NO20011912L - Fremgangsmåte for fremstilling av kirale karboksylsyrer fra nitriler ved hjelp av en nitrilase eller mikroorganismer sominneholder et gen for nitrilasen - Google Patents

Fremgangsmåte for fremstilling av kirale karboksylsyrer fra nitriler ved hjelp av en nitrilase eller mikroorganismer sominneholder et gen for nitrilasen

Info

Publication number
NO20011912L
NO20011912L NO20011912A NO20011912A NO20011912L NO 20011912 L NO20011912 L NO 20011912L NO 20011912 A NO20011912 A NO 20011912A NO 20011912 A NO20011912 A NO 20011912A NO 20011912 L NO20011912 L NO 20011912L
Authority
NO
Norway
Prior art keywords
nucleic acid
nitrilase
acid sequences
carboxylic acids
nitriles
Prior art date
Application number
NO20011912A
Other languages
English (en)
Other versions
NO327857B1 (no
NO20011912D0 (no
Inventor
Marion Ress-Loeschke
Thomas Friedrich
Bernhard Hauer
Ralf Mattes
Dirk Engels
Original Assignee
Basf Ag
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 Basf Ag filed Critical Basf Ag
Publication of NO20011912L publication Critical patent/NO20011912L/no
Publication of NO20011912D0 publication Critical patent/NO20011912D0/no
Publication of NO327857B1 publication Critical patent/NO327857B1/no

Links

Classifications

    • 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
    • C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09—Recombinant DNA-technology
    • C12N15/11—DNA or RNA fragments; Modified forms thereof; Non-coding nucleic acids having a biological activity
    • C12N15/52—Genes encoding for enzymes or proenzymes
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H21/00—Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic 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
    • 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
    • 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
    • C12P7/42—Hydroxy-carboxylic acids

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Genetics & Genomics (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Biochemistry (AREA)
  • Biotechnology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Health & Medical Sciences (AREA)
  • Molecular Biology (AREA)
  • General Engineering & Computer Science (AREA)
  • Microbiology (AREA)
  • Biomedical Technology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Analytical Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • Biophysics (AREA)
  • Plant Pathology (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Micro-Organisms Or Cultivation Processes Thereof (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Enzymes And Modification Thereof (AREA)
NO20011912A 1998-10-19 2001-04-18 Isolert nukleinsyresekvens kodende for et polypeptid med nitrilaseaktivitet, aminosyresekvens, nukleinsyrekonstruksjon, vektor, mikroorganisme samt fremgangsmate for fremstilling av chirale karboksylsyrer. NO327857B1 (no)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE19848129A DE19848129A1 (de) 1998-10-19 1998-10-19 Verfahren zur Herstellung chiraler Carbonsäuren aus Nitrilen mit Hilfe einer Nitrilase oder Mikroorganismen, die ein Gen für die Nitrilase enthalten
PCT/EP1999/007679 WO2000023577A1 (de) 1998-10-19 1999-10-13 Verfahren zur herstellung chiraler carbonsäuren aus nitrilen mit hilfe einer nitrilase oder mikroorganismen, die ein gen für die nitrilase enthalten

Publications (3)

Publication Number Publication Date
NO20011912L true NO20011912L (no) 2001-04-18
NO20011912D0 NO20011912D0 (no) 2001-04-18
NO327857B1 NO327857B1 (no) 2009-10-05

Family

ID=7884933

Family Applications (1)

Application Number Title Priority Date Filing Date
NO20011912A NO327857B1 (no) 1998-10-19 2001-04-18 Isolert nukleinsyresekvens kodende for et polypeptid med nitrilaseaktivitet, aminosyresekvens, nukleinsyrekonstruksjon, vektor, mikroorganisme samt fremgangsmate for fremstilling av chirale karboksylsyrer.

Country Status (21)

Country Link
US (1) US6869783B1 (no)
EP (1) EP1123386B1 (no)
JP (1) JP4489298B2 (no)
KR (1) KR100715744B1 (no)
CN (1) CN100422319C (no)
AT (1) ATE349517T1 (no)
AU (1) AU765480B2 (no)
BR (1) BR9914629A (no)
CA (1) CA2347521C (no)
CZ (1) CZ302494B6 (no)
DE (2) DE19848129A1 (no)
DK (1) DK1123386T3 (no)
EE (1) EE05008B1 (no)
ES (1) ES2280125T3 (no)
HU (1) HU228092B1 (no)
ID (1) ID29136A (no)
IL (2) IL142397A0 (no)
NO (1) NO327857B1 (no)
PT (1) PT1123386E (no)
WO (1) WO2000023577A1 (no)
ZA (1) ZA200104066B (no)

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US20040002147A1 (en) * 1999-12-29 2004-01-01 Desantis Grace Nitrilases
DE10010149A1 (de) * 2000-03-03 2001-09-06 Basf Ag Nitrilase aus Rhodococcus rhodochrous NCIMB 11216
US6562603B2 (en) 2000-08-04 2003-05-13 E. I. Du Pont De Nemours And Company 3-hydroxycarboxylic acid production and use in branched polymers
US6455730B1 (en) 2000-08-04 2002-09-24 E. I. Du Pont De Nemours & Company Preparation of dicarboxylic acid monoesters from cyanocarboxylic acid esters
WO2002029079A2 (en) * 2000-10-04 2002-04-11 Maxygen, Inc. Enantioselective production of amino carboxylic acids
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
EP2039762A3 (en) 2001-06-21 2009-07-29 Verenium Corporation Nitralases
ITMI20011826A1 (it) * 2001-08-30 2003-03-02 Istituto Biochimico Italiano Microorganismo dotato di attivita' nitrile-idratasica/amidasica enantioselettiva e regioselettiva
ES2288630T3 (es) 2002-12-02 2008-01-16 Basf Aktiengesellschaft Sistema de expresion, que puede ser inducido por medio de la l-ramnosa.
US8815569B2 (en) 2003-01-08 2014-08-26 Basf Se Methods for preserving and/or storing cells having a nitrilase or nitrile hydratase activity
AT412092B (de) * 2003-02-27 2004-09-27 Dsm Fine Chem Austria Gmbh Verfahren zur herstellung chiraler alpha-hydroxycarbonsäuren durch enzymatische hydrolyse von chiralen cyanhydrinen
EP1599584B1 (en) * 2003-02-27 2009-07-01 Basf Se Modified nitrilases and their use in methods for the production of carboxylic acids
CN102796770B (zh) * 2004-12-22 2014-06-04 纳幕尔杜邦公司 乙醇酸的酶促生产
US20100267100A1 (en) * 2007-03-21 2010-10-21 Ling Hua Enzymatic synthesis of optically pure beta-hydroxy carboxylic acids and their derivatives
US20090004720A1 (en) * 2007-06-26 2009-01-01 Ling Hua Smart Biocatalysts For Organic Synthesis
EP2338987A1 (en) * 2009-11-16 2011-06-29 ZYRUS Beteiligungsgesellschaft mbH & Co. Patente I KG Whole cell biocatalyst
JP2013162746A (ja) * 2010-05-24 2013-08-22 Mitsui Chemicals Inc アミド化合物の製造方法
WO2012069434A1 (de) 2010-11-24 2012-05-31 Basf Se Verfahren zur herstellung n-heterozyklischer optisch aktiver alkohole
KR101223665B1 (ko) * 2011-01-26 2013-01-17 재단법인 경북해양바이오산업연구원 나이트릴레이즈 rmn2을 이용한 카르복실산의 제조방법
KR101223664B1 (ko) * 2011-01-26 2013-01-17 재단법인 경북해양바이오산업연구원 나이트릴레이즈 rmn1을 이용한 카르복실산의 제조방법
KR101223663B1 (ko) * 2011-01-26 2013-01-21 재단법인 경북해양바이오산업연구원 나이트릴레이즈 vmn1을 이용한 카르복실산의 제조방법
KR101223666B1 (ko) * 2011-01-26 2013-01-17 재단법인 경북해양바이오산업연구원 나이트릴레이즈 orn을 이용한 카르복실산의 제조방법
JP2023526068A (ja) 2020-05-15 2023-06-20 ビーエーエスエフ ソシエタス・ヨーロピア イソプレノイド生成の改善方法
JP2024545115A (ja) 2021-12-10 2024-12-05 ビーエーエスエフ ソシエタス・ヨーロピア アルキルホスフィナートの除草活性
EP4444731A1 (en) 2021-12-10 2024-10-16 Basf Se Enzymatic decarbamoylation of glufosinate derivatives
IL313405A (en) 2021-12-10 2024-08-01 Basf Se Synthesis of glufosinate using a hydantoinase-based process
EP4634395A1 (en) 2022-12-16 2025-10-22 Basf Se New ethylenediamine-n,n'-disuccinic acid (edds) synthases
CN121335908A (zh) 2023-06-13 2026-01-13 巴斯夫欧洲公司 使用基于酰胺酶的工艺的草铵膦合成
WO2025104224A1 (en) 2023-11-17 2025-05-22 Basf Se Edds synthase variants
CN122422291A (zh) 2023-11-17 2026-07-17 巴斯夫欧洲公司 S,s-乙二胺-n,n’-二琥珀酸的结晶形式、相应制备方法及用途
EP4556568A1 (en) 2023-11-17 2025-05-21 Basf Se Biocatalytical methods for producing ethylenediamine-n,n'-disuccinic acid
WO2025219238A1 (en) 2024-04-15 2025-10-23 Basf Se Process for producing l-glufosinate from a diol or diol derivative
WO2025219237A1 (en) 2024-04-15 2025-10-23 Basf Se A process for the preparation of 2-oxo-4-(hydroxy(methyl)phosphinoyl)butyric acid

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US5283193A (en) 1988-06-27 1994-02-01 Asahi Kasei Kogyo K.K. Process for producing optically active α-substituted organic acid and microorganism and enzyme used therefor
JP2623345B2 (ja) 1988-06-27 1997-06-25 旭化成工業株式会社 光学活性なα―置換有機酸の製造方法
JPH0219577A (ja) 1988-07-04 1990-01-23 Nippon Saafuakutanto Kogyo Kk 反応染料用均染剤組成物
DE69131217T2 (de) * 1990-03-30 1999-09-23 Mitsubishi Rayon Co., Ltd. Verfahren zur Herstellung von R(-)Mandelsäure und deren Derivaten
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
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Also Published As

Publication number Publication date
KR100715744B1 (ko) 2007-05-08
ZA200104066B (en) 2002-07-01
HUP0104802A2 (hu) 2002-04-29
DE19848129A1 (de) 2000-04-20
ATE349517T1 (de) 2007-01-15
IL142397A0 (en) 2002-03-10
CA2347521A1 (en) 2000-04-27
PT1123386E (pt) 2007-03-30
CN1331743A (zh) 2002-01-16
EP1123386A1 (de) 2001-08-16
EE200100232A (et) 2002-08-15
AU6470899A (en) 2000-05-08
CA2347521C (en) 2010-02-23
NO327857B1 (no) 2009-10-05
AU765480B2 (en) 2003-09-18
ES2280125T3 (es) 2007-09-01
CZ20011382A3 (cs) 2002-03-13
HUP0104802A3 (en) 2005-10-28
EE05008B1 (et) 2008-04-15
US6869783B1 (en) 2005-03-22
KR20010085938A (ko) 2001-09-07
CZ302494B6 (cs) 2011-06-15
HU228092B1 (en) 2012-10-29
WO2000023577A1 (de) 2000-04-27
JP2002527106A (ja) 2002-08-27
DE59914102D1 (de) 2007-02-08
IL142397A (en) 2008-03-20
DK1123386T3 (da) 2007-05-07
ID29136A (id) 2001-08-02
CN100422319C (zh) 2008-10-01
BR9914629A (pt) 2001-06-26
NO20011912D0 (no) 2001-04-18
JP4489298B2 (ja) 2010-06-23
EP1123386B1 (de) 2006-12-27

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