DK2847214T3 - Konstruerede iminreduktaser og fremgangsmåder til den reduktive aminering af keton- og aminforbindelser - Google Patents

Konstruerede iminreduktaser og fremgangsmåder til den reduktive aminering af keton- og aminforbindelser Download PDF

Info

Publication number
DK2847214T3
DK2847214T3 DK13724127.9T DK13724127T DK2847214T3 DK 2847214 T3 DK2847214 T3 DK 2847214T3 DK 13724127 T DK13724127 T DK 13724127T DK 2847214 T3 DK2847214 T3 DK 2847214T3
Authority
DK
Denmark
Prior art keywords
compound
polypeptide
engineered
seq
sequence
Prior art date
Application number
DK13724127.9T
Other languages
English (en)
Inventor
Jeffrey Moore
Steven J Collier
Jovana Nazor
Gregory Hughes
Jacob Janey
Gjalt Huisman
Scott Novick
Nicholas Agard
Oscar Alvizo
Gregory Cope
Stefanie Ng Minor
Haibin Chen
Derek Smith
Wan Lin Yeo
Joly Sukumaran
Original Assignee
Codexis Inc
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 Codexis Inc filed Critical Codexis Inc
Application granted granted Critical
Publication of DK2847214T3 publication Critical patent/DK2847214T3/da

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
    • C12P13/02Amides, e.g. chloramphenicol or polyamides; Imides or polyimides; Urethanes, i.e. compounds comprising N-C=O structural element or polyurethanes
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N9/00Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
    • C12N9/0004Oxidoreductases (1.)
    • C12N9/0012Oxidoreductases (1.) acting on nitrogen containing compounds as donors (1.4, 1.5, 1.6, 1.7)
    • C12N9/0026Oxidoreductases (1.) acting on nitrogen containing compounds as donors (1.4, 1.5, 1.6, 1.7) acting on CH-NH groups of donors (1.5)
    • C12N9/0028Oxidoreductases (1.) acting on nitrogen containing compounds as donors (1.4, 1.5, 1.6, 1.7) acting on CH-NH groups of donors (1.5) with NAD or NADP as acceptor (1.5.1)
    • 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
    • C12P13/04Alpha- 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
    • C12P17/00Preparation of heterocyclic carbon compounds with only O, N, S, Se or Te as ring hetero atoms
    • C12P17/10Nitrogen as only ring hetero atom
    • 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
    • C12P17/00Preparation of heterocyclic carbon compounds with only O, N, S, Se or Te as ring hetero atoms
    • C12P17/10Nitrogen as only ring hetero atom
    • C12P17/12Nitrogen as only ring hetero atom containing a six-membered hetero ring
    • 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
    • C12P17/00Preparation of heterocyclic carbon compounds with only O, N, S, Se or Te as ring hetero atoms
    • C12P17/16Preparation of heterocyclic carbon compounds with only O, N, S, Se or Te as ring hetero atoms containing two or more hetero rings
    • C12P17/165Heterorings having nitrogen atoms as the only ring heteroatoms
    • 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
    • C12P17/00Preparation of heterocyclic carbon compounds with only O, N, S, Se or Te as ring hetero atoms
    • C12P17/18Preparation of heterocyclic carbon compounds with only O, N, S, Se or Te as ring hetero atoms containing at least two hetero rings condensed among themselves or condensed with a common carbocyclic ring system, e.g. rifamycin
    • C12P17/185Heterocyclic compounds containing sulfur atoms as ring hetero atoms in the condensed system
    • 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
    • C12P17/00Preparation of heterocyclic carbon compounds with only O, N, S, Se or Te as ring hetero atoms
    • C12P17/18Preparation of heterocyclic carbon compounds with only O, N, S, Se or Te as ring hetero atoms containing at least two hetero rings condensed among themselves or condensed with a common carbocyclic ring system, e.g. rifamycin
    • C12P17/188Heterocyclic compound containing in the condensed system at least one hetero ring having nitrogen atoms and oxygen atoms as the only ring heteroatoms
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12YENZYMES
    • C12Y105/00Oxidoreductases acting on the CH-NH group of donors (1.5)
    • C12Y105/01Oxidoreductases acting on the CH-NH group of donors (1.5) with NAD+ or NADP+ as acceptor (1.5.1)
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12YENZYMES
    • C12Y105/00Oxidoreductases acting on the CH-NH group of donors (1.5)
    • C12Y105/01Oxidoreductases acting on the CH-NH group of donors (1.5) with NAD+ or NADP+ as acceptor (1.5.1)
    • C12Y105/01023Tauropine dehydrogenase (1.5.1.23)
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12YENZYMES
    • C12Y105/00Oxidoreductases acting on the CH-NH group of donors (1.5)
    • C12Y105/01Oxidoreductases acting on the CH-NH group of donors (1.5) with NAD+ or NADP+ as acceptor (1.5.1)
    • C12Y105/01024N5-(Carboxyethyl)ornithine synthase (1.5.1.24)
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12YENZYMES
    • C12Y105/00Oxidoreductases acting on the CH-NH group of donors (1.5)
    • C12Y105/01Oxidoreductases acting on the CH-NH group of donors (1.5) with NAD+ or NADP+ as acceptor (1.5.1)
    • C12Y105/01028Opine dehydrogenase (1.5.1.28)
    • 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/50Improvements relating to the production of bulk chemicals
    • Y02P20/52Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts

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)
  • Genetics & Genomics (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Health & Medical Sciences (AREA)
  • General Engineering & Computer Science (AREA)
  • Biochemistry (AREA)
  • Microbiology (AREA)
  • Biotechnology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Molecular Biology (AREA)
  • Medicinal Chemistry (AREA)
  • Biomedical Technology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Micro-Organisms Or Cultivation Processes Thereof (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Enzymes And Modification Thereof (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Claims (11)

1. Konstrueret polypeptid med iminreduktaseaktivitet, omfattende en aminosyresekvens med mindst 80% sekvensidentitet til SEQ ID NO: 2 og én eller flere restforskelle som sammenlignet med sekvensen af SEQ ID NO: 2 ved restpositioner valgt blandt X198, Xlll, X136, X156, X197, X201, X259, X280, X292, og X293 der er i stand til at: i) omdanne substratforbindelse (la) pyruvat,
og substratforbindelse (2b) butylamin
til produktforbindelse (3b), N-2-(butylamino)propansyre,
under egnede reaktionsbetingelser hvor polypeptidet har forbedret iminreduktaseaktivitet sammenlignet med polypeptidet af SEQ ID NO: 2; ii) omdanne substratforbindelse (lb) cyclohexanon,
og substratforbindelse (2a) L-norvalin
til produktforbindelse (3c), (S)-2-(cyclohexylamino)pentansyre,
under egnede reaktionsbetingelser hvor polypeptidet har forbedret iminreduktaseaktivitet sammenlignet med polypeptidet af SEQ ID NO: 2; eller iii) omdanne substratforbindelse (lb) cyclohexanon,
og substratforbindelse (2b) butylamin
til produktforbindelse (3d), N-butylcyclohexanamin,
under egnede reaktionsbetingelser hvor polypeptidet har forbedret iminreduktaseaktivitet sammenlignet med polypeptidet af SEQ ID NO: 2. . Konstrueret polypeptid ifølge krav 1 hvor restforskellene er valgt blandt 198E/A/H/P/S, X111M/Q/S, X136G, X156G/I/Q/S/T/V, X197I/P, X201L, 259E/H/I/L/M/S/T, X280L, X292C/G/I/P/S/T/V/Y, og X293H/I/K/IVN/Q/T/V. . Konstrueret polypeptid ifølge krav 1 hvor aminosyresekvensen omfatter mindst n kombination af restforskellene valgt fra: (a) X111M, X156T, X198H, X259M, X280L, X292V, og X293H; (b) X156T, X197P, X198H, X259H, X280L, X292P, og X293H; (C) X111M, X136G, X156S, X197I, X198H, X201L, X259H, X280L, X292V, og X293H; (d) X197I, X198E, X259M, og X280L; (e) X156T, X197I, X198E, X201L, X259H, X280L, X292V, og X293H; (f) X111M, X136G, X198H, X259M, X280L, X292S, og X293H; og (g) X156V, X197P, X198E, X201L, X259M, X280L, og X292T.
4. Konstrueret polypeptid ifølge et hvilket som helst af kravene 1 til 3 der yderligere omfatter én eller flere restforskelle som sammenlignet med sekvensen af SEQ ID NO: 2 ved restpositioner valgt blandt X4, X5, X14, X20, X29, X37, X67, X71, X74, X82, X94, X97, X100, Xlll, X124, X137, X141, X143, X149, X153, X154, X157, X158, X160, X163, X177, X178, X183, X184, X185, X186, X220, X223, X226, X232, X243, X246, X256, X258, X259, X260, X261, X265, X266, X270, X273, X274, X277, X279, X283, X284, X287, X288, X294, X295, X296, X297, X308, X311, X323, X324, X326, X328, X332, X353, og X356.
5. Konstrueret polypeptid ifølge krav 4 hvor: i) restforskellene er valgt blandt X4H/L/R, X5T, X14P, X20T, X29R/T, X37H, X67A/D, X71C/V, X74R, X82P, X94K/R/T, X97P, X100W, X111R, X124IVN, X137N, X141W, X143W, X149L, X153V/Y, X154F/M/Q/Y, X157D/H/L/M/N/R, X158K, X160N, X163T, X177C/H, X178E, X183C, X184K/Q/R, X185V, X186K/R, X220D/H, X223T, X226L, X232A/R, X243G, X246W, X256V, X258D, X259V/W, X260G, X261A/G/I/K/R/S/T, X265G/L/Y, X266T, X270G, X273W, X274M, X277A/I, X279F/L/V/Y, X283V, X284K/L/M/Y, X287S/T, X288G/S, X294A/I/V, X295R/S, X296IVN/V/W, X297A, X308F, X311C/T/V, X323C/I/M/T/V, X324IVT, X326V, X328A/G/E, X332V, X353E, og X356R; ii) aminosyresekvensen omfatter mindst én kombination af restforskellene valgt fra: (a) X29R, X184R, X223T, X261S, X284M, og X287T; (b) X29R, X157R, X184Q, X220H, X223T, X232A, X261I, X284M, X287T, X288S, X324L, X332V, og X353E; (c) X29R, X157R, X184Q, X220H, X223T, X232A, X259V, X261I, X284M, X287T, X288S, X324L, X332V, og X353E; (d) X29R, X94K, XIHR, X137N, X157R, X184Q, X220H, X223T, X232A, X259V, X261I, X279V, X284M, X287T, X288S, X324L, X332V, og X353E; og (e) X29R, X94K, XIHR, X137N, X157R, X184Q, X220H, X223T, X232A, X259V, X261I, X266T, X279V, X284M, X287T, X288S, X295S, X311V, X324L, X328E, X332V, og X353E; iii) aminosyresekvensen omfatter kombinationen af restforskellene X156T, X197I, X198E, X201L, X259H, X280L, X292V, og X293H og én eller flere restforskelle valgt blandt X29R/T, X94K/R/T, XIHR, X137N, X157D/H/L/M/N/R, X184K/Q/R, X220D/H, X223T, X232A/R, X259V/W, X261A/G/I/K/R/S/T, X266T, X279F/L/V/Y, X284K/L/M/Y, X287S/T, X288G/S, X295S, X311V, X324L/T, X328E, X332V, og X353E; eller iv) aminosyresekvensen omfatter kombinationen af restforskellene X156T, X197I, X198E, X201L, X259H, X280L, X292V, og X293H mindst én kombination af restforskellene valgt fra: (a) X29R, X184R, X223T, X261S, X284M, og X287T; (b) X29R, X157R, X184Q, X220H, X223T, X232A, X261I, X284M, X287T, X288S, X324L, X332V, og X353E; (c) X29R, X157R, X184Q, X220H, X223T, X232A, X259V, X261I, X284M, X287T, X288S, X324L, X332V, og X353E; (d) X29R, X94K, XIHR, X137N, X157R, X184Q, X220H, X223T, X232A, X259V, X261I, X279V, X284M, X287T, X288S, X324L, X332V, og X353E; og (e) X29R, X94K, XIHR, X137N, X157R, X184Q, X220H, X223T, X232A, X259V, X261I, X266T, X279V, X284M, X287T, X288S, X295S, X311V, X324L, X328E, X332V, og X353E.
6. Konstrueret polypeptid ifølge krav 4 der er i stand til at: i) omdanne substratforbindelse (li),
og substratforbindelse (2b)
til produktforbindelse (3d),
under egnede reaktionsbetingelser; eller ii) omdanne substratforbindelse (lj),
og substratforbindelse (2b)
til produktforbindelse (3o),
under egnede reaktionsbetingelser.
7. Konstrueret polypeptid ifølge krav 1, hvor aminosyresekvensen omfatter en sekvens valgt fra gruppen bestående af de lige-nummererede sekvensidentifi-katorer af SEQ ID NO: 4 - 100, og 112 - 750.
8. Polynukleotid der koder for et konstrueret polypeptid ifølge et hvilket som helst af kravene 1 til 7, eventuelt hvor polynukleotidet omfatter en nukleinsyresekvens valgt fra gruppen bestående af de ulige-nummererede sekvensidentifikatorer af SEQ ID NO: 3 - 99, og 111 - 749.
9. Ekspressionsvektor omfattende polynukleotidet ifølge krav 8.
10. Værtscelle omfattende polynukleotidet ifølge krav 8 eller ekspressionsvektoren ifølge krav 9.
11. Fremgangsmåde til fremstilling af et konstrueret polypeptid med imin-reduktaseaktivitet, omfattende dyrkning af værtscellen ifølge krav 10 under betingelser der er egnede for ekspression af polypeptidet, eventuelt yderligere omfattende isolering af det konstruerede polypeptid.
12. Fremgangsmåde til fremstilling af en forbindelse med formel (III),
hvor R1- og R2-grupperne er uafhængigt valgt fra et hydrogenatom, og eventuelt substitueret alkyl, alkenyl, alkynyl, alkoxy, carboxy, aminocarbonyl, heteroalkyl, heteroalkenyl, heteroalkynyl, carboxyalkyl, aminoalkyl, haloalkyl, alkylthioalkyl, cycloalkyl, aryl, arylalkyl, heterocycloalkyl, heteroaryl, og heteroarylalkyl; og eventuelt R1 og R2 er bundet for at danne en 3-leddet til 10-leddet ring; R3- og R4-grupperne er uafhængigt valgt fra et hydrogenatom, og eventuelt substitueret alkyl, alkenyl, alkynyl, alkoxy, carboxy, aminocarbonyl, heteroalkyl, heteroalkenyl, heteroalkynyl, carboxyalkyl, aminoalkyl, haloalkyl, alkylthioalkyl, cycloalkyl, aryl, arylalkyl, heterocycloalkyl, heteroaryl, og heteroarylalkyl, med det forbehold at begge R3 og R4 kan ikke være hydrogen; og eventuelt R3 og R4 er bundet for at danne en 3-leddet til 10-leddet ring; og eventuelt, er carbonatomet og/eller nitrogenet indikeret med * er kiralt; fremgangsmåden omfatter at bringe en forbindelse med formel (I),
hvor R1, og R2 er som defineret ovenfor; og en forbindelse med formel (II),
hvor R3, og R4 er som defineret ovenfor; i kontakt med et konstrueret polypeptid med iminreduktaseaktivitet i tilstedeværelse af en cofaktor under egnede reaktionsbetingelser, hvor det konstruerede polypeptid er et konstrueret polypeptid ifølge et hvilket som helst af kravene 1 til 7.
13. Fremgangsmåden ifølge krav 12 hvor: i) R3 og R4 er bundet for at danne en 3-leddet til 10-leddet ring; ii) substratforbindelsen med formel (II) er valgt fra methylamin, dimethylamin, isopropylamin, butylamin, isobutylaminl, L-norvalin, anilin, (S)-2-aminopent-4-enoensyre, pyrrolidin, og hydroxypyrrolidin; iii) mindst én af R1 og R2 af forbindelsen med formel (I) er bundet til mindst én af R3 og R4 af aminforbindelsen med formel (II), hvorved fremgangsmåden til fremstilling af aminforbindelsen med formel (III) omfatter en intramolekylær reaktion; eller iv) de egnede reaktionsbetingelser omfatter (a) substratpåfyldning ved ca. 10 g/l til 100 g/l; (b) ca. 0,1 g/l til ca. 50 g/l af det konstruerede polypeptid; (c) ca. 0,05 g/l (0,001 M) til ca. 2,5 g/l (0,050 M) NAD(P)H; (d) en pH på ca. 6 til 10; (e) temperatur på ca. 20° til 50°C; og (f) reaktionstid på 2-120 timer.
DK13724127.9T 2012-05-11 2013-05-09 Konstruerede iminreduktaser og fremgangsmåder til den reduktive aminering af keton- og aminforbindelser DK2847214T3 (da)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201261646100P 2012-05-11 2012-05-11
PCT/US2013/040377 WO2013170050A1 (en) 2012-05-11 2013-05-09 Engineered imine reductases and methods for the reductive amination of ketone and amine compounds

Publications (1)

Publication Number Publication Date
DK2847214T3 true DK2847214T3 (da) 2018-03-12

Family

ID=48468843

Family Applications (1)

Application Number Title Priority Date Filing Date
DK13724127.9T DK2847214T3 (da) 2012-05-11 2013-05-09 Konstruerede iminreduktaser og fremgangsmåder til den reduktive aminering af keton- og aminforbindelser

Country Status (8)

Country Link
US (16) US9193957B2 (da)
EP (1) EP2847214B1 (da)
CN (2) CN107904216B (da)
DK (1) DK2847214T3 (da)
HU (1) HUE036947T2 (da)
IL (1) IL235292A (da)
SG (1) SG11201407297VA (da)
WO (1) WO2013170050A1 (da)

Families Citing this family (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
HUE036947T2 (hu) 2012-05-11 2018-08-28 Codexis Inc Átalakított iminreduktázok és eljárások keton- és aminvegyületek reduktív aminálására
CN106232619B (zh) 2013-11-13 2022-09-09 科德克希思公司 工程化的亚胺还原酶和用于酮和胺化合物的还原胺化的方法
US10370648B2 (en) 2014-11-25 2019-08-06 Codexis, Inc. Engineered imine reductases and methods for the reductive amination of ketone and amine compounds
EP3297442A4 (en) 2015-05-18 2018-11-07 Zymtronix, LLC Magnetically immobilized microbiocidal enzymes
CA2992261A1 (en) 2015-07-15 2017-01-19 Zymtronix, Llc Automated bionanocatalyst production
WO2018034877A1 (en) 2016-08-13 2018-02-22 Zymtronix, Llc Magnetically immobilized biocidal enzymes and biocidal chemicals
US11046936B2 (en) * 2016-08-26 2021-06-29 Codexis, Inc. Engineered imine reductases and methods for the reductive amination of ketone and amine compounds
CN108504701B (zh) * 2018-04-26 2021-05-14 中南林业科技大学 一种异丙甲草胺中间体的合成方法
CN109355266B (zh) * 2018-11-06 2020-11-27 华东理工大学 亚胺还原酶突变体及其在光学活性1-取代-四氢异喹啉衍生物合成中的应用
PL3653617T3 (pl) 2018-11-16 2021-04-06 Zanoprima Lifesciences Limited Sposób otrzymywania (s)-nikotyny z miozminy
US20220145339A1 (en) 2018-12-10 2022-05-12 MAX-PLANCK-Gesellschaft zur Förderung der Wissenschaften e.V. Method for preparation of primary amine compounds
CA3137734A1 (en) * 2019-05-01 2020-11-05 Codexis, Inc. Engineered glucose dehydrogenases and methods for the reductive amination of ketone and amine compounds
CN114127272A (zh) * 2019-05-01 2022-03-01 科德克希思公司 工程化亚胺还原酶和用于酮和胺化合物的还原胺化的方法
US10947253B2 (en) 2019-08-05 2021-03-16 Ankh Life Sciences Limited Fused polycyclic dimers
MX2022002473A (es) 2019-08-30 2022-08-02 Codexis Inc Variantes de lipasa modificadas geneticamente.
CN110564788B (zh) * 2019-09-30 2021-05-04 江南大学 一种利用亚胺还原酶生产麻黄碱的方法
CN110951705B (zh) * 2019-12-20 2020-09-25 中国科学院苏州生物医学工程技术研究所 胺脱氢酶突变体、酶制剂、重组载体、重组细胞及其制备方法和应用
CN112795603B (zh) * 2020-12-14 2022-06-24 山东金城医药化工有限公司 一种制备(s)-2-(3-吡啶)-吡咯烷的方法
CN112409327A (zh) * 2020-11-18 2021-02-26 山东金城医药化工有限公司 一种高光学纯度烟碱的制备方法
CN112779300B (zh) * 2020-12-15 2022-10-21 上海合全药物研发有限公司 生物催化制备(s)-3-丁炔-2-胺的方法
TW202342741A (zh) * 2021-12-28 2023-11-01 日商中外製藥股份有限公司 多胜肽及使用其之胺基酸的製造方法
CN114717211B (zh) * 2022-03-23 2023-06-02 江苏集萃分子工程研究院有限公司 亚胺还原酶突变体m5及其在合成氮杂环手性胺中的应用
CN114686537B (zh) * 2022-04-14 2023-10-10 华南理工大学 一种多酶级联催化l-氨基酸生成n-甲基-l-氨基酸的方法及其应用

Family Cites Families (37)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5538867A (en) 1988-09-13 1996-07-23 Elf Aquitaine Process for the electrochemical regeneration of pyridine cofactors
KR100356926B1 (ko) 1993-09-07 2003-01-10 교와 핫꼬 고교 가부시끼가이샤 트랜스-4-히드록시-l-프롤린의제조법
US6117679A (en) 1994-02-17 2000-09-12 Maxygen, Inc. Methods for generating polynucleotides having desired characteristics by iterative selection and recombination
US6335160B1 (en) 1995-02-17 2002-01-01 Maxygen, Inc. Methods and compositions for polypeptide engineering
US5605793A (en) 1994-02-17 1997-02-25 Affymax Technologies N.V. Methods for in vitro recombination
US5837458A (en) 1994-02-17 1998-11-17 Maxygen, Inc. Methods and compositions for cellular and metabolic engineering
MX9606013A (es) 1994-06-03 1997-12-31 Novo Nordisk Biotech Inc Lacasas purificadas de myceliophthora y acidos nucleicos que codifican para las mismas.
EP0777737B1 (en) 1994-06-30 2005-05-04 Novozymes Biotech, Inc. Non-toxic, non-toxigenic, non-pathogenic fusarium expression system and promoters and terminators for use therein
FI104465B (fi) 1995-06-14 2000-02-15 Valio Oy Proteiinihydrolysaatteja allergioiden hoitamiseksi tai estämiseksi, niiden valmistus ja käyttö
IL136574A0 (en) 1997-12-08 2001-06-14 California Inst Of Techn A method for forming a polynucleotide of desired properties
US6495023B1 (en) 1998-07-09 2002-12-17 Michigan State University Electrochemical methods for generation of a biological proton motive force and pyridine nucleotide cofactor regeneration
JP4221100B2 (ja) 1999-01-13 2009-02-12 エルピーダメモリ株式会社 半導体装置
US6376246B1 (en) 1999-02-05 2002-04-23 Maxygen, Inc. Oligonucleotide mediated nucleic acid recombination
DE60042090D1 (de) 1999-03-11 2009-06-04 Eastman Chem Co Enzymatische Reduktion mit Hydrogen mittels metallkatalysierter Kofaktorregenerierung
AU4964101A (en) 2000-03-30 2001-10-15 Maxygen Inc In silico cross-over site selection
US7049485B2 (en) 2000-10-20 2006-05-23 Board Of Trustees Of Michigan State University Transgenic plants containing ligninase and cellulase which degrade lignin and cellulose to fermentable sugars
US7202070B2 (en) 2000-10-31 2007-04-10 Biocatalytics, Inc. Method for reductive amination of a ketone using a mutated enzyme
EP1479762B1 (en) 2002-02-28 2011-09-28 Mitsubishi Chemical Corporation Novel dehydrogenase and gene encoding the same
US20050084907A1 (en) 2002-03-01 2005-04-21 Maxygen, Inc. Methods, systems, and software for identifying functional biomolecules
BRPI0413501A (pt) 2003-08-11 2006-10-10 Codexis Inc polipetìdeo, polinucleotìdeo isolado ou recombinante, vetor de expressão, célula hospedeira, e, método de preparar um polipetìdeo de hhdh
KR20060064620A (ko) 2003-08-11 2006-06-13 코덱시스, 인코포레이티드 개선된 글루코스 데히드로게나제 폴리펩티드 및 관련폴리뉴클레오티드
WO2005017135A1 (en) 2003-08-11 2005-02-24 Codexis, Inc. Improved ketoreductase polypeptides and related polynucleotides
MXPA06001718A (es) 2003-08-11 2006-05-19 Codexis Inc Procedimiento enzimatico para la produccion de derivados de acido 3-hidroxibutirico 4-sustituido y esteres de acido carboxilico sustituido con ciano e hidroxi vecinales.
KR101234439B1 (ko) 2003-09-25 2013-02-18 몬산토 테크놀로지 엘엘씨 단백질 내로의 비―표준 아미노산의 도입 방지
KR101502634B1 (ko) 2007-02-08 2015-03-16 코덱시스, 인코포레이티드 케토 환원 효소 및 이의 용도
EP2118281A2 (en) 2007-02-12 2009-11-18 Codexis, Inc. Structure-activity relationships
WO2009029554A2 (en) 2007-08-24 2009-03-05 Codexis, Inc. Improved ketoreductase polypeptides for the stereoselective production of (r)-3-hydroxythiolane
JP5973131B2 (ja) 2007-09-13 2016-08-23 コデクシス, インコーポレイテッド アセトフェノンの還元のためのケトレダクターゼポリペプチド
KR20100061571A (ko) * 2007-09-28 2010-06-07 코덱시스, 인코포레이티드 케토리덕타제 폴리펩티드 및 이의 용도
EP2205727B1 (en) 2007-10-01 2015-06-24 Codexis, Inc. Ketoreductase polypeptides for the production of azetidinone
US20090312196A1 (en) 2008-06-13 2009-12-17 Codexis, Inc. Method of synthesizing polynucleotide variants
WO2010027710A2 (en) 2008-08-27 2010-03-11 Codexis, Inc. Ketoreductase polypeptides and uses thereof
WO2010025287A2 (en) 2008-08-27 2010-03-04 Codexis, Inc. Ketoreductase polypeptides for the production of 3-aryl-3-hydroxypropanamine from a 3-aryl-3-ketopropanamine
HUE026181T2 (en) 2008-08-27 2016-05-30 Codexis Inc Ketoreductase polypeptide for the preparation of 3-aryl-3-hydroxypropanamine from 3-aryl-3-ketopropanamine
CN102186972B (zh) 2008-08-29 2014-08-20 科德克希思公司 用于立体选择性生产(4s)-3-[(5s)-5-(4-氟苯基)-5-羟基戊酰基]-4-苯基-1,3-噁唑烷-2-酮的酮还原酶多肽
US20110262977A1 (en) * 2008-09-01 2011-10-27 Daicel Chemical Industries, Ltd. Process for production of optically active amine derivative
HUE036947T2 (hu) 2012-05-11 2018-08-28 Codexis Inc Átalakított iminreduktázok és eljárások keton- és aminvegyületek reduktív aminálására

Also Published As

Publication number Publication date
US10787689B2 (en) 2020-09-29
WO2013170050A1 (en) 2013-11-14
US20200385768A1 (en) 2020-12-10
US20170022527A1 (en) 2017-01-26
CN104428313B (zh) 2017-11-17
US10494656B2 (en) 2019-12-03
US20160168545A1 (en) 2016-06-16
HUE036947T2 (hu) 2018-08-28
EP2847214B1 (en) 2017-12-27
US9193957B2 (en) 2015-11-24
US20210054422A1 (en) 2021-02-25
US20190078124A1 (en) 2019-03-14
US10947572B2 (en) 2021-03-16
EP2847214A1 (en) 2015-03-18
US20160040140A1 (en) 2016-02-11
US9695451B2 (en) 2017-07-04
CN107904216B (zh) 2021-06-29
US11377673B2 (en) 2022-07-05
US9803224B2 (en) 2017-10-31
US9487760B2 (en) 2016-11-08
US9296993B2 (en) 2016-03-29
US20190249209A1 (en) 2019-08-15
US10066250B2 (en) 2018-09-04
US10160983B1 (en) 2018-12-25
US20170268028A1 (en) 2017-09-21
US20230295673A1 (en) 2023-09-21
CN107904216A (zh) 2018-04-13
US20180066292A1 (en) 2018-03-08
US20200032303A1 (en) 2020-01-30
IL235292A (en) 2017-12-31
SG11201407297VA (en) 2014-12-30
US20180187221A1 (en) 2018-07-05
US20130302859A1 (en) 2013-11-14
US20180346945A1 (en) 2018-12-06
US11618911B2 (en) 2023-04-04
CN104428313A (zh) 2015-03-18
US9828614B1 (en) 2017-11-28
US10308966B2 (en) 2019-06-04
US20220315961A1 (en) 2022-10-06
US9932613B2 (en) 2018-04-03

Similar Documents

Publication Publication Date Title
US11618911B2 (en) Engineered imine reductases and methods for the reductive amination of ketone and amine compounds
US11060072B2 (en) Engineered imine reductases and methods for the reductive amination of ketone and amine compounds
EP3224354B1 (en) Engineered imine reductases and methods for the reductive amination of ketone and amine compounds