PL1963516T3 - Sposób enancjoselektywnej enzymatycznej redukcji związków hydroksyketonowych - Google Patents

Sposób enancjoselektywnej enzymatycznej redukcji związków hydroksyketonowych

Info

Publication number: PL1963516T3
Authority: PL; Poland
Prior art keywords: hydroxy ketone; alkyl; general formula; enzymatic reduction; enantioselective enzymatic
Prior art date: 2005-12-19

Application number

PL06819032T

Other languages

English (en)

Inventor

Antje Gupta

Maria Bobkova

Anke Tschentscher

Original Assignee

Iep Gmbh

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.)

2005-12-19

Filing date

2006-12-14

Publication date

2011-07-29

2006-12-14 Application filed by Iep Gmbh filed Critical Iep Gmbh

2011-07-29 Publication of PL1963516T3 publication Critical patent/PL1963516T3/pl

Links

230000002255 enzymatic effect Effects 0.000 title abstract 2
238000000034 method Methods 0.000 title abstract 2
150000001875 compounds Chemical class 0.000 title 1
BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 abstract 4
125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 2
102000004316 Oxidoreductases Human genes 0.000 abstract 2
108090000854 Oxidoreductases Proteins 0.000 abstract 2
XJLXINKUBYWONI-DQQFMEOOSA-N [[(2r,3r,4r,5r)-5-(6-aminopurin-9-yl)-3-hydroxy-4-phosphonooxyoxolan-2-yl]methoxy-hydroxyphosphoryl] [(2s,3r,4s,5s)-5-(3-carbamoylpyridin-1-ium-1-yl)-3,4-dihydroxyoxolan-2-yl]methyl phosphate Chemical compound NC(=O)C1=CC=C[N+]([C@@H]2[C@H]([C@@H](O)[C@H](COP([O-])(=O)OP(O)(=O)OC[C@@H]3[C@H]([C@@H](OP(O)(O)=O)[C@@H](O3)N3C4=NC=NC(N)=C4N=C3)O)O2)O)=C1 XJLXINKUBYWONI-DQQFMEOOSA-N 0.000 abstract 2
229930027945 nicotinamide-adenine dinucleotide Natural products 0.000 abstract 2
230000003647 oxidation Effects 0.000 abstract 2
238000007254 oxidation reaction Methods 0.000 abstract 2
150000003333 secondary alcohols Chemical class 0.000 abstract 2
125000004209 (C1-C8) alkyl group Chemical group 0.000 abstract 1
238000006243 chemical reaction Methods 0.000 abstract 1
150000002009 diols Chemical class 0.000 abstract 1
229910052739 hydrogen Inorganic materials 0.000 abstract 1
239000001257 hydrogen Substances 0.000 abstract 1
125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 1
BOPGDPNILDQYTO-NNYOXOHSSA-N nicotinamide-adenine dinucleotide Chemical compound C1=CCC(C(=O)N)=CN1[C@H]1[C@H](O)[C@H](O)[C@@H](COP(O)(=O)OP(O)(=O)OC[C@@H]2[C@H]([C@@H](O)[C@@H](O2)N2C3=NC=NC(N)=C3N=C2)O)O1 BOPGDPNILDQYTO-NNYOXOHSSA-N 0.000 abstract 1

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
- C12P7/24—Preparation of oxygen-containing organic compounds containing a carbonyl group
- C12P7/26—Ketones
- 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
- C12P13/00—Preparation of nitrogen-containing organic compounds
- C12P13/002—Nitriles (-CN)
- 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
- 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
- C12P41/002—Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture by oxidation/reduction reactions
- 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
- C12P7/62—Carboxylic acid esters
- 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
- C12N9/0004—Oxidoreductases (1.)
- C12N9/0008—Oxidoreductases (1.) acting on the aldehyde or oxo group of donors (1.2)

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Engineering & Computer Science (AREA)
Life Sciences & Earth Sciences (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)
Analytical Chemistry (AREA)
Preparation Of Compounds By Using Micro-Organisms (AREA)
Enzymes And Modification Thereof (AREA)
Medicines Containing Plant Substances (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

PL06819032T 2005-12-19 2006-12-14 Sposób enancjoselektywnej enzymatycznej redukcji związków hydroksyketonowych PL1963516T3 (pl)

Applications Claiming Priority (3)

Application Number	Priority Date	Filing Date	Title
AT0202705A AT503017B1 (de)	2005-12-19	2005-12-19	Verfahren zur enantioselektiven enzymatischen reduktion von hydroxyketoverbindungen
PCT/EP2006/012037 WO2007073875A1 (de)	2005-12-19	2006-12-14	Verfahren zur enantioselektiven enzymatischen reduktion von hydroxyketoverbindungen
EP06819032A EP1963516B1 (de)	2005-12-19	2006-12-14	Verfahren zur enantioselektiven enzymatischen reduktion von hydroxyketoverbindungen

Publications (1)

Publication Number	Publication Date
PL1963516T3 true PL1963516T3 (pl)	2011-07-29

Family

ID=37900660

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
PL06819032T PL1963516T3 (pl)	2005-12-19	2006-12-14	Sposób enancjoselektywnej enzymatycznej redukcji związków hydroksyketonowych

Country Status (17)

Country	Link
US (2)	US8980592B2 (pl)
EP (1)	EP1963516B1 (pl)
JP (1)	JP5328365B2 (pl)
KR (1)	KR101344605B1 (pl)
CN (1)	CN101432435A (pl)
AT (2)	AT503017B1 (pl)
AU (1)	AU2006331069B2 (pl)
CA (1)	CA2633583C (pl)
DE (1)	DE502006008961D1 (pl)
DK (1)	DK1963516T3 (pl)
ES (1)	ES2363374T3 (pl)
PL (1)	PL1963516T3 (pl)
PT (1)	PT1963516E (pl)
SI (1)	SI1963516T1 (pl)
TW (1)	TWI408234B (pl)
WO (1)	WO2007073875A1 (pl)
ZA (1)	ZA200805336B (pl)

Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
AT504542B1 (de) *	2006-12-07	2008-09-15	Iep Gmbh	Verfahren zur enantioselektiven enzymatischen reduktion von secodionderivaten
TWI601825B (zh) *	2007-09-27	2017-10-11	Ｉｅｐ有限公司	對映異構選擇性酶催化還原中間產物之方法
CN101429514B (zh) *	2007-11-08	2011-06-15	陈依军	一种双羰基还原酶、其基因及其应用
EP2226386A1 (de) *	2009-03-05	2010-09-08	IEP GmbH	Verfahren zur stereoselektiven enzymatischen Reduktion von Ketoverbindungen
PL2445890T3 (pl)	2009-06-22	2016-02-29	Sk Biopharmaceuticals Co Ltd	Sposób wytwarzania estru (R)-1-arylo-2-tetrazoliloetylowego kwasu karbaminowego
US8404461B2 (en) *	2009-10-15	2013-03-26	SK Biopharmaceutical Co. Ltd.	Method for preparation of carbamic acid (R)-1-aryl-2-tetrazolyl-ethyl ester
CN103228658A (zh) *	2010-10-08	2013-07-31	卡迪拉保健有限公司	用于通过酶促转化制备西他列汀的中间体的方法
KR102023208B1 (ko) *	2010-12-16	2019-09-19	파마젤 게엠베하	신규한 7β-히드록시스테로이드 데히드로게나제 돌연변이체 및 우르소데옥시콜산의 제조 방법
EP2861750B1 (en) *	2012-06-18	2016-11-23	Laboratorio Chimico Internazionale S.p.A.	Process for producing chiral 1-substituted 3-piperidinols employing oxidoreductases
CN102978249A (zh) *	2012-11-19	2013-03-20	苏州汉酶生物技术有限公司	6-氰基-（3r,5r）-二羟基己酸叔丁酯的生物制备方法
CN103146591B (zh) *	2013-01-30	2014-08-27	浙江工业大学	生物还原制备他汀侧链6-氰基-(3r,5r)-二羟基己酸叔丁酯及菌株
CN104342410B (zh) *	2013-07-26	2017-04-19	南京朗恩生物科技有限公司	一种酮还原酶突变体及其制备方法
CN105713884A (zh) *	2014-12-02	2016-06-29	安琪酵母股份有限公司	生物催化氢化组合物及其合成罗素伐他汀手性中间体方法
US10746586B2 (en)	2015-05-28	2020-08-18	Sonicu, Llc	Tank-in-tank container fill level indicator
US10745263B2 (en)	2015-05-28	2020-08-18	Sonicu, Llc	Container fill level indication system using a machine learning algorithm
CN109913514A (zh) *	2019-03-12	2019-06-21	江苏理工学院	一种固定化酶流化床连续催化合成ats-7的方法

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US5324662A (en)	1992-05-15	1994-06-28	E. R. Squibb & Sons, Inc.	Stereoselective microbial or enzymatic reduction of 3,5-dioxo esters to 3-hydroxy-5-oxo, 3-oxo-5-hydroxy, and 3,5-dihydroxy esters
GB9512837D0 (en) *	1995-06-23	1995-08-23	Zeneca Ltd	reduction of ketone groups
JP4510351B2 (ja) *	1999-12-03	2010-07-21	株式会社カネカ	新規カルボニル還元酵素、その遺伝子、およびその利用法
GB0011120D0 (en)	2000-05-09	2000-06-28	Avecia Ltd	Process
JP2005520517A (ja)	2002-03-18	2005-07-14	チバ　スペシャルティ　ケミカルズ　ホールディング　インコーポレーテッド	高い溶媒および温度安定性を有するアルコールデヒドロゲナーゼ
DE10327454A1 (de) *	2003-06-18	2005-01-20	Juelich Enzyme Products Gmbh	Oxidoreduktase aus Pichia capsulata
AT413541B (de)	2004-05-10	2006-03-15	Iep Gmbh	Verfahren zur herstellung von 2-butanol

2005
- 2005-12-19 AT AT0202705A patent/AT503017B1/de not_active IP Right Cessation
2006
- 2006-12-14 JP JP2008546207A patent/JP5328365B2/ja not_active Expired - Fee Related
- 2006-12-14 US US12/086,704 patent/US8980592B2/en active Active
- 2006-12-14 AU AU2006331069A patent/AU2006331069B2/en not_active Ceased
- 2006-12-14 DE DE502006008961T patent/DE502006008961D1/de active Active
- 2006-12-14 WO PCT/EP2006/012037 patent/WO2007073875A1/de not_active Ceased
- 2006-12-14 AT AT06819032T patent/ATE499447T1/de active
- 2006-12-14 CN CNA2006800477546A patent/CN101432435A/zh active Pending
- 2006-12-14 ZA ZA200805336A patent/ZA200805336B/xx unknown
- 2006-12-14 DK DK06819032.1T patent/DK1963516T3/da active
- 2006-12-14 PL PL06819032T patent/PL1963516T3/pl unknown
- 2006-12-14 ES ES06819032T patent/ES2363374T3/es active Active
- 2006-12-14 CA CA2633583A patent/CA2633583C/en active Active
- 2006-12-14 SI SI200631010T patent/SI1963516T1/sl unknown
- 2006-12-14 PT PT06819032T patent/PT1963516E/pt unknown
- 2006-12-14 EP EP06819032A patent/EP1963516B1/de active Active
- 2006-12-18 TW TW095147521A patent/TWI408234B/zh not_active IP Right Cessation
2008
- 2008-07-15 KR KR1020087017190A patent/KR101344605B1/ko not_active Expired - Fee Related
2015
- 2015-02-04 US US14/613,863 patent/US9228214B2/en active Active

Also Published As

Publication number	Publication date
EP1963516B1 (de)	2011-02-23
AT503017B1 (de)	2007-07-15
TW200801196A (en)	2008-01-01
EP1963516A1 (de)	2008-09-03
US9228214B2 (en)	2016-01-05
DE502006008961D1 (de)	2011-04-07
WO2007073875A1 (de)	2007-07-05
CN101432435A (zh)	2009-05-13
AU2006331069A1 (en)	2007-07-05
US8980592B2 (en)	2015-03-17
US20090221044A1 (en)	2009-09-03
CA2633583C (en)	2016-06-21
AT503017A4 (de)	2007-07-15
ATE499447T1 (de)	2011-03-15
JP2009519722A (ja)	2009-05-21
ZA200805336B (en)	2009-12-30
KR101344605B1 (ko)	2013-12-26
SI1963516T1 (sl)	2011-06-30
PT1963516E (pt)	2011-05-25
ES2363374T3 (es)	2011-08-02
CA2633583A1 (en)	2007-07-05
TWI408234B (zh)	2013-09-11
DK1963516T3 (da)	2011-06-06
JP5328365B2 (ja)	2013-10-30
KR20080087000A (ko)	2008-09-29
US20150152451A1 (en)	2015-06-04
AU2006331069B2 (en)	2012-04-05

Publication	Publication Date	Title
PL1963516T3 (pl)	2011-07-29	Sposób enancjoselektywnej enzymatycznej redukcji związków hydroksyketonowych
Kroutil et al.	2004	Recent advances in the biocatalytic reduction of ketones and oxidation of sec-alcohols
Kroutil et al.	2004	Biocatalytic oxidation of primary and secondary alcohols
Lutz et al.	2004	Bioorganometallic chemistry: biocatalytic oxidation reactions with biomimetic NAD+/NADH co-factors and [Cp* Rh (bpy) H]+ for selective organic synthesis
PH12014501770A1 (en)	2014-11-10	Method for enzymatic redox cofactor regeneration
Sucharitakul et al.	2008	Detection of a C4a-hydroperoxyflavin intermediate in the reaction of a flavoprotein oxidase
Rodriguez et al.	2012	Recent advances in cofactor regeneration systems applied to biocatalyzed oxidative processes
EP1179595A4 (en)	2004-12-08	(R) -2-OCTANOL DEHYDROGENASES, METHOD FOR THE PRODUCTION OF THESE ENZYMS, DNA ENCODING THESE ENZYMES, AND METHOD FOR THE PRODUCTION OF ALCOHOLS BY USE OF THE ENZYMES
ATE515571T1 (de)	2011-07-15	Verfahren zur herstellung von optisch aktiven sekundären alkoholen aus ketonen unter verwendung einer adsorbierten carbonylreduktase-aktivität
EP2438179B1 (en)	2016-12-21	A process for the enzymatic reduction of enoates
BR0316552A (pt)	2005-10-04	Microorganismos metabolicamente engenheirado e geneticamente transformado, e, método para produzir um produto metabólico desejado
Sokolova et al.	2024	Exploiting hydrogenases for biocatalytic hydrogenations
RU2002134073A (ru)	2004-03-27	Способ, включающий непрямую электрохимическую регенерацию n a d (p) h
Martı́nez et al.	2000	Preparation of halohydrin β-blocker precursors using yeast-catalysed reduction
WO2024215747A3 (en)	2025-03-06	Improved methods of cell-free synthesis
Velonia et al.	2000	Dismutation of aldehydes catalyzed by alcohol dehydrogenases
Musa	2014	Enzymatic production of both enantiomers of rhododendrol
JIN et al.	2005	Electrochemical regeneration of FAD by catalytic electrode without electron mediator and biochemical reducing power
DE102004037669A1 (de)	2005-03-10	(R)- und (S)-1,4-Dichlor-butan-2-ol und Verfahren zu deren Herstellung durch enantioselektive enzymatische Reduktion von 1,4-Dichlor-butan-2-on
Jang et al.	2003	Complete In Vitro Conversion of n-Xylose to Xylitol by Coupling Xylose Reductase and Formate Dehydrogenase
ID23839A (id)	2000-05-25	Pembuatan mikroba aktinol
ES2619338T3 (es)	2017-06-26	Procedimiento para la producción de 3-piperidinoles quirales sustituidos en posición 1 empleando oxidorreductasas
JP7565304B2 (ja)	2024-10-10	酵素触媒作用によりスルホンを調製するための選択的プロセス
Tanihata et al.	2012	Oxidative degradation of 4-hydroxyacetophenone in Arthrobacter sp. TGJ4
US20220259624A1 (en)	2022-08-18	Selective process for preparing sulfoxides by enzymatic catalysis