HUP9801621A2 - Új eszteráz és eljárás optikailag aktív chromanvegyületek előállítására - Google Patents
Új eszteráz és eljárás optikailag aktív chromanvegyületek előállításáraInfo
- Publication number
- HUP9801621A2 HUP9801621A2 HU9801621A HUP9801621A HUP9801621A2 HU P9801621 A2 HUP9801621 A2 HU P9801621A2 HU 9801621 A HU9801621 A HU 9801621A HU P9801621 A HUP9801621 A HU P9801621A HU P9801621 A2 HUP9801621 A2 HU P9801621A2
- Authority
- HU
- Hungary
- Prior art keywords
- esterase
- optically active
- production
- acetic acid
- methods
- Prior art date
Links
- 108090000371 Esterases Proteins 0.000 title abstract 5
- 238000000034 method Methods 0.000 title abstract 3
- 238000004519 manufacturing process Methods 0.000 title abstract 2
- VZWXIQHBIQLMPN-UHFFFAOYSA-N chromane Chemical class C1=CC=C2CCCOC2=C1 VZWXIQHBIQLMPN-UHFFFAOYSA-N 0.000 title 1
- KGDUETQEJCATNN-UHFFFAOYSA-N 2-(3,4-dihydro-2h-chromen-3-yl)acetic acid Chemical compound C1=CC=C2CC(CC(=O)O)COC2=C1 KGDUETQEJCATNN-UHFFFAOYSA-N 0.000 abstract 2
- 239000000843 powder Substances 0.000 abstract 2
- KGDUETQEJCATNN-QMMMGPOBSA-N 2-[(3s)-3,4-dihydro-2h-chromen-3-yl]acetic acid Chemical class C1=CC=C2C[C@@H](CC(=O)O)COC2=C1 KGDUETQEJCATNN-QMMMGPOBSA-N 0.000 abstract 1
- 241000894006 Bacteria Species 0.000 abstract 1
- 108090000790 Enzymes Proteins 0.000 abstract 1
- 102000004190 Enzymes Human genes 0.000 abstract 1
- 108090000604 Hydrolases Proteins 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 150000001412 amines Chemical class 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- 244000005700 microbiome Species 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
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
- C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
- C12N9/14—Hydrolases (3)
- C12N9/16—Hydrolases (3) acting on ester bonds (3.1)
-
- 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
- C12N9/14—Hydrolases (3)
- C12N9/16—Hydrolases (3) acting on ester bonds (3.1)
- C12N9/18—Carboxylic ester hydrolases (3.1.1)
-
- 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
- C12P17/06—Oxygen as only ring hetero atoms containing a six-membered hetero ring, e.g. fluorescein
-
- 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
- C12P41/003—Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture by ester formation, lactone formation or the inverse reactions
- C12P41/005—Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture by ester formation, lactone formation or the inverse reactions by esterification of carboxylic acid groups in the enantiomers or the inverse reaction
-
- 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
- C12P41/003—Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture by ester formation, lactone formation or the inverse reactions
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Zoology (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Microbiology (AREA)
- Biotechnology (AREA)
- Biochemistry (AREA)
- General Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Biomedical Technology (AREA)
- Molecular Biology (AREA)
- Medicinal Chemistry (AREA)
- Analytical Chemistry (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Enzymes And Modification Thereof (AREA)
Abstract
A találmány szerinti eljárással őptikailag aktív krőmán-3-ecetsavat ésőptikailag aktív krőmán-3-ecetsav-észtereket lehet előállítani úgy,hőgy ha az (I) általánős képletű (3R)- és (3S)-krőmán-3-ecetsav-észterek keverékét - a képletben R1 jelentése 1-5 szénatőmős, egyenes vagy elágazó láncú alkilcsőpőrt,az R2 jelentése hidrőgénatőm vagy szűbsztitűált vagy szűbsztitűálatlanaminőcsőpőrt - őptikailag szelektív hidrőlízisaktivitással rendelkezőészter-hidrőlázzal, vagy az észterázt tartalmazó mikrőőrganizműsőkkal,vagy az abból készült enzimpreparátűmmal kezelik. szterázkéntelőnyösen Pseűdőnőcardia nemzetséghez tartőzó baktériűmból származó,új észterázt alkalmaznak. A találmány tárgyát képezi a fent említettúj észteráz és előállítására vőnatkőzó eljárás. ŕ
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP19394997 | 1997-07-18 | ||
JP21975897 | 1997-08-01 | ||
JP31999597 | 1997-11-20 |
Publications (3)
Publication Number | Publication Date |
---|---|
HU9801621D0 HU9801621D0 (en) | 1998-09-28 |
HUP9801621A2 true HUP9801621A2 (hu) | 1999-08-30 |
HUP9801621A3 HUP9801621A3 (en) | 2001-08-28 |
Family
ID=27326840
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
HU9801621A HUP9801621A3 (en) | 1997-07-18 | 1998-07-17 | Novel esterase and methods for the production of optically active chroman compounds |
Country Status (6)
Country | Link |
---|---|
US (2) | US6060290A (hu) |
EP (1) | EP0892044B1 (hu) |
KR (1) | KR100300443B1 (hu) |
CN (1) | CN1218110A (hu) |
DE (1) | DE69828338T2 (hu) |
HU (1) | HUP9801621A3 (hu) |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0892044B1 (en) * | 1997-07-18 | 2004-12-29 | Mitsui Chemicals, Inc. | Esterase and its use for the production of optically active chroman compounds |
KR20030012964A (ko) * | 2001-08-06 | 2003-02-14 | 주식회사 제노포커스 | 광학활성 α-치환 헤테로시클릭카르복실산 에스테르의제조방법 |
WO2008000738A1 (de) | 2006-06-27 | 2008-01-03 | Basf Se | Proteine mit esterase-aktivität |
NO2171061T3 (hu) * | 2007-07-04 | 2018-02-24 | ||
US8206969B2 (en) | 2007-12-20 | 2012-06-26 | Basf Se | CALB muteins and their use |
CN101979528B (zh) * | 2010-10-21 | 2012-05-30 | 北京农业生物技术研究中心 | 一种酯酶及其编码基因与应用 |
EP3572523A1 (en) * | 2018-05-25 | 2019-11-27 | Bayer Aktiengesellschaft | Novel carboxyesterhydrolases |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE4430089A1 (de) * | 1994-08-25 | 1996-02-29 | Bayer Ag | Verfahren zur enzymatischen Herstellung von enantiomerenreinen Chroman-2-carbonsäuren und deren Derivaten |
US5658796A (en) * | 1995-06-07 | 1997-08-19 | Seprachem, Inc. | Optical resolution of alkyl chroman-2-carboxylates |
TW363051B (en) * | 1995-08-31 | 1999-07-01 | Mitsui Toatsu Chemicals | Substituted amidine derivatives and platelet aggregation inhibitor containing the same |
EP0892044B1 (en) * | 1997-07-18 | 2004-12-29 | Mitsui Chemicals, Inc. | Esterase and its use for the production of optically active chroman compounds |
-
1998
- 1998-07-15 EP EP98305608A patent/EP0892044B1/en not_active Expired - Lifetime
- 1998-07-15 DE DE69828338T patent/DE69828338T2/de not_active Expired - Fee Related
- 1998-07-17 US US09/118,275 patent/US6060290A/en not_active Expired - Fee Related
- 1998-07-17 HU HU9801621A patent/HUP9801621A3/hu unknown
- 1998-07-18 KR KR1019980029029A patent/KR100300443B1/ko not_active IP Right Cessation
- 1998-07-18 CN CN98117243A patent/CN1218110A/zh active Pending
-
2000
- 2000-03-13 US US09/524,760 patent/US6303349B1/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
CN1218110A (zh) | 1999-06-02 |
KR19990013989A (ko) | 1999-02-25 |
EP0892044A3 (en) | 2001-05-02 |
EP0892044A2 (en) | 1999-01-20 |
DE69828338T2 (de) | 2005-06-02 |
HU9801621D0 (en) | 1998-09-28 |
US6303349B1 (en) | 2001-10-16 |
KR100300443B1 (ko) | 2001-09-06 |
EP0892044B1 (en) | 2004-12-29 |
HUP9801621A3 (en) | 2001-08-28 |
DE69828338D1 (de) | 2005-02-03 |
US6060290A (en) | 2000-05-09 |
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