ATE141952T1 - Enzymkatalysiertes verfahren zur herstellung von optisch aktiven karbonsäuren - Google Patents

Enzymkatalysiertes verfahren zur herstellung von optisch aktiven karbonsäuren

Info

Publication number
ATE141952T1
ATE141952T1 AT92200030T AT92200030T ATE141952T1 AT E141952 T1 ATE141952 T1 AT E141952T1 AT 92200030 T AT92200030 T AT 92200030T AT 92200030 T AT92200030 T AT 92200030T AT E141952 T1 ATE141952 T1 AT E141952T1
Authority
AT
Austria
Prior art keywords
carboxylic acid
carboxic
acids
optically active
enzyme
Prior art date
Application number
AT92200030T
Other languages
English (en)
Inventor
Dooren Theodorus Johannes Van
Den Tweel Wilhelmus Johann Van
Original Assignee
Dsm Nv
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 Nv filed Critical Dsm Nv
Application granted granted Critical
Publication of ATE141952T1 publication Critical patent/ATE141952T1/de

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12PFERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P41/00Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture
    • C12P41/006Processes 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
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12PFERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P13/00Preparation of nitrogen-containing organic compounds
    • C12P13/04Alpha- or beta- amino acids
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S435/00Chemistry: molecular biology and microbiology
    • Y10S435/8215Microorganisms
    • Y10S435/822Microorganisms using bacteria or actinomycetales
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S435/00Chemistry: molecular biology and microbiology
    • Y10S435/8215Microorganisms
    • Y10S435/822Microorganisms using bacteria or actinomycetales
    • Y10S435/824Achromobacter

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Zoology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Wood Science & Technology (AREA)
  • Biotechnology (AREA)
  • Microbiology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Health & Medical Sciences (AREA)
  • Biochemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Analytical Chemistry (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
AT92200030T 1991-01-11 1992-01-07 Enzymkatalysiertes verfahren zur herstellung von optisch aktiven karbonsäuren ATE141952T1 (de)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
NL9100038A NL9100038A (nl) 1991-01-11 1991-01-11 Enzym-gekatalyseerde bereiding van optisch aktieve carbonzuren.

Publications (1)

Publication Number Publication Date
ATE141952T1 true ATE141952T1 (de) 1996-09-15

Family

ID=19858714

Family Applications (1)

Application Number Title Priority Date Filing Date
AT92200030T ATE141952T1 (de) 1991-01-11 1992-01-07 Enzymkatalysiertes verfahren zur herstellung von optisch aktiven karbonsäuren

Country Status (9)

Country Link
US (1) US5248608A (de)
EP (1) EP0494716B1 (de)
JP (1) JP3135653B2 (de)
AT (1) ATE141952T1 (de)
CA (1) CA2059075A1 (de)
DE (1) DE69213033T2 (de)
DK (1) DK0494716T3 (de)
ES (1) ES2093764T3 (de)
NL (1) NL9100038A (de)

Families Citing this family (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1995016786A1 (en) * 1993-12-17 1995-06-22 Dsm N.V. Phenylserine amides and the preparation of phenylserines/phenylserine amides
US6551618B2 (en) 1994-03-15 2003-04-22 University Of Birmingham Compositions and methods for delivery of agents for neuronal regeneration and survival
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
WO1995034525A1 (fr) * 1994-06-13 1995-12-21 Mitsubishi Rayon Co., Ltd. DERIVE D'ACIDE CARBOXYLIQUE OPTIQUEMENT ACTIF A SUBSTITUTION α ET PROCEDE DE PRODUCTION DUDIT DERIVE
WO1997044480A1 (de) 1996-05-20 1997-11-27 Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. Enzymatische synthese optisch aktiver hydroxamsäuren und ihre umsetzung zu optisch aktiven primären aminen durch lossen-umlagerung
DE19634446A1 (de) * 1996-05-20 1997-11-27 Fraunhofer Ges Forschung Enzymatische Synthese optisch aktiver Hydroxamsäuren und ihre Umsetzung zu optisch aktiven primären Aminen durch Lossen-Umlagerung
GB9615852D0 (en) 1996-07-29 1996-09-11 Allied Colloids Ltd Production of amino acids and enzymes used therefor
CA2272554C (en) * 1996-11-22 2001-08-28 Pioneer Hi-Bred International, Inc. Moniliformin detoxification compositions and methods
WO2000063354A1 (en) 1999-04-16 2000-10-26 Mitsubishi Rayon Co., Ltd. Novel amidase gene
US7732404B2 (en) 1999-12-30 2010-06-08 Dexcel Ltd Pro-nanodispersion for the delivery of cyclosporin
EP1170375A3 (de) * 2000-06-27 2002-01-16 Nissan Chemical Industries Ltd. Mikrobielles Umwandlungsverfahren für hydroxyaromatische Verbindungen
JP3951126B2 (ja) 2000-12-11 2007-08-01 三菱瓦斯化学株式会社 光学活性(4r)−1,3−チアゾリジン−4−カルボン酸の製造方法
ATE365216T1 (de) 2001-07-23 2007-07-15 Dsm Ip Assets Bv Nucleinsäuresequenzen kodierend für enantioselektive amidasen
ATE362544T1 (de) * 2002-06-14 2007-06-15 Dsm Ip Assets Bv Polypeptide mit alpha-h alpha amino acid amide racemase aktivitität und nukleinsäuren kodierend dafür
ES2552226T3 (es) 2003-06-27 2015-11-26 DePuy Synthes Products, Inc. Reparación y regeneración de cartílago y hueso utilizando células derivadas posparto
US9572840B2 (en) 2003-06-27 2017-02-21 DePuy Synthes Products, Inc. Regeneration and repair of neural tissue using postpartum-derived cells
US8790637B2 (en) 2003-06-27 2014-07-29 DePuy Synthes Products, LLC Repair and regeneration of ocular tissue using postpartum-derived cells
US20060223177A1 (en) 2003-06-27 2006-10-05 Ethicon Inc. Postpartum cells derived from umbilical cord tissue, and methods of making and using the same
US9592258B2 (en) 2003-06-27 2017-03-14 DePuy Synthes Products, Inc. Treatment of neurological injury by administration of human umbilical cord tissue-derived cells
JP5289970B2 (ja) 2005-12-16 2013-09-11 エシコン・インコーポレイテッド 組織適合性不適合な移植における逆免疫反応を抑制するための組成物および方法
US9125906B2 (en) 2005-12-28 2015-09-08 DePuy Synthes Products, Inc. Treatment of peripheral vascular disease using umbilical cord tissue-derived cells
EP2089511B1 (de) 2006-11-13 2014-09-17 DePuy Synthes Products, LLC In-vitro-expansion von postpartalen zellen mittels mikroträgern
CN107028983A (zh) * 2008-12-19 2017-08-11 德普伊新特斯产品有限责任公司 肺部疾病和病症的治疗
US10179900B2 (en) 2008-12-19 2019-01-15 DePuy Synthes Products, Inc. Conditioned media and methods of making a conditioned media
US8722034B2 (en) 2009-03-26 2014-05-13 Depuy Synthes Products Llc hUTC as therapy for Alzheimer's disease
US20120329107A1 (en) * 2009-12-04 2012-12-27 Mitsubishi Gas Chemical Company, Inc. Method for preparing optically active amino acids and optically active amino acid amides

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5713000A (en) * 1980-06-24 1982-01-22 Ube Ind Ltd Preparation of optical active tryptophane
JPS57186495A (en) * 1981-05-14 1982-11-16 Ube Ind Ltd Preparation of l-alpha-methylphenylalanine
DE3683512D1 (de) * 1985-02-25 1992-03-05 Mitsubishi Gas Chemical Co Verfahren zur optischen isomerisierung von optisch aktiver aminosaeure und verfahren zur herstellung von optisch aktiver aminosaeure.
JPS6255097A (ja) * 1985-09-04 1987-03-10 Nitto Chem Ind Co Ltd L−アミノ酸の製造法
EP0383403A1 (de) * 1989-02-16 1990-08-22 Stamicarbon B.V. Verfahren zur Herstellung von organischen chemischen Produkten

Also Published As

Publication number Publication date
DE69213033T2 (de) 1997-04-03
DK0494716T3 (de) 1997-02-10
US5248608A (en) 1993-09-28
JPH0530992A (ja) 1993-02-09
ES2093764T3 (es) 1997-01-01
EP0494716A3 (en) 1992-10-07
NL9100038A (nl) 1992-08-03
CA2059075A1 (en) 1992-07-12
EP0494716B1 (de) 1996-08-28
DE69213033D1 (de) 1996-10-02
JP3135653B2 (ja) 2001-02-19
EP0494716A2 (de) 1992-07-15

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Legal Events

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UEP Publication of translation of european patent specification
REN Ceased due to non-payment of the annual fee