DE68925002T2 - Verfahren zur Herstellung von optisch-aktiven alpha-substituierten organischen Säuren und Mikroorganismen und Enzyme, die dafür verwendet werden. - Google Patents

Verfahren zur Herstellung von optisch-aktiven alpha-substituierten organischen Säuren und Mikroorganismen und Enzyme, die dafür verwendet werden.

Info

Publication number
DE68925002T2
DE68925002T2 DE68925002T DE68925002T DE68925002T2 DE 68925002 T2 DE68925002 T2 DE 68925002T2 DE 68925002 T DE68925002 T DE 68925002T DE 68925002 T DE68925002 T DE 68925002T DE 68925002 T2 DE68925002 T2 DE 68925002T2
Authority
DE
Germany
Prior art keywords
microorganisms
production
organic acids
optically active
enzymes used
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 - Fee Related
Application number
DE68925002T
Other languages
English (en)
Other versions
DE68925002D1 (de
Inventor
Keizou Yamamoto
Kazumasa Otsubo
Kazuhiko Oishi
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Asahi Kasei Corp
Asahi Chemical Industry Co Ltd
Original Assignee
Asahi Chemical Industry Co Ltd
Asahi Kasei Kogyo KK
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 Asahi Chemical Industry Co Ltd, Asahi Kasei Kogyo KK filed Critical Asahi Chemical Industry Co Ltd
Publication of DE68925002D1 publication Critical patent/DE68925002D1/de
Application granted granted Critical
Publication of DE68925002T2 publication Critical patent/DE68925002T2/de
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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
    • C12P7/00—Preparation of oxygen-containing organic compounds
    • C12P7/40—Preparation of oxygen-containing organic compounds containing a carboxyl group including Peroxycarboxylic acids
    • 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
    • C12N9/14—Hydrolases (3)
    • C12N9/78—Hydrolases (3) acting on carbon to nitrogen bonds other than peptide bonds (3.5)
    • 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
    • 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
    • C12P41/00—Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture
    • C12P41/006—Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture by reactions involving C-N bonds, e.g. nitriles, amides, hydantoins, carbamates, lactames, transamination reactions, or keto group formation from racemic mixtures

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Zoology (AREA)
  • Wood Science & Technology (AREA)
  • Health & Medical Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Health & Medical Sciences (AREA)
  • Biochemistry (AREA)
  • General Engineering & Computer Science (AREA)
  • Microbiology (AREA)
  • Biotechnology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Analytical Chemistry (AREA)
  • Medicinal Chemistry (AREA)
  • Molecular Biology (AREA)
  • Biomedical Technology (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Micro-Organisms Or Cultivation Processes Thereof (AREA)
DE68925002T 1988-06-27 1989-06-27 Verfahren zur Herstellung von optisch-aktiven alpha-substituierten organischen Säuren und Mikroorganismen und Enzyme, die dafür verwendet werden. Expired - Fee Related DE68925002T2 (de)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP15691188 1988-06-27

Publications (2)

Publication Number Publication Date
DE68925002D1 DE68925002D1 (de) 1996-01-18
DE68925002T2 true DE68925002T2 (de) 1996-08-29

Family

ID=15638079

Family Applications (1)

Application Number Title Priority Date Filing Date
DE68925002T Expired - Fee Related DE68925002T2 (de) 1988-06-27 1989-06-27 Verfahren zur Herstellung von optisch-aktiven alpha-substituierten organischen Säuren und Mikroorganismen und Enzyme, die dafür verwendet werden.

Country Status (4)

Country Link
EP (1) EP0348901B1 (de)
JP (1) JP2623345B2 (de)
DE (1) DE68925002T2 (de)
DK (1) DK314989A (de)

Families Citing this family (38)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0356912A3 (de) * 1988-08-29 1991-09-18 Idemitsu Kosan Company Limited Verfahren zur Herstellung von 2-substituierter, optisch aktiver Karbonsäure
US5238828A (en) * 1988-08-29 1993-08-24 Idemitsu Kosan Company Limited Method for the preparation of an optically active 2-substituted carboxylic acid
JP2696127B2 (ja) * 1990-03-22 1998-01-14 旭化成工業株式会社 光学活性な２―ヒドロキシカルボン酸の製造法
JP2698936B2 (ja) * 1990-08-16 1998-01-19 日東化学工業株式会社 Ｒ（‐）―マンデル酸誘導体の製造法
DE69131217T2 (de) * 1990-03-30 1999-09-23 Mitsubishi Rayon Co Verfahren zur Herstellung von R(-)Mandelsäure und deren Derivaten
DK161690D0 (da) * 1990-07-05 1990-07-05 Novo Nordisk As Fremgangsmaade til fremstilling af enantiomere forbindelser
US5242816A (en) * 1990-07-10 1993-09-07 Lonza Ltd. Microbiological oxidation of alkyl groups in heterocycles
JP2974737B2 (ja) * 1990-08-16 1999-11-10 三菱レイヨン株式会社 光学活性乳酸の製造法
US5593871A (en) * 1990-09-20 1997-01-14 E. I. Du Pont De Nemours And Company Process for the preparation of enantiometric 2-alkanoic acid amides from nitriles
ES2085487T3 (es) * 1990-09-20 1996-06-01 Du Pont Un procedimiento para la preparacion de acidos 2-alcanoicos enantiomericos.
SG48037A1 (en) * 1990-11-14 1998-04-17 Nitto Chemical Industry Co Ltd Biology process for production-alpha-hydroxyamide or alpha-hydroxy acid
JPH04341185A (ja) * 1990-12-11 1992-11-27 Asahi Chem Ind Co Ltd 新規ニトリラーゼ
JP2676568B2 (ja) * 1991-06-26 1997-11-17 日東化学工業株式会社 Ｒ（−）−マンデル酸およびその誘導体の製造法
US5258305A (en) * 1991-09-13 1993-11-02 Nitto Chemical Industry Co., Ltd. Manufacture of optically active 2-phenylpropionic acid and 2-phenylpropionamide from the nitrile using Rhodococcus equi
JP2720140B2 (ja) * 1993-02-03 1998-02-25 日東化学工業株式会社 フェニル基を有する光学活性α−ヒドロキシカルボン酸の製造法
JP3218133B2 (ja) * 1993-02-03 2001-10-15 三菱レイヨン株式会社 フェニル基を有する光学活性α−ヒドロキシカルボン酸の製造法
US5597716A (en) * 1993-11-18 1997-01-28 Mitsubishi Rayon Co., Ltd. Process for producing D-lactic acid and L-lactamide
CA2150526C (en) * 1994-06-09 2005-11-15 Andreas Kiener Biotechnological process for the preparation of cyclic s-.alpha.-amino carboxylic acids and r-.alpha.-amino carboxamides
JP3235934B2 (ja) 1994-08-04 2001-12-04 三菱レイヨン株式会社 ロドコッカス属細菌由来カナマイシン耐性遺伝子
ES2126313T3 (es) * 1994-09-22 1999-03-16 Rhone Poulenc Nutrition Animal Hidrolisis enzimatica de los 4-metiltiobutironitrilos.
FR2724931B1 (fr) * 1994-09-22 1996-12-20 Rhone Poulenc Nutrition Animal Hydrolyse enzymatique des 4-methylthiobutyronitrile
EP0773297B2 (de) 1995-11-10 2008-04-23 Mitsubishi Rayon Co., Ltd. Verfahren zur Herstellung einer alpha-Hydroxy-säure oder eines alpha-Hydroxy-amids mittels Mikroorganismen
JPH10179183A (ja) * 1996-12-20 1998-07-07 Daicel Chem Ind Ltd カルボン酸の製造方法
US5866379A (en) * 1997-01-28 1999-02-02 Novus International Enzymatic conversion of α-hydroxynitriles to the corresponding .alpha.
DE19848129A1 (de) 1998-10-19 2000-04-20 Basf Ag Verfahren zur Herstellung chiraler Carbonsäuren aus Nitrilen mit Hilfe einer Nitrilase oder Mikroorganismen, die ein Gen für die Nitrilase enthalten
DE60042364D1 (de) * 1999-04-16 2009-07-23 Mitsubishi Rayon Co Neue amidasegene
DE10010149A1 (de) * 2000-03-03 2001-09-06 Basf Ag Nitrilase aus Rhodococcus rhodochrous NCIMB 11216
JP4544695B2 (ja) * 2000-04-28 2010-09-15 旭化成ケミカルズ株式会社 グリシンの微生物学的な製造法
FR2822460B1 (fr) * 2001-03-26 2005-04-29 Rhodia Chimie Sa Procede de preparation enantioselectif d'acides carboxyliques optiquement actifs par hydrolyse enzymatique de nitriles
JP4584242B2 (ja) 2003-02-27 2010-11-17 ビーエーエスエフ ソシエタス・ヨーロピア 改変されたニトリラーゼおよびカルボン酸の製造方法におけるその使用
JP4493011B2 (ja) * 2004-06-11 2010-06-30 三菱レイヨン株式会社 ロドコッカス属細菌由来トリメトプリム耐性ジヒドロ葉酸還元酵素及びその遺伝子
GB0413322D0 (en) * 2004-06-15 2004-07-14 Avecia Ltd Process
JP4929700B2 (ja) * 2005-12-15 2012-05-09 住友化学株式会社 カルボン酸の製造法
JP2007295821A (ja) * 2006-04-28 2007-11-15 Asahi Kasei Chemicals Corp 生体触媒を用いたα−ヒドロキシ酸或いはα−ヒドロキシ酸アンモニウムの製造方法
EP1881077A1 (de) * 2006-07-19 2008-01-23 Solvay Organics GmbH Verfahren zur Herstellung von fluorhaltigen alpha-Hydroxycarbonsäuren
EP2574667A1 (de) 2011-10-02 2013-04-03 Technische Universität Graz Enzymvarianten
CN114236024B (zh) * 2021-12-07 2023-12-29 江苏宝众宝达药业股份有限公司 一种同时测定4-氟-3-硝基苯腈及其异构体含量的方法
CN117050922B (zh) * 2023-10-11 2023-12-08 江苏聚庚科技股份有限公司 一种含氟苯腈类化合物降解菌及其在环境治理中的应用

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR1342844A (fr) * 1961-09-16 1963-11-15 Bayer Ag Procédé de préparation d'acides phénoxyacétiques substitués, optiquement actifs
JPS5414668B2 (de) * 1972-09-05 1979-06-08
DK261685A (da) * 1985-06-11 1986-12-12 Novo Industri As Fremgangsmaade til fremstilling af optisk aktive, organiske forbindelser
JPS6255098A (ja) * 1985-09-04 1987-03-10 Nitto Chem Ind Co Ltd 光学活性α−オキシ酸の製造法
FR2626289B1 (fr) * 1988-01-27 1990-06-08 Rhone Poulenc Sante Procede de preparation d'acides aryl-2 alkanoiques optiquement actifs
FR2626288B1 (de) * 1988-01-27 1990-05-18 Rhone Poulenc Sante
FR2631975B1 (fr) * 1988-05-26 1990-11-30 Rhone Poulenc Chimie Procede de preparation d'acides aryloxy-2 ou arylthio-2 alkanoiques optiquement actifs

Also Published As

Publication number Publication date
EP0348901A3 (de) 1991-07-24
JP2623345B2 (ja) 1997-06-25
EP0348901B1 (de) 1995-12-06
JPH0284198A (ja) 1990-03-26
DE68925002D1 (de) 1996-01-18
DK314989D0 (da) 1989-06-26
DK314989A (da) 1989-12-28
EP0348901A2 (de) 1990-01-03

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Legal Events

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8364 No opposition during term of opposition
8339 Ceased/non-payment of the annual fee