ES2593811T3 - Producción microbiana de ácido L-ascórbico - Google Patents
Producción microbiana de ácido L-ascórbico Download PDFInfo
- Publication number
- ES2593811T3 ES2593811T3 ES10184019.7T ES10184019T ES2593811T3 ES 2593811 T3 ES2593811 T3 ES 2593811T3 ES 10184019 T ES10184019 T ES 10184019T ES 2593811 T3 ES2593811 T3 ES 2593811T3
- Authority
- ES
- Spain
- Prior art keywords
- microorganism
- ifo
- cells
- ascorbic acid
- production
- Prior art date
- Legal status (The legal status 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 status listed.)
- Expired - Lifetime
Links
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 title abstract description 86
- 238000004519 manufacturing process Methods 0.000 title abstract description 29
- 239000002211 L-ascorbic acid Substances 0.000 title abstract description 24
- 235000000069 L-ascorbic acid Nutrition 0.000 title abstract description 24
- 229960005070 ascorbic acid Drugs 0.000 title abstract description 24
- 230000000813 microbial effect Effects 0.000 title 1
- 244000005700 microbiome Species 0.000 abstract description 35
- 238000000034 method Methods 0.000 abstract description 30
- ZZZCUOFIHGPKAK-UHFFFAOYSA-N D-erythro-ascorbic acid Natural products OCC1OC(=O)C(O)=C1O ZZZCUOFIHGPKAK-UHFFFAOYSA-N 0.000 abstract description 19
- 229930003268 Vitamin C Natural products 0.000 abstract description 19
- 235000019154 vitamin C Nutrition 0.000 abstract description 19
- 239000011718 vitamin C Substances 0.000 abstract description 19
- DCNMIDLYWOTSGK-KVQBGUIXSA-N L-xylo-hexos-2-ulose Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)C(=O)C=O DCNMIDLYWOTSGK-KVQBGUIXSA-N 0.000 abstract description 9
- 108010053002 L-sorbosone dehydrogenase Proteins 0.000 abstract description 6
- 241000589220 Acetobacter Species 0.000 abstract description 5
- 241000589236 Gluconobacter Species 0.000 abstract description 5
- 239000002773 nucleotide Substances 0.000 abstract description 5
- 125000003729 nucleotide group Chemical group 0.000 abstract description 5
- 102000004196 processed proteins & peptides Human genes 0.000 abstract description 3
- 108090000765 processed proteins & peptides Proteins 0.000 abstract description 3
- FWMNVWWHGCHHJJ-SKKKGAJSSA-N 4-amino-1-[(2r)-6-amino-2-[[(2r)-2-[[(2r)-2-[[(2r)-2-amino-3-phenylpropanoyl]amino]-3-phenylpropanoyl]amino]-4-methylpentanoyl]amino]hexanoyl]piperidine-4-carboxylic acid Chemical compound C([C@H](C(=O)N[C@H](CC(C)C)C(=O)N[C@H](CCCCN)C(=O)N1CCC(N)(CC1)C(O)=O)NC(=O)[C@H](N)CC=1C=CC=CC=1)C1=CC=CC=C1 FWMNVWWHGCHHJJ-SKKKGAJSSA-N 0.000 abstract description 2
- 241000588722 Escherichia Species 0.000 abstract description 2
- 241000589516 Pseudomonas Species 0.000 abstract description 2
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- 229920001184 polypeptide Polymers 0.000 abstract 2
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- 210000004027 cell Anatomy 0.000 description 55
- 241000589232 Gluconobacter oxydans Species 0.000 description 33
- 230000000284 resting effect Effects 0.000 description 28
- 230000012010 growth Effects 0.000 description 24
- 238000000909 electrodialysis Methods 0.000 description 17
- 238000006243 chemical reaction Methods 0.000 description 13
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 12
- 239000012528 membrane Substances 0.000 description 12
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 9
- 239000002253 acid Substances 0.000 description 9
- 239000002609 medium Substances 0.000 description 9
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 8
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 8
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 8
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 8
- 239000000047 product Substances 0.000 description 8
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- 244000235858 Acetobacter xylinum Species 0.000 description 6
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- 229920001817 Agar Polymers 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 6
- 238000005342 ion exchange Methods 0.000 description 6
- 235000010355 mannitol Nutrition 0.000 description 6
- 244000283763 Acetobacter aceti Species 0.000 description 5
- 241000589234 Acetobacter sp. Species 0.000 description 5
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 5
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 5
- -1 Dsorbitol Chemical compound 0.000 description 5
- LKDRXBCSQODPBY-AMVSKUEXSA-N L-(-)-Sorbose Chemical compound OCC1(O)OC[C@H](O)[C@@H](O)[C@@H]1O LKDRXBCSQODPBY-AMVSKUEXSA-N 0.000 description 5
- 239000008272 agar Substances 0.000 description 5
- 229940041514 candida albicans extract Drugs 0.000 description 5
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- 235000014680 Saccharomyces cerevisiae Nutrition 0.000 description 4
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
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- 230000014759 maintenance of location Effects 0.000 description 4
- 239000000594 mannitol Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- LWIHDJKSTIGBAC-UHFFFAOYSA-K tripotassium phosphate Chemical compound [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 240000008042 Zea mays Species 0.000 description 3
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 3
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 3
- 239000012736 aqueous medium Substances 0.000 description 3
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 3
- 239000004202 carbamide Substances 0.000 description 3
- 239000013611 chromosomal DNA Substances 0.000 description 3
- 235000005822 corn Nutrition 0.000 description 3
- 238000001914 filtration Methods 0.000 description 3
- 238000004128 high performance liquid chromatography Methods 0.000 description 3
- HEBKCHPVOIAQTA-UHFFFAOYSA-N meso ribitol Natural products OCC(O)C(O)C(O)CO HEBKCHPVOIAQTA-UHFFFAOYSA-N 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 235000015097 nutrients Nutrition 0.000 description 3
- 238000000746 purification Methods 0.000 description 3
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- 238000004064 recycling Methods 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 239000000523 sample Substances 0.000 description 3
- 238000012163 sequencing technique Methods 0.000 description 3
- 159000000000 sodium salts Chemical group 0.000 description 3
- 238000001179 sorption measurement Methods 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- NWUYHJFMYQTDRP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;1-ethenyl-2-ethylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CCC1=CC=CC=C1C=C.C=CC1=CC=CC=C1C=C NWUYHJFMYQTDRP-UHFFFAOYSA-N 0.000 description 2
- 235000002837 Acetobacter xylinum Nutrition 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- 108010023063 Bacto-peptone Proteins 0.000 description 2
- 241000195493 Cryptophyta Species 0.000 description 2
- CIWBSHSKHKDKBQ-DUZGATOHSA-N D-isoascorbic acid Chemical compound OC[C@@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-DUZGATOHSA-N 0.000 description 2
- 108090000790 Enzymes Proteins 0.000 description 2
- 102000004190 Enzymes Human genes 0.000 description 2
- 241000588724 Escherichia coli Species 0.000 description 2
- 241001646716 Escherichia coli K-12 Species 0.000 description 2
- 108091028043 Nucleic acid sequence Proteins 0.000 description 2
- 239000001888 Peptone Substances 0.000 description 2
- 108010080698 Peptones Proteins 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 238000000246 agarose gel electrophoresis Methods 0.000 description 2
- PYMYPHUHKUWMLA-LMVFSUKVSA-N aldehydo-D-ribose Chemical compound OC[C@@H](O)[C@@H](O)[C@@H](O)C=O PYMYPHUHKUWMLA-LMVFSUKVSA-N 0.000 description 2
- 150000001413 amino acids Chemical class 0.000 description 2
- LFVGISIMTYGQHF-UHFFFAOYSA-N ammonium dihydrogen phosphate Chemical compound [NH4+].OP(O)([O-])=O LFVGISIMTYGQHF-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 239000003729 cation exchange resin Substances 0.000 description 2
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- 229940099596 manganese sulfate Drugs 0.000 description 2
- 239000011702 manganese sulphate Substances 0.000 description 2
- 235000007079 manganese sulphate Nutrition 0.000 description 2
- SQQMAOCOWKFBNP-UHFFFAOYSA-L manganese(II) sulfate Chemical compound [Mn+2].[O-]S([O-])(=O)=O SQQMAOCOWKFBNP-UHFFFAOYSA-L 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 235000019319 peptone Nutrition 0.000 description 2
- 229910000160 potassium phosphate Inorganic materials 0.000 description 2
- 235000011009 potassium phosphates Nutrition 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- VWDWKYIASSYTQR-UHFFFAOYSA-N sodium nitrate Chemical compound [Na+].[O-][N+]([O-])=O VWDWKYIASSYTQR-UHFFFAOYSA-N 0.000 description 2
- 239000006228 supernatant Substances 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- 230000009897 systematic effect Effects 0.000 description 2
- 238000000108 ultra-filtration Methods 0.000 description 2
- 238000000825 ultraviolet detection Methods 0.000 description 2
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- RFSUNEUAIZKAJO-VRPWFDPXSA-N D-Fructose Natural products OC[C@H]1OC(O)(CO)[C@@H](O)[C@@H]1O RFSUNEUAIZKAJO-VRPWFDPXSA-N 0.000 description 1
- HEBKCHPVOIAQTA-QWWZWVQMSA-N D-arabinitol Chemical compound OC[C@@H](O)C(O)[C@H](O)CO HEBKCHPVOIAQTA-QWWZWVQMSA-N 0.000 description 1
- 239000004386 Erythritol Substances 0.000 description 1
- UNXHWFMMPAWVPI-UHFFFAOYSA-N Erythritol Natural products OCC(O)C(O)CO UNXHWFMMPAWVPI-UHFFFAOYSA-N 0.000 description 1
- RFSUNEUAIZKAJO-ARQDHWQXSA-N Fructose Chemical compound OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@@H]1O RFSUNEUAIZKAJO-ARQDHWQXSA-N 0.000 description 1
- 241000206672 Gelidium Species 0.000 description 1
- SQUHHTBVTRBESD-UHFFFAOYSA-N Hexa-Ac-myo-Inositol Natural products CC(=O)OC1C(OC(C)=O)C(OC(C)=O)C(OC(C)=O)C(OC(C)=O)C1OC(C)=O SQUHHTBVTRBESD-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical group C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 241000320429 Ketogulonicigenium vulgare Species 0.000 description 1
- 238000012408 PCR amplification Methods 0.000 description 1
- JVWLUVNSQYXYBE-UHFFFAOYSA-N Ribitol Natural products OCC(C)C(O)C(O)CO JVWLUVNSQYXYBE-UHFFFAOYSA-N 0.000 description 1
- 238000002105 Southern blotting Methods 0.000 description 1
- 229930006000 Sucrose Natural products 0.000 description 1
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
- TVXBFESIOXBWNM-UHFFFAOYSA-N Xylitol Natural products OCCC(O)C(O)C(O)CCO TVXBFESIOXBWNM-UHFFFAOYSA-N 0.000 description 1
- 238000002835 absorbance Methods 0.000 description 1
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- 229910021529 ammonia Inorganic materials 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
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- PYMYPHUHKUWMLA-UHFFFAOYSA-N arabinose Natural products OCC(O)C(O)C(O)C=O PYMYPHUHKUWMLA-UHFFFAOYSA-N 0.000 description 1
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- 239000001110 calcium chloride Substances 0.000 description 1
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- 238000007444 cell Immobilization Methods 0.000 description 1
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- 238000010908 decantation Methods 0.000 description 1
- 238000004925 denaturation Methods 0.000 description 1
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- UNXHWFMMPAWVPI-ZXZARUISSA-N erythritol Chemical compound OC[C@H](O)[C@H](O)CO UNXHWFMMPAWVPI-ZXZARUISSA-N 0.000 description 1
- 235000019414 erythritol Nutrition 0.000 description 1
- 229940009714 erythritol Drugs 0.000 description 1
- ZMMJGEGLRURXTF-UHFFFAOYSA-N ethidium bromide Chemical compound [Br-].C12=CC(N)=CC=C2C2=CC=C(N)C=C2[N+](CC)=C1C1=CC=CC=C1 ZMMJGEGLRURXTF-UHFFFAOYSA-N 0.000 description 1
- 229960005542 ethidium bromide Drugs 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- FBPFZTCFMRRESA-GUCUJZIJSA-N galactitol Chemical compound OC[C@H](O)[C@@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-GUCUJZIJSA-N 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- CDAISMWEOUEBRE-GPIVLXJGSA-N inositol Chemical compound O[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@H](O)[C@@H]1O CDAISMWEOUEBRE-GPIVLXJGSA-N 0.000 description 1
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- 102000004169 proteins and genes Human genes 0.000 description 1
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- HEBKCHPVOIAQTA-ZXFHETKHSA-N ribitol Chemical compound OC[C@H](O)[C@H](O)[C@H](O)CO HEBKCHPVOIAQTA-ZXFHETKHSA-N 0.000 description 1
- CDAISMWEOUEBRE-UHFFFAOYSA-N scyllo-inosotol Natural products OC1C(O)C(O)C(O)C(O)C1O CDAISMWEOUEBRE-UHFFFAOYSA-N 0.000 description 1
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- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000000811 xylitol Substances 0.000 description 1
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- HEBKCHPVOIAQTA-SCDXWVJYSA-N xylitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)CO HEBKCHPVOIAQTA-SCDXWVJYSA-N 0.000 description 1
- 229960002675 xylitol Drugs 0.000 description 1
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
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
- C12N9/0004—Oxidoreductases (1.)
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
- C12N9/0004—Oxidoreductases (1.)
- C12N9/0006—Oxidoreductases (1.) acting on CH-OH groups as donors (1.1)
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
- C12N9/0004—Oxidoreductases (1.)
- C12N9/0008—Oxidoreductases (1.) acting on the aldehyde or oxo group of donors (1.2)
-
- 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
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- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Zoology (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Genetics & Genomics (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Microbiology (AREA)
- Biotechnology (AREA)
- Biochemistry (AREA)
- General Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Biomedical Technology (AREA)
- Molecular Biology (AREA)
- Medicinal Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
- Enzymes And Modification Thereof (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP03017677 | 2003-08-14 | ||
| EP03017677 | 2003-08-14 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2593811T3 true ES2593811T3 (es) | 2016-12-13 |
Family
ID=34178381
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES10184019.7T Expired - Lifetime ES2593811T3 (es) | 2003-08-14 | 2004-08-16 | Producción microbiana de ácido L-ascórbico |
| ES04738146T Expired - Lifetime ES2421294T3 (es) | 2003-08-14 | 2004-08-16 | Producción microbiana de ácido L-ascórbico |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES04738146T Expired - Lifetime ES2421294T3 (es) | 2003-08-14 | 2004-08-16 | Producción microbiana de ácido L-ascórbico |
Country Status (9)
| Country | Link |
|---|---|
| US (3) | US7700723B2 (enExample) |
| EP (2) | EP1664303B1 (enExample) |
| JP (1) | JP4896718B2 (enExample) |
| KR (1) | KR101311562B1 (enExample) |
| CN (2) | CN104004776A (enExample) |
| BR (1) | BRPI0413542A (enExample) |
| EA (1) | EA009287B1 (enExample) |
| ES (2) | ES2593811T3 (enExample) |
| WO (2) | WO2005017159A2 (enExample) |
Families Citing this family (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101151365B (zh) * | 2005-02-11 | 2012-05-23 | 帝斯曼知识产权资产管理有限公司 | 基因sms02 |
| WO2006084733A1 (en) * | 2005-02-11 | 2006-08-17 | Dsm Ip Assets B.V. | Gene rcs 21 |
| WO2006084643A2 (en) * | 2005-02-11 | 2006-08-17 | Dsm Ip Assets B.V. | Novel gene vcs 07 |
| WO2006084645A1 (en) * | 2005-02-11 | 2006-08-17 | Dsm Ip Assets B.V. | Novel gene rcs 10 |
| WO2006084737A1 (en) * | 2005-02-11 | 2006-08-17 | Dsm Ip Assets B.V. | Gene rcs 23 |
| WO2006084735A1 (en) * | 2005-02-11 | 2006-08-17 | Dsm Ip Assets B.V. | Gene for coenzyme pqq synthesis protein b from gluconobacter oxydans |
| US20080193972A1 (en) * | 2005-02-11 | 2008-08-14 | Bastian Chevreux | Gene Rcs 25 |
| EP1846554A1 (en) * | 2005-02-11 | 2007-10-24 | DSMIP Assets B.V. | Fermentive vitamin c production |
| WO2006084724A1 (en) * | 2005-02-11 | 2006-08-17 | Dsm Ip Assets B.V. | Novel gene rcs 28 |
| WO2007028602A1 (en) | 2005-09-08 | 2007-03-15 | Dsm Ip Assets B.V. | Novel gene sms 37 |
| EP1931785A2 (en) * | 2005-09-09 | 2008-06-18 | DSMIP Assets B.V. | Novel gene gms 01 |
| US8137940B2 (en) | 2005-09-09 | 2012-03-20 | Dsm Ip Assets B.V. | Method for production of biomass using a gluconobacter oxydans comprising an inactivated NADP dependent glucose dehydrogenase gene |
| FR2906817B1 (fr) * | 2006-10-04 | 2012-04-06 | Gervais Danone Sa | Procede de culture pour favoriser la production de vitamine k2 par les bacteries lactiques et ses applications a la preparation de produits alimentaires |
| EP1918383A1 (en) * | 2006-11-02 | 2008-05-07 | DSMIP Assets B.V. | Semi-continuous fermentation process for pantothenate production |
| EP1918382A1 (en) * | 2006-11-02 | 2008-05-07 | DSMIP Assets B.V. | Semi-continuous cascade fermentation process for pantothenate production |
| US20100323412A1 (en) * | 2008-01-10 | 2010-12-23 | Bastien Chevreux | Novel gene sms 44 |
| CN103073601B (zh) * | 2013-02-01 | 2015-08-19 | 东北制药集团股份有限公司 | 一种2-酮基-l-古龙酸溶液加晶种的可控浓缩结晶方法 |
| NZ743055A (en) * | 2013-03-08 | 2020-03-27 | Xyleco Inc | Equipment protecting enclosures |
| CN105392892A (zh) | 2013-03-27 | 2016-03-09 | 六品科技公司 | 重组噬菌体和细菌检测方法 |
| JP2016521996A (ja) * | 2013-06-19 | 2016-07-28 | サンプルシックス テクノロジーズ，インコーポレイティド | ファージベースの細菌検出アッセイ |
| CN105683210B (zh) | 2013-08-23 | 2020-07-14 | 贝林格尔·英格海姆Rcv两合公司 | 用于细胞破碎和/或回收生物分子的微粒 |
| EP3122870B1 (en) * | 2014-03-25 | 2022-06-29 | Ginkgo Bioworks Inc. | Methods and genetic systems for cell engineering |
| CN116053017B (zh) * | 2022-11-04 | 2023-08-22 | 医波(厦门)科技有限公司 | 一种复合磁性微球及其制备方法和应用 |
Family Cites Families (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5082785A (en) | 1987-01-30 | 1992-01-21 | Hoffmann-La Roche Inc. | Biosynthesis of 2 keto-l-gulonic acid |
| WO1989006688A2 (en) | 1988-01-14 | 1989-07-27 | F. Hoffmann-La Roche & Co. Aktiengesellschaft | Novel enzyme |
| ATE180831T1 (de) * | 1990-09-17 | 1999-06-15 | Hoffmann La Roche | L-gulono-gamma-lacton dehydrogenase |
| US5376544A (en) * | 1992-09-08 | 1994-12-27 | Rutgers The State University Of New Jersey | Enzymes for the production of 2-keto-L-gulonic acid |
| AU6731896A (en) * | 1995-07-17 | 1997-02-18 | Fraunhofer-Gesellschaft Zur Forderung Der Angewandten Forschung E.V. | Cyclitol |
| EP0922759B1 (en) * | 1997-12-01 | 2004-01-28 | F. Hoffmann-La Roche Ag | Aldehyde dehydrogenase |
| US20020012979A1 (en) * | 1998-06-08 | 2002-01-31 | Alan Berry | Vitamin c production in microorganisms and plants |
| GB0119864D0 (en) * | 2001-08-15 | 2001-10-10 | Cerestar Holding Bv | Process for the manufacture of 2-keto-L-gulonic acid |
| AU2003229663A1 (en) * | 2002-04-22 | 2003-11-03 | Dsm Ip Assets B.V. | Aldehyde dehydrogenase ii |
| AU2003274096A1 (en) * | 2002-06-06 | 2003-12-22 | Dsm Ip Assets B.V. | Aldehyde dehydrogenase |
| AU2003280338A1 (en) * | 2002-09-27 | 2004-04-19 | Dsm Ip Assets B.V. | Process for producing vitamin c |
| DE60322921D1 (de) | 2002-09-27 | 2008-09-25 | Dsm Ip Assets Bv | Aldehyddehyrdrogenase-gen |
| CN100357446C (zh) * | 2002-09-27 | 2007-12-26 | 帝斯曼知识产权资产管理有限公司 | 维生素c的微生物生产方法 |
| CN1914326B (zh) * | 2004-01-30 | 2012-04-18 | 帝斯曼知识产权资产管理有限公司 | 维生素c的微生物生产方法 |
| US20080226126A1 (en) * | 2005-01-31 | 2008-09-18 | Yoshinori Ohno | Object-Tracking Apparatus, Microscope System, and Object-Tracking Program |
| EP1846554A1 (en) * | 2005-02-11 | 2007-10-24 | DSMIP Assets B.V. | Fermentive vitamin c production |
-
2004
- 2004-08-16 EA EA200600408A patent/EA009287B1/ru not_active IP Right Cessation
- 2004-08-16 ES ES10184019.7T patent/ES2593811T3/es not_active Expired - Lifetime
- 2004-08-16 CN CN201410171433.3A patent/CN104004776A/zh active Pending
- 2004-08-16 ES ES04738146T patent/ES2421294T3/es not_active Expired - Lifetime
- 2004-08-16 JP JP2006522868A patent/JP4896718B2/ja not_active Expired - Fee Related
- 2004-08-16 EP EP04738146.2A patent/EP1664303B1/en not_active Expired - Lifetime
- 2004-08-16 EP EP10184019.7A patent/EP2348113B1/en not_active Expired - Lifetime
- 2004-08-16 US US10/567,763 patent/US7700723B2/en not_active Expired - Lifetime
- 2004-08-16 CN CN200480023361.2A patent/CN1882691B/zh not_active Expired - Fee Related
- 2004-08-16 WO PCT/CH2004/000511 patent/WO2005017159A2/en not_active Ceased
- 2004-08-16 KR KR1020067003014A patent/KR101311562B1/ko not_active Expired - Fee Related
- 2004-08-16 WO PCT/CH2004/000512 patent/WO2005017172A1/en not_active Ceased
- 2004-08-16 BR BRPI0413542-3A patent/BRPI0413542A/pt not_active Application Discontinuation
-
2010
- 2010-02-08 US US12/701,748 patent/US8338144B2/en not_active Expired - Fee Related
-
2012
- 2012-11-21 US US13/683,487 patent/US20130217080A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| CN1882691A (zh) | 2006-12-20 |
| US20130217080A1 (en) | 2013-08-22 |
| ES2421294T3 (es) | 2013-08-30 |
| EP2348113A3 (en) | 2012-11-14 |
| EA009287B1 (ru) | 2007-12-28 |
| JP4896718B2 (ja) | 2012-03-14 |
| US20100203598A1 (en) | 2010-08-12 |
| WO2005017159A2 (en) | 2005-02-24 |
| CN104004776A (zh) | 2014-08-27 |
| EA200600408A1 (ru) | 2006-08-25 |
| US8338144B2 (en) | 2012-12-25 |
| KR101311562B1 (ko) | 2013-09-26 |
| US7700723B2 (en) | 2010-04-20 |
| EP2348113B1 (en) | 2016-06-29 |
| EP2348113A2 (en) | 2011-07-27 |
| JP2007502102A (ja) | 2007-02-08 |
| EP1664303B1 (en) | 2013-04-24 |
| WO2005017159A3 (en) | 2005-11-03 |
| BRPI0413542A (pt) | 2006-10-17 |
| US20070184534A1 (en) | 2007-08-09 |
| KR20060064629A (ko) | 2006-06-13 |
| EP1664303A2 (en) | 2006-06-07 |
| WO2005017172A1 (en) | 2005-02-24 |
| CN1882691B (zh) | 2014-05-28 |
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