WO2006084725A1 - Nouveau gene sts 16 - Google Patents

Nouveau gene sts 16 Download PDF

Info

Publication number
WO2006084725A1
WO2006084725A1 PCT/EP2006/001220 EP2006001220W WO2006084725A1 WO 2006084725 A1 WO2006084725 A1 WO 2006084725A1 EP 2006001220 W EP2006001220 W EP 2006001220W WO 2006084725 A1 WO2006084725 A1 WO 2006084725A1
Authority
WO
WIPO (PCT)
Prior art keywords
microorganism
vitamin
production
polynucleotide
sts
Prior art date
Application number
PCT/EP2006/001220
Other languages
English (en)
Inventor
Bastien Chevreux
Anne Françoise MAYER
Anja Meury
Nigel John Mouncey
Masako Shinjoh
Original Assignee
Dsm Ip Assets B.V.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Dsm Ip Assets B.V. filed Critical Dsm Ip Assets B.V.
Publication of WO2006084725A1 publication Critical patent/WO2006084725A1/fr

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P17/00—Preparation of heterocyclic carbon compounds with only O, N, S, Se or Te as ring hetero atoms
    • C12P17/02—Oxygen as only ring hetero atoms
    • C12P17/04—Oxygen as only ring hetero atoms containing a five-membered hetero ring, e.g. griseofulvin, vitamin C
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/195—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from bacteria
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P7/00—Preparation of oxygen-containing organic compounds
    • C12P7/40—Preparation of oxygen-containing organic compounds containing a carboxyl group including Peroxycarboxylic acids
    • C12P7/58—Aldonic, ketoaldonic or saccharic acids
    • C12P7/60—2-Ketogulonic acid

Definitions

  • the present invention relates to newly identified genes that encode proteins that are involved in the synthesis of L-ascorbic acid (hereinafter also referred to as Vitamin C).
  • the invention also features polynucleotides comprising the full-length polynucleotide sequences of the novel genes and fragments thereof, the novel polypeptides encoded by the polynucleotides and fragments thereof, as well as their functional equivalents.
  • the present invention also relates to the use of said polynucleotides and polypeptides as biotechnological tools in the production of Vitamin C from microorganisms, whereby a modification of said polynucleotides and/or encoded polypeptides has a direct or indirect impact on yield, production, and/or efficiency of production of the fermentation product in said microorganism. Also included are methods/processes of using the polynucleotides and modified polynucleotide sequences to transform host microorganisms. The invention also relates to genetically engineered microorganisms and their use for the direct production of Vitamin C.
  • Vitamin C is one of very important and indispensable nutrient factors for human beings. Vitamin C is also used in animal feed even though some farm animals can synthesize it in their own body.
  • Vitamin C has been produced industrially from D-glucose by the well-known Reichstein method. All steps in this process are chemical except for one (the conversion of D-sorbitol to L-sorbose), which is carried out by microbial conversion. Since its initial implementation for industrial production of Vitamin C, several chemical and technical modifications have been used to improve the efficiency of the Reichstein method. Recent developments of Vitamin C production are summarized in Ullmann's Encyclopedia of Industrial Chemistry, 5 th Edition, Vol. A27 (1996), pp. 547ff.
  • 2-keto-L-gulonic acid an intermediate compound that can be chemically converted into Vitamin C by means of an alkaline rearrangement reaction
  • 2-KGA 2-keto-L-gulonic acid
  • L-sorbose or D-sorbitol an intermediate compound that can be chemically converted into Vitamin C by means of an alkaline rearrangement reaction
  • strains belonging e.g. to the Ketogulonicigenium or Gluconobacter genera or by an alternative fermentation process
  • Vitamin C Current chemical production methods for Vitamin C have some undesirable characteristics such as high-energy consumption and use of large quantities of organic and inorganic solvents. Therefore, over the past decades, other approaches to manufacture Vitamin C using microbial conversions, which would be more economical as well as ecological, have been investigated.
  • Direct Vitamin C production from a number of substrates including D-sorbitol, L-sorbose and L-sorbosone has been reported in several microorganisms, such as algae, yeast and acetic acid bacteria, using different cultivation methods.
  • bacteria able to directly produce Vitamin C include, for instance, strains from the genera of Gluconobacter, Gluconacetobacter, Acetobacter, Ketogulonicigenium, Pantoea, Pseudomonas or Escherichia.
  • yeast or algae include, e.g., Candida, Saccharomyces, Zygosaccharomyces, Schizosaccharomyces, Kluyveromyces or Chlorella.
  • Microorganisms able to assimilate D-sorbitol for growth usually possess enzymes able to oxidize this compound into a universal assimilation substrate such as D-fructose. Also microorganisms able to grow on L-sorbose possess an enzyme, NAD(P)H-dependent L- sorbose reductase, which is able to reduce this compound to D-sorbitol, which is then further oxidized into D-fructose.
  • D-fructose is an excellent substrate for the growth of many microorganisms, after it has been phosphorylated by means of a D-fructose kinase.
  • acetic acid bacteria which are obligate aerobe, gram-negative microorganisms belonging to the genus Acetobacter, Gluconobacter, and Gluconacetobacter
  • these microorganisms are able to transport D-sorbitol into the cytosol and convert it into D-fructose by means of a cytosolic NAD-dependent D-sorbitol dehydrogenase.
  • Some individual strains such as Gluconobacter oxydans IFO 3292, and IFO 3293, are able as well to transport L-sorbose into the cytosol and reduce it to D- sorbitol by means of a cytosolic NAD(P)H-dependent L-sorbose reductase, which then is further oxidized into D-fructose.
  • the Embden-Meyerhof-Parnas pathway, as well as the tricarboxyclic acid cycle are not fully active, and the main pathway channeling sugars into the central metabolism is the pentose phosphate pathway.
  • D- fructose-6-phosphate obtained from D-fructose by a phosphorylation reaction enters the pentose phosphate pathway, being further metabolized and producing reducing power in the form of NAD(P)H and tricarboxylic compounds necessary for growth and maintenance.
  • NAD(P)H NAD(P)H
  • tricarboxylic compounds necessary for growth and maintenance.
  • Acetic acid bacteria are well known for their ability to incompletely oxidize different substrates such as alcohols, sugars, sugar alcohols and aldehydes. These processes are generally known as oxidative fermentations or incomplete oxidations, and they have been well established for a long time in the food and chemical industry, especially in vinegar and in L-sorbose production.
  • a useful product known to be obtained from incomplete oxidations of D-sorbitol or L-sorbose using strains belonging to the Gluconobacter genus is 2-KGA.
  • Acetic acid bacteria accomplish these incomplete oxidation reactions by means of different dehydrogenases located either in the periplasmic space, on the periplasmic membrane as well as in the cytoplasm.
  • Different co-factors are employed by the different dehydrogenases, the most common being PQQ and FAD for membrane-bound or periplasmic enzymes, and NAD/NADP for cytoplasmic enzymes.
  • Proteins, in particular transporters, that are active in the transportation of sugar such as e.g. glucose, sugar alcohols and related compounds across the cellular membrane are herein referred to as being involved in the Sugar Transport System.
  • sugar such as e.g. glucose, sugar alcohols and related compounds across the cellular membrane
  • STS proteins Proteins, in particular transporters, that are active in the transportation of sugar such as e.g. glucose, sugar alcohols and related compounds across the cellular membrane are herein referred to as being involved in the Sugar Transport System.
  • STS proteins Proteins, in particular transporters, that are active in the transportation of sugar such as e.g. glucose, sugar alcohols and related compounds across the cellular membrane.
  • STS proteins Proteins, in particular transporters, that are active in the transportation of sugar such as e.g. glucose, sugar alcohols and related compounds across the cellular membrane.
  • STS proteins are in general membrane-bound or are associated to membrane-bound structures and are functional as single proteins or as subunits in protein complexes such as permeases or active transporters. STS proteins are known to be responsible for selectively facilitating, assisting or enabling the transport of compounds such as sugars, sugar alcohols, sugar ketones or sugar aldehydes across the cellular or periplasmatic membrane.
  • STS proteins can be divided into three types on the basis of their mechanisms.
  • the first class of transporters uses energy from the proton-motive force to transport molecules against a concentration gradient. These symport and antiport systems couple the movement of two different molecules across the membrane (via permeases having two separate binding sites for the two different molecules); in symport, both molecules are transported in the same direction, while in antiport, one molecule is imported while the other is exported. - 4 - 24595
  • the second class of transporters is energized by the transfer of a high-energy phosphate group from phosphoenolpyruvate, through various protein components, to the substrate which is phosphorylated upon import as its phosphoester form.
  • PTS phosphotransferase system
  • the third class of transporters couples the hydrolysis of ATP to substrate translocation. These systems are termed the ATP-binding cassette (ABC) type transporters.
  • the ABC- transport system consists of a substrate specific binding protein which is located in the periplasm in gram-negative bacteria or which is membrane associated in gram-positive ' bacteria, an integral membrane domain and a cytoplasmic-facing ATP hydrolyzing domain.
  • An object of the present invention is to improve the yields and or productivity of Vitamin C production.
  • STS proteins of the present invention are selected from transferases [EC 2], preferably transferases transferring phosphorus-containing groups [EC 2.7], more preferably phosphotransferases with an alcohol group as acceptor [EC 2.7.1] and phosphotransferases with a nitrogenous group as acceptor [EC 2.7.3], most preferably protein-np-phosphohistidine-sugar phosphotransferase [EC 2.7.1.69] and phosphoenolpyruvate-protein phosphotransferase [EC 2.7.3.9] or from hydrolases [EC 3], preferably hydrolases acting on acid anhydrides [EC 3.6].
  • the STS proteins of the present invention maybe selected from sugar transporters and/or sugar alcohol transporters, preferably transporter proteins and periplasmic binding/transfer proteins, more preferably, periplasmic sorbitol-binding proteins, periplasmic solute-binding proteins, periplasmic D-allose-binding proteins, trehalose/maltose ABC transporters including subunits like membrane components, - 5 - 24595 mannitol/sorbitol ABC-type transporter including subunits like MtIK ATPase or membrane (MtIG or MtIF) components, and proteins involved in PTS including Ptsl enzyme I, Hpr protein, enzyme IIA Man , P-loop ATPase protein family or Hpr kinases.
  • periplasmic sorbitol-binding proteins preferably periplasmic solute-binding proteins
  • periplasmic D-allose-binding proteins trehalose/maltose ABC transporters including subunits like membrane
  • STS proteins encoded by polynucleotides having a nucleotide sequence that hybridizes preferably under highly stringent conditions to a sequence shown in SEQ ID NO:1 play an important role in the biotechnological production of Vitamin C. It has also been found, that by genetically altering the expression level of nucleotides according to the invention in a microorganism capable of directly producing Vitamin C, such as for example Gluconobacter, the direct fermentation of Vitamin C by said microorganism can be even greatly improved.
  • the invention relates to a polynucleotide selected from the group consisting of:
  • polynucleotides comprising a nucleotide sequence obtainable by nucleic acid amplification such as polymerase chain reaction, using genomic DNA from a microorganism as a template and a primer set according to SEQ ID NO: 3 and SEQ ID NO:4;
  • polynucleotides comprising a nucleotide sequence encoding a fragment or derivative of a polypeptide encoded by a polynucleotide of any of (a) to (c) wherein in said derivative one or more amino acid residues are conservatively substituted compared to said polypeptide, and said fragment or derivative has the activity of a sugar transporter and/or sugar alcohol transporter, preferably STS 16 activity;
  • polynucleotides the complementary strand of which hybridizes under stringent conditions to a polynucleotide as defined in any one of (a) to (d) and which encode a sugar transporter and/or sugar alcohol transporter, preferably a STS 16 polypeptide;
  • polynucleotides which are at least 70%, such as 85, 90 or 95% identical to a polynucleotide as defined in any one of (a) to (d) and which encode a sugar transporter and/or sugar alcohol transporter, preferably a STS 16 polypeptide;
  • the STS protein as isolated from Gluconobacter oxydans DSM 17078 shown in SEQ ID NO:2 and described herein was found to be a particularly useful STS protein, since it appeared that it performs a crucial function in the direct Vitamin C production in microorganisms, in particular in bacteria, such as acetic acid bacteria, such as Gluconobacter, Acetobacter and Gluconacetobacter.
  • the invention relates to a polynucleotide encoding a polypeptide according to SEQ ID NO:2.
  • This protein may be encoded by a nucleotide sequence as shown in SEQ ID NO: 1.
  • the invention therefore also relates to polynucleotides comprising the nucleotide sequence according to SEQ ID NO:1.
  • the nucleotide and amino acid sequences determined above were used as a "query sequence" to perform a search with Blast2 program (version 2 or BLAST from National Center for Biotechnology [NCBI] against the database PRO SW-SwissProt (full release plus incremental updates). From the searches, the STS 16 polynucleotide according to SEQ ID NO:1 was annotated as encoding a MtIG membrane component of the mannitol/sorbitol ABC-type transporter.
  • a nucleic acid according to the invention may be obtained by nucleic acid amplification using cDNA, mRNA or alternatively, genomic DNA, as a template and appropriate oligonucleotide primers such as the nucleotide primers according to SEQ ID NO: 3 and SEQ ID NO: 4 according to standard PCR amplification techniques.
  • the nucleic acid thus amplified may be cloned into an appropriate vector and characterized by DNA sequence analysis.
  • the template for the reaction may be cDNA obtained by reverse transcription of mRNA prepared from strains known or suspected to comprise a polynucleotide according to the invention.
  • the PCR product may be subcloned and sequenced to ensure that the amplified sequences represent the sequences of a new nucleic acid sequence as described herein, or a functional equivalent thereof.
  • the PCR fragment may then be used to isolate a full length cDNA clone by a variety of known methods.
  • the amplified fragment may be labeled and used to screen a bacteriophage or cosmid cDNA library.
  • the labeled fragment may be used to screen a genomic library.
  • the invention relates to polynucleotides comprising a nucleotide sequence obtainable by nucleic acid amplification such as polymerase chain reaction, using DNA such as genomic DNA from a microorganism as a template and a primer set according to SEQ ID NO:3 and SEQ ID NO:4. - 7 - 24595
  • the invention also relates to polynucleotides comprising a nucleotide sequence encoding a fragment or derivative of a polypeptide encoded by a polynucleotide as described herein wherein in said derivative one or more amino acid residues are conservatively substituted compared to said polypeptide, and said fragment or derivative has the activity of a STS polypeptide, preferably a STS 16 polypeptide.
  • the invention also relates to polynucleotides the complementary strand of which hybridizes under stringent conditions to a polynucleotide as defined herein and which encode a STS polypeptide, preferably a STS 16 polypeptide.
  • the invention also relates to polynucleotides which are at least 70% identical to a polynucleotide as defined herein and which encode a STS polypeptide; and the invention also relates to polynucleotides being the complementary strand of a polynucleotide as defined herein above.
  • the invention also relates to microorganisms wherein the activity of a STS polypeptide, preferably a STS 16 polypeptide, is enhanced and/or improved so that the yield of Vitamin C which is directly produced from D-sorbitol or L-sorbose is increased.
  • This may be accomplished, for example, by transferring a polynucleotide according to the invention into a recombinant or non-recombinant microorganism that may or may not contain an endogenous equivalent of the STS 16 gene.
  • a STS protein preferably a STS 16 protein.
  • Such may be for instance accomplished by either genetically modifying the host organism in such a way that it produces more or more stable copies of the STS protein, preferably the STS 16 protein, than the wild type organism or by increasing the specific activity of the STS protein, preferably the STS 16 protein.
  • Modifications in order to have the organism produce more copies of the STS 16 gene, i.e. overexpressing the gene, and/or protein may include the use of a strong promoter, or the mutation (e.g. insertion, deletion or point mutation) of (parts of) the STS 16 gene or its regulatory elements. It may also involve the insertion of multiple copies of the gene into a suitable microorganism.
  • An increase in the specific activity of an STS 16 protein may also be accomplished by methods known in the art. Such methods may include the mutation (e.g. insertion, deletion or point mutation) of (parts of) the STS 16 gene.
  • a gene is said to be "overexpressed” if the level of transcription of said gene is enhanced in comparison to - 8 - 24595 the wild type gene.
  • a gene is overexpressed if the amount of generated mRNA is increased by at least 1%, 2%, 5% 10%, 25%, 50%, 75%, 100%, 200% or even more than 500%, compared to the amount of mRNA generated from a wild-type gene.
  • the STS 16 protein may be expressed and tested for activity in the presence of compounds suspected to enhance the activity of the STS 16 protein.
  • the activity of the STS 16 protein may also be increased by stabilizing the messenger RNA encoding STS 16.
  • Such methods are also known in the art, see for example, in Sambrook et al., 1989, Molecular Cloning, A Laboratory Manual, Cold Spring Harbor Press, N. Y.; and Ausubel et al. (eds.), 1995, Current Protocols in Molecular Biology, (John Wiley & Sons, N. Y.).
  • the invention may be performed in any microorganism carrying a STS 16 gene or homologue thereof.
  • Suitable microorganisms may be selected from the group consisting of yeast, algae and bacteria, either as wild type strains, mutant strains derived by classic mutagenesis and selection methods or as recombinant strains.
  • yeast may be, e.g., Candida, Saccharomyces, Zygosaccharomyces, Schizosaccharomyces, or Kluyveromyces.
  • An example of such algae may be, e.g., Chlorella.
  • bacteria may be, e.g., Gluconobacter, Acetohacter, Gluconacetobacter, Ketogulonicigenium, Pantoea, Pseudomonas, such as, e.g., Pseudomonas putida, and Escherichia, such as, e.g., Escherichia coli.
  • Gluconobacter oxydans DSM 17078 (formerly known as Gluconobacter oxydans N44-1) has been deposited at Deutsche Sammlung von Mikroorganismen und Zellkulturen (DSMZ), Mascheroder Weg IB, D-38124 Braunschweig, Germany according to the Budapest Treaty on 26. January 2005.
  • DSMZ Deutsche Sammlung von Mikroorganismen und Zellkulturen
  • Microorganisms which can be used for the present invention may be publicly available from different sources, e.g., Deutsche Sammlung von Mikroorganismen und Zellkulturen (DSMZ), Mascheroder Weg IB, D-38124 Braunschweig, Germany, American Type Culture Collection (ATCC), P.O. Box 1549, Manassas, VA 20108 USA or Culture Collection Division, NITE Biological Resource Center, 2-5-8, Kazusakamatari, Kisarazu- shi, Chiba, 292-0818, Japan (formerly: Institute for Fermentation, Osaka (IFO), 17-85, Juso-honmachi 2-chome,Yodogawa-ku, Osaka 532-8686, Japan).
  • Examples of preferred bacteria deposited with IFO are for instance Gluconobacter oxydans (formerly known as - 9 - 24595
  • G. melanogenus IFO 3293 Gluconobacter oxydans (formerly known as G. melanogenus) IFO 3292, Gluconobacter oxydans (formerly known as G. rubiginosus) IFO 3244, Gluconobacter frateurii (formerly known as G. industrius) IFO 3260, Gluconobacter cerinus IFO 3266, Gluconobacter oxydans IFO 3287, and Acetobacter aceti subsp. orleanus IFO 3259, which were all deposited on April 05, 1954; Acetobacter aceti subsp. xylinum IFO 13693 deposited on October 22, 1975, and Acetobacter aceti subsp.
  • strain Acetobacter sp. ATCC 15164 which is also an example of a preferred bacterium, was deposited with ATCC.
  • Strain Gluconobacter oxydans (formerly known as G. melanogenus) N 44-1 as another example of a preferred bacterium is a derivative of the strain IFO 3293 and is described in Sugisawa et al, Agric. Biol. Chem. 54: 1201-1209, 1990.
  • a microorganism as of the present invention may carry further modifications either on the DNA or protein level (see above), as long as such modification has a direct impact on the yield, production and/or efficiency of the direct production of Vitamin C from substrates like e.g. D-sorbitol or L-sorbose.
  • Such further modifications may for instance affect other genes encoding STS proteins as described above, in particular genes encoding membrane- bound L-sorbosone dehydrogenases, such as L-sorbosone dehydrogenase SNDHai, or membrane-bound PQQ bound D-sorbitol dehydrogenases.
  • Methods of performing such modifications are known in the art, with some examples further described herein.
  • SNDHai for direct production of vitamin C as well as the nucleotide and amino acid sequence thereof we refer to WO 2005/017159 which is incorporated herein by reference.
  • the invention also relates to processes for the expression of endogenous genes in a microorganism, to processes for the production of polypeptides as defined above in a microorganism and to processes for the production of microorganisms capable of producing Vitamin C. All these processes may comprise the step of altering a microorganism, wherein "altering” as used herein encompasses the process for "genetically altering” or “altering the composition of the cell culture media and/or methods used for culturing” in such a way that the yield and/or productivity of the fermentation product can be improved compared to the wild-type organism.
  • improved yield of Vitamin C means an increase of at least 5%, 10%, 25%, 30%, 40%, 50%, 75%, 100%, 200% or even more than 500%, compared to a wild-type microorganism, i.e. a microorganism which is not genetically altered. - 10 - 24595
  • genetically engineered or “genetically altered” means the scientific alteration of the structure of genetic material in a living organism. It involves the production and use of recombinant DNA. More in particular it is used to delineate the genetically engineered or modified organism from the naturally occurring organism. Genetic engineering may be done by a number of techniques known in the art, such as e.g. gene replacement, gene amplification, gene disruption, transfection, transformation using plasmids, viruses, or other vectors.
  • a genetically modified organism e.g. genetically modified microorganism, is also often referred to as a recombinant organism, e.g. recombinant microorganism.
  • the present invention provides a process for the direct production of Vitamin C comprising converting a substrate into Vitamin C. This may for instance be done in a medium comprising a microorganism, which may be a resting or a growing microorganism, preferably a resting microorganism.
  • substrates may be used as a carbon source in a process of the present invention, i.e. a process for direct conversion of a given substrate into Vitamin C such as e.g. mentioned above.
  • Particularly suited carbon sources are those that are easily obtainable from the D- glucose or D-sorbitol metabolization pathway such as, for example, D-glucose, D-sorbitol, L-sorbose, L-sorbosone, 2-keto-L-gulonate, D-gluconate, 2-keto-D-gluconate or 2,5- diketo-gluconate.
  • the substrate is selected from for instance D-glucose, D- sorbitol, L-sorbose or L-sorbosone, more preferably from D-glucose, D-sorbitol or L- sorbose, and most preferably from D-sorbitol, L-sorbose or L-sorbosone.
  • substrate and "production substrate” in connection with the above process using a microorganism is used interchangeably herein.
  • a medium as used herein for the above process using a microorganism may be any suitable medium for the production of Vitamin C.
  • the medium is an aqueous medium comprising for instance salts, substrate(s), and a certain pH.
  • the medium in which the substrate is converted into Vitamin C is also referred to as the production medium.
  • “Fermentation” or “production” or “fermentation process” as used herein may be the use of growing cells using media, conditions and procedures known to the skilled person, or the use of non-growing so-called resting cells, after they have been cultivated by using media, conditions and procedures known to the skilled person, under appropriate conditions for the conversion of suitable substrates into desired products such as Vitamin C.
  • resting cells are used for the production of Vitamin C. - 11 - 24595
  • direct fermentation is intended to mean that a microorganism is capable of the conversion of a certain substrate into the specified product by means of one or more biological conversion steps, without the need of any additional chemical conversion step.
  • direct conversion of D-sorbitol into Vitamin C is intended to describe a process wherein a microorganism is producing Vitamin C and wherein D-sorbitol is offered as a carbon source without the need of an intermediate chemical conversion step.
  • a single microorganism capable of directly fermenting Vitamin C is preferred. Said microorganism is cultured under conditions which allow such conversion from the substrate as defined above.
  • microorganisms also include synonyms or basonyms of such species having the same physiological properties, as defined by the International Code of Nomenclature of Prokaryotes.
  • the nomenclature of the microorganisms as used herein is the one officially accepted (at the filing date of the priority application) by the
  • IJSEM International Committee on Systematics of Prokaryotes and the Bacteriology and Applied Microbiology Division of the International Union of Microbiological Societies, and published by its official publication vehicle International Journal of Systematic and Evolutionary Microbiology (IJSEM).
  • IJSEM International Committee on Systematics of Prokaryotes and the Bacteriology and Applied Microbiology Division of the International Union of Microbiological Societies, and published by its official publication vehicle International Journal of Systematic and Evolutionary Microbiology (IJSEM).
  • resting cells refer to cells of a microorganism which are for instance viable but not actively growing, or which are growing at low specific growth rates, for instance, growth rates that are lower than 0.02 h "1 , preferably lower than 0.01 h "1 . Cells which show the above growth rates are said to be in a "resting cell mode”.
  • step (a) or growth phase a first step
  • step (b) the growth rate of the microorganism
  • step (b) the production of Vitamin C from the substrate using the (b)
  • Growth and production phase as performed in the above process using a microorganism may be performed in the same vessel, i.e., only one vessel, or in two or more different vessels, with an optional cell separation step between the two phases.
  • Vitamin C can be recovered from the cells by any suitable means. Recovering means for - 12 - 24595 instance that the produced Vitamin C may be separated from the production medium. Optionally, the thus produced Vitamin C may be further processed.
  • growth phase For the purpose of the present invention relating to the above process using a microorganism, the terms “growth phase”, “growing step”, “growth step” and “growth period” are used interchangeably herein. The same applies for the terms “production phase”, “production step”, “production period”.
  • One way of performing the above process using a microorganism as of the present invention may be a process wherein the microorganism is grown in a first vessel, the so- called growth vessel, as a source for the resting cells, and at least part of the cells are transferred to a second vessel, the so-called production vessel.
  • the conditions in the production vessel may be such that the cells transferred from the growth vessel become resting cells as defined above. Vitamin C is produced in the second vessel and recovered therefrom.
  • the growing step can be performed in an aqueous medium, i.e. the growth medium, supplemented with appropriate nutrients for growth under aerobic conditions.
  • the cultivation may be conducted, for instance, in batch, fed-batch, semi-continuous or continuous mode.
  • the cultivation period may vary depending on for instance the host, pH, temperature and nutrient medium to be used, and maybe for instance about 10 h to about 10 days, preferably about 1 to about 10 days, more preferably about 1 to about 5 days when run in batch or fed-batch mode, depending on the microorganism.
  • the residence time maybe for instance from about 2 to about 100 h, preferably from about 2 to about 50 h, depending on the microorganism.
  • the cultivation may be conducted for instance at a pH of about 3.0 to about 9.0, preferably about 4.0 to about 9.0, more preferably about 4.0 to about 8.0, even more preferably about 5.0 to about 8.0.
  • algae or yeast are used, the cultivation may be conducted, for instance, at a pH below about 7.0, preferably below about 6.0, more preferably below about 5.5, and most preferably below about 5.0.
  • a suitable temperature range for carrying out the cultivation using bacteria may be for instance from about 13°C to about 40°C, preferably from about 18°C to about 37°C, more preferably from about 13°C to about 36 0 C, and most preferably from about 18 0 C to about 33°C.
  • a suitable temperature range for carrying out the cultivation maybe for instance from about 15 0 C to about 40 0 C, preferably from about 20°C to about 45°C, more preferably from about 25°C to about 40 0 C, even more preferably from about 25°C to about 38 0 C, and most preferably from about 30 0 C to about 38°C.
  • the culture medium for growth usually may contain such nutrients as assimilable carbon sources, e.g., glycerol, D-mannitol, D-sorbitol, L-sorbose, erythritol, ribitol, xylitol, - 13 - 24595 arabitol, inositol, dulcitol, D-ribose, D-fructose, D-glucose, sucrose, and ethanol, preferably L-sorbose, D-glucose, D-sorbitol, D-mannitol, glycerol and ethanol; and digestible nitrogen sources such as organic substances, e.g., peptone, yeast extract and amino acids.
  • assimilable carbon sources e.g., glycerol, D-mannitol, D-sorbitol, L-sorbose, erythritol, ribitol, xylitol
  • the media may be with or without urea and/or corn steep liquor and/or baker's yeast.
  • Various inorganic substances may also be used as nitrogen sources, e.g., nitrates and ammonium salts.
  • the growth medium usually may contain inorganic salts, e.g., magnesium sulfate, manganese sulfate, potassium phosphate, and calcium carbonate.
  • inorganic salts e.g., magnesium sulfate, manganese sulfate, potassium phosphate, and calcium carbonate.
  • Cells obtained using the procedures described above can then be further incubated at essentially the same modes, temperature and pH conditions as described above, in the presence of substrates such as D-sorbitol, L-sorbose, or D-glucose, in such a way that they convert these substrates directly into Vitamin C.
  • Incubation can be done in a nitrogen-rich medium, containing, for example, organic nitrogen sources, e.g., peptone, yeast extract, baker's yeast, urea, amino acids, and corn steep liquor, or inorganic nitrogen sources, e.g., nitrates and ammonium salts, in which case cells will be able to further grow while producing Vitamin C.
  • organic nitrogen sources e.g., peptone, yeast extract, baker's yeast, urea, amino acids, and corn steep liquor
  • inorganic nitrogen sources e.g., nitrates and ammonium salts
  • incubation can be done in a nitrogen-poor medium, in which case cells will not grow substantially, and will be in a resting cell mode, or biotransformation mode.
  • the incubation medium may also contain inorganic salts, e.g., magnesium sulfate, manganese sulfate, potassium phosphate, and calcium chloride.
  • the specific growth rates are for instance at least 0.02 h "1 .
  • the growth rate depends on for instance the composition of the growth medium, pH, temperature, and the like.
  • the growth rates maybe for instance in a range from about 0.05 to about 0.2 h "1 , preferably from about 0.06 to about 0.15 h "1 , and most preferably from about 0.07 to about 0.13 h "1 .
  • resting cells may be provided by cultivation of the respective microorganism on agar plates thus serving as growth vessel, using essentially the same conditions, e.g., cultivation period, pH, temperature, nutrient medium as described above, with the addition of agar agar.
  • the cells from the growth phase may be harvested or concentrated and transferred to a second vessel, the so-called production vessel.
  • This vessel may contain an aqueous medium supplemented with any applicable production substrate that can be converted to Vitamin C by the cells.
  • Cells from the growth vessel can be harvested or concentrated by any suitable operation, such as for instance centrifugation, membrane crossflow ultrafiltration or microfiltration, filtration, decantation, flocculation.
  • the cells thus obtained may also be transferred to the - 14 - 24595 production vessel in the form of the original broth from the growth vessel, without being harvested, concentrated or washed, i.e. in the form of a cell suspension.
  • the cells are transferred from the growth vessel to the production vessel in the form of a cell suspension without any washing or isolating step in-between.
  • cells may be grown under appropriate conditions to the desired cell density followed by a replacement of the growth medium with the production medium containing the production substrate.
  • Such replacement may be, for instance, the feeding of production medium to the vessel at the same time and rate as the withdrawal or harvesting of supernatant from the vessel.
  • operations for cell recycling or retention may be used, such as for instance cell recycling steps.
  • recycling steps include but are not limited to methods using centrifuges, filters, membrane crossflow microf ⁇ ltration of ultrafiltration steps, membrane reactors, flocculation, or cell immobilization in appropriate porous, non-porous or polymeric matrixes.
  • the aqueous medium in the production vessel as used for the production step in connection with the above process using a microorganism, hereinafter called production medium may contain only the production substrate(s) to be converted into Vitamin C, or may contain for instance additional inorganic salts, e.g., sodium chloride, calcium chloride, magnesium sulfate, manganese sulfate, potassium phosphate, calcium phosphate, and calcium carbonate.
  • the production medium may also contain digestible nitrogen sources such as for instance organic substances, e.g., peptone, yeast extract, urea, amino acids, and corn steep liquor, and inorganic substances, e.g.
  • the medium may be with or without urea and/or corn steep liquor and/or baker's yeast.
  • the production step may be conducted for instance in batch, fed-batch, semi-continuous or continuous mode. In case of fed-batch, semi-continuous or continuous mode, both cells from the growth vessel and production medium can be fed continuously or intermittently to the production vessel at appropriate feed rates. Alternatively, only production medium may be fed continuously or intermittently to the production vessel, while the cells coming from the growth vessel are transferred at once to the production vessel.
  • the cells coming from the growth vessel may be used as a cell suspension within - 15 - 24595 the production vessel or may be used as for instance flocculated or immobilized cells in any solid phase such as porous or polymeric matrixes.
  • the production period defined as the period elapsed between the entrance of the substrate into the production vessel and the harvest of the supernatant containing Vitamin C, the so-called harvest stream, can vary depending for instance on the kind and concentration of cells, pH, temperature and nutrient medium to be used, and is preferably about 2 to about 100 h.
  • the pH and temperature can be different from the pH and temperature of the growth step, but is essentially the same as for the growth step.
  • the production step is conducted in continuous mode, meaning that a first feed stream containing the cells from the growth vessel and a second feed stream containing the substrate is fed continuously or intermittently to the production vessel.
  • the first stream may either contain only the cells isolated/separated from the growth medium or a cell suspension, coming directly from the growth step, i.e. cells suspended in growth medium, without any intermediate step of cell separation, washing and/or isolating.
  • the second feed stream as herein defined may include all other feed streams necessary for the operation of the production step, e.g. the production medium comprising the substrate in the form of one or several different streams, water for dilution, and base for pH control.
  • the ratio of the feed rate of the first stream to feed rate of the second stream may vary between about 0.01 and about 10, preferably between about 0.01 and about 5, most preferably between about 0.02 and about 2. This ratio is dependent on the concentration of cells and substrate in the first and second stream, respectively.
  • Another way of performing the process as above using a microorganism of the present invention may be a process using a certain cell density of resting cells in the production vessel.
  • the cell density is measured as absorbance units (optical density) at 600 nm by methods known to the skilled person.
  • the cell density in the production step is at least about 10, more preferably between about 10 and about 200, even more preferably between about 15 and about 200, even more preferably between about 15 to about 120, and most preferably between about 20 and about 120.
  • any means known in the art may be used, such as for instance cell recycling by centrifugation, filtration, membrane crossflow ultrafiltration of microfiltration, decantation, flocculation, cell retention in the vessel by membrane devices or cell immobilization.
  • the production step is - 16 - 24595 performed in continuous or semi-continuous mode and cells are continuously or intermittently fed from the growth vessel
  • the cell density in the production vessel may be kept at a constant level by, for instance, harvesting an amount of cells from the production vessel corresponding to the amount of cells being fed from the growth vessel.
  • the produced Vitamin C contained in the so-called harvest stream is recovered/harvested from the production vessel.
  • the harvest stream may include, for instance, cell-free or cell-containing aqueous solution coming from the production vessel, which contains Vitamin C as a result of the conversion of production substrate by the resting cells in the production vessel.
  • Cells still present in the harvest stream may be separated from the Vitamin C by any operations known in the art, such as for instance filtration, centrifugation, decantation, membrane crossflow ultrafiltration or microfiltration, tangential flow ultrafiltration or microf ⁇ ltration or dead end filtration. After this cell separation operation, the harvest stream is essentially free of cells.
  • the process of the present invention may be combined with further steps of separation and/or purification of the produced Vitamin C from other components contained in the harvest stream, i.e., so-called downstream processing steps.
  • steps may include any means known to a skilled person, such as, for instance, concentration, crystallization, precipitation, adsorption, ion exchange, electrodialysis, bipolar membrane electrodialysis and/or reverse osmosis.
  • Vitamin C may be further purified as the free acid form or any of its known salt forms by means of operations such as for instance treatment with activated carbon, ion exchange, adsorption and elution, concentration, crystallization, filtration and drying.
  • a first separation of Vitamin C from other components in the harvest stream might be performed by any suitable combination or repetition of, for instance, the following methods: two- or three-compartment electrodialysis, bipolar membrane electrodialysis, reverse osmosis or adsorption on, for instance, ion exchange resins or non-ionic resins. If the resulting form of Vitamin C is a salt of L-ascorbic acid, conversion of the salt form into the free acid form maybe performed by for instance bipolar membrane electrodialysis, ion exchange, simulated moving bed chromatographic techniques, and the like.
  • Combination of the mentioned steps, e.g., electrodialysis and bipolar membrane electrodialysis into one step might be also used as well as combination of the mentioned steps e.g. several steps of ion exchange by using simulated moving bed chromatographic methods. Any of these procedures alone or in combination constitute a convenient means for isolating and purifying the product, i.e. Vitamin C.
  • the product thus obtained may further be isolated in a manner such as, e.g. by concentration, crystallization, precipitation, washing and drying of the crystals and/or further purified by, for instance, treatment with activated carbon, ion exchange and/or re-crystallization. - 17 - 24595
  • Vitamin C is purified from the harvest stream by a series of downstream processing steps as described above without having to be transferred to a nonaqueous solution at any time of this processing, i.e. all steps are performed in an aqueous environment.
  • Such preferred downstream processing procedure may include for instance the concentration of the harvest stream coming from the production vessel by means of two- or three-compartment electrodialysis, conversion of Vitamin C in its salt form present in the concentrated solution into its acid form by means of bipolar membrane electrodialysis and/or ion exchange, purification by methods such as for instance treatment with activated carbon, ion exchange or non-ionic resins, followed by a further concentration step and crystallization. These crystals can be separated, washed and dried. If necessary, the crystals may be again re-solubilized in water, treated with activated carbon and/or ion exchange resins and recrystallized. These crystals can then be separated, washed and dried.
  • sequence of the gene comprising a nucleotide sequence according to SEQ ID NO:1 encoding a STS 16 protein was determined by sequencing a genomic clone obtained from Gluconobacter oxydans DSM 17078.
  • the invention also relates to a polynucleotide encoding at least a biologically active fragment or derivative of a STS 16 polypeptide as shown in SEQ ID NO:2.
  • biologically active fragment or derivative means a polypeptide which retains essentially the same biological function or activity as the polypeptide shown in SEQ ID NO:2.
  • biological activity may for instance be enzymatic activity, signaling activity or antibody reactivity.
  • synthetic biological function or
  • “functional equivalent” as used herein means that the protein has essentially the same biological activity, e.g. enzymatic, signaling or antibody reactivity, as a polypeptide shown in SEQ ID NO:2.
  • polypeptides and polynucleotides of the present invention are preferably provided in an isolated form, and preferably are purified to homogeneity.
  • isolated means that the material is removed from its original environment ⁇ e.g., the natural environment if it is naturally occurring).
  • a naturally-occurring polynucleotide or polypeptide present in a living microorganism is not isolated, but the same polynucleotide or polypeptide, separated from some or all of the coexisting materials in the natural system, is isolated.
  • Such polynucleotides could be part of a vector and/or - 18 - 24595 such polynucleotides or polypeptides could be part of a composition and still be isolated in that such vector or composition is not part of its natural environment.
  • An isolated polynucleotide or nucleic acid as used herein may be a DNA or RNA that is not immediately contiguous with both of the coding sequences with which it is immediately contiguous (one on the 5'-end and one on the 3 '-end) in the naturally occurring genome of the organism from which it is derived.
  • a nucleic acid includes some or all of the 5'-non-coding (e.g., promoter) sequences that are immediately contiguous to the coding sequence.
  • isolated polynucleotide therefore includes, for example, a recombinant DNA that is incorporated into a vector, into an autonomously replicating plasmid or virus, or into the genomic DNA of a prokaryote or eukaryote, or which exists as a separate molecule (e.g., a cDNA or a genomic DNA fragment produced by PCR or restriction endonuclease treatment) independent of other sequences. It also includes a recombinant DNA that is part of a hybrid gene encoding an additional polypeptide that is substantially free of cellular material, viral material, or culture medium (when produced by recombinant DNA techniques), or chemical precursors or other chemicals (when chemically synthesized). Moreover, an "isolated nucleic acid fragment” is a nucleic acid fragment that is not naturally occurring as a fragment and would not be found in the natural state.
  • polynucleotide As used herein, the terms “polynucleotide”, “gene” and “recombinant gene” refer to nucleic acid molecules which may be isolated from chromosomal DNA, which include an open reading frame encoding a protein, e.g. G. oxydans DSM 17078 STS proteins.
  • a polynucleotide may include a polynucleotide sequence as shown in SEQ ID NO:1 or fragments thereof and regions upstream and downstream of the gene sequences which may include, for example, promoter regions, regulator regions and terminator regions important for the appropriate expression and stabilization of the polypeptide derived thereof.
  • a gene may include coding sequences, non-coding sequences such as for instance untranslated sequences located at the 3'- and 5'-ends of the coding region of a gene, and regulatory sequences. Moreover, a gene refers to an isolated nucleic acid molecule as defined herein. It is furthermore appreciated by the skilled person that DNA sequence polymorphisms that lead to changes in the amino acid sequences of STS proteins may exist within a population, e.g., the Gluconobacter oxydans population. Such genetic polymorphism in the STS 16 gene may exist among individuals within a population due to natural variation or in cells from different populations. Such natural variations can typically result in 1-5% variance in the nucleotide sequence of the STS 16 gene. Any and all such nucleotide variations and the resulting amino acid polymorphism in STS 16 are the result of natural variation and that do not alter the functional activity of STS proteins are intended to be within the scope of the invention. - 19 - 24595
  • nucleic acid molecule As used herein, the terms "polynucleotide” or “nucleic acid molecule” are intended to include DNA molecules ⁇ e.g., cDNA or genomic DNA) and RNA molecules ⁇ e.g., mRNA) and analogs of the DNA or RNA generated using nucleotide analogs.
  • the nucleic acid molecule may be single-stranded or double-stranded, but preferably is double-stranded DNA.
  • the nucleic acid may be synthesized using oligonucleotide analogs or derivatives ⁇ e.g., inosine or phosphorothioate nucleotides). Such oligonucleotides maybe used, for example, to prepare nucleic acids that have altered base-pairing abilities or increased resistance to nucleases.
  • sequence information as provided herein should not be so narrowly construed as to require inclusion of erroneously identified bases.
  • the specific sequences disclosed herein may be readily used to isolate the complete gene from a recombinant or non-recombinant microorganism capable of converting a given carbon source directly into Vitamin C, in particular Gluconobacter oxydans, preferably Gluconobacter oxydans DSM 17078 which in turn may easily be subjected to further sequence analyses thereby identifying sequencing errors.
  • nucleotide sequences determined by sequencing a DNA molecule herein were determined using an automated DNA sequencer and all amino acid sequences of polypeptides encoded by DNA molecules determined herein were predicted by translation of a DNA sequence determined as above. Therefore, as is known in the art for any DNA sequence determined by this automated approach, any nucleotide sequence determined herein may contain some errors. Nucleotide sequences determined by automation are typically at least about 90% identical, more typically at least about 95% to at least about 99.9% identical to the actual nucleotide sequence of the sequenced DNA molecule. The actual sequence may be more precisely determined by other approaches including manual DNA sequencing methods well known in the art.
  • a single insertion or deletion in a determined nucleotide sequence compared to the actual sequence will cause a frame shift in translation of the nucleotide sequence such that the predicted amino acid sequence encoded by a determined nucleotide sequence will be completely different from the amino acid sequence actually encoded by the sequenced DNA molecule, beginning at the point of such an insertion or deletion.
  • a nucleic acid molecule according to the invention may comprise only a portion or a fragment of the nucleic acid sequence provided by the present invention, such as for instance the sequence shown in SEQ ID NO:1, for example a fragment which may be used as a probe or primer such as for instance SEQ ID NO:3 or SEQ ID NO:4 or a fragment - 20 - 24595 encoding a portion of a protein according to the invention.
  • the nucleotide sequence determined from the cloning of the STS 16 gene allows for the generation of probes and primers designed for use in identifying and/or cloning other STS 16 family members, as well as STS 16 homologues from other species.
  • the probe/primer typically comprises substantially purified oligonucleotides which typically comprises a region of nucleotide sequence that hybridizes preferably under highly stringent conditions to at least about 12 or 15, preferably about 18 or 20, more preferably about 22 or 25, even more preferably about 30, 35, 40, 45, 50, 55, 60, 65, or 75 or more consecutive nucleotides of a nucleotide sequence shown in SEQ TD NO:1 or a fragment or derivative thereof.
  • a nucleic acid molecule encompassing all or a portion of the nucleic acid sequence of SEQ ID NO: 1 may be also isolated by the polymerase chain reaction (PCR) using synthetic oligonucleotide primers designed based upon the sequence information contained herein.
  • PCR polymerase chain reaction
  • a nucleic acid of the invention may be amplified using cDNA, mRNA or alternatively, genomic DNA, as a template and appropriate oligonucleotide primers according to standard PCR amplification techniques.
  • the nucleic acid thus amplified may be cloned into an appropriate vector and characterized by DNA sequence analysis.
  • Fragments of a polynucleotide according to the invention may also comprise polynucleotides not encoding functional polypeptides. Such polynucleotides may function as probes or primers for a PCR reaction.
  • Nucleic acids according to the invention may be used as hybridization probes or polymerase chain reaction (PCR) primers.
  • Uses of the nucleic acid molecules of the present invention that do not encode a polypeptide having a STS 16 activity include, inter alia, (1) isolating the gene encoding the protein of the present invention, or allelic variants thereof from a cDNA library, e.g., from other organisms than Gluconobacter oxydans and (2) Northern blot analysis for detecting expression of mRNA of said protein in specific cells or (3) use in enhancing and/or improving the function or activity of homologous STS 16 genes in said other organisms.
  • Probes based on the nucleotide sequences provided herein may be used to detect transcripts or genomic sequences encoding the same or homologous proteins for instance in other organisms.
  • Nucleic acid molecules corresponding to natural variants and non-G. oxydans homologues of the G. oxydans STS 16 DNA of the invention which are also embraced by the present invention may be isolated based on their homology to the G. oxydans STS 16 nucleic acid disclosed herein using the G. oxydans DNA, or a portion - 21 - 24595 thereof, as a hybridization probe according to standard hybridization techniques, preferably under highly stringent hybridization conditions.
  • the probe further comprises a label group attached thereto, e.g., the label group can be a radioisotope, a fluorescent compound, an enzyme, or an enzyme cofactor.
  • the label group can be a radioisotope, a fluorescent compound, an enzyme, or an enzyme cofactor.
  • Homologous gene sequences may be isolated, for example, by performing PCR using two degenerate oligonucleotide primer pools designed on the basis of nucleotide sequences as taught herein.
  • the template for the reaction may be cDNA obtained by reverse transcription of mRNA prepared from strains known or suspected to express a polynucleotide according to the invention.
  • the PCR product may be subcloned and sequenced to ensure that the amplified sequences represent the sequences of a new nucleic acid sequence as described herein, or a functional equivalent thereof.
  • the PCR fragment may then be used to isolate a full length cDNA clone by a variety of known methods.
  • the amplified fragment may be labeled and used to screen a bacteriophage or cosmid cDNA library.
  • the labeled fragment may be used to screen a genomic library.
  • RNA may be isolated, following standard procedures, from an appropriate cellular or tissue source.
  • a reverse transcription reaction may be performed on the RNA using an oligonucleotide primer specific for the most 5'-end of the amplified fragment for the priming of first strand synthesis.
  • RNA/DNA hybrid may then be "tailed" ⁇ e.g., with guanines) using a standard terminal transferase reaction, the hybrid may be digested with RNaseH, and second strand synthesis may then be primed ⁇ e.g., with a poly-C primer).
  • RNaseH RNaseH
  • second strand synthesis may then be primed ⁇ e.g., with a poly-C primer.
  • nucleic acids encoding other STS 16 family members which thus have a nucleotide sequence that differs from a nucleotide sequence according to SEQ ID NO:1 are within the scope of the invention.
  • nucleic acids encoding STS 16 proteins from different species which thus may have a nucleotide sequence which differs from a nucleotide sequence shown in SEQ ID NO:1 are within the scope of the invention. - 22 - 24595
  • the invention also relates to an isolated polynucleotide hybridisable under stringent conditions, preferably under highly stringent conditions, to a polynucleotide as of the present invention, such as for instance a polynucleotide shown in SEQ ID NO:1.
  • a polynucleotide as of the present invention, such as for instance a polynucleotide shown in SEQ ID NO:1.
  • such polynucleotide may be obtained from a microorganism capable of converting a given carbon source directly into Vitamin C, in particular Gluconobacter oxydans, preferably Gluconobacter oxydans DSM 17078.
  • hybridizing is intended to describe conditions for hybridization and washing under which nucleotide sequences at least about 50%, at least about 60%, at least about 70%, more preferably at least about 80%, even more preferably at least about 85% to 90%, most preferably at least 95% homologous to each other typically remain hybridized to each other.
  • a nucleic acid of the invention is at least 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or more homologous to a nucleic acid sequence shown in SEQ ID NO:1 or the complement thereof.
  • a preferred, non-limiting example of stringent hybridization conditions are hybridization in 6x sodium chloride/sodium citrate (SSC) at about 45°C, followed by one or more washes in Ix SSC, 0.1% SDS at 50 0 C, preferably at 55°C, more preferably at 60 0 C and even more preferably at 65 0 C.
  • SSC 6x sodium chloride/sodium citrate
  • Highly stringent conditions include incubations at 42 0 C for a period of several days, such as 2-4 days, using a labeled DNA probe, such as a digoxigenin (DIG)-labeled DNA probe, followed by one or more washes in 2x SSC, 0.1% SDS at room temperature and one or more washes in 0.5x SSC, 0.1% SDS or O.lx SSC, 0.1% SDS at 65-68°C.
  • highly stringent conditions include, for example, 2 h to 4 days incubation at 42°C using a DIG-labeled DNA probe (prepared by e.g.
  • an isolated nucleic acid molecule of the invention that hybridizes under preferably highly stringent conditions to a nucleotide sequence of the invention corresponds to a naturally-occurring nucleic acid molecule.
  • a "naturally- - 23 - 24595 occurring" nucleic acid molecule refers to an RNA or DNA molecule having a nucleotide sequence that occurs in nature (e.g., encodes a natural protein).
  • the nucleic acid encodes a natural G. oxydans STS 16 protein.
  • a polynucleotide which hybridizes only to a poly (A) sequence would not be included in a polynucleotide of the invention used to specifically hybridize to a portion of a nucleic acid of the invention, since such a polynucleotide would hybridize to any nucleic acid molecule containing a poly (A) stretch or the complement thereof (e.g., practically any double-stranded cDNA clone).
  • genomic DNA or cDNA libraries constructed from other organisms e.g. microorganisms capable of converting a given carbon source directly into Vitamin C, in particular other Gluconobacter species may be screened.
  • Gluconobacter strains may be screened for homologous polynucleotides by Southern and/or Northern blot analysis.
  • DNA libraries may be constructed from RNA isolated from the appropriate strain, utilizing standard techniques well known to those of skill in the art.
  • a total genomic DNA library may be screened using a probe hybridisable to a polynucleotide according to the invention.
  • a nucleic acid molecule of the present invention such as for instance a nucleic acid molecule shown in SEQ ID NO: 1 or a fragment or derivative thereof, may be isolated using standard molecular biology techniques and the sequence information provided herein.
  • nucleic acid molecules according to the invention may be isolated using standard hybridization and cloning techniques (e.g., as described in Sambrook, J., Fritsh, E. F. , and Maniatis, T. Molecular Cloning : A Laboratory Manual. 2nd, ed. , Cold Spring Harbor Laboratory, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY, 1989).
  • oligonucleotides corresponding to or hybridisable to nucleotide sequences according to the invention may be prepared by standard synthetic techniques, e.g., using an automated DNA synthesizer. - 24 - 24595
  • the terms “homology” or “percent identity” are used interchangeably herein. For the purpose of this invention, it is defined here that in order to determine the percent identity of two amino acid sequences or of two nucleic acid sequences, the sequences are aligned for optimal comparison purposes (e.g., gaps may be introduced in the sequence of a first amino acid or nucleic acid sequence for optimal alignment with a second amino or nucleic acid sequence). The amino acid residues or nucleotides at corresponding amino acid positions or nucleotide positions are then compared. When a position in the first sequence is occupied by the same amino acid residue or nucleotide as the corresponding position in the second sequence, then the molecules are identical at that position.
  • the two sequences are the same length.
  • the skilled person will be aware of the fact that several different computer programs are available to determine the homology between two sequences. For instance, a comparison of sequences and determination of percent identity between two sequences may be accomplished using a mathematical algorithm. In a preferred embodiment, the percent identity between two amino acid sequences is determined using the Needleman and Wunsch (J. MoI. Biol. (48): 444-453 (1970) ) algorithm which has been incorporated into the GAP program in the GCG software package (available at http://www.accehys.com), using either a Blossom 62 matrix or a PAM250 matrix, and a gap weight of 16, 14, 12, 10, 8, 6 or 4 and a length weight of 1, 2, 3, 4, 5 or 6. The skilled person will appreciate that all these different parameters will yield slightly different results but that the overall percentage identity of two sequences is not significantly altered when using different algorithms.
  • the percent identity between two nucleotide sequences is determined using the GAP program in the GCG software package (available at http://www.accelrys.com), using a NWSgapdna.CMP matrix and a gap weight of 40, 50, 60, 70 or 80 and a length weight of 1, 2, 3, 4, 5 or 6.
  • the percent identity between two amino acid or nucleotide sequences is determined using the algorithm of E. Meyers and W.
  • nucleic acid and protein sequences of the present invention may further be used as a "query sequence" to perform a search against public databases to, for example, identify other family members or related sequences.
  • search may be performed using the BLASTN and BLASTX programs (version 2.0) of Altschul, et al. (1990) J. MoI. Biol. - 25 - 24595
  • Gapped BLAST may be utilized as described in Altschul et al, (1997) Nucleic Acids Res. 25 (17): 3389-3402.
  • the default parameters of the respective programs (e.g., BLASTX and BLASTN) may be used. See http ://www.ncbi .nlm.nih. gov.
  • an isolated nucleic acid molecule of the invention comprises a nucleic acid molecule which is the complement of a nucleotide sequence as of the present invention, such as for instance the sequence shown in SEQ ID NO: 1.
  • a nucleic acid molecule, which is complementary to a nucleotide sequence disclosed herein, is one that is sufficiently complementary to a nucleotide sequence shown in SEQ ID NO:1 such that it may hybridize to said nucleotide sequence thereby forming a stable duplex.
  • a nucleic acid of the invention as shown in SEQ ED NO:1 or the complement thereof contains at least one mutation leading to a gene product with modified function/activity.
  • the at least one mutation may be introduced by methods described herein.
  • the at least one mutation leads to a STS 16 protein whose function and/or activity compared to the wild type counterpart is enhanced or improved. Methods for introducing such mutations are well known in the art.
  • the term "increase" of activity as used herein encompasses increasing activity of one or more polypeptides in the producing organism, which in turn are encoded by the corresponding polynucleotides described herein.
  • the STS 16 protein There are a number of methods available in the art to accomplish increase of activity of a given protein, in this case the STS 16 protein, hi general, the specific activity of a protein may be increased or the copy number of the protein may be increased.
  • the term increase of activity or equivalent expressions also encompasses the situation wherein STS 16 protein activity is introduced in a cell that did not contain this activity before, e.g. by introducing a gene encoding STS 16 in a cell that did not contain an equivalent of this gene before, or that could not express an active form of the corresponding protein before.
  • the copy number of the genes corresponding to the polynucleotides described herein may be increased.
  • a strong promoter may be used to direct the expression of the polynucleotide.
  • the promoter, regulatory region and/or the ribosome binding site upstream of the gene can be altered to increase the expression.
  • the expression may also be enhanced or increased by - 26 - 24595 increasing the relative half-life of the messenger RNA.
  • the activity of the polypeptide itself may be increased by employing one or more mutations in the polypeptide amino acid sequence, which increase the activity. For example, altering the affinity of the polypeptide for its corresponding substrate may result in improved activity.
  • the relative half-life of the polypeptide may be increased.
  • the improvement may be achieved by altering the composition of the cell culture media and/or methods used for culturing.
  • "Enhanced expression” or “improved activity” as used herein means an increase of at least 5%, 10%, 25%, 50%, 75%, 100%, 200% or even more than 500%, compared to a wild-type protein, polynucleotide, gene; or the activity and/or the concentration of the protein present before the polynucleotides or polypeptides are enhanced and/or improved.
  • the activity of the STS 16 protein may also be enhanced by contacting the protein with a specific or general enhancer of its activity.
  • vectors containing a nucleic acid encoding a protein according to the invention or a functional equivalent or portion thereof.
  • vector refers to a nucleic acid molecule capable of transporting another nucleic acid to which it has been linked.
  • plasmid refers to a circular double stranded DNA loop into which additional DNA segments may be ligated.
  • viral vector Another type of vector is a viral vector, wherein additional DNA segments may be ligated into the viral genome.
  • Certain vectors are capable of autonomous replication in a host cell into which they are introduced (e.g., bacterial vectors having a bacterial origin of replication). Other vectors are integrated into the genome of a host cell upon introduction into the host cell, and thereby are replicated along with the host genome.
  • vectors are capable of directing the expression of genes to which they are operatively linked. Such vectors are referred to herein as "expression vectors".
  • expression vectors of utility in recombinant DNA techniques are often in the form of plasmids.
  • plasmid and vector can be used interchangeably herein as the plasmid is the most commonly used form of vector.
  • the invention is intended to include such other forms of expression vectors, such as viral vectors (e.g., replication defective retroviruses, adenoviruses and adeno-associated viruses), which serve equivalent functions.
  • the recombinant vectors of the invention comprise a nucleic acid of the invention in a form suitable for expression of the nucleic acid in a host cell, which means that the recombinant expression vector includes one or more regulatory sequences, selected on the basis of the host cells to be used for expression, which is operatively linked to the nucleic acid sequence to be expressed.
  • "operatively linked" is intended to mean that the nucleotide sequence of interest is linked to the - 27 - 24595 regulatory sequence(s) in a manner which allows for expression of the nucleotide sequence (e.g., in an in vitro transcription/translation system or in a host cell when the vector is introduced into the host cell).
  • regulatory sequence is intended to include promoters, enhancers and other expression control elements (e.g., attenuator). Such regulatory sequences are described, for example, in Goeddel; Gene Expression Technology: Methods in Enzymology 185, Academic Press, San Diego, CA (1990). Regulatory sequences include those which direct constitutive or inducible expression of a nucleotide sequence in many types of host cells and those which direct expression of the nucleotide sequence only in a certain host cell (e.g. tissue-specific regulatory sequences). It will be appreciated by those skilled in the art that the design of the expression vector can depend on such factors as the choice of the host cell to be transformed, the level of expression of protein desired, etc.
  • the expression vectors of the invention may be introduced into host cells to thereby produce proteins or peptides, encoded by nucleic acids as described herein, including, but not limited to, mutant proteins, fragments thereof, variants or functional equivalents thereof, and fusion proteins, encoded by a nucleic acid as described herein, e.g., STS 16 proteins, mutant forms of STS 16 proteins, fusion proteins and the like.
  • the recombinant expression vectors of the invention maybe designed for expression of STS 16 proteins in a suitable microorganism.
  • a protein according to the invention may be expressed in bacterial cells such as strains belonging to the genera Gluconobacter, Gluconacetobacter or Acetobacter.
  • Expression vectors useful in the present invention include chromosomal-, episomal- and virus-derived vectors e.g., vectors derived from bacterial plasmids, bacteriophage, and vectors derived from combinations thereof, such as those derived from plasmid and bacteriophage genetic elements, such as cosmids and phagemids.
  • the DNA insert may be operatively linked to an appropriate promoter, which may be either a constitutive or inducible promoter.
  • an appropriate promoter which may be either a constitutive or inducible promoter.
  • the skilled person will know how to select suitable promoters.
  • the expression constructs may contain sites for transcription initiation, termination, and, in the transcribed region, a ribosome binding site for translation.
  • the coding portion of the mature transcripts expressed by the constructs may preferably include an initiation codon at the beginning and a termination codon appropriately positioned at the end of the polypeptide to be translated.
  • Vector DNA may be introduced into suitable host cells via conventional transformation or transfection techniques.
  • transformation transformation
  • transconjugation and “transfection” are intended to refer to a variety of art-recognized techniques for introducing foreign nucleic acid (e.g., DNA) into a host cell, including calcium phosphate or calcium chloride co-precipitation, DEAE-dextran-mediated transfection, transduction, - 28 - 24595 infection, lipofection, cationic lipidmediated transfection or electroporation.
  • Suitable methods for transforming or transfecting host cells may be found in Sambrook, et al. (supra), Davis et al., Basic Methods in Molecular Biology (1986) and other laboratory manuals.
  • a gene that encodes a selectable marker is generally introduced into the host cells along with the gene of interest.
  • selectable markers include those that confer resistance to drugs, such as kanamycin, tetracycline, ampicillin and streptomycin.
  • a nucleic acid encoding a selectable marker is preferably introduced into a host cell on the same vector as that encoding a protein according to the invention or can be introduced on a separate vector such as, for example, a suicide vector, which cannot replicate in the host cells. Cells stably transfected with the introduced nucleic acid can be identified by drug selection (e.g., cells that have incorporated the selectable marker gene will survive, while the other cells die).
  • the invention provides also an isolated polypeptide having the amino acid sequence shown in SEQ ID NO:2 or an amino acid sequence obtainable by expressing a polynucleotide of the present invention, such as for instance a polynucleotide sequence shown in SEQ ID NO:1 in an appropriate host.
  • Polypeptides according to the invention may contain only conservative substitutions of one or more amino acids in the amino acid sequence represented by SEQ ID NO:2 or substitutions, insertions or deletions of non-essential amino acids.
  • a nonessential amino acid is a residue that may be altered in the amino acid sequences shown in SEQ ID NO:2 without substantially altering the biological function.
  • amino acid residues that are conserved among the proteins of the present invention are predicted to be particularly unamenable to alteration.
  • amino acids conserved among the proteins according to the present invention and other STS 16 proteins are not likely to be amenable to alteration.
  • substitution is intended to mean that a substitution in which the amino acid residue is replaced with an amino acid residue having a similar side chain.
  • These families are known in the art and include amino acids with basic side chains (e.g., lysine, arginine and histidine), acidic side chains (e.g., aspartic acid, glutamic acid), uncharged polar side chains (e.g., glycine, asparagine, glutamine, serine, threonine, tyrosine, cysteine), non-polar side chains (e.g., alanine, valine, leucine, isoleucine, proline, phenylalanine, methionine, tryptophan), beta-branched side chains (e.g., threonine, valine, isoleucine) and aromatic side chains (e.g., tyrosine, phenylalanine, tryptophan, histidine).
  • basic side chains e.g., lysine
  • the polynucleotides of the invention maybe utilized in the genetic engineering of a suitable host cell to make it better and more efficient in the fermentation, for example in a direct fermentation process for Vitamin C.
  • a genetically engineered/recombinantly produced host cell (also referred to as recombinant cell or transformed cell) carrying such a modified polynucleotide wherein the function of the linked protein is significantly modified in comparison to a wild-type cell such that the yield, production and/or efficiency of production of one or more fermentation products such as Vitamin C is improved.
  • the host cell may be selected from a microorganism capable of directly producing one or more fermentation products such as for instance Vitamin C from a given carbon source, in particular Gluconobacter oxydans, preferably G. oxydans DSM 17078.
  • a “transformed cell” or “recombinant cell” is a cell into which (or into an ancestor of which) has been introduced, by means of recombinant DNA techniques, a nucleic acid according to the invention, or wherein the activity of the STS 16 protein has been increased and/or enhanced.
  • Suitable host cells include cells of microorganisms capable of producing a given fermentation product, e.g., converting a given carbon source directly into Vitamin C.
  • strains from the genera Pseudomonas, Pantoea, Escherichia, Corynebacterium, Ketogulonicigenium and acetic acid bacteria like e.g., Gluconobacter, Acetobacter or Gluconacetobacter, preferably Acetobacter sp., Acetobacter aceti, Gluconobacter frateurii, Gluconobacter cerinus, Gluconobacter thailandicus, Gluconobacter oxydans, more preferably G. oxydans, most preferably G. oxydans DSM 17078.
  • Improved gene expression may also be achieved by modifying the STS 16 gene, e.g., by introducing one or more mutations into the STS 16 gene wherein said modification leads to a STS 16 protein with a function which is significantly improved in comparison to the wild-type protein.
  • the polynucleotide carrying the at least one mutation is derived from a polynucleotide as represented by SEQ ID NO:1 or equivalents thereof.
  • a mutation as used herein may be any mutation leading to a more functional or more stable polypeptide, e.g. more functional or more stable STS 16 gene products. This may include for instance an alteration in the genome of a microorganism, which improves the synthesis of STS 16 or leads to the expression of a STS 16 protein with an altered amino acid sequence whose function compared with the wild type counterpart having a non- altered amino acid sequence is improved and/or enhanced. The improvement may occur at the transcriptional, translational or post-translational level. - 30 - 24595
  • the alteration in the genome of the microorganism may be obtained e.g. by replacing through a single or double crossover recombination a wild type DNA sequence by a DNA sequence containing the alteration.
  • the alteration may, e.g. be a DNA sequence encoding an antibiotic resistance marker or a gene complementing a possible auxotrophy of the microorganism. Mutations include, but are not limited to, deletion- insertion mutations.
  • An alteration in the genome of the microorganism leading to a more functional polypeptide may also be obtained by randomly mutagenizing the genome of the microorganism using e.g. chemical mutagens, radiation or transposons and selecting or screening for mutants which are better or more efficient producers of one or more fermentation products. Standard methods for screening and selection are known to the skilled person.
  • a repressor of the STS 16 gene of the present invention i.e., wherein its repressor gene expression is artificially suppressed in order to improve the yield, productivity, and/or efficiency of production of the fermentation product when introduced into a suitable host cell.
  • Methods of providing knockouts as well as microorganisms carrying such suppressed genes are well known in the art.
  • the suppression of the repressor gene may be induced by deleting at least a part of the repressor gene or the regulatory region thereof.
  • "suppression of the gene expression” includes complete and partial suppression, as well as suppression under specific conditions and also suppression of the expression of either one of the two alleles.
  • the aforementioned mutagenesis strategies for STS 16 proteins may result in increased yields of a desired compound in particular Vitamin C.
  • This list is not meant to be limiting; variations on these mutagenesis strategies will be readily apparent to one of ordinary skill in the art.
  • the nucleic acid and protein molecules of the invention may be utilized to generate microorganisms such as Gluconobacter oxydans or related strains of bacteria expressing mutated STS 16 nucleic acid and protein molecules such that the yield, productivity, and/or efficiency of production of a desired compound such as Vitamin C is improved.
  • the process of the present invention leads to yields of Vitamin C which are in general at least about more than 5.7 g/1, such as 10 g/1, 20 g/1, 50 g/1, 100 g/1, 200 g/1, 300 g/1, 400 g/1 or more than 600 g/1.
  • the yield of Vitamin C produced by the process of the present invention is in the range of from about more than 5.7 to about 600 g/1.
  • Vitamin C refers to the concentration of Vitamin C in the harvest stream coming directly out of the production vessel, i.e. the cell-free supernatant comprising the Vitamin C.
  • microorganisms in particular from the genera of Gluconobacter, Gluconacetobacter and Acetobacter are provided that are able to directly produce Vitamin C from a suitable carbon source like D-sorbitol and/or L-sorbose.
  • a microorganism capable of directly producing Vitamin C in quantities of 300 mg/1 when starting from D-sorbitol or more or 800 mg/1 or more when starting from L-sorbose, respectively when for instance measured in a resting cell method after an incubation period of 20 hours.
  • Such may be achieved by increasing the activity of a STS polypeptide, preferably a STS 16 polypeptide.
  • the yield of Vitamin C produced from D-sorbitol may even be as high as 400, 600, 1000 mg/1 or even exceed 1.5, 2, 4, 10, 20, 50 g/1.
  • the yield of Vitamin C produced from L-sorbose may even be as high as 1000 mg/1 or even exceed 1.5, 2, 4, 10, 20, 50 g/1.
  • these amounts of Vitamin C can be achieved when measured by resting cell method after an incubation period of 20 hours.
  • measurement in a "resting cell method” comprises (i) growing the cells by means of any method well know to the person skilled in the art, (ii) harvesting the cells from the growth broth, and (iii) incubating the harvested cells in a medium containing the substrate which is to be converted into the desired product, e.g. Vitamin C, under conditions where the cells do not grow any longer, i.e. there is no increase in the amount of biomass during this so-called conversion step.
  • a medium containing the substrate which is to be converted into the desired product e.g. Vitamin C
  • the recombinant microorganism carrying e.g. a modified STS 16 gene and which is able to produce the fermentation product in significantly higher yield, productivity, and/or efficiency may be cultured in an aqueous medium supplemented with appropriate nutrients under aerobic conditions as described above.
  • nucleic acid molecules, polypeptides, vectors, primers, and recombinant microorganisms described herein maybe used in one or more of the following methods: identification of Gluconobacter oxydans and related organisms; mapping of genomes of organisms related to Gluconobacter oxydans; identification and localization of Gluconobacter oxydans sequences of interest; evolutionary studies; determination of STS 16 protein regions required for function; modulation of a STS 16 protein activity or function; modulation of the activity of a STS pathway; and modulation of cellular production of a desired compound, such as Vitamin C. - 32 - 24595
  • the invention provides methods for screening molecules which modulate the activity of a STS 16 protein, either by interacting with the protein itself or a substrate or binding partner of the STS 16 protein, or by modulating the transcription or translation of a STS 16 nucleic acid molecule of the invention.
  • a microorganism expressing one or more STS 16 proteins of the invention is contacted with one or more test compounds, and the effect of each test compound on the activity or level of expression of the STS 16 protein is assessed.
  • the biological, enzymatic or other activity of STS proteins can be measured by methods well known to a skilled person, such as, for example, by incubating a membrane fraction containing the STS protein with the radioactively marked sugar or sugar alcohol which can be actively transported by the STS protein.
  • the incorporation of radioactivity into the cell mass is directly proportional to the activity of the transporter.
  • the activity of a transporter can be measured in an assay where intact cells containing the specific transporter are incubated in the presence of phosphate buffer at pH 6 and the radioactively marked carbon source such as e.g. glucose.
  • the rate of assimilation of radioactive carbon source such as e.g. glucose by the cells can be measured by methods known to the skilled person, and is directly proportional to the STS protein activity present in the membrane fraction.
  • the fermentation product of the methods according to the invention may not be limited to Vitamin C alone.
  • the "desired compound” or “fermentation product” as used herein may be any natural product of Gluconobacter oxydans, which includes the final products and intermediates of biosynthesis pathways, such as for example L-sorbose, L-sorbosone, D-gluconate, 2-keto- D-gluconate, 5-keto-D-gluconate, 2,5-diketo-D-gluconate and 2-keto-L-gulonate (2- KGA), in particular the biosynthetic generation of Vitamin C.
  • the present invention is directed to the use of a polynucleotide, polypeptide, vector, primer and recombinant microorganism as described herein in the production of Vitamin C, i.e., the direct conversion of a carbon source into Vitamin C.
  • a modified polynucleotide, polypeptide, vector and recombinant microorganism as described herein is used for improving the yield, productivity, and/or efficiency of the production of Vitamin C.
  • production or “productivity” are art-recognized and include the concentration of the fermentation product (for example, Vitamin C) formed within a given time and a given fermentation volume (e.g., kg product per hour per liter).
  • efficiency of production includes the time required for a particular level of production to be achieved (for example, how long it takes for the cell to attain a particular rate of output of a - 33 - 24595 fermentation product).
  • yield is art-recognized and includes the efficiency of the conversion of the carbon source into the product ⁇ i.e., Vitamin C). This is generally written as, for example, kg product per kg carbon source.
  • biosynthesis or a “biosynthetic pathway” are art-recognized and include the synthesis of a compound, preferably an organic compound, by a cell from intermediate compounds in what may be a multistep and highly regulated process.
  • metabolic is art-recognized and includes the totality of the biochemical reactions that take place in an organism.
  • the metabolism of a particular compound comprises the overall biosynthetic, modification, and degradation pathways in the cell related to this compound.
  • the language "transport” or “import” is art-recognized and includes the facilitated movement of one or more molecules across a cellular membrane through which the molecule would otherwise either be unable to pass or be passed inefficiently.
  • Vitamin C as used herein may be any chemical form of L-ascorbic acid found in aqueous solutions, such as for instance undissociated, in its free acid form or dissociated as an anion.
  • the solubilized salt form of L-ascorbic acid maybe characterized as the anion in the presence of any kind of cations usually found in fermentation supernatants, such as for instance potassium, sodium, ammonium, or calcium.
  • isolated crystals of the free acid form of L-ascorbic acid are called by their corresponding salt name, i.e. sodium ascorbate, potassium ascorbate, calcium ascorbate and the like.
  • the present invention is related to a process for the production of Vitamin C wherein a nucleotide according to the invention or a modified polynucleotide sequence as described above is introduced into a suitable microorganism, the recombinant microorganism is cultured under conditions that allow the production of Vitamin C in high productivity, yield, and/or efficiency, the produced fermentation product is isolated from the culture medium and optionally further purified.
  • Example 1 Preparation of chromosomal DNA and amplification of DNA fragment by PCR
  • Chromosomal DNA of Gluconobacter oxydans DSM 17078 was prepared from the cells cultivated at 30°C for 1 day in mannitol broth (MB) liquid medium consisting of 25 g/1 mannitol, 5 g/1 of yeast extract (Difco), and 3 g/1 of Bactopeptone (Difco) by the method described by Sambrook et al (1989) "Molecular Cloning: A Laboratory Manual/Second Edition", Cold Spring Harbor Laboratory Press).
  • a DNA fragment was prepared by PCR with the chromosomal DNA prepared above and a set of primers, Pf(SEQ DD NO:3) and Pr (SEQ ID NO:4).
  • the Expand High Fidelity PCR kit (Roche Diagnostics) and 10 ng of the chromosomal DNA was used in total volume of 100 ⁇ according to the supplier's instruction to have the PCR product containing STS 16 DNA sequence (SEQ ID NO:1).
  • the PCR product was recovered from the reaction and its correct sequence confirmed.
  • an overexpression system using an integrative construct may be used.
  • the STS 16 gene is fused to a strong constitutive promoter, and the construct is then introduced into G. oxydans DSM 17078.
  • the overexpression of the STS 16 gene may be determined through standard methods known to those skilled in the art, such as transcript analysis using Northern Blot, RT-PCR or other technology, protein expression determination using Western Blot, two- dimensional gel electrophoresis, protein activity determination using specific enzyme assays or through direct measurement of product formation or substrate conversion.
  • the promoter can be any promoter that exhibits strong constitutive activity in Gluconobacter oxydans such as the tufB promoter from Escherichia coli, the tufB promoter from Gluconobacter oxydans, the dnaA promoter from Gluconobacter oxydans, or the sndh promoter from Gluconobacter oxydans.
  • the promoter of the STS 16 gene may be replaced by the strong constitutive modified P sndh promoter (SEQ ID NO:5).
  • SEQ ID NO:5 the strong constitutive modified P sndh promoter
  • a DNA fragment is built up by Long Flanking Homology (LFH)-PCR consisting of 500-bp of the upstream region of the STS 16 gene, a kanamycin-resistance cassette, the P sndh -promoter fused to a modified ribosome binding site and the first 500-bp of the STS 16 gene.
  • LDH Long Flanking Homology
  • the single parts are amplified by PCR using the GC-rich PCR kit (Roche Molecular Biochemicals).
  • the STS 16 DNA upstream region is amplified using primer pair STS 16US+1 (SEQ ID NO:6) and KmSTS 16US-1 (SEQ ID NO:7) containing complementary kanamycin-resistance cassette - 35 - 24595 overhang sequence at 5'-end.
  • the P sndh promoter fragment is amplified using primer pair KmPsndh+1 (SEQ ID NO: 8) containing complementary kanamycin-resistance cassette overhang sequence at 5'-end and STS 16Psndh-l (SEQ ID NO:9) containing complementary STS 16 DNA overhang sequence at 5'-end.
  • the first 500-bp of the STS 16 gene is amplified using primer pair PsndhSTS 16+1 (SEQ ID NO: 10) containing complementary P snd h promoter overhang sequence at 5'-end and STS 16-1 (SEQ ID NO: 11).
  • PsndhSTS 16+1 SEQ ID NO: 10
  • SEQ ID NO: 11 complementary P snd h promoter overhang sequence at 5'-end and STS 16-1
  • G. oxydans DSM 17078 genomic DNA is used as a template.
  • the kanamycin-resistance cassette is amplified using plasmid pUC4K (Amersham Bioscience, accession No. X06404) as a template and primer pair Km+ 1 (SEQ E) NO: 12) and Km-I (SEQ E) NO:13).
  • the PCR conditions consist of 35 cycles of denaturation at 94°C for 30 sec, annealing at 50°C for 30 sec and extension at 72°C for 1 min.
  • the individual PCR fragments are gel-purified, mixed and re-amplified using the primer pair STS 16US+1 / STS 16-1 to amplify a full length product whereby the P sndh promoter is inserted upstream of the STS 16 gene,
  • the PCR reaction conditions for the second round reaction consist of 94°C, 2 min, then 10 cycles of [94°C, 30 sec, 63°C, 30 sec, 68 0 C, 6 min], followed by 20 cycles of [94°C, 30 sec, 63°C, 30 sec, 68°C, 6 min with an additional 20 sec per cycle] and a final extension at 68°C for 10 min.
  • the PCR product is transformed directly into competent G. oxydans DSM 17078 cells and transformants are selected on mannitol broth agar medium containing kanamycin to a final concentration of 50 ⁇ g ml "1 . Several putative transformants are observed of which several are then analyzed by PCR using primer pair STS 16US+1 / STS 16-1 to verify that the DNA fragment has inserted into the genome via a double crossover. Strains showing the correct size PCR product have the PCR product sequenced. Strains with the correct sequence are named G. oxydans DSM 17078-STS 16upl and G. oxydans DSM 17078-STS 16up2.
  • G. oxydans DSM 17078, G. oxydans DSM 17078-STS 16upl and G. oxydans DSM 17078-STS 16up2 are grown at 27 0 C for 3 days on No. 3BD agar medium containing 70 g/1 D-sorbitol, 0.5 g/1 glycerol, 7.5 g/1 yeast extract (Difco), 2.5 g/1 MgSO 4 -7H 2 O, 10 g/1 CaCO 3 and 18 g/1 agar (Difco).
  • the identification of the L-ascorbic acid is done using an amino-column (YMC-Pack Polyamine-II, YMC, Inc., Kyoto, Japan) with UV detection at 254 nm.
  • the mobile phase is 50 mM NH 4 H 2 PO 4 and acetonitrile (40:60).
  • MS HPLC-mass spectrometry
  • the supernatants of the reaction mixtures incubated with cells of G. oxydans DSM 17078- STS 16u ⁇ l and G. oxydans DSM 17078-STS 16u ⁇ 2 contain at least 20% more Vitamin C than the supernatant of the reaction mixture incubated with cells of G. oxydans DSM 17078.
  • SEQ ID NO: 1 The presence of SEQ ID NO: 1 and/or equivalents in other organisms than the ones disclosed herein before, e.g. organisms as mentioned in Table 1, maybe determined by a simple DNA hybridization experiment.
  • Acetobacter aceti subsp. xylinum IFO 13693 and IFO 13773 are grown at 27°C for 3 days on No. 350 medium containing 5 g/1 Bactopeptone (Difco), 5 g/1 yeast extract (Difco), 5 g/1 glucose, 5 g/1 mannitol, 1 g/1 MgSO 4 -7H 2 O, 5 ml/1 ethanol, and 15 g/1 agar.
  • Gluconacetobacter and all Gluconobacter strains are grown at 27°C for 3 days on mannitol broth (MB) agar medium containing 25 g/1 mannitol, 5 g/1 yeast extract (Difco), 3 g/1 Bactopeptone (Difco), and 18 g/1 agar (Difco).
  • E. coli K- 12 is grown on Luria Broth agar medium. The other strains are grown on medium recommended by the suppliers or according to methods known in the art. Genomic DNA is extracted as described by e.g. Sambrook et al., 1989, "Molecular Cloning: A Laboratory Manual/Second Edition", Cold Spring Harbor Laboratory Press) from a suitable organism as, e.g. mentioned in Table 1.
  • Genomic DNA preparations are digested with restriction enzymes such as Ec ⁇ Bl or Hindis., and 1 ⁇ g of the DNA fragments are separated by agarose gel electrophoresis (1% - 37 - 24595 agarose).
  • the gel is treated with 0.25 N HCl for 15 min and then 0.5 N NaOH for 30 min, and then blotted onto nitrocellulose or a nylon membrane with Vacuum Blotter Model 785 (BIO-RAD Laboratories AG, Switzerland) according to the instruction of the supplier.
  • the resulting blot is then brought into contact/hybridized with a solution wherein the probe, such as e.g.
  • a DIG-labeled probe e.g. SEQ ID NO:1
  • SEQ ID NO:1 may be prepared according to Example 1 by using the PCR-DIG labeling kit (Roche Diagnostics) and a set of primers, SEQ ID NO:3 and SEQ ED NO:4. A result of such a blot is depicted in Table 1.
  • the hybridization may be performed under stringent or highly stringent conditions.
  • a preferred, non-limiting example of such conditions are hybridization in 6x sodium chloride/sodium citrate (SSC) at about 45°C, followed by one or more washes in Ix SSC, 0.1% SDS at 50°C, preferably at 55 0 C, more preferably at 60°C and even more preferably at 65°C.
  • SSC 6x sodium chloride/sodium citrate
  • Highly stringent conditions include, for example, 2 h to 4 days incubation at 42°C in a solution such as DigEasyHyb solution (Roche Diagnostics GmbH) with or without 100 ⁇ g/ml salmon sperm DNA, or a solution comprising 50% formamide, 5x SSC (150 mM NaCl, 15 mM trisodium citrate), 0.02% sodium dodecyl sulfate, 0.1% N- lauroylsarcosine, and 2% blocking reagent (Roche Diagnostics GmbH), followed by washing the filters twice for 5 to 15 min in 2x SSC and 0.1% SDS at room temperature and then washing twice for 15-30 min in 0.5x SSC and 0.1% SDS or O.lx SSC and 0.1% SDS at 65-68 0 C. To detect DNA fragments with lower identity to the probe DNA, final washing steps can be done at lower temperatures such as 50-65°C and for shorter washing time such as 1-15 min.
  • a solution such as DigEasyHy
  • the genes corresponding to the positive signals within the respective organisms shown in Table 1 can be cloned by a PCR method well known in the art using genomic DNA of such an organism together with a suitable primer set, such as e.g. SEQ ID NO:3 and SEQ ID NO:4 under conditions as described in Example 1 or as follows: 5 to 100 ng of genomic DNA is used per reaction (total volume 50 ⁇ l).
  • a suitable primer set such as e.g. SEQ ID NO:3 and SEQ ID NO:4 under conditions as described in Example 1 or as follows: 5 to 100 ng of genomic DNA is used per reaction (total volume 50 ⁇ l).
  • Expand High Fidelity PCR system (Roche Diagnostics) can be used with reaction conditions consisting of 94°C for 2 min; 30 cycles of (i) denaturation step at 94 0 C for 15 sec, (ii) annealing step at 60 0 C for 30 sec, (iii) synthesis step at 72 0 C for 0.5 to 5 min depending to the target DNA length (1 min /1 kb); extension at 72 0 C for 7 min.
  • PCR with degenerate primers, which can be synthesized based on SEQ ID NO:2 or amino acid sequences as consensus sequences selected by aligning several amino acid sequences obtained by a sequence search program such as BLASTP (or BLASTX when nucleotide sequence is used as a "query sequence") to find proteins having a similarity to the protein of SEQ ID - 38 - 24595
  • temperature of the second annealing step (see above) can be lowered to 55°C, or even to 50-45°C.
  • a result of such an experiment is shown in Table 1.
  • Consensus sequences mentioned above might be amino acid sequences belonging to certain categories of several protein domain/family databases such as PROSITE (database of protein families and domains), COGs (Cluster of Ortholog Groups), CDD (Conserved Domain Databases), pfam (large collection of multiple sequence alignments and hidden Markov models covering many common protein domains and families).
  • PROSITE database of protein families and domains
  • COGs Cluster of Ortholog Groups
  • corresponding DNA encoding the protein can be amplified by PCR using the protein sequence or its nucleotide sequence when it is available in public databases.
  • organisms may further provide genes,
  • campestris ATCC 33913 Xanthomonas oryzaepv. oryzae KLACC 10331, Agrobacterium tumefaciens C58, Bradyrhizobium japonicwn USDA 110, Sinorhizobium meliloti 1021 or Ralstonia solanacearuni GMI 1000.
  • the STS 16 gene and equivalents as, e.g. a PCR product obtained in Example 4, referred to herein as gene X can be used in an overexpression system according to Example 2 or can be cloned into pCR2.1-TOPO Qnvitrogen, Carlsbad, CA, USA) and used to transform E. coli TGl to have a Apr transformant carrying pCR2.1-TOPO-gene X, i.e. carrying a PCR product obtained in Example 4.
  • the insert is amplified with a set of primers, PfNdeI [SEQ ID NO:3 with CCCAT at the 5'-end] and PrHindm [SEQ ID NO:4 with CCAAGCTT at the 5'-end], by PCR.
  • Resulting PCR product is digested with Ndel and Hmdm and the fragment is inserted together with PcrtE-SD (Shine-Dalgarno) fragment (WO 02/099095) digested with Xliol and Ndel into pVKlOO (ATCC 37156) between the sites of Xhol and HindHL E.
  • coli TGl is transformed with the ligation product to have Tc r transformant carrying plasmid pVK-PcrtE-SD-gene X, which is then used to transform a suitable host, e.g. G. oxydans DSM 17078 by electroporation to have e.g. Tc r G. oxydans DSM 17078/pVK- PcrtE-SD-gene X. - 39 - 24595
  • Vitamin C Production of Vitamin C using the recombinant cells of e.g. G. oxydans strains DSM 17078 and the corresponding wild-type strain are performed according to Example 3.
  • the recombinant cells can produce at least more than 20% Vitamin C compared to the wild-type strain.
  • Signal 1 Detection of DNA on a blot with genomic DNA of different strains and SEQ ID NO: 1 as labeled probe.
  • Signal 2 Detection of DNA of different strains in a PCR reaction using primer pair SEQ ID NO:3 and SEQ ID NO:4.
  • Signal 3 Detection of DNA of different strains in a PCR reaction using degenerate primers. For more explanation refer to the text.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Health & Medical Sciences (AREA)
  • Zoology (AREA)
  • Wood Science & Technology (AREA)
  • Genetics & Genomics (AREA)
  • General Health & Medical Sciences (AREA)
  • Biochemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Engineering & Computer Science (AREA)
  • Microbiology (AREA)
  • Biotechnology (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Biophysics (AREA)
  • Medicinal Chemistry (AREA)
  • Molecular Biology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Micro-Organisms Or Cultivation Processes Thereof (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)

Abstract

La présente invention a trait à des gènes nouvellement identifiés codant pour des protéines qui sont impliquées dans la synthèse de l'acide L-ascorbique (désigné ci-après Vitamine C). Le gène cloné code pour une sous-unité de liaison d'adénosine triphosphate (ATP) du transporteur de sorbitol/mannitol. L'invention a également trait à des polynucléotides comportant des séquences polynucléotidiques pleine longueur des nouveaux gènes et des fragments de ceux-ci, aux nouveaux polypeptides codés par les polynucléotides et des fragments de ceux-ci, ainsi qu'à leurs équivalents fonctionnels. La présente invention a trait en outre à l'utilisation desdits polynucléotides et polypeptides comme outils biotechnologiques dans la production de la Vitamine C à partir de micro-organismes, selon lequel une modification desdits polynucléotides et/ou polypeptides codés ont un impact direct ou indirect sur le rendement, la production et/ou l'efficacité de production du produit de fermentation dans ledit micro-organisme. L'invention a trait en outre à des procédés/processus d'utilisation des polynucléotides et de séquences polynucléotidiques modifiées pour la transformation de micro-organismes hôtes. Enfin, l'invention a trait à des micro-organismes génétiquement modifiés et à leur utilisation pour la production directe de la Vitamine C.
PCT/EP2006/001220 2005-02-11 2006-02-10 Nouveau gene sts 16 WO2006084725A1 (fr)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
EP05405066 2005-02-11
EP05405082 2005-02-11
EP05405066.1 2005-02-11
EP05405082.8 2005-02-11

Publications (1)

Publication Number Publication Date
WO2006084725A1 true WO2006084725A1 (fr) 2006-08-17

Family

ID=36441384

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/EP2006/001220 WO2006084725A1 (fr) 2005-02-11 2006-02-10 Nouveau gene sts 16

Country Status (1)

Country Link
WO (1) WO2006084725A1 (fr)

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2002012481A2 (fr) * 2000-08-04 2002-02-14 Genencor International, Inc. Renforcement de production industrielle par augmentation du transport substratique
WO2004029235A2 (fr) * 2002-09-27 2004-04-08 Dsm Ip Assets B.V. Gene de l'aldehyde deshydrogenase

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2002012481A2 (fr) * 2000-08-04 2002-02-14 Genencor International, Inc. Renforcement de production industrielle par augmentation du transport substratique
WO2004029235A2 (fr) * 2002-09-27 2004-04-08 Dsm Ip Assets B.V. Gene de l'aldehyde deshydrogenase

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
BRUNKER P ET AL: "Structure and function of the genes involved in mannitol, arabitol and glucitol utilization from Pseudomonas fluorescens DSM50106", GENE: AN INTERNATIONAL JOURNAL ON GENES AND GENOMES, ELSEVIER, AMSTERDAM, NL, vol. 206, no. 1, 5 January 1998 (1998-01-05), pages 117 - 126, XP004102880, ISSN: 0378-1119 *
DATABASE GENBANK 21 January 2005 (2005-01-21), "Complete genome sequence of the acetogenic bacterium Gluconobacter oxydans", XP002383346, retrieved from NCBI Database accession no. CP000009 *
PRUST C ET AL: "Complete genome sequence of the acetic acid bacterium Gluconobacter oxydans", NATURE BIOTECHNOLOGY, NATURE PUBLISHING GROUP, NEW YORK, NY, US, vol. 23, no. 2, 21 January 2005 (2005-01-21), pages 195 - 200, XP002334906, ISSN: 1087-0156 *

Similar Documents

Publication Publication Date Title
WO2006084719A1 (fr) Production de vitamine c par voie fermentative
US9079951B2 (en) Method for production of vitamin C
US8053218B2 (en) Gene STS 18
US20080113417A1 (en) Gene Sms 12
WO2006084701A1 (fr) Gene phosphotransferase a partir de gluconobacter oxydans
WO2006084703A2 (fr) Nouveau gene sts 24
EP1853715A1 (fr) Gene rcs 23
WO2006084735A1 (fr) Gene pour la proteine b de synthese de la coenzyme pqq a partir de gluconobacter oxydans
WO2006084725A1 (fr) Nouveau gene sts 16
US20090215135A1 (en) Novel Gene STS 22
WO2006084722A2 (fr) Nouveau gene sts 15
WO2006084704A2 (fr) Nouveau gene sts 01
WO2006084730A1 (fr) Gene d'oxydoreductase tire du systeme de la chaine respiratoire de gluconobacter oxydans
WO2006084723A1 (fr) Gene sts 17
WO2006084702A2 (fr) Nouveau gene sts 23
WO2006084720A2 (fr) Nouveau gene sts 25
US20100151516A1 (en) Gene SMS 13
WO2006084705A2 (fr) Nouveau gene sts 06
WO2006084706A2 (fr) Nouveau gene sts 07
WO2006084734A1 (fr) Gene rcs 25
WO2006084733A1 (fr) Gene rcs 21
EP1859032A1 (fr) Gene sms 14
WO2006084727A1 (fr) Gene rcs 05
EP1846552A2 (fr) Nouveau gene rcs 06
WO2006084732A2 (fr) Nouveau gene rcs 07

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application
NENP Non-entry into the national phase

Ref country code: DE

122 Ep: pct application non-entry in european phase

Ref document number: 06706846

Country of ref document: EP

Kind code of ref document: A1

WWW Wipo information: withdrawn in national office

Ref document number: 6706846

Country of ref document: EP