Introduction Propionibacteria are Gram-positive bacteria capable of producing various useful compounds in a variety of industrial processes. For example, several Propionibacterium species are known to produce vitamin Bl2 (cobalamin) in large scale fermentation processes. Other species are used in dairy applications such as cheese manufacturing where they contribute, and in many cases even are mainly responsible, for the specific flavour and texture of the cheese. Many Propionibacterium species are considered safe for inclusion, as live organisms, into food and animal feed.

To be able to fully exploit the biotechnological potential of Propionibacterium, efficient and flexible genetic engineering techniques are required. Such techniques rely on the availability of a suitable plasmid to express a protein from a heterologous gene in Propionibacterium.

EP-A-0400931 (Nippon Oil) refers to an endogenous plasmid (pTY-1) from Propionibacterium pentosaceum (ATCC 4875) but does not describe its sequence or exemplify how it may be used to express a heterologous gene.

JP 08-56673 refers to the plasmid pTY-1 for producing vitamin B12 but does not provide any evidence that the plasmid remains as a freely replicating extrachromosomal element nor that the plasmid is stable inside the transformed cells.

The invention therefore seeks to provide vectors that are more efficient than those in the prior art, and can remain extrachromosomal and/or are stable. In particular the invention aims to provide an efficient vector for the cloning or expression of Propionibacterium or foreign genomic fragments or genes into a (Propionibacterium) host strain. This may enable host specific restriction enzymes to be circumvented and thereby avoid the host treating the plasmid as a foreign polynucleotide.

Summary of the invention Accordingly, the present invention in a first aspect provides a polynucleotide comprising a sequence capable of hybridising selectively to (a) SEQ ID NO: 1 or the complement thereof ; (b) a sequence from the 3.6 kb plasmid of Propionibacterium freudenreichii CBS 101022; (c) a sequence from the 3.6 kb plasmid of Propionibacterium freudenreichii CBS 101023; or (d) a sequence that encodes a polypeptide of the invention, such as (at least part of) the amino acid sequence of SEQ ID NO: 2 or SEQ ID No: 3, or the complement thereof.

SEQ ID NO: 1 sets out the DNA sequence of the endogenous plasmid of Propionibacterium LMG 16545 which the inventors have discovered. The first coding sequence runs from nucleotide 273 to nucleotide 1184 and the predicted amino acid sequence of this coding sequence is shown in SEQ ID NO: 2. The second coding sequence runs from nucleotides 1181 to 1483 and the predicted amino acid sequence of this coding sequence is shown in SEQ ID No: 3.

The inventors screened a large collection of Propionibacterium isolates and identified two strains both harboring cryptic plasmids with a size of 3.6 kb. One of the strains is Propionibacterium freudenreichii LMG 16545 which was deposited at Centraalbureau voor Schimmelcultures (CBS), Oosterstraat 1, Postbus 273, NL-3740 AG Baarn, Netherlands, in the name of Gist-brocades B. V. of Wateringseweg 1, P. O. Box 1,2600 MA Delft, The Netherlands, on 19 June 1998 under the terms of the Budapest Treaty and was given accession number CBS 101022. The other strain is Propionibacterium freudenreichii LMG 16546 which was also deposited by the same depositor on 19 June 1998 under the terms of the Budapest Treaty at CBS and was given accession number CBS 101023.

Through full characterization and computer assisted analysis of the nucleotide sequence of LMG 16545 the inventors have been able to identify insertion sites for foreign DNA fragments. These sites have allowed construction of plasmids that are still capable of autonomous replication in Propionibacterium.

Surprisingly it was found that an erythromycin resistance gene from the actinomycete Saccharopolyspora erythraea is efficiently expressed in Propionibacterium and thus can be used as a selection marker for transformed cells.

Also constructed are bifunctional vectors, stably maintainable and selectable in both E. coli and Propionibacterium. This allows the use of E. coli for vector construction, as well as functional expression of homologous or heterologous genes in Propionibacterium.

Vector construction using E. coli is comparatively easy and can be done quickly.

The polynucleotide of the invention may be autonomously replicating or extrachromosomal, for example in a bacterium such as a Propionibacterium.

Hence another aspect the invention provides a vector which comprises a polynucleotide of the invention.

The invention also provides a process for the preparation of a polypeptide, the process comprising cultivating a host cell transformed or transfected with a vector of the invention under conditions to provide for expression of the polypeptide.

The invention additionally provides a polypeptide which comprises the sequence set out in SEQ ID NO: 2 or 3 or a sequence substantially homologous to that sequence, or a fragment of either sequence, or a protein encoded by a polynucleotide of the invention.

Detailed Description of the Invention Polynucleotides A polynucleotide of the invention may be capable of hybridising selectively with the sequence of SEQ ID NO: 1, or a portion of SEQ ID No: 1, or to the sequence complementary to that sequence or portion of the sequence. The polynucleotide of the invention may be capable of hybridising selectively to the sequence of the 3.6 kb plasmid of P. freudenreichii CBS 101022 or CBS 101023, or to a portion of the sequence of either plasmid. Typically, a polynucleotide of the invention is a contiguous sequence of nucleotides which is capable of selectively hybridizing to the sequence of SEQ ID. No: 1 or of either 3.6 kb plasmid, or portion of any of these sequences, or to the complement of these sequences or portion of any of these sequences.

A polynucleotide of the invention and the sequence of SEQ ID NO: 1, or either

of the 3.6 kb plasmids, or a sequence encoding a polypeptide, or a portion of these sequences, can hydridize at a level significantly above background. Background hybridization may occur, for example, because of other polynucleotides present in the preparation. The signal level generated by the interaction between a polynucleotide of the invention and the sequence of SEQ ID NO: 1 or of either 3.6 kb plasmid, or portion of these sequences, is typically at least 10 fold, preferably at least 100 fold, as intense as interactions between other polynucleotides and the coding sequence of SEQ ID NO: 1 or of either 3.6 kb plasmid, or a sequence encoding the polypeptide, or portion of these sequences. The intensity of interaction <BR> may be measured, for example, by radiolabelling the probe, e. g. with 3zip. Selective hybridisation is typically achieved using conditions of medium stringency (for example 0.3M sodium chloride and 0.03M sodium citrate at about 50°C) to high stringency (same conditions but at about 60°C).

Polynucleotides included in the invention can be generally at least 70%, preferably at least 80 or 90%, more preferably at least 95%, and optimally at least 98% homologous (to the sequences (a) to (d)) over a region of at least 20, preferably at least 30, for instance at least 40,60 or 100 or more contiguous nucleotides.

Any combination of the above mentioned degrees of homology and minimum sizes may be used to define polynucleotides of the invention, with the more stringent combinations (i. e. higher homology over longer lengths) being preferred. Thus for example a polynucleotide which is at least 80% or 90% homologous over 25, preferably over 30 nucleotides forms one embodiment of the invention, as does a polynucleotide which is at least 90% or 95% homologous over 40 nucleotides.

The portions referred to above may be the coding sequences of SEQ ID No: 1 or of either 3.6 kb plasmid. Other preferred portions of SEQ ID No: 1 are the replication origin, promoter or regulatory sequences, or sequences capable of effecting or assisting autonomous replication in a host cell, such as a Propionibacterium.

It has been found that the portion of the plasmid from the restriction site SalI to AlwNI appears to be the region that is required for replication of the plasmid. Other parts of the plasmid have been deleted and yet replication does not appear to have been adversely affected. Therefore in the invention sequence (b) and (c) can be the

region delineated by the restriction sites SalI and AlwNI. This is approximately 1.7b in length. Alternatively, sequences (b) or (c) can be replaced by the sequence corresponding to nucleotides 1 to 1,800, such as 100 to 1,700, suitably 150 to 1,500, advantageously 200 to 1,300 and optimally 250 to 1,200 of SEQ. ID. No. 1.

The proteins (SEQ. ID. Nos. 2 and 3) encoded by ORF1 and ORF2 respectively, are thought to both help the plasmid replicate. The plasmid replicates by the known rolling circle replication method where the original ds DNA plasmid is cut by either of the proteins which assists production of a copy of the outer strand using the inner strand as a template. The copy of the outer ring is removed and the ends joined. The host then replicates a new inner ring using the generated outer ring as a template.

The coding sequences of the invention may be modified by nucleotide substitutions, for example from 1,2 or 3 to 10,25,50 or 100 substitutions. The polynucleotides of sequences (a) to (d) may alternatively or additionally be modified by one or more insertions or deletions and/or by an extension at either or both ends.

Degenerate substitutions may be made and/or substitutions may be made which would result in a conservative amino acid substitution when the modified sequence is translated, for example as discussed later with relation to the polypeptides of the invention.

Polynucleotides of the invention may comprise DNA or RNA. They may also be polynucleotides which include within them synthetic or modified nucleotides. A number of different types of modification to polynucleotides are known in the art.

These include methylphosphonate and phosphorothioate backbones, addition of acridine or polylysine chains at the 3'and/or 5'ends of the molecule. For the purposes of the present invention, it is to be understood that the polynucleotides described herein may be modified by any method available in the art. Such modifications may be carried out in order to enhance in vivo activity or lifespan.

Polynucleotides of the invention may be used as a primer, e. g. a PCR (polymerase chain reaction) primer, a primer for an alternative amplification reaction, a probe e. g. labelled with a revealing label by conventional means using radioactive or non-radioactive labels, or the polynucleotides may be incorporated or cloned into vectors.

Such primers, probes and other fragments will be at least 15, preferably at least

20, for example at least 25,30 or 40 nucleotides in length. They will typically be up to 40,50,60,70,100 or 150 nucleotides in length. Probes and fragments can be longer than 150 nucleotides, for example up to 200,300,500,1,000 or 1,500 nucleotides in length, or even up to a few nucleotides, such as 5 or 10 nucleotides, short of any of the sequences (a) to (d).

Polynucleotides such as a DNA polynucleotide and primers according to the invention may be produced recombinantly, synthetically, or by any means available to those of skill in the art. They may also be cloned by standard techniques. The polynucleotides are typically provided in isolated and/or purified form.

In general, primers will be produced by synthetic means, involving a step wise manufacture of the desired nucleic acid sequence one nucleotide at a time.

Techniques for accomplishing this using automated techniques are readily available in the art.

Longer polynucleotides will generally be produced using recombinant means, for example using PCR cloning techniques. This will involve making a pair of primers (e. g. of about 15-30 nucleotides) to the region of SEQ ID No: 1 or of either 3.6 kb plasmid which it is desired to clone, bringing the primers into contact with DNA obtained from a Propionibacterium, performing a polymerase chain reaction under conditions which bring about amplification of the desired region, isolating the amplified fragment (e. g. by purifying the reaction mixture on an agarose gel) and recovering the amplified DNA. The primers may be designed to contain suitable restriction enzyme recognition sites so that the amplified DNA can be cloned into a suitable cloning vector. Such techniques may be used to obtain all or part of SEQ ID No: 1 or either 3.6 kb plasmid.

The techniques mentioned herein are well known in the art'°.

Polynucleotides which are not 100% homologous to SEQ ID No: 1 or either 3.6 kb plasmid but fall within the scope of the invention can be obtained in a number of ways.

Homologous polynucleotides of SEQ ID NO: 1 or of either 3.6 kb plasmid may be obtained for example by probing genomic DNA libraries made from a range of Propionibacteria, such as P. freudenreichii, Pjensenii, P. thoenii, P. acidipropionici, or other strains of bacteria of the class Actinomycetes, or other gram positive bacteria,

or those that are G: C rich. All these organisms are suitable sources of homologous or heterologous genes, promoters, enhancers, or host cells, for use in the invention.

Such homologues and fragments thereof in general will be capable of selectively hybridizing to the coding sequence of SEQ ID NO: 1 or its complement or of either 3.6 kb plasmid. Such sequences may be obtained by probing genomic DNA libraries of the Propionibacterium with probes comprising all or part of the coding sequence SEQ ID NO: 1 or of either 3.6 kb plasmid under conditions of medium to high stringency (for example 0.03M sodium chloride and 0.3M sodium citrate at from about 50°C to about 60°C).

Homologues may also be obtained using degenerate PCR which will use primers designed to target conserved sequences within the homologues. Conserved sequences can be predicted from aligning SEQ ID No: 1 or the sequence of either 3.6 kb plasmid with their homologues. The primers will contain one or more degenerate positions and will be used at stringency conditions lower than those used for cloning sequences with single sequence primers against known sequences.

Alternatively, such polynucleotides may be obtained by site directed mutagenesis of SEQ ID No: 1 or of either 3.6 kb plasmid, or their homologues. This may be useful where for example silent codon changes are required to sequences to optimise codon preferences for a particular host cell in which the polynucleotide sequences are being expressed. Other sequence changes may be desired in order to introduce restriction enzyme recognition sites, or to alter the property or function of the polypeptides encoded by the polynucleotides.

Methods of measuring polynucleotide homology are well known in the art. For example the UWGCG package provides the BESTFIT programme which can be used to calculate homology, for example used on its default setting'. For amino acid homology with regard to polypeptides of the invention which are discussed later, one can employ BLAST (Basic Local Alignment Search Tool'), which produces alignments of amino acid sequences (and nucleotide sequences if necessary) to determine sequence similarity. BLAST can thus be used to determine exact matches or to identify homologues, and is particularly useful for those matches which do not contain gaps. The BLAST technique uses the algorithm based on the High-scoring Segment Pair (HSP).

The invention includes double stranded polynucleotides comprising a polynucleotide sequence of the invention and its complement.

Polynucleotides (e. g. probes or primers) of the invention may carry a revealing <BR> <BR> <BR> <BR> <BR> label. Suitable labels include radioisotopes such as"P or"S, enzyme labels, or other protein labels such as biotin. Detection techniques for these labels are known per se.

The polynucleotides (labelled or unlabelled) may be used in nucleic acid-based tests for detecting or sequencing another polynucleotide of the invention, in a sample.

Polynucleotides of the invention include variants of the sequence of SEQ ID NO: 1 or of either 3.6 kb plasmid which are capable of autonomously replicating or remaining extrachromosomally in a host cell. Such variants may be stable in a bacterium such as a Propionibacterium.

Generally the polynucleotide will comprise the replication origin and/or coding region (s) of SEQ ID No: 1 or of either 3.6 kb plasmid, or homologues of these sequences. A polynucleotide of the invention which is stable in a host cell, such as Propionibacterium, or E. coli is one which is not lost from the host within five generations, such as fifteen generations, preferably thirty generations. Generally such a polynucleotide would be inherited by both daughter cells every generation.

The polynucleotide may comprise a promoter or an origin of replication (e. g. upstream of any sequences encoding a replication protein).

The polynucleotide of the invention can be transformed or transfected into a bacterium, such as a Propionibacterium, or E. coli, for example by a suitable method". It may be present in a bacterium at a copy number of 5 to 500, such as 10 to 100.

The polynucleotide may be capable of autonomous replication in a bacterium other than a Propionibacterium. Such a bacterium may be E. coli, or a gram positive or G: C rich bacterium or one of the class Actinomycetes. Such a polynucleotide will generally comprise sequences which enable the polynucleotide to be autonomously replicated in that bacterium. Such sequences can be derived from plasmids which are able to replicate in that bacterium.

A polynucleotide of the invention may be one which has been produced by replication in a Propionibacterium. Alternatively it may have been produced by

replication in another bacterium, such as E. coli. The polynucleotide may be able to circumvent the host restriction systems of Propionibacterium.

Vectors A second aspect of the invention relates to a vector comprising a polynucleotide of the first aspect. The vector may be capable of replication in a host cell, such as a bacterium, for examples Actinomycetes, e. g. Propionibacterium or E. coli. The vector may be a linear polynucleotide or, more usually, a circular polynucleotide.

The vector may be a hybrid of the polynucleotide of the invention and another vector. The other vector may be an E. coli vector, such as pBR322, or a vector of the pUC family, RI, ColD or RSF1010 or a vector derived therefrom.

The polynucleotide or vector of the invention may be a plasmid. Such a plasmid may have a restriction map the same as or substantially similar to the restriction maps shown in Figure 1,2a or 2b.

The polynucleotide or vector may have a size of 1 kb to 20 kb, such as from 2 to 10 kb, optimally from 3 to 7 kb.

The polynucleotide or vector may comprise multiple functional cloning sites.

Such cloning sites generally comprise the recognition sequences of restriction enzymes. The polynucleotide or vector may comprise the sequence shown in SEQ ID No: 1 and/or contains restriction enzyme recognition sites for EcoRI, SacI, AlwN1, BsmI, BsaBI, Bcll, ApaI, HindIII, SalI, HpaI, PstI, SphI, BamHI, Acc65I, EcoRV and BglII. The polynucleotide or vector may thus comprise one, more than one or all of these restriction enzyme sites, generally in the order shown in the Figures.

Preferably, when present in a bacterium, such as a Propionibacterium or E. coli, the polynucleotide or vector of the invention does not integrate into the chromosome of the bacterium. Generally the polynucleotide or vector does not integrate within 5 generations, preferably 20 or 30 generations.

The polynucleotide or vector may be an autonomously replicating plasmid that can remain extrachromosomal inside a host cell, which plasmid is derived from an endogenous Propionibacterium plasmid, and when comprising a heterologous gene (to the host) is capable of expressing that gene inside the host cell. The term"derived

from"means that the autonomously replicating plasmid includes a sequence the same as the polynucleotide of the invention.

The vector of the invention may comprise a selectable marker. The selectable marker may be one which confers antibiotic resistance, such as ampicillin, kanamycin or tetracylin resistance genes. The selectable marker may be an erythromycin resistance gene. The erythromycin resistance gene may be from Actinomycetes, such as Saccharopolyspora erythraea, for example from Saccharopolyspora erythraea NRRL2338. Other selectable markers which may be present in the vector include genes conferring resistance to chloramphenicol, thiostrepton, viomycin, neomycin, apramycin, hygromycin, bleomycin or streptomycin.

The vector may be an expression vector, and so may comprise a heterologous gene (which does not naturally occur in the host cell, e. g. Propionibacteria), or an endogenous or homologous gene of the host cell, e. g. Propionibacteria. In the expression vector the gene to be expressed is usually operably linked to a control sequence which is capable of providing for the expression of the gene in a host cell.

The term"operably linked"refers to a juxtaposition wherein the components described are in a relationship permitting them to function in their intended manner.

A controlled sequence"operably linked"to a coding sequence is ligated in such a way that expression of the coding sequence is achieved under conditions compatible with the control sequences.

The heterologous or endogenous gene may be inserted between nucleotides 1 and 200 or between nucleotides 1500 to 3555 of SEQ ID No: 1 or at an equivalent position in a homologous polynucleotide.

Such genes may comprise homologous or endogenous genes such as for elongation factors, promoters regulatory sequences or elements, and replication proteins. Other genes (which may be heterologous to the host) include those encoding for or assisting in the production of nutritional factors, immunomodulators, hormones, proteins and enzymes (e. g. proteases, amylases, peptidases, lipases), texturing agents, flavouring substances (e. g. diacetyl, acetone), gene clusters, antimicrobial agents (e. g. nisin), substances for use in foodstuffs (e. g. in sausages, cheese) metabolic enzymes, vitamins (e. g. B, 2), uroporphyrinogen (III)

methyltransferase (UP III MT), cobA, antigens and (e. g. for vaccines) therapeutic agents. As will be seen, the hosts can produce a wide variety of substances, not just polypeptides, which may be either the desired product or may be used to produce the desired product.

The heterologous gene may have a therapeutic effect on a human or animal.

Such a gene may comprise an antigen, for example from a pathogenic organism. The host, such as Propionibacterium, comprising a polynucleotide with such a heterologous gene may be used as or in a vaccine, and may provide protection against the pathogens.

The heterologous antigen may be a complete protein or a part of a protein containing an epitope. The antigen may be from a bacterium, a virus, a yeast or a fungus.

Host cells and expression The host cell forms the third aspect of the invention and comprises a polynucleotide or vector of the first or second aspect. The host cell may be a bacterium e. g. of the class Actinomycetes. The bacterium may be a Propionibacterium or E. coli. The Propionibacterium may be P. freudenreichii, P. jensenii, P. thoenii or P. acidipropionici.

In a fourth aspect the invention provides a process for producing a host cell of the third aspect, the process comprising transforming or transfecting a host cell with a polynucleotide or vector of the first or second aspect, e. g. with known transformation techniques".

In a fifth aspect the invention provides a process for the preparation of a polypeptide encoded by the polynucleotide or vector of invention present in host cell of the invention comprising placing or culturing the host cell in conditions where expression of the polypeptide occurs.

This aspect of the invention thus provides a process for the preparation of a polypeptide encoded by a given gene, which process comprises cultivating a host cell transformed or transfected with an expression vector comprising the gene, under conditions to provide for an expression of the said polypeptide, and optionally recovering the expressed polypeptide. The host cell may be of the class

Actinomycetes, or a gram positive bacteria such as Propionibacterium or E. coli.

Promoters, translation initiators, translation terminators, elongation factor genes, ribosomal RNA, antibiotic resistance genes, synthetic promoters (e. g. designed on consensus sequences) to other expression regulation signals present in the polynucleotide or vector can be those which are compatible with expression in the host cell. Such promoters include the promoters of the endogenous genes of the host cell.

Culturing conditions may be aerobic or anaerobic conditions, depending on the host. For a fermentation process the host cell would be placed in anaerobic, and then possibly aerobic, conditions. The compound produced, such as an expressed polypeptide, may then be recovered, e. g. from the host cell or fermentation medium.

The expressed polypeptide may be secreted from the host cell. Alternatively the polypeptide may not be secreted from the host cell. In such a case the polypeptide may be expressed on the surface of the host cell. This may be desirable, for example, if the polypeptide comprises an antigen to which an immune response is desired in human or animal.

A homologous gene that may be present in the vector of the invention may be cobA. A host cell comprising this vector may therefore be capable of producing a compound such as vitamin B, 2 from a substrate or the compound may be the product of an enzyme. The invention specifically provides a process for the preparation of vitamin B12 comprising cultivating or fermenting such a host cell under conditions in which the UP (III) MT gene is expressed. The expressed enzyme can be contacted with a suitable substrate under conditions in which the substrate is converted to vitamin B, 2. This may result in increased production of vitamin B, 2.

Therapeutics As described above the polynucleotide of the invention may comprise a heterologous gene which is a therapeutic gene. Thus the invention includes a host cell comprising a vector of the invention which comprises a therapeutic gene for use in a method of treatment of the human or animal body by therapy. Such a host cell may be Propionibacterium. The host cell may be alive or dead.

The host cell can be formulated for clinical administration by mixing them with

a pharmaceutically acceptable carrier or diluent. For example they can be formulated for topical, parenteral, intravenous, intramuscular, subcutaneous, oral or transdermal administration. The host cell may be mixed with any vehicle which is pharmaceutically acceptable and appropriate for the desired route of administration.

The pharmaceutically acceptable carrier or diluent for injection may be, for example, a sterile or isotonic solution such as Water for injection or physiological saline.

The dose of the host cells may be adjusted according to various parameters, especially according to the type of the host cells used, the age, weight and condition of the patient to be treated; the mode of administration used; the condition to be treated; and the required clinical regimen. As a guide, the number of host cells administered, for example by oral administration, is from 10'to 10"host cells per dose for a 70 kg adult human.

The routes of administration and dosages described are intended only as a guide since a skilled practitioner will be able to determine readily the optimum route of administration and dosage of any particular patient and condition.

Polypeptides A sixth aspect of the invention provides a polypeptide of the invention comprising one of the amino acid sequences set out in SEQ ID NO: 2 or 3 or a substantially homologous sequence, or of a fragment of either of these sequences.

The polypeptide may be one encoded by a polynucleotide of the first aspect. In general, the naturally occurring amino acid sequences shown in SEQ ID NO: 2 or 3 are preferred. However, the polypeptides of the invention include homologues of the natural sequences, and fragments of the natural sequences and their homologues, which have the activity of the naturally occurring polypeptides. One such activity may be to effect the replication of the polynucleotide of the invention. In particular, a polypeptide of the invention may comprise: (a) the protein of SEQ ID No: 2 or 3; or (b) a homologue thereof from Actinomycetes, such as Propionibacterium freudenreichii or other Propionibacterium strains; or (c) a protein at least 70% homologous to (a) or (b).

A homologue may occur naturally in a Propionibacterium and may function in a

substantially similar manner to a polypeptide of SEQ ID NO: 2 or 3. Such a homologue may occur in Actinomycetes or gram positive bacteria.

A protein at least 70% homologous to the proteins of SEQ ID NO: 2 or 3 or a homologue thereof will be preferably at least 80 or 90% and more preferably at least 95%, 97% or 99% homologous thereto over a region of at least 20, preferably at least 30, for instance at least 40,60 or 100 or more contiguous amino acids. Methods of measuring protein homology are well known in the art and it will be understood by those of skill in the art that in the present context, homology is calculated on the basis of amino acid identity (sometimes referred to as"hard homology").

The sequences of the proteins of SEQ ID NO: 2 and 3 and of homologues can thus be modified to provide other polypeptides within the invention.

Amino acid substitutions may be made, for example from 1,2 or 3 to 10,20 or 30 substitutions. The modified polypeptide generally retains its natural activity.

Conservative substitutions may be made, for example according to the following Table. Amino acids in the same block in the second column and preferably in the same line in the third column may be substituted for each other: ALIPHATIC Non-polar GAP ILV Polar-uncharged C S T M NQ Polar-charged D E KR AROMATIC H F W Y Polypeptides of the invention also include fragments of the above-mentioned full length polypeptides and variants thereof, including fragments of the sequences set out in SEQ ID NO: 2 or 3. Such fragments can retain the natural activity of the full-length polypeptide.

Suitable fragments will be at least about 5, e. g. 10,12,15 or 20 amino acids in size. Polypeptide fragments of SEQ ID No: 2 and 3 and homologues thereof may contain one or more (e. g. 2,3,5, or 10) substitutions, deletions or insertions,

including conserved substitutions.

Polypeptides of the invention may be in a substantially isolated form. A polypeptide of the invention may also be in a substantially purified form, in which case it will generally comprise the polypeptide in a preparation in which more than 90%, e. g. 95%, 98% or 99% of the polypeptide in the preparation is a polypeptide of the invention.

A polypeptide of the invention may be labelled with a revealing label. The revealing label may be any suitable label which allows the polypeptide to be detected. Suitable labels include radioisotopes, e. g.'ZSi, 35S, enzymes, antibodies, polynucleotides and linkers such as biotin.

Industrial Applications As will be apparent from the discussion, the host cells of the third aspect can be used to produce not only the recombinant proteins, but also other compounds of interest, including non-proteins such as inorganic chemicals, in particular vitamins.

A seventh aspect of the present invention therefore relates to a process for the production of a compound, the process comprising culturing or fermenting host cells of the third aspect under conditions whereby the desired compound is produced.

Although this compound may be a polypeptide, for example a polypeptide of the sixth aspect, it may also be one of the compounds mentioned in the previous discussion concerning genes to be expressed. Clearly inorganic compounds will not be expressed by a gene, but they may be produced by an enzyme, or the polypeptide or enzyme may assist the host cell in the production of the desired compound. These compounds may be produced inside the cell, and later isolated, for example following lysis of the host cell, or they may pass through the wall of the host cell into a surrounding medium, which may be a fermentation medium, for example an aqueous solution. In this way, the host cells can be cultured in an aqueous medium that comprises cells and nutrients for the cells, for example assimilable sources of carbon and/or nitrogen.

The polypeptides so produced may have therapeutic uses. They may be drugs or other pharmacologically active compounds, or may be antigenic or immunogenic, in which case they may find use in vaccines.

The invention additionally encompasses compounds produced by this process, whether or not it is a recombinant polypeptide. Compounds specifically contemplated are vitamins, such as vitamin B, 2 (cobalamin).

In some cases the compound need not be isolated either from the fermentation medium or from the host cells. The host cells may themselves be used in particular applications, for example in, or in the manufacturing of, foodstuffs such as sausages, or in cheese making, or the host cells may for example be included in an animal feed, such as when the host cells contain a compound to be ingested by the animal in question. The invention therefore extends to the use of these compounds or the host cells, in the production of foodstuffs such as cheeses and sausages. The invention also contemplates foodstuffs or animal feed comprising host cells or a compound produced by the invention.

In a particularly preferred embodiment of the present invention the host cells can be used in a cheese making process, and so the invention additionally includes a process for manufacturing cheese where the microorganisms employed are host cells of the invention. The host cells may be used instead of or in addition to, other bacteria, such as lactic acid bacteria. Propionic acid bacteria are currently used in cheese making processes, for example with mesophilic cultures (Maasdam type of cheese) as well as thermophilic cultures (Emmental). Both mesophilic and thermophilic organisms can be responsible for the acidification of the milk or cheese.

In this way the host cells of the invention can be not only used for cheese but also for the production of other fermented dairy products (e. g. yoghurts). Propionic acid bacterium are employed in cheese making because of their ability to convert lactate and carbohydrates to propionic acid, acetic acid and carbon dioxide. The host cells of the invention, especially if they are propionibacteria, can be employed because they can be less sensitive to nitrates and salt, which may allow the reduction or omission of bactofugation of the milk (usually employed to reduce the levels of Clostridia).

The fermentation of the host cells may have one or two phases or stages. These may be for example a growth and/or production phase, or anaerobic and/or aerobic phase. Preferably, there will be a growth and/or anaerobic phase, and suitably also (e. g. afterwards) a production and/or aerobic phase.

Both the carbon and/or nitrogen sources may be complex sources or individual compounds. For carbon, it is preferred that this is glucose. For nitrogen, appropriate sources include yeast extract or ammonia or ammonium ions.

Preferred features and characteristics of one aspect of the invention are suitable for another aspect mutatis mutandis.

Figures The invention is illustrated by the accompanying drawings in which: Figure 1 is a restriction map of a vector within the invention, p545 obtained from P. freudenreichii LMG 16545 (CBS 101022); and Figures 2a and 2b each contain two maps of two vectors, all four vectors being within the invention.

The invention will now be described, by way of example, by reference to the following Examples, which are not to be construed as being limiting.

EXAMPLE 1 Screening of Propionibacterium strains A collection of 75 nonpathogenic strains of Propionibacterium was screened for the presence of indigenous plasmids. The majority of strains were obtained from the BCCM/LMG culture collection (Ghent, Belgium), although some strains were obtained from ATCC (Rockville, Md., USA) or from DSM (Braunschweig, Germany). Screening was performed using a small scale plasmid isolation procedure.

First bacteria were cultivated anaerobically in MRS medium6 for 48 hrs at 30°C.

Plasmids were then purified from the bacteria using a plasmid DNA isolation procedure originally developed for E. coli4 with some modifications: cells from a 5 ml culture were washed in a 25% sucrose, 50 mM Tris-HCl pH8 solution, resuspended in 250 TENS (25% sucrose + 50mM NaCl + 50 mM Tris-HCl + 5mM EDTA pH8), containing 1 Omg/ml lysozyme (Boehringer Mannheim), and incubated at 37°C for 20-30 minutes. The bacterial cells were then lysed in 500ut of 0.2 N NaOH/1% SDS (2-5 minute incubation on ice). After addition of400ul 3M NaAc pH4.8 (5 minutes on ice) and subsequent extraction with phenol/chloroform, the DNA was precipitated by addition of isopropanol.

The DNA was analysed by electrophoresis on 1 % agarose gels, and visualised by ethidium bromide. Whereas most strains were negative, i. e. did not reveal the presence of indigenous plasmids in this analysis, the majority of strains that proved positive contained large (220 kb) plasmids. Smaller plasmids were observed in 6 strains. Of these, P. jensenii LMG16453, P. acidipropionici ATCC4875, P. acidipropionici LMG16447 and a nonspecified Propionibacterium strain (LMG16550) contained a plasmid in the size range of 6-10 kb. Two strains (P. freudenreichii LMG16545 and P. freudenreichii LMG16546) showed an identical plasmid profile of 2 plasmids. One plasmid was large (size not determined) and the other was smaller, more abundantly present and had a size of 3.6 kb. These 3.6 kb plasmids from LMG16545 and LMG16546 were chosen for further analysis.

EXAMPLE 2 Analysis of an indigenous plasmid from strains LMG16545 and LMG16546 The 3.6 kb plasmids were isolated from both strains and further purified by CsCI-ethidium bromide density gradient ultracentrifugation". Limited restriction maps were made of both preparations and these turned out to be identical". The restriction map of the 3.6 kb plasmid is shown in Fig. 1. Restriction enzymes and T4 ligase were obtained from New England Biolabs or GIBCO BRL.

The 3.6 kb plasmid from strain LMG16545 (from here on referred to as p545) was radioactively labelled and used in Southern blot hybridization experiments.

Hybridisation conditions were 0.2 x SSC, 65°C. It reacted equally well with both LMG16545 and LMG16546 plasmid DNA extracts, supporting the close relationship of these strains, whereas a plasmid DNA extract from P. acidipropionici ATCC4875, that harbors a 6.6 kb plasmid called pTY1 or pRG018 failed to react.

The DNA sequence of plasmid p545 was determined with fluorescent dye labelled dideoxyribonucleotides in an Applied Biosystems 373A automatic sequencer, and is included as SEQ ID No: 1 in the sequence listing. Sequence analysis was performed on plasmid DNA that had been linearized with EcoRI and inserted into EcoRI digested pBluescript SKII+ DNA (Stratagene, La Jolla, Ca., USA). Computer assisted analysis of the sequence thus obtained using BLAST search'revealed homologies to proteins involved in replication of plasmids from several GC-rich organisms (e. g., pAL5000 encoded repA and repB from Mycobacteriumfortuitum814 show 28-30% identity and 34-38% similarity with the respective putative replication proteins from plasmid p545; pXZ10142 from Corynebacterium glutamicum [PIR Accession Number S32701] is another example of plasmids encoding replication proteins homologous to the p545 putative replication proteins). The results of the database comparisons with homologous sequences are detailed in Examples 7 and 8.

EXAMPLE 3 Construction of E. colilPropionibacterium shuttle vectors E. coli plasmid pBR322 was digested with EcoRI and AvaI and the smaller

fragment thus generated (measuring 1.4 kb and encompassing the tetracyclin resistance conferring gene) was replaced by a synthetic duplex DNA. The synthetic duplex DNA was designed so as to link EcoRI and Aval ends and to supply a number of unique restriction enzyme recognition sites: 5'- AATTCAAGCTTGTCGACGTTAACCTGCAGGCATGCGGATCCGGTACCGAT ATCAGATCT-3' (SEQ. ID. NO. 4) 3'- GTTCGAACAGCTGCAATTGGACGTCCGTACGCCTAGGCCATGGCTATAGT CTAGAAGCC-5' (SEQ. ID. NO. 5) The following restriction enzyme recognition sites were supplied in this way: EcoRI (restored), HindIII, SalI, HpaI, PstI, SphI, BamHI, Acc65I, EcoRV, BglII (AvaI is not restored).

This synthetic DNA was ligated to the large fragment and the ligation mixture transferred back to E. coli (T4 ligase was used). A plasmid of the expected composition was obtained (pBR322AI). The multiple cloning site can be used to introduce a selection marker as well as plasmid p545 DNA.

As an example the construction of an E. colil Propionibacterium shuttle plasmid conferring resistance to erythromycin was performed as will now be described.

A 1.7 kb Acc65I fragment from the Saccharopolyspora erythraea NRRL2338 erythromycin biosynthesis cluster and containing the erythromycin resistance conferring genel52 was inserted into Acc65I linearized pBR322AI. Then the newly derived construct, named pBRES, was linearized with EcoRV and ligated to p545 DNA that had been digested with BsaBI. E. coli transformants were found to harbor a vector with the correct insert, in both orientations. The resulting plasmid vectors were named pBRESP36B1 and pBRESP36B2 (Figs. 2a and 2b).

Plasmid vector constructs were also obtained with p545 DNA linearized in an other restriction site situated outside the putative replication region, namely AlwNI.

For this construction the pBRES vector had to be provided with a suitable cloning site. An adaptor was designed consisting of two complementary oligonucleotides of

the following composition (SEQ. ID. Nos 6 and 7): 5'GTACCGGCCGCTGCGGCCAAGCTT 3' 5'GATCAAGCTTGGCCGCAGCGGCCG 3' Annealing of these oligo's created a double stranded DNA fragment with Acc65I and BglII cohesive ends respectively, which moreover contains an internal SfiI restriction site, that provides ends compatible to the AlwNI digested p545 plasmid.

This adaptor was cloned in pBRES between the BgIII and the proximal Acc65I site.

The pBRES-Sfi vector thus obtained was subsequently digested by SfiI and ligated to AlwNI digested p545. Transformation of E. coli yielded transformants with the correct vector as confirmed by restriction enzyme analysis. The vector obtained was named pBRESP36A (Fig. 2).

EXAMPLE 4 Transformation of Propionibacterium with E. coli/Propionibacterium shuttle vectors Transformation of Propionibacterium freudenreichii strain ATCC6207 with pBRESP36B1 will be described.

The bacterial cells are cultivated in SLB (sodium lactate broth"at 30°C to a stationary growth phase, and subsequently diluted 1: 50 in fresh SLB. After incubation at 30°C for around 20 hours, cells (now in the exponential growth phase) were harvested and washed extensively in cold 0.5M sucrose. Subsequently cells were washed once in the electroporation buffer, consisting of 0.5M sucrose, buffered by lrnM potassiumacetate, pH5.5, and finally resuspended in this electroporation buffer in about 1/100 of the original culture volume. Cells were kept on ice during the whole procedure.

For the electroporation (apparatus from BIORAD), 80-100 pl of cell suspension was mixed with +1 Fg of DNA (or smaller amounts), in a cooled 1 or 2 mm electroporation cuvette, and an electric pulse delivered. Optimal pulse conditions were found to be 25kV/cm at 200 K2 resistance and 25aF capacitance. However, lower and higher voltages (also at 10092) also yield transformants.

Immediately after the pulse, 900 ul cold SLB containing 0.5 M sucrose was added to the pulsed cell suspension and these are subsequently incubated for 2.5 to 3 hours at 30°C before plating appropriate dilutions on SLB/agar plates containing 0.5 M sucrose and 10>g/ml erythromycin. After a 5 to 7 day incubation period at 30°C under anaerobic conditions, transformants were detected.

DNA isolated from E. coli DH5a (Promega) yielded a transformation efficiency of 20-30 transformants per pg DNA. A 10-100 fold higher efficiency is achieved when DNA is isolated from E. coli JM110 (damri, dcrri strain). E. coli transformation was done according to BIORAD instructions.

Transformants contained the authentic vectors, indistinguishable from the original plasmid DNA used for transformation of ATCC6207. This was shown by restriction enzyme analysis of plasmid DNA isolated from the transformants by the small scale plasmid DNA isolation procedure refered to before.

Vectors were exclusively present as autonomously replicating plasmids.

Southern blot hybridization'3 with total DNA isolates showed that chromosomal DNA did not hybridise to the vector DNA used as a probe, indicating that no chromosomal integration of plasmid DNA occured.

Transformation was also successful with vectors pBRESP36B2 and pBRESP36A, indicating that functionality of the vector was independent of the orientation of p545 or the cloning site used. Also in this case the authenticity of the vectors was confirmed.

Moreover, transformation of P. freudenreichii strain ATCC6207 with DNA isolated from a Propionibacterium transformant resulted in a 105-106 fold increased transformation efficiency as compared to that obtained with DNA isolated from E. coli DH5a.

Transformation of another P. freudenreichii strain, LMG16545 (the same strain from which the p545 plasmid was obtained), resulted in a transformation efficiency comparable to that of the ATCC strain.

The results of the transformations, and the effect on vitamin B, 2 production, is shown in the following Table.

Eight out of 10 transformants gave up to a 50% higher vitamin B, 2content than the control strain.

StrainID Transformed plasmid Vitamin B, Z (mg/gdry matter) COB 1 pBRES36COB 0.57 COB2 pBRES36COB 0.67 COB3 pBRES36COB 0.83 COB4 pBRES36COB 0.68 COB5 pBRES36COB 0.69 COB6 pBRES36COB 0. 61 COB7 pBRES36COB 0. 53 COB8 pBRES36COB 0.64 COB9 pBRES36COB 0.50 COB 10 pBRES36COB 0.74 recATCC6207 pBRESP36B2 0. 54 EXAMPLE 5 Construction of plasmid vector containing the cobA gene The construction and application of a plasmid vector to increase the level of vitamin B, 2 (cobalamin) synthesis in P. freudenreichii strain ATCC6207 will be described.

The promoter region of the gene conferring erythromycin resistance in Saccharopolyspora erythraea2 3 was generated by PCR using the following primers (SEQ. ID. NOs 8 and 9): forward primer: (5'-3') AAACTGCAGCTGCTGGCTTGCGCCCGATGCTAGTC

reverse primer: (5'-3') AAACTGCAGCAGCTGGGCAGGCCGCTGGACGGCCTGCCCTCGAGCTCGT CTAGAATGTGCTGCCGATCCTGGTTGC The PCR fragment thus generated contained an AIwNI site at the 5'end followed by the authentic promoter region and the first 19 amino acids of the coding region of the erythromycin resistance gene, to ensure proper transcription and translation initiation. At the 3'end XbaI and XhoI sites were provided (for insertion of the cobA gene in a later stage), a terminator sequence as present downstream from the erythromycin resistance gene, and an AIwNI site.

The PCR product was digested by AIwNI and ligated to pBRESP36B2, partially digested with AIwNI. Of the two AIwNI sites present in pBRESP36B2, only the one present in the p545 specific part of the vector will accommodate the fragment. E. coli transformants were obtained harboring the expected construct, named pBRES36pEt. This vector was used for further constructions as described below.

The coding sequence of cobA, the gene encoding uroporphyrinogen III methyltransferase, was generated by PCR from Propionibacterium freudenreichii strain ATCC6207, using the following primers (SEQ. ID. NOs 10 and 11): forward: (5'-3') CTAGTCTAGACACCGATGAGGAAACCCGATGA reverse: (5'-3') CCCAAGCTTCTCGAGTCAGTGGTCGCTGGGCGCGCG The cobA gene thus amplified carries an site at the N terminal coding region, and HindIII and XhoI sites at the C terminal coding region.

The functionality of this cobA gene was confirmed by cloning the PCR product as an XbaI-HindIII fragment in pUC18, and subsequent transformation of E. coli strain JM109. Transformants with a functional cobA gene show a bright red fluorescence when illuminated with LTV light. Plasmid DNA isolated from such a transformant was digested with XbaI and XhoI, ligated to likewise digested pBRESP36B2. DNA and used for transformation of E. coli. DNA from several transformants was analysed by restriction enzyme digestion and gel electrophoresis.

Transformants were found to bear the correct insert in the expression vector. This

new vector was named pBRES36COB. This vector was subsequently transferred to P. freudenreichii ATCC6207 following the protocol described before. Ten of the transformants obtained were analysed and were found to harbor the pBRES36COB vector, which was again indistinguishable from the original vector used for transformation, as shown by analysis of the restriction enzyme digests. In these ten transformants the level of vitamin B, 2 synthesis was determined as follows.

Frozen cultures of Propionibacterium Propionibacterium transformants 10, through well as well control strain containing only the vector plasmid pBRESP36B2, were inoculated in 100 ml flasks containing 50 ml of BHI (Brain Heart Infusion) medium (Difco) and incubated for 72 hrs at 28°C without shaking. From this preculture 4 ml were transferred to 200 ml of production medium consisting of Difco yeast extract 15 g/l, Nalactate 30 g/l, KH2PO4 0.5g/l, MnSO4 0.01 g/l, and CoCl2 0.005 g/1 in a 500 ml shake flask and incubated at 28°C for 56 hrs without shaking, followed by 48 hrs in a New Brunswick rotary shaker at 200 rpm.

Vitamin B, 2 titres were measured using a known HPLC method5. Nine out of 10 transformants showed an approx. 25% higher vitamin B'2 production than the control strain.

EXAMPLE 6 Stability of the plasmids All three shuttle vectors pBRESP36A, pBRESP36Bl, and pBRESP36B2 were stably maintained over 30 generations of culturing of the respective transformants: no loss of erythromycin resistance was observed as determined by viability counts on selective (erythromycin containing) and non-selective agar plates. The structural stability of the plasmid in the transformant population after 30 generations was established by plasmid DNA isolation and characterisation by restriction enzyme mapping as described above: only restriction fragments similar to those of the authentic plasmid were observed.

EXAMPLE 7 Database sequence homology analysis for predicted polypeptide encoded by the first open readme frame (SEQ. ID. No. 2 ! MDSFETLFPESWLPRKPLASAEKSGAYRHVTRQRALELPYIEANPLVMQSLV ITDRDASDADWAADLAGLPSPSYVSMNRVTTTGHIVYALKNPVCLTDAARR RPINLLARVEQGLCDVLGGDASYGHRITKNPLSTAHATLWGPADALYELRA <BR> <BR> <BR> <BR> LAHTLDEIHALPEAGNPRRNVTRSTVGRNVTLFDTTRMWAYRAVRHSWGG PVAEWEHTVFEHIHLLNETIIAD The above 227 amino acid sequence (ORF 1) was aligned and compared with several other protein sequences (target NBRF-PIR, release PIR R52.0 March 1997, cut-off 45, KTUP: 2).

With a protein from Mycobacterium fortuitum plasmid pAL 5,000 (JS0052) a match of 37.1 % was found over 194 amino acids (INIT 167,292). With a protein from Corynebacterium glutamicum (S32701) a match 32.0% over 125 amino acids was found (INIT 125,116). A match of 29.9% over 221 amino acids (INIT 86,259) was found with the ColE2 protein from E. coli (S04455). Precisely the same match over the same number of amino acids was found for the ColE3 protein, also from E. coli (S04456).

EXAMPLE 8 Database sequence homology analysis for predicted polypeptide encoded by the second reading frame (SEO. ID. No. 3) MTTRERLPRN GYSIAAAAKK LGVSESTVKR WTSEPREEFV ARVAARHARI RELRSEGQSM RAIAAEVGVS VGTVHYALNK NRTDA The second protein (ORF2) was also aligned and compared with another protein, using the same parameters and software as described for Example 7. This sequence however is only 85 amino acids in length.

The ORF2 sequence was compared with a protein from Mycobacterium fortuitum (S32702) and a 53.3% match over 75 amino acids was found (INIT 207, 207).

EXAMPLE 9 Functional analysis of plasmid p545 In order to improve the vector system further, the plasmid functions essential for replication and stability were delineated more precisely through deletion of large regions of the original plasmid p545. The result, a smaller cloning vector, will allow the use of the p545 based vector system for cloning larger DNA fragments.

To this end vector pBRESP36A (Figure 2) was digested with SstII and BcII, resulting in a 1.7 kb and a 6.5 kb fragment. The 1.7 kb fragment, in fact the 1.6 kb AlwNI-BcII fragment of plasmid p545, was replaced by a synthetic duplex DNA, composed of SEQ. ID. No. 12 and SEQ. ID. No. 13 with SstII and BclJ compatible ends and a number of unique restriction enzyme recognition sites.

SEQ. ID. No. 12 5'GGAGATCTAGATCGATATCTCGAG 3' SEQ. ID. No. 13 5'GATCCTCGAGATATCGATCTAGATCTCCGC 3' The following restriction enzyme recognition sites were supplied in this way: SstII (restored), BgllI, XbaI, ClaI, EcoRV, XhoI, (BcII is not restored). The ligation mixture was transferred to E. coli, and transformants were selected containing a vector of the expected composition. The vector was named pBRESAhS- B. Subsequent successful transformation of P. fi eudenreichEi strain ATCC6207 with this vector indicated that the 1.6 kb region between AlwNI and Bcll in p545 is not essential for replication of the plasmid.

A further deletion was made by removal of the 240 bp corresponding to the region between SalI and BcII in plasmid p545. This was achieved by digestion of pBRESAAS-B with SalI-SstI, and SstI-XhoI respectively, and isolation of the 1.3 kb SalI-SstI fragment, and the 6.6 kb SstI-XhoI fragment. The fragments were ligated, and the ligation mixture was transferred to P. freudenreichii ATCC6207, yielding numerous transformants. The newly derived construct, named

pBRESAAS-S, was isolated and its structure confirmed by restriction enzyme mapping.

Thus all essential information for replication of plasmid p545 is located on a fragment of 1.7 kb delimited by the restriction sites SalI and AlwNI and encompassing the predicted replication proteins encoded by ORF 1 and ORF2, and that 1.8 kb can be deleted without obviously disturbing replication or stability of the plasmid.

EXAMPLE 10 Expression of a chloramphenicol resistance gene from Corynebacterium.

A chloramphenicol resistance gene (cul) from Corynebacterium'8 has been identified as encoding a chloramphenicol export protein. This gene was inserted in the Propionibacterium-E. coli shuttle vector pBRESP36B2. This vector was digested with BgIII and HindIII, and with BgIII and HpaI respectively. The 2.9 kb BglII-HindIII and 5.2 kb BglII-HpaI fragments were isolated.

The fragment containing the cml gene, including its own promoter, was obtained by digestion with PvuII and HindIII, and the 3.3 kb fragment containing the gene was isolated. The two vector-specific fragments and the cml fragment were ligated: PvuII and HpaI ends are blunt, thus inserting the cml gene as well as restoring the ermE gene of the parent vector. The ligation mixture was transferred to E. coli, and a transformant was selected, in which the vector contained the correct cml insert. The vector was named pBRESBCM.

Transformation of P. freudenreichii ATCC6207 with this vector, and selection on plates containing 1 Oug/ml erythromycin, or 5ug/ml chloramphenicol, yielded erythromycin and chloramphenicol resistant colonies, respectively, indicating that apart from the erythromycin resistance gene (shown earlier with the Propionibacterium-E. coli shuttle vectors), also the chloramphenicol resistance gene is expressed in Propionibacterium. Transformants could be cultivated in liquid medium containing up to 20 Zg/ml chloramphenicol.

EXAMPLE 11 Expression of lipase (gehA) gene from P. acnes To illustrate efficient cloning and expression of an extracellular protein using the present vector system, a lipase gene gehA from P. acnes was used'9. Vector pUL6001, harbouring gehA on a XhoI fragment, was digested with XhoI, and the 2.75 kb fragment containing the gene was isolated. Vector pBRESAAS-B (from Example 9) was linearized by XhoI, and the ends dephosphorylated using Calf Intestine Phosphatase to avoid self ligation. Linearized vector and the gehA containing fragment were ligated and the ligation mixture was transferred to E. coli.

Transformants were analysed by restriction enzyme analysis for the presence of the correct recombinant plasmid, named pBRESALIP. This plasmid was subsequently transferred to P. freudenreichii strain ATCC6207. Transformants were screened for the expression of the lipase gene, using agar plates containing tributyrin as the indicator for increased lipase expression. P. freudenreichii transformants harbouring pBRESALIP showed significantly increased halo sizes in this assay as compared to untransformed strains or strains transformed with the parent vector.

REFERENCES 1. Altschul et al, J. Mol. Biol. 215: 403-410 (1990) 2. Bibb et al., Gene 38,215 (1985) 3. Bibb et al., Mol. Microbiol. 14 (3), 533 (1984) 4. Birnboim and Doly, Nucleic Acids Res. 7,1513 (1979) 5. Blanche, Anal. Biochem. 189,24 (1990) 6. DeMan et al, J. Appl. Bacteriol. 36,130 (1960) 7. Deveraux et al, Nucleic Acids Research. 12: 387-395 (1984) 8. Labidi et al, Plasmid 27,130 (1992) 9. Rehberger and Glatz, Appl. Environ. Microbiol. 59,83 (1990) 10. Rossi et al, Res. Microbiol. 147,133 (1996) 11. Sambrook et al, Molecular Cloning, Cold Spring Harbor Laboratory Press (1989) 12. Sattler et al, J. Bact. 177,1564 (1995) 13. Southern, J. Mol. Biol. 98,503 (1975) 14. Stolt and Stoker, Microbiol. 142,2795 (1996) 15. Thompson et al, Gene 20,51 (1982) 16. Uchijama and Weisblum, Gene 38,103 (1985) 17. de Vries et al, J. Gen. Microbiol. 71,515 (1972) 18. Tauch et al, Plasmid 40 (2): 126 (1998) 19. Miskin et al, Microbiol 143: 1745 (1997) SUMMARY OF SEQUENCES 1. DNA sequence of plasmid LMG 16545 (CBS 101022), 3.6 kb.

2. amino acid of protein of ORF1 (303 residues, bases 273-1184).

3. amino acid of protein of ORF2 (85 residues, bases 1181-1438).

4-13. DNA primers/oligonuceotides