobacterium daecheongense, Chryseobacterium rhizosphaerae, Duganella radicis, Exiguobacteriuni antarcticum, Exiguobacterium sibiriciim, Frigidibacter albus ("previously Deifuiviimonas dentrificans) Leifsonia lickenia, Massilia kyonggiensis, Novosphingobium sediminicola, Novosphingobium lindaniclasticum, Pantoea agglomerans (recently reassigned to Pantoea vagans), Pedobacter ierrae, Pseudomonas fluorescens, Pseudomonas kelmanticensis, Pseudomonas oryzihabitans, Pseudomonas putida, Rahnella aquatiiis, Rkizobium etli, Rhodococcus erytkropolis, Stenotrophomonas maltopkilia and TumebaciHus permanentifrigoris .

[0170] In some embodiments, the disclosure provides consortia, comprising: at least two novel isolated microbial strains of species, selected from the group consisting of: Ackromohacter pulmonis, Agrobacterium fabrum previously Rkizobium pusense), Artkrohacter nicotinovorans, Azotobacter ckroococcum., Chryseobacterium daecheongense, Chryseobacterium rhizosphaerae, Duganella radicis, Exiguobacterium antarcticum, Exiguobacterium sibiricum, Frigidibacter albus (previously Delfulviimonas dentrificans) Leifsonia lickenia, Massilia kyonggiensis, Novosphingobium sediminicola, Novosphingobium lindaniclasticum, Pantoea agglomerans (recently reassigned to Pantoea vagans), Pedobacter terrae, Pseudomonas fluorescens, Pseudomonas kelmanticensis, Pseudomonas oryzihabitans, Pseudomonas putida, Rahnella aquatiiis, Rkizobium etli, Rkodococcus erytkropolis, Stenotrophomonas maltopkilia and TumebaciHus permanentifrigoris.Vaxt ular novel strains of these aforementioned species can be found in Tables 1-4.

[0171] In some embodiments, the disclosure provides consortia, comprising: at least two isolated microbial species selected from Tables 1-4, and further comprising a Bradyrhizobium species . [0172] In particular aspects, the disclosure provides microbial consortia, comprising species as grouped in Tables 5-11. With respect to Tables-5-11, the letters A through I represent a non-limiting selection of microbes of the present disclosure, defined as:

[0173] A ^: = Rahnella aquatilis and associated novel strains identified in Table 1;

[0174] B = Bacillus megatarium and associated novel strains identified in Table 2;

[0175] C ^:=: Bacillus niacini and associated novel strains identified in Table 3;

[0176] D = Chryseobacterium rhizosphaerae and associated novel strains identified in Table 4;

[0177] E = Frigidihacter alhus or Delfulviimonas dentrificans (In Taxonomic Flux) and associated novel strains identified in Table 4;

[0178] F = Pedobacter terrae and associated novel strains identified in Table 4;

[0179] G ^: = Leifsonia lichenia and associated novel strains identified in Table 4;

[0180] H = Tumebacillus permanentifrigoris and associated novel strains identified in Table 4; and

[0181] 1 = Novosphingobium sediminicola and associated novel strains identified in Table 4.

Table 5: Eight and Nine Strain Consortia

Table 6: Seven Strain Consortia

Table 7: Six Strain Consortia

A,B,C,D,E,F A,B,C,D,E,G A,B,C,D,E,H A,B,C,D,E,I A,B,C,D,F,G A,B,C,D,F,H A,B,C,D,F,I

A,B,C,D,G,H A,B,C,D,G,I A,B,C,D,H,I A,B,C,E,F,G A,B,C,E,F,H A,B,C,E,F,I A,B,C,E,G,H

A,B,C,E,G, I A,B,C,E,H,I A,B,C,F,G,H A,B,CF,G,I A,B,C,F,H,I A,3,C,G,H,i A,B,D,E,F,G

A,B,D,E,F,H A,B,D,E,F,I A,B,D,E,G,H A,B,D,E,G,I A,B,D,E,H,I A,B,D,F,G,H A,B,D, F,G,I

D,E,F,G,H,I C,E,F,G,H,I A,B,D,F,H,I A,B,D,G,H,I A,B,E,F,G,H A,B,E,F,G,I A,B,E,F,H,I A,B,E,G,H,I A,B,F,G,H,I A,C,D,E,F,G A,C,D,E,F,H A,C,D,E,F,I A,C,D,E,G,H A,C,D,E,G,I

A,C,D,E,H,I A,C,D,F,G,H A,C,D,F,G,I A,C,D,F,H,I A,C,D,G,H,I A,C,E,F,G,H A,C,E,F,G,I

A,C,E,F,H, I A,C, E,G,H,I A,C,F,G,H,i A,D,E, F,G,H A,D,E,F,G,I A,D,E,F,H,I A,D,E,G,H,I

A,D,F,G,H,I A,E,F,G,H,I B,C,D,E,F,G B,C,D,E,F,H 1 B,C,D,E,F,I B,C,D,E,G,H B,C,D,E,G,I

B,C,D,E,H,I B,C,D,F,G,H B,C,D,F,G,I B,C,D,F,H,I B,C,D,G,H,I B,C,E,F,G,H B,C,E,F,G,I

B,C,E,F,H,i B,C,E,G,H,I B,C,F,G,H,i B,D,E,F,G,H B,D,E,F,G,I B,D,E,F,H,I B,D,E,G,H,I

B,D,F,G,H,I B,E,F,G,HJ C,D,E,F,G,H C,D,E,F,G C,D,E,F,H,I C,D,E,G,H,I C,D,F,G,H,I

Table 8: Five Strain Consortia

Table 9: Four Strain Consortia

A,B,C, D A,B,C,E A,B,C,F A,B,C,G A,B,C,H A,B,CJ A,B,D,E A,B,D,F D,G,H,\

A,B,D,G A,B,D,H A,B,D,I A,B,E,F A,B,E,G Α,Β,Ε,Η Α,Β,Ε,Ι A,B,F,G E,F,G,H

A,B,F,H A,D,F,H A,D,F,I A,D,G,H A,D,G,I A,D,H,I A,E,F,G A,E,F,H E,F,G,I

A,B,F,I A,B,G,H A,B,G,I Α,Β,Η,Ι A,C,D,E A,C,D,F A,C,D,G A,C,D,H E,F,H,i

A, CD,! A,C,E,F A,C,E,G A,C,E,H A,Q E,I A,C,F,G A,C,F,H A,C,F,I E,G,H,I

A,C,G,H A,C,G,I A,C,H,I A, D, E, F A,D,E,G A,D,E,H A,D,E,I A,D,F,G F,G,H,I

A,E,F,I A,E,G,H A,E,G,I Α,Ε,Η,Ι A,F,G,H A,F,G,I A,F,H,I A,G,H,I D,E,F,H

B,C,D,E B,C,D,F B,C,D,G B,C,D,H B,C,D,i B,C,E,F 3,C,E,G B,C,E,H D,E,F,I

B,C,E,! B,C,F,G B,C,F,H B,C,F,I B,C,G,H B,C,G,I B,C,HJ B,D,E,F D,E,G,H

B,D,E,G Β,Ο,Ε,Η B,D,E,I B,D,F,G B,D,F,H B,D,F,I B,D,G,H B,D,G,I D,E,G,I

Β,Ο,Η,Ι B,E,F,G B,E,F,H B,E,F,I B,E,G,H B,E,G,I Β,Ε,Η,Ι B,F,G,H D,E,H,!

B,F,G,I B,F,H,I B,G,H,I C,D,E,F C,D,E,G C,D,E,H C,D,E,I C,D,F,G D,F,G,H

C, D,F,H C,D,F,I C, D,G,H C,D,G,I C,D,H,I C,E,F,G C,E,F,H C,E,FJ D,F,GJ

C,E,G, H C, E,G,I C,E,H,I C,F,G,H C,F,G,I ςρ,Η,ι C,G,H,I D,E,F,G D,F,H,I Table 10: Three Strain Consortia

Table 11 : Two Strain Consortia

[0182] In some embodiments, the microbial consortia may be selected from any member group from Tables 5-11.

Isolated Microbes - Source Material

[0183] The microbes of the present disclosure were obtained, among other places, at various locales in New Zealand and the United States.

Isolated Microbes - Microbial Culture Techniques

[0184] The microbes of Tables 1-4 were identified by utilizing standard microscopic techniques to characterize the microbes' phenotype, which was then utilized to identify the microbe to a taxonomically recognized species.

[0185] The isolation, identification, and culturing of the microbes of the present disclosure can be effected using standard microbiological techniques. Examples of such techniques may be found in Gerhardt, P. (ed.) Methods for General and Molecular Microbiology, American Society for Microbiology, Washington, D.C. ( 1994) and Lennette, E. H. (ed.) Manual of Clinical Microbiology, Third Edition. American Society for Microbiology, Washington, D.C. (1980), each of which is incorporated by reference.

[0186] Isolation can be effected by streaking the specimen on a solid medium {e.g. , nutrient agar plates) to obtain a single colony, which is characterized by the phenotypie traits described hereinabove (e.g., Gram positive/negative, capable of forming spores aerobically/anaerobically, cellular morphology, carbon source metabolism, acid/base production, enzyrne secretion, metabolic secretions, etc.) and to reduce the likelihood of working with a culture which has become contaminated.

[0187] For example, for isolated bacteria of the disclosure, biologically pure isolates can be obtained through repeated subculture of biological samples, each subculture followed by streaking onto solid media to obtain individual colonies. Methods of preparing, thawing, and growing lyophilized bacteria are commonly known, for example, Gherna, R. L. and C. A. Reddy. 2007. Culture Preservation, p 1019-1033. In C. A. Reddy, T. J. Beveridge, J. A. Breznak, G. A. Marziuf, T. M. Schmidt, and L. R. Snyder, eds. American Society for Microbiology, Washington, D.C., 1033 pages; herein incorporated by reference. Thus freeze dried liquid formulations and cultures stored long term at -70° C in solutions containing glycerol are contemplated for use in providing formulations of the present inventions.

[0188] The bacteria of the disclosure can be propagated in a liquid medium under aerobic conditions. Medium for growing the bacterial strains of the present disclosure includes a carbon source, a nitrogen source, and inorganic salts, as well as specially required substances such as vitamins, amino acids, nucleic acids and the like. Examples of suitable carbon sources which can be used for growing the bacterial strains include, but are not limited to, starch, peptone, yeast extract, amino acids, sugars such as glucose, arabinose, rnannose, glucosamine, maltose, and the like; salts of organic acids such as acetic acid, fumaric acid, adipic acid, propionic acid, citric acid, gluconic acid, malic acid, pyruvic acid, malonic acid and the like; alcohols such as ethanoi and glycerol and the like; oil or fat such as soybean oil, rice bran oil, olive oil, corn oil, sesame oil. The amount of the carbon source added varies according to the kind of carbon source and is typically between 1 to 100 gram(s) per liter of medium. Preferably, glucose, starch, and/or peptone is contained in the medium as a major carbon source, at a concentration of 0.1-5% (W/V). Examples of suitable nitrogen sources which can be used for growing the bacterial strains of the present invention include, but are not limited to, am ino acids, yeast extract, tryptone, beef extract, peptone, potassium nitrate, ammonium nitrate, ammonium chloride, ammonium sulfate, ammonium phosphate, ammonia or combinations thereof. The amount of nitrogen source varies according to the type of nitrogen source, typically between 0.1 to 30 gram per liter of medium. The inorganic salts, potassium dihydrogen phosphate, dipotassium hydrogen phosphate, di sodium hydrogen phosphate, magnesium sulfate, magnesium chloride, ferric sulfate, ferrous sulfate, ferric chloride, ferrous chloride, manganous sulfate, manganous chloride, zinc sulfate, zinc chloride, cupric sulfate, calcium chloride, sodium chloride, calcium carbonate, sodium carbonate can be used alone or in combination, llie amount of inorganic acid varies according to the kind of the inorganic salt, typically between 0.001 to 10 gram per liter of medium. Examples of specially required substances include, but are not limited to, vitamins, nucleic acids, yeast extract, peptone, meat extract, malt extract, dried yeast and combinations thereof. Cultivation can be effected at a temperature, which allows the growth of the bacterial strains, essentially, betw een 20°C and 46°C. In some aspects, a temperature range is 30°C-37°C. For optimal growth, in some embodiments, the medium can be adjusted to pH 7.0-7.4. It will be appreciated that commercially available media may also be used to culture the bacterial strains, such as Nutrient Broth or Nutrient Agar available from Difco, Detroit, MI. It will be appreciated that cultivation time may differ depending on the type of culture medium used and the concentration of sugar as a major carbon source.

[0189] In aspects, cultivation lasts between 24-96 hours. Bacterial cells thus obtained are isolated using methods, which are well known in the art. Examples include, but are not limited to, membrane filtration and centrifugal separation. The pH may be adjusted using sodium hydroxide and the like and the culture may be dried using a freeze dryer, until the water content becomes equal to 4% or less. Microbial co-cultures may be obtained by- propagating each strain as described hereinabove. It will be appreciated that the microbial strains may be cultured together when compatible culture conditions can be employed.

Isolated Microbes - Microbial Strains

[0190] Microbes can be distinguished into a genus based on polyphasic taxonomy, which incorporates all available phenotypic and genotypic data into a consensus classification (Vandamme et al. 1996. Polyphasic taxonomy, a consensus approach to bacterial systematics. Microbiol Rev 1996, 60:407-438). One accepted genotypic method for defining species is based on overall genomic relatedness, such that strains which share approximately 70% or more relatedness using DNA-DNA hybridization, with 5°C or less Aim (the difference in the melting temperature between homologous and heterologous hybrids), under standard conditions, are considered to be members of the same species. Thus, populations that share greater than the aforementioned 70% threshold can be considered to be variants of the same species. [0191] The 16S rRNA sequences are often used for making distinctions between species, in that if a 16S rRNA sequence shares less than a specified % sequence identit - from a reference sequence, then the two organisms from, which the sequences were obtained are said to be of different species.

[0192] Thus, one could consider microbes to be of the same species, if they share at least 80%, 85%, 90%, 95%, 97%, 98%, or 99% sequence identity across the 16S or 18S rRNA or rDNA sequence. In some aspects, a microbe could be considered to be the same species only if it shares at least 95% identity.

[0193] Further, one could define microbial strains of a species, as those that share at least 80%, 85%, 90%, 95%, 97%, 98%, or 99% sequence identity across the 16S rRNA sequence. Comparisons may also be made with 23S rRNA sequences against reference sequences. In some aspects, a microbe could be considered to be the same strain only if it shares at least 95% identity. In some embodiments, "substantially similar genetic characteristics" means a microbe sharing at least 95% identity.

[0194] In one embodiment, microbial strains of the present disclosure include those that comprise polynucleotide sequences that share at least 70%, 75%, 80%, 81%, 82%, 83%, 84%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or 100% sequence identity with any one of SEQ ID NOs: l, 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, 39, 30, 31, 32, 33, 34, or 307; or any one of SEQ ID NOs:35-306.

[0195] In one embodiment, microbes of the present disclosure include those that comprise polynucleotide sequences that share at least 70%, 75%, 80%, 81%, 82%, 83%, 84%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or 100% sequence identity with any one of SEQ ID N0s: L 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, 39, 30, 31, 32, 33, 34, or 307; or any one of SEQ ID NOs:35-306.

[0196] In one embodiment, microbial consortia of the present disclosure include two or more microbes those that comprise polynucleotide sequences that share at least 70%, 75%, 80%, 81%, 82%, 83%, 84%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or 100% sequence identity with any one of SEQ ID NOs: l, 2, 3, 4, 5, 6, 7, 8, 9, 10, 1 1, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 39, 30, 31, 32, 33, 34, and/or 307; or any one of SEQ ID NQs:35-306.

[0197] Unculturable microbes often cannot be assigned to a definite species in the absence of a phenotype determination, the microbes can be given a candidates designation within a genus provided their 16S rR A sequences subscribes to the principles of identity with known species.

[0198] One approach is to observe the distribution of a large number of strains of closely related species in sequence space and to identify clusters of strains that are well resolved from other clusters. This approach has been developed by using the concatenated sequences of multiple core (house-keeping) genes to assess clustering patterns, and has been called multilocus sequence analysis (MLSA) or multilocus sequence phylogenetic analysis. MLSA has been used successfully to explore clustering patterns among large numbers of strains assigned to very closely related species by current taxonomic methods, to look at the relationships between small numbers of strains within a genus, or within a broader taxonomic grouping, and to address specific taxonomic questions. More generally, the method can be used to ask whether bacterial species exist - that is, to observe whether large populations of similar strains invariably fall into well-resolved clusters, or whether in some cases there is a genetic continuum in which clear separation into clusters is not observed.

[0199] In order to more accurately make a determination of genera, a determination of phenotypic traits, such as morphological, biochemical, and physiological characteristics are made for comparison with a reference genus archetype. The colony morphology can include color, shape, pigmentation, production of slime, etc. Features of the cell are described as to shape, size, Gram reaction, extracellular material, presence of endospores, flagella presence and location, motility, and inclusion bodies. Biochemical and physiological features describe growth of the organism at different ranges of temperature, pH, salinity and atmospheric conditions, growth in presence of different sole carbon and nitrogen sources. One of ordinary skill in the art would be reasonably apprised as to the phenotypic traits that define the genera of the present disclosure. For instance, colony color, form, and texture on a particular agar (e.g. YMA) was used to identify species of Rhizobium.

[0200] In one embodiment, the microbes taught herein were identified utilizing 16S rRNA gene sequences. It is known in the art that 16S rRNA contains hypervariable regions that can provide species/strain-specific signature sequences useful for bacterial identification. In the present disclosure, many of the microbes were identified via partial (500 - 1200 bp) 16S rRNA sequence signatures. In aspects, each strain represents a pure colony isolate that was selected from an agar plate. Selections were made to represent the diversity of organisms present based on any defining morphological characteristics of colonies on agar medium. The medium used, in embodiments, was R2A, PDA, Nitrogen-free semi-solid medium, or MRS agar. Colony descriptions of each of the 'picked' isolates were made after 24-hour growth and then entered into our database. Sequence data was subsequently obtained for each of the isolates.

[0201] Pliylogenetic analysis using the 16S rRNA gene was used to define "substantially similar" species belonging to common genera and also to define "substantially similar" strains of a given taxonomic species. Further, we recorded physiological and/or biochemical properties of the isolates that can be utilized to highlight both minor and significant differences between strains that could lead to advantageous behavior on plants.

Agricultural Compositions

[0202] In some embodiments, the microbes of the disclosure are combined into agricultural compositions. In some embodiments, the agricultural compositions of the present disclosure include, but are not limited to: wetters, compatibilizmg agents (also referred to as "compatibility agents"), antifoam agents, cleaning agents, sequestering agents, drift reduction agents, neutralizing agents and buffers, corrosion inhibitors, dyes, odorants, spreading agents (also referred to as "spreaders"), penetration aids (also referred to as "penetrants"), sticking agents (also referred to as "stickers" or "binders"), dispersing agents, thickening agents (also referred to as "thickeners"), stabilizers, emulsifiers, freezing point depressants, antimicrobial agents, and the like.

[0203] in some embodiments, the agricultural compositions of the present disclosure are solid. Where solid compositions are used, it may be desired to include one or more carrier materials with the active isolated microbe or consortia. In some embodiments, the present disclosure teaches the use of carriers including, but not limited to: mineral earths such as silicas, silica gels, silicates, talc, kaolin, attaclay, limestone, chalk, loess, clay, dolomite, diatomaceous earth, calcium sulfate, magnesium sulfate, magnesium oxide, ground synthetic materials, fertilizers such as ammonium sulfate, ammonium phosphate, ammonium nitrate, thiourea and urea, products of vegetable origin such as cereal meals, tree bark meal, wood meal and nutshell meal, cellulose powders, attapulgites, montmorillonites, mica, vermiculites, synthetic silicas and synthetic calcium silicates, or compositions of these.

[0204] In some embodiments, the agricultural compositions of the present disclosure are liquid. Urns in some embodiments, the present disclosure teaches that the agricultural compositions disclosed herein can include compounds or salts such as monoethanolatnine salt, sodium sulfate, potassium sulfate, sodium chloride, potassium chloride, sodium acetate, ammonium hydrogen sulfate, ammonium chloride, ammonium acetate, ammonium formate, ammonium oxalate, ammonium carbonate, ammonium hydrogen carbonate, ammonium thiosulfate, ammonium hydrogen diphosphate, ammonium dihydrogen monophosphate, ammonium sodium hydrogen phosphate, ammonium thiocyanate, ammonium sulfamate or ammonium carbamate.

[0205] In some embodiments, the present disclosure teaches that agricultural compositions can include binders such as: polyvinylpyrrolidone, polyvinyl alcohol, partially hydrolyzed polyvinyl acetate, carboxymethylceiiuiose, starch, vinylpyrrolidone/vmyl acetate copolymers and polyvinyl acetate, or compositions of these; lubricants such as magnesium stearate, sodium stearate, talc or polyethylene glycol, or compositions of these; antifoams such as silicone emulsions, long-chain alcohols, phosphoric esters, acetylene diols, fatty acids or organofluorine compounds, and compiexing agents such as: salts of ethylenediaminetetraacetic acid (EDTA), salts of trinitrilotriacetic acid or salts of polyphosphoric acids, or compositions of these.

[0206] In some embodiments, the agricultural compositions comprise surface-active agents. In some embodiments, the surface -active agents are added to liquid agricultural compositions. In other embodiments, the surface-active agents are added to solid formulations, especially those designed to be diluted with a carrier before application. Thus, in some embodiments, the agricultural compositions comprise surfactants. Surfactants are sometimes used, either alone or with other additives, such as mineral or vegetable oils as adjuvants to spray-tank mixes to improve the biological performance of the microbes on the target. The types of surfactants used for bioenhancement depend generally on the nature and mode of action of the microbes. The surface -active agents can be anionic, cation ic. or nonionic in character, and can be employed as emulsifying agents, wetting agents, suspending agents, or for other purposes. In some embodiments, the surfactants are non- ionics such as: alky ethoxylates, linear aliphatic alcohol ethoxylates, and aliphatic amine ethoxylates. Surfactants conventionally used in the art of formulation and which may also be used in the present formulations are described, in McCutcheon 's Detergents and Emulsifiers Annual, MC Publishing Corp., Ridgewood, N.J., 1998, and in Encyclopedia of Surfactants , Vol. I-III, Chemical Publishing Co., New York, 1980-81 . In some embodiments, the present disclosure teaches the use of surfactants including alkali metal, alkaline earth metal or ammonium salts of aromatic sulfonic acids, for example, ligno-, phenol-, naphthalene- and dibutylnaphtiialenesulfonic acid, and of fatty acids of aryl sulfonates, of alkyl ethers, of lauryl ethers, of fatty alcohol sulfates and of fatty alcohol glycol ether sulfates, condensates of sulfonated naphthalene and its derivatives with formaldehyde, condensates of naphthalene or of the naphthalenesulfonic acids with phenol and formaldehyde, condensates of phenol or phenolsulfonic acid with formaldehyde, condensates of phenol with formaldehyde and sodium sulfite, polyoxyethylene octylphenyl ether, ethoxylated isooctyl-, octyl- or nonylphenol, tributylphenyl polyglycoi ether, alkyiaryl polyether alcohols, isotridecyi alcohol, ethoxylated castor oil, ethoxylated triarylphenols, salts of phosphated triarylphenolethoxylates, lauryl alcohol polyglycoi ether acetate, sorbitol esters, lignin-sulfite waste liquors or methylcellulose, or compositions of these.

[0207] In some embodiments, the present disclosure teaches other suitable surface-active agents, including salts of alkyl sulfates, such as diethanolammonium lauryl sulfate; alkylarylsulfonate salts, such as calcium dodecylbenzene sulfonate; alkylphenol-alkylene oxide addition products, such as nonylphenol-Ci g ethoxylate; alcohol-alkylene oxide addition products, such as tridecyl alcohoI-Cie ethoxylate; soaps, such as sodium stearate; alkylnaphthalene-sulfonate salts, such as sodium dibutyl-naphthalenesulfonate; dialkyl esters of sulfosuccinate salts, such as sodium di(2-ethylhexyl)sulfosuccinate; sorbitol esters, such as sorbitol oleate; quaternary amines, such as lauryl tri methyl ammonium chloride; polyethylene glycol esters of fatty acids, such as polyethylene glycol stearate; block copolymers of ethylene oxide and propylene oxide; salts of mono and dialkyl phosphate esters; vegetable oils such as soybean oil, rapeseed/canola oil, olive oil, castor oil, sunflower seed oil, coconut oil, corn oil, cottonseed oil, linseed oil, palm oil, peanut oil, safflower oil, sesame oil, rung oil and the like; and esters of the above vegetable oils, particularly methyl esters.

[0208] In some embodiments, the agricultural compositions comprise wetting agents. A wetting agent is a substance that when added to a liquid increases the spreading or penetration power of the liquid by reducing the interfacial tension between the liquid and the surface on which it is spreading. Wetting agents are used for two main functions in agrochemical formulations: during processing and manufacture to increase the rate of wetting of powders in water to make concentrates for soluble liquids or suspension concentrates; and during mixing of a product with water in a spray tank or other vessel to reduce the wetting time of wettable powders and to improve the penetration of water into water-dispersible granules. In some embodiments, examples of wetting agents used in the agricultural compositions of the present disclosure, including wettable powders, suspension concentrates, and water-dispersible granule formulations are: sodium lauryl sulphate; sodium dioctyl sulphosuccinate; alkyl phenol ethoxylates; and aliphatic alcohol ethoxylates.

[0209] In some embodiments, the agricultural compositions of the present disclosure comprise dispersing agents. A dispersing agent is a substance which adsorbs onto the surface of particles and helps to preserve the state of dispersion of the particles and prevents them from re-aggregating. In some embodiments, dispersing agents are added to agricultural compositions of the present disclosure to facilitate dispersion and suspension during manufacture, and to ensure the particles redisperse into water in a spray tank. In some embodiments, dispersing agents are used in wettable powders, suspension concentrates, and water-dispersible granules. Surfactants that are used as dispersing agents have the ability to adsorb strongly onto a particle surface and provide a charged or steric barrier to re- aggregation of particles. In some embodiments, the most commonly used surfactants are anionic, non-ionic, or mixtures of the two types.

[0210] In some embodiments, for wettable powder formulations, the most common dispersing agents are sodium lignosulphonates. In some embodiments, suspension concentrates provide very good adsorption and stabilization using polyelectrolytes, such as sodium naphthalene sulphonate formaldehyde condensates. In some embodiments, tristyrylphenol ethoxylate phosphate esters are also used. In some embodiments, such as alkylarylethylene oxide condensates and EO-PO block copolymers are sometimes combined with anionics as dispersing agents for suspension concentrates.

[0211] In some embodiments, the agricultural compositions of the present disclosure comprise polymeric surfactants. In some embodiments, the polymeric surfactants have very long hydrophobic 'backbones' and a large number of ethylene oxide chains forming the 'teeth' of a 'comb' surfactant. In some embodiments, these high molecular weight polymers can give very good long-term stability to suspension concentrates, because the hydrophobic backbones have many anchoring points onto the particle surfaces. In some embodiments, examples of dispersing agents used in agricultural compositions of the present disclosure are: sodium lignosulphonates; sodium naphthalene sulphonate formaldehyde condensates; tristyrylphenol ethoxylate phosphate esters; aliphatic alcohol ethoxylat.es; alky et.hoxylat.es; EO-PO block copolymers; and graft copolymers.

[0212] In some embodiments, the agricultural compositions of the present, disclosure comprise emulsifying agents. An emulsifying agent is a substance, which stabilizes a suspension of droplets of one liquid phase in another liquid phase. Without the emulsifying agent the two liquids would separate into two immiscible liquid phases. In some embodiments, the most commonly used emulsifier blends include alkylphenol or aliphatic alcohol with 12 or more ethylene oxide units and the oil-soluble calcium salt of dodecylbenzene sulphonic acid. A range of hydrophile-Iipophile balance ("HLB") values from 8 to 18 will normally provide good stable emulsions. In some embodiments, emulsion stability can sometimes be improved by the addition of a small amount of an EO-PO block copolymer surfactant.

[0213] In some embodiments, the agricultural compositions of the present disclosure comprise soiubilizing agents. A solubilizing agent is a surfactant, which will form micelles in water at concentrations above the critical micelle concentration. The micelles are then able to dissolve or soiubilize water-insoluble materials inside the hydrophobic past of the micelle. The types of surfactants usually used for solubilization are non-ionics: sorbitan monooleates; sorbitan monooleate ethoxyiates; and methyl oleate esters.

[0214] In some embodiments, the agricultural compositions of the present disclosure comprise organic solvents. Organic solvents are used mainly in the formulation of emulsifiabie concentrates, ULV formulations, and to a lesser extent granular formulations. Sometimes mixtures of solvents are used. In some embodiments, the present disclosure teaches the use of solvents including aliphatic paraffmic oils such as kerosene or refined paraffins. In other embodiments, the present disclosure teaches the use of aromatic solvents such as xylene and higher molecular weight fractions of C9 and C IO aromatic solvents. In some embodiments, chlorinated hydrocarbons are useful as co-solvents to prevent crystallization of pesticides when the formulation is emulsified into water. Alcohols are sometimes used as co-solvents to increase solvent power. [0215] In some embodiments, the agricultural compositions comprise gelling agents. Thickeners or gelling agents are used mainly in the formulation of suspension concentrates, emulsions, and suspoemulsions to modify the rheoiogy or flow properties of the liquid and to prevent separation and settling of the dispersed particles or droplets. Thickening, gelling, and anti-settling agents generally fall into two categories, namely water-insoluble particulates and water-soluble polymers. It is possible to produce suspension concentrate formulations using clays and silicas. In some embodiments, the agricultural compositions comprise one or more thickeners including, but not limited to: montmorillonite, e.g. bentonite; magnesium aluminum silicate; and attapulgite. In some embodiments, the present disclosure teaches the use of polysaccharides as thickening agents. The types of polysaccharides most commonly used are natural extracts of seeds and seaweeds or synthetic derivatives of cellulose. Some embodiments utilize xanthan and some embodiments utilize cellulose. In some embodiments, the present disclosure teaches the use of thickening agents including, but are not limited to: guar gum; locust bean gum; carrageenam; alginates; methyl cellulose; sodium carboxymethyl cellulose (SCMC); hydroxyethyl cellulose (HEC). In some embodiments, the present disclosure teaches the use of other types of anti-settling agents such as modified starches, polyacrylates, polyvinyl alcohol, and polyethylene oxide. Another good anti-settling agent is xanthan gum ,

[0216] In some embodiments, the presence of surfactants, which lower mterfaciai tension, can cause water-based formulations to foam during mixing operations in production and in application through a spray tank. Thus, in some embodiments, in order to reduce the tendency to foam, anti-foam agents are often added either during the production stage or before filling into bottles/spray tanks. Generally, there are two types of anti-foam, agents, namely silicones and non-silicones. Silicones are usually aqueous emulsions of dimethyl polysiloxane, while the non-silicone anti-foam agents are water-insoluble oils, such as octanol and nonanol, or silica. In both cases, the function of the anti-foam agent is to displace the surfactant from the air-water interface.

[0217] In some embodiments, the agricultural compositions comprise a preseivative.

[0218] Further, the individual microbes, or microbial consortia, or microbial communities, developed according to the disclosed methods can be combined with known actives available in the agricultural space, such as: pesticide, herbicide, bactericide, fungicide, insecticide, virucide, miticide, nemataicide, acaricide, plant growth regulator, rodenticide, anti-algae agent, biocontrol or beneficial agent. Further, the microbes, microbial consortia, or microbial communities developed according to the disclosed methods can be combined with known fertilizers. Such combinations may exhibit synergistic properties. Further still, the individual microbes, or microbial consortia, or microbial communities, developed according to the disclosed methods can be combined with inert ingredients. Also, in some aspects, the disclosed microbes are combined with biological active agents.

Metabolites Produced by Microbes and Consortia of the Disclosure

[0219] In some cases, the microbes of the present disclosure may produce one or more compounds and/or have one or more activities, e.g., one or more of the following: production of a metabolite, production of a phytohormone such as auxin, production of acetoin, production of an antimicrobial compound, production of a siderophore, production of a ceiiuiase, production of a pectinase, production of a chitinase, production of a xylanase, nitrogen fixation, or mineral phosphate solubilization.

[0220] For example, a microbe of the disclosure may produce a phytohormone selected from the group consisting of an auxin, a cytokinm, a gibberellin, ethylene, a brassinosteroid, and abseisie acid.

[0221 ] Thus, a '"metabolite produced by" a microbe of the disclosure, is intended to capture any molecule (small molecule, vitamin, mineral, protein, nucleic acid, lipid, fat, carbohydrate, etc.) produced by the microbe. Often, the exact mechanism of action, whereby a microbe of the disclosure imparts a beneficial trait upon a given plant species is not known. It is hypothesized, that in some instances, the microbe is producing a metabolite that is beneficial to the plant. Thus, in some aspects, a cell-free or inactivated preparation of microbes is beneficial to a plant, as the microbe does not have to be alive to impart a beneficial trait upon the given plant species, so long as the preparation includes a metabolite that was produced by said microbe and which is beneficial to a plant.

[0222] In one embodiment, the microbes of the disclosure may produce auxin (e.g., indole-3- acetic acid (IAA)). Production of auxin can be assayed. Many of the microbes described herein may be capable of producing the plant hormone auxin indole -3 -acetic acid (IAA) when grown in culture. Auxin plays a key role in altering the physiology of the plant, including the extent of root growth.

[0223] Therefore, in an embodiment, the microbes of the disclosure are present as a population disposed on the surface or within a tissue of a given plant species. The microbes mav produce a metabolite in an amount effective to cause a detectable increase in the amount of metabolite that is found on or within the plant, when compared to a reference plant not treated with the microbes or ceil-free or inactive preparations of the disclosure. The metabolites produced by said microbial population may be beneficial to the plant species.

Plant Growth Regulators and BiostimuSants

[0224] In some embodiments, the agricultural compositions of the present disclosure comprise plant growth regulators and/or biostimulants, used in combination with the taught microbes.

[0225] In some embodiments, the individual microbes, or microbial consortia, or microbial communities, developed according to the disclosed methods can be combined with known plant growth regulators in the agricultural space, such as: auxins, gibberellins, cytokinins, ethylene generators, growth inhibitors, and growth retardants.

[0226] For example, in some embodiments, the present disclosure teaches agricultural compositions comprising one or more of the following active ingredients including: ancymidol, butralin, alcohols, chloromequat chloride, cytokinin, daminozide, ethepohon, flurprimidol, giberrelic acid, gibberellin mixtures, indole-3-butryic acid (IBA), maleic hydrazide, mefludide, mepiquat chloride, mepiquat pentaborate, naphthalene -acetic acid (NAA), 1-napthaleneacetemide, (NAD), n-decanol, placlobutrazol, prohexadione calcium, trinexapac-ethyl, uniconazole, salicylic acid, abscisic acid, ethylene, brassmosteroids, jasmonates, poivamines, nitric oxide, strigolaciones, or karrikms among others.

[0227] In some embodiments, the individual microbes, or microbial consortia, or microbial communities, developed according to the disclosed methods can be combined with seed inoculants known in the agricultural space, such as: QUICKRQQTS ^® , VAULT ⁴ ', RH1ZO- STICK ^® , N ODULATOR ^® , DORMAL ^® , SAB REX ^® , among others. In some embodiments, a Bradyrhizohium inoculant is utilized in combination with any single microbe or microbial consortia disclosed here. In particular aspects, a synergistic effect is observed when one combines one of the aforementioned inoculants, e.g. QUICKROOTS ^® or Brad rhizobium, with a microbe or microbial consortia as taught herein .

[0228] In some embodiments, the agricultural compositions of the present disclosure comprise a plant growth regulator, which contains: kinetin, gibberellic acid, and indole butyric acid, along with copper, manganese, and zinc. [0229] In some aspects, the agricultural compositions comprising microbes of the disclosure (e.g. any microbe or combination thereof from Tables 1-4) and kinetin, gibbereilic acid, and indole butyric acid, along with copper, manganese, and zinc, exhibit the ability to act synergistically together.

[0230] In some embodiments, the present disclosure teaches agricultural compositions comprising one or more commercially available plant growth regulators, including but not limited to: Abide®, A-Rest®, Butralin®, Fair®, Royaltac M®, Sucker-Plucker®, Off- Shoot®, Contact-85®, Citadel®, Cycocel®, E-Pro®, Conkiin®, Culbac®, Cytoplex®, Early Harvest®, Foli-Zyme®, Goldengro®, Happygro®, Incite®, Megagro®, Ascend®, Radiate®, Stimulate®, Suppress®, Validate®, X-Cyte®, B-Nine®, Compress®, Dazide®, Boll Buster®, BoilD®, Cerone®, Cotton Quik®, Ethrel®, Finish®:', Flash®, Hurel « . Mature®, MFX®, Prep®, Proxy®, Quali-Pro®, SA-50®, Setup®, Super Boll®, Whiteout®, Gutless®, Legacy®, Mastiff®, Topflor®, Ascend®, Cytoplex®, Ascend®, Early Harvest®, Falgro®, Florgib®, Foli-Zyme®, GA3®, GibGro®, Green Sol® ⁾ , Incite®, N-Large®, PGR IV®, Pro- Gibfa®, Release® ⁾ , Rouse®, Ryzup®, Stimulate®, BVB®, Chrysal®, Fascination®, Procone®, Fair®, Rite-Hite®, Royal®, Sucker Stuff®, Embark®, Sta-Lo®, Pix®, Pentia®, DipN Grow®, Goldengro® ⁾ , Hi-Yield® ⁾ , Rootone®, Antac®, FST-7®, Royaltac®, Bonzi®, Cambistat®, Cutdown®, Downsize ¹ ®, Florazol®, Paclo®, Paczol®, Piccolo® ⁾¹ , Profile®, Shortstop®, Tnmmit®, Turf Enhancer® ⁾ , Apogee® ⁾ , Armor Tech®, Goldwing®, Governor®, Groom®, Legacy®, Primeraone®, Primo®, Provair®, Solace®, T-Nex®, T-Pac®, Concise®, and Sumagic®.

[0231] In some embodiments, the present invention teaches a synergistic use of the presently disclosed microbes or microbial consortia with plant growth regulators and/or stimulants such as phytohormones or chemicals that influence the production or disruption of plant growth regulators.

[0232] In some embodiments, the present invention teaches that phytohormones can include: Auxins (e.g., Indole acetic acid IAA), Gibberellins, Cytokinins (e.g., Kinetin), Abscisic acid, Ethylene (and its production as regulated by ACC synthase and disrupted by ACC deaminase).

[0233] In some embodiments, the present invention teaches additional plant-growth promoting chemicals that may act in synergy with the microbes and microbial consortia disclosed herein, such as: humic acids, fulvic acids, amino acids, polyphenols and protein hydroly sates.

[0234] In some embodiments, the present disclosure teaches that the individual microbes, or microbial consortia, or microbial communities, developed according to the disclosed methods— including any single microorganism or combination of microorganisms disclosed in Tables 1-4 of the specification— can be combined with Ascend® or other similar plant growth regulators. Ascend® is described as comprising 0.090% cytokinin as kinetin, 0.030% gibberellic acid, 0.045% indole butyric acid, and 99.835% other ingredients.

[0235] Thus, in some embodiments, the disclosure provides for the application of the taught microbes in combination with Ascend® upon any crop. Further, the disclosure provides for the application of the taught microbes in combination with Ascend® upon any crop and utilizing any method or application rate.

[0236] In some embodiments, the present disclosure teaches agricultural compositions with biostimulants.

[0237] As used herein, the term "biostimulant" refers to any substance that acts to stimulate the growth of microorganisms that may be present in soil or other plant growing medium.

[0238] The level of microorganisms in the soil or growing medium is directly correlated to plant health. Microorganisms feed on biodegradable carbon sources, and therefore plant health is also correlated with the quantity of organic matter in the soil. While fertilizers provide nutrients to feed and grow plants, in some embodiments, biostimulants provide biodegradable carbon, e.g., molasses, carbohydrates, e.g., sugars, to feed and grow microorganisms. Unless clearly stated otherwise, a biostimulant may comprise a single ingredient, or a combination of several different ingredients, capable of enhancing microbial activity or plant growth and development, due to the effect of one or more of the ingredients, either acting independently or in combination.

[0239] In some embodiments, biostimulants are compounds that produce non-nutritional plant growth responses. In some embodiments, many important benefits of biostimulants are based on tlieir ability to influence hormonal activity. Hormones in plants (phytohormones) are chemical messengers regulating normal plant development as well as responses to the environment. Root and shoot growth, as well as other growth responses are regulated by phytohormones. In some embodiments, compounds in biostimulants can alter the hormonal status of a plant and exert large influences over its growth and health. Thus, in some embodiments, the present disclosure teaches sea kelp, humic acids, fill vie acids, and B Vitamins as common components of biostimulants. In some embodiments, the biostimulants of the present disclosure enhance antioxidant activity, which increases the plant's defensive system. In some embodiments, vitamin C, vitamin E, and amino acids such as glycine are antioxidants contained in biostimulants.

[0240] In other embodiments, biostimulants may act to stimulate the growth of microorganisms that are present in soil or oilier plant growing medium. Prior studies have shown that when certain biostimulants comprising specific organic seed extracts (e.g., soybean) were used in combination with a microbial inoculant, the biostimulants were capable of stimulating growth of microbes included in the microbial inoculant. Thus, in some embodiments, the present disclosure teaches one or more biostimulants that, when used with a microbial inoculant, is capable of enhancing the population of both native microbes and inoculant microbes. For a review of some popular uses of biostimulants, please see Calvo et al., 2014, Plant Soil 383:3-41.

[0241 ] In some embodiments, the present disclosure teaches that the individual microbes, or microbial consortia, or microbial communities, developed according to the disclosed methods— including any single microorganism or combination of microorganisms disclosed in Tables 1-4 of the specification— can be combined with any plant biostimulant.

[0242] In some embodiments, the present disclosure teaches agricultural compositions comprising one or more commercially available biostimulants, including but not limited to: Vitazyme®, Diehard™ Biorush®, Diehard™ Biorush® Fe, Diehard™ Soluble Kelp, Diehard™ Humate SP, Phocon®, Foliar Plus™, Plant Pius™, Accomplish LM®, Titan®, Soil Builder™, Nutri Life, Soil Solution TM, Seed Coat TM PercPlus TM, Plant Power, CropKarb®, Thrust™, Fast2Grow®, Baccarat®, and Potente® among others.

[0243] In some embodiments, the present disclosure teaches that the individual microbes, or microbial consortia, or microbial communities, developed according to the disclosed methods— including any single microorganism or combination of microorganisms disclosed in Tables 1-4 of the specification— can be combined with ProGibb® or other similar plant growth regulators. ProGibb® is described as comprising 4.0% Gibberellic Acid and 96.00% other ingredients. [0244] In some embodiments, the present disclosure teaches that the individual microbes, or microbial consortia, or microbial communities, developed according to the disclosed methods— including any single microorganism or combination of microorganisms disclosed in Tables 1-4 of the specification— can be combined with Release® or other similar plant growth regulators. Release R is described as comprising 10.0% Gibbereilic Acid and 90.00% other ingredients.

[0245] In some embodiments, the present disclosure teaches that the individual microbes, or microbial consortia, or microbial communities, developed according to the disclosed methods— including any single microorganism or combination of microorganisms disclosed in Tables 1-4 of the specification— can be combined with RyzUp SmartGrass® or other similar plant growth regulators. RyzUp SmartGrass® is described as comprising 40.0% Gibberellin A3 and 60.00% other ingredients.

[0246] In some embodiments, the present disclosure teaches that the individual microbes, or microbial consortia, or microbial communities, developed according to the disclosed methods— including any single microorganism or combination of microorganisms disclosed in Tables 1 -4 of the specification— can be combined with X-CYTE™ or other similar plant growth regulators. X-CYTE™ is described as comprising 0.04% Cytokinin, as kinetin and 99.96% oilier ingredients.

[0247] In some embodiments, the present disclosure teaches that the individual microbes, or microbial consortia, or microbial communities, developed according to the disclosed methods— including any single microorganism or combination of microorganisms disclosed in Tables 1 -4 of the specification— can be combined with N-Large™ or other similar plant growth regulators. N-Large™ is described as comprising 4.0% Gibberellin A ₃ and 96.00% other ingredients.

[0248] In some embodiments, when the microbe or microbial consortia identified according to die taught methods is combined with an active chemical agent one witnesses an additive effect on a plant phenotypic trait of interest. In other embodiments, when the microbe or microbial consortia identified according to the taught methods is combined with an active chemical agent one witness a synergistic effect on a plant phenotypic trait of interest.

[0249] In some embodiments, when the microbe or microbial consortia identified according to the taught methods is combined with a fertilizer one witnesses an additive effect on a plant phenotvpic trait of interest. In other embodiments, when the microbe or microbial consortia identified according to the taught methods is combined with a fertilizer one witness a synerg stic effect on a plant phenotvpic trait of interest.

[0250] In some embodiments, when the microbe or microbial consortia identified according to the taught methods is combined with a plant growth regulator, one witnesses an additive effect on a plant phenotvpic trait of interest. In some embodiments, when the microbe or microbial consortia identified according to the taught methods is combined with a plant growth regulator, one witnesses a synergistic effect. In some aspects, the microbes of the present disclosure are combined with Ascend* ^' and a synergistic effect is observed for one or more phenotvpic traits of interest.

[0251] In some embodiments, when the microbe or microbial consortia identified according to the taught methods is combined with a biostimulant, one witnesses an additive effect on a plant phenotvpic trait of interest. In some embodiments, when the microbe or microbial consortia identified according to the taught methods is combined with a biostimulant, one witnesses a synergistic effect.

[0252] The synergistic effect obtained by the taught methods can be quantified according to Colby's formula (i.e. (E) ~X+Y-(X*Y/100). See Colby, R. S., ' ^" Calculating Synergistic and Antagonistic Responses of Herbicide Combinations," 1967 Weeds, vol. 15, pp. 20-22, incorporated herein by reference in its entirety. Thus, by "synergistic" is intended a component which, by virtue of its presence, increases the desired effect by more than an additive amount.

[0253] The isolated microbes and consortia of the present disclosure can synergistically increase the effectiveness of agricultural active compounds and also agricultural auxiliary compounds.

[0254] In other embodiments, when the microbe or microbial consortia identified according to the taught methods is combined with a fertilizer one witnesses a synergistic effect.

[0255] Furthermore, in certain embodiments, the disclosure utilizes synergistic interactions to define microbial consortia. That is, in certain aspects, the disclosure combines together certain isolated microbial species, which act synergistically, into consortia that impart a beneficial trait upon a plant, or which are correlated with increasing a beneficial plant trait. [0256] The agricultural compositions developed according to the disclosure can be formulated with certain auxiliaries, in order to improve the activity of a known active agricultural compound. This has the advantage that the amounts of active ingredient in the formulation may be reduced while maintaining the efficacy of the active compound, thus allowing costs to be kept as low as possible and any official regulations to be followed. In individual cases, it may also possible to widen the spectrum of action of the active compound since plants, where the treatment with a particular active ingredient without addition was insufficiently successful, can indeed be treated successfully by the addition of certain auxiliaries along with the disclosed microbial isolates and consortia. Moreover, the performance of the active may be increased in individual cases by a suitable formulation when the environmental conditions are not favorable.

[0257] Such auxiliaries that can be used in an agricultural composition can be an adjuvant. Frequently, adjuvants take the form of surface-active or salt-like compounds. Depending on their mode of action, they can roughly be classified as modifiers, activators, fertilizers, pH buffers, and the like. Modifiers affect the wetting, sticking, and spreading properties of a formulation. Activators break up the waxy cuticle of the plant and improve the penetration of the active ingredient into the cuticle, both short-term (over minutes) and long-term (over hours). Fertilizers such as ammonium sulfate, ammonium nitrate or urea improve the absorption and solubility of the active ingredient and may reduce the antagonistic behavior of active ingredients. pH buffers are conventionally used for bringing the formulation to an optimal pH.

[0258] For further embodiments of agricultural compositions of the present disclosure, See "Chemistry and Technology of Agrochemical Formulations," edited by D. A. Knowles, copyright 1998 by Kluwer Academic Publishers, hereby incorporated by reference.

Seed Treatments

[0259] In some embodiments, the present disclosure also concerns the discovery that treating seeds before they are sown or planted with a combination of one or more of the microbes or agricultural compositions of the present disclosure can enhance a desired plant trait, e.g. plant growth, plant health, and/or plant resistance to pests.

[0260] Thus, in some embodiments, the present disclosure teaches the use of one or more of the microbes or microbial consortia as seed treatments. The seed treatment can be a seed coating applied directly to an untreated and "naked" seed. However, the seed treatment can be a seed overcoat that is applied to a seed that has already been coated with one or more previous seed coatings or seed treatments. The previous seed treatments may include one or more active compounds, either chemical or biological, and one or more inert ingredients.

[0261] The term "seed treatment ^" ' generally refers to application of a material to a seed prior to or during the time it is planted in soil . Seed treatment with microbes, and other agricultural compositions of the present disclosure, has the advantages of delivering the treatments to the locus at which the seeds are planted shortly before germination of tl e seed and emergence of a seedling.

[0262] In other embodiments, the present disclosure also teaches that the use of seed treatments minimizes the amount of microbe or agricultural composition that is required to successfully treat the plants, and further limits the amount of contact of workers with the microbes and compositions compared to application techniques such as spraying over soil or over emerging seedlings.

[0263] Moreover, in some embodiments, the present disclosure teaches that the microbes disclosed herein are important for enhancing the early stages of plant life (e.g. , within the first thirty days following emergence of the seedling). Thus, in some embodiments, delivery of the microbes and/or compositions of the present disclosure as a seed treatment places the microbe at the locus of action at a critical time for its activity.

[0264] In some embodiments, the microbial compositions of the present disclosure are formulated as a seed treatment. In some embodiments, it is contemplated that the seeds can be substantially uniformly coated with one or more layers of the microbes and/or agricultural compositions disclosed herein, using conventional methods of mixing, spraying, or a combination thereof through the use of treatment, application equipment that is specifically designed and manufactured to accurately, safely, and efficiently apply seed treatment products to seeds. Such equipment uses various types of coating technology such as rotary coaters, drum coaters, fluidized bed techniques, spouted beds, rotary mists, or a combination thereof. Liquid seed treatments such as those of the present disclosure can be applied via either a spinning "atomizer" disk or a spray nozzle, which evenly distributes the seed treatment onto the seed as it moves though tlie spray pattem. In aspects, the seed is then mixed or tumbled for an additional period of time to achieve additional treatment distri bution a d drying. [0265] The seeds can be primed or unprimed before coating with the microbial compositions to increase the uniformity of germination and emergence. In an alternati ve embodiment, a dry powder formulation can be metered onto the moving seed and allowed to mix until completely distributed.

[0266] In some embodiments, the seeds have at least part of the surface area coated with a microbiological composition, according to the present disclosure. In some embodiments, a seed coat comprising the microbial composition is applied directly to a naked seed. In some embodiments, a seed overcoat comprising the microbial composition is applied to a seed that already has a seed coat applied thereon. In some aspects, the seed may have a seed coat comprising, e.g. clothianidin and/or Bacillus firmusA- \5%2, upon which the present composition will be applied on top of, as a seed overcoat. In some aspects, the taught microbial compositions are applied as a seed overcoat to seeds that have already been treated with PONCHO™ VOTiVO™. In some aspects, the seed may have a seed coat comprising, e.g. Metalaxyl, and/or clothianidin, and/or Bacillus firmus-\-\ 582, upon which the present composition will be applied on top of, as a seed overcoat. In some aspects, the taught microbial compositions are applied as a seed overcoat to seeds that have already been treated with ACCELERON™.

[0267] In some embodiments, the microorganism-treated seeds have a microbial spore concentration, or microbial cell concentration, from about: 10 to 1G' ² , i0 ³ to 10", 10 ³ to l O ¹⁰ , 10 ³ to 10 ⁹ , 10 ³ to 10 ⁸ , 10 ³ to 10 ⁷ , 10 ³ to 10 ⁶ , 10 ³ to 10 ^s , or 10 ³ to 10 ⁴ per seed.

[0268] In some embodiments, the microorganism-treated seeds have a microbial spore concentration, or microbial cell concentration, from about: i0 ⁴ to I 0 ^l2 , 10* to 10 ¹¹ , 10 ⁴ to 10 ¹⁰ , 10 ⁴ to 10 ⁹ , 10 ⁴ to 10 ⁸ , 10 ⁴ to 10 ⁷ , 10 ⁴ to 10 ⁶ , or 10 ⁴ to 10 ^s per seed.

[0269] In some embodiments, the microorganism-treated seeds have a microbial spore concentration, or microbial cell concentration, from about: 10 ⁵ to 10 ^l2 , 10 ⁵ to 10", I 0 ⁵ to 10 ¹⁰ , 10 ⁵ to 10 ⁹ , 10 ⁵ to 10 ⁸ , 10 ⁵ to 10 ⁷ , or 10 ⁵ to 10 ⁶ per seed.

[0270] In some embodiments, the microorganism-treated seeds have a microbial spore concentration, or microbial cell concentration, from about: 10 ⁵ to 10 ⁹ per seed.

[0271] In some embodiments, the microorganism-treated seeds have a microbial spore concentration, or microbial cell concentration, of at least about: 1 χ 10 ^J , or 1 χ I0 ⁴ , or 1 χ 10 ^s , or 1 10 ⁶ , or 1 ^χ 10 ⁷ , or 1 χ 10 ⁸ , or 1 χ 10 ⁹ per seed. [0272] In some embodiments, the amount of one or more of the microbes and/or agricultural compositions applied to the seed depend on the final formulation, as well as size or type of the plant or seed utilized. In some embodiments, one or more of the microbes are present in about 2% w/w/ to about 80% w/w of the entire formulation. In some embodiments, the one or more of the microbes employed in the compositions is about 5% w/w to about 65% w/w, or 10% w/w to about 60% w/w by weight of the entire formulation.

[0273] In some embodiments, the seeds may also have more spores or microbial cells per seed, such as, for example about 10 ² , 10 ³ , 10 , 10 ⁵ , 10 ⁶ , I0 ⁷ , I0 ⁸ , 10 ^" . 10 ¹⁰ , 10 ¹¹ , 10 '. 10 ¹³ , 10 ¹⁴ , 10 ¹⁵ , 10' ⁶ , or 10 ¹ ' spores or cells per seed.

[0274] In some embodiments, the seed coats of the present disclosure can be up to 10um, 20μηι, 30μηι, 40μηι, 50μιη, 60μιη, 70 τη, 80μm, 90μηι, lOOiim, l lOiim, 120ιιηι, Ι30μηι, 140μιη, 150μιη, 160μηι, 170μηι, 180μιη, 190μηι, 200μηι, 210μιη, 220μιη, 230μηι, 240μηι, 250μιη, 260μηι, 270μηι, 280μιη, 290μτη, 3()0μηι, 310μηι, 320μιη, 330μιπι, 340μηι, 350μπι, 360μιη, 370μηι, 380μπι, 390μιη, 400μηι, 410μηι, 420μιη, 430μιη, 440μηι, 450um. 460μιη, 470μηι, 480μηι, 490μιη, 500μηι, 510μηι, 520μιη, 530μιη, 540μηι, 550μηι, 560μιη, 570μηι, 580μηι, 590μηι, 600μιη, 610μηι, 620μηι, 630μηι, 640μπι, 650μηι, 660μηι, 670μηι, 680μπι, 690μηι, 700μηι, 710μτη, 72()μηι, 730μηι, 740μιη, 750μιπι, 760μιηι, 770μηι, 780μιη, 790μιηι,

ΝΟΟμηι. S ί ΐθμιη, 820μιηι, 830μηι, 840μιη _: , 850μιη, 860μηι, 87 Όμηι, 880μ .in, 890μιη , 900μιηι,

910μιη, 920μηι, 930μπι, 940μιη, 950| am, 960μιη, 970μηι, 980μm, 990μιη, ΙΟΟΟμηι,

ΙΟΙΟμιηι, 1020μιη, 1030μηι, 104ί)μτη, 1050μιη, ΙΟόΟμηι, 1070μηι, 1080μτη, 1090μιη,

Ι ΙΟΟμιηι, Ι Ι ΙΟμιη, 1120μπι, Ι 130μηι, 1140μιιη, 1150μιη, 1160μηι, 1 Γ70μιηι, 1180μιη,

1190μηι, 1200μηι, 1210μηι, 1220μηι, 1230μηι, 1240μιη, 1250μm, 1260μιηι, 1270μιη,

1280μηι, 1290μτη, 1300μιη, 13 ΙΟμηι, 1320μηι, 1330 m, 1340μηι, 1350μηι, 1360μιηι,

1370μηι, 1380μηι, 1390μτη, 1400μιη, 1410μηι, 1420μιπι, 1430μιη, 1440μηι, 145ί)μτη,

1460μιη, 1470μηι, 1480μιηι, 1490μιη, 1500μm, 1510μιηι, 1520μιη, 1530μηι, 1540μηι,

1550μιη, 1560μπι, 1570μηι, 1580μιη, 1590μιη, 1600μηι, 1610μηι, 1620μιη, 1630μηι,

1640μηι, 1650μηι, 1660μηι, 1670μιηι, 1680μηι, 1690μηι, ΠΟΟμτη, 1710μιη, 1720μm,

1730μιτη, 1740μιη, 1750μηι, 1760μηι, 1770μιη, 1780μηι, 1790μηι, 1800μτη, 1810μπι,

1820μιηι, 1830μιη, 1840μηι, 1850μηι, 1860 ιιη, 1870μιη, 1880μηι, 1890μιηι, 1900μιη,

19Ι0μηι, 1920μτη, 1930μιη, 1940μιη, 1950μηι, 1960μηι, 1970μηι, 1980μηι, 1990μηι,

2000μιη, 2010μηι, 2020μτη, 2030μιη, 2040μηι, 2050μιτη, 2060μιη, 2070μηι, 208ί)μτη,

2090μιη, 2100μηι, 21 ΙΟμιηι, 2120μιη, 2130μm, 2140μιηι, 2150μιη, 2160μηι, 2Ι70μηι, 2180μιη, 2190μιη, 2200μτη, 2210μιη, 2220μιη, 2230μιτι, 2240μπι, 2250μτη, 2260μιτι,

2270μηι, 2280μιη, 2290μπη, 2300μηι, 2310μιη, 2320μηι, 2330μηι, 2340μηι, 2350μιη,

2360μηι, 2370μηι, 2380μπι, 2390μιη, 2400μηι, 2410μηι, 2420μηι, 2430μτη, 2440μκι,

2450μηι, 2460μτη, 2470μιη, 2480μηι, 2490μηι, 2500μηι, 251 Ομπι, 2520μηι, 2530μιτί,

2540μτη, 2550μπι, 2560μτη, 2570μηι, 2580μηι, 2590μτη, 2600μιη, 26 ΙΟμιτι, 262ί)μϊΤί,

2630μηι, 2640μηι, 2650μηι, 2660μηι, 2670μηι, 2680μηι, 2690μιη, 2700μιτι, 2710μηι,

2720μηι, 2730μηι, 2740μτη, 2750μηι, 2760μιη, 2770μηι, 2780μιη, 2790μπι, 2800μιη,

2810μπϊ, 2820μιη, 2830μιτι, 284ί)μτη, 2850μιη, 2860μτη, 2870μηι, 2880μτη, 2890μιη,

2900μηι, 2910μιη, 2920μΐϊΐ, 2930μηι, 2940μιη, 2950μπι, 2960μηι, 2970μηι, 2980μιη,

2990μηι, or 3000μηι thick.

[0275] In some embodiments, the seed coats of the present disclosure can be 0.5mm, 1mm, 1.5mm, 2mm, 2.5mm, 3mm, 3.5mm, 4mm, 4.5mm, or 5mm thick.

[0276] In some embodiments, the seed coats of the present disclosure can be at least 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%, 10.5%, 1 1%, 11.5%, 12%, 12.5%, 13%, 13.5%, 14%, 14.5%, 15%, 15.5%, 16%, 16,5%, 17%, 17,5%, 18%, 18.5%, 19%, 19.5%, 20%, 20.5%, 21%, 21.5%, 22%, 22.5%, 23%, 23.5%, 24%, 24.5%, 25%, 25.5%, 26%, 26.5%, 27%, 27.5%, 28%, 28.5%, 29%, 29.5%, 30%, 30.5%, 31%, 31.5%, 32%, 32.5%, 33%, 33.5%, 34%, 34.5%, 35%, 35.5%, 36%, 36.5%, 37%, 37,5%, 38%, 38,5%, 39%, 39,5%, 40%, 40.5%, 41%, 41.5%, 42%, 42.5%, 43%, 43.5%, 44%, 44.5%, 45%, 45.5%, 46%, 46.5%, 47%, 47.5%, 48%, 48.5%, 49%, 49.5%, or 50% of the uncoated seed weight.

[0277] In some embodiments, the microbial spores and/or cells can be coated freely onto the seeds or they can be formulated in a liquid or solid composition before being coated onto the seeds. For example, a solid composition comprising the microorganisms can be prepared by mixing a solid carrier with a suspension of the spores until the solid carriers are impregnated with the spore or cell suspension. This mixture can then be dried to obtain the desired particles.

[0278] In some other embodiments, it is contemplated that the solid or liquid microbial compositions of the present disclosure further contain functional agents e.g., activated carbon, nutrients (fertilizers), and other agents capable of improving the germination and quality of the products or a combination thereof. [0279] Seed coating methods and compositions that are known in the art can be particularly useful when they are modified by the addition of one of the embodiments of the present disclosure. Such coating methods and apparatus for their application are disclosed in, for example: U.S. Pat. Nos. 5,916,029; 5,918,413; 5,554,445; 5,389,399; 4,759,945; 4,465,017, and U.S. Pat. App. No. 13/260,310, each of which is incorporated by reference herein.

[0280] Seed coating compositions are disclosed in, for example: U.S. Pat. Nos. 5,939,356; 5,876,739, 5,849,320; 5,791,084, 5,661,103; 5,580,544, 5,328,942; 4,735,015; 4,634,587; 4,372,080, 4,339,456; and 4,245,432, each of which is incorporated by reference herein.

[0281 ] In some embodiments, a variety of additives can be added to the seed treatment formulations comprising the inventive compositions. Binders can be added and include those composed of an adhesive polymer that can be natural or synthetic without phytotoxic effect on the seed to be coated. The binder may be selected from polyvinyl acetates; polyvinyl acetate copolymers; ethylene vinyl acetate (EVA) copolymers; polyvinyl alcohols; polyvinyl alcohol copolymers; celluloses, including ethylceiluioses, methylcelluloses, hydroxymethyl celluloses, hydroxypropylcelluloses and carboxymethylcellulose ; polyvinylpyrolidones; polysaccharides, including starch, modified starch, dextrins, maltodextrins, alginate and chitosans; fats; oils; proteins, including gelatin and zeins; gum arables; shellacs; vmy dene chloride and vmyiidene chloride copolymers; calcium lignosulfonates; acrylic copolymers; polyvinylacryiates; polyethylene oxide; acrylamide polymers and copolymers; polyhydroxy ethyl acrylate, methylacrylamide monomers; and polychioroprene.

[0282] Any of a variety of colorants may be employed, including organic chromophores classified as nitroso; nitro; azo, including monoazo, bisazo and polyazo; acridine, anthraquinone, azine, diphenylmethane, indamine, indophenol, methine, oxazine, phthalocyanine, thiazine, thiazole, triarylmethane, xanthene. Other additives that can be added include trace nutrients such as salts of iron, manganese, boron, copper, cobalt, molybdenum and zinc.

[0283] A polymer or other dust control agent can be applied to retain the treatment on the seed surface.

[0284] In some specific embodiments, in addition to the microbial cells or spores, the coating can further comprise a layer of adherent. The adherent should be non-toxic, biodegradable, and adhesive. Examples of such materials include, but are not limited to, polyvinyl acetates; polyvinyl acetate copolymers; polyvinyl alcohols; polyvinyl alcohol copolymers; celluloses, such as methyl celluloses, hydroxymethyl celluloses, and hydroxymethyl propyl celluloses; dextrins; alginates; sugars; molasses; polyvinyl pyrrolidones; polysaccharides; proteins; fats; oils; gum arables; gelatins; syrups; and starches. More examples can be found in, for example, U.S. Pat. No. 7,213,367, incorporated herein by reference.

[0285] Various additives, such as adherents, dispersants, surfactants, and nutrient and buffer ingredients, can also be included in the seed treatment formulation. Other conventional seed treatment additives include, but are not limited to: coating agents, wetting agents, buffering agents, and polysaccharides. At least one agriculturally acceptable carrier can be added to the seed treatment formulation such as water, solids, or dry powders. The dry powders can be derived from a variety of materials such as calcium carbonate, gypsum, vermiculite, talc, humus, activated charcoal, and various phosphorous compounds.

[0286] In some embodiments, the seed coating composition can comprise at least one filler, which is an organic or inorganic, natural or synthetic component with which the active components are combined to facilitate its application onto the seed, in aspects, the filler is an inert solid such as clays, natural or synthetic silicates, silica, resins, waxes, solid fertilizers (for example ammonium salts), natural soil minerals, such as kaolins, clays, talc, lime, quartz, attapuigite, montmorillonite, bentonite or diatomaceous earths, or synthetic minerals, such as silica, alumina or silicates, in particular aluminium or magnesium silicates.

[0287] In some embodiments, the seed treatment formulation may further include one or more of the following ingredients: other pesticides, including compounds that act only below the ground; fungicides, such as captan, tliiram, metalaxyl, fludioxonil, oxadixyi, and isomers of each of those materials, and the like; herbicides, including compounds selected from glyphosate, carbamates, thiocarbamates, acetamides, triazines, dinitroamiines, glycerol ethers, pyridazinones, uracils, phenoxys, ureas, and benzoic acids; herbicidal safeners such as benzoxazine, benzhydryl derivatives, N,N-diallyl dichloroacetamide, various dihaloacyl, oxazoiidinyl and thiazoiidmyl compounds, ethanone, naphthaiic anhydride compounds, and oxime derivatives; chemicai fertilizers; biological fertilizers; and biocontrol agents such as other naturally -occurring or recombinant bacteria and fungi from the genera Rhizobium, Bacillus, Pseudomonas, Serratia, Trichoderma, Glomus, Gliocladium and mycorrhizal fungi. These ingredients may be added as a separate layer on the seed, or alternatively may be added as part of the seed coating composition of the disclosure.

[0288] In some embodiments, the formulation that is used to treat the seed in the present disclosure can be in the form of a suspension: emulsion; sluny of particles in an aqueous medium (e.g., water); ettable powder; ettable granules (dry flowable); and dry granules. If formulated as a suspension or slurry, the concentration of the active ingredient in the formulation can be about 0.5% to about 99% by weight (w/w), or 5-40%, or as otherwise formulated by those skilled in the art.

[0289] As mentioned above, other conventional inactive or inert ingredients can be incorporated into the formulation. Such inert ingredients include, but are not limited to: conventional sticking agents; dispersing agents such as methylcellulose, for example, serve as combined dispersant/sticking agents for use in seed treatments; polyvinyl alcohol; lecithin, polymeric dispersants (e.g., polyvinylpyrrolidone/vinyl acetate); thickeners (e.g., clay thickeners to improve viscosity and reduce settling of particle suspensions); emulsion stabilizers; surfactants; antifreeze compounds (e.g., urea), dyes, colorants, and the like. Further inert ingredients useful in the present disclosure can be found in McCutcheon's, vol . 1, "Ernulsifiers and Detergents," MC Publishing Company, Glen Rock, N.J., U.S.A., 1996, incorporated by reference herein.

[0290] The seed coating formulations of the present disclosure can be applied to seeds by a variety of methods, including, but not limited to: mixing in a container (e.g., a bottle or bag), mechanical application, tumbling, spraying, and immersion. A variety of active or inert material can be used for contacting seeds with microbial compositions according to the present disclosure.

[0291] In some embodiments, the amount of the microbes or agricultural composition that is used for the treatment of the seed will vary depending upon the type of seed and the type of active ingredients, but the treatment will comprise contacting the seeds with an agriculturally effective amount of the inventive composition.

[0292] As discussed above, an effective amount means that amount of the inventive composition that is sufficient to affect beneficial or desired results. An effective amount can be administered in one or more administrations. [0293] In sorne embodiments, in addition to the coating layer, the seed may be treated with one or more of the following ingredients: other pesticides including fungicides and herbicides; herbicidal safeners; fertilizers and/or biocontrol agents, Tliese ingredients may be added as a separate layer or alternatively may be added in the coating layer.

[0294] In some embodiments, the seed coating formulations of the present disclosure may be applied to the seeds using a variety of techniques and machines, such as ffuidized bed techniques, the roller mill method, rotostatic seed treaters, and drum coaters. Other methods, such as spouted beds may also be useful. The seeds may be pre-sized before coating. After coating, the seeds are typically dried and then transferred to a sizing machine for sizing. Such procedures are known in the art.

[0295] In some embodiments, the microorganism-treated seeds may also be enveloped with a film, overcoating to protect the coating. Such overcoatings are known in the art and may be applied using fiuidized bed and drum film coating techniques.

[0296] In other embodiments of the present disclosure, compositions according to the present disclosure can be introduced onto a seed by use of solid matrix priming. For example, a quantity of an inventive composition can be mixed with a solid matrix material and then the seed can be placed into contact with the solid matrix material for a period to allow the composition to be introduced to the seed. The seed can then optionally be separated from the solid matrix material and stored or used, or the mixture of solid matrix material plus seed can be stored or planted directly. Solid matrix materials which are useful in the present disclosure include poiyacrylamide, starch, clay, silica, alumina, soil, sand, polyurea, polyacrylate, or any other material capable of absorbing or adsorbing the inventive composition for a time and releasing that composition into or onto the seed. It is useful to make sure that the inventive composition and the solid matrix material are compatible with each other. For example, the solid matrix material should be chosen so that it can release the composition at a reasonable rate, for example over a period of minutes, hours, or days.

Microorganisms

[0297] As used herein the term "microorganism" should be taken broadly. It includes, but is not limited to, the two prokaryotic domains, Bacteria and Archaea, as well as eukaryotic fungi and protists. [0298] By way of example, the microorganisms may include: Proteobacteria (such as Pseudomonas, Enterobacter, Stenotrophomonas, Burkholderia. Rhizobium, HerbaspMllum, Pantoea, Serratia, Rahnella, Azospirillum, Azorhizobium, Azotobacter, Duganella, Delftia, Bradyrhizohiun, Sinorhizobium and Halomonas), Firmicutes (such as Bacillus, Paeni bacillus, Lactobacillus, Mycoplasma, and Acetobacterium), Actinobacteria (such as Streptomyces, Rhodococcus, Microhacterium, and Curtobacterium), and the fungi Ascomycota (such as Trichoderma, Ampelomyces, Coniothyrium, Paecoelomyces, Penicillium, Cladosporium, Hypocrea, Beauveria, Metarhizium, Ver!icu!lium, Cordyceps, Pichea, and Candida, Basidiomycota (such as Coprinus, Corticium, and Agaricus) and Oomycota (such as Pythium, Mucor, and Mortierella) ,

[0299] In a particular embodiment, the microorganism is an endophyte, or an epiphyte, or a microorganism inhabiting the plant rhizosphere or rhizosheath. That is, the microorganism may be found present in the soil material adhered to the roots of a plant or in the area immediately adjacent a plant's roots. In one embodiment, the microorganism is a seed-borae endophyte.

[0300] Endophytes may benefit host plants by preventing pathogenic organisms from colonizing them. Extensive colonization of the plant tissue by endophytes creates a "barrier effect," where the local endophytes outcompete and prevent pathogenic organisms from taking hold. Endophytes may also produce chemicals which inhibit the growth of competitors, including pathogenic organisms.

[0301] In certain embodiments, the microorganism is unculturable. This should be taken to mean that the microorganism is not known to be culturable or is difficult to culture using methods known to one skilled in the art.

[0302] Microorganisms of the present disclosure may be collected or obtained from any source or contained within and/or associated with material collected from any source.

[0303] In an embodiment, the microorganisms are obtained from any general terrestrial environment, including its soils, plants, fungi, animals (including invertebrates) and other biota, including the sediments, water and biota of lakes and rivers; from the marine environment, its biota and sediments (for example sea water, marine muds, marine plants, marine invertebrates (for example sponges), marine vertebrates (for example, fish)); the terrestrial and marine geosphere (regolith and rock, for example crushed subterranean rocks, sand and clays); the cryosphere and its meltwater; the atmosphere (for example, filtered aerial dusts, cloud and rain droplets); urban, industrial and other man-made environments (for example, accumulated organic and mineral matter on concrete, roadside gutters, roof surfaces, road surfaces),

[0304] In another embodiment the microorganisms are collected from a source likely to favor the selection of appropriate microorganisms. By way of example, the source may be a particular environment in which it is desirable for other plants to grow, or which is thought to be associated with terroir. In another example, the source may be a plant having one or more desirable traits, for example a plant which naturally grows in a particular environment or under certain conditions of interest. By way of example, a certain plant may naturally grow in sandy soil or sand of high salinity, or under extreme temperatures, or with little water, or it may be resistant to certain pests or disease present in the environment, and it may be desirable for a commercial crop to be grown in such conditions, particularly if they are, for example, the only conditions available in a particular geographic location . By way of further example, the microorganisms may be collected from commercial crops grown in such environments, or more specifically from individual crop plants best displaying a trait of interest amongst a crop grown in any specific environment, for example the fastest-growing plants amongst a crop grown in saline-limiting soils, or the least damaged plants in crops exposed to severe insect damage or disease epidemic, or plants having desired quantities of certain metabolites and other compounds, including fiber content, oil content, and the like, or plants displaying desirable colors, taste, or smell. The microorganisms may be collected from a plant of interest or any material occurring in the environment of interest, including fungi and other animal and plant biota, soil, water, sediments, and other elements of the environment as referred to previously. In certain embodiments, the microorganisms are individual isolates separated from different environments.

[0305] In one embodiment, a microorganism or a combination of microorganisms, of use in the methods of the disclosure may be selected from a pre-existing collection of individual microbial species or strains based on some knowledge of their likely or predicted benefit to a plant. For example, the microorganism may be predicted to: improve nitrogen fixation; release phosphate from the soil organic matter; release phosphate from the inorganic forms of phosphate (e.g. rock phosphate); "fix carbon" in the root microsphere; live in the rhizosphere of the plant thereby assisting the plant in absorbing nutrients from the surrounding soil and then providing these more readily to the plant; increase the number of nodules on the plant roots and thereby increase the number of symbiotic nitrogen fixing bacteria (e.g. Rhizobium species) per plant and the amount of nitrogen fixed by the plant; elicit plant defensive responses such as ISR (induced systemic resistance) or SAR (systemic acquired resistance) which help the plant resist the invasion and spread of pathogenic microorganisms; compete with microorganisms deleterious to plant growth or health by antagonism, or competitive utilization of resources such as nutrients or space; change the color of one or more part of the plant, or change the chemical profile of the plant, its smell, taste or one or more other quality.

[0306] In one embodiment a microorganism or combination of microorganisms is selected from a pre-existing collection of individual microbial species or strains that provides no knowledge of their likely or predicted benefit to a plant. For example, a collection of unidentified microorganisms isolated from plant tissues without any knowledge of their ability to improve plant growth or health, or a collection of microorganisms collected to explore their potential for producing compounds that could lead to the development of pharmaceutical drugs.

[0307] In one embodiment, the microorganisms are acquired from the source material (for example, soil, rock, water, air, dust, plant or other organism) in which they naturally reside. The microorganisms may be provided in any appropriate form, having regard to its intended use in the methods of the disclosure. However, by way of example only, the microorganisms may be provided as an aqueous suspension, gel, homogenate, granule, powder, slurry, live organism or dried material.

[0308] The microorganisms of the disclosure may be isolated in substantially pure or mixed cultures. They may be concentrated, diluted, or provided in the natural concentrations in which they are found in the source material. For example, microorganisms from saline sediments may be isolated for use in this disclosure by suspending the sediment in fresh water and allowing the sediment to fall to the bottom. The water containing the bulk of the microorganisms may be removed by decantation after a suitable period of settling and either applied directly to the plant growth medium, or concentrated by filtering or centnfugation, diluted to an appropriate concentration and applied to the plant growth medium with the bulk of the salt removed. By way of further example, microorganisms from mineralized or toxic sources may be similarly treated to recover the microbes for application to the plant growth material to minimize the potential for damage to the plant. [0309] In another embodiment, the microorganisms are used in a cmde form, in which they are not isolated from the source material in which they naturally reside. For example, the microorganisms are provided in combination with the source material in which they reside; for example, as soil, or the roots, seed or foliage of a plant. In this embodiment, the source material may include one or more species of microorganisms.

[0310] In some embodiments, a mixed population of microorganisms is used in the methods of the disclosure.

[0311] In embodiments of the disclosure where the microorganisms are isolated from a source material (for example, the material in which they naturally reside), any one or a combination of a number of standard techniques which will be readily known to skilled persons may be used. However, by way of example, these in general employ processes by which a solid or liquid culture of a single microorganism can be obtained in a substantially pure form, usually by physical separation on the surface of a solid microbial growth medium or by volumetric dilutive isolation into a liquid microbial growth medium. These processes may include isolation from dry material, liquid suspension, slurries or homogenates in which the material is spread in a thin layer over an appropriate solid gel growth medium, or serial dilutions of the material made into a sterile medium and inoculated into liquid or solid culture media.

[0312] Whilst not essential, in one embodiment, the material containing the microorganisms may be pre-treated prior to the isolation process in order to either multiply all microorganisms in the material, or select portions of the microbial population, either by enriching the material with microbial nutrients (for example, by pasteurizing the sample to select for microorganisms resistant to heat exposure (for example, bacilli), or by exposing the sample to low concentrations of an organic solvent or sterilant (for example, household bleach) to enhance the survival of spore-forming or solvent-resistant microorganisms). Microorganisms can then be isolated from the enriched materials or materials treated for selective survival, as above.

[0313] In an embodiment of the disclosure, endophytic or epiphytic microorganisms are isolated from plant material. Any number of standard techniques known in the art may be used and the microorganisms may be isolated from any appropriate tissue in the plant, including for example root, stem and leaves, and plant reproductive tissues. By way of example, conventional methods for isolation from plants typically include the sterile excision of the plant material of interest (e.g. root or stem lengths, leaves), surface sterilization with an appropriate solution (e.g. 2% sodium hypochlorite), after which the plant material is placed on nutrient medium for microbial growth (See, for example, Strobel G and Daisy B (2003) Microbiology and Molecular Biology Reviews 67 (4): 491-502; Zinniel DK et a/. (2002) Applied and Environmental Microbiology 68 (5): 2198-2208).

[0314] In one embodiment of the disclosure, the microorganisms are isolated from root tissue. Further methodology for isolating microorganisms from plant material are detailed hereinafter.

[0315] In one embodiment, the microbial population is exposed (prior to the method or at any stage of the method) to a selective pressure. For example, exposure of the microorganisms to pasteurisation before their addition to a plant growth medium (preferably sterile) is likely to enhance the probability that the plants selected for a desired trait will be associated with spore-fonning microbes that can more easily survive in adverse conditions, in commercial storage, or if applied to seed as a coating, in an adverse environment.

[0316] In certain embodiments, as mentioned herein before, the microorganism(s) may be used in crude form and need not be isolated from a plant or a media. For example, plant material or growth media which includes the microorganisms identified to be of benefit to a selected plant may be obtained and used as a crude source of microorganisms for the next round of the method or as a crude source of microorganisms at the conclusion of the method. For example, whole plant material could be obtained and optionally processed, such as mulched or crashed. Alternatively, individual tissues or parts of selected plants (such as leaves, stems, roots, and seeds) may be separated from the plant and optionally processed, such as mulched or crashed. In certain embodiments, one or more part of a plant which is associated with the second set of one or more microorganisms may be removed from one or more selected plants and, where any successive repeat of the method is to be conducted, grafted on to one or more plant used in any step of the plant breeding methods.

Plants Thai Are Able to Benefit from the Application of the Disclosed Microbes, Consortia, and Compositions Comprising the Same

[0317] Any number of a variety of different plants, including mosses and lichens and algae, may be used in the methods of the disclosure. In embodiments, the plants have economic, social, or environmental value. For example, the plants may include those used as: food crops, fiber crops, oil crops, in the forestry industry, in the pulp and paper industry, as a feedstock for biofuel production, and as ornamental plants.

[0318] In other embodiments, the plants may be economically, socially, or environmentally undesirable, such as weeds. The following is a list of non-limiting examples of the types of plants the methods of the disclosure may be applied to:

Food crops:

[0319] Cereals e.g maize, rice, wheat, barley, sorghum, millet, oats, rye, triticale, and buckwheat;

[0320] Leafy vegetables e.g, brassicaceous plants such as cabbages, broccoli, bok choy, rocket: salad greens such as spinach, cress, and lettuce;

[0321] Fruiting and flowering vegetables e.g. avocado, sweet com, artichokes; curcubits e.g. squash, cucumbers, melons, courgettes, pumpkins; solanaceous vegetables/fruits e.g. tomatoes, eggplant, and capsicums;

[0322] Podded vegetables e.g. groundnuts, peanuts, peas, soybeans, beans, lentils, chickpea, okra;

[0323] Bulbed and stem vegetables e.g. asparagus, celery, Allium crops e.g garlic, onions, and leeks;

[0324] Roots and tuberous vegetables e.g. carrots, beet, bamboo shoots, cassava, yams, ginger, Jerusalem artichoke, parsnips, radishes, potatoes, sweet potatoes, taro, turnip, and wasabi;

[0325] Sugar crops including sugar beet {Beta vulgaris), sugar cane (Saccharum officinarum);

[0326] Crops grown for the production of non-alcoholic beverages and stimulants e.g. coffee, black, herbal, and green teas, cocoa, marijuana, and tobacco;

[0327] Fruit crops such as true berry fruits (e.g. kiwifruit, grape, currants, gooseberry, guava, feijoa, pomegranate), citms fruits (e.g. oranges, lemons, limes, grapefruit), epigynous fmits (e.g. bananas, cranberries, blueberries), aggregate fruit (blackberry, raspberry, boysenberry), multiple fruits (e.g. pineapple, fig), stone fruit crops (e.g. apricot, peach, cherry, plum), pip- fruit (e.g. apples, pears) and others such as strawberries, sunflower seeds; [0328] Culinary and medicinal herbs e.g. rosemary, basil, bay laurel, coriander, mint, dill, Hypericum, foxglove, alovera, rosehips, and cannabis;

[0329] Crop plants producing spices e.g. black pepper, cumin cinnamon, nutmeg, ginger, cloves, saffron, cardamom, mace, paprika, rnasalas, star anise;

[0330] Crops grown for the production of nuts e.g. almonds and walnuts, Brazil nut, cashew nuts, coconuts, chestnut, macadamia nut, pistachio nuts; peanuts, pecan nuts;

[0331] Crops grown for production of beers, wines and other alcohoiic beverages e.g grapes, and hops;

[0332] Oilseed crops e.g. soybean, peanuts, cotton, olives, sunflower, sesame, lupin species and brassicaeous crops (e.g. canola/oilseed rape); and, edible fungi e.g. white mushrooms, Shiitake and oyster mushrooms;

Plants used m pastoral agriculture:

[0333] Legumes: Trifblium species, Medicago species, and Lotus species; White clover (T.repens); Red clover (T. pratense); Caucasian clover (T. ambigum); subterranean clover (T.subterraneum); Alfalfa/Lucerne (Medicago sativum); annual medics; barrel medic; black medic; Sainfoin (Onobrychis viciifolia); Birdsfoot trefoil (Lotus corniculatus); Greater Birdsfoot trefoil (Lotus pedunculatus);

[0334] Seed legumes/pulses including Peas (Pisum sativum), Common bean (Phaseolus vulgaris), Broad beans (Vicia faba), Mung bean ( Vigna radiata), Cowpea (Vigna unguiculata), Chick pea (Cicer arietum), Lupins {Lupinus species); Cereals including Maize/com (Zea mays), Sorghum (Sorghum spp.), Millet (Panicum miliaceum, P. sumatrense). Rice (Oryza sativa indica, Oryza sativa japonica). Wheat (Triticum sativa). Barley (Hordeum vulgare), Rye (Secale cereale), Triticale (Triticum X Secale), Oats (Averia sativa);

[0335] Forage and Amenity grasses: Temperate grasses such as Lolium species; Festuca species; Agrostis spp., Perennial ryegrass (Lolium perenne); hybrid ryegrass (Lolium hybridum); annual ryegrass (Lolium multiflorum), tall fescue (Festuca arundinacea); meadow fescue (Festuca pratensis); red fescue (Festuca rubra); Festuca ovina; Festuioliums (Lolium

X Festuca crosses); Cocksfoot (Dactylis glome rata); Kentucky bluegrass Poa pratensis; Poa palustris; Poa nemoralis; Poa trivialis; Poa compresa; Bromus species; Phalaris (Phleu species); Arrhenaiherum elatius; Agropyron species; Avena strigosa; Setaria italic; [0336] Tropical grasses such as: Phalaris species: Brachiaria species; Eragrosiis species; Pamcum species; Bahai grass (Paspalum notatum); Brachypodium species; and, grasses used for biofuel production such as Switchgrass (Pamcum virgatum) and Miscanthus species;

Fiber crops:

[0337] Cotton, hemp, jute, coconut, sisal, flax (Linum spp.), New Zealand flax (Phormium spp.); plantation and natural forest species harvested for paper and engineered wood fiber products such as coniferous and broadieafed forest species;

Tree and shrub species used in plantation forestry and bio-foel crops:

[0338] Pine (Finns species); Fir (Pseudotsuga species); Spruce (Picea species); Cypress (Cupressus species); Wattle (Acacia species); Alder (Alnus species); Oak species (Quercus species); Redwood (Sequoiadendron species); willow (Salix species); birch (Betula species); Cedar (Cedurus species); Ash (Fraxinus species); Larch (Larix species); Eucalyptus species; Bamboo (Bambuseae species) and Poplars (Populus species).

Plants grown for conversion to energy, biofuels or industrial products by extractive, biological, physical or biochemical treatment:

[0339] Oil-producing plants such as oil palm, jatropha, soybean, cotton, linseed; Latex- producing plants such as the Para Rubber tree, Hevea brasiliensis and the Panama Rubber Tree Castilla elastica; plants used as direct or indirect feedstocks for the production of biofuels i.e. after chemical, physical (e.g. thermal or catalytic) or biochemical (e.g. enzymatic pre -treatment) or biological (e.g. microbial fermentation) transformation during the production of biofuels, industrial solvents or chemical products e.g. ethanol or butanol, propane dials, or other fuel or industrial material including sugar crops (e.g. beet, sugar cane), starch producing crops (e.g. C3 and C4 cereal crops and tuberous crops), celluiosic crops such as forest trees (e.g. Pines, Eucalypts) and Graminaceous and Poaceous plants such as bamboo, switch grass, miscanthus; crops used in energy, biofuel or industrial chemical production via gasification and/or microbial or catalytic conversion of the gas to biofuels or other industrial raw materials such as solvents or plastics, with or without the production of biochar (e.g. biomass crops such as coniferous, eucalypt, tropical or broadleaf forest trees, graminaceous and poaceous crops such as bamboo, switch grass, miscanthus, sugar cane, or hemp or softwoods such as poplars, willows; and, biomass crops used in the production of biochar; Crops producing natural products useful for the pharmaceutical. Agricultural nutraceutical and cosmeceutical industries:

[0340] Crops producing pharmaceutical precursors or compounds or nutraceutical and cosmeceutical compounds and materials for example, star anise (shikimic acid), Japanese knotweed (resveratroi), kiwifruit (soluble fiber, proteolytic enzymes):

Floricultural, Ornamental and Amenity plants grown for their aesthetic or environmental properties:

[0341] Flowers such as roses, tulips, chrysanthemums;

[0342] Ornamental shrubs such as Buxus, Hebe, Rosa, Rhododendron, Hedera

[0343] Amenity plants such as Piatanus, Choisya, Escallonia, Euphorbia, Carex

[0344] Mosses such as sphagnum moss

Plants grown for bioremediation:

[0345] Helianthus, Brassica, Salix, Populus, Eucalyptus

Hybrid and GM Plant Improvement

[0346] In certain aspects, the microbes of the present disclosure are applied to hybrid plants to increase beneficial traits of said hybrids. In other aspects, tlie microbes of tlie present disclosure are applied to genetically modified plants to increase beneficial traits of said GM plants. The microbes taught herein are able to be applied to hybrids and GM plants and thus maximize the elite genetics and trait technologies of these plants.

[0347] It should be appreciated that a plant may be provided in the form of a seed, seedling, cutting, propagule, or any other plant material or tissue capable of growing. In one embodiment the seed may be surface-sterilised with a material such as sodium hypochlorite or mercuric chloride to remove surface-contaminating microorganisms. In one embodiment, the propagule is grown in axenic culture before being placed in the plant growth medium, for example as sterile plantlets in tissue culture.

Methods of Application

[0348] The microorganisms may be applied to a plant, seedling, cutting, propagule, or the like and/or the growth medium, containing said plant, using any appropriate technique k now n in the art. [0349] However, by way of example, an isolated microbe, consortia, or composition comprising the same may be applied to a plant, seedling, cutting, propagule, or the like, by spraying or dusting.

[0350] In another embodiment, the isolated microbe, consortia, or composition comprising the same may applied directly to a plant seed prior to sowing.

[0351] In another embodiment, the isolated microbe, consortia, or composition comprising the same may applied directly to a plant seed, as a seed coating.

[0352] In one embodiment of the present disclosure, the isolated microbe, consortia, or composition comprising the same is supplied in the form of granules, or plug, or soil drench that is applied to the plant growth media.

[0353] In other embodiments, the the isolated microbe, consortia, or composition comprising the same are supplied in the form of a foliar application, such as a foliar spray or liquid composition. The foliar spray or liquid application may be applied to a growing plant or to a growth media, e.g. soil.

[0354] In another embodiment, the isolated microbe, consortia, or composition comprising the same may be formulated into granules and applied alongside seeds during planting. Or the granules may be applied after planting. Or the granules may be applied before planting.

[0355] In some embodiments, the isolated microbe, consortia, or composition comprising the same are administered to a plant or growth media as a topical application and/or drench application to improve crop growth, yield, and quality. The topical application may be via utilization of a dry mix or powder or dusting composition or may be a liquid based formulation.

[0356] In embodiments, the the isolated microbe, consortia, or composition comprising the same can be formulated as: (1) solutions; (2) wettable powders; (3) dusting powders; (4) soluble powders; (5) emulsions or suspension concentrates; (6) seed dressings or coatings, (7) tablets; (8) water-dispersible granules; (9) water soluble granules (slow or fast release); (10) microencapsulated granules or suspensions; and (11) as irrigation components, among others. In in certain aspects, the compositions may be diluted in an aqueous medium prior to conventional spray application. The compositions of the present disclosure can be applied to the soil, plant, seed, rhizosphere, rhizosheath, or other area to which it would be beneficial to apply the microbial compositions. Further still, ballistic methods can be utilized as a means for introducing endophytic microbes.

[0357] In aspects, the compositions are applied to the foliage of plants. The compositions may be applied to the foliage of plants in the form of an emulsion or suspension concentrate, liquid solution, or foliar spray. The application of the compositions may occur in a laboratory, growth chamber, greenhouse, or in the field.

[0358] In another embodiment, microorganisms may be inoculated into a plant by cutting the roots or stems and exposing the plant surface to the microorganisms by spraying, dipping, or otherwise applying a liquid microbial suspension, or gel, or powder.

[0359] In another embodiment, the microorganisms may be injected directly into foliar or root tissue, or otherwise inoculated directly into or onto a foliar or root cut, or else into an excised embryo, or radicle, or coleoptile. These inoculated plants may then be further exposed to a growth media containing further microorganisms; however, this is not necessary.

[0360] In other embodiments, particularly where the microorganisms are unculturable, the microorganisms may be transferred to a plant by any one or a combination of grafting, insertion of explants, aspiration, electroporation, wounding, root pruning, induction of stomatal opening, or any physical, chemical or biological treatment that provides the opportunity for microbes to enter plant cells or the intercellular space. Persons of skill in the art may readily appreciate a number of alternative techniques that may be used.

[0361] In one embodiment, the microorganisms infiltrate parts of the plant such as the roots, stems, leaves and/or reproductive plant parts (become endophytic), and/or grow upon the surface of roots, stems, leaves and/or reproductive plant parts (become epiphytic) and/or grow in the plant rhizosphere. In one embodiment, the microorganisms form a symbiotic relationship with the plant.

EXAMPLES

I. Increased Yield in Agriculturally Important Crops

[0362] In certain embodiments of the disclosure, the present methods aim to increase yields for a given crop. [0363] The methodologies presented herein— based upon utilizing the disclosed isolated microbes, consortia, and compositions comprising the same— have the potential to increase the yield of important agricultural crops. These yield increases can be realized without the need for further fertilizer addition.

Example 1: Increasing Ryegrass Biomass with Isolated Microbes and Microbiai

Consortia

A. Seed Treatment with Isolated Microbe

[0364] In this example, an isolated microbe from Tables 1-4 will be applied as a seed coating to seeds of ryegrass (Lolium perenne). Upon applying the isolated microbe as a seed coating, the ryegrass will be planted and cultivated in the standard manner.

[0365] A control plot of ryegrass seeds, which did not have the isolated microbe applied as a seed coating, will also be planted.

[0366] It is expected that the ryegrass plants grown from the seeds treated with the seed coating will exhibit a quantiflably higher biomass than the control ryegrass plants.

[0367] The biomass from the treated plants may be about 1 -10% higher, 10-20% higher, 20- 30% higher, 30-40% higher, 40-50% higher, 50-60% higher, 60-70% higher, 70-80% higher, 80-90% higher, or more.

[0368] The biomass from the treated plants may equate to about a 1 bushel per acre increase over the controls, or a 2 bushel per acre increase, or a 3 bushel per acre increase, or a 4 bushel per acre increase, or a 5 bushel per acre increase, or more.

[0369] In some aspects, the biomass increase is statistically significant. In other aspects, the biomass increase is not statistically significant, but is still quantifiable.

B, Seed Treatment with Microbial Consortia

[0370] In this example, a microbial consortium, comprising at least two microbes from Tables 1 -4 will be applied as a seed coating to seeds of ryegrass (Lolium perenne). Upon applying the microbial consortium as a seed coating, the ryegrass will be planted and cultivated in the standard manner.

[0371] A con trol plot of ryegrass seeds, which did not have the microbial consortium applied as a seed coating, will also be planted. [0372] It is expected that the ryegrass plants grown from the seeds treated with the seed coating will exhibit a quantifiably higher biomass than the control ryegrass plants.

[0373] The biomass from the treated plants may be about 1 -10% higher, 10-20% higher, 20- 30% higher, 30-40% higher, 40-50% higher, 50-60% higher, 60-70% higher, 70-80% higher, 80-90% higher, or more.

[0374] The biomass from the treated plants may equate to about a 1 bushel per acre increase over the controls, or a 2 bushel per acre increase, or a 3 bushel per acre increase, or a 4 bushel per acre increase, or a 5 bushel per acre increase, or more.

[0375] In some aspects, the biomass increase is statistically significant. In other aspects, the biomass increase is not statistically significant, but is still quantifiable.

C. Treatment with Agricultural Composition Comprisin Isolated Microbe

[0376] In this example, an isolated microbe from Tables 1-4 will be applied as an agricultural composition, administered to the ryegrass seed at the time of sowing.

[0377] For example, it is anticipated that a farmer will apply the agricultural composition to the ryegrass seeds simultaneously upon broadcasting said seeds into the field. This can be accomplished, for example, by applying the agricultural composition to a hopper or spreader, which contains the ryegrass seeds and which is configured to broadcast the same.

[0378] A control plot of ryegrass seeds, which are not administered the agricultural composition, will also be planted.

[0379] it is expected that the ryegrass plants grown from the seeds treated with the agricultural composition will exhibit a quantifiably higher biomass than the control ryegrass plants.

[0380] The biomass from the treated plants may be about 1 -10% higher, 10-20% higher, 20- 30% higher, 30-40% higher, 40-50% higher, 50-60% higher, 60-70% higher, 70-80% higher, 80-90% higher, or more.

[0381] The biomass from the treated plants may equate to about a 1 bushel per acre increase over the controls, or a 2 bushel per acre increase, or a 3 bushel per acre increase, or a 4 bushel per acre increase, or a 5 bushel per acre increase, or more.

[0382] In some aspects, the biomass increase is statistically significant. In other aspects, the biomass increase is not statistically significant, but is still quantifiable. D. Treatment with Agricultural Composition Comprising Microbial Consortia

[0383] In this example, a microbial consortium, comprising at least two microbes from Tables 1-4 will be applied as an agricultural composition, administered to the ryegrass seed at the time of sowing.

[0384] For example, it is anticipated that a farmer will apply the agricultural composition to the ryegrass seeds simultaneously upon broadcasting said seeds into the field. This can be accomplished, for example, by applying the agricultural composition to a hopper or spreader, which contains the ryegrass seeds and which is configured to broadcast the same.

[0385] A control plot of ryegrass seeds, which are not administered the agricultural composition, will also be planted.

[0386] It is expected that the ryegrass plants grown from the seeds treated with the agricultural composition will exhibit a quantitiabiy higher biomass than the control ryegrass plants.

[0387] The biomass from the treated plants may be about 1 -10% higher, 10-20% higher, 20- 30% higher, 30-40% higher, 40-50% higher, 50-60% higher, 60-70% higher, 70-80% higher, 80-90% higher, or more.

[0388] The biomass from the treated plants may equate to about a 1 bushel per acre increase over the controls, or a 2 bushel per acre increase, or a 3 bushel per acre increase, or a 4 bushel per acre increase, or a 5 bushel per acre increase, or more.

[0389] In some aspects, the biomass increase is statistically significant. In other aspects, the biomass increase is not statistically significant, but is still quantifiable.

Example 2: Increasing Maize Biomass with Isolated Microbes and Microbial

Consortia

A. Seed Treatment with Isolated Microbe

[0390] In this example, an isolated microbe from Tables 1-4 will be applied as a seed coating to seeds of com (Zea mays). Upon applying the isolated microbe as a seed coating, the com will be planted and cultivated in the standard manner.

[0391] A control plot of corn seeds, which did not have the isolated microbe applied as a seed coating, will also be planted. [0392] It is expected that the corn plants grown from the seeds treated with the seed coating will exhibit a quantifiably higher biomass than the control corn plants.

[0393] The biomass from the treated plants may be about 1 -10% higher, 10-20% higher, 20- 30% higher, 30-40% higher, 40-50% higher, 50-60% higher, 60-70% higher, 70-80% higher, 80-90% higher, or more.

[0394] The biomass from the treated plants may equate to about a 1 bushel per acre increase over the controls, or a 2 bushel per acre increase, or a 3 bushel per acre increase, or a 4 bushel per acre increase, or a 5 bushel per acre increase, or more.

[0395] In some aspects, the biomass increase is statistically significant. In other aspects, the biomass increase is not statistically significant, but is still quantifiable.

B, Seed Treatment with Microbial Consortia

[0396] In this example, a microbial consortium, comprising at least two microbes from Tables 1-4 will be applied as a seed coating to seeds of com (Zea mays). Upon applying the microbial consortium as a seed coating, the corn will be planted and cultivated in the standard manner.

[0397] A control plot of corn seeds, which did not have the microbial consortium applied as a seed coating, will also be planted.

[0398] It is expected that the com plants grown from the seeds treated with the seed coating will exhibit a quantifiably higher biomass than the control com plants.

[0399] The biomass from the treated plants may be about 1-10% higher, 10-20% higher, 20- 30% higher, 30-40% higher, 40-50% higher, 50-60% higher, 60-70% higher, 70-80% higher, 80-90% higher, or more.

[0400] The biomass from the treated plants may equate to about a 1 bushel per acre increase over the controls, or a 2 bushel per acre increase, or a 3 bushel per acre increase, or a 4 bushel per acre increase, or a 5 bushel per acre increase, or more.

[0401] In some aspects, the biomass increase is statistically significant. In other aspects, the biomass increase is not statistically significant, but is still quantifiable. C. Treatment with Agricultural Composition Comprising Isolated Microbe

[0402] In this example, an isolated microbe from Tables 1-4 will be applied as an agricultural composition, administered to the com seed at the time of sowing.

[0403] For example, it is anticipated that a fanner will apply the agricultural composition to the com seeds simultaneously upon planting the seeds into the field. This can be accomplished, for example, by applying the agricultural composition to a hopper/bulk tank on a standard 16 row planter, which contains the com seeds and which is configured to plant the same into rows. Alternatively, the agricultural composition can be contained in a separate bulk tank on the planter and sprayed into the rows upon planting the com seed.

[0404] A control plot of corn seeds, winch are not administered the agricultural composition, will also be planted.

[0405] It is expected that the corn plants grown from the seeds treated with the agricultural composition will exhibit a quantifiah!y higher biomass than the control corn plants.

[0406] The biomass from the treated plants may be about 1 -10% higher, 10-20% higher, 20- 30% higher, 30-40% higher, 40-50% higher, 50-60% higher, 60-70% higher, 70-80% higher, 80-90% higher, or more.

[0407] The biomass from the treated plants may equate to about a 1 bushel per acre increase over the controls, or a 2 bushel per acre increase, or a 3 bushel per acre increase, or a 4 bushel per acre increase, or a 5 bushel per acre increase, or more.

[0408] In some aspects, the biomass increase is statistically significant. In other aspects, the biomass increase is not statistically significant, but is still quantifiable.

D. Treatment with Agricultural Composition Comprising Microbial Consortia

[0409] In this example, a microbial consortium, comprising at least two microbes from Tables 1-4 will be applied as an agricultural composition, administered to the corn seed at the time of sowing.

[0410] For example, it is anticipated that a farmer will apply the agricultural composition to the com seeds simultaneously upon planting the seeds into the field. This can be accomplished, for example, by applying the agricultural composition to a hopper/bulk tank on a standard 16 row planter, which contains the com seeds and which is configured to plant the same into rows. Alternatively, the agricultural composition can be contained in a separate bulk tank on the planter and sprayed into the rows upon planting the corn seed.

[041.1] A control plot of corn seeds, which are not administered the agricultural composition, will also be planted.

[0412] It is expected that the corn plants grown from the seeds treated with the agricultural composition will exhibit a quantifiably higher biomass than the control corn plants.

[0413] The biomass from the treated plants may be about 1 -10% higher, 10-20% higher, 20- 30% higher, 30-40% higher, 40-50% higher, 50-60% higher, 60-70% higher, 70-80% higher, 80-90% higher, or more.

[0414] The biomass from the treated plants may equate to about a 1 bushel per acre increase over the controls, or a 2 bushel per acre increase, or a 3 bushel per acre increase, or a 4 bushel per acre increase, or a 5 bushel per acre increase, or more.

[0415] In some aspects, the biomass increase is statistically significant. In other aspects, the biomass increase is not statistically significant, but is still quantifiable.

h Isolated Microbes and Microbial

[0416] In this example, an isolated microbe from Tables 1-4 will be applied as a seed coating to seeds of soybean (Glycine max). Upon applying the isolated microbe as a seed coating, the soybean will be planted and cultivated in the standard manner.

[0417] A control plot of soybean seeds, which did not have the isolated microbe applied as a seed coating, will also be planted.

[0418] It is expected that the soybean plants grown from the seeds treated with the seed coating will exhibit a quantifiably higher biomass than the control soybean plants.

[0419] The biomass from the treated plants may be about 1 -10% higher, 10-20% higher, 20- 30% higher, 30-40% higher, 40-50% higher, 50-60% higher, 60-70% higher, 70-80% higher, 80-90% higher, or more.

[0420] The biomass from the treated plants may equate to about a 1 bushel per acre increase over the controls, or a 2 bushel per acre increase, or a 3 bushel per acre increase, or a 4 bushel per acre increase, or a 5 bushel per acre increase, or more. [0421] In some aspects, the biomass increase is statistically significant. In other aspects, the biomass increase is not statistically significant, but is still quantifiable.

B. Seed Treatment with Microbial Consortia

[0422] In this example, a microbial consortium., comprising at least two microbes from Tables 1 -4 will be applied as a seed coating to seeds of soybean {Glycine max). Upon applying the microbial consortium as a seed coating, the soybean will be planted and cultivated in the standard manner.

[0423] A control plot of soybean seeds, which did not have the microbial consortium applied as a seed coating, will also be planted.

[0424] It is expected that the soybean plants grown from the seeds treated with the seed coating will exhibit a quantifiably higher biomass than the control soybean plants.

[0425] The biomass from the treated plants may be about 1 -10% higher, 10-20% higher, 20- 30% higher, 30-40% higher, 40-50% higher, 50-60% higher, 60-70% higher, 70-80% higher, 80-90% higher, or more.

[0426] The biomass from the treated plants may equate to about a 1 bushel per acre increase over the controls, or a 2 bushel per acre increase, or a 3 bushel per acre increase, or a 4 bushel per acre increase, or a 5 bushel per acre increase, or more.

[0427] In some aspects, the biomass increase is statistically significant. In other aspects, the biomass increase is not statistically significant, but is still quantifiable.

C. Treatment with Agricultu al Composition Comprisin Isolated Microbe

[0428] In this example, an isolated microbe from Tables 1-4 will be applied as an agricultural composition, administered to the soybean seed at the time of sowing.

[0429] For example, it is anticipated that a farmer will apply the agricultural composition to the soybean seeds simultaneously upon planting the seeds into the field. This can be accomplished, for example, by applying the agricultural composition to a hopper/bulk tank on a standard 16 row planter, which contains the soybean seeds and which is configured to plant the same into rows. Alternatively, the agricultural composition can be contained in a separate bulk tank on the planter and sprayed into the rows upon planting the soybean seed.

[0430] A control plot of soybean seeds, which are not administered the agricultural composition, will also be planted. [0431] t is expected that the soybean plants grown from the seeds treated with the agricultural composition will exhibit a quantifiably higher biomass than the control soybean plants.

[0432] The biomass from the treated plants may be about 1 -10% higher, 10-20% higher, 20- 30% higher, 30-40% higher, 40-50% higher, 50-60% higher, 60-70% higher, 70-80% higher, 80-90% higher, or more.

[0433] The biomass from the treated plants may equate to about a 1 bushel per acre increase over the controls, or a 2 bushel per acre increase, or a 3 bushel per acre increase, or a 4 bushel per acre increase, or a 5 bushel per acre increase, or more.

[0434] In some aspects, the biomass increase is statistically significant. In other aspects, the biomass increase is not statistically significant, but is still quantifiable.

D. Treatment with Agricultural Composition Comprising Microbial Consortia

[0435] In this example, a microbial consortium, comprising at least two microbes from Tables 1-4 will be applied as an agricultural composition, administered to the soybean seed at the time of sowing.

[0436] For example, it is anticipated that a farmer will apply the agricultural composition to the soybean seeds simultaneously upon planting the seeds into the field. This can be accomplished, for example, by applying the agricultural composition to a hopper/bulk tank on a standard 16 row planter, which contains the soybean seeds and which is configured to plant the same into rows. Alternatively, the agricultural composition can be contained in a separate bulk tank on the planter and sprayed into the rows upon planting the soybean seed.

[0437] A control plot of soybean seeds, which are not administered the agricultural composition, will also be planted.

[0438] It is expected that the soybean plants grown from the seeds treated with the agricultural composition will exhibit a quantifiably higher biomass than the control soybean plants.

[0439] The biomass from the treated plants may be about 1-10% higher, 10-20% higher, 20- 30% higher, 30-40% higher, 40-50% higher, 50-60% higher, 60-70% higher, 70-80% higher, 80-90% higher, or more. [0440] The biomass from the treated plants may equate to about a 1 bushel per acre increase over the controls, or a 2 bushel per acre increase, or a 3 bushel per acre increase, or a 4 bushel per acre increase, or a 5 bushel per acre increase, or more.

[0441] In some aspects, the biomass increase is statistically significant. In other aspects, the biomass increase is not statistically significant, but is still quantifiable.

Example 4: Modifying Wheat Seedling Biomass with Isolated Microbes

A. Seed Treatment with Isolated Microbe

[0442] In this example, wheat seeds were inoculated with individual microbial strains (BCIs), and allowed to germinate (Figure 5).

[0443] The seeds were inoculated and placed on wet paper towels and rolled. The rolls were then incubated at 25 °C in plastic bins covered with wet towels. Each strain appearing in Figure 5 was tested in triplicate, with 20 seeds per replicate test.

[0444] Total biomass was measured at seven days post treatment. An uninoculated 'water' control treatment was run and measured simultaneously. The solid line parallel to the x axis and bisecting the bars near the top of the y~axis of figure 5 represents uninoculated control seeds. Some of the inoculated strains revealed relative increases in biomass at seven days post inoculation (DPI) compared to untreated control in vitro.

[0445] Table 12 provides a breakout of the biomass increase in wheat having been inoculated as described above, relative to a water-only treatment control (H20) and an untreated (Unt) control. The two columns immediately to the right of the species reflect the percentage increase over control (%IOC) for the water-only treatment control and the untreated control. Both increases and decreases in the hiomasses are reflected in the data of table 12. A smaller plant reflects potential for in-field conservation of nutrients and water where these resources may be limited by drought or local conditions, thus decreases are hypothesized to be yield relevant.

[0446] The results demonstrated that -19 strains caused a relative increase in total biomass of wheat at seven days post inoculation (DPI) compared to the water-only and untreated controls in vitro. Eight strains showed greater than a 5% increase over both controls, whereas 19 strains showed greater than a 5% decrease in biomass over the water control. Table 12

Pseudomonas

55530 or/zihabitans 11.6 -1.9 68 Dyadobacter soli -1.8 -13.8

Exig uob acterium Achromobacter

81 sp. 10.9 -2.6 49 pulmonis -5.0 -16.5

Pseudomonas

804 jinjuensis 10.4 -3.0

Example 5: Modifying Wheat Seedling Shoot and Root Biomass with Isolated Microbes A. Seed Treatment with Isolated Microbe

[0447] In this example, wheat seeds were inoculated with individual microbial strains (BCIs), and subjected to a germination test (Figure 6 A and Figure 6 B).

[0448] The seeds were inoculated, placed on wet germination paper, and rolled. The rolls were then incubated at 25°C in plastic bins. Each strain in Figure 6 was tested in triplicate, with 30 seeds per replicate.

[0449] Shoot and root biomass was measured at six days post treatment. An uninoculated 'water ^" control treatment was run and measured simultaneously. The solid line parallel to the x axis and bisecting the bars near the top of the y-axis in each figure represents the average of values for the water-treated control seeds. Some of the inoculated strains revealed relative increases in shoot and/or root biomass at six days post inoculation (DPI) compared to untreated control in vitro.

[0450] Table 13 provides a breakout of the shoot and root biomass increase in wheat having been inoculated and treated as described above, relative to a water-only control (H20). The two columns immediately to the right of the species reflect the percentage increase over control (%IOC). Both increases and decreases in biomass are reflected in the data of table 13. A smaller plant reflects potential for in-field conservation of nutrients and water where these resources may be limited by drought or local conditions, thus decreases are hypothesized to be yield relevant.

[0451] The results demonstrated that 16 strains caused a relative increase in shoot biomass of wheat at six days post inoculation (DPI) compared to the water-only controls in vitro. Twelve strains showed greater than a 5% increase over water control, whereas 10 strains showed greater than a 5% decrease in shoot biomass over the water control.

[0452] The results demonstrated that 26 strains caused a relative increase in root biomass of wheat at six days post inoculation (DPI) compared to the water-only control in vitro. Eighteen strains showed greater than a 5% increase over control, whereas 2 strains showed greater than a 5% decrease in biomass relative to the water control.

Table 13

Shoot Root

BiGmas5% Biomass%

BC! SOC SOC

Strain # Crop Species Control Control

49 Wheat Achromobacter pulmonis 9.03 18.55

Agrobacterium fabrum or Rhizobium

pusense (In Taxonomic Flux)

46 Wheat (previously Rhizobium sp.) 3.31 18.55

Agrobacterium fabrum or Rhizobium

pusense (Irs Taxonomic Flux)

958 Wheat ( ^' previously Rhizobium sp.) 13.55 21.26

Agrobacterium fabrum or Rhizobium

pusense (In Taxonomic Flux)

5222 Wheat (previously Rhizobium sp,) -10.54 0.90

717 Wheat Arthrobacter nicotinovorans 13.85 11.76

3189 Wheat Arthrobacter nicotinovorans 2.41 19.90

3444 Wheat Arthrobacter nicotinovorans -3.32 4.07

45 Wheat Chryseobacterium daecheongense -2.41 5.88

191 Wheat Chryseobacterium daecheongense -3.92 2.71

774 Wheat Chryseobacterium daecheongense -8.14 0.90

597 Wheat Chryseobacterium rhizosphaerae -1.81 6.78

615 Wheat Chryseobacterium rhizosphaerae -17.17 -4.98

1075 Wheat Chryseobacterium rhizosphaerae 5.42 4.97

Frigidibacter aibus or Deifuiviimonas

402 Wheat dentrif icons (In Taxonomic Flux) -7.23 8.14

Frigidibacter aibus or Deifuiviimonas

745 Wheat dentrif icons (In Taxonomic Flux) -19.28 -2.27

3 Wheat Duganeila radicis -15.97 -8.60

105 Wheat Duganella radicis 6.32 22.62

63 Wheat Exiguobacterium antarcticum -6.03 -5.43

Exiguobacterium sibircum or

718 Wheat antarcticum 12.04 18.55

116 Wheat Exiguobacterium sibiricum 11.14 12.66

225 Wheat Exiguobacterium soli -10.24 -3.17

712 Wheat Frigidibacter aibus 1.20 15.83

3231 Wheat M ass ilia kyonggiensis 12.04 21.71

94 Wheat MassiHa kyonggiensis 9.94 11.31

97 Wheat Massilia kyonggiensis 1.51 0.90 138 Wheat Novosphingohium sediminicoia -3,32 5.43

53 Wheat Pedobacter terrae 5.72 12.21

91 Wheat Pedobacter terrae -10.24 -0.91

110 Wheat Pedobacter terrae -7.83 4.52

616 Wheat Pseud omon as h elm an ticen sis 9.33 15.38

800 Wheat Pseudomonas he!manticensis 8.73 14.47

2945 Wheat Pseudomonas heimanticensis 0.60 4.97

Example 6: Modif ying Corn Seedling Shoot and Root Bio mass with Is oSated Micr

A. Seed Treatment with Isolated Microbe

[0453] In this example, com seeds were inoculated with individual microbial strains (BCIs), and subjected to a germination test (Figures 7 A, 7 B, 8 A and 8 B).

[0454] The seeds were inoculated, placed on wet germination paper, and roiled. The rolls were then incubated at 25°C in plastic bins. Each strain appearing in Figures 7 A, 7 B, 8 A and 8 B was tested in triplicates, with 30 seeds per replicate test. Due to the amount of samples tested, rolls were placed in two independent bins with a respective water control, represented individually in Figures 7 A, 7 B, 8 A and 8 B,

[0455] Shoot and root biomass was measured at six days post treatment. An uninoculated 'water' control treatment was run and measured simultaneously. The solid line parallel to the x axis and bisecting the bars near the top of the y-axis in each figure represents the average of values for the water-treated control seeds. Some of the inoculated strains revealed relative increases in shoot and/or root biomass at six days post inoculation (DPI) compared to untreated control in vitro.

[0456] Table 14 provides a breakout of the shoot and root biomass changes in com having been inoculated and treated as described above, relative to a water-only control (H20). The two columns immediately to the right of the species reflect the percentage increase over control (%IOC). Both increases and decreases in the biomasses are reflected in the data of table 14. A smaller plant reflects potential for in-field conservation of nutrients and water where these resources may be limited by drought or local conditions, thus decreases are hypothesized to be yield relevant.

[0457] The results demonstrated that 25 strains caused a relative increase in shoot biomass of com at six days post inoculation (DPI) compared to the water-only control in vitro. Twenty - two strains showed greater than a 10% increase, whereas 7 strains caused a decrease in biomass relative the water control.

[0458] The results demonstrated that 15 strains caused a relative increase in root biomass of corn at six days post inoculation (DPI) compared to the water-only control in vitro. Eight strains showed greater than a 5% increase over water control, whereas 1 1 strams showed greater than a 5% decrease in root biomass over the water control.

[0459] Results demonstrated that a number of strains isolated from superior plants caused a significant increase over the water control in root and/or shoot biomass (p<0.05 Dimnett's Multiple Comparisons Test). Statistically significant results are labeled with an asterisk. In one embodiment, superior plants are defined as a subset of individual plants observed in an AMS process to exhibit a phenotype of interest that is improved relative to the plurality of plants screened in the same assay. Phenotype s of interest may be screened in the absence or presence of biotic or abiotic stress and include early vigor, as manifested by improved germination rate, foliar and or root biomass; chlorophyll content; leaf canopy temperature; and water use efficiency.

Table 14

BCf Root Strain Shoot Biomass% Biomass% # Crop Species IOC !OC

49 Corn Achromobacter pulmonis -4.28 -16.12

Agrobacterium fabrum or Rhizobium

pusense (in Taxonomic Flux) (previously

46 Corn Rhizobium so.) 15.10 -4.41

Agrobacterium fabrum or Rhizobium

pusense (In Taxonomic Flux) (previously

958 Corn Rhizobium sp.) 17.31 -0.63

Agrobacterium fabrum or Rhizobium

pusense (in Taxonomic Flux) (previously

5222 Corn Rhizobium sp.) 22.22 -2.52

717 Corn Arthrobacter nicotinovorans 26.21 22.61*

3189 Corn Arthrobacter nicotinovorans 74.15* 14.05

3444 Corn Arthrobacter nicotinovorans 6.48 -15.54

45 Corn Chryseobacterium daecheongense 31.48 -3.60

191 Corn Chryseobacterium daecheongense 19.44 -14.86

774 Corn Chryseobacterium daecheongense 21.58 1.17

597 Corn Chryseobacterium rhizosphaerae 15.53 3.15 615 Corn Chryseobacterium rhizosphaerae 17.52 1.89

1075 Corn Chryseobacteriurn rhizosphaerae 73.79* 11.26

Frigidibacter aibus or De!fu!viimonas

402 Corn dentrif icons (in Taxonomic Flux) 11.25 2.97

Frigidibacter aibus or Deifuiviimonas

745 Corn dentrif icons (in Taxonomic Flux) 8.76 -17.75

31 Corn Duganeiia radicis 35.68* -2.07

105 Corn Duganeiia radicis 19.73 5.05

63 Corn Exiguobacterium an tarcticum 17.17 2.61

718 Corn Exiguobacterium sibircurn or antarcticum 1.29 -12.27

116 Corn Exiguobacterium sibiricum 77,56* 24.05*

225 Corn Exiguobacterium soii 15.67 -7.75

138 Corn Exiguobacterium sp. 16.31 0.81

712 Corn Frigidibacter aibus 15.24 4.77

3231 Corn Masss ^' ii a kyonggiensis -12.84 -10.53

94 Corn Massiiia kyonggiensis -6.44 -8.54

97 Corn MassiHa kyonggiensis -2.29 -13.74

53 Corn Pedobacter terrae -7.90 ^■ 14.58

91 Corn Pedobacter terrae 50.64* 23.87*

110 Corn Pedobacter terrae -0.17 -7.64

616 Corn Pseudomonas heimanticensis 16.67 14.05

800 Corn Pseudomonas heimanticensis -3.21 -2.88

2945 Corn Pseudomonas heimanticensis 14.60 5.68

* Statistical y significant results

Examp !e 7: increasing Root and Shoot Length of Maiz e, Wheat, and Tomato with bes

A. Seec Treat* neot with Isolated Microbe

[0460] In this example, seeds of maize, wheat, and tomato were inoculated with individual microbial strains (BDNZ strains), and allowed to germinate.

[0461] The seeds were inoculated,placed on wet paper towels and rolled. The rolls were then incubated at 25 °C in sealed plastic bags. Each strain appearing in table 15 was tested in germination tests in duplicate, with 30 seeds per replicate test for wheat and maize and 50 seeds for tomato,

[0462] Root length and shoot length (RL and SL) were measured at four days post treatment. Some of the inoculated strains revealed relative increases in root and/or shoot length at four days point inoculation (DPI) compared to untreated control . [0463] Each strain applied to maize seed was tested in duplicates of 30 seeds each. Results show that while germination rates w ^f ere good for all strains tested, some strains caused a relative increase in root and/or shoot length at 4 days post inoculation (DPI) compared to the water control in vitro (See Figures 9 and 10).

[0464] Each strain applied to wheat seed was tested in duplicates of 30 seeds each. Root and shoot length were measured at 4 days post treatment. Results show that germination rates were good for all strains tested (>90%), and some strains caused a relative increase in root and/or shoot length at 4 days post inoculation (DPI) compared to the water control in vitro (See Figures 11 and 12).

[0465] Each strain applied to tomato seed was tested in duplicates of 50 seeds each. Root and shoot length were measured at 4 days post inoculation (DPI). Results show that germination rates were good for all strains tested, and some strains caused a relative increase in root and/or shoot length at 4 days post inoculation (DPI) compared to the water control in vitro (See Figures 13 and 14).

[0466] Table 15 provides a breakout of the root and shoot length increase (in mm) after inoculation and treatment as described above, relative to a water-only control (H20). The columns immediately to the right of the species reflect the percentage increase over control (%IOC) for the water-only control. Both increases and decreases are reflected in the data. A smaller plant reflects potential for in-field conservation of nutrients and water where these resources may be limited by drought or local conditions, thus decreases are hypothesized to be yield relevant.

[0467] The results demonstrated that a number of strains isolated from superior plants caused a significant mcrease over the water control in root and/or shoot length (p<0.1, Fisher's LSD) at four days post inoculation (DPI). Twenty strains isolated from superior plants caused a significant increase over the water control in maize root length and 19 caused a significant increase in maize shoot length. Four strains caused a significant increase over control in root and shoot length of wheat. Four strains caused a significant increase o ver control in root and shoot length of tomato. Table 15

68741 !■. >:ί :. :1> · Stenotrophomonas terrae 15.8 20.3

[0468] In table 15, the root and shoot length were assessed to evaluate the effect of the microbe treatments on early plant development. Both increases and decreases in biomass have been noted to reflect the possibility that decreases are hypothesized to be yield relevant; for example a smaller plant reflects potential for in-field conservation of nutrients and water where these may be limited by drought or local conditions. Results show that of all strains tested, some 40 strains caused a relative increase in root length at 4 days post inoculation (DPI) and 35 strains caused a relative increase in shoot length compared to water controls in vitro. Four tomato strains, three wheat strains and 17 maize strains caused a significant increase in both shoot length and root length ( 0.1. Fishers least squared difference). Example 8: Modifying Root and Shoot Length of Corn with Isolated Microbes

A. Seed Treatment with Isolated Microbe

[0469] In this example, corn seeds were inoculated with individual microbial strains and allowed to germinate (Figures 15 A, 15B, 16A and 16B).

[0470] The seeds were inoculated, placed on wet germination paper, and rolled. The rolls were then incubated at 25°C in plastic bins. Each strain appearing in figures 15 and 16 was tested in germination tests in triplicates, with 30 seeds per replicate. Due to the amount of samples tested, rolls were placed in two independent bins with a respective water control, represented individually in Figures 15 and 16 by graphs A and B.

[0471] Root length and shoot length (RL and SL) were measured at six days post treatment. A control treatment was included comprising seeds treated with water in the absence of a microbial inoculant of the present disclosure. Some of the inoculated strains revealed relative increases in root and/or shoot length at six days point inoculation (DPI) compared to untreated control (Figures 15 and 16).

[0472] Table 16 provides a breakout of the root and shoot length increase (in mm) after inoculation and treatment as described above, relative to a water-only control (H20). The columns immediately to the right of the species reflect the percentage increase over control (%IOC). Both increases and decreases are reflected in the data. A smaller plant reflects potential for in-field conservation of nutrients and water where these resources may be limited by drought or local conditions, thus decreases are hypothesized to be yield relevant.

[0473] Results demonstrated that a number of strains listed in Table 16 which were origaniy isolated from superior plants caused a significant increase, over the water-only control, in root and/or shoot length (p<0.05, Fisher's LSD) at six days post inoculation (DPI). Statistically significant results are labeled with an asterisk. Ten strains isolated from superior plants caused a significant increase over the water control in com shoot length and 5 caused a significant increase in corn root length. Table 16

% IOC % soc

Strain Crop Species SL RL

49 Corn Achromobacter pulmonis 23.30 ^■ 0.84

Agrobacterium fabrum or Rhizobium

pusense (In Taxonomic Fiux) fpreviousiy

46 Corn Rhizobium sp.) 21.79 1.56

Agrobacterium fabrum or Rhizobium

pusense (In Taxonomic Flux) fpreviousiy

958 Corn Rhizobium sp.) 47.76* 6.25

Agrobacterium fabrum or Rhizobium

pusense (In Taxonomic Flux) fpreviousiy

5222 Corn Rhizobium sp.) 38.31* 17.55*

717 Corn Arthrobacter nicotinovorans 60.20* 53.32*

3189 Corn Arthrobacter nicotinovorans N/A N/A

3444 Corn Arthrobacter nicotinovorans 21.04 3.36

45 Corn Chryseobacterium daecheongense 39.99* 11.43

191 Corn Chryseobacterium daecheongense 17.91 1.62

774 Corn Chryseobacterium daecheongense 45.65* 6.84

597 Corn Chryseobacterium rhizosphaerae 20.90 5.29

615 Corn Chryseobacterium rhizosphaerae 25.57 9.98

1075 Corn Chryseobacterium rhizosphaerae N/A N/A

Frigidibacter aibus or Delfulviimonas

402 Corn dentrificans (in Taxonomic F!ux) 44.78* 18.96*

Frigidibacter aibus or Delfulviimonas

745 Corn dentrificans (in Taxonomic Fiux) 15.92 -0.36

31 Corn Duganeiia radicis 22.39 12.81

105 Corn Duganelia radicis 36.02 7.51

63 Corn Exiguobacterium antarcticum 42.29* 4.59

718 Corn Exiguobacterium sibircum or antarcticum 18.12 -6.56

116 Corn Exiguobacterium sibiricum N/A N/A

225 Corn Exiguobacterium soli 23.88 9.48

138 Corn Exiguobacterium sp. 37.11 20.56*

712 Corn Frigidibacter aibus 38.81* 10.24

3231 Corn Massilia kyonggiensis -13.92 -10.76

94 Corn Massiiia kyonggiensis 16.50 -9.92

97 Corn Massilia kyonggiensis 11.72 -4.68

53 Corn Pedobacter terrae 3.88 4.33

91 Corn Pedobacter terrae N/A N/A

110 Corn Pedobacter terrae 12.30 4.87

616 Corn Pseudomonas helmanticensis 42.79* 56.95* 800 Corn Pseudomonas helmanticensis 6.97 2.62

2945 Corn Pseudomonas helmanticensis 38.81* 8.22

* Statistically significant results

[0474] In table 16, the root and shoot length were assessed to evaluate the effect of the microbe treatments on early plant development. Both increases and decreases have been noted to reflect the possibility that decreases are hypothesized to be yield relevant: for example a smaller plant reflects potential for in-field conservation of nutrients and water where these may be limited by drought or local conditions. Results show that of all strains tested, some 21 strains caused a relative increase in root length at six days post inoculation (DPI) and 27 strains caused a relative increase in shoot length compared to water controls in vitro, A total of six strains tested on com caused a significant increase in both shoot length and root length (p<0.1, Fishers least squared difference). Asterisks show significance (p<0.1, Dunnette's Multtiple-Comparison Test).

Example 9: Biochemical Characterization of Microbial Isolates

A. In vitro analysis of plant beneficial properties of a microbe in US trials

[0475] In this example, isolated microbes from Table 4 were grown on minimal or nutrient- deficient agar plates supplemented with insoluble nutrient substrates to determine biochemical activity (Table 17).

[0476] Isolates were tested, in triplicate, for phosphate, potassium, and zinc solubilization, siderophore production and the ability to grow on low nitrogen media. Plates were incubated at 25 °C for six days.

[0477] Table 17 provides a summary of the growth response of each isolate, having been grown as described above. Tests are abbreviated as follows: Mica (K solubilization) - isolates were grown on modified Alexandrov medium supplemented with Mica (Parmar and Smdhu 2013); P04 - isolates were grown on NBRIP media (Nautiyal, 1999) containing insoluble tri- calcium phosphate as the sole source of P; ZnO and Zn03 (Zn solubilization) - isolates were grown on minimal media supplemented with insoluble Zn as described by Goteti et al., (2013); NfA - isolates were grown on Nfb media (Dobereiner et al., 1976) without Bromothymol blue, solidified with 12.5% agar; CAS agar - isolates were grown on Chrome Azurol-s agar for detection of iron chelation according to the method of Perez-Miranda et al (2007). [0478] Within table 17, a (+) symbol represents an isolates ability to grow under the test conditions and solubilize the respective element, (---) symbol represents a lack of solubilization, (N/A) represents no isolate growth observed on the respective media.

[0479] Results show that microbes on table 4 exhibit a broad spectrum of known plant- beneficial biochemical activities (Rana et aL, 2012, Rodriguez and Revnaldo, 1999) including solubilization of mineral nutrients and chelation of micronutrients. By enhancing nutrient availability for plant growth promotion, the microbes exhibit a potential for increasing plant yields.

Table 17

Strain Species Media

Mica CAS

BCi # (K) P04 ZrsO ZnC03 Mf A agar

49 Achromobacter pulmonis N/A + + + + -

Agrobacterium fabrum or

46 Rhizobium pusense - - + - + -

Agrobacterium fabrum or

958 Rhizobium pusense - - + + + -

717 A rth robac ter n ico tin o varans - + + + +

3189 Art rob a cter n ico tin o vorans - + + + -

3444 A rth robac ter n ico tin o vorans - + + + + -

Chryseobacteriurn

774 daecheongense - N/A N/A N/A N/A -

615 Chryseobacteriurn rhizosphaerae N/A N/A N/A N/A N/A +

1075 Chryseobacteriurn rhizosphaerae N/A N/A N/A N/A N/A +

597 Chryseobacteriurn rhizosphaerae N/A N/A N/A N/A N/A +

Frigidibacter albus or

Deifuiviimonas dentrificans (in

402 Taxonomic Fiux) - N/A N/A +

Frigidibacter aibus or

Deifuiviimonas dentrificans (In

745 Taxonomic Flux) - - N/A N/A + -

31 Duganei!a radicis - N/A + + + -

105 Duganella radicis - N/A + + + -

712 Frigidibacter aibus - N/A N/A +

3231 Massiiia kyonggiensis - + N/A N/A -

94 Massiiia kyonggiensis - + + + + -

97 Massiiia kyonggiensis - - N/A N/A N/A +

53 Pedobacter terrae - N/A + + + -

91 Pedobacter terrae - - + + -

110 Pedobacter terrae - - + + + -

616 Pseudomonas heimanticensis + + N/A N/A + - 800 Pseud orn anas h elm an tic en sis + + N/A N/A + -

2945 Pseudomonas helmanticensis + + N/A + + +

Agrobacterium fabrum or

5222 Rbizobium pusense

B. In vitro analysis of plant beneficial properties of a microbe on New Zealand trials [0480] Microbes from Table 18 were grown on minimal or nutrient-deficient agar plates supplemented with insoluble nutrient substrates to determine biochemical activity.

[0481] Phosphate solubilization was determined using NBRIP media containing 5 g/L tri- calcium phosphate according to the method Islam et al., (2007). The ability to use phytate as the sole source of phosphorus for growth was assessed using media containing (g/L): phytic acid (10) NaNQ ₃ (3); KC1 (0.5); FeS0 ₄ .7H ₂ 0 (0.01); MgS0 ₄ .7H ₂ 0 (0.5); glucose (10) and noble agar (15), pH 7.5. Growth on low-nitrogen media (Low N) was assessed using NfA media as described above.

[0482] Within table 18, a (+) symbol represents an isolates ability to grow under the test conditions and solubilize the respective element, (---) symbol represents a lack of solubilization.

Table 18

II. Increased Brought Tolerance and H¾0 Use Efficiency in Agriculturally Important Crops

[0483] In certain embodiments of the disclosure, the present methods aim to increase the drought tolerance and water use efficiency for a given crop.

[0484] The methodologies presented herein— based upon utilizing the disclosed isolated microbes, consortia, and compositions comprising the same— have the potential to increase the drought tolerance and water use efficiency of important agricultural crops. This will enable a more sustainable agricultural system and increase the regions of the world that are suitable for growing important crops.

Example 1: Increasing Ryegrass Drought Tolerance and I¾0 Use Efficiency with

Isolated Microbes and Microbial Consortia

A. Seed Treatment with Isolated Microbe

[0485] In this example, an isolated microbe from Tables 1 -4 will be applied as a seed coating to seeds of ryegrass (Lolium perenne). Upon applying the isolated microbe as a seed coating, the ryegrass will be planted and cultivated in the standard manner.

[0486] A control plot of ryegrass seeds, which did not have the isolated microbe applied as a seed coating, will also be planted.

[0487] it is expected that the ryegrass plants grown from the seeds treated with the seed coating will exhibit a quantifiable and superior ability to tolerate drought conditions and/or exhibit superior water use efficiency, as compared to the control ryegrass plants.

[0488] The drought tolerance and/or water use efficiency can be based on any number of standard tests from the art, e.g leaf water retention, turgor loss point, rate of photosynthesis, leaf color and other phenotypic indications of drought stress, yield performance, and various root morphological and growth patterns.

B. Seed Treatment with Microbial Consortia

[0489] In this example, a microbial consortium, comprising at least two microbes from Tables 1-4 will be applied as a seed coating to seeds of ryegrass {Lolium perenne). Upon applying the microbial consortium as a seed coating, the ryegrass will be planted and cultivated in the standard manner.

[0490] A control plot of ryegrass seeds, which did not have the microbial consortium applied as a seed coating, will also be planted.

[0491] It is expected that the ryegrass plants grown from the seeds treated with the seed coating will exhibit a quantifiable and superior ability to tolerate drought conditions and/or exhibit superior water use efficiency, as compared to the control ryegrass plants.

[0492] The drought tolerance and/or water use efficiency can be based on any number of standard tests from the art, e.g leaf water retention, turgor loss point, rate of photosynthesis, leaf color and other phenotypic indications of drought stress, yield performance, and various root morphological and growth patterns.

C. Treatment with Agricultural Composition Comprising Isolated Microbe

[0493] In this example, an isolated microbe from Tables 1-4 will be applied as an agricultural composition, administered to the ryegrass seed at the time of sowing.

[0494] For example, it is anticipated that a farmer will apply the agricultural composition to the ryegrass seeds simultaneously upon broadcasting said seeds into the field. This can be accomplished, for example, by applying the agricultural composition to a hopper or spreader, which contains the ryegrass seeds and which is configured to broadcast the same.

[0495] A control plot of ryegrass seeds, which are not administered the agricultural composition, will also be planted.

[0496] It is expected that the ryegrass plants grown from the seeds treated with the with the agricultural composition will exhibit a quantifiable and superior ability to tolerate drought conditions and/or exhibit superior water use efficiency, as compared to the control ryegrass plants.

[0497] The drought tolerance and/or water use efficiency can be based on any number of standard tests from the art, e.g leaf water retention, turgor loss point, rate of photosynthesis, leaf color and other phenotypic indications of drought stress, yield performance, and various root morphological and growth patterns.

D. Treatment with Agricultural Composition Comprising Microbial Consortia

[0498] In this example, a microbial consortium, comprising at least two microbes from Tables 1-4 will be applied as an agricultural composition, administered to the ryegrass seed at the time of sowing.

[0499] For example, it is anticipated that a farmer will apply the agricultural composition to the ryegrass seeds simultaneously upon broadcasting said seeds into the field. This can be accomplished, for example, by applying the agricultural composition to a hopper or spreader, which contains the ryegrass seeds and which is configured to broadcast the same.

[0500] A control plot of ryegrass seeds, which are not administered the agricultural composition, will also be planted. [0501] It is expected thai the ryegrass plants grown from the seeds treated with the with the agricultural composition will exhibit a quantifiable and superior ability to tolerate drought conditions and/or exhibit superior water use efficiency, as compared to the control ryegrass plants.

[0502] The drought tolerance and/or water use efficiency can be based on any number of standard tests from the art, e.g leaf water retention, turgor loss point, rate of photosynthesis, leaf color and other phenoiypic indications of drought stress, yield performance, and various root morphological and growth patterns.

Example 2: Increasing Maize Drought Tolerance and I¾0 Use Efficiency with Isolated

Microbes and Microbial Consortia

A. Seed Treatment with Isolated Microbe

[0503] In this example, an isolated microbe from Tables 1-4 will be applied as a seed coating to seeds of corn (Zea mays). Upon applying the isolated microbe as a seed coating, the corn will be planted and cultivated in the standard manner.

[0504] A control plot of corn seeds, which did not have the isolated microbe applied as a seed coating, will also be planted.

[0505] It is expected that the corn plants grown from the seeds treated with the seed coating will exhibit a quantifiable and superior ability to tolerate drought conditions and/or exhibit superior water use efficiency, as compared to the control corn plants.

[0506] The drought tolerance and/or water use efficiency can be based on any number of standard tests from the art, e.g leaf water retention, turgor loss point, rate of photosynthesis, leaf color and other phenoiypic indications of drought stress, yield performance, and various root morphological and growth patterns.

B, Seed Treatment with Microbial Consortia

[0507] In this example, a microbial consortium, comprising at least two microbes from Tables 1-4 will be applied as a seed coating to seeds of com (Zea mays). Upon applying the microbial consortium as a seed coating, the corn will be planted and cultivated in the standard manner.

[0508] A control plot of com seeds, which did not have the microbial consortium applied as a seed coating, will also be planted. [0509] It is expected that the corn plants grown from the seeds treated with the seed coating will exliibit a quantifiable and superior ability to tolerate drought conditions and/or exhibit superior water use efficiency, as compared to the control com plants.

[0510] The drought tolerance and/or water use efficiency can be based on any number of standard tests from the art, e.g leaf water retention, turgor loss point, rate of photosynthesis, leaf color and other phenotypic indications of drought stress, yield performance, and various root morphological and growth patterns.

C. Treatment with Agricultural Composition Comprising Isolated Microbe

[0511] In this example, an isolated microbe from Tables 1-4 will be applied as an agricultural composition, administered to the corn seed at the time of sowing.

[0512] For example, it is anticipated that a fanner will apply the agricultural composition to the corn seeds simultaneously upon planting the seeds into the field. This can be accomplished, for example, by applying the agricultural composition to a hopper/bulk tank on a standard 16 row planter, which contains the com seeds and which is configured to plant the same into rows. Alternatively, the agricultural composition can be contained in a separate bulk tank on the planter and sprayed into the rows upon planting the corn seed.

[0513] A control plot of com seeds, which are not administered the agricultural composition, will also be planted.

[0514] It is expected that the com plants grown from the seeds treated with the with the agricultural composition will exliibit a quantifiable and superior ability to tolerate drought conditions and/or exhibit superior water use efficiency, as compared to the control corn plants.

[0515] The drought tolerance and/or water use efficiency can be based on any number of standard tests from the art, e.g leaf water retention, turgor loss point, rate of photosynthesis, leaf color and other phenotypic indications of drought stress, yield performance, and various root morphological and growth patterns.

D. Treatment with Agricultural Composition Comprisin Microbial Consortia

[0516] In this example, a microbial consortium, comprising at least two microbes from Tables 1-4 will be applied as an agricultural composition, administered to the com seed at the time of sowing. [0517] For example, it is anticipated that a farmer will apply the agricultural composition to the corn seeds simultaneously upon planting the seeds into the field. This can be accomplished, for example, by applying the agricultural composition to a hopper/bulk tank on a standard 16 row planter, which contains the com seeds and which is configured to plant the same into rows. Alternatively, the agricultural composition can be contained in a separate bulk tank on the planter and sprayed into the ro s upon planting the corn seed.

[0518] A control plot of com seeds, which are not administered the agricultural composition, will also be planted.

[0519] It is expected that the com plants grown from the seeds treated with the with the agricultural composition will exliibit a quantifiable and superior ability to tolerate drought conditions and/or exhibit superior water use efficiency, as compared to the control corn plants.

[0520] The drought tolerance and/or water use efficiency can be based on any number of standard tests from the art, e.g leaf water retention, turgor loss point, rate of photosynthesis, leaf color and other phenotypic indications of drought stress, yield performance, and various root morphological and growth patterns.

Example 3: Increasing Soybean Drought Tolerance and ¾0 Use Efficiency with Isolated Microbes and Microbial Consortia

A. Seed Treatment with Isolated Microbe

[0521] In this example, an isolated microbe from Tables 1-4 will be applied as a seed coating to seeds of soybean (Glycine max). Upon applying the isolated microbe as a seed coating, the soybean will be planted and cultivated in the standard manner.

[0522] A control plot of soybean seeds, which did not have the isolated microbe applied as a seed coating, will also be planted.

[0523] It is expected that the soybean plants grown from the seeds treated with the seed coating will exliibit a quantifiable and superior ability to tolerate drought conditions and/or exhibit superior water use efficiency, as compared to the control soybean plants.

[0524] The drought tolerance and/or water use efficiency can be based on any number of standard tests from the art, e.g leaf water retention, turgor loss point, rate of photosynthesis, leaf color and other phenotypic indications of drought stress, yield performance, and various root morphological and growth patterns. B. Seed Treatment with Microbial Consortia

[0525] In this example, a microbial consortium, comprising at least two microbes from Tables 1-4 will be applied as a seed coating to seeds of soybean (Glycine max). Upon applying the microbial consortium as a seed coating, the soybean will be planted and cultivated in the standard manner.

[0526] A control plot of soybean seeds, which did not have the microbial consortium applied as a seed coating, will also be planted.

[0527] It is expected that the soybean plants grown from the seeds treated with the seed coating will exhibit a quantifiable and superior ability to tolerate drought conditions and/or exhibit superior water use efficiency, as compared to the control soybean plants.

[0528] The drought tolerance and/or water use efficiency can be based on any number of standard tests from the art, e.g leaf water retention, turgor loss point, rate of photosynthesis, leaf color and other phenotypic indications of drought stress, yield performance, and various root morphological and growth patterns.

C. Treatment with Agricultural Composition Comprising Isolated Microbe

[0529] In this example, an isolated microbe from Tables 1-4 will be applied as an agricultural composition, administered to the soybean seed at the time of sowing.

[0530] For example, it is anticipated that a farmer will apply the agricultural composition to the soybean seeds simultaneously upon planting the seeds into the field. This can be accomplished, for example, by applying the agricultural composition to a hopper/bulk tank on a standard 16 row? planter, which contains the soybean seeds and which is configured to plant the same into rows. Alternatively, the agricultural composition can be contained in a separate bulk tank on the planter and sprayed into the rows upon planting the soybean seed.

[0531 ] A control plot of soybean seeds, which are not administered the agricultural composition, will also be planted.

[0532] It is expected that the soybean plants grown from the seeds treated with the with the agricultural composition will exhibit a quantifiable and superior ability to tolerate drought conditions and/or exhibit superior water use efficiency, as compared to the control soybean plants. [0533] The drought tolerance and/or water use efficiency can be based on any number of standard tests from the art, e.g leaf water retention, turgor loss point, rate of photosynthesis, leaf color and other phenotypic indications of drought stress, yield performance, and various root morphological and growth patterns,

D. Treatment with Agricultural Composition Comprising Microbial Consortia

[0534] In this example, a microbial consortium, comprising at least two microbes from Tables 1-4 will be applied as an agricultural composition, administered to the soybean seed at the time of sowing.

[0535] For example, it is anticipated that a farmer will apply the agricultural composition to the soybean seeds simultaneously upon planting the seeds into the field. This can be accomplished, for example, by applying the agricultural composition to a hopper/bulk tank on a standard 16 row planter, which contains the soybean seeds and which is configured to plant the same into rows. Alternatively, the agricultural composition can be contained in a separate bulk tank on the planter and sprayed into the rows upon planting the soybean seed.

[0536] A control plot of soybean seeds, which are not administered the agricultural composition, will also be planted.

[0537] It is expected that the soybean plants grown from the seeds treated with the with the agricultural composition will exhibit a quantifiable and superior ability to tolerate drought conditions and/or exhibit superior water use efficiency, as compared to the control soybean plants.

[0538] The drought tolerance and/or water use efficiency can be based on any number of standard tests from the art, e.g leaf water retention, turgor loss point, rate of photosynthesis, leaf color and other phenotypic indications of drought stress, yield performance, and various root morphological and growth patterns.

III. Increased Nitrogen Use Efficiency in Agriculturally Important Crops

[0539] In certain embodiments of the disclosure, the present methods aim to decrease the amount of nitrogen that must be deposited into a given agricultural system and yet achieve the same or better yields for a given crop.

[0540] The methodologies presented herein— based upon utilizing the disclosed isolated microbes, consortia, and compositions comprising the same— have the potential to reduce the amount of nitrogen fertilizer that is lost by farmers every year due to nitrogen leaching into the air, soil, and waterways. This will enable a more sustainable agricultural system that is still able to produce yield results consistent with today's agricultural expectations.

Example 1: Increasing Ryegrass NUE with Isolated Microbes and Microbial

Consortia

A. Seed Treatment with Isolated Microbe

[0541] In this example, an isolated microbe from Tables 1 -4 will be applied as a seed coating to seeds of ryegrass (Lolium perenne). Upon applying the isolated microbe as a seed coating, the ryegrass will be planted and cultivated in the standard manner.

[0542] A control plot of ryegrass seeds, which did not have the isolated microbe applied as a seed coating, will also be planted.

[0543] It is expected that the ryegrass plants grown from the seeds treated with the seed coating will exhibit a quantifiable and superior ability to utilize nitrogen, as compared to the control ryegrass plants.

[0544] The nitrogen use efficiency can be quantified by recording a measurable change in any of the main nitrogen metabolic pool sizes in the assimilation pathways (e.g., a measurable change in one or more of the following: nitrate, nitrite, ammonia, glutamic acid, aspartic acid, glutamine, asparagine, lysine, leucine, threonine, methionine, glycine, tryptophan, tyrosine, total protein content of a plant part, total nitrogen content of a plant part, and/or chlorophyll content), or where the treated plant is shown to provide the same or elevated biomass or harvestable yield at lower nitrogen fertilization levels compared to the control plant, or where the treated plant is shown to provide elevated biomass or harvestable yields at the same nitrogen fertilization levels compared to a control plant.

B. Seed Treatment with Microbial Consortia

[0545] In this example, a microbial consortium, comprising at least two microbes from Tables 1-4 will be applied as a seed coating to seeds of ryegrass (Lolium perenne). Upon applying the microbial consortium as a seed coating, the ryegrass \\ ill be planted and cultivated in the standard manner.

[0546] A control plot of ryegrass seeds, w hich did not have the microbial consortium applied as a seed coating, will also be planted. [0547] It is expected that the ryegrass plants grown from the seeds treated with the seed coating will exhibit a quantifiable and superior ability to utilize nitrogen, as compared to the control ryegrass plants,

[0548] The nitrogen use efficiency can be quantified by recording a measurable change in any of the mam nitrogen metabolic pool sizes in the assimilation pathways (e.g. , a measurable change in one or more of the following: nitrate, nitrite, ammonia, glutamic acid, aspartic acid, glutamine, asparagine, lysine, leucine, threonine, methionine, glycine, tryptophan, tyrosine, total protein content of a plant part, total nitrogen content of a plant part, and/or chlorophyll content), or where the treated plant is shown to provide the same or elevated biomass or harvestable yield at lower nitrogen fertilization levels compared to the control plant, or where the treated plant is shown to provide elevated biomass or harvestable yields at the same nitrogen fertilization levels compared to a control plant.

C. Treatment with Agricultural Composition Comprisin Isolated Microbe

[0549] In this example, an isolated microbe from Tables 1-4 will be applied as an agricultural composition, administered to the ryegrass seed at the time of sowing.

[0550] For example, it is anticipated that a farmer will apply the agricultural composition to the ryegrass seeds simultaneously upon broadcasting said seeds into the field. This can be accomplished, for example, by applying the agricultural composition to a hopper or spreader, which contains the ryegrass seeds and which is configured to broadcast the same.

[0551] A control plot of ryegrass seeds, which are not administered the agricultural composition, will also be planted.

[0552] it is expected that the ryegrass plants grown from the seeds treated with the agricultural composition will exhibit a quantifiable and superior ability to utilize nitrogen, as compared to the control ryegrass plants.

[0553] The nitrogen use efficiency can be quantified by recording a measurable change in any of the main nitrogen metabolic pool sizes in the assimilation pathways (e.g. , a measurable change in one or more of the following: nitrate, nitrite, ammonia, glutamic acid, aspartic acid, glutamine, asparagine, lysine, leucine, threonine, methionine, glycine, tryptophan, tyrosine, total protein content of a plant part, total nitrogen content of a plant part, and/or chlorophyll content), or where the treated plant is shown to provide the same or elevated biomass or harvestable yield at lower nitrogen fertilization levels compared to the control plant, or where the treated plant is shown to provide elevated biomass or harvestable yields at the same nitrogen fertilization levels compared to a control plant.

D. Treatment with Agricultural Composition Comprising Microbial Consortia

[0554] In this example, a microbial consortium, comprising at least two microbes from Tables 1 -4 will be applied as an agricultural composition, administered to the ryegrass seed at the time of sowing.

[0555] For example, it is anticipated that a farmer will apply the agricultural composition to the ryegrass seeds simultaneously upon broadcasting said seeds into the field. This can be accomplished, for example, by applying the agricultural composition to a hopper or spreader, which contains the ryegrass seeds and which is configured to broadcast the same.

[0556] A control plot of ryegrass seeds, which are not administered the agricultural composition, will also be planted.

[0557] It is expected that the ryegrass plants grown from the seeds treated with the agricultural composition will exhibit a quantifiable and superior ability to utilize nitrogen, as compared to the control ryegrass plants.

[0558] The nitrogen use efficiency can be quantified by recording a measurable change in any of the main nitrogen metabolic pool sizes in the assimilation pathways (e.g., a measurable change in one or more of the following: nitrate, nitrite, ammonia, glutamic acid, aspartic acid, glutamine, asparagine, lysine, leucine, threonine, methionine, glycine, tryptophan, tyrosine, total protein content of a plant part, total nitrogen content of a plant part, and/or chlorophyll content), or where the treated plant is shown to provide the same or elevated biomass or harvestable yield at lower nitrogen fertilization levels compared to the control plant, or where the treated plant is shown to provide elevated biomass or harvestable yields at the same nitrogen fertilization levels compared to a control plant.

Example 2: Increasing Maize NUE with Isolated Microbes and Microbial

Consortia

A. Seed Treatment with Isolated Microbe

[0559] In this example, an isolated microbe from Tables 1-4 will be applied as a seed coating to seeds of corn (Zea mays). Upon applying the isolated microbe as a seed coating, the corn will be planted and cultivated in the standard manner. [0560] A control plot of corn seeds, which did not have the isolated microbe applied as a seed coating, will also be planted.

[0561 ] It is expected that the com plants grown from the seeds treated with the seed coating will exhibit a quantifiable and superior ability to utilize nitrogen, as compared to the control corn plants.

[0562] The nitrogen use efficiency can be quantified by recording a measurable change in any of the main nitrogen metabolic pool sizes in the assimilation pathways {e.g., a measurable change in one or more of the following: nitrate, nitrite, ammonia, glutamic acid, aspartic acid, glutamine, asparagine, lysine, leucine, threonine, methionine, glycine, tryptophan, tyrosine, total protein content of a plant part, total nitrogen content of a plant part, and/or chlorophyll content), or where the treated plant is shown to provide the same or elevated biomass or harvestable yield at lower nitrogen fertilization levels compared to the control plant, or where the treated plant is shown to provide elevated biomass or harvestable y ields at the same nitrogen fertilization levels compared to a control plant.

B. Seed Treatment with Microbial Consortia

[0563] In this example, a microbial consortium, comprising at least two microbes from Tables 1-4 will be applied as a seed coating to seeds of corn (Zea mays). Upon applying the microbial consortium as a seed coating, the com will be planted and cultivated in the standard manner.

[0564] A control plot of com seeds, which did not have the microbial consortium applied as a seed coating, will also be planted.

[0565] It is expected that the corn plants grown from the seeds treated with the seed coating will exhibit a quantifiable and superior ability to utilize nitrogen, as compared to the control corn plants.

[0566] The nitrogen use efficiency can be quantified by recording a measurable change in any of the main nitrogen metabolic pool sizes in the assimilation pathways (e.g., a measurable change in one or more of the following: nitrate, nitrite, ammonia, glutamic acid, aspartic acid, glutamine, asparagine, lysine, leucine, threonine, methionine, glycine, tryptophan, tyrosine, total protein content of a plant part, total nitrogen content of a plant part, and/or chlorophyll content), or where the treated plant is shown to provide the same or elevated biomass or harvestable yield at lower nitrogen fertilization levels compared to the control plant, or where the treated plant is shown to provide elevated biomass or harvestable yields at the same nitrogen fertilization levels compared to a control plant.

C. Treatment with Agricultural Composition Comprising Isolated Microbe

[0567] In this example, an isolated microbe from Tables 1-4 will be applied as an agricultural composition, administered to the corn seed at the time of sowing.

[0568] For example, it is anticipated that a farmer will apply the agricultural composition to the com. seeds simultaneously upon planting the seeds into the field. This can be accomplished, for example, by applying the agricultural composition to a hopper/bulk tank on a standard 16 row planter, which contains the com seeds and which is configured to plant the same into rows. Alternatively, the agricultural composition can be contained in a separate bulk tank on the planter and sprayed into the rows upon planting the corn seed.

[0569] A control plot of corn seeds, which are not administered the agricultural composition, will also be planted.

[0570] It is expected that the com plants grown from the seeds treated with the agricultural composition will exhibit a quantifiable and superior ability to utilize nitrogen, as compared to the control corn plants.

[0571] The nitrogen use efficiency can be quantified by recording a measurable change in any of the main nitrogen metabolic pool sizes in the assimilation pathways [e.g., a measurable change in one or more of the following: nitrate, nitrite, ammonia, glutamic acid, aspartic acid, glutamine, asparagine, lysine, leucine, threonine, methionine, glycine, tiyptophan, tyrosine, total protein content of a plant part, total nitrogen content of a plant part, and/or chlorophyll content), or where the treated plant is shown to provide the same or elevated biomass or harvestable yield at lower nitrogen fertilization levels compared to the control plant, or where the treated plant is shown to provide elevated biomass or harvestable y ields at the same nitrogen fertilization levels compared to a control plant.

D. Treatment with Agricultural Composition Comprising Microbial Consortia

[0572] In this example, a microbial consortium., comprising at least two microbes from Tables 1-4 will be applied as an agricultural composition, administered to the com seed at the time of sowing. [0573] For example, it is anticipated that a farmer will apply the agricultural composition to the corn seeds simultaneously upon planting the seeds into the field. This can be accomplished, for example, by applying the agricultural composition to a hopper/bulk tank on a standard 16 row planter, which contains the com seeds and which is configured to plant the same into rows. Alternatively, the agricultural composition can be contained in a separate bulk tank on the planter and sprayed into the rows upon planting the corn seed.

[0574] A control plot of com seeds, which are not administered the agricultural composition, will also be planted.

[0575] It is expected that the com plants grown from the seeds treated with the agricultural composition will exhibit a quantifiable and superior ability to utilize nitrogen, as compared to the control corn plants.

[0576] The nitrogen use efficiency can be quantified by recording a measurable change in any of the main nitrogen metabolic pool sizes in the assimilation pathways [e.g., a measurable change in one or more of the following: nitrate, nitrite, ammonia, glutamic acid, aspartic acid, glutamine, asparagine, lysine, leucine, threonine, methionine, glycine, tiyptophan, tyrosine, total protein content of a plant part, total nitrogen content of a plant part, and/or chlorophyll content), or where the treated plant is shown to provide the same or elevated biomass or harvestable yield at lower nitrogen fertilization levels compared to the control plant, or where the treated plant is shown to provide elevated biomass or harvestable yields at the same nitrogen fertilization levels compared to a control plant.

Example 3: Increasing Soybean NUE with Isolated Microbes and Microbial

Consortia

A. Seed Treatment with Isolated Microbe

[0577] In this example, an isolated microbe from Tables 1-4 will be applied as a seed coating to seeds of soybean (Glycine max). Upon applying the isolated microbe as a seed coating, the soybean will be planted and cultivated in the standard manner.

[0578] A control plot of soybean seeds, which did not have the isolated microbe applied as a seed coating, will also be planted. [0579] It is expected that the soybean plants grown from the seeds treated with the seed coating will exhibit a quantifiable and superior ability to utilize nitrogen, as compared to the control soybean plants.

[0580] The nitrogen use efficiency can be quantified by recording a measurable change in any of the mam nitrogen metabolic pool sizes in the assimilation pathways (e.g., a measurable change in one or more of the following: nitrate, nitrite, ammonia, glutamic acid, aspartic acid, glutamine, asparagine, lysine, leucine, threonine, methionine, glycine, tryptophan, tyrosine, total protein content of a plant part, total nitrogen content of a plant part, and/or chlorophyll content), or where the treated plant is shown to provide the same or elevated biomass or harvestable yield at lower nitrogen fertilization levels compared to the control plant, or where the treated plant is shown to provide elevated biomass or harvestable yields at the same nitrogen fertilization levels compared to a control plant.

B, Seed Treatment with Microbial Consortia

[0581] In this example, a microbial consortium, comprising at least two microbes from Tables 1-4 will be applied as a seed coating to seeds of soybean (Glycine max). Upon applying the microbial consortium as a seed coating, the soybean will be planted and cultivated in the standard manner.

[0582] A control plot of soybean seeds, which did not have the microbial consortium applied as a seed coating, will also be planted.

[0583] It is expected that the soybean plants grown from the seeds treated with the seed coating will exhibit a quantifiable and superior ability to utilize nitrogen, as compared to the control soybean plants.

[0584] The nitrogen use efficiency can be quantified by recording a measurable change in any of the main nitrogen metabolic pool sizes in the assimilation pathways (e.g., a measurable change in one or more of the following: nitrate, nitrite, ammonia, glutamic acid, aspartic acid, glutamine, asparagine, lysine, leucine, threonine, methionine, glycine, tryptophan, tyrosine, total protein content of a plant part, total nitrogen content of a plant part, and/or chlorophyll content), or where the treated plant is shown to provide the same or elevated biomass or harvestable yield at lower nitrogen fertilization levels compared to the control plant, or where the treated plant is shown to provide elevated biomass or harvestable yields at the same nitrogen fertilization levels compared to a control plant. C. Treatment with Agricultural Composition Comprising Isolated Microbe

[0585] In this example, an isolated microbe from Tables 1-4 will be applied as an agricultural composition, administered to the soybean seed at the time of sowing.

[0586] For example, it is anticipated that a fanner will apply the agricultural composition to the soybean seeds simultaneously upon planting the seeds into the field. This can be accomplished, for example, by applying the agricultural composition to a hopper/bulk tank on a standard 16 row planter, which contains the soybean seeds and which is configured to plant the same into rows. Alternatively, the agricultural composition ca be contained in a separate bulk tank on the planter and sprayed into the rows upon planting the soybean seed.

[0587] A control plot of soybean seeds, which are not administered the agricultural composition, will also be planted.

[0588] It is expected that the soybean plants grown from the seeds treated with the agricultural composition will exhibit a quantifiable and superior ability to utilize nitrogen, as compared to the control soybean plants.

[0589] The nitrogen use efficiency can be quantified by recording a measurable change in any of the main nitrogen metabolic pool sizes in the assimilation pathways (e.g., a measurable change in one or more of the following: nitrate, nitrite, ammonia, glutamic acid, aspartic acid, glutamine, asparagine, lysine, leucine, threonine, methionine, glycine, tryptophan, tyrosine, total protein content of a plant part, total nitrogen content of a plant part, and/or chlorophyll content), or where the treated plant is shown to provide the same or elevated biornass or harvestabie yield at lower nitrogen fertilization levels compared to the control plant, or where the treated plant is shown to provide elevated biomass or harvestabie yields at the same nitrogen fertilization levels compared to a control plant.

D. Treatment with Agricultural Composition Comprising Microbial Consortia

[059Θ] In this example, a microbial consortium, comprising at least two microbes from Tables 1-4 will be applied as an agricultural composition, administered to the soybean seed at the time of sowing.

[0591] For example, it is anticipated that a farmer will apply the agricultural composition to the soybean seeds simultaneously upon planting the seeds into the field. This can be accomplished, for example, by applying the agricultural composition to a hopper/bulk tank on a standard 16 row planter, which contains the soybean seeds and which is configured to plant the same into rows. Alternatively, the agricultural composition can he contained in a separate bulk tank on the planter and sprayed into the rows upon planting the soybean seed.

[0592] A control plot of soybean seeds, which are not administered the agricultural composition, will also be planted.

[0593] It is expected that the soybean plants grown from the seeds treated with the agricultural composition will exhibit a quantifiable and superior ability to utilize nitrogen, as compared to the control soybean plants.

[0594] The nitrogen use efficiency can be quantified by recording a measurable change in any of the main nitrogen metabolic pool sizes in the assimilation pathways (e.g., a measurable change in one or more of the following: nitrate, nitrite, ammonia, glutamic acid, aspartic acid, glutamine, asparagine, lysine, leucine, threonine, methionine, glycine, tryptophan, tyrosine, total protein content of a plant part, total nitrogen content of a plant part, and/or chlorophyll content), or where the treated plant is shown to provide the same or elevated biomass or harvestable yield at lower nitrogen fertilization levels compared to the control plant, or where the treated plant is shown to provide elevated biomass or harvestable yields at the same nitrogen fertilization levels compared to a control plant.

IV. Increased Metabolite Expression in Agriculturally Important Crops

[0595] In certain embodiments of the disclosure, the present methods aim to increase the production of a metabolite of interest for a given crop.

[0596] The methodologies presented herein— based upon utilizing the disclosed isolated microbes, consortia, and compositions comprising the same— have the potential to increase the production of a metabolite of interest for a given crop.

Example 1: Increasing Sugar Content in Basil with Isolated Microbes and Microbial Consortia

A. Seed Treatment with Isolated Microbe

[0597] In this example, an isolated microbe from Tables 1-4 will be applied as a seed coating to seeds of basil (Ocium basilicum). Upon applying the isolated microbe as a seed coating, the basil will be planted and cultivated in the standard manner.

[0598] A control plot of basil seeds, which did not have the isolated microbe applied as a seed coating, will also be planted. [0599] It is expected that the basil plants grown from the seeds treated with the seed coating will exhibit a quantifiable increase in water-soluble carbohydrate content, as compared to the control basil plants.

B. Seed Treatment with Microbial Consortia

[0600] In this example, a microbial consortium, comprising at least two microbes from Tables 1-4 will be applied as a seed coating to seeds of basil (Ocium basilicum). Upon applying the microbial consortium as a seed coating, the basil will be planted and cultivated in the standard manner.

[0601] A controi plot of basil seeds, which did not have the microbial consortium applied as a seed coating, will also be planted.

[0602] It is expected that the basil plants grown from the seeds treated with the seed coating will exhibit a quantifiable increase in water-soluble carbohydrate content, as compared to the control basil plants.

V. Synergistic Effect Achievable with Combination of Microbes and Ascend®

A. Seed Treatment with Isolated Microbe Combined with Ascend®

[0603] In this example, an isolated microbe from Tables 1-4 will be combined with Ascend® and applied as a seed coating to seeds of a plant. Upon applying the isolated microbe/Ascend© combination as a seed coating, the plant will be planted and cultivated in the standard manner.

[0604] A control plot of plant seeds, which did not have the isolated microbe/Ascend© combination applied as a seed coating, will also be planted.

[0605] It is expected that the plants grown from the seeds treated with the seed coating will exhibit a quantifiable increase in a phenotypic trait of interest, as compared to the control plants. It is expected that a synergistic effect may be observed for the phenotypic trait of interest.

B, Seed Treatment with Microbial Consortia Combined with Ascend®

[0606] In this example, a microbial consortium, comprising at least two microbes from

Tables 1-4 will be combined with Ascend® and then applied as a seed coating to seeds of a plant. Upon applying the microbial consortium/ Ascend® combination as a seed coating, the plant will be planted and cultivated in the standard manner. 7] A control plot of plant seeds, which did not have the microbial consortium/Ascend® combination applied as a seed coating, will also be planted.

[0608] It is expected that the plants grown from the seeds treated with the seed coating will exhibit a quantifiable increase in a phenotypic trait of interest, as compared to the control plants. It is expected that a synergistic effect may be observed for the phenotypic trait of interest.

VI, Microbial Consortia

The microbial consortia utilized in the examples are presented in Table 18 in a non- limiting matter, while recognizing that the microbial consostia may comprise any one or more microbes presented in tables 1-4.

Table 19: Consortia Compositions

Rliodococcus erythropohs BDNZ

Stenotrophomonas maltophilia

54093

BDNZ 54073

Pseudomonas oryzihabiians

Rliodococcus erythropohs BDNZ

BDNZ 55530

54093

Rahnella aquatilis BDNZ 56532

Panioea vagans BDNZ 55529

Pseudomonas otyzihabitans BDNZ

55530

Stenotrophomonas maltophilia Stenotrophomonas maltophilia BDNZ 54073 BDNZ 54073

Rhodococcus erythropohs BDNZ Rhodococcus erythropohs

54093 54093

Panioea vagans BDNZ 55529 Pseudomonas fluorescens BDNZ

56530

Rahnella aauaiihs BDNZ 56532

Panioea agglomerans BDNZ 57547

Rhodococcus erythropohs BDNZ Rahnella aquatilis BDNZ 57157 54093

Rahnella aquatilis BDNZ 58013

Pseudomonas fluorescens BDNZ

56530 Rhizobium etli BDNZ 60473

Panioea agglomerans BDNZ 57547

D7 Stenotrophomonas ahophilia D8 Stenotrophomonas mahophilia.

BDNZ 54073 BDNZ 54073

Rhodococciis erythropolis BDNZ Rhodococciis erythropolis BDNZ 54093 54093

Pantoea vagans BDNZ 55529 Pantoea vagans BDNZ 55529

Pseudomonas oryzihabitans BDNZ Pseudomonas oryzihabitans 55530 BDNZ 55530

RahneUa aquatilis BDNZ 56532 RahneUa aquatilis BDNZ 57157

RahneUa aquatilis BDNZ 58013 Rhizobium eth BDNZ 60473

RakneHa aquatilis BDNZ 56532

D9 10 Rhodococcus erythropolis BDNZ

54093

Pantoea vagans BDNZ 5 529

Pseudomonas oryzihabitans BDNZ 55530

RahneUa aquatilis BDNZ 56532

Exiguobacterium aurantiacum BCl

Dl l RahneUa aquatilis BCl 29

D12

50 ^"

Duganella radicis BCl 31

Duganella radicis BCl 105

Exiguobacteriu sibiricum BCl Rhizobium pusense BCl 106 116

Kosakonia radicincitans BCl 107 Novosphingobiiim sediminicola

BCl 130

Delflia lacustris BCl 124

Ensifer sp. BCl 131

Microbacterium oleivorans BCl 132

Chitinophaga terrae BCl 79

D13 D14 Exiguobacterium acetylicum BCl

23 ^~

Exiguobacterium so. BCl 81

RahneUa aquatilis BCl 29

Novosphingobium sediminicola BCI 82 Rhizobium lemnae BCI 34

Exiguobacierium acetvlicum BCI Achromobacter spanius BCI 385 83

Variovorax ginsengisoli BCI 137

Dyadobacter soli BCI 68

D15 Rhodococcus erythropolis BDNZ

D16

54093

Chiiinophaga ierrae BCI 79

Pantoea vagans BDNZ 55529 Pedobacter ierrae BCI 91

Pseudomonas orvzihabitans Massilia albidiflava BCI 97 BDNZ 55530

Novosphingobhim sediminicola

BCI 136

D17 Rhodococcus erythropolis BDNZ Exiguobacierium acetylicum

D18

54093 BCI 125

Rahnella aquatilis BDNZ 56532 Bacillus megaterium BCI 255

Ra wlla aquatilis BDNZ 58013 Paenibacilhis glycanilvticus BCI

418

Rhizobium etli BDNZ 60473

D19 Agrobacterium fabrum BCI 608 Arthrobacter pascens BCI 682

D20

Acidovorax soh BCI 690 Novosphingobium

lindaniclasiicum BCI 684

Rhizobium graha ii BCI 691

Β<¾'ί¾' robiniae BCI 688

Bacillus subtilis BCI 989

Microbacterium maritypicum BCI 689

Spkingopyxis alaskensis BCI 914

Chryseobacterium rhizosphaerae

D21 D22 Novosphingobhim resinovorum BCI 615 BCI 557

Hydrogenopnaga atypica BCI 687 Arthrobacter mysorens BCI 700

Bosea robiniae BCI 689 So.y<¾? thiooxidans BCI 703

Microbacterium maritypicum BCI Bacillus oleronius BCI 1071 688

Agrobacterium fabrum. BCI 958

D23 Pedobacter rhizosphaerae BCI 598 Novosphingobium sediminicola

D24

BCI 130 Bacillus sp. BCI 715 Ensifer sp. BCI 131

Pseudomonas jinjuensis BQ 804 Microbacterium oleivorans BCS

132

Pseudomonas p tida BCI 805

D2S Arthrobacter cupressi BO 59

D26 Bosea rohiniae BCI 689

Dyadobacter soli BCI 68 Bosea thiooxidans BCI 703

Bosea eneae BCI 1267

D27 Pseudomonas helmanticemis BCI Chryseobacterium rhizosphaerae

D28

616 BCI 597

Arthrobacter pascens BCI 682 Defluviimonas demtrificans BCI

712

Bosea robitvae BCT 689

Arthrobacter nicotinovorans BCI Pseudomonas putida BCI 791 717

Agrobacterium fabrum BCI 958 Pseudomonas putida BCI 802

Pseudomonas florescens BDNZ

D29 D30 Rhodococcus erythropolis BDNZ 71627 74552

Novosphingobium sediminicola I ^' umebaciilus permanentifrigoris BDNZ 71628 BDNZ 74542

Microbacterium azadirachtae

BDNZ 7 629

D31 Turnebacillus permanentifrigoris

D32 Rhodococcus erythropolis BNDZ BDNZ 72229 72250

Bacillus megatarium BDNZ 72242 Leifsonia lichenia BDNZ 72243

Bacillus megatarium BDNZ 72242 Novosphingobium

D33 D34

iiridaniclasticum BDNZ 71222 Leifionia lic enia BDNZ 72243

Bacillus arvabhattai BDNZ 72259

Rhodococcus erythropolis BDNZ

D35 D36 Bacillus cereus BDNZ 71220 7122

Rhodococcus etyihropohs BNDZ

Novosphingobium lindaniclasiicum 71221

BDNZ 71222

Novosphingobium

Microbacterium azadirachtae lindaniclasticum BDNZ 71222 BDNZ 71663 D37 Massiiia kyonggiensis BDNZ

D38 Vanovorax paradoxus BDNZ 73021 72150

Microbacterium azadirachtae Tumebacilhis permanentifrigoris BDNZ 72996 BDNZ 72366

Rhizobium tibeticum BDNZ 72135

D39 7 'umebacillus permanentifrigoris

BDNZ 72287

Bacillus rnegaiarium BDNZ 72255

Sienotrophomonas maltophilia

A l Flavobacterium glaciei BDNZ

A2

BDNZ 54073 66487

Rhodococcus erythropolis BDNZ Massilia niastensis BDNZ 55184 54093

Pseudomonas fluoresceins BDNZ

P toea vagans BDNZ 55529 54480

Psendo onas oryzihabitam

BDNZ55530

A3 Azospirillum lipoferum BDNZ Janthinobacterium sp. BDNZ

A4

57661 54456

Herbaspirilium huttiense BDNZ Mucilagmibacter dorafii BDNZ 54487 66513

Pantoea agglomerans BDNZ Pseudomonas psyckrotolercms 54499 BDNZ 54517

Pseudomonas fluorescerts BDNZ

54480

AS Janthinobacterium sp. BDNZ Rhizobium eta BDNZ 61443

A6

54456

Caulobacter henrici BDNZ 66341

Mucilagmibacter dorajii BDNZ

66513 ^" Duganella violaceinigra BDNZ

66361

Pseudomonas psych rotolerans

BDNZ 54 17

A7 Duganella violaceinigra BDNZ

AS Ramlibacter henchirensis BDNZ 66361 66331

Rhizobium. pisi BDNZ 66326

Mucilagmibacter gosvpii BDNZ 66321

Paenibacillus amviolvticus BDNZ 66316

Polar omonas girisengisoh BDNZ Sphingobium quisquiliarum

A9 A10

66373 BDNZ 66576

Bacillus subtilis BDNZ 66347

Azospirillum lipoferurn BDNZ 66297

Rhodoferax ferrireducens BDNZ Rhodococcus erythropolis BDNZ

All A12

66374 54093

Mucilagmibacter gosypii BDNZ Pseudomonas oryzihabitans 66321 BDNZ 55530

Paenibacillus amylolyticus BDNZ Rahneila aquatilis BDNZ 56532 66316

Azospirillum lipoferurn

BDNZ66315

Rhodococcus erythropohs BDNZ Rhodococcus erythropolis

A13

54093 BDNZ54299

Rahneila aquatilis BDNZ 57157 Rahneila aquatilis BDNZ58013

Azoiobacter chroococcum Herbaspirillum huttiense BDNZ BDNZ57597 65600 ^'

Rhodococcus erythropohs BDNZ

A15

54093

Pseudomonas oryzihabitans BDNZ

55530

Rahneila aauaiilis BDNZ 56532

VII. Effects of Microbial Consortia on Plant Phenotvpes

Example !: Evaluation of Phenotype of Plants Exposed to Microbial Consortia in U.S. Trials

[0610] Plants disclosed in Table 20 were grown in a controlled environment in a rooting volume of 167ml and typically in a soil substrate. The chamber photopenod was set to 16 hours for all experiments on all species. The light intensity ranged from 180 μηιοΐ PAR m ^" s ^{" 1} to approximately 200 μηιοΐ PAR m ^"2 s ^{" !} as plant height increased during experiments.

[0611] The air temperature was typically 28°C during the photopenod, decreasing to 23°C during the night for Zea mays, Glycine max, and Sorghum bicolor experiments. Air temperature was typically 24°C during the photoperiod, decreasing to 20°C during the night for Triticum aestivum experiments.

[0612] Phenotypes were measured during early vegetative growth, typically before the V3 developmental stage.

[0613] Leaf chlorophyll content was measured midway along the youngest fully-expanded leaf non-destructively using a meter providing an index of leaf chlorophyll content (CCM- 200, Opti Sciences, Hudson, NH, US).

[0614] Whole plant, shoot, and root dry weight was measured after plants had been dried to a constant weight in a diying oven set to 80°C. At least 10 replicate plants were measured for each phenotype measured in each experiment.

[Θ615] For evaluations on Glycine max, the number of nodules were counted.

[0616] A control treatment of umnoculated seeds was run in each experiment for comparison with plants grown from seeds inoculated with microbial consortia.

Controlled Environ merit Efficacy {¾}

[0617] The data presented in table 20 describes the percentage of time (efficiency) a particular consortium changed a phenotype of interest relative to a control nm in the same experiment. The measured phenotypes were whole plant dry weight (plant), shoot dry weight (shoot), root dry weight (root), leaf chlorophyll content (chlorophyll), leaf temperature (Tleaf), and nodulation.

[0618] The data presented is averaged across the number of times a specific consortium was tested against a control (evaluations). For consortia where different phenotypes were measured in a different number of evaluations, an asterisk was placed next to data points to match the phenotype with the number of evaluations. Evaluations have been broken down and displayed for specific crop species (crop).

[0619] The presented data identifies consortia that have increased a phenotype of interest in greater than 60% of evaluations (hit rate >59) and consortia that decreased a phenotype of interest in greater than 60% of evaluations (hit rate<41). Both increases and decreases in a phenotype of interest were recorded to reflect the possibility that decreases in select phenotypes of interest are yield relevant. Improvement in canopy photosynthesis through decreased leaf chlorophyll, and improvement in drought tolerance through decreased shoot biornass constitute two examples.

Example 2: Evaluation of Phenotype of Plants Exposed to Microbial Consortia in New Zealand Trials

[0620] A. Seed Treatment with Microbial Consortia

[0621] The inoculants were prepared from isolates grown as spread plates on R2A incubated at 25°C for 48 to 72 hours. Colonies were harvested by blending with sterile distilled water (SDW) which was then transferred into sterile containers. Serial dilutions of the harvested cells were plated and incubated at 25°C for 24 hours to estimate the number of colony forming units (CPU) in each suspension. Dilutions were prepared using individual isolates or blends of isolates (consortia) to deliver ~lxl 0 ^s cfii/microbe/seed and seeds inoculated by either imbibition in the liquid suspension or by overtreatment with 5% vegetable gum and oil.

[0622] Seeds corresponding to the plants of table 21 were planted within 24 to 48 hours of treatment in agricultural soil, potting media or inert growing media. Plants were grown in small pots (28 niL to 200 mL) in either a controlled environment or in a greenhouse. Chamber photoperiod was set to 16 hours for all experiments on all species. Air temperature was typically maintained between 22-24°C.

[0623] Unless otherwise stated, all plants were watered with tap water 2 to 3 times weekly. Growth conditions were varied according to the trait of interest and included manipulation of applied fertilizer, watering regime and salt stress as follows:

• Low N - seeds planted in soil potting media or inert growing media with no applied N fertilizer

* Moderate N - seeds planted in soil or growing media supplemented with commercial N fertilizer to equivalent of 135 kg/ha applied N

« Insol P - seeds planted in potting media or inert growth substrate and watered with quarter strength Pikovskaya's liquid medium containing tri -calcium phosphate as the only form phosphate fertilizer.

* Cold Stress - seeds planted in soil, potting media or inert growing media and incubated at 10"C for one week before being transferred to the plant growth room.

• Salt stress - seeds planted in soil, potting media or inert growing media and watered with a solution containing between 100 to 200 mg/L NaCl.

[0624] Untreated (no applied microbe) controls were prepared for each experiment. Plants were randomized on trays throughout the growth environment. Between 10 and 30 replicate plants were prepared for each treatment in each experiment. Phenot pes were measured during early vegetative growth, typically before the V3 developmental stage and between 3 and 6 weeks after sowing. Foliage was cut and weighed. Roots were washed, blotted dry and weighed. Results indicate performance of treatments against the untreated control.

[0625] The data presented in table 21 describes the efficacy with which a microbial species or strain can change a phenotype of interest relative to a control run in the same experiment. Phenotypes measured were shoot fresh weight and root fresh weight for plants growing either in the absence of presence of a stress (assay). For each microbe species, an overall efficacy- score indicates the percentage of times a strain of that species increased a both shoot and root fresh weight in independent evaluations. For each species, the specifics of each independent assay is given, providing a strain ID (strain) and the crop species the assay was performed on (crop). For each independent assay the percentage increase in shoot and root fresh weight over the controls is given.

B. Seed Treatment with Microbial Consortia

[0626] The inocuiants were prepared from isolates grown as spread plates on R2A incubated at 25°C for 48 to 72 hours. Colonies were harvested by blending with sterile distilled water (SDW) which was then transferred into sterile containers. Serial dilutions of the harvested cells were plated and incubated at 25°C for 24 hours to estimate the number of colony forming units (CPU) in each suspension. Dilutions were prepared using individual isolates or blends of isolates (consortia) to deliver ~lxl(f cfu/microbe/seed and seeds inoculated by either imbibition in the liquid suspension or by overtreatment in combination with 0.1 - 1 % vegetable gum..

[0627] Seeds corresponding to the plants of table 22 were planted within 24 to 48 hours of treatment in agricultural soil, potting media or inert growing media. Plants were grown in small pots (28 niL) in a controlled environment. The chamber photoperiod was set to 16 hours for all experiments on all species. Air temperature was typically maintained between 22-24°C.

[0628] All plants were watered with tap water 2 to 3 times weekly. Plants were subjected to either no stress (NS) or limited nitrogen to investigate nitrogen use efficiency (NUE). Growth conditions were varied according to the trait of interest and included manipulation of applied fertilizer as follows:

* Low N - seeds planted in soil potting media or inert growing media with no applied N fertilizer

* Moderate N - seeds planted in soil or growing media supplemented with commercial N fertilizer to equivalent of 135 kg/ha applied N [0629] Untreated (no applied microbe) controls were prepared for each experiment. Plants were randomized on trays throughout the growth environment. Between 10 and 30 replicate plants were prepared for each treatment in each experiment. Phenotypes were measured during early vegetative growth, typically before the V3 developmental stage and between 3 and 6 weeks after sowing. Fresh foliar weight was measured 18h after watering substrate to saturation. Dry root weight was measured after drying to a constant weight at 80°C. Results indicate performance of treatments against the untreated control.

Table 22

[0630] The data presented in table 22 describes the percentage of time a particular consortium changed a phenotype of interest relative to an inert-only control run in the same experiment. The measured phenotypes were fresh shoot weight, measured 18 hours after watering to saturation, and dry root weight, measured after drying to a constant state at 80 degrees Celsius.

[0631] The presented data identifies consortia that have increased a phenotype of interest in greater than 60% of evaluations (hit rate >59) and consortia that decreased a phenotype of interest in greater than 60% of evaluations (hit rate<41). Both increases and decreases in a phenotype of interest were recorded to reflect the possibility that decreases in select phenotypes of interest are yield relevant. Example 3: Evaluation of Yield Effect of Maize Exposed to Microbial Consortia in U.S. Field Trials

[0632] The data presented in Table 23 summarizes the changes in final yield relative to a control for six consortia tested in eight locations in the mid- West of the United States. Also presented is final yield data from two drought trials performed in California in the United States. Data is expressed as the percentage of trials in which a yield effect in bushels per acre of a particular magnitude was obsen/ed. All field trials were run in accordance with standard agronomic practices.

Table 23

Example 4: Evaluate Yield Effect of Maize Exposed to Microbial Consortia in New Zealand Field Trials

[0633] The data presented in Table 24 summarizes the results of New Zealand field trials for select consortia. The presented data describes the number of trials in which a particular consortia has been tested relative to a control, and the number of trials in which the consortia treatment increased the final yield relative to the control treatment. All field trials were run in accordance with standard agronomic practices.

Table 24

Example 5: Microbes Deposited with the ARS Culture Collection (NRRL)

[0634] In one experimental embodiment, the inventors utilized the following microbial species in applications of the present disclosure. Table 25 details microbial species of the present disclosure which have been deposited with the United States Department of Agriculture ARS Culture Collection (NRRL).

Table 25

Taxonomy BCi BD Z Deposited Accession USDA

(US) (NZ) date number Viabi!ity

Date

1 Acidovorax soli 648 12.29.2015 NRRL B-67181 1.4.2016

2 Aciciovorax soli 690 12.29.2015 NRRL B-67182 1.4.2016

3 Arthrobacter 59 12,29.2015 NRRL B-67183 1.4.2016

cupressi

4 Arthrobacter 62 12,29.2015 NRRL B-67184 1.4.2016

cupressi

5 Bosea eneae 1267 12,29.2015 NRRL B-67185 1.4.2016

6 Bosea robiniae 689 12.29.2015 NRRL B-67186 1.4.2016

7 Bosea thiooxidans 703 12.29.2015 NRRL B-67187 1.4.2016

8 Chitinophaga 79 12,29.2015 NRRL B-67188 1.4.2016

terrae

9 Chitinophaga 109 12.29.2015 NRRL B-67189 1.4.2016

terrae

10 Delftia iacustris 124 12.29.2015 NRRL B-67190 1.4.2016

11 Deiftia Iacustris 2350 12.29.2015 NRRL B-67191 1.4.2016

12 Duganella radicis 105 12,29.2015 NRRL B-67192 1.4.2016

13 Duganeiia 2204 12.29.2015 NRRL B-67193 1.4.2016

violaceinigra

14 Dyadobacter soii 68 12.29.2015 NRRL B-67194 1.4.2016

15 Dyadobacter soli 96 12.29.2015 NRRL B-67195 1.4.2016

16 Flavobacterium 4005 12.29.2015 NRRL B-67196 1.4.2016

glacei

17 Herbaspiriilum 162 12.29.2015 NRRL B-67197 1.4.2016

chlorophenolicum

18 Massilia 97 12.29.2015 NRRL B-67198 1.4.2016

kyonggiensis

(deposited as

Massilia

aibidiflava)

19 Massilia niastensis 1217 12.29.2015 NRRL B-67199 1.4.2016

20 Novosphingobium 684 12.29.2015 NRRL B-67201 1.4.2016

lindaniclasticum

21 Novosphingobium 608 12.29.2015 NRRL B-67200 1.4.2016

lindaniclasticum

22 Novosphingobium 557 12,29.2015 NRRL B-672G2 1.4.2016

resinovorum Novosphingobium 3709 12,29.2015 W! L B-67203 1.4.2016 resinovorum

Paenibacillus 418 12.29.2015 N!RRL B-67204 1.4.2016 glycanilyticus

Pedobacter 598 12.29.2015 N!RRL B-67205 1.4.2016 rhizosphaerae

(deposited as

Pedobacter soli)

Pedobacter terrae 91 12,29.2015 W!RRL B-67206 1.4.2016

Pseudomonas 804 12.29.2015 NRRL B-67207 1.4.2016 jinjuensis

Ramlibacter 739 12.29.2015 NRRL B-67208 1.4.2016 henchirensis

Ramlibacter 1959 12.29.2015 NRRL B-67209 1.4.2016 henchirensis

Rhizobium 34 12.29.2015 HRRl B-67210 1.4.2016 rhizoryzae

(previously R.

lemnae)

Rhizobium 661 12.29.2015 fc!RRL B-67211 1.4.2016 rhizoryzae

(previously R.

lemnae)

Rhizobium sp. 106 12.29.2015 RRL B-67212 1.4.2016

Sinorhizobium 111 12.29.2015 H i B-67213 1.4.2016

Chiapanecum (now

Ensifer adhaerens)

Sphingopyxis 412 12,29.2015 NRRL B-67214 1.4.2016 aiaskensis

Sphingopyxis 914 12,29.2015 RRL B-67215 1.4.2016 aiaskensis

Variovorax 137 12,29.2015 fc!RRL B-67216 1.4.2016 ginsengisoli

Variovorax 3078 12,29.2015 fc!RRL B-67217 1.4.2016 ginsengisoli

Achromobacter 49 12, 18.15 W!RRL B-67174 12.21.2015 pulmonis

Chryseobacterlum 45 12, 18.15 RRL B-67172 12.21.2015 daecheongense

Duganella radicis 31 1.13.16 RRL B-67166 1.15.2016

Exiguobacterium 50 12.18.15 HRRl B-67175 12,2 x.2013 aurantiacum

Exiguobacterium 116 12.18.15 HRRl B-67167 12,2 x. 013 sibiricum

osakonia 44 12.18.15 H i B-67171 12,2 x. 013 radicincitans

Microbacterium 132 12.18.15 MRRL B-67170 12.21.2015 oleivorans

Novosphingobium 130 12.18.15 MRRL B-67168 12.21.2015 sediminicola

Pedobacter terrae 53 12.18,15 H i B-67176 12,2 x.20X3

RahneNa aquatilis 29 12, 18.15 NRRL B-67165 12.21.2015

Agrobacterium 46 12, 18.15 N!RRL B-67173 12.21.2015 fa brum or

Rhizobium pusense

(In Taxonomic Flux)

(previously

Rhizobium sp.)

Sinorhizobium 131 12.18.15 N!RRL B-67169 12.21.2015 chiapanecum

(Ensifer adhaerens

- current

classification)

Pantoea vagans 55529 1.29.2016 RRL B-67224 2.4.2016

Pseudomonas 55530 1,29.2016 NRRL B-67225 oryzihabitans 2,4,2016

Stenotrophomonas 54073 1,29.2016 HRRl B-67226 maltophilia 2,4,2016

Rahnella aquatilis 58013 1,29.2016 H i B-67229 2.4.2016 ahnella aquatilis 56532 1.2.9,2016 RRL B-67228 2.4.2016

Rhodococcus 54093 1.29.2016 fc!RRL B-67227 erythropolis 2.4.2016

Herbaspirillum 58 2,8.2016 MRRL B-67236 chlorophenoiicum 2.10.2016

Bacillus niacini 4718 2,8.2016 MRRL B-67230 2.10.2016

Polaromonas 66373 2.8.2016 N!RRL B-67231 ginsengisoii 2.10.2016

Polaromonas 66821 2.8.2016 RRL B-67234 ginsengisoii 2.10.2016

Duganella 66361 2.8.2016 RRL B-67232 vioiaceinigra 2.10.2016

Duganella 58291 2.8.2016 RRL B-67233 vioiaceinigra 2.10.2016 assilia niastensis 55184 2.8.2016 RRL B-67235 2.10.2016

Agrobacterium 958 7.14.2016 fc!RRL B-67286 7.17.2016 fabrum or

Rhizobium pusense

Arthrobacter 717 7,14.2016 MRRL B-67289 7.17,2016 nicotinovorans

Arthrobacter 3189 7,14.2016 MRRL B-67290 7.17,2016 nicotinovorans

Chryseobacterium 191 7.14.2016 RRL B-67291 7.17.2016 daecheongense

Chryseobacterium 597 7.14.2016 RRL B-67288 7.17.2016 rhizosphaerae

Chryseobacterium 615 7.14.2016 N!RRL B-67287 7.17.2016 rhizosphaerae 69 Frigidibacter a!hus 712 7.14,2016 W! L B-67285 7.17.2016 or Delfulviimonas

dent rif icons (In

Taxonomic Flux)

70 Frigidibacter a!bus 402 7.14,2016 NRRL B-67283 7.17.2016

or Delfulviimonas

dentrif leans (in

Taxonomic Flux)

71 Frigidibacter aibus 745 7.14.2016 N!RRL B-67284 7.17.2016

or Delfulviimonas

dentrif icans (in

Taxonomic Flux)

72 Exiguobacterium 63 7,14.2016 H i B-67292 7.17,2016

antarcticum

73 Exiguobacterium 225 7,14.2016 NRRL B-67293 7.17.2016

antarcticum

74 Exiguobacterium 718 7,14.2016 NRRL B-67294 7.17.2016

sibiricum

75 Pseudomonas 616 7,14,2016 NRRL B-67295 7.17.2016

helmanticensis

76 Pseudomonas 2945 7,14,2016 NRRL B-67296 7.17.2016

helmanticensis

77 Pseudomonas 800 7.14.2016 N!RRL B-67297 7.17.2016

helmanticensis

78 Leifsonia !ichenia 72243 7.21.2016 N!RRL B-67298 7.22.2016

79 Leifsonia lichenia 72289 7.21.2016 RRL B-67299 7.22.2016

80 Tumebacillus 72229 7,21.2016 HRRl B-673G2 In process

permanetifrigoris

81 Tumebacillus 74542 7,21.2016 H i B-673G0 In process

permanetifrigoris

82 Tumebacillus 72366 7,22.2016 HRRl B-673G3 In process

permanetifrigoris

83 Tumebacillus 72287 7,21.2016 MRRL B-67301 In process

permanetifrigoris

*In process notes that viability testing has been conducted and outcome is awaiting transmittal

Example 6: Novel Microbial Species Deposited with the ARS Culture Collection (NRRL)

[0635] In one experimental embodiment, the inventors utilized the following microbial species in applications of the present disclosure.

Table 26

Taxonomy BC1 (US) BDMZ {HZ}

Achromobacter pulmonis 49

Acidovorax soli 648

Acidovorax soli 690 Agrobacterium fabrum or

Rhizobium pusense (in Taxonomix

flux) 46

Agrobacterium fabrum or

Rhizobium pusense (in Taxonomix

flux) 958

Arthrobacter cupressi 59

Arthrobacter cupressi 62

Arthrobacter nicotinovorans 717

Arthrobacter nicotinovorans 3189

Bacillus niacini 4718

Bosea eneae 1267

Bosea robiniae 689

Bosea thiooxidans 703

Chitinophaga terrae 79

Chitinophaga terrae 109

Chryseobacterium

daecheongense 45

Chryseobacterium

daecheongense 191

Chryseobacterium rhizospaerae 597

Chryseobacterium rhizospaerae 615

Delftia lacustris 124

Delftia lacustris 2350

Frigidibacter albas or

Delfulvlimonas dentrificans (In

Taxonomic Flux) 712

Frigidibacter a!bus or

Delfulviimonas dentrificans (in

Taxonomic Flux) 402

Frigidibacter a!bus or

Delfulviimonas dentrificans (in

Taxonomic Flux) 745

Duganella radicis 105

Duganelia radicis 31

Duganella violaceinigra 2204

Duganella violaceinigra 66361

Duganelia violaceinigra 58291

Dyadobacter soli 68

Dyadobacter soli 96

Exiguobacterium antarcticum 63

Exiguobacierium antarcticum 225

Exiguobacterium aurantiacum 50

Exiguobacterium sibiricum 116

Exiguobacterium sibiricum 718

Flavobacterium giacei 4005

Herbaspirillum chlorophenolicum 162

Herbaspirillum chlorophenolicum 58

Kosakonia radicincitans 44 Leifsonia iichenia 72243

Leifsonia iichenia 72289

Massilia kyonggiensis (deposited

as assiiia aibidifiava; new

taxonomy is kyonggiensis) 97

Massiiia niastensis 1217

Massiiia niastensis 55184

■vlicrobacterium o!eivorans 132

Novosphingobium

iindaniclasticum 684

Novosphingobium

iindaniclasticum 608

Novosphingobium resinovorum 557

Novosphingobium resinovorum 3709

Novosphingobium sediminicola 130

Paenibaciiius glycaniiyticus 418

Pantoea vagans 55529

Pedobacter rhizosphaerae

(deposited as Pedobacter soli) 598

Pedobacter terrae 91

Pedobacter terrae 53

Poiaromonas ginsengisoii 66373

Polaromonas ginsengisoii 66821

Pseudomonas helmanticensis 616

Pseudomonas helmanticensis 2945

Pseudomonas helmanticensis 800

Pseudomonas jinjuensis 804

Pseudomonas oryzihabitans 55530

Rahneiia aquatilis 29

Rahnelia aquatilis 58013

Rahneiia aquatilis 56532

Ramiibacter henchirensis 739

Ramiibacter henchirensis 1959

Rhizobium rhizoryzae 34

Rhizobium rhizoryzae 661

Rhizobium sp. 106

Rhodococcus erythropolis 54093

Sinorhizobium chiapanecum (now

Ensifer adhaerens) 131

Sinorhizobium Chiapanecum (now

Ensifer adhaerens) 111

Sphingopyxis aiaskensis 412

Sphingopyxis alaskensis 914

Stenotrophomonas maitophilia 54073

Tumebacillus permanentifrigoris 72229

Tumebacillus permanentifrigoris 74542

Tumebacillus permanentifrigoris 72366

Tumebacillus permanentifrigoris 72287

Variovorax ginsengisoii 137 Variovorax ginsengisoli 3078

Example 7: Deposited Microbial Species Novel to Agriculture

[0636] In one experimental embodiment, the inventors utilized the following microbial species in applications of the present disclosure. Table 27 notes microbial organisms of the present disclosure which have been deposited with the NRRL, ATCC, and/or DSMZ depositories with the respective accession numbers.

Species novel to

Agriculture fin Tables 1, 2, NRRL # DS Z # ATTC #

3, 4 and 25}

Achromobacter pulmonis NRRL B-67174 DS 29617

Acidovorax soil NRRL B-67181

NRRL B-67182

Agrobacterium fabrum or NRRL B-67173 DSM22668

Rhizobium pusense (in NRRL B-67286

Taxonomic Flux) (previously

Rhizobium sp.)

Arthrobacter cupressi NRRL B-67183

NRRL B-67184

Arthrobacter NRRL B-67289 DSM420 49919

nicotinovorans NRRL B-67290

Bosea eneae NRRL B-67185

Bosea minatitlanensis DSM-13099 700918

Bosea robinae NRRL B-67186

Caulobacter henricii DSM-4730 15253

Chitinophaga arvensicola DS -3695 51264

Chitinophaga terrae NRRL B-67188

Chryseobacterium NRRL B-67172 DS 15235

daecheongense NRRL B-67291

Chryseobacterium NRRL B-67288

rhizophaerae NRRL B-67287

Delftia lacustris NRRL B-67190

NRRL B-67191

Frigidibacter albas or NRRL B-67285

Delfulvlimonas dentrificans NRRL B-67283

(In Taxonomic Flux) NRRL B-67284

Duganelia radicis NRRL B-67192

NRRL B-67166

Duganelia violaceinigra NRRL B-67193

(Pseudoduganeila NRRL B-67232

violaceinigra) NRRL B-67233

Dyadobacter soli NRRL B-67193

NRRL B-67194

Exiguobacierium NRRL B-67292 DS 14480 antarcticum NRRL B-67293

txiguobacterium sibiricum NRRL B-67167 DSM 17290

NRRL B-67294

Flavobacterium glaciei NRRL B-67196

Frateuria aurantia DSM-6220

Frateuria terrea DSM-26515

Herbaspirillum NRRL B-67197

chlorophenolicum NRRL B-67236

.ianthinobacterium DSM-9628 agaricidamnosum

.ianthinobacterium lividum DSM-1522

Leifsonia lichenia NRRL B-67298

NRRL B-67299

Luteibacter yeojuensis DSM-17673

Massilia kyongggiensis NRRL B-67198 DSM 101532

(previously assilia

albidiflava)

Massilia niastensis NRRL B-67199

NRRL B-67235

Microbacterium sp. DSM-16050 31001

(OLI EVORANS DEPOSITED)

Novosphingobium NRRL B-67201 DSM25409 lindaniclasticum NRRL B-67200

Novosphingobium NRRL B-67202

resinovorum NRRL B-67203

Novosphingobium rosa DSM-7285 51837

Novosphingobium NRRL B-67168 DSM 27057 sediminicola

Paenibacillus amylolyticus DSM-11730 9995

Paenibacilius chondroitinus DS -5051 51184

Paenibacillus glycanilyticus NRRL B-67204

Pedobacter rhizosphaerae NRRL B-67205

(Pedobacter soil)

Pedobacter terrae NRRL B-67206

NRRL B-67176

Polaromonas ginsengisoli NRRL B-67231

NRRL B-67234

Pseudomonas NRRL B-67295 DSM28442 helmanticensis NRRL B-67296

NRRL B-67297

Pseudomonas jinjuensis NRRL B-67207

Ramlibacter henchirensis NRRL B-67208

Rhizobium rhizoryzae NRRL B-67210

NRRL B-67211

Rhodoferax ferrireducens DSM-15236 BAA-621

Sinorhizobium NRRL B-67213

chiapanecum (Ensifer NRRL B-67169

adhaerens) Sphingobium quisquiliarum DSM-24952

Sphingopyxis alaskensis NRRL B-67214

RL B-67215

Stenotrophomonas terrae DSM-18941

Tumebacillus NRRL B-67302 DSM 118773

permanentifrigoris RRL B-67300

NRRL B-67303

NRRL B-67301

Variovorax ginsengisoli NRRL B-67216

RRL B-67217

Example 8: Microbial Consortia Embodiments

[0637] In one experimental embodiment, the inventors utilized the following microbial consortia in applications of the present disclosure. Table 28 notes microbial consortia D12, D21, D27, D28, D30, D31, D32, D33, and D34 of the present disclosure. Underneath each of the consortia designations are the specific strain numbers that identify the microbes present in each of the consortia.

Table 28

Strain Si rain Consortia*

BC!# BDISfZ# Microbe identity D12 D21 D27 D28 D30 D31 D32 D33 D34

Duganelia radicis

31 (31) 31

Exiguobacterium

116 sibiricum (116) 116

Novosphingobium

130 sediminicola (130) 130

Agro bacterium

fabrum or

Rhizobium

pusense (ini

958 taxonomix flux) 958 958 -

Pseudomonas

helmanticensis

616 (616) 616

Chryseobacterium

rhizosphaerae

615 (615) 615

Tumebacillus

permanentifrigoris

74542 (74542) 74542

Tumebacillus

permanentifrigoris

72229 (72229) 72229 Leifsonia lichenia

72243 (72243) 72243 72243

Chryseobacterium

rhizosphaerae

597 (597) 597

F gidibacter a!bus

or Delfulviimonas

dentri j leans (In

Taxonomic F!ux)

712 (712) 712

Arthrobacter

nicotinovorans

717 (717) 717

Novosphingobium

lindaniclasticum

71222 (71222) 71222

Example 9: Microbial Strain and Microbial Species Embodiments

[0638] In one experimental embodiment, the inventors utilized the following microbial species and/or strains in applications of the present disclosure. Table 29 notes specific microbial species and strains utilized in experimental studies which are novel to agriculture and have exhibited positive results in controlled environment screening experiments of the present disclosure.

Table 29

individual species of

Strain Strai individual strains of note Strain Strain note

Species BDMZ# BC!# Species BDMZ# BCi#

Dugane!!a violaceinigra 66361 Arthrobacter nicotinovorans 3189

Chryseobacterium 45

54522 703

Bosea thiooxidans daecheongense

Chryseobacterium 191

55184 1217

Massiiia niastensis daecheongense

Polaromonas 597

66373

ginsengisoli Chryseobacterium rhizosphaerae

N o vosph in g obi urn 615

557

resinovorum Chryseobacterium rhizosphaerae

Frigidibacter albus or 712

2204 Delfulviimonas dentrificans (In

Duganeiia violaceinigra Taxonomic Flux)

Frigidibacter albus or 402

Exiguobacterium 50 Delfulviimonas dentrificans (In

aurantiacum Taxonomic Flux)

Exiguobacterium Frigidibacter albus or 745

116

sibiricum Delfulviimonas dentrificans (In Taxonomic Flux)

Variovorax ginsengisoli 3078 Exiguobacterium antarcticum 63

Pedobacter 225

598

rhizosphaerae Exiguobacterium antarcticum

Duganei!a radicis 31 Exiguobacterium sibiricum 116

Paenibacillus 718

418

g!ycani!yticus Exiguobacterium sibiricum

Bacillus niacin 1718 Leifsonia lichenia 72243

St en o troph om onas 72289 maitophilia 54073 Leifsonia lichenia

Rhodococcus 53 erythropolis 54093 Pedobacter terrae -

Pantoea vagans 55529 Pseudomonas heimanticensis 616

Pseudomonas 2945 oryzihabitans 55530 Pseudomonas heimanticensis

Achromobacter 49 800 pulmonis Pseudomonas heimanticensis

Agrobactenum fabrurn 46

or Rbizobium pusense

(In Taxonomic Flux)

(previously Rhizobium

sp.) Tumeba cilius p er anen tifrig oris 72229

Agrobactenum fabrurn 958

or Rhizobium pusense

(In Taxonomic Flux)

(previously Rhizobium

sp.) Tumeba cill us perm anen tifrig or is 74542

Arthrobacter 717

nicotlnovorans Tumeba cill us perm anen tifrig or is 72366

Tumeba cilius permanen tifrig oris 72287

INCORPORATION BY REFERENCE

[0639] All references, articles, publications, patents, patent publications, and patent applications cited herein are incorporated by reference in their entireties for all purposes.

[0640] However, mention of any reference, article, publication, patent, patent publication, and patent application cited herein is not, and should not be taken as, an acknowledgment or any form of suggestion that they constitute valid prior art or form part of the common general knowledge in any country in the world.

REFERENCES

[0641] Ascend® plant growth regulator product sheet. EPA reg. No. 9776-335 [0642] Calvo, P., Nelson, L., Kloepper, J. W., 2014 Agricultural uses of plant biostimulants. Plant soil 383, 3-41.

[0643] '"Chemistr ' and Technology of Agrochemical Formulations," edited by D. A. Knowles, copyright 1998 by Kluwer Academic Publishers.

[0644] Colby, R. S., "Calculating Synergistic and Antagonistic Responses of Herbicide Combinations, 1967 Weeds, vol. 5, pp. 20-22.

[0645] Current Protocols in Molecular Biology (F.M. Ausubel et ai , eds., 1987).

[0646] Crameri 1997) Nature Biotech. 15:436-438.

[0647] Crameri et al. \99%) Nature 391 :288-291.

[0648] De Almeida et al., (1989) Mol. Gen. Genetics 218:78-86).

[0649] Dobereiner J, Marriel E and Nery M 1976 Ecological distribution of Spirillum lipoferum Beijerinck. Can. J. Microbiol. 22, 1464--- 1473.

[0650] Faliraeus, G. (1957). J. Ger, \ Microbiol. 16: 374-381.

[0651] Gerhardt, P. (ed.) Methods for General and Molecular Microbiology. American Society for Microbiology, Washington, D.C. (1994).

[0652] Gherna, R. L. and C. A. Reddy. 2007. Culture Preservation, p 1019-1033. In C. A. Redely, T. J. Beveridge, J. A. Breznak, G. A. Marzluf, T. M. Schmidt, and L. R. Snyder, eds. American Society for Microbiology, Washington, D.C, 1033 pages.

[0653] Goteti, P. K. et al., (2013). International Journal of Microbiology 2013: 1-7 Article ID 869697.

[0654] Hartmann A., Baidani J.I. The genus Azospirillum // The Prokaryotes, V. 5: Proteobacteria Alpha and Beta Subclasses //' Eds. M. Dworkin, S. Faikow, E. Rosenberg, K.H. Schleifer, E. Stackebrandt, - Springer Verlag, New York, USA, 2006. p. 11 -140.

[0655] Innis et al , eds. ( 1990) PCR Protocols: A Guide to Methods and Applications (Academic Press, New York).

[0656] Innis and Gelfand, eds. (1995) PCR Strategies (Academic Press, New Y ork).

[0657] In re Bergstrom, 427 F.2d 1394, (CCPA 1970),

[0658] In re Bergy, 596 F.2d 952 (CCPA 1979). [0659] Islam, M. T., Deora, A., Hashidoko, Y, Rahman, A., Ito, T., and Tahara, S. (2007) Isolation and Identification of Potential Phosphate Solubilizing Bacteria from the Rhizopiane of Oryza sativa L. cv. BR29 of Bangladesh. Zeitschrift fur Naturforsehung C 62(1-2): 103-10.

[0660] Jones et al , (1985) EMBO J. 4:241 1-2418.

[0661] Lennette, E. H. (ed.) Manual of Clinical Microbiology, Third Edition, American Society for Microbiology, Washington, D.C. (1980).

[0662] McCutcheon's Detergents and Emidsifiers Annual, MC Publishing Corp., Ridgewood, N.J,, 1998, and in Encyclopedia of Surfactants, Vol. Ι-ΠΙ, Chemical Publishing Co., New York, 1980-81.

[0663] McCutcheon's, vol . 1, "Emulsifiers and Detergents," MC Publishing Company, Glen Rock, N.J., U.S.A., 1996.

[0664] Merck & Co. v. Olin Mathieson Chemical Corp . 253 F.2d 156 (4th Cir. 1958),

[0665] Miche, L and Balandreau, J (2001). Effects of rice seed surface sterilisation with hypochlorite on inoculated Burkholderia vietamiensis . Appl. Environ. Microbiol..67(7): p3046-3052.

[0666] Moore er a/. (1997) J. Mol. Biol. 272:336-347.

[0667] Nautiyal, C.S. (1999), FEMS Microbiology Letters 170 (1999) 265-270.

[0668] N-Large™ plant growth regulator product sheet. EPA Reg. No. 57538-18.

[0669] Parke-Davis & Co. v. H.K. Mulford & Co., 189 F. 95 (S.D.N.Y. 1911).

[0670] Parmar, P. and Sindhu, S. S. (2013) Potassium Solubilization by Rhizosphere Bacteria: Influence of Nutritional and Environmental Conditions. Journal of Microbiology Research, 3(1): 25-31 ,

[0671] PCT/NZ2012/000041, published on September 20, 2012, as International Publication No. WO 2012125050 Al .

[0672] PCT/NZ2013/000171, published on March 27, 2014, as International Publication No. WO 2014046553 Al .

[0673] Perez-Miranda, S. et al,, (2007). Journal of Microbiological Methods 70: 127-131.

[0674] Pikovskava RI (1948). Mobilization of phosphoms in soil connection with the vital activity of some microbial species. Microbiologic! 17:362-370. [0675] ProGibb® plant growth regulator product sheet. EPA Reg. No. 73049-15.

[0676] Rana, A. et al. (2012) Enhancing Micronutrient Uptake and Yield of Wheat Through Bacterial PGPR Consortia, Soil Science and Plant Nutrition, 58:5, 573-582.

[0677] Release® plant growth regulator product sheet. EPA Reg. No. 73049-6.

[0678] Rodriguez, H. and Reynaldo, F. (1999). Phosphate Solubilizing Bacteria and their Role in Plant Growth Promotion. Biotechnology Advances. 17. 319-339.

[0679] Ruth Eckford, R, Cook, F.D., Saul, D., Aislabie J., and J. Foght (2002) Free-living Heterotrophic Bacteria Isolated from Fuel-Contaminated Antarctic Soils. Appl. Environ. Microbiol 68(10):5181.

[0680] RyzUp SmartGrass® plant growth regulator product sheet. EPA Reg. No. 73049-1.

[0681] Sambrook et al (1989) Molecular Cloning: A Laboratory Manual (2nd ed., Cold Spring Harbor Laboratory Press, Plainview, New Y ork).

[0682] Shanware, A.S. et al., 2014 Int.J.Curr.Microbiol.App.Sci 3(9) 622-629.

[0683] Stemmer (1994) Nature 370:389-391.

[0684] Stemmer ( 1994) PNAS 91 : 10747- 10751.

[0685] Strobel G and Daisy B (2003) Microbiology and Molecular Biology Reviews 67 (4): 491-502.

[0686] U.S. Pat. No. 8,652,490 'Tasteuria Strain" issued February 18, 2014,

[0687] U.S. Pat. No. 8,383,097 ''Bacteria Cultures and Compositions Comprising Bacteria Cultures" issued February 26, 2013.

[0688] Vandamme et al. 1996. Polyphasic taxonomy, a consensus approach to bacterial systematics. Microbiol Rev 1996, 60:407-438.

[0689] Bergey's Manual of Systematic Bacteriology 2 ^nd Edition Volume 1 (2001) The Archaea and the deeply branching and phototrophic Bacteria. Editor-in-Chief: George M. Garrity. Editors: David R. Boone and Richard W. Castenhoiz. ISBN 0-387-98771-1.

[0690] Bergey's Manual of Systematic Bacteriology 2 ^nd Edition Volume 2 (2005) The Proteobacteria. Editor-in-Chief: George M. Garrity. Editors: Don J. Brenner, Noel R. Krieg and James T. Staley. ISBN 0-387-95040-0, [0691] Bergey ^' s Manual of Systematic Bacteriology 2 ⁿ Edition Volume 3 (2009) The Firmicutes. Editors: Paul De Vos, George Garrity, Dorothy Jones, Noel R. Krieg, Wolfgang Ludwig, Fred A, Rainey, Karl-Heinz Schleifer and William B. Whitman. ISBN 0-387-95041 -

9,

[0692] Bergey's Manual of Systematic Bacteriology 2 ^nd Edition Volume 4 (2011) The Bacteroidetes, Spirochaetes, Tenericutes (Mollicutes), Acidobacteria, Fibrobacteres, Fusobacteria, Dictyoglomi, Gemmatimonadetes, Lentisphaerae, Verrucomicrobia,

Chiamydiae, and Planctomycetes. Editors: Noel R. Krieg, James T. Staley, Daniel R. Brown, Brian P. Hedlund, Bruce J. Paster, Naomi L. Ward, Wolfgang Ludwig and William. B. Whitman. ISBN 0-387-95042-6

[0693] Bergey's Manual of Systematic Bacteriology 2 ^nd Edition Volume 5 (2012) The Actinobactena. Editors: Michael Goodfellow, Peter Kampfer, Hans-Jiirgen Busse, Martha E. Trujillo, Ken-ichiro Suzuki, Wolfgang Ludwig and William B. Whitman. ISBN 0-387- 95042-7.

[0694] Yemra and Willis (Biochem. J. 1954, 57: 508-514).

[0695] X-CYTE™ plant growth regulator product sheet. EPA Reg. No. 57538-15.

[0696] Zhang et al(\99T} PNAS 94:4504-4509,

[0697] Zinniel DK et a/. (2002) Applied and Environmental Microbiology 68 (5): 2198- 2208).

[0698] Pikovskava RI (1948). Mobilization of phosphorus in soil connection with the vital activity of some microbial species. Microbiologic! 17:362-370.