HUP0101056A3 - Improvements in the enzymatic synthesis of chiral amines - Google Patents

Improvements in the enzymatic synthesis of chiral amines

Info

Publication number
HUP0101056A3
HUP0101056A3 HU0101056A HUP0101056A HUP0101056A3 HU P0101056 A3 HUP0101056 A3 HU P0101056A3 HU 0101056 A HU0101056 A HU 0101056A HU P0101056 A HUP0101056 A HU P0101056A HU P0101056 A3 HUP0101056 A3 HU P0101056A3
Authority
HU
Hungary
Prior art keywords
enzymatic synthesis
chiral amines
chiral
amines
enzymatic
Prior art date
Application number
HU0101056A
Other languages
English (en)
Original Assignee
Celgro Annandale
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 Celgro Annandale filed Critical Celgro Annandale
Publication of HUP0101056A2 publication Critical patent/HUP0101056A2/hu
Publication of HUP0101056A3 publication Critical patent/HUP0101056A3/hu

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
    • C12P13/00Preparation of nitrogen-containing organic compounds
    • 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
    • C12P13/001Amines; Imines
    • 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
    • C12P13/005Amino acids other than alpha- or beta amino acids, e.g. gamma amino acids
    • 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
    • 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
    • C12P13/06Alanine; Leucine; Isoleucine; Serine; Homoserine
    • 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
    • C12P13/12Methionine; Cysteine; Cystine
    • 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

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)
  • General Engineering & Computer Science (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Biotechnology (AREA)
  • Biochemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Microbiology (AREA)
  • General Health & Medical Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Analytical Chemistry (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
HU0101056A 1998-03-11 1999-03-10 Improvements in the enzymatic synthesis of chiral amines HUP0101056A3 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US7752098P 1998-03-11 1998-03-11
PCT/US1999/005150 WO1999046398A1 (en) 1998-03-11 1999-03-10 Improvements in the enzymatic synthesis of chiral amines

Publications (2)

Publication Number Publication Date
HUP0101056A2 HUP0101056A2 (hu) 2001-07-30
HUP0101056A3 true HUP0101056A3 (en) 2006-03-28

Family

ID=22138554

Family Applications (1)

Application Number Title Priority Date Filing Date
HU0101056A HUP0101056A3 (en) 1998-03-11 1999-03-10 Improvements in the enzymatic synthesis of chiral amines

Country Status (24)

Country Link
EP (1) EP1075534B8 (hu)
JP (1) JP2002505884A (hu)
KR (1) KR20010034561A (hu)
CN (1) CN1154746C (hu)
AT (1) ATE295424T1 (hu)
AU (1) AU753904B2 (hu)
BR (1) BR9908797A (hu)
CA (1) CA2322605A1 (hu)
CZ (1) CZ295882B6 (hu)
DE (1) DE69925267T2 (hu)
ES (1) ES2243051T3 (hu)
FI (1) FI20001805A (hu)
HK (1) HK1035000A1 (hu)
HU (1) HUP0101056A3 (hu)
MX (1) MXPA00008573A (hu)
NO (1) NO319671B1 (hu)
NZ (1) NZ506405A (hu)
PL (1) PL342882A1 (hu)
PT (1) PT1075534E (hu)
RU (1) RU2213142C2 (hu)
SK (1) SK284352B6 (hu)
TR (1) TR200002604T2 (hu)
UA (1) UA64784C2 (hu)
WO (1) WO1999046398A1 (hu)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1038953B1 (en) * 1999-03-19 2004-09-22 Sumitomo Chemical Company, Limited Stereoselective transaminase, gene encoding said protein and use thereof
JP2001190298A (ja) * 2000-01-13 2001-07-17 Kanegafuchi Chem Ind Co Ltd 光学活性n−メチルアミノ酸の製造方法
EP1818411A1 (en) * 2006-02-13 2007-08-15 Lonza AG Process for the preparation of optically active chiral amines
DE102007042600A1 (de) 2007-09-07 2009-03-12 Evonik Degussa Gmbh Verfahren zur Herstellung von enantiomerenangereichten Aminen
SG172891A1 (en) 2009-01-08 2011-08-29 Codexis Inc Transaminase polypeptides
JP5707344B2 (ja) 2009-02-26 2015-04-30 コデクシス, インコーポレイテッド トランスアミナーゼ生体触媒
CN102597226B (zh) 2009-06-22 2015-08-19 科德克希思公司 转氨酶反应
ES2599644T3 (es) * 2009-09-02 2017-02-02 Lonza Ag Un proceso para la identificación y preparación de una omega-transaminasa (R)-específica
US8852900B2 (en) 2010-06-17 2014-10-07 Codexis, Inc. Biocatalysts and methods for the synthesis of (S)-3-(1-aminoethyl)-phenol
US8932836B2 (en) 2010-08-16 2015-01-13 Codexis, Inc. Biocatalysts and methods for the synthesis of (1R,2R)-2-(3,4-dimethoxyphenethoxy)cyclohexanamine
JP6275642B2 (ja) * 2011-08-16 2018-02-07 エンバイオ・リミテツド 光学活性キラルアミンの酵素的合成
CN104630170A (zh) * 2013-11-08 2015-05-20 中国科学院天津工业生物技术研究所 一种来源于里氏木霉的新(r)-转氨酶及其应用
CN114134126B (zh) * 2021-10-28 2023-12-05 浙江大学杭州国际科创中心 转氨酶及其突变体在制备(s)-1-甲氧基-2-丙胺中的应用

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5300437A (en) * 1989-06-22 1994-04-05 Celgene Corporation Enantiomeric enrichment and stereoselective synthesis of chiral amines
DE69635082T2 (de) * 1995-10-23 2006-06-01 Kaneka Corp. Verfahren zur herstellung optisch aktiver aminoverbindungen

Also Published As

Publication number Publication date
EP1075534A1 (en) 2001-02-14
RU2213142C2 (ru) 2003-09-27
BR9908797A (pt) 2000-12-12
CA2322605A1 (en) 1999-09-16
NO20004036L (no) 2000-10-27
WO1999046398A1 (en) 1999-09-16
EP1075534A4 (en) 2003-07-09
NO319671B1 (no) 2005-09-05
DE69925267T2 (de) 2006-01-26
JP2002505884A (ja) 2002-02-26
PL342882A1 (en) 2001-07-16
AU2993899A (en) 1999-09-27
ATE295424T1 (de) 2005-05-15
HK1035000A1 (en) 2001-11-09
ES2243051T3 (es) 2005-11-16
CZ20003177A3 (cs) 2000-12-13
UA64784C2 (en) 2004-03-15
AU753904B2 (en) 2002-10-31
CN1154746C (zh) 2004-06-23
HUP0101056A2 (hu) 2001-07-30
KR20010034561A (ko) 2001-04-25
CN1292828A (zh) 2001-04-25
FI20001805A (fi) 2000-08-15
EP1075534B1 (en) 2005-05-11
PT1075534E (pt) 2005-09-30
SK13382000A3 (sk) 2001-05-10
MXPA00008573A (es) 2003-07-14
CZ295882B6 (cs) 2005-11-16
SK284352B6 (sk) 2005-02-04
NO20004036D0 (no) 2000-08-11
DE69925267D1 (de) 2005-06-16
EP1075534B8 (en) 2005-07-06
NZ506405A (en) 2003-08-29
TR200002604T2 (tr) 2000-11-21

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Legal Events

Date Code Title Description
FD9A Lapse of provisional protection due to non-payment of fees