ES2834978T3 - Proceso de fermentación de dos fases para la producción de un isoprenoide - Google Patents
Proceso de fermentación de dos fases para la producción de un isoprenoide Download PDFInfo
- Publication number
- ES2834978T3 ES2834978T3 ES14761704T ES14761704T ES2834978T3 ES 2834978 T3 ES2834978 T3 ES 2834978T3 ES 14761704 T ES14761704 T ES 14761704T ES 14761704 T ES14761704 T ES 14761704T ES 2834978 T3 ES2834978 T3 ES 2834978T3
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- Prior art keywords
- oxygen
- phase
- isoprenoid
- fermentation
- phase system
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- USDOQCCMRDNVAH-UHFFFAOYSA-N sigma-cadinene Natural products C1C=C(C)CC2C(C(C)C)CC=C(C)C21 USDOQCCMRDNVAH-UHFFFAOYSA-N 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 229940032094 squalane Drugs 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- MCRAOCBPZAIHJQ-QBYKVAOYSA-N stemar-13-ene Chemical compound CC([C@@H]1CC2)(C)CCC[C@]1(C)[C@]1(C3)[C@@H]2C=C(C)[C@@H]3CC1 MCRAOCBPZAIHJQ-QBYKVAOYSA-N 0.000 description 1
- QFVOYBUQQBFCRH-VQSWZGCSSA-N steviol Chemical compound C([C@@]1(O)C(=C)C[C@@]2(C1)CC1)C[C@H]2[C@@]2(C)[C@H]1[C@](C)(C(O)=O)CCC2 QFVOYBUQQBFCRH-VQSWZGCSSA-N 0.000 description 1
- 229940032084 steviol Drugs 0.000 description 1
- 229930182488 steviol glycoside Natural products 0.000 description 1
- 235000019411 steviol glycoside Nutrition 0.000 description 1
- 150000008144 steviol glycosides Chemical class 0.000 description 1
- 235000019202 steviosides Nutrition 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- DKPFODGZWDEEBT-QFIAKTPHSA-N taxane Chemical class C([C@]1(C)CCC[C@@H](C)[C@H]1C1)C[C@H]2[C@H](C)CC[C@@H]1C2(C)C DKPFODGZWDEEBT-QFIAKTPHSA-N 0.000 description 1
- 229930006978 terpinene Natural products 0.000 description 1
- 150000003507 terpinene derivatives Chemical class 0.000 description 1
- 229940116411 terpineol Drugs 0.000 description 1
- 150000003534 tetranortriterpenoids Chemical class 0.000 description 1
- 150000003535 tetraterpenes Chemical class 0.000 description 1
- 235000009657 tetraterpenes Nutrition 0.000 description 1
- 229930007110 thujone Natural products 0.000 description 1
- 229960000790 thymol Drugs 0.000 description 1
- ZRVDANDJSTYELM-FXAWDEMLSA-N totarol Chemical compound CC([C@@H]1CC2)(C)CCC[C@]1(C)C1=C2C(C(C)C)=C(O)C=C1 ZRVDANDJSTYELM-FXAWDEMLSA-N 0.000 description 1
- 229940074347 totarol Drugs 0.000 description 1
- CRDAMVZIKSXKFV-UHFFFAOYSA-N trans-Farnesol Natural products CC(C)=CCCC(C)=CCCC(C)=CCO CRDAMVZIKSXKFV-UHFFFAOYSA-N 0.000 description 1
- ZHYZQXUYZJNEHD-UHFFFAOYSA-N trans-geranic acid Natural products CC(C)=CCCC(C)=CC(O)=O ZHYZQXUYZJNEHD-UHFFFAOYSA-N 0.000 description 1
- ZRVDANDJSTYELM-UHFFFAOYSA-N trans-totarol Natural products C1CC2C(C)(C)CCCC2(C)C2=C1C(C(C)C)=C(O)C=C2 ZRVDANDJSTYELM-UHFFFAOYSA-N 0.000 description 1
- YKUJZZHGTWVWHA-UHFFFAOYSA-N triptolide Natural products COC12CC3OC3(C(C)C)C(O)C14OC4CC5C6=C(CCC25C)C(=O)OC6 YKUJZZHGTWVWHA-UHFFFAOYSA-N 0.000 description 1
- 229930195735 unsaturated hydrocarbon Natural products 0.000 description 1
- 238000009834 vaporization Methods 0.000 description 1
- 230000008016 vaporization Effects 0.000 description 1
- GUAUUIHVMRMGCT-MISXGVKJSA-N velleral Chemical compound C[C@H]1C=C(C=O)C(C=O)=C[C@@H]2CC(C)(C)C[C@H]12 GUAUUIHVMRMGCT-MISXGVKJSA-N 0.000 description 1
- DCSCXTJOXBUFGB-UHFFFAOYSA-N verbenone Natural products CC1=CC(=O)C2C(C)(C)C1C2 DCSCXTJOXBUFGB-UHFFFAOYSA-N 0.000 description 1
- NLUGUZJQJYVUHS-IDXDZYHTSA-N verrucarin A Chemical compound C([C@@]12[C@@]3(C)[C@@]45CCC(C)=C[C@H]4O[C@@H]1C[C@H]3OC(=O)\C=C/C=C/C(=O)OCC[C@H]([C@@H](C(=O)OC5)O)C)O2 NLUGUZJQJYVUHS-IDXDZYHTSA-N 0.000 description 1
- NLUGUZJQJYVUHS-UHFFFAOYSA-N verrucarina A Natural products C1OC(=O)C(O)C(C)CCOC(=O)C=CC=CC(=O)OC2CC3OC4C=C(C)CCC41C2(C)C31CO1 NLUGUZJQJYVUHS-UHFFFAOYSA-N 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 239000012855 volatile organic compound Substances 0.000 description 1
- 239000012138 yeast extract Substances 0.000 description 1
- 229930001895 zingiberene Natural products 0.000 description 1
- KKOXKGNSUHTUBV-LSDHHAIUSA-N zingiberene Chemical compound CC(C)=CCC[C@H](C)[C@H]1CC=C(C)C=C1 KKOXKGNSUHTUBV-LSDHHAIUSA-N 0.000 description 1
- USDOQCCMRDNVAH-KKUMJFAQSA-N β-cadinene Chemical compound C1C=C(C)C[C@H]2[C@H](C(C)C)CC=C(C)[C@@H]21 USDOQCCMRDNVAH-KKUMJFAQSA-N 0.000 description 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
- C12P5/00—Preparation of hydrocarbons or halogenated hydrocarbons
- C12P5/007—Preparation of hydrocarbons or halogenated hydrocarbons containing one or more isoprene units, i.e. terpenes
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Zoology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Microbiology (AREA)
- General Chemical & Material Sciences (AREA)
- Biotechnology (AREA)
- Health & Medical Sciences (AREA)
- Biochemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP13003384 | 2013-07-04 | ||
| PCT/NL2014/000020 WO2015002528A1 (en) | 2013-07-04 | 2014-07-04 | Two-phase fermentation process for the production of an organic compound |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2834978T3 true ES2834978T3 (es) | 2021-06-21 |
Family
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|---|---|---|---|
| ES14761704T Active ES2834978T3 (es) | 2013-07-04 | 2014-07-04 | Proceso de fermentación de dos fases para la producción de un isoprenoide |
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| Country | Link |
|---|---|
| US (2) | US20160168595A1 (https=) |
| EP (1) | EP3017050B1 (https=) |
| BR (1) | BR112015032968B1 (https=) |
| ES (1) | ES2834978T3 (https=) |
| HU (1) | HUE051864T2 (https=) |
| SI (1) | SI3017050T1 (https=) |
| WO (1) | WO2015002528A1 (https=) |
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| US9902979B2 (en) * | 2013-09-05 | 2018-02-27 | Niigata University | Method for producing ambrein |
| JP6579544B2 (ja) * | 2015-07-02 | 2019-09-25 | 学校法人金沢工業大学 | 物質変換方法、バイオリアクターの製造方法、バイオリアクター |
| AU2018221742B2 (en) | 2017-02-15 | 2022-12-01 | Magic Leap, Inc. | Projector architecture incorporating artifact mitigation |
| AU2018260710B2 (en) | 2017-04-26 | 2022-07-21 | Teewinot Technologies Limited | Apparatus, methods and composition for synthesis of cannabinoid compounds |
| EP3861101A4 (en) * | 2018-10-05 | 2022-07-20 | Manus Bio Inc. | BIOSYNTHESIS AND RECOVERY OF SECONDARY METABOLITES |
| WO2020264400A2 (en) * | 2019-06-26 | 2020-12-30 | Zymergen Inc. | Compositions and methods for synthesis of terpenoids |
| KR20220119408A (ko) | 2019-12-20 | 2022-08-29 | 바스프 에스이 | 터펜의 독성 감소 및 미생물에서 생산 잠재성 증가 |
| EP3922727A1 (en) | 2020-06-12 | 2021-12-15 | Basf Se | Method for separating biomass from a solution comprising biomass and at least one aroma compound |
| EP4015626A1 (en) | 2020-12-18 | 2022-06-22 | Isobionics B.V. | Enzymes and methods for fermentative production of monoterpene esters |
| US11299700B1 (en) | 2021-02-19 | 2022-04-12 | Acequia Biotechnology, Llc | Bioreactor containers and methods of growing hairy roots using the same |
| CN113201463B (zh) * | 2021-05-12 | 2022-10-25 | 天津大学 | 一种快速筛选藏红花酸高产菌株的方法及其构建方法 |
| CN114480312B (zh) * | 2022-01-19 | 2024-04-16 | 首都医科大学附属北京世纪坛医院 | 一种松香烷型三环二萜类化合物c-14位羟化酶 |
| WO2025063999A2 (en) * | 2023-04-24 | 2025-03-27 | Amyris, Inc. | Methods for improved cell culture performance and product recovery |
| WO2026003190A1 (en) | 2024-06-27 | 2026-01-02 | Basf Se | Means and methods for alpha-farnesene production |
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| US20100145116A1 (en) * | 2007-03-08 | 2010-06-10 | Frederik Van Keulen | Production of High-Purity Carotenoids by Fermenting Selected Bacterial Strains |
| AU2008305655B2 (en) | 2007-09-20 | 2013-10-31 | Amyris, Inc. | Production of isoprenoids |
| CN102812129B (zh) | 2009-11-10 | 2015-08-26 | 麻省理工学院 | 用于从类异戊二烯途径生产化学和医药产品的微生物工程 |
| EP2336310A1 (en) | 2009-12-16 | 2011-06-22 | Isobionics B.V. | Valencene synthase |
| WO2011074965A1 (en) | 2009-12-17 | 2011-06-23 | Stichting Sanquin Bloedvoorziening | Methods and means for counteracting an activity of an fc domain |
| WO2013090769A2 (en) * | 2011-12-14 | 2013-06-20 | Kiverdi, Inc. | Method and apparatus for growing microbial cultures that require gaseous electron donors, electron acceptors, carbon sources, or other nutrients |
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2014
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- 2014-07-04 HU HUE14761704A patent/HUE051864T2/hu unknown
- 2014-07-04 EP EP14761704.7A patent/EP3017050B1/en active Active
- 2014-07-04 ES ES14761704T patent/ES2834978T3/es active Active
- 2014-07-04 SI SI201431719T patent/SI3017050T1/sl unknown
- 2014-07-04 WO PCT/NL2014/000020 patent/WO2015002528A1/en not_active Ceased
- 2014-07-04 BR BR112015032968-3A patent/BR112015032968B1/pt active IP Right Grant
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2019
- 2019-01-25 US US16/257,709 patent/US11072805B2/en active Active
Also Published As
| Publication number | Publication date |
|---|---|
| EP3017050B1 (en) | 2020-09-09 |
| SI3017050T1 (sl) | 2021-02-26 |
| US11072805B2 (en) | 2021-07-27 |
| HUE051864T2 (hu) | 2021-03-29 |
| WO2015002528A1 (en) | 2015-01-08 |
| BR112015032968B1 (pt) | 2022-01-25 |
| EP3017050A1 (en) | 2016-05-11 |
| BR112015032968A2 (https=) | 2017-07-25 |
| US20160168595A1 (en) | 2016-06-16 |
| US20190225994A1 (en) | 2019-07-25 |
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