CA2796438A1 - Method for purifying bio-organic compounds from fermentation broth containing surfactants by temperature-induced phase inversion - Google Patents
Method for purifying bio-organic compounds from fermentation broth containing surfactants by temperature-induced phase inversion Download PDFInfo
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- CA2796438A1 CA2796438A1 CA2796438A CA2796438A CA2796438A1 CA 2796438 A1 CA2796438 A1 CA 2796438A1 CA 2796438 A CA2796438 A CA 2796438A CA 2796438 A CA2796438 A CA 2796438A CA 2796438 A1 CA2796438 A1 CA 2796438A1
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- Prior art keywords
- composition
- emulsion
- bio
- oil
- temperature
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- 239000001257 hydrogen Substances 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 238000011081 inoculation Methods 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 238000005511 kinetic theory Methods 0.000 description 1
- 229930007744 linalool Natural products 0.000 description 1
- 238000004811 liquid chromatography Methods 0.000 description 1
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 1
- 239000000347 magnesium hydroxide Substances 0.000 description 1
- 229910001862 magnesium hydroxide Inorganic materials 0.000 description 1
- 239000001630 malic acid Substances 0.000 description 1
- 235000011090 malic acid Nutrition 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 230000001404 mediated effect Effects 0.000 description 1
- VOVZXURTCKPRDQ-CQSZACIVSA-N n-[4-[chloro(difluoro)methoxy]phenyl]-6-[(3r)-3-hydroxypyrrolidin-1-yl]-5-(1h-pyrazol-5-yl)pyridine-3-carboxamide Chemical compound C1[C@H](O)CCN1C1=NC=C(C(=O)NC=2C=CC(OC(F)(F)Cl)=CC=2)C=C1C1=CC=NN1 VOVZXURTCKPRDQ-CQSZACIVSA-N 0.000 description 1
- WASNIKZYIWZQIP-AWEZNQCLSA-N nerolidol Natural products CC(=CCCC(=CCC[C@@H](O)C=C)C)C WASNIKZYIWZQIP-AWEZNQCLSA-N 0.000 description 1
- GSGDTSDELPUTKU-UHFFFAOYSA-N nonoxybenzene Chemical compound CCCCCCCCCOC1=CC=CC=C1 GSGDTSDELPUTKU-UHFFFAOYSA-N 0.000 description 1
- 150000007823 ocimene derivatives Chemical class 0.000 description 1
- 229920002114 octoxynol-9 Polymers 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 230000008520 organization Effects 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 238000010979 pH adjustment Methods 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 229920000259 polyoxyethylene lauryl ether Polymers 0.000 description 1
- 150000008442 polyphenolic compounds Chemical class 0.000 description 1
- 235000013824 polyphenols Nutrition 0.000 description 1
- 230000001376 precipitating effect Effects 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000002731 protein assay Methods 0.000 description 1
- 229930006696 sabinene Natural products 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 238000007655 standard test method Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- UUCCCPNEFXQJEL-UHFFFAOYSA-L strontium dihydroxide Chemical compound [OH-].[OH-].[Sr+2] UUCCCPNEFXQJEL-UHFFFAOYSA-L 0.000 description 1
- 229910001866 strontium hydroxide Inorganic materials 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- 229930006978 terpinene Natural products 0.000 description 1
- 150000003507 terpinene derivatives Chemical class 0.000 description 1
- 238000000954 titration curve Methods 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
- XJPBRODHZKDRCB-UHFFFAOYSA-N trans-alpha-ocimene Natural products CC(=C)CCC=C(C)C=C XJPBRODHZKDRCB-UHFFFAOYSA-N 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 238000010977 unit operation Methods 0.000 description 1
- WCTNXGFHEZQHDR-UHFFFAOYSA-N valencene Natural products C1CC(C)(C)C2(C)CC(C(=C)C)CCC2=C1 WCTNXGFHEZQHDR-UHFFFAOYSA-N 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 210000005253 yeast cell Anatomy 0.000 description 1
- GVJHHUAWPYXKBD-IEOSBIPESA-N α-tocopherol Chemical compound OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-IEOSBIPESA-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
- C12P5/02—Preparation of hydrocarbons or halogenated hydrocarbons acyclic
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C7/00—Purification; Separation; Use of additives
- C07C7/11—Purification; Separation; Use of additives by absorption, i.e. purification or separation of gaseous hydrocarbons with the aid of liquids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C7/00—Purification; Separation; Use of additives
- C07C7/10—Purification; Separation; Use of additives by extraction, i.e. purification or separation of liquid hydrocarbons with the aid of liquids
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
- C11B1/00—Production of fats or fatty oils from raw materials
-
- 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
-
- 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
-
- Y—GENERAL 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E50/00—Technologies for the production of fuel of non-fossil origin
- Y02E50/30—Fuel from waste, e.g. synthetic alcohol or diesel
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Biotechnology (AREA)
- Biochemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Engineering & Computer Science (AREA)
- Microbiology (AREA)
- Genetics & Genomics (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Analytical Chemistry (AREA)
- Water Supply & Treatment (AREA)
- Colloid Chemistry (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
- Cosmetics (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US37387610P | 2010-08-16 | 2010-08-16 | |
| US61/373,876 | 2010-08-16 | ||
| PCT/US2011/047616 WO2012024186A1 (en) | 2010-08-16 | 2011-08-12 | Method for purifying bio-organic compounds from fermentation broth containing surfactants by temperature-induced phase inversion |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2796438A1 true CA2796438A1 (en) | 2012-02-23 |
Family
ID=44515045
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA2796438A Abandoned CA2796438A1 (en) | 2010-08-16 | 2011-08-12 | Method for purifying bio-organic compounds from fermentation broth containing surfactants by temperature-induced phase inversion |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US20120040396A1 (enExample) |
| EP (1) | EP2606018A1 (enExample) |
| JP (1) | JP2013534144A (enExample) |
| KR (1) | KR20130108064A (enExample) |
| CN (1) | CN103052612A (enExample) |
| AU (1) | AU2011292231B2 (enExample) |
| BR (1) | BR112012027462A2 (enExample) |
| CA (1) | CA2796438A1 (enExample) |
| MX (1) | MX2012012705A (enExample) |
| WO (1) | WO2012024186A1 (enExample) |
| ZA (1) | ZA201207717B (enExample) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20150087039A1 (en) * | 2012-03-07 | 2015-03-26 | Abengoa Bioenergy New Technologies, Llc | Methods for enhancing the recovery of oil during biofuel production |
| JP6611136B2 (ja) | 2014-02-28 | 2019-11-27 | デルフト アドヴァンスト バイオフューエルズ ベー．フェー． | 脂質または炭化水素の回収のための方法 |
| WO2019030073A1 (en) * | 2017-08-07 | 2019-02-14 | Total Raffinage Chimie | PROCESS FOR RECOVERING ISOPRENOIDS PRODUCED BY MICROORGANISMS |
| WO2020006251A1 (en) * | 2018-06-29 | 2020-01-02 | Amyris, Inc. | Methods for recovering water-immiscible isoprenoid compounds from microbial biomass |
| EP3766982A1 (en) | 2019-07-18 | 2021-01-20 | Delft Advanced Biofuels B.V. | Integrated system for biocatalytically producing and recovering an organic substance |
| EP4646426A1 (en) | 2023-01-03 | 2025-11-12 | Amyris, Inc. | Host cells capable of producing sequiterpenoids and methods of use thereof |
Family Cites Families (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2427326A (en) * | 1945-02-13 | 1947-09-09 | Socony Vacuum Oil Co Inc | Treatment of mineral oil emulsions |
| US2782244A (en) * | 1952-01-24 | 1957-02-19 | Phillips Petroleum Co | Isomerizing hydrocarbons with the catalyst in the continuous phase inverting the phases and separating the catalyst employing phase inversion |
| US4725287A (en) * | 1986-11-24 | 1988-02-16 | Canadian Occidental Petroleum, Ltd. | Preparation of stable crude oil transport emulsions |
| US5730905A (en) * | 1994-06-21 | 1998-03-24 | Betzdearborn Inc. | Method of resolving oil and water emulsions |
| US6431370B1 (en) * | 1995-01-27 | 2002-08-13 | Genencor International, Inc. | Direct enzyme agglomeration process |
| KR100819187B1 (ko) * | 1999-03-25 | 2008-04-04 | 발티온 테크닐리넨 투트키무스케스쿠스 | 단백질 분배 방법 |
| DE10035930A1 (de) * | 2000-07-21 | 2002-01-31 | Clariant Gmbh | Feinemulsionen |
| US7179311B2 (en) * | 2003-01-31 | 2007-02-20 | Chevron U.S.A. Inc. | Stable olefinic, low sulfur diesel fuels |
| CN1246451C (zh) * | 2003-08-07 | 2006-03-22 | 上海来益生物药物研究开发中心有限责任公司 | 浊点系统在生物转化中的应用 |
| EP3031924A1 (en) | 2006-05-26 | 2016-06-15 | Amyris, Inc. | Production of isoprenoids |
| MY163029A (en) | 2006-05-26 | 2017-07-31 | Amyris Inc | Apparatus for making bio-organic compounds |
| BRPI0713105B8 (pt) * | 2006-05-26 | 2021-05-25 | Amyris Biotechnologies Inc | método para produzir um isoprenóide |
| US7846222B2 (en) * | 2006-10-10 | 2010-12-07 | Amyris Biotechnologies, Inc. | Fuel compositions comprising farnesane and farnesane derivatives and method of making and using same |
| CA2670307C (en) | 2006-11-21 | 2013-06-25 | Amyris Biotechnologies, Inc. | Jet fuel compositions and methods of making and using same |
| CA2670280A1 (en) | 2006-11-21 | 2008-11-06 | Amyris Biotechnologies, Inc. | Jet fuel compositions and methods of making and using same |
| CN101260137B (zh) * | 2007-03-07 | 2010-12-08 | 中国科学院过程工程研究所 | 用微波辅助浊点萃取从甘草中提纯并精制甘草酸的方法 |
| US8110093B2 (en) | 2007-03-14 | 2012-02-07 | Ls9, Inc. | Process for producing low molecular weight hydrocarbons from renewable resources |
| EP3546588A3 (en) | 2007-06-01 | 2019-12-18 | Corbion Biotech, Inc. | Recombinant microalgal cell and method of producing lipids using said cell |
| AU2008279775B2 (en) | 2007-07-20 | 2012-09-13 | Amyris, Inc. | Fuel compositions comprising tetramethylcyclohexane |
| WO2009134946A1 (en) | 2008-05-02 | 2009-11-05 | Amyris Biotechnologies, Inc. | Fuel compositions comprising an amorphane or a stereoisomer thereof and methods of making and using same |
| US7655739B1 (en) | 2009-06-26 | 2010-02-02 | Amyris Biotechnologies, Inc. | Adhesive compositions comprising a polyfarnesene |
| US7589243B1 (en) | 2008-09-17 | 2009-09-15 | Amyris Biotechnologies, Inc. | Jet fuel compositions |
| US7592295B1 (en) | 2008-10-10 | 2009-09-22 | Amyris Biotechnologies, Inc. | Farnesene dimers and/or farnesane dimers and compositions thereof |
-
2011
- 2011-08-05 US US13/198,711 patent/US20120040396A1/en not_active Abandoned
- 2011-08-12 CN CN2011800374729A patent/CN103052612A/zh active Pending
- 2011-08-12 ZA ZA201207717A patent/ZA201207717B/xx unknown
- 2011-08-12 BR BR112012027462A patent/BR112012027462A2/pt not_active IP Right Cessation
- 2011-08-12 JP JP2013524893A patent/JP2013534144A/ja active Pending
- 2011-08-12 AU AU2011292231A patent/AU2011292231B2/en not_active Ceased
- 2011-08-12 MX MX2012012705A patent/MX2012012705A/es not_active Application Discontinuation
- 2011-08-12 EP EP11749297.5A patent/EP2606018A1/en not_active Withdrawn
- 2011-08-12 WO PCT/US2011/047616 patent/WO2012024186A1/en not_active Ceased
- 2011-08-12 CA CA2796438A patent/CA2796438A1/en not_active Abandoned
- 2011-08-12 KR KR1020127028294A patent/KR20130108064A/ko not_active Withdrawn
Also Published As
| Publication number | Publication date |
|---|---|
| WO2012024186A1 (en) | 2012-02-23 |
| BR112012027462A2 (pt) | 2016-07-19 |
| EP2606018A1 (en) | 2013-06-26 |
| AU2011292231A1 (en) | 2012-12-13 |
| KR20130108064A (ko) | 2013-10-02 |
| MX2012012705A (es) | 2012-11-29 |
| CN103052612A (zh) | 2013-04-17 |
| US20120040396A1 (en) | 2012-02-16 |
| JP2013534144A (ja) | 2013-09-02 |
| AU2011292231B2 (en) | 2013-11-21 |
| ZA201207717B (en) | 2013-12-23 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FZDE | Discontinued |
Effective date: 20160812 |