KR20150010932A - 카바페넴의 무세포 제조법 - Google Patents
카바페넴의 무세포 제조법 Download PDFInfo
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- KR20150010932A KR20150010932A KR1020147009054A KR20147009054A KR20150010932A KR 20150010932 A KR20150010932 A KR 20150010932A KR 1020147009054 A KR1020147009054 A KR 1020147009054A KR 20147009054 A KR20147009054 A KR 20147009054A KR 20150010932 A KR20150010932 A KR 20150010932A
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- 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
- C12P17/18—Preparation 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
- C12P17/182—Heterocyclic compounds containing nitrogen atoms as the only ring heteroatoms in the condensed system
- C12P17/184—Heterocyclic compounds containing nitrogen atoms as the only ring heteroatoms in the condensed system containing a beta-lactam ring, e.g. thienamycin
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
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- 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
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
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- C12N9/0004—Oxidoreductases (1.)
- C12N9/0008—Oxidoreductases (1.) acting on the aldehyde or oxo group of donors (1.2)
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
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Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BRPI0811530B1 (pt) | 2007-05-14 | 2019-01-02 | Research Foundation Of State Univ Of New York | composição compreendendo indutor(es) de resposta fisiológica à dispersão ácido decanóico, superfície, solução, método ex vivo de tratamento ou inibição da formação de um biofilme sobre uma superfície |
| US9637746B2 (en) | 2008-12-15 | 2017-05-02 | Greenlight Biosciences, Inc. | Methods for control of flux in metabolic pathways |
| ES2718844T3 (es) | 2010-05-07 | 2019-07-04 | Greenlight Biosciences Inc | Métodos para controlar el flujo en rutas metabólicas mediante la reubicación de enzimas |
| US8916358B2 (en) | 2010-08-31 | 2014-12-23 | Greenlight Biosciences, Inc. | Methods for control of flux in metabolic pathways through protease manipulation |
| RU2015129774A (ru) | 2012-12-21 | 2017-02-01 | Гринлайт Байосайенсиз, Инк. | Бесклеточная система для преобразования метана в топливо, пируват или изобутанол |
| JP6483687B2 (ja) | 2013-08-05 | 2019-03-13 | グリーンライト バイオサイエンシーズ インコーポレーテッドGreenlight Biosciences,Inc. | プロテアーゼ切断部位を有する操作されたタンパク質 |
| BR112017020690A2 (pt) | 2015-03-30 | 2018-06-26 | Greenlight Biosciences Inc | produção livre de células de ácido ribonucleico |
| CN109196109B (zh) | 2016-04-06 | 2024-06-25 | 绿光生物科技股份有限公司 | 无细胞生成核糖核酸 |
| NL2017636B1 (en) | 2016-10-18 | 2018-04-26 | Univ Delft Tech | Methods for increasing production of carbapenem antibiotics and derivatives in bacteria |
| AU2018205503A1 (en) | 2017-01-06 | 2019-07-25 | Greenlight Biosciences, Inc. | Cell-free production of sugars |
| CN107630054A (zh) * | 2017-04-13 | 2018-01-26 | 绍兴百茵生物技术有限公司 | 培南类药物中间体的生物转化方法 |
| BR112020007068A2 (pt) | 2017-10-11 | 2020-10-06 | Greenlight Biosciences, Inc. | métodos e composições para produção de nucleosídeo trifosfato e ácido ribonucleico |
| US11319320B2 (en) | 2017-11-06 | 2022-05-03 | Snap Bio, Inc. | PIM kinase inhibitor compositions, methods, and uses thereof |
| NL2020614B1 (en) | 2018-03-19 | 2019-09-30 | Univ Delft Tech | Method for producing cell wall-targeting antibiotics in susceptible bacteria |
Family Cites Families (130)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| USRE28886E (en) | 1969-08-04 | 1976-06-29 | Kyowa Hakko Kogyo Co., Ltd. | Method for preparing cytidine diphosphate choline |
| JPS4841555B1 (enExample) | 1969-08-04 | 1973-12-07 | ||
| US4006060A (en) | 1974-11-25 | 1977-02-01 | Merck & Co., Inc. | Thienamycin production |
| US3950357A (en) | 1974-11-25 | 1976-04-13 | Merck & Co., Inc. | Antibiotics |
| US4194047A (en) | 1975-11-21 | 1980-03-18 | Merck & Co., Inc. | Substituted N-methylene derivatives of thienamycin |
| US4266034A (en) | 1978-04-14 | 1981-05-05 | Exxon Research And Engineering Company | Method for producing microbial cells and use thereof to produce oxidation products |
| US4248966A (en) | 1979-05-17 | 1981-02-03 | Massachusetts Institute Of Technology | Synthesis of isopenicillin derivatives in the absence of living cells |
| US4270537A (en) | 1979-11-19 | 1981-06-02 | Romaine Richard A | Automatic hypodermic syringe |
| US4458066A (en) | 1980-02-29 | 1984-07-03 | University Patents, Inc. | Process for preparing polynucleotides |
| US4329481A (en) | 1980-06-25 | 1982-05-11 | Merck & Co., Inc. | Process for the preparation of N-protected N-formimidoyl 2-aminoethanethiol |
| US4292436A (en) | 1980-06-25 | 1981-09-29 | Merck & Co., Inc. | Process for the preparation of N-protected N-formimidoyl 2-aminoethanethiol |
| US4374772A (en) | 1981-03-19 | 1983-02-22 | Merck & Co., Inc. | Process for the preparation of N-formimidoyl thienamycin and reagents therefor |
| JPS585189A (ja) | 1981-07-01 | 1983-01-12 | Sanraku Inc | 新規なアミドヒドロラ−ゼ |
| US4460689A (en) | 1982-04-15 | 1984-07-17 | Merck & Co., Inc. | DNA Cloning vector TG1, derivatives, and processes of making |
| JPS617788A (ja) | 1984-06-22 | 1986-01-14 | Sony Corp | 静止画記録再生装置 |
| US4596556A (en) | 1985-03-25 | 1986-06-24 | Bioject, Inc. | Hypodermic injection apparatus |
| EP0202094B1 (en) | 1985-05-13 | 1988-09-21 | Unitika Ltd. | Process for producing physiologically active substance |
| JPS61260895A (ja) | 1985-05-13 | 1986-11-19 | Unitika Ltd | 生理活性物質の製造方法 |
| US5672497A (en) | 1986-03-21 | 1997-09-30 | Eli Lilly And Company | Method for increasing the antibiotic-producing ability of antibiotic-producing microorganisms |
| US4886499A (en) | 1986-12-18 | 1989-12-12 | Hoffmann-La Roche Inc. | Portable injection appliance |
| US4946783A (en) | 1987-01-30 | 1990-08-07 | President And Fellows Of Harvard College | Periplasmic protease mutants of Escherichia coli |
| GB8704027D0 (en) | 1987-02-20 | 1987-03-25 | Owen Mumford Ltd | Syringe needle combination |
| US4790824A (en) | 1987-06-19 | 1988-12-13 | Bioject, Inc. | Non-invasive hypodermic injection device |
| US4941880A (en) | 1987-06-19 | 1990-07-17 | Bioject, Inc. | Pre-filled ampule and non-invasive hypodermic injection device assembly |
| US4940460A (en) | 1987-06-19 | 1990-07-10 | Bioject, Inc. | Patient-fillable and non-invasive hypodermic injection device assembly |
| US4950603A (en) | 1987-11-02 | 1990-08-21 | Eli Lilly And Company | Recombinant DNA expression vectors and DNA compounds that encode isopenicillin N synthetase from Streptomyces lipmanii |
| JPH01228473A (ja) | 1988-03-08 | 1989-09-12 | Hikari Kimura | 新規な組み換え体dnaおよびグルタチオンの製造法 |
| US5339163A (en) | 1988-03-16 | 1994-08-16 | Canon Kabushiki Kaisha | Automatic exposure control device using plural image plane detection areas |
| US5070020A (en) | 1988-05-09 | 1991-12-03 | Eli Lilly And Company | Recombinant dna expression vectors and dna compounds that encode deacetoxycephalosporin c synthetase |
| FR2638359A1 (fr) | 1988-11-03 | 1990-05-04 | Tino Dalto | Guide de seringue avec reglage de la profondeur de penetration de l'aiguille dans la peau |
| CA2005649A1 (en) | 1988-12-22 | 1990-06-22 | Matthew B. Tobin | Recombinant dna expression vectors and dna compounds that encode isopenicillin n epimerase (racemase) activity |
| US5312335A (en) | 1989-11-09 | 1994-05-17 | Bioject Inc. | Needleless hypodermic injection device |
| US5064413A (en) | 1989-11-09 | 1991-11-12 | Bioject, Inc. | Needleless hypodermic injection device |
| IL97000A0 (en) | 1990-01-26 | 1992-03-29 | Lilly Co Eli | Recombinant dna expression vectors and dna compounds that encode isopenicillin n epimerase activity |
| US5190521A (en) | 1990-08-22 | 1993-03-02 | Tecnol Medical Products, Inc. | Apparatus and method for raising a skin wheal and anesthetizing skin |
| US5527288A (en) | 1990-12-13 | 1996-06-18 | Elan Medical Technologies Limited | Intradermal drug delivery device and method for intradermal delivery of drugs |
| GB9118204D0 (en) | 1991-08-23 | 1991-10-09 | Weston Terence E | Needle-less injector |
| SE9102652D0 (sv) | 1991-09-13 | 1991-09-13 | Kabi Pharmacia Ab | Injection needle arrangement |
| KR0177841B1 (ko) | 1992-01-30 | 1999-04-01 | 나까무라 간노스께 | 시티딘 디인산 콜린의 제조방법 |
| US5328483A (en) | 1992-02-27 | 1994-07-12 | Jacoby Richard M | Intradermal injection device with medication and needle guard |
| US5383851A (en) | 1992-07-24 | 1995-01-24 | Bioject Inc. | Needleless hypodermic injection device |
| US5569189A (en) | 1992-09-28 | 1996-10-29 | Equidyne Systems, Inc. | hypodermic jet injector |
| US5334144A (en) | 1992-10-30 | 1994-08-02 | Becton, Dickinson And Company | Single use disposable needleless injector |
| US5319122A (en) | 1992-11-12 | 1994-06-07 | Merck & Co., Inc. | Process for the preparation of benzylformimidate |
| EP0679189B1 (en) | 1993-01-15 | 2003-06-04 | Genetics Institute, LLC | Cloning of enterokinase and method of use |
| US6746859B1 (en) | 1993-01-15 | 2004-06-08 | Genetics Institute, Llc | Cloning of enterokinase and method of use |
| US5436131A (en) | 1993-04-02 | 1995-07-25 | Merck & Co., Inc. | Color screening assay for identifying inhibitor resistant HIV protease mutants |
| WO1995024176A1 (en) | 1994-03-07 | 1995-09-14 | Bioject, Inc. | Ampule filling device |
| US5466220A (en) | 1994-03-08 | 1995-11-14 | Bioject, Inc. | Drug vial mixing and transfer device |
| KR0131166B1 (ko) | 1994-05-04 | 1998-04-11 | 최차용 | 무세포시스템에서 단백질을 제조하는 방법 |
| GB9410142D0 (en) * | 1994-05-20 | 1994-07-06 | Univ Warwick | Carbapenems |
| US5599302A (en) | 1995-01-09 | 1997-02-04 | Medi-Ject Corporation | Medical injection system and method, gas spring thereof and launching device using gas spring |
| JPH08196284A (ja) | 1995-01-19 | 1996-08-06 | Canon Inc | 酵素反応素子およびその製造方法、酵素反応器ならびに酵素反応方法 |
| US5730723A (en) | 1995-10-10 | 1998-03-24 | Visionary Medical Products Corporation, Inc. | Gas pressured needle-less injection device and method |
| WO1997002358A1 (en) | 1995-07-06 | 1997-01-23 | The Leland Stanford Junior University | Cell-free synthesis of polyketides |
| US6537776B1 (en) | 1999-06-14 | 2003-03-25 | Diversa Corporation | Synthetic ligation reassembly in directed evolution |
| US5893397A (en) | 1996-01-12 | 1999-04-13 | Bioject Inc. | Medication vial/syringe liquid-transfer apparatus |
| GB9607549D0 (en) | 1996-04-11 | 1996-06-12 | Weston Medical Ltd | Spring-powered dispensing device |
| KR100205768B1 (en) | 1996-08-24 | 1999-07-01 | Choongwae Pharm Co | Stereo-selective composition of 4-acetoxyazetidinone |
| GB9622516D0 (en) | 1996-10-29 | 1997-01-08 | Univ Cambridge Tech | Enzymic cofactor cycling |
| US20020160459A1 (en) | 1997-01-14 | 2002-10-31 | Alan Berry | Process for production of n-glucosamine |
| US5993412A (en) | 1997-05-19 | 1999-11-30 | Bioject, Inc. | Injection apparatus |
| IT1298087B1 (it) | 1998-01-08 | 1999-12-20 | Fiderm S R L | Dispositivo per il controllo della profondita' di penetrazione di un ago, in particolare applicabile ad una siringa per iniezioni |
| GB9815666D0 (en) * | 1998-07-17 | 1998-09-16 | Smithkline Beecham Plc | Novel compounds |
| US6613552B1 (en) | 1999-01-29 | 2003-09-02 | Board Of Trustees Operating Michigan State University | Biocatalytic synthesis of shikimic acid |
| US6994986B2 (en) | 1999-03-17 | 2006-02-07 | The Board Of Trustees Of The Leland Stanford University | In vitro synthesis of polypeptides by optimizing amino acid metabolism |
| CA2365668C (en) | 1999-03-17 | 2014-05-20 | The Board Of Trustees Of The Leland Stanford Junior University | In vitro macromolecule biosynthesis methods using exogenous amino acids and a novel atp regeneration system |
| US6168931B1 (en) | 1999-03-17 | 2001-01-02 | The Board Of Trustees Of The Leland Stanford Junior University | Enhanced in vitro synthesis of biological macromolecules using a novel ATP regeneration system |
| WO2000062804A2 (en) | 1999-04-15 | 2000-10-26 | The Regents Of The University Of California | Identification of sortase gene |
| US6284483B1 (en) | 1999-10-06 | 2001-09-04 | Board Of Trustees Operating Michigan State University | Modified synthetases to produce penicillins and cephalosporins under the control of bicarbonate |
| CA2293852A1 (fr) | 1999-12-30 | 2001-06-30 | Purecell Technologies Inc. | Procede de preparation d'extraits de plantes actifs et utiles a la capture de radicaux libres; les extraits, et compositions et dispositifs les comprenant |
| US6548276B2 (en) | 2000-09-06 | 2003-04-15 | The Board Of Trustees Of The Leland Stanford Junior University | Enhanced in vitro synthesis of active proteins containing disulfide bonds |
| US7041479B2 (en) | 2000-09-06 | 2006-05-09 | The Board Of Trustess Of The Leland Stanford Junior University | Enhanced in vitro synthesis of active proteins containing disulfide bonds |
| KR20080113283A (ko) | 2001-04-04 | 2008-12-29 | 제넨코 인터내셔날 인코포레이티드 | 숙주 세포에서의 생산물의 생산 방법 |
| WO2002088325A2 (en) | 2001-05-02 | 2002-11-07 | University Of South Florida | Vector system for selection of genes encoding secreted proteins and membrane-bound proteins |
| RU2294370C2 (ru) | 2001-09-06 | 2007-02-27 | Адзиномото Ко., Инк. | Способ получения спирта с использованием микроорганизма |
| AU2002326884B2 (en) | 2001-09-13 | 2007-10-18 | Genentech, Inc. | Aminopeptidase |
| AU2002363144A1 (en) | 2001-10-30 | 2003-05-12 | The Board Of Trustees Of The Leland Stanford Junior University | Enhanced in vitro nucleic acid synthesis using nucleoside monophosphates |
| US20040038250A1 (en) | 2002-04-04 | 2004-02-26 | Astur-Pharma, S.A. | Gene cluster for thienamycin biosynthesis, genetic manipulation and utility |
| DE10219714A1 (de) | 2002-05-02 | 2003-11-27 | Holland Sweetener Co | Verfahren zur mikrobielien Herstellung von aromatischen Aminosäuren und anderen Metaboliten des aromatischen Aminosäurebiosyntheseweges |
| US20050164359A1 (en) | 2002-05-08 | 2005-07-28 | Hashimoto Shin-Ichi | Process for producing cytidine 5'-diphosphate choline |
| MXPA04012978A (es) | 2002-07-01 | 2005-09-12 | Arkion Life Sciences Llc D B A | Proceso y material para la produccion de glucosamina y n-acetilglucosamina. |
| CA2496437C (en) | 2002-08-19 | 2013-01-08 | The Board Of Trustees Of The Leland Stanford Junior University | Improved methods of in vitro protein synthesis |
| US7223390B2 (en) | 2003-05-09 | 2007-05-29 | Research Development Foundation | Insertion of furin protease cleavage sites in membrane proteins and uses thereof |
| US7341852B2 (en) | 2003-07-18 | 2008-03-11 | The Board Of Trustees Of The Leland Stanford Junior University | Methods of decoupling reaction scale and protein synthesis yield in batch mode |
| US20050054044A1 (en) | 2003-07-18 | 2005-03-10 | The Board Of Trustees Of The Leland Stanford Junior University | Method of alleviating nucleotide limitations for in vitro protein synthesis |
| WO2005030949A1 (en) | 2003-09-24 | 2005-04-07 | Board Of Trustees Operating Michigan State University | Methods and materials for the production of shikimic acid |
| CN101014716B (zh) | 2003-11-20 | 2015-06-10 | 小利兰·斯坦福大学托管委员会 | 体外蛋白质合成的改进方法 |
| EA010837B1 (ru) | 2004-03-25 | 2008-12-30 | Зе Боард Оф Трастиз Оф Зе Лилэнд Стэнфорд Джуниор Юниверсити | Повышение выхода экспрессии протеина в системах бесклеточного синтеза протеинов путём добавления антипенных присадок |
| US8257943B2 (en) | 2004-06-25 | 2012-09-04 | Kyowa Hakko Bio Co., Ltd. | Process for producing dipeptides or dipeptide derivatives |
| EP1819813A2 (en) | 2004-12-10 | 2007-08-22 | DSMIP Assets B.V. | Production of beta-lactam antibiotics by genetically modified non-naturally producing microorganisms |
| WO2006090385A2 (en) | 2005-02-22 | 2006-08-31 | Ramot At Tel-Aviv University Ltd. | Protease inhibitors and method of screening thereof |
| US7351563B2 (en) | 2005-06-10 | 2008-04-01 | The Board Of Trustees Of The Leland Stanford Junior University | Cell-free extracts and synthesis of active hydrogenase |
| US7312049B2 (en) | 2005-06-14 | 2007-12-25 | The Board Of Trustees Of The Leland Stanford Junior University | Total amino acid stabilization during cell-free protein synthesis |
| TW200741005A (en) | 2005-08-10 | 2007-11-01 | Kyowa Hakko Kogyo Kk | A purification method of cytidine diphosphate |
| US7517680B2 (en) | 2005-09-09 | 2009-04-14 | Johns Hopkins University | Production of clavulanic acid by genetic engineering of Streptomyces clavuligerus |
| US8183010B2 (en) | 2005-10-31 | 2012-05-22 | The Board Of Trustees Of The Leland Stanford Junior University | Cell-free synthesis of membrane bound polypeptides |
| WO2007137144A2 (en) | 2006-05-17 | 2007-11-29 | University Of Medicine And Dentistry Of New Jersey | Single protein production in living cells facilitated by a messenger rna interferase |
| WO2007140816A1 (en) | 2006-06-09 | 2007-12-13 | Metabolic Explorer | Glycolic acid production by fermentation from renewable resources |
| WO2007144018A1 (en) | 2006-06-12 | 2007-12-21 | Metabolic Explorer | Ethanolamine production by fermentation |
| US20110129438A1 (en) | 2006-06-28 | 2011-06-02 | James Robert Swartz | Immunogenic protein constructs |
| WO2008002661A2 (en) | 2006-06-28 | 2008-01-03 | The Board Of Trustees Of The Leland Stanford Junior University | Fusion protein constructs |
| AU2007325952B8 (en) | 2006-06-29 | 2013-06-27 | The Board Of Trustees Of The Leland Stanford Junior University | Cell-free synthesis of proteins containing unnatural amino acids |
| WO2008002673A2 (en) | 2006-06-29 | 2008-01-03 | The Board Of Trustees Of The Leland Stanford Junior University | Cell-free synthesis of virus like particles |
| US8293894B2 (en) | 2006-11-20 | 2012-10-23 | Orchid Chemicals & Pharmaceuticals Limited | Process for the preparation of carbapenem antibiotic |
| KR100832740B1 (ko) | 2007-01-17 | 2008-05-27 | 한국과학기술원 | 분지쇄 아미노산 생성능이 개선된 변이 미생물 및 이를이용한 분지쇄 아미노산의 제조방법 |
| US7871794B2 (en) | 2007-01-18 | 2011-01-18 | The Board Of Trustees Of The Leland Stanford Junior University | Enhanced cell-free synthesis of active proteins containing disulfide bonds |
| WO2008094546A2 (en) | 2007-01-31 | 2008-08-07 | The Regents Of The University Of California | Genetically modified host cells for increased p450 activity levels and methods of use thereof |
| US20090124012A1 (en) | 2007-08-08 | 2009-05-14 | Mazef Biosciences, Llc | Toxin/antitoxin systems and methods for regulating cellular growth, metabolic engineering and production of recombinant proteins |
| EP2242842A1 (en) | 2008-02-14 | 2010-10-27 | Wageningen Universiteit | Nucleotide sequences coding for cis-aconitic decarboxylase and use thereof |
| SI2262901T1 (sl) | 2008-03-05 | 2019-02-28 | Genomatica, Inc. | Primarni alkohol producirajoči organizmi |
| JP2011519561A (ja) | 2008-05-01 | 2011-07-14 | ジェノマティカ, インコーポレイテッド | メタクリル酸の産生のための微生物 |
| JP5750370B2 (ja) | 2008-07-28 | 2015-07-22 | ブレイン・バイオテクノロジー・リサーチ・アンド・インフォメーション・ネットワーク・アクチェンゲゼルシャフト | 生産方法 |
| GB0819563D0 (en) | 2008-10-24 | 2008-12-03 | Isis Innovation | Methods for preparing heterocyclic rings |
| BRPI0914521A2 (pt) | 2008-10-27 | 2016-07-26 | Butamax Advanced Biofuels Llc | célula hospedeira microbiana recombinante, método de aumento da produção de isobutanol e método de produção de isobutanol |
| WO2010051527A2 (en) | 2008-10-31 | 2010-05-06 | Gevo, Inc. | Engineered microorganisms capable of producing target compounds under anaerobic conditions |
| US9637746B2 (en) | 2008-12-15 | 2017-05-02 | Greenlight Biosciences, Inc. | Methods for control of flux in metabolic pathways |
| CN105132387A (zh) * | 2008-12-22 | 2015-12-09 | 绿光生物科学公司 | 用于制造化合物的组合物和方法 |
| EP2204453B1 (en) | 2008-12-30 | 2013-03-13 | Süd-Chemie IP GmbH & Co. KG | Process for cell-free production of chemicals |
| US8597923B2 (en) | 2009-05-06 | 2013-12-03 | SyntheZyme, LLC | Oxidation of compounds using genetically modified Candida |
| WO2010141468A1 (en) | 2009-06-01 | 2010-12-09 | Way Jeffrey C | Methods and molecules for yield improvement involving metabolic engineering |
| EP2462221B1 (en) | 2009-08-05 | 2017-02-22 | Genomatica, Inc. | Semi-synthetic terephthalic acid via microorganisms that produce muconic acid |
| EP2513112A4 (en) | 2009-12-11 | 2013-05-08 | Univ Johns Hopkins | PROCEDURE FOR LATE ADDITION OF THE (8R) -HYDROXYL GROUP TO THE CARBAPENEM BETA-LACTAM ANTIBIOTICASYNTHESIS |
| US9040253B2 (en) | 2010-04-14 | 2015-05-26 | Sutro Biopharma, Inc. | Method for enhancing recombinant protein production by cell-free protein expression system |
| ES2718844T3 (es) | 2010-05-07 | 2019-07-04 | Greenlight Biosciences Inc | Métodos para controlar el flujo en rutas metabólicas mediante la reubicación de enzimas |
| US8916358B2 (en) * | 2010-08-31 | 2014-12-23 | Greenlight Biosciences, Inc. | Methods for control of flux in metabolic pathways through protease manipulation |
| WO2012135902A1 (en) | 2011-04-08 | 2012-10-11 | James Cook University | Protease activity assay |
| RU2015129774A (ru) | 2012-12-21 | 2017-02-01 | Гринлайт Байосайенсиз, Инк. | Бесклеточная система для преобразования метана в топливо, пируват или изобутанол |
| AU2014274932A1 (en) | 2013-06-05 | 2015-12-17 | Greenlight Biosciences, Inc. | Control of metabolic flux in cell-free biosynthetic systems |
| JP6483687B2 (ja) | 2013-08-05 | 2019-03-13 | グリーンライト バイオサイエンシーズ インコーポレーテッドGreenlight Biosciences,Inc. | プロテアーゼ切断部位を有する操作されたタンパク質 |
-
2012
- 2012-09-07 CA CA2846893A patent/CA2846893A1/en not_active Abandoned
- 2012-09-07 CN CN201280054408.6A patent/CN104093848A/zh active Pending
- 2012-09-07 US US13/606,911 patent/US9469861B2/en not_active Expired - Fee Related
- 2012-09-07 EP EP12766509.9A patent/EP2753702B1/en not_active Not-in-force
- 2012-09-07 KR KR1020147009054A patent/KR20150010932A/ko not_active Withdrawn
- 2012-09-07 JP JP2014529904A patent/JP2014526250A/ja active Pending
- 2012-09-07 SG SG2014014377A patent/SG2014014377A/en unknown
- 2012-09-07 WO PCT/US2012/054195 patent/WO2013036787A2/en not_active Ceased
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2014
- 2014-02-17 IL IL231010A patent/IL231010A0/en unknown
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2016
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| EP2753702B1 (en) | 2021-12-15 |
| US9469861B2 (en) | 2016-10-18 |
| IL231010A0 (en) | 2014-03-31 |
| JP2014526250A (ja) | 2014-10-06 |
| SG2014014377A (en) | 2014-05-29 |
| CN104093848A (zh) | 2014-10-08 |
| HK1199909A1 (en) | 2015-07-24 |
| EP2753702A2 (en) | 2014-07-16 |
| US20170096692A1 (en) | 2017-04-06 |
| US20130065878A1 (en) | 2013-03-14 |
| WO2013036787A2 (en) | 2013-03-14 |
| CA2846893A1 (en) | 2013-03-14 |
| WO2013036787A3 (en) | 2013-06-13 |
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