SK176397A3 - A method for immobilization of enzymes - Google Patents
A method for immobilization of enzymes Download PDFInfo
- Publication number
- SK176397A3 SK176397A3 SK1763-97A SK176397A SK176397A3 SK 176397 A3 SK176397 A3 SK 176397A3 SK 176397 A SK176397 A SK 176397A SK 176397 A3 SK176397 A3 SK 176397A3
- Authority
- SK
- Slovakia
- Prior art keywords
- enzyme
- lipase
- immobilized
- carrier
- aqueous phase
- Prior art date
Links
- 102000004190 Enzymes Human genes 0.000 title claims abstract description 82
- 108090000790 Enzymes Proteins 0.000 title claims abstract description 82
- 238000000034 method Methods 0.000 title claims abstract description 40
- 108090001060 Lipase Proteins 0.000 claims abstract description 58
- 102000004882 Lipase Human genes 0.000 claims abstract description 58
- 239000004367 Lipase Substances 0.000 claims abstract description 57
- 235000019421 lipase Nutrition 0.000 claims abstract description 57
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 26
- 239000008346 aqueous phase Substances 0.000 claims abstract description 24
- 108010093096 Immobilized Enzymes Proteins 0.000 claims abstract description 23
- 230000008569 process Effects 0.000 claims abstract description 22
- 238000000855 fermentation Methods 0.000 claims abstract description 20
- 230000004151 fermentation Effects 0.000 claims abstract description 20
- 239000012071 phase Substances 0.000 claims abstract description 19
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 claims abstract description 19
- 239000007787 solid Substances 0.000 claims abstract description 18
- 230000002209 hydrophobic effect Effects 0.000 claims abstract description 16
- 108010064785 Phospholipases Proteins 0.000 claims abstract description 15
- 102000015439 Phospholipases Human genes 0.000 claims abstract description 15
- 238000009884 interesterification Methods 0.000 claims abstract description 14
- 239000000839 emulsion Substances 0.000 claims abstract description 12
- 239000002245 particle Substances 0.000 claims abstract description 9
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 26
- 150000003904 phospholipids Chemical class 0.000 claims description 17
- 238000006243 chemical reaction Methods 0.000 claims description 16
- 230000007062 hydrolysis Effects 0.000 claims description 16
- 238000006460 hydrolysis reaction Methods 0.000 claims description 16
- 239000000126 substance Substances 0.000 claims description 11
- ZIIUUSVHCHPIQD-UHFFFAOYSA-N 2,4,6-trimethyl-N-[3-(trifluoromethyl)phenyl]benzenesulfonamide Chemical compound CC1=CC(C)=CC(C)=C1S(=O)(=O)NC1=CC=CC(C(F)(F)F)=C1 ZIIUUSVHCHPIQD-UHFFFAOYSA-N 0.000 claims description 10
- 238000002360 preparation method Methods 0.000 claims description 10
- 150000003626 triacylglycerols Chemical class 0.000 claims description 9
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 8
- 229930195729 fatty acid Natural products 0.000 claims description 8
- 239000000194 fatty acid Substances 0.000 claims description 8
- 150000004665 fatty acids Chemical class 0.000 claims description 8
- OGBUMNBNEWYMNJ-UHFFFAOYSA-N batilol Chemical class CCCCCCCCCCCCCCCCCCOCC(O)CO OGBUMNBNEWYMNJ-UHFFFAOYSA-N 0.000 claims description 5
- 230000003197 catalytic effect Effects 0.000 claims description 4
- 238000002156 mixing Methods 0.000 claims description 4
- 241000223258 Thermomyces lanuginosus Species 0.000 claims description 3
- -1 diglycerides Chemical class 0.000 claims description 3
- 230000003100 immobilizing effect Effects 0.000 claims description 3
- 235000000346 sugar Nutrition 0.000 claims description 3
- 150000008163 sugars Chemical group 0.000 claims description 3
- 239000006228 supernatant Substances 0.000 claims description 3
- 229920002307 Dextran Polymers 0.000 claims description 2
- 241000235403 Rhizomucor miehei Species 0.000 claims description 2
- 241000235545 Rhizopus niveus Species 0.000 claims description 2
- 229920002472 Starch Polymers 0.000 claims description 2
- 239000001913 cellulose Substances 0.000 claims description 2
- 229920002678 cellulose Polymers 0.000 claims description 2
- 230000002255 enzymatic effect Effects 0.000 claims description 2
- 125000005313 fatty acid group Chemical group 0.000 claims description 2
- 235000019698 starch Nutrition 0.000 claims description 2
- 239000008107 starch Substances 0.000 claims description 2
- 239000003921 oil Substances 0.000 abstract description 37
- 239000007788 liquid Substances 0.000 abstract description 3
- 239000002028 Biomass Substances 0.000 abstract description 2
- 239000000463 material Substances 0.000 abstract 1
- 235000019198 oils Nutrition 0.000 description 34
- 235000021588 free fatty acids Nutrition 0.000 description 16
- 230000000694 effects Effects 0.000 description 12
- 238000005886 esterification reaction Methods 0.000 description 12
- 238000011065 in-situ storage Methods 0.000 description 11
- 238000004519 manufacturing process Methods 0.000 description 9
- 229920002125 Sokalan® Polymers 0.000 description 8
- 239000000203 mixture Substances 0.000 description 8
- 108010048733 Lipozyme Proteins 0.000 description 7
- 239000012530 fluid Substances 0.000 description 7
- FCCDDURTIIUXBY-UHFFFAOYSA-N lipoamide Chemical compound NC(=O)CCCCC1CCSS1 FCCDDURTIIUXBY-UHFFFAOYSA-N 0.000 description 7
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 239000003054 catalyst Substances 0.000 description 6
- 235000019626 lipase activity Nutrition 0.000 description 6
- 229940057917 medium chain triglycerides Drugs 0.000 description 6
- 230000009467 reduction Effects 0.000 description 5
- 238000001035 drying Methods 0.000 description 4
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 3
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 3
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- 239000005642 Oleic acid Substances 0.000 description 3
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 3
- 235000019486 Sunflower oil Nutrition 0.000 description 3
- 239000000969 carrier Substances 0.000 description 3
- 238000005119 centrifugation Methods 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 230000032050 esterification Effects 0.000 description 3
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 3
- 239000002808 molecular sieve Substances 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 3
- 230000007420 reactivation Effects 0.000 description 3
- 238000000926 separation method Methods 0.000 description 3
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 3
- 239000000758 substrate Substances 0.000 description 3
- 239000002600 sunflower oil Substances 0.000 description 3
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- UYXTWWCETRIEDR-UHFFFAOYSA-N Tributyrin Chemical compound CCCC(=O)OCC(OC(=O)CCC)COC(=O)CCC UYXTWWCETRIEDR-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 229910003460 diamond Inorganic materials 0.000 description 2
- 239000010432 diamond Substances 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 239000003925 fat Substances 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- KJFMBFZCATUALV-UHFFFAOYSA-N phenolphthalein Chemical compound C1=CC(O)=CC=C1C1(C=2C=CC(O)=CC=2)C2=CC=CC=C2C(=O)O1 KJFMBFZCATUALV-UHFFFAOYSA-N 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- 239000012429 reaction media Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 101000968489 Rhizomucor miehei Lipase Proteins 0.000 description 1
- 241000209140 Triticum Species 0.000 description 1
- 235000021307 Triticum Nutrition 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 238000010923 batch production Methods 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 238000010924 continuous production Methods 0.000 description 1
- 238000007872 degassing Methods 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000004945 emulsification Methods 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 150000004676 glycans Chemical class 0.000 description 1
- 125000005456 glyceride group Chemical group 0.000 description 1
- 239000012510 hollow fiber Substances 0.000 description 1
- 239000003262 industrial enzyme Substances 0.000 description 1
- 210000003734 kidney Anatomy 0.000 description 1
- 239000002609 medium Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 230000002906 microbiologic effect Effects 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen(.) Chemical compound [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 235000014593 oils and fats Nutrition 0.000 description 1
- 238000005192 partition Methods 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 230000008929 regeneration Effects 0.000 description 1
- 238000011069 regeneration method Methods 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 230000003381 solubilizing effect Effects 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 238000005809 transesterification reaction Methods 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 125000005457 triglyceride group Chemical group 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 239000012610 weak anion exchange resin Substances 0.000 description 1
- 230000003442 weekly effect Effects 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
- C12P7/00—Preparation of oxygen-containing organic compounds
- C12P7/64—Fats; Fatty oils; Ester-type waxes; Higher fatty acids, i.e. having at least seven carbon atoms in an unbroken chain bound to a carboxyl group; Oxidised oils or fats
- C12P7/6436—Fatty acid esters
- C12P7/6445—Glycerides
- C12P7/6458—Glycerides by transesterification, e.g. interesterification, ester interchange, alcoholysis or acidolysis
-
- 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
- C12N11/00—Carrier-bound or immobilised enzymes; Carrier-bound or immobilised microbial cells; Preparation thereof
- C12N11/02—Enzymes or microbial cells immobilised on or in an organic carrier
-
- 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
- C12N11/00—Carrier-bound or immobilised enzymes; Carrier-bound or immobilised microbial cells; Preparation thereof
- C12N11/02—Enzymes or microbial cells immobilised on or in an organic carrier
- C12N11/10—Enzymes or microbial cells immobilised on or in an organic carrier the carrier being a carbohydrate
-
- 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
- C12P7/00—Preparation of oxygen-containing organic compounds
- C12P7/64—Fats; Fatty oils; Ester-type waxes; Higher fatty acids, i.e. having at least seven carbon atoms in an unbroken chain bound to a carboxyl group; Oxidised oils or fats
- C12P7/6436—Fatty acid esters
- C12P7/6445—Glycerides
- C12P7/6454—Glycerides by esterification
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Engineering & Computer Science (AREA)
- Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Genetics & Genomics (AREA)
- Biochemistry (AREA)
- Microbiology (AREA)
- Biotechnology (AREA)
- General Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Biomedical Technology (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Molecular Biology (AREA)
- Immobilizing And Processing Of Enzymes And Microorganisms (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Fats And Perfumes (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP95201738 | 1995-06-27 | ||
PCT/EP1996/002587 WO1997001632A1 (en) | 1995-06-27 | 1996-06-14 | Immobilized enzyme and its use for the processing of triglyceride oils |
Publications (1)
Publication Number | Publication Date |
---|---|
SK176397A3 true SK176397A3 (en) | 1998-07-08 |
Family
ID=8220419
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SK1763-97A SK176397A3 (en) | 1995-06-27 | 1996-06-14 | A method for immobilization of enzymes |
Country Status (13)
Country | Link |
---|---|
US (1) | US6162623A (ja) |
EP (1) | EP0835304A1 (ja) |
JP (1) | JP3403202B2 (ja) |
AU (1) | AU720776B2 (ja) |
BR (1) | BR9609381A (ja) |
CA (1) | CA2225475A1 (ja) |
CZ (1) | CZ286747B6 (ja) |
MX (1) | MX9800035A (ja) |
PL (1) | PL324288A1 (ja) |
SK (1) | SK176397A3 (ja) |
TR (1) | TR199701705T1 (ja) |
WO (1) | WO1997001632A1 (ja) |
ZA (1) | ZA965375B (ja) |
Families Citing this family (42)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CZ221899A3 (cs) * | 1996-12-19 | 1999-11-17 | Unilever N. V. | Způsob imobilizace enzymu |
KR20020043349A (ko) * | 2000-12-04 | 2002-06-10 | 김병기 | 고정화 포스포리파제 a-2 및 이를 이용한 인지질 또는그를 포함하는 레시틴의 가수분해방법 |
US7226771B2 (en) | 2002-04-19 | 2007-06-05 | Diversa Corporation | Phospholipases, nucleic acids encoding them and methods for making and using them |
AU2003243157C1 (en) | 2002-04-19 | 2008-09-04 | Verenium Corporation | Phospholipases, nucleic acids encoding them and methods for making and using them |
SE0201581D0 (sv) * | 2002-05-29 | 2002-05-29 | Scandinavian Biotechnology Res | New improved acyltransferase |
CA2515583C (en) | 2003-03-07 | 2015-07-14 | Diversa Corporation | Hydrolases, nucleic acids encoding them and methods for making and using them |
DE10340739A1 (de) * | 2003-09-04 | 2005-04-07 | Satia Gmbh | Verfahren zur enzymatischen Herstellung von Mono- und Diacylglycerid-haltigen Emulgatoren |
CN101432292B (zh) | 2004-06-16 | 2013-03-13 | 维莱尼姆公司 | 对叶绿素进行酶促脱色的组合物和方法 |
US20080070291A1 (en) * | 2004-06-16 | 2008-03-20 | David Lam | Compositions and Methods for Enzymatic Decolorization of Chlorophyll |
US7390522B2 (en) * | 2004-10-26 | 2008-06-24 | Loders Croklaan Usa Llc | Composition and coated bakery products |
US7931778B2 (en) | 2005-11-04 | 2011-04-26 | Cargill, Incorporated | Lecithin-starches compositions, preparation thereof and paper products having oil and grease resistance, and/or release properties |
MY140578A (en) * | 2005-12-07 | 2009-12-31 | Malaysian Agricultural Res And Dev Inst Mardi | Modified coconut oils with broad antimicrobial spectrum |
EP1987142A4 (en) | 2006-02-02 | 2009-07-15 | Verenium Corp | ESTERASES AND ASSOCIATED NUCLEIC ACIDS AND METHODS |
EP1840203A1 (en) | 2006-03-31 | 2007-10-03 | Cargill, Inc. | Enzymatic modification in a continuously regenerated packed bed column |
WO2008036863A2 (en) | 2006-09-21 | 2008-03-27 | Verenium Corporation | Phospholipases, nucleic acids encoding them and methods for making and using them |
UA97127C2 (uk) | 2006-12-06 | 2012-01-10 | Бандж Ойлз, Инк. | Спосіб безперервної ферментативної обробки композиції, що містить ліпід, та система для його здійснення |
GB0700074D0 (en) | 2007-01-03 | 2007-02-07 | Danisco | process |
IL180598A0 (en) * | 2007-01-08 | 2007-07-04 | Basheer Sobhi | Immobilized interfacial enzymes of improved and stabilized activity |
TWI438279B (zh) | 2007-03-16 | 2014-05-21 | Nisshin Oillio Group Ltd | 脂肪酶粉末製劑,其製造方法及使用 |
CN101689638A (zh) * | 2007-05-04 | 2010-03-31 | 埃克民公司 | 固定化酶及其用途 |
DK2177608T3 (en) * | 2007-07-31 | 2015-12-14 | Fuji Oil Co Ltd | Immobilized lipase and process for producing the same |
US8076123B2 (en) * | 2007-10-26 | 2011-12-13 | Oilseeds Biorefinery Corporation | Emulsification-free degumming of oil |
AR077042A1 (es) | 2009-06-12 | 2011-07-27 | Danisco | Metodo para tratar una composicion que contiene pirofiofitina |
UA109884C2 (uk) | 2009-10-16 | 2015-10-26 | Поліпептид, що має активність ферменту фосфатидилінозитол-специфічної фосфоліпази с, нуклеїнова кислота, що його кодує, та спосіб його виробництва і застосування | |
UA111708C2 (uk) | 2009-10-16 | 2016-06-10 | Бандж Ойлз, Інк. | Спосіб рафінування олії |
WO2011110967A1 (en) | 2010-03-12 | 2011-09-15 | Danisco A/S | Process |
EP2582809A1 (en) | 2010-06-17 | 2013-04-24 | DuPont Nutrition Biosciences ApS | Process |
DE102010025764A1 (de) * | 2010-07-01 | 2012-01-05 | Süd-Chemie AG | Phospholipase-Träger-Komplex |
DK2678438T3 (en) | 2011-02-23 | 2017-10-02 | Dupont Nutrition Biosci Aps | ENZYME TREATMENT OF CHLOROPHYL IN PLANT OILS |
WO2012114232A1 (en) | 2011-02-23 | 2012-08-30 | Dupont Nutrition Biosciences Aps | Process |
WO2013104659A2 (en) | 2012-01-13 | 2013-07-18 | Dupont Nutrition Biosciences Aps | Process |
WO2013104660A1 (en) | 2012-01-13 | 2013-07-18 | Dupont Nutrition Biosciences Aps | Process for treating a plant oil comprising hydrolysing chlorophyll or a chlorophyll derivative and involving partial caustic neutralisation |
WO2013160372A1 (en) | 2012-04-27 | 2013-10-31 | Dupont Nutrition Biosciences Aps | Process for treating plant oil involving addition of serial doses of chlorophyll or chlorophyll derivative degrading enzyme |
WO2013160374A1 (en) | 2012-04-27 | 2013-10-31 | Dupont Nutrition Biosciences Aps | Process for refining crude plant oil involving enzymatic hydrolysis and gum recycling |
US20150353970A1 (en) | 2012-12-31 | 2015-12-10 | Trans Bio-Diesel Ltd. | Enzymatic transesterification/esterification processing systems and processes employing lipases immobilzed on hydrophobic resins |
JP2016523095A (ja) * | 2013-06-27 | 2016-08-08 | ネステク ソシエテ アノニム | エマルション安定性の改善された組成物及び栄養製品 |
WO2015017045A1 (en) | 2013-07-03 | 2015-02-05 | Keclon Sa | Modified bacillus cereus phospholipase c protein and method of processing vegetable oil |
WO2015140275A1 (en) | 2014-03-19 | 2015-09-24 | Novozymes A/S | Polypeptides having phospholipase c activity and polynucleotides encoding same |
CN106459934A (zh) | 2014-05-15 | 2017-02-22 | 诺维信公司 | 包括具有磷脂酶c活性的多肽的组合物及其应用 |
CN109628211A (zh) * | 2018-12-26 | 2019-04-16 | 广东省农业科学院蚕业与农产品加工研究所 | 一种去除油脂中游离脂肪酸的方法 |
CN113355369B (zh) * | 2020-03-02 | 2022-11-15 | 大连医诺生物股份有限公司 | 一种采用流加方式的固定化脂肪酶催化制备共轭亚油酸的方法及应用 |
CN116286731B (zh) * | 2023-04-19 | 2024-06-11 | 中国农业科学院农产品加工研究所 | 蛋白基固定化酶及其制备方法及高效制备甘油二酯的方法 |
Family Cites Families (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5584397A (en) * | 1978-12-20 | 1980-06-25 | Ajinomoto Kk | Fat and oil ester exchange using lipase |
DE3163939D1 (en) * | 1980-03-08 | 1984-07-12 | Fuji Oil Co Ltd | Method for enzymatic interesterification of lipid and enzyme used therein |
JPS6034189A (ja) * | 1983-08-02 | 1985-02-21 | Kanegafuchi Chem Ind Co Ltd | 油脂のエステル交換法 |
DK402583D0 (da) * | 1983-09-05 | 1983-09-05 | Novo Industri As | Fremgangsmade til fremstilling af et immobiliseret lipasepraeparat og anvendelse deraf |
US4940845A (en) * | 1984-05-30 | 1990-07-10 | Kao Corporation | Esterification process of fats and oils and enzymatic preparation to use therein |
US4629742A (en) * | 1986-01-27 | 1986-12-16 | Akzo America Inc. | Hydrolysis of fats |
DK399387D0 (da) * | 1987-07-31 | 1987-07-31 | Novo Industri As | Immobiliseret lipase og dennes anvendelse |
US5219744A (en) * | 1987-08-26 | 1993-06-15 | Ajinomoto Co., Inc. | Process for modifying fats and oils |
EP0382767B1 (en) * | 1987-09-28 | 1993-12-15 | Novo Nordisk A/S | Method for immobilizing lipase |
ES2073405T3 (es) * | 1987-12-09 | 1995-08-16 | Kao Corp | Enzima inmovilizada y esterificacion e interesterificacion de la misma. |
US5316927A (en) * | 1988-10-04 | 1994-05-31 | Opta Food Ingredients, Inc. | Production of monoglycerides by enzymatic transesterification |
DK638688D0 (da) * | 1988-11-16 | 1988-11-16 | Novo Industri As | Partikelformet immobiliseret lipase-praeparat, fremgangsmaade til fremstilling deraf og anvendelse deraf |
GB8915299D0 (en) * | 1989-07-04 | 1989-08-23 | Cerestar Holding Bv | Carbohydrate refining process and a supported enzyme for use therein |
US5288619A (en) * | 1989-12-18 | 1994-02-22 | Kraft General Foods, Inc. | Enzymatic method for preparing transesterified oils |
DE4027290C2 (de) * | 1990-08-29 | 1995-03-23 | Forschungszentrum Juelich Gmbh | Verfahren zur Gewinnung von Enzymen aus enzymhaltigen Suspensionen |
US5182201A (en) * | 1990-10-26 | 1993-01-26 | Uop | Lipase immobilization without covalent bonding on an amphiphilic support containing lipophilic alkyl chains |
DE4115938A1 (de) * | 1991-05-16 | 1992-11-19 | Metallgesellschaft Ag | Enzymatisches verfahren zur verminderung des gehaltes an phosphorhaltigen bestandteilen in pflanzlichen und tierischen oelen |
JP3194792B2 (ja) * | 1992-06-12 | 2001-08-06 | 天野エンザイム株式会社 | 酵素を用いた脂肪族ポリエステルの分解法 |
ATE247707T1 (de) * | 1994-02-21 | 2003-09-15 | Novozymes As | Verfahren zur herstellung einer immobilisierten enzympräparation und ihre verwendung |
CZ221899A3 (cs) * | 1996-12-19 | 1999-11-17 | Unilever N. V. | Způsob imobilizace enzymu |
-
1996
- 1996-06-14 WO PCT/EP1996/002587 patent/WO1997001632A1/en not_active Application Discontinuation
- 1996-06-14 EP EP96921996A patent/EP0835304A1/en not_active Withdrawn
- 1996-06-14 CA CA002225475A patent/CA2225475A1/en not_active Abandoned
- 1996-06-14 AU AU63036/96A patent/AU720776B2/en not_active Ceased
- 1996-06-14 SK SK1763-97A patent/SK176397A3/sk unknown
- 1996-06-14 TR TR97/01705T patent/TR199701705T1/xx unknown
- 1996-06-14 CZ CZ19974187A patent/CZ286747B6/cs not_active IP Right Cessation
- 1996-06-14 US US08/983,085 patent/US6162623A/en not_active Expired - Fee Related
- 1996-06-14 PL PL96324288A patent/PL324288A1/xx unknown
- 1996-06-14 BR BR9609381A patent/BR9609381A/pt not_active Application Discontinuation
- 1996-06-14 JP JP50413097A patent/JP3403202B2/ja not_active Expired - Fee Related
- 1996-06-25 ZA ZA9605375A patent/ZA965375B/xx unknown
-
1998
- 1998-01-07 MX MX9800035A patent/MX9800035A/es unknown
Also Published As
Publication number | Publication date |
---|---|
WO1997001632A1 (en) | 1997-01-16 |
US6162623A (en) | 2000-12-19 |
MX9800035A (es) | 1998-11-29 |
ZA965375B (en) | 1997-12-25 |
PL324288A1 (en) | 1998-05-11 |
CZ418797A3 (cs) | 1998-06-17 |
JPH11500319A (ja) | 1999-01-12 |
AU720776B2 (en) | 2000-06-08 |
EP0835304A1 (en) | 1998-04-15 |
TR199701705T1 (xx) | 1998-04-21 |
CA2225475A1 (en) | 1997-01-16 |
BR9609381A (pt) | 1999-05-18 |
CZ286747B6 (en) | 2000-06-14 |
JP3403202B2 (ja) | 2003-05-06 |
AU6303696A (en) | 1997-01-30 |
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