ES2699747T3 - Microorganismos recombinantes para la producción potenciada de mevalonato, isopreno e isoprenoides - Google Patents
Microorganismos recombinantes para la producción potenciada de mevalonato, isopreno e isoprenoides Download PDFInfo
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- ES2699747T3 ES2699747T3 ES12720353T ES12720353T ES2699747T3 ES 2699747 T3 ES2699747 T3 ES 2699747T3 ES 12720353 T ES12720353 T ES 12720353T ES 12720353 T ES12720353 T ES 12720353T ES 2699747 T3 ES2699747 T3 ES 2699747T3
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Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201161481121P | 2011-04-29 | 2011-04-29 | |
| PCT/US2012/035687 WO2012149491A2 (en) | 2011-04-29 | 2012-04-27 | Recombinant microorganisms for enhanced production of mevalonate, isoprene, and isoprenoids |
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| Publication Number | Publication Date |
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| ES2699747T3 true ES2699747T3 (es) | 2019-02-12 |
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| ES12720353T Active ES2699747T3 (es) | 2011-04-29 | 2012-04-27 | Microorganismos recombinantes para la producción potenciada de mevalonato, isopreno e isoprenoides |
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| EP (1) | EP2702140B1 (enExample) |
| JP (2) | JP6301827B2 (enExample) |
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| US8647642B2 (en) | 2008-09-18 | 2014-02-11 | Aviex Technologies, Llc | Live bacterial vaccines resistant to carbon dioxide (CO2), acidic PH and/or osmolarity for viral infection prophylaxis or treatment |
| US9121038B2 (en) | 2011-04-29 | 2015-09-01 | The Goodyear Tire & Rubber Company | Recombinant microorganisms for enhanced production of mevalonate, isoprene, and isoprenoids |
| EP2794851A2 (en) * | 2011-12-23 | 2014-10-29 | Danisco US Inc. | Enhanced production of isoprene using marine bacterial cells |
| WO2013181647A2 (en) * | 2012-06-01 | 2013-12-05 | Danisco Us Inc. | Compositions and methods of producing isoprene and/or industrrial bio-products using anaerobic microorganisms |
| RU2723620C2 (ru) * | 2012-07-13 | 2020-06-16 | Калиста, Инк. | Система, способы и композиции для биопереработки |
| CN104540949B (zh) * | 2012-08-07 | 2018-05-29 | 阿迈瑞斯公司 | 用于稳定乙酰-辅酶a衍生化合物生成的方法 |
| MY171958A (en) * | 2013-03-15 | 2019-11-08 | Amyris Inc | Use of phosphoketolase and phosphotransacetylase for production of acetyl-coenzyme a derived compounds |
| ES2735331T3 (es) | 2013-04-10 | 2019-12-18 | Goodyear Tire & Rubber | Fosfocetolasas para mejorar la producción de metabolitos derivados de acetil-coenzima A, isopreno, precursores de isoprenoides e isoprenoides |
| JP6139244B2 (ja) * | 2013-04-23 | 2017-05-31 | 住友ゴム工業株式会社 | ポリイソプレノイド増産方法、およびそのための増産剤、かかる方法で製造されたポリイソプレノイド |
| RU2013146377A (ru) | 2013-10-17 | 2015-04-27 | Закрытое акционерное общество "Научно-исследовательский институт Аджиномото-Генетика" (ЗАО "АГРИ") | СПОСОБ ПОЛУЧЕНИЯ ИЗОПРЕНА С ИСПОЛЬЗОВАНИЕМ БАКТЕРИИ РОДА Bacillus |
| US20160237442A1 (en) * | 2013-10-18 | 2016-08-18 | University Of Washington Through Its Center For Commercialization | Modified group i methanotrophic bacteria and uses thereof |
| US20160237398A1 (en) * | 2013-10-18 | 2016-08-18 | University Of Washington Through Its Center For Commercialization | Methods of microbial production of excreted products from methane and related bacterial strains |
| US20160376600A1 (en) | 2013-11-25 | 2016-12-29 | Genomatica, Inc. | Methods for enhancing microbial production of specific length fatty alcohols in the presence of methanol |
| PL3077501T3 (pl) | 2013-12-03 | 2022-01-31 | Genomatica, Inc. | Mikroorganizmy i sposoby poprawy wydajności produktu na metanolu z użyciem syntezy acetylo-coa |
| CN104164457B (zh) * | 2014-07-15 | 2016-05-04 | 青岛农业大学 | 一种利用新mva途径合成异戊二烯的方法及其相应重组细胞和应用 |
| JP6470532B2 (ja) * | 2014-09-17 | 2019-02-13 | 積水化学工業株式会社 | 組換え細胞、並びに、有機化合物の生産方法 |
| CN104593405A (zh) * | 2014-11-24 | 2015-05-06 | 安徽大学 | 一种高产丙氨酸的枯草杆菌工程菌的构建方法 |
| KR101776375B1 (ko) * | 2015-03-18 | 2017-09-08 | 씨제이제일제당 (주) | 피루브산 디하이드로게나아제 변이체, 이를 포함하는 미생물 및 이를 이용한 l-아미노산 생산 방법 |
| US10676723B2 (en) | 2015-05-11 | 2020-06-09 | David Gordon Bermudes | Chimeric protein toxins for expression by therapeutic bacteria |
| CN105624180B (zh) * | 2016-02-06 | 2018-12-28 | 中国热带农业科学院橡胶研究所 | HbCS3基因在提高原核表达菌生长速率、研究橡胶树抗逆境胁迫和产胶能力中的应用 |
| CN105647953A (zh) * | 2016-03-18 | 2016-06-08 | 黑龙江大学 | 高产2,3-丁二醇的产酸克雷伯氏基因工程菌株的构建方法及其发酵方法 |
| CN105647954A (zh) * | 2016-03-18 | 2016-06-08 | 黑龙江大学 | 高产2,3-丁二醇的产酸克雷伯氏基因工程菌株的构建方法及其发酵方法 |
| CN106148262B (zh) * | 2016-07-01 | 2019-09-03 | 江南大学 | 提高乙酰氨基葡萄糖产量的重组枯草芽孢杆菌及其构建方法 |
| US11180535B1 (en) | 2016-12-07 | 2021-11-23 | David Gordon Bermudes | Saccharide binding, tumor penetration, and cytotoxic antitumor chimeric peptides from therapeutic bacteria |
| US11129906B1 (en) | 2016-12-07 | 2021-09-28 | David Gordon Bermudes | Chimeric protein toxins for expression by therapeutic bacteria |
| CN109234216B (zh) * | 2017-07-10 | 2022-05-20 | 上海医药工业研究院 | 一种生产鲨烯的基因工程菌及其方法 |
| CN107937431A (zh) * | 2017-10-28 | 2018-04-20 | 国际竹藤中心 | 一种提高酿酒酵母合成芳樟醇能力的方法 |
| CN109722403B (zh) * | 2017-10-30 | 2020-12-04 | 中国石油化工股份有限公司 | 一种利用纤维素制备金合欢烯的工程菌株及方法 |
| CN108179114B (zh) * | 2017-11-27 | 2021-08-20 | 南京晓庄学院 | 产抗厌氧菌化合物的菌株和发酵方法、抗厌氧菌化合物提取及制备方法和使用方法 |
| CA3084263A1 (en) | 2017-12-07 | 2019-06-13 | Zymergen Inc. | Engineered biosynthetic pathways for production of (6e)-8-hydroxygeraniol by fermentation |
| CN111868047A (zh) | 2017-12-21 | 2020-10-30 | 齐默尔根公司 | 荆芥内半缩醛氧化还原酶、荆芥内半缩醛合酶和能够产生荆芥内酯的微生物 |
| HUE065696T2 (hu) | 2018-03-06 | 2024-06-28 | Danisco Us Inc | Acetát-termelés csökkentése PAB1-et túltermelõ élesztõvel |
| CN110964679B (zh) * | 2018-09-29 | 2022-06-28 | 中国石油化工股份有限公司 | 一种利用纤维素制备金合欢烯的工程菌株及方法 |
| CN110964680B (zh) * | 2018-09-29 | 2022-06-28 | 中国石油化工股份有限公司 | 利用纤维素制备金合欢烯的工程菌株及方法 |
| WO2020071538A1 (en) | 2018-10-05 | 2020-04-09 | Ajinomoto Co., Inc. | Method for producing target substance by bacterial fermentation |
| US11845940B2 (en) * | 2020-02-27 | 2023-12-19 | The Regents Of The University Of California | Genetically modified fungal cells and methods useful for producing prespatane |
| AU2021305200A1 (en) * | 2020-07-08 | 2023-02-16 | The Regents Of The University Of California | Modified yeast host cells useful for producing isoprenol |
| WO2022032084A1 (en) * | 2020-08-06 | 2022-02-10 | Synlogic Operating Company, Inc. | Recombinant bacteria for production of d-lactate and/or l-lactate and uses thereof |
| CN115704038B (zh) * | 2021-08-10 | 2025-08-15 | 西北农林科技大学 | 一种基因、重组载体、工程菌及其应用 |
| JP2023105728A (ja) * | 2022-01-19 | 2023-07-31 | 旭化成株式会社 | 改変微生物及び化合物の製造方法 |
| CN115948444A (zh) * | 2022-10-21 | 2023-04-11 | 江南大学 | 一种利用硝酸盐和全局厌氧调节因子Fnr提高地衣芽孢杆菌厌氧活性的方法 |
| CN116925991B (zh) * | 2023-07-28 | 2024-08-09 | 天津大学 | 高产甲羟戊酸的重组盐单胞菌菌株及构建方法与应用 |
| CN119286752B (zh) * | 2024-12-10 | 2025-07-11 | 杭州合碳创物科技有限公司 | 一种生产甲瓦龙酸的重组大肠杆菌及其应用 |
Family Cites Families (40)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE19629568C1 (de) | 1996-07-15 | 1998-01-08 | Fraunhofer Ges Forschung | Verfahren zur Herstellung von Isopren |
| WO2000078935A1 (en) | 1999-06-22 | 2000-12-28 | Smithkline Beecham Corporation | Mevalonate pathway genes |
| US7172886B2 (en) | 2001-12-06 | 2007-02-06 | The Regents Of The University Of California | Biosynthesis of isopentenyl pyrophosphate |
| US20050287655A1 (en) | 2002-05-10 | 2005-12-29 | Kyowa Hakko Kogyo Co., Ltd. | Process for producing mevalonic acid |
| AU2003287028B2 (en) | 2002-10-04 | 2008-09-04 | E.I. Du Pont De Nemours And Company | Process for the biological production of 1,3-propanediol with high yield |
| JP4168870B2 (ja) * | 2003-08-14 | 2008-10-22 | トヨタ自動車株式会社 | プレニルアルコールの製造方法 |
| RU2004124226A (ru) | 2004-08-10 | 2006-01-27 | Закрытое акционерное общество "Научно-исследовательский институт Аджиномото-Генетика" (ЗАО АГРИ) (RU) | Использование фосфокетолазы для продукции полезных метаболитов |
| CA2651747C (en) * | 2006-05-26 | 2017-10-24 | Amyris Biotechnologies, Inc. | Production of isoprenoids |
| US7947478B2 (en) | 2006-06-29 | 2011-05-24 | The Regents Of The University Of California | Short chain volatile hydrocarbon production using genetically engineered microalgae, cyanobacteria or bacteria |
| JP4986547B2 (ja) | 2006-09-04 | 2012-07-25 | 株式会社Adeka | 新規なアセトアセチルCoA合成酵素、それをコードするDNA配列、当該酵素の製造方法および当該酵素を利用したメバロン酸の製造方法 |
| MX2009004221A (es) * | 2006-10-20 | 2009-09-10 | Univ Arizona State | Cianobacterias modificadas. |
| US7947483B2 (en) * | 2007-08-10 | 2011-05-24 | Genomatica, Inc. | Methods and organisms for the growth-coupled production of 1,4-butanediol |
| BRPI0823506A8 (pt) | 2007-12-13 | 2018-05-15 | Danisco Us Inc Genencor Div | composições e métodos para a produção de isoprene |
| WO2009100231A2 (en) | 2008-02-06 | 2009-08-13 | The Regents Of The University Of California | Short chain volatile isoprene hydrocarbon production using the mevalonic acid pathway in genetically engineered yeast and fungi |
| CN102015995B (zh) * | 2008-03-03 | 2014-10-22 | 焦耳无限科技公司 | 产生碳基目的产物的二氧化碳固定工程微生物 |
| JP2011518564A (ja) | 2008-04-23 | 2011-06-30 | ダニスコ・ユーエス・インク | 改良された微生物によるイソプレン産出用のイソプレンシンターゼ変異体 |
| US7632995B2 (en) | 2008-05-09 | 2009-12-15 | Monsanto Technology Llc | Plants and seeds of hybrid corn variety CH852179 |
| US10100334B2 (en) * | 2008-05-23 | 2018-10-16 | Nucelis Inc. | Production of squalene using yeast |
| EP2310490B1 (en) | 2008-07-02 | 2019-01-02 | Danisco US Inc. | Methods for producing isoprene |
| HU3516U (en) | 2008-07-31 | 2008-11-28 | Zoltan Kuthi | Anti-theft protection of draining for fuel tanks |
| CA2737082A1 (en) * | 2008-09-15 | 2010-03-18 | Danisco Us Inc. | Increased isoprene production using mevalonate kinase and isoprene synthase |
| MY156562A (en) | 2008-09-15 | 2016-02-26 | Danisco Us Inc | Increased isoprene production using the archaeal lower mevalonate pathway |
| WO2010031079A1 (en) | 2008-09-15 | 2010-03-18 | Danisco Us Inc. | Systems using cell culture for production of isoprene |
| CA2737223A1 (en) | 2008-09-15 | 2010-03-18 | Danisco Us Inc. | Reduction of carbon dioxide emission during isoprene production by fermentation |
| BRPI0918936A2 (pt) | 2008-09-15 | 2019-09-24 | Danisco Us Inc | conversão de derivados de prenila em isopreno |
| CN102333866B (zh) | 2008-12-30 | 2015-04-29 | 丹尼斯科美国公司 | 生产异戊二烯和共同产物的方法 |
| US20100297749A1 (en) | 2009-04-21 | 2010-11-25 | Sapphire Energy, Inc. | Methods and systems for biofuel production |
| EP2421966A2 (en) | 2009-04-23 | 2012-02-29 | Danisco US Inc. | Three-dimensional structure of isoprene synthase and its use thereof for generating variants |
| JP4760951B2 (ja) | 2009-05-08 | 2011-08-31 | トヨタ自動車株式会社 | ブタノール生産能を有する組換え微生物及びブタノールの製造方法 |
| TWI434921B (zh) | 2009-06-17 | 2014-04-21 | Danisco Us Inc | 從生物異戊二烯組合物製造燃料成分之方法及系統 |
| TW201412988A (zh) | 2009-06-17 | 2014-04-01 | Danisco Us Inc | 使用dxp及mva途徑之改良之異戊二烯製造 |
| CA2773675A1 (en) | 2009-09-15 | 2011-03-24 | Sapphire Energy, Inc. | A system for transformation of the chloroplast genome of scenedesmus sp. and dunaliella sp. |
| JP5978132B2 (ja) * | 2009-11-23 | 2016-08-24 | ニューセリス インコーポレイテッド | 酵母を用いるスクアレン生成のための方法および組成物 |
| CN102884028B (zh) | 2009-12-18 | 2015-08-19 | 丹尼斯科美国公司 | 从可再生资源中纯化异戊二烯 |
| AU2010336342B2 (en) | 2009-12-23 | 2015-02-26 | Danisco Us Inc. | Compositions and methods for the increased production of isoprene and other products with 6 - phosphogluconolactonase (PGL) |
| WO2012019169A1 (en) * | 2010-08-06 | 2012-02-09 | Danisco Us Inc. | Production of isoprene under neutral ph conditions |
| JP2014502148A (ja) | 2010-10-27 | 2014-01-30 | ダニスコ・ユーエス・インク | イソプレン生産の向上を目的としたイソプレン合成酵素変異体 |
| EP2655606A1 (en) * | 2010-12-22 | 2013-10-30 | Danisco US Inc. | Compositions and methods for improved isoprene production using two types of ispg enzymes |
| US9121038B2 (en) | 2011-04-29 | 2015-09-01 | The Goodyear Tire & Rubber Company | Recombinant microorganisms for enhanced production of mevalonate, isoprene, and isoprenoids |
| JP2014519811A (ja) * | 2011-04-29 | 2014-08-21 | ダニスコ・ユーエス・インク | チオラーゼ、HMG−CoA合成酵素及びHMG−CoA還元酵素活性を有するポリペプチドをコードしている遺伝子を使用するメバロン酸、イソプレン、及びイソプレノイドの生産 |
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| US20190153479A1 (en) | 2019-05-23 |
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