JP2017501709A - 微生物細胞から微生物油を入手する方法 - Google Patents
微生物細胞から微生物油を入手する方法 Download PDFInfo
- Publication number
- JP2017501709A JP2017501709A JP2016541284A JP2016541284A JP2017501709A JP 2017501709 A JP2017501709 A JP 2017501709A JP 2016541284 A JP2016541284 A JP 2016541284A JP 2016541284 A JP2016541284 A JP 2016541284A JP 2017501709 A JP2017501709 A JP 2017501709A
- Authority
- JP
- Japan
- Prior art keywords
- volume
- oil
- cell composition
- lysed cell
- weight
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 230000000813 microbial effect Effects 0.000 title claims abstract description 118
- 238000000034 method Methods 0.000 title claims abstract description 116
- 239000000203 mixture Substances 0.000 claims abstract description 248
- 235000020777 polyunsaturated fatty acids Nutrition 0.000 claims abstract description 53
- 230000002934 lysing effect Effects 0.000 claims abstract description 20
- 239000003921 oil Substances 0.000 claims description 159
- 239000003995 emulsifying agent Substances 0.000 claims description 71
- YZXBAPSDXZZRGB-DOFZRALJSA-N arachidonic acid Chemical compound CCCCC\C=C/C\C=C/C\C=C/C\C=C/CCCC(O)=O YZXBAPSDXZZRGB-DOFZRALJSA-N 0.000 claims description 60
- MBMBGCFOFBJSGT-KUBAVDMBSA-N all-cis-docosa-4,7,10,13,16,19-hexaenoic acid Chemical compound CC\C=C/C\C=C/C\C=C/C\C=C/C\C=C/C\C=C/CCC(O)=O MBMBGCFOFBJSGT-KUBAVDMBSA-N 0.000 claims description 43
- 238000003756 stirring Methods 0.000 claims description 32
- 235000021342 arachidonic acid Nutrition 0.000 claims description 30
- 229940114079 arachidonic acid Drugs 0.000 claims description 30
- 150000003839 salts Chemical class 0.000 claims description 27
- 235000020669 docosahexaenoic acid Nutrition 0.000 claims description 25
- 238000000855 fermentation Methods 0.000 claims description 25
- 230000004151 fermentation Effects 0.000 claims description 25
- 229940090949 docosahexaenoic acid Drugs 0.000 claims description 21
- 238000010438 heat treatment Methods 0.000 claims description 21
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 claims description 20
- 239000010779 crude oil Substances 0.000 claims description 19
- 241000235575 Mortierella Species 0.000 claims description 16
- 239000002585 base Substances 0.000 claims description 16
- -1 anionic carboxylate Chemical class 0.000 claims description 15
- 125000000129 anionic group Chemical group 0.000 claims description 15
- 239000003960 organic solvent Substances 0.000 claims description 12
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims description 11
- JAZBEHYOTPTENJ-JLNKQSITSA-N all-cis-5,8,11,14,17-icosapentaenoic acid Chemical compound CC\C=C/C\C=C/C\C=C/C\C=C/C\C=C/CCCC(O)=O JAZBEHYOTPTENJ-JLNKQSITSA-N 0.000 claims description 11
- 235000020673 eicosapentaenoic acid Nutrition 0.000 claims description 10
- 229960005135 eicosapentaenoic acid Drugs 0.000 claims description 10
- JAZBEHYOTPTENJ-UHFFFAOYSA-N eicosapentaenoic acid Natural products CCC=CCC=CCC=CCC=CCC=CCCCC(O)=O JAZBEHYOTPTENJ-UHFFFAOYSA-N 0.000 claims description 10
- YUFFSWGQGVEMMI-JLNKQSITSA-N (7Z,10Z,13Z,16Z,19Z)-docosapentaenoic acid Chemical compound CC\C=C/C\C=C/C\C=C/C\C=C/C\C=C/CCCCCC(O)=O YUFFSWGQGVEMMI-JLNKQSITSA-N 0.000 claims description 9
- 239000002245 particle Substances 0.000 claims description 9
- 235000021294 Docosapentaenoic acid Nutrition 0.000 claims description 8
- 241001467333 Thraustochytriaceae Species 0.000 claims description 7
- 239000012874 anionic emulsifier Substances 0.000 claims description 7
- 239000007788 liquid Substances 0.000 claims description 7
- 241000199913 Crypthecodinium Species 0.000 claims description 6
- 229910019142 PO4 Inorganic materials 0.000 claims description 6
- 241000233671 Schizochytrium Species 0.000 claims description 6
- 239000012634 fragment Substances 0.000 claims description 6
- 241000907999 Mortierella alpina Species 0.000 claims description 5
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 5
- 235000020660 omega-3 fatty acid Nutrition 0.000 claims description 5
- 150000002978 peroxides Chemical class 0.000 claims description 5
- 229910052698 phosphorus Inorganic materials 0.000 claims description 5
- 239000011574 phosphorus Substances 0.000 claims description 5
- 229940083575 sodium dodecyl sulfate Drugs 0.000 claims description 5
- DVSZKTAMJJTWFG-SKCDLICFSA-N (2e,4e,6e,8e,10e,12e)-docosa-2,4,6,8,10,12-hexaenoic acid Chemical compound CCCCCCCCC\C=C\C=C\C=C\C=C\C=C\C=C\C(O)=O DVSZKTAMJJTWFG-SKCDLICFSA-N 0.000 claims description 4
- GZJLLYHBALOKEX-UHFFFAOYSA-N 6-Ketone, O18-Me-Ussuriedine Natural products CC=CCC=CCC=CCC=CCC=CCC=CCCCC(O)=O GZJLLYHBALOKEX-UHFFFAOYSA-N 0.000 claims description 4
- OPGOLNDOMSBSCW-CLNHMMGSSA-N Fursultiamine hydrochloride Chemical compound Cl.C1CCOC1CSSC(\CCO)=C(/C)N(C=O)CC1=CN=C(C)N=C1N OPGOLNDOMSBSCW-CLNHMMGSSA-N 0.000 claims description 4
- KAUVQQXNCKESLC-UHFFFAOYSA-N docosahexaenoic acid (DHA) Natural products COC(=O)C(C)NOCC1=CC=CC=C1 KAUVQQXNCKESLC-UHFFFAOYSA-N 0.000 claims description 4
- 229940098330 gamma linoleic acid Drugs 0.000 claims description 4
- VZCCETWTMQHEPK-QNEBEIHSSA-N gamma-linolenic acid Chemical compound CCCCC\C=C/C\C=C/C\C=C/CCCCC(O)=O VZCCETWTMQHEPK-QNEBEIHSSA-N 0.000 claims description 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims description 4
- 239000010452 phosphate Substances 0.000 claims description 4
- 239000011734 sodium Substances 0.000 claims description 4
- JIWBIWFOSCKQMA-UHFFFAOYSA-N stearidonic acid Natural products CCC=CCC=CCC=CCC=CCCCCC(O)=O JIWBIWFOSCKQMA-UHFFFAOYSA-N 0.000 claims description 4
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 claims description 4
- 240000004808 Saccharomyces cerevisiae Species 0.000 claims description 3
- 241000233675 Thraustochytrium Species 0.000 claims description 3
- 229910052783 alkali metal Inorganic materials 0.000 claims description 3
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims description 3
- BTBJBAZGXNKLQC-UHFFFAOYSA-N ammonium lauryl sulfate Chemical group [NH4+].CCCCCCCCCCCCOS([O-])(=O)=O BTBJBAZGXNKLQC-UHFFFAOYSA-N 0.000 claims description 3
- 229940063953 ammonium lauryl sulfate Drugs 0.000 claims description 3
- SMVRDGHCVNAOIN-UHFFFAOYSA-L disodium;1-dodecoxydodecane;sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O.CCCCCCCCCCCCOCCCCCCCCCCCC SMVRDGHCVNAOIN-UHFFFAOYSA-L 0.000 claims description 3
- 235000020665 omega-6 fatty acid Nutrition 0.000 claims description 3
- BHAAPTBBJKJZER-UHFFFAOYSA-N p-anisidine Chemical compound COC1=CC=C(N)C=C1 BHAAPTBBJKJZER-UHFFFAOYSA-N 0.000 claims description 3
- 229910052708 sodium Inorganic materials 0.000 claims description 3
- 239000000341 volatile oil Substances 0.000 claims description 3
- HOBAELRKJCKHQD-UHFFFAOYSA-N (8Z,11Z,14Z)-8,11,14-eicosatrienoic acid Natural products CCCCCC=CCC=CCC=CCCCCCCC(O)=O HOBAELRKJCKHQD-UHFFFAOYSA-N 0.000 claims description 2
- HOBAELRKJCKHQD-QNEBEIHSSA-N dihomo-γ-linolenic acid Chemical compound CCCCC\C=C/C\C=C/C\C=C/CCCCCCC(O)=O HOBAELRKJCKHQD-QNEBEIHSSA-N 0.000 claims description 2
- 230000002538 fungal effect Effects 0.000 claims description 2
- VZCCETWTMQHEPK-UHFFFAOYSA-N gamma-Linolensaeure Natural products CCCCCC=CCC=CCC=CCCCCC(O)=O VZCCETWTMQHEPK-UHFFFAOYSA-N 0.000 claims description 2
- 229940012843 omega-3 fatty acid Drugs 0.000 claims description 2
- 239000006014 omega-3 oil Substances 0.000 claims description 2
- 229940033080 omega-6 fatty acid Drugs 0.000 claims description 2
- 238000007670 refining Methods 0.000 claims description 2
- 229940057950 sodium laureth sulfate Drugs 0.000 claims description 2
- SXHLENDCVBIJFO-UHFFFAOYSA-M sodium;2-[2-(2-dodecoxyethoxy)ethoxy]ethyl sulfate Chemical compound [Na+].CCCCCCCCCCCCOCCOCCOCCOS([O-])(=O)=O SXHLENDCVBIJFO-UHFFFAOYSA-M 0.000 claims description 2
- 150000003467 sulfuric acid derivatives Chemical class 0.000 claims description 2
- 230000001580 bacterial effect Effects 0.000 claims 1
- 210000004027 cell Anatomy 0.000 description 359
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 63
- 229910052799 carbon Inorganic materials 0.000 description 42
- 235000002639 sodium chloride Nutrition 0.000 description 39
- 239000000243 solution Substances 0.000 description 25
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 24
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 22
- 239000012071 phase Substances 0.000 description 19
- 239000000839 emulsion Substances 0.000 description 18
- 239000002028 Biomass Substances 0.000 description 13
- 239000007787 solid Substances 0.000 description 13
- 239000011780 sodium chloride Substances 0.000 description 12
- 239000000126 substance Substances 0.000 description 12
- 238000011282 treatment Methods 0.000 description 12
- 239000000843 powder Substances 0.000 description 11
- 230000009089 cytolysis Effects 0.000 description 10
- 235000014113 dietary fatty acids Nutrition 0.000 description 9
- 229930195729 fatty acid Natural products 0.000 description 9
- 239000000194 fatty acid Substances 0.000 description 9
- 238000000265 homogenisation Methods 0.000 description 9
- 239000002609 medium Substances 0.000 description 9
- 244000005700 microbiome Species 0.000 description 9
- 102000004190 Enzymes Human genes 0.000 description 8
- 108090000790 Enzymes Proteins 0.000 description 8
- 238000013019 agitation Methods 0.000 description 8
- 229940088598 enzyme Drugs 0.000 description 8
- 150000004665 fatty acids Chemical class 0.000 description 8
- 239000002253 acid Substances 0.000 description 7
- 238000001035 drying Methods 0.000 description 7
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 7
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
- 235000020978 long-chain polyunsaturated fatty acids Nutrition 0.000 description 6
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
- 235000010482 polyoxyethylene sorbitan monooleate Nutrition 0.000 description 6
- 229920000053 polysorbate 80 Polymers 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- 241001465754 Metazoa Species 0.000 description 5
- 241000598397 Schizochytrium sp. Species 0.000 description 5
- 235000013336 milk Nutrition 0.000 description 5
- 239000008267 milk Substances 0.000 description 5
- 210000004080 milk Anatomy 0.000 description 5
- 238000002156 mixing Methods 0.000 description 5
- 235000021317 phosphate Nutrition 0.000 description 5
- 238000000926 separation method Methods 0.000 description 5
- 241000894007 species Species 0.000 description 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
- LZZYPRNAOMGNLH-UHFFFAOYSA-M Cetrimonium bromide Chemical compound [Br-].CCCCCCCCCCCCCCCC[N+](C)(C)C LZZYPRNAOMGNLH-UHFFFAOYSA-M 0.000 description 4
- 241000195493 Cryptophyta Species 0.000 description 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
- 108010059820 Polygalacturonase Proteins 0.000 description 4
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 4
- 102000005158 Subtilisins Human genes 0.000 description 4
- 108010056079 Subtilisins Proteins 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- 239000008346 aqueous phase Substances 0.000 description 4
- 238000005119 centrifugation Methods 0.000 description 4
- 235000013601 eggs Nutrition 0.000 description 4
- 238000005259 measurement Methods 0.000 description 4
- 150000003904 phospholipids Chemical class 0.000 description 4
- 238000012545 processing Methods 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 241000233866 Fungi Species 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- 241000235395 Mucor Species 0.000 description 3
- 108091005804 Peptidases Proteins 0.000 description 3
- 102000035195 Peptidases Human genes 0.000 description 3
- 239000004365 Protease Substances 0.000 description 3
- 102000016679 alpha-Glucosidases Human genes 0.000 description 3
- 108010028144 alpha-Glucosidases Proteins 0.000 description 3
- 125000002091 cationic group Chemical group 0.000 description 3
- 210000002421 cell wall Anatomy 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 230000001419 dependent effect Effects 0.000 description 3
- 230000002255 enzymatic effect Effects 0.000 description 3
- 108010093305 exopolygalacturonase Proteins 0.000 description 3
- 239000012530 fluid Substances 0.000 description 3
- 235000013372 meat Nutrition 0.000 description 3
- 239000007764 o/w emulsion Substances 0.000 description 3
- 238000011084 recovery Methods 0.000 description 3
- 230000002829 reductive effect Effects 0.000 description 3
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 2
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 2
- 108010084185 Cellulases Proteins 0.000 description 2
- 102000005575 Cellulases Human genes 0.000 description 2
- 241000199914 Dinophyceae Species 0.000 description 2
- 235000021292 Docosatetraenoic acid Nutrition 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- NPPQSCRMBWNHMW-UHFFFAOYSA-N Meprobamate Chemical compound NC(=O)OCC(C)(CCC)COC(N)=O NPPQSCRMBWNHMW-UHFFFAOYSA-N 0.000 description 2
- 241001219224 Mortierella elongata Species 0.000 description 2
- 241000233639 Pythium Species 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 241001491678 Ulkenia Species 0.000 description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 239000011324 bead Substances 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 229960000686 benzalkonium chloride Drugs 0.000 description 2
- 229960001950 benzethonium chloride Drugs 0.000 description 2
- UREZNYTWGJKWBI-UHFFFAOYSA-M benzethonium chloride Chemical compound [Cl-].C1=CC(C(C)(C)CC(C)(C)C)=CC=C1OCCOCC[N+](C)(C)CC1=CC=CC=C1 UREZNYTWGJKWBI-UHFFFAOYSA-M 0.000 description 2
- CADWTSSKOVRVJC-UHFFFAOYSA-N benzyl(dimethyl)azanium;chloride Chemical compound [Cl-].C[NH+](C)CC1=CC=CC=C1 CADWTSSKOVRVJC-UHFFFAOYSA-N 0.000 description 2
- 239000012620 biological material Substances 0.000 description 2
- 238000004061 bleaching Methods 0.000 description 2
- 239000001110 calcium chloride Substances 0.000 description 2
- 229910001628 calcium chloride Inorganic materials 0.000 description 2
- 235000011148 calcium chloride Nutrition 0.000 description 2
- 235000014633 carbohydrates Nutrition 0.000 description 2
- 150000001720 carbohydrates Chemical class 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 230000001413 cellular effect Effects 0.000 description 2
- YMKDRGPMQRFJGP-UHFFFAOYSA-M cetylpyridinium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC[N+]1=CC=CC=C1 YMKDRGPMQRFJGP-UHFFFAOYSA-M 0.000 description 2
- 229960001927 cetylpyridinium chloride Drugs 0.000 description 2
- WOWHHFRSBJGXCM-UHFFFAOYSA-M cetyltrimethylammonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC[N+](C)(C)C WOWHHFRSBJGXCM-UHFFFAOYSA-M 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 150000001982 diacylglycerols Chemical class 0.000 description 2
- 235000015872 dietary supplement Nutrition 0.000 description 2
- PSLWZOIUBRXAQW-UHFFFAOYSA-M dimethyl(dioctadecyl)azanium;bromide Chemical compound [Br-].CCCCCCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCCCCCCCC PSLWZOIUBRXAQW-UHFFFAOYSA-M 0.000 description 2
- 238000004090 dissolution Methods 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 235000013305 food Nutrition 0.000 description 2
- 230000005484 gravity Effects 0.000 description 2
- 238000000227 grinding Methods 0.000 description 2
- 230000000670 limiting effect Effects 0.000 description 2
- 230000033001 locomotion Effects 0.000 description 2
- 150000004668 long chain fatty acids Chemical class 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000012528 membrane Substances 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 150000002759 monoacylglycerols Chemical class 0.000 description 2
- 235000015097 nutrients Nutrition 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 239000008188 pellet Substances 0.000 description 2
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 description 2
- 239000000244 polyoxyethylene sorbitan monooleate Substances 0.000 description 2
- 229940068968 polysorbate 80 Drugs 0.000 description 2
- 239000001103 potassium chloride Substances 0.000 description 2
- 235000011164 potassium chloride Nutrition 0.000 description 2
- 235000018102 proteins Nutrition 0.000 description 2
- 102000004169 proteins and genes Human genes 0.000 description 2
- 108090000623 proteins and genes Proteins 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- 235000014102 seafood Nutrition 0.000 description 2
- 239000007790 solid phase Substances 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- DCXXMTOCNZCJGO-UHFFFAOYSA-N tristearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCCCCCCCC)COC(=O)CCCCCCCCCCCCCCCCC DCXXMTOCNZCJGO-UHFFFAOYSA-N 0.000 description 2
- 239000012855 volatile organic compound Substances 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- 239000002699 waste material Substances 0.000 description 2
- FPRKGXIOSIUDSE-SYACGTDESA-N (2z,4z,6z,8z)-docosa-2,4,6,8-tetraenoic acid Chemical compound CCCCCCCCCCCCC\C=C/C=C\C=C/C=C\C(O)=O FPRKGXIOSIUDSE-SYACGTDESA-N 0.000 description 1
- TWSWSIQAPQLDBP-CGRWFSSPSA-N (7e,10e,13e,16e)-docosa-7,10,13,16-tetraenoic acid Chemical compound CCCCC\C=C\C\C=C\C\C=C\C\C=C\CCCCCC(O)=O TWSWSIQAPQLDBP-CGRWFSSPSA-N 0.000 description 1
- JGTNAGYHADQMCM-UHFFFAOYSA-M 1,1,2,2,3,3,4,4,4-nonafluorobutane-1-sulfonate Chemical compound [O-]S(=O)(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F JGTNAGYHADQMCM-UHFFFAOYSA-M 0.000 description 1
- YFSUTJLHUFNCNZ-UHFFFAOYSA-M 1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-heptadecafluorooctane-1-sulfonate Chemical compound [O-]S(=O)(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F YFSUTJLHUFNCNZ-UHFFFAOYSA-M 0.000 description 1
- HNSDLXPSAYFUHK-UHFFFAOYSA-N 1,4-bis(2-ethylhexyl) sulfosuccinate Chemical compound CCCCC(CC)COC(=O)CC(S(O)(=O)=O)C(=O)OCC(CC)CCCC HNSDLXPSAYFUHK-UHFFFAOYSA-N 0.000 description 1
- BMYNFMYTOJXKLE-UHFFFAOYSA-N 3-azaniumyl-2-hydroxypropanoate Chemical compound NCC(O)C(O)=O BMYNFMYTOJXKLE-UHFFFAOYSA-N 0.000 description 1
- CDOUZKKFHVEKRI-UHFFFAOYSA-N 3-bromo-n-[(prop-2-enoylamino)methyl]propanamide Chemical compound BrCCC(=O)NCNC(=O)C=C CDOUZKKFHVEKRI-UHFFFAOYSA-N 0.000 description 1
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- UHPMCKVQTMMPCG-UHFFFAOYSA-N 5,8-dihydroxy-2-methoxy-6-methyl-7-(2-oxopropyl)naphthalene-1,4-dione Chemical compound CC1=C(CC(C)=O)C(O)=C2C(=O)C(OC)=CC(=O)C2=C1O UHPMCKVQTMMPCG-UHFFFAOYSA-N 0.000 description 1
- 229940046305 5-bromo-5-nitro-1,3-dioxane Drugs 0.000 description 1
- 241000251468 Actinopterygii Species 0.000 description 1
- 241000143060 Americamysis bahia Species 0.000 description 1
- USFZMSVCRYTOJT-UHFFFAOYSA-N Ammonium acetate Chemical compound N.CC(O)=O USFZMSVCRYTOJT-UHFFFAOYSA-N 0.000 description 1
- 239000005695 Ammonium acetate Substances 0.000 description 1
- 239000004382 Amylase Substances 0.000 description 1
- 108010065511 Amylases Proteins 0.000 description 1
- 102000013142 Amylases Human genes 0.000 description 1
- 241000235349 Ascomycota Species 0.000 description 1
- 102000035101 Aspartic proteases Human genes 0.000 description 1
- 108091005502 Aspartic proteases Proteins 0.000 description 1
- 241000228212 Aspergillus Species 0.000 description 1
- 241000206761 Bacillariophyta Species 0.000 description 1
- 241000894006 Bacteria Species 0.000 description 1
- 241000221198 Basidiomycota Species 0.000 description 1
- 102100026189 Beta-galactosidase Human genes 0.000 description 1
- 108010022172 Chitinases Proteins 0.000 description 1
- 102000012286 Chitinases Human genes 0.000 description 1
- 102100037328 Chitotriosidase-1 Human genes 0.000 description 1
- 241000195628 Chlorophyta Species 0.000 description 1
- 241000206751 Chrysophyceae Species 0.000 description 1
- 241000222290 Cladosporium Species 0.000 description 1
- 241001480517 Conidiobolus Species 0.000 description 1
- 241000238424 Crustacea Species 0.000 description 1
- 241000199912 Crypthecodinium cohnii Species 0.000 description 1
- 102000005927 Cysteine Proteases Human genes 0.000 description 1
- 108010005843 Cysteine Proteases Proteins 0.000 description 1
- 241001480508 Entomophthora Species 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- 241000223218 Fusarium Species 0.000 description 1
- 102100028496 Galactocerebrosidase Human genes 0.000 description 1
- 108010093031 Galactosidases Proteins 0.000 description 1
- 102000002464 Galactosidases Human genes 0.000 description 1
- 108010042681 Galactosylceramidase Proteins 0.000 description 1
- 102000004547 Glucosylceramidase Human genes 0.000 description 1
- 108010017544 Glucosylceramidase Proteins 0.000 description 1
- 108010060309 Glucuronidase Proteins 0.000 description 1
- 102000053187 Glucuronidase Human genes 0.000 description 1
- 108010000540 Hexosaminidases Proteins 0.000 description 1
- 102000002268 Hexosaminidases Human genes 0.000 description 1
- 241000282412 Homo Species 0.000 description 1
- 108010003272 Hyaluronate lyase Proteins 0.000 description 1
- 102000009066 Hyaluronoglucosaminidase Human genes 0.000 description 1
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 1
- 108010003381 Iduronidase Proteins 0.000 description 1
- 102000004627 Iduronidase Human genes 0.000 description 1
- WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical compound OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 description 1
- 108010059881 Lactase Proteins 0.000 description 1
- 235000019687 Lamb Nutrition 0.000 description 1
- 102000005741 Metalloproteases Human genes 0.000 description 1
- 108010006035 Metalloproteases Proteins 0.000 description 1
- 241000048020 Mortierella exigua Species 0.000 description 1
- 241000907923 Mortierella schmuckeri Species 0.000 description 1
- 108010014251 Muramidase Proteins 0.000 description 1
- 102000016943 Muramidase Human genes 0.000 description 1
- 108010062010 N-Acetylmuramoyl-L-alanine Amidase Proteins 0.000 description 1
- 108010006232 Neuraminidase Proteins 0.000 description 1
- 102000005348 Neuraminidase Human genes 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- 241000228143 Penicillium Species 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-L Phosphate ion(2-) Chemical compound OP([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-L 0.000 description 1
- 241000233614 Phytophthora Species 0.000 description 1
- 101710184309 Probable sucrose-6-phosphate hydrolase Proteins 0.000 description 1
- 241000197220 Pythium insidiosum Species 0.000 description 1
- 241000223252 Rhodotorula Species 0.000 description 1
- 102000012479 Serine Proteases Human genes 0.000 description 1
- 108010022999 Serine Proteases Proteins 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- 229930182558 Sterol Natural products 0.000 description 1
- 241001466451 Stramenopiles Species 0.000 description 1
- 102400000472 Sucrase Human genes 0.000 description 1
- 101710112652 Sucrose-6-phosphate hydrolase Proteins 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 1
- 238000010306 acid treatment Methods 0.000 description 1
- 239000012190 activator Substances 0.000 description 1
- TWSWSIQAPQLDBP-UHFFFAOYSA-N adrenic acid Natural products CCCCCC=CCC=CCC=CCC=CCCCCCC(O)=O TWSWSIQAPQLDBP-UHFFFAOYSA-N 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 125000005599 alkyl carboxylate group Chemical group 0.000 description 1
- 150000008051 alkyl sulfates Chemical class 0.000 description 1
- 125000005211 alkyl trimethyl ammonium group Chemical group 0.000 description 1
- HQPCSDADVLFHHO-LTKCOYKYSA-N all-cis-8,11,14,17-icosatetraenoic acid Chemical compound CC\C=C/C\C=C/C\C=C/C\C=C/CCCCCCC(O)=O HQPCSDADVLFHHO-LTKCOYKYSA-N 0.000 description 1
- AHANXAKGNAKFSK-PDBXOOCHSA-N all-cis-icosa-11,14,17-trienoic acid Chemical compound CC\C=C/C\C=C/C\C=C/CCCCCCCCCC(O)=O AHANXAKGNAKFSK-PDBXOOCHSA-N 0.000 description 1
- 108010061314 alpha-L-Fucosidase Proteins 0.000 description 1
- 102000012086 alpha-L-Fucosidase Human genes 0.000 description 1
- 102000019199 alpha-Mannosidase Human genes 0.000 description 1
- 108010012864 alpha-Mannosidase Proteins 0.000 description 1
- DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 description 1
- 235000019257 ammonium acetate Nutrition 0.000 description 1
- 229940043376 ammonium acetate Drugs 0.000 description 1
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 1
- 235000011130 ammonium sulphate Nutrition 0.000 description 1
- 235000019418 amylase Nutrition 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 235000008452 baby food Nutrition 0.000 description 1
- 235000015173 baked goods and baking mixes Nutrition 0.000 description 1
- 235000015278 beef Nutrition 0.000 description 1
- 108010005774 beta-Galactosidase Proteins 0.000 description 1
- 102000006995 beta-Glucosidase Human genes 0.000 description 1
- 108010047754 beta-Glucosidase Proteins 0.000 description 1
- 235000013361 beverage Nutrition 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- XVBRCOKDZVQYAY-UHFFFAOYSA-N bronidox Chemical compound [O-][N+](=O)C1(Br)COCOC1 XVBRCOKDZVQYAY-UHFFFAOYSA-N 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- 239000002775 capsule Substances 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 150000007942 carboxylates Chemical class 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000003518 caustics Substances 0.000 description 1
- 230000006037 cell lysis Effects 0.000 description 1
- 150000001793 charged compounds Chemical class 0.000 description 1
- 235000013351 cheese Nutrition 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 108010057052 chitotriosidase Proteins 0.000 description 1
- 238000003843 chloralkali process Methods 0.000 description 1
- XTEGARKTQYYJKE-UHFFFAOYSA-N chloric acid Chemical compound OCl(=O)=O XTEGARKTQYYJKE-UHFFFAOYSA-N 0.000 description 1
- 229940005991 chloric acid Drugs 0.000 description 1
- QBWCMBCROVPCKQ-UHFFFAOYSA-N chlorous acid Chemical compound OCl=O QBWCMBCROVPCKQ-UHFFFAOYSA-N 0.000 description 1
- 229940077239 chlorous acid Drugs 0.000 description 1
- KRVSOGSZCMJSLX-UHFFFAOYSA-L chromic acid Substances O[Cr](O)(=O)=O KRVSOGSZCMJSLX-UHFFFAOYSA-L 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 235000013365 dairy product Nutrition 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 238000004332 deodorization Methods 0.000 description 1
- 230000001877 deodorizing effect Effects 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-M dihydrogenphosphate Chemical compound OP(O)([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-M 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- REZZEXDLIUJMMS-UHFFFAOYSA-M dimethyldioctadecylammonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCCCCCCCC REZZEXDLIUJMMS-UHFFFAOYSA-M 0.000 description 1
- 235000019329 dioctyl sodium sulphosuccinate Nutrition 0.000 description 1
- 229940018602 docusate Drugs 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 239000008157 edible vegetable oil Substances 0.000 description 1
- PRHHYVQTPBEDFE-UHFFFAOYSA-N eicosatrienoic acid Natural products CCCCCC=CCC=CCCCCC=CCCCC(O)=O PRHHYVQTPBEDFE-UHFFFAOYSA-N 0.000 description 1
- 238000005868 electrolysis reaction Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 125000004494 ethyl ester group Chemical group 0.000 description 1
- 210000003527 eukaryotic cell Anatomy 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 235000019197 fats Nutrition 0.000 description 1
- 239000006052 feed supplement Substances 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- UQSQSQZYBQSBJZ-UHFFFAOYSA-N fluorosulfonic acid Chemical compound OS(F)(=O)=O UQSQSQZYBQSBJZ-UHFFFAOYSA-N 0.000 description 1
- 235000012041 food component Nutrition 0.000 description 1
- 239000005417 food ingredient Substances 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 235000013350 formula milk Nutrition 0.000 description 1
- 235000021588 free fatty acids Nutrition 0.000 description 1
- AWJWCTOOIBYHON-UHFFFAOYSA-N furo[3,4-b]pyrazine-5,7-dione Chemical compound C1=CN=C2C(=O)OC(=O)C2=N1 AWJWCTOOIBYHON-UHFFFAOYSA-N 0.000 description 1
- 229930195712 glutamate Natural products 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 108010002430 hemicellulase Proteins 0.000 description 1
- 229960002773 hyaluronidase Drugs 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
- 229940071870 hydroiodic acid Drugs 0.000 description 1
- GPRLSGONYQIRFK-UHFFFAOYSA-N hydron Chemical compound [H+] GPRLSGONYQIRFK-UHFFFAOYSA-N 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- QWPPOHNGKGFGJK-UHFFFAOYSA-N hypochlorous acid Chemical compound ClO QWPPOHNGKGFGJK-UHFFFAOYSA-N 0.000 description 1
- 235000015243 ice cream Nutrition 0.000 description 1
- 230000000415 inactivating effect Effects 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 235000011073 invertase Nutrition 0.000 description 1
- 150000008040 ionic compounds Chemical class 0.000 description 1
- FBAFATDZDUQKNH-UHFFFAOYSA-M iron chloride Chemical compound [Cl-].[Fe] FBAFATDZDUQKNH-UHFFFAOYSA-M 0.000 description 1
- 229910000358 iron sulfate Inorganic materials 0.000 description 1
- BAUYGSIQEAFULO-UHFFFAOYSA-L iron(2+) sulfate (anhydrous) Chemical compound [Fe+2].[O-]S([O-])(=O)=O BAUYGSIQEAFULO-UHFFFAOYSA-L 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 229940116108 lactase Drugs 0.000 description 1
- 235000020667 long-chain omega-3 fatty acid Nutrition 0.000 description 1
- 235000010335 lysozyme Nutrition 0.000 description 1
- 239000004325 lysozyme Substances 0.000 description 1
- 229960000274 lysozyme Drugs 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 150000004667 medium chain fatty acids Chemical class 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000004702 methyl esters Chemical class 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- LPUQAYUQRXPFSQ-DFWYDOINSA-M monosodium L-glutamate Chemical compound [Na+].[O-]C(=O)[C@@H](N)CCC(O)=O LPUQAYUQRXPFSQ-DFWYDOINSA-M 0.000 description 1
- 239000004223 monosodium glutamate Substances 0.000 description 1
- 235000013923 monosodium glutamate Nutrition 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000012454 non-polar solvent Substances 0.000 description 1
- 239000012875 nonionic emulsifier Substances 0.000 description 1
- SMGTYJPMKXNQFY-UHFFFAOYSA-N octenidine dihydrochloride Chemical compound Cl.Cl.C1=CC(=NCCCCCCCC)C=CN1CCCCCCCCCCN1C=CC(=NCCCCCCCC)C=C1 SMGTYJPMKXNQFY-UHFFFAOYSA-N 0.000 description 1
- 230000036961 partial effect Effects 0.000 description 1
- 238000009928 pasteurization Methods 0.000 description 1
- UZUFPBIDKMEQEQ-UHFFFAOYSA-N perfluorononanoic acid Chemical class OC(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F UZUFPBIDKMEQEQ-UHFFFAOYSA-N 0.000 description 1
- SNGREZUHAYWORS-UHFFFAOYSA-N perfluorooctanoic acid Chemical class OC(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F SNGREZUHAYWORS-UHFFFAOYSA-N 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 235000015277 pork Nutrition 0.000 description 1
- OTYBMLCTZGSZBG-UHFFFAOYSA-L potassium sulfate Chemical compound [K+].[K+].[O-]S([O-])(=O)=O OTYBMLCTZGSZBG-UHFFFAOYSA-L 0.000 description 1
- 229910052939 potassium sulfate Inorganic materials 0.000 description 1
- 235000011151 potassium sulphates Nutrition 0.000 description 1
- 244000144977 poultry Species 0.000 description 1
- 235000013594 poultry meat Nutrition 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
- 238000005086 pumping Methods 0.000 description 1
- 235000014438 salad dressings Nutrition 0.000 description 1
- 108700004121 sarkosyl Proteins 0.000 description 1
- 150000004671 saturated fatty acids Chemical class 0.000 description 1
- 235000003441 saturated fatty acids Nutrition 0.000 description 1
- 239000012047 saturated solution Substances 0.000 description 1
- 235000015067 sauces Nutrition 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 238000010517 secondary reaction Methods 0.000 description 1
- 235000021391 short chain fatty acids Nutrition 0.000 description 1
- 150000004666 short chain fatty acids Chemical class 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 235000017550 sodium carbonate Nutrition 0.000 description 1
- KSAVQLQVUXSOCR-UHFFFAOYSA-M sodium lauroyl sarcosinate Chemical compound [Na+].CCCCCCCCCCCC(=O)N(C)CC([O-])=O KSAVQLQVUXSOCR-UHFFFAOYSA-M 0.000 description 1
- 229940045885 sodium lauroyl sarcosinate Drugs 0.000 description 1
- RYYKJJJTJZKILX-UHFFFAOYSA-M sodium octadecanoate Chemical compound [Na+].CCCCCCCCCCCCCCCCCC([O-])=O RYYKJJJTJZKILX-UHFFFAOYSA-M 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- PNGLEYLFMHGIQO-UHFFFAOYSA-M sodium;3-(n-ethyl-3-methoxyanilino)-2-hydroxypropane-1-sulfonate;dihydrate Chemical compound O.O.[Na+].[O-]S(=O)(=O)CC(O)CN(CC)C1=CC=CC(OC)=C1 PNGLEYLFMHGIQO-UHFFFAOYSA-M 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 235000003702 sterols Nutrition 0.000 description 1
- 150000003432 sterols Chemical class 0.000 description 1
- 230000000153 supplemental effect Effects 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
- 150000003626 triacylglycerols Chemical class 0.000 description 1
- 238000002604 ultrasonography Methods 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 235000013618 yogurt Nutrition 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C57/00—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms
- C07C57/02—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms with only carbon-to-carbon double bonds as unsaturation
- C07C57/03—Monocarboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/42—Separation; Purification; Stabilisation; Use of additives
- C07C51/48—Separation; Purification; Stabilisation; Use of additives by liquid-liquid treatment
-
- 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
- C11B1/02—Pretreatment
- C11B1/025—Pretreatment by enzymes or microorganisms, living or dead
-
- 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
- C11B1/10—Production of fats or fatty oils from raw materials by extracting
-
- 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
- C11B3/00—Refining fats or fatty oils
-
- 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
- C11B3/00—Refining fats or fatty oils
- C11B3/02—Refining fats or fatty oils by chemical reaction
- C11B3/06—Refining fats or fatty oils by chemical reaction with bases
-
- 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
- C12P7/6463—Glycerides obtained from glyceride producing microorganisms, e.g. single cell oil
-
- 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
- C12P7/6472—Glycerides containing polyunsaturated fatty acid [PUFA] residues, i.e. having two or more double bonds in their backbone
-
- 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
- C12N1/00—Microorganisms, e.g. protozoa; Compositions thereof; Processes of propagating, maintaining or preserving microorganisms or compositions thereof; Processes of preparing or isolating a composition containing a microorganism; Culture media therefor
- C12N1/12—Unicellular algae; Culture media therefor
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Zoology (AREA)
- Microbiology (AREA)
- Biochemistry (AREA)
- Health & Medical Sciences (AREA)
- Biotechnology (AREA)
- General Chemical & Material Sciences (AREA)
- Genetics & Genomics (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Cell Biology (AREA)
- Botany (AREA)
- Medicinal Chemistry (AREA)
- Tropical Medicine & Parasitology (AREA)
- Virology (AREA)
- Biomedical Technology (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Fats And Perfumes (AREA)
Abstract
Description
[0001] 本出願は、2013年12月20日に出願された米国仮特許出願第61/918,953号明細書の出願日の利益を主張し、上記特許出願の開示は参照により本明細書に組み込まれる。
[0002] 本明細書で開示されているのは、1種または複数種の微生物細胞から1種または複数種の多価不飽和脂肪酸(PUFA)を含む微生物油を入手するための方法であって、細胞を溶解して溶解細胞組成物を形成し、次いでこの溶解細胞組成物から油を回収することによる方法である。本明細書でさらに開示されているのは、本明細書に記載した少なくとも1つの方法により微生物細胞から回収される、1種または複数種のPUFAを含む微生物油である。
であり、塩基であるBのKbは下記のように定義される。
[実施例1]
[00102] 微生物細胞(モルティエレラ(Mortierella))を含む細胞ブロス(250mL)を30秒にわたり剪断ミキサーを通して送り、次いでこのブロスをMicrofluidics M−110Yマイクロフルイダイザー(Microfluidics(マサチューセッツ州ニュートン(Newton,MA))に2回通すことにより、機械的にホモジナイズして細胞を溶解した。このマイクロフルイダイザーに1回目も2回目も10,000psiで通した。溶解細胞組成物に、この溶解細胞組成物の1重量%の量でドデシル硫酸ナトリウム(SDS)粉末を添加した。溶解細胞組成物を、3時間にわたり180rpmの速度で撹拌しつつ90℃に加熱した。NaOHの12.5重量/重量%溶液を溶解細胞組成物の2重量%〜4重量%で添加することにより、溶解細胞組成物のpHを8.42に調整した。固体のNaClを溶解細胞組成物の2重量%の量で添加し、この組成物を30時間にわたり90℃にて180rpmで撹拌した。撹拌中、溶解細胞組成物のpHが低下し、NaOHの12.5重量/重量%溶液を溶解細胞組成物の2重量%〜4重量%で添加してpHを8に調整した。溶解細胞組成物を5分にわたり8,000gで遠心分離して粗油を生成し、この粗油から(ARA重量で)69.7%のARAを得た。この粗油のアニシジン値(AV)は27.9であった。
[00103] 微生物細胞(モルティエレラ(Mortierella))を含む細胞ブロス(250mL)を30秒にわたり剪断ミキサーを通して送り、次いでこのブロスをMicrofluidics M−110Yマイクロフルイダイザー(Microfluidics(マサチューセッツ州ニュートン)に2回通すことにより、機械的にホモジナイズして細胞を溶解した。このマイクロフルイダイザーに1回目も2回目も10,000psiで通した。NaOHの12.5重量/重量%溶液を溶解細胞組成物の4重量%〜8重量%で添加することにより、溶解細胞組成物のpHを10.02に調整した。SDS粉末を溶解細胞組成物の1重量%の量で添加し、この組成物を3時間にわたり180rpmの速度で撹拌しつつ90℃に加熱した。溶解細胞組成物のpHが8.5に低下し、このpHで固体のNaClを溶解細胞組成物の2重量%の量で添加し、この組成物を40時間にわたり90℃にて180rpmで撹拌した。撹拌中、溶解細胞組成物のpHが低下し、NaOHの12.5重量/重量%溶液を溶解細胞組成物の2重量%〜4重量%で添加してpHを8に調整した。次いで、溶解細胞組成物を5分にわたり8,000gで遠心分離して粗油を生成し、この粗油から(ARA重量で)78.9%のARAを得た。この粗油のAVは11.2であった。
[00104] 微生物細胞(モルティエレラ(Mortierella))を含む細胞ブロス(716kg)をGEA Niroホモジナイザー(GEA Niro Soavi North America、ニューハンプシャー州ベドフォード(Bedford,NH))に2回通すことにより、このブロスを機械的にホモジナイズして細胞を溶解して溶解細胞組成物を形成した。このマイクロフルイダイザーに1回目も2回目も10,000psiで通した。SDS粉末を溶解細胞組成物の1重量%の量で添加し、この組成物を3時間にわたり180rpmの速度で撹拌しつつ90℃に加熱した。NaOHの50重量/重量%溶液を1.3kg添加して溶解細胞組成物のpHを約8.5に調整した。固体のNaClを溶解細胞組成物の2重量%の量で添加し、この組成物を60時間にわたり90℃で撹拌した。撹拌中、溶解細胞組成物のpHが低下し、その後、NaOHの50重量/重量%溶液を溶解細胞組成物の0.5重量%〜1重量%で添加してpHを8に調整した。この組成物を40kg/分の供給速度にて6,000rpmで遠心分離(Westfalia RSE−110遠心分離機(Westfalia Separator AG、ドイツ)を使用した)して粗油を生成し、この粗油から(ARA重量で)85%のARAを得た。粗油のAVは48.9であり、リン含有量は3.2ppmであった。
[00105] 微生物細胞(モルティエレラ(Mortierella))を含む細胞ブロス(1,600kg)を60分にわたり剪断ミキサーを通して送り、次いでこのブロスをMicrofluidics M−110Yマイクロフルイダイザー(Microfluidics、マサチューセッツ州ニュートン)に2回通すことにより、機械的にホモジナイズして細胞を溶解して溶解細胞組成物を形成した。このマイクロフルイダイザーに1回目も2回目も10,000psiで通した。NaOHの50重量/重量%溶液を溶解細胞組成物の1重量%で添加して溶解細胞組成物のpHを約10に調整した。SDSの30重量/重量%溶液を溶解細胞組成物の3重量%の量で添加し、この組成物を3時間にわたり180rpmの速度で撹拌しつつ90℃に加熱した。溶解細胞組成物のpHが約8.5に低下し、このpHで固体のNaClを溶解細胞組成物の2重量%の量で添加し、この組成物を100時間にわたり90℃にて180rpmで撹拌した。撹拌中、溶解細胞組成物のpHが低下し、NaOHの50重量/重量%溶液を溶解細胞組成物の0.5重量%〜1重量%で添加してpHを8に調整した。この組成物を8L/分の供給速度にて11,000rpmで遠心分離(Seital SR 1010遠心分離機(Seital srl、イタリア)を使用した)して粗油を生成し、この粗油から(ARA重量で)66.9%のARAを得た。粗油のAVは14.6であり、リン含有量は1ppmであった。
[00106] 微生物細胞(モルティエレラ(Mortierella))を含む細胞ブロス(250g)を30秒にわたり剪断ミキサーを通して送り、このブロスをMicrofluidics M−110Yマイクロフルイダイザー(Microfluidics、マサチューセッツ州ニュートン)に2回通すことにより、機械的にホモジナイズして細胞を溶解した。このマイクロフルイダイザーに1回目も2回目も10,000psiで通した。NaOHの12.5重量/重量%溶液を添加して溶解細胞組成物のpHを10に調整した。溶解細胞組成物に、この溶解細胞組成物の1重量%の量でTween80(ポリソルベート80)を添加し、この組成物を3時間にわたり250rpmの速度で撹拌しつつ90℃に加熱した。溶解細胞組成物のpHが8.3に低下し、このpHで固体のNaClを溶解細胞組成物の2重量%の量で添加し、この組成物を20時間にわたり90℃にて250rpmで撹拌した。20時間の撹拌期間全体を通して試料を採取し、5分にわたり8,000gで遠心分離した。油が分離する兆候はなかった。Tween80(ポリソルベート80)を溶解細胞組成物の2重量%の量で添加して実験を繰り返した。油が分離する兆候はなかった。SDSは実施例1〜4の溶解細胞組成物からの油の分離を促進し、これは、SDSがイオン性乳化剤であり(Tween80は非イオン性乳化剤である)、Tween80(1310g/mol)と比べて分子量が小さい(288g/mol)ためであると考えられる。
[00107] 微生物細胞(シゾキトリウム(Schizochytrium)種)を含む細胞ブロス(300g)を、60℃で1時間にわたり低温殺菌した。この細胞ブロスを180RPMの速度で撹拌し、60℃に加熱した。50重量%のNaOH溶液を添加して未洗浄のブロスのpHを7〜7.5に調整し、Alcalase(登録商標)2.4 FG(Novozymes(ノースカロライナ州フランクリントン(Franklinton,NC))から入手可能である)を、ブロス重量を基準として0.5%の量で添加することにより、細胞を溶解した。このブロスを2時間にわたり反応させ、次いで12.5重量%のNaOH溶液を添加してpHを10〜11に調整した。同時に、SDS粉末を溶解細胞組成物の2重量%の量で添加し、この組成物を2〜5時間にわたり80〜90℃に加熱した。この保持時間後に、固体のNaClを溶解細胞組成物の2重量%の量で添加し、この組成物を19時間にわたり90℃に加熱した。溶解細胞組成物を5分にわたり8000RPMで遠心分子(Thermo Scientific Sorvell ST40R Centrifuge)して粗油を生成し、この粗油から(DHA重量で)51.44%のDHAを得た。
[00108] 微生物細胞(シゾキトリウム(Schizochytrium)種)を含む細胞ブロス(300g)を、60℃で1時間にわたり低温殺菌した。未洗浄の細胞ブロスをMicrofluidics M−110Yマイクロフルイダイザー(Microfluidics、マサチューセッツ州ニュートン)に10,000psiで1回通すことにより、このブロスを機械的にホモジナイズして細胞を溶解した。溶解細胞組成物を180RPMの速度で撹拌しつつ、12.5重量%のNaOH溶液を添加してこの組成物のpHを10〜11に調整した。同時に、SDS粉末を溶解細胞組成物の2重量%の量で添加し、この組成物を2〜5時間にわたり80〜90℃に加熱した。この保持時間後に、固体のNaClを溶解細胞組成物の2重量%の量で添加し、この組成物を90℃に加熱して数時間にわたり保持した。溶解細胞組成物を5分にわたり8000RPMで遠心分子(Thermo Scientific Sorvell ST40R Centrifuge)して粗油を生成し、この粗油から(DHA重量で)59.32%のDHAを得た。
[00109] 微生物細胞(シゾキトリウム(Schizochytrium)種)を含む細胞ブロス(300g)を、60℃で1時間にわたり低温殺菌した。この細胞ブロスを180RPMの速度で撹拌し、60℃に加熱した。50重量%のNaOH溶液を添加して未洗浄のブロスのpHを7〜7.5に調整し、Alcalase(登録商標)2.4 FG(Novozymes(ノースカロライナ州フランクリントン)から入手可能である)を、ブロス重量を基準として0.5%の量で添加することにより、細胞を溶解した。撹拌を維持しつつ、12.5重量%のNaOH溶液を添加して溶解細胞組成物のpHを10〜11に調整した。同時に、SDS粉末を溶解細胞組成物の1重量%の量で添加し、この組成物を1.5時間にわたり80〜90℃に加熱した。この保持時間後に、固体のNaClを溶解細胞組成物の2重量%の量で添加し、この組成物を90℃に加熱して数時間にわたり保持した。溶解細胞組成物を5分にわたり8000RPMで遠心分子(Thermo Scientific Sorvell ST40R Centrifuge)して、粗油を生成した。
[00110] 微生物細胞(シゾキトリウム(Schizochytrium)種)を含む細胞ブロス(300g)を、60℃で1時間にわたり低温殺菌した。この細胞ブロスを180RPMの速度で撹拌し、60℃に加熱した。50重量%のNaOH溶液を添加して未洗浄のブロスのpHを7〜7.5に調整し、Alcalase(登録商標)2.4 FG(Novozymes(ノースカロライナ州フランクリントン)から入手可能である)を、ブロス重量を基準として0.5%の量で添加することにより、細胞を溶解した。撹拌を維持しつつ、12.5重量%のNaOH溶液を添加して溶解細胞組成物のpHを10〜11に調整した。同時に、SDS粉末を溶解細胞組成物の0.5重量%の量で添加し、この組成物を2時間にわたり80〜90℃に加熱した。この保持時間後に、固体のNaClを溶解細胞組成物の2重量%の量で添加し、この組成物を90℃に加熱して18時間にわたり保持した。溶解細胞組成物を5分にわたり8000RPMで遠心分子(Thermo Scientific Sorvell ST40R Centrifuge)して80%の粗油を得て、この粗油から(DHA重量で)85%のDHAを得た。
[00111] 微生物細胞(シゾキトリウム(Schizochytrium)種)を含む細胞ブロス(300g)を、60℃で1時間にわたり低温殺菌した。この細胞ブロスを180RPMの速度で撹拌し、60℃に加熱した。50重量%のNaOH溶液を添加して未洗浄のブロスのpHを7〜7.5に調整し、Alcalase(登録商標)2.4 FG(Novozymes(ノースカロライナ州フランクリントン)から入手可能である)を、ブロス重量を基準として0.5%の量で添加することにより、細胞を溶解した。撹拌を維持しつつ、12.5重量%のNaOH溶液を添加して溶解細胞組成物のpHを10〜11に調整した。同時に、SDS粉末を溶解細胞組成物の1重量%の量で添加し、この組成物を90℃に加熱した。90℃での2.5時間後に、この組成物を5分にわたり8000RPMで遠心分子(Thermo Scientific Sorvell ST40R Centrifuge)して粗油を生成し、この粗油から(DHA重量で)92%のDHAを得た。
Claims (37)
- 1種または複数種の微生物細胞から1種または複数種の多価不飽和脂肪酸を含む微生物油を入手するための方法であって、
(a)前記微生物油を含む前記細胞を溶解して溶解細胞組成物を形成する工程;
(b)前記溶解細胞組成物を解乳化して解乳化溶解細胞組成物を形成する工程;
(c)前記解乳化溶解細胞組成物から前記油を分離する工程;および
(d)前記油を回収する工程
を含み、(b)が、工程(a)の前に、工程(a)の最中にまたは工程(a)の後に乳化剤を添加する工程を含む、方法。 - (a)または(b)の少なくとも一方が、前記細胞または前記組成物を少なくとも70℃に加熱する工程をさらに含む、請求項1に記載の方法。
- (a)または(b)の少なくとも一方が、前記細胞または前記組成物を約70℃〜約100℃に加熱する工程をさらに含む、請求項1または2に記載の方法。
- (b)が、前記溶解細胞組成物に塩基を添加する工程をさらに含む、請求項1〜3のいずれか一項に記載の方法。
- (b)が、前記溶解細胞組成物のpHを約8以上に上昇させる工程をさらに含む、請求項1〜4のいずれか一項に記載の方法。
- (b)が、前記溶解細胞組成物の約0.05重量%〜約20重量%の量で塩を添加する工程をさらに含む、請求項1〜5のいずれか一項に記載の方法。
- (b)が、前記溶解細胞組成物を撹拌する工程をさらに含む、請求項1〜6のいずれか一項に記載の方法。
- (a)が、前記細胞を撹拌する工程をさらに含む、請求項1〜7のいずれか一項に記載の方法。
- (a)の前記細胞が未洗浄である、請求項1〜8のいずれか一項に記載の方法。
- (a)の前記細胞が発酵ブロスに含まれている、請求項1〜9のいずれか一項に記載の方法。
- (c)が、前記解乳化溶解細胞組成物を遠心分離する工程を含む、請求項1〜10のいずれか一項に記載の方法。
- 前記多価不飽和脂肪酸が、ω−3脂肪酸、ω−6脂肪酸およびそれらの混合物から選択される、請求項1〜11のいずれか一項に記載の方法。
- 前記多価不飽和脂肪酸が、ドコサヘキサエン酸(DHA)、エイコサペンタエン酸(EPA)、ドコサペンタエン酸(DPA)、アラキドン酸(ARA)、γ−リノール酸(GLA)、ジホモ−γ−リノール酸(DGLA)、ステアリドン酸(SDA)およびそれらの混合物から選択される、請求項1〜12のいずれか一項に記載の方法。
- 前記多価不飽和脂肪酸がドコサヘキサエン酸(DHA)である、請求項13に記載の方法。
- 前記多価不飽和脂肪酸がアラキドン酸(ARA)である、請求項13に記載の方法。
- 前記微生物細胞が、藻類、酵母、真菌類、抵抗または細菌の細胞である、請求項1〜15のいずれか一項に記載の方法。
- 前記微生物細胞が、モルティエレラ(Mortierella)属、クリプテコディニウム(Crypthecodinium)属またはスラウストキトリアレス(Thraustochytriales)目に由来する、請求項1〜16のいずれか一項に記載の方法。
- 前記微生物細胞がスラウストキトリアレス(Thraustochytriales)目に由来する、請求項16に記載の方法。
- 前記微生物細胞が、トラウストキトリウム(Thraustochytrium)属、シゾキトリウム(Schizochytrium)属またはそれらの混合物に由来する、請求項17に記載の方法。
- 前記微生物細胞がモルティエレラ・アルピナ(Mortierella Alpina)に由来する、請求項16に記載の方法。
- 前記溶解細胞組成物が、液体、細胞断片および微生物油を含む、請求項1〜20のいずれか一項に記載の方法。
- 前記油を前記細胞から入手するために有機溶媒が使用されない、請求項1〜21のいずれか一項に記載の方法。
- 前記解乳化溶解細胞組成物の平均粒径が少なくとも10ミクロンである、請求項1〜22のいずれか一項に記載の方法。
- 前記乳化剤がイオン性乳化剤である、請求項1〜23のいずれか一項に記載の方法。
- 前記イオン性乳化剤が、アニオン性硫酸塩乳化剤、アニオン性スルホン酸塩乳化剤、アニオン性リン酸塩乳化剤、アニオン性カルボン酸塩乳化剤およびこれらの組み合わせから選択されるアニオン性乳化剤である、請求項24に記載の方法。
- 前記アニオン性乳化剤がアニオン性硫酸塩乳化剤である、請求項25に記載の方法。
- 前記アニオン性硫酸塩乳化剤が、ラウリル硫酸アンモニウム、ドデシル硫酸ナトリウム、ラウレス硫酸ナトリウム、ラウリルエーテル硫酸ナトリウム、ミレス硫酸ナトリウムおよびこれらの組み合わせから選択される、請求項25に記載の方法。
- 前記乳化剤が前記溶解細胞組成物の0.2重量%〜10重量%の量で添加される、請求項1〜27のいずれか一項に記載の方法。
- 前記塩が、アルカリ金属塩、アルカリ土類金属塩、硫酸塩およびそれらの組み合わせからなる群から選択される、請求項6〜28のいずれか一項に記載の方法。
- (d)の前記油が粗油である、請求項1〜29のいずれか一項に記載の方法。
- (d)が、前記粗油を精製して精油を入手する工程をさらに含む、請求項30に記載の方法。
- 前記油が少なくとも30重量%のアラキドン酸を含む、請求項1〜31のいずれか一項に記載の方法。
- 前記油が少なくとも30重量%のドコサヘキサエン酸を含む、請求項1〜32のいずれか一項に記載の方法。
- 前記油のアニシジン値が約50未満である、請求項1〜33のいずれか一項に記載の方法。
- 前記油のリン含量が約8ppm以下である、請求項1〜34のいずれか一項に記載の方法。
- 前記油の過酸化物値が約5meq/kg未満である、請求項1〜35のいずれか一項に記載の方法。
- 請求項1〜36のいずれか一項に記載の方法により入手される油。
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2019212553A JP6989094B2 (ja) | 2013-12-20 | 2019-11-25 | 微生物細胞から微生物油を入手する方法 |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201361918953P | 2013-12-20 | 2013-12-20 | |
US61/918,953 | 2013-12-20 | ||
PCT/US2014/071461 WO2015095690A2 (en) | 2013-12-20 | 2014-12-19 | Processes for obtaining microbial oil from microbial cells |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2019212553A Division JP6989094B2 (ja) | 2013-12-20 | 2019-11-25 | 微生物細胞から微生物油を入手する方法 |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2017501709A true JP2017501709A (ja) | 2017-01-19 |
JP2017501709A5 JP2017501709A5 (ja) | 2018-02-08 |
Family
ID=53403890
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2016541284A Pending JP2017501709A (ja) | 2013-12-20 | 2014-12-19 | 微生物細胞から微生物油を入手する方法 |
JP2019212553A Active JP6989094B2 (ja) | 2013-12-20 | 2019-11-25 | 微生物細胞から微生物油を入手する方法 |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2019212553A Active JP6989094B2 (ja) | 2013-12-20 | 2019-11-25 | 微生物細胞から微生物油を入手する方法 |
Country Status (13)
Country | Link |
---|---|
US (1) | US10472316B2 (ja) |
EP (1) | EP3082792A4 (ja) |
JP (2) | JP2017501709A (ja) |
KR (1) | KR102552228B1 (ja) |
CN (1) | CN105939710B (ja) |
AR (1) | AR098896A1 (ja) |
AU (1) | AU2014369042B2 (ja) |
CA (1) | CA2934491C (ja) |
IL (2) | IL278961B2 (ja) |
MX (1) | MX370606B (ja) |
SG (1) | SG11201605033UA (ja) |
TW (1) | TWI708836B (ja) |
WO (1) | WO2015095690A2 (ja) |
Families Citing this family (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2295595B1 (en) | 2000-01-19 | 2019-05-01 | DSM IP Assets B.V. | Solventless extraction process |
EP3617318A1 (en) | 2010-06-01 | 2020-03-04 | DSM IP Assets B.V. | Extraction of lipid from cells and products therefrom |
CA2934491C (en) | 2013-12-20 | 2023-09-26 | Dsm Ip Assets B.V. | Processes for obtaining microbial oil from microbial cells |
US11124736B2 (en) | 2013-12-20 | 2021-09-21 | Dsm Ip Assets B.V. | Processes for obtaining microbial oil from microbial cells |
CN105960235B (zh) | 2013-12-20 | 2021-01-08 | 帝斯曼知识产权资产管理有限公司 | 用于从微生物细胞获得微生物油的方法 |
JP2017504318A (ja) | 2013-12-20 | 2017-02-09 | ディーエスエム アイピー アセッツ ビー.ブイ. | 微生物細胞から微生物油を入手するための方法 |
US11419350B2 (en) * | 2016-07-01 | 2022-08-23 | Corbion Biotech, Inc. | Feed ingredients comprising lysed microbial cells |
JP6998935B2 (ja) | 2016-07-13 | 2022-01-18 | エボニック オペレーションズ ゲーエムベーハー | 溶解された脂質含有バイオマスから脂質を分離する方法 |
CN109477122B (zh) * | 2016-07-13 | 2023-03-14 | 帝斯曼知识产权资产管理有限公司 | 从含有产油微生物的发酵液中提取包含多不饱和脂肪酸的微生物油的方法 |
ES2872009T3 (es) | 2016-12-27 | 2021-11-02 | Evonik Degussa Gmbh | Método de aislamiento de lípidos a partir de una biomasa que contiene lípidos |
CN108570484A (zh) * | 2017-03-07 | 2018-09-25 | 武汉普赛特膜技术循环利用有限公司 | 一种使用三次发酵法由藻发酵液中纯化富集dha油脂的方法 |
EP3470502A1 (en) | 2017-10-13 | 2019-04-17 | Evonik Degussa GmbH | Method of separating lipids from a lysed lipids containing biomass |
EP3527664A1 (en) | 2018-02-15 | 2019-08-21 | Evonik Degussa GmbH | Method of isolating lipids from a lipids containing biomass |
US11666062B2 (en) | 2017-12-22 | 2023-06-06 | Dsm Ip Assets B.V. | Oil comprising at least one polyunsaturated fatty acid having at least 20 carbon atoms (LC-PUFA) |
BR112020019920A2 (pt) * | 2018-03-30 | 2021-01-05 | Dsm Ip Assets B.V. | Método de redução de emulsão por lavagem de caldo |
BR112020019931A2 (pt) * | 2018-03-30 | 2021-03-30 | Dsm Ip Assets B.V. | Método de redução de emulsão através da manutenção de uma baixa concentração de carboidrato |
US11976253B2 (en) | 2018-05-15 | 2024-05-07 | Evonik Operations Gmbh | Method of isolating lipids from a lysed lipids containing biomass by emulsion inversion |
CA3101855C (en) | 2018-05-15 | 2023-06-20 | Evonik Operations Gmbh | Method of isolating lipids from a lipids containing biomass with aid of hydrophobic silica |
WO2020016363A1 (en) | 2018-07-20 | 2020-01-23 | Total Raffinage Chimie | Wet process for recovering oil produced by microorganism |
BR112021013014A2 (pt) * | 2019-01-03 | 2021-09-14 | Corbion Biotech Inc. | Processo para fabricar uma suspensão de células lisadas |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2004504849A (ja) * | 2000-08-02 | 2004-02-19 | デーエスエム・ナムローゼ・フェンノートシャップ | 微生物由来の油の単離方法 |
WO2006046943A2 (en) * | 2004-10-22 | 2006-05-04 | Martek Biosciences Corporation | Methods for producing lipids by liberation from biomass |
JP2013532964A (ja) * | 2010-06-01 | 2013-08-22 | ディーエスエム アイピー アセッツ ビー.ブイ. | 細胞からの脂質の抽出およびそれに由来する生産物 |
Family Cites Families (151)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2753362A (en) | 1951-05-18 | 1956-07-03 | Standard Brands Inc | Process of extracting lipids from plant and animal tissue |
GB808128A (en) | 1955-12-01 | 1959-01-28 | Nat Res Dev | A method of increasing the fatty contents of such micro-organisms as yeasts, bacteria and moulds |
US3089821A (en) | 1959-10-28 | 1963-05-14 | Merck & Co Inc | Process for the preparation of lipids |
DE2056896B2 (de) | 1970-02-18 | 1979-12-06 | Veb Schwermaschinenbau Kombinat Ernst Thaelmann Magdeburg, Ddr 3011 Magdeburg | Verfahren zur gleichzeitigen Gewinnung von Fett und Protein aus pflanzlichen, ölhaltigen Rohstoffen und Zwischenprodukten |
US3878232A (en) | 1970-09-28 | 1975-04-15 | Staley Mfg Co A E | Extraction process to improve the quality and yield of crude vegetable oils |
GB1466853A (en) | 1973-05-22 | 1977-03-09 | Simon Rosedowns Ltd | Extraction |
US4504473A (en) | 1982-06-30 | 1985-03-12 | Ribi Immunochem Research, Inc. | Pyridine soluble extract of a microorganism |
DE3248167A1 (de) | 1982-12-27 | 1984-06-28 | Wintershall Ag, 3100 Celle | Trehaloselipidtetraester |
DE3587044T2 (de) | 1985-01-22 | 1993-06-03 | Agency Ind Science Techn | Verfahren zur herstellung von lipiden aus fungusmassen. |
JPS61170397A (ja) | 1985-01-22 | 1986-08-01 | Agency Of Ind Science & Technol | モルテイエレラ属糸状菌体の多段抽出処理方法 |
US4792418A (en) | 1985-08-14 | 1988-12-20 | Century Laboratories, Inc. | Method of extraction and purification of polyunsaturated fatty acids from natural sources |
JPS6244170A (ja) | 1985-08-19 | 1987-02-26 | Agency Of Ind Science & Technol | モルテイエレラ属糸状菌体の超臨界流体による抽出方法 |
US4680314A (en) | 1985-08-30 | 1987-07-14 | Microbio Resources, Inc. | Process for producing a naturally-derived carotene/oil composition by direct extraction from algae |
JPS62278987A (ja) | 1986-05-26 | 1987-12-03 | Kanegafuchi Chem Ind Co Ltd | 酵素反応生成物の回収方法 |
DK199887D0 (da) | 1987-04-15 | 1987-04-15 | Danisco Bioteknologi As | Gaerstamme |
JPS63304990A (ja) | 1987-06-04 | 1988-12-13 | Meiji Seika Kaisha Ltd | 菌体内有効成分の抽出方法 |
FR2621327B1 (fr) | 1987-10-06 | 1990-01-05 | Commissariat Energie Atomique | Procede de production et d'extraction de polysaccharides a partir d'une culture de porphyridium cruentum et dispositif pour la mise en oeuvre du procede |
JPH0198494A (ja) | 1987-10-09 | 1989-04-17 | Agency Of Ind Science & Technol | バイオリアクター |
US5340594A (en) | 1988-09-07 | 1994-08-23 | Omegatech Inc. | Food product having high concentrations of omega-3 highly unsaturated fatty acids |
US5340742A (en) | 1988-09-07 | 1994-08-23 | Omegatech Inc. | Process for growing thraustochytrium and schizochytrium using non-chloride salts to produce a microfloral biomass having omega-3-highly unsaturated fatty acids |
US6451567B1 (en) | 1988-09-07 | 2002-09-17 | Omegatech, Inc. | Fermentation process for producing long chain omega-3 fatty acids with euryhaline microorganisms |
US5130242A (en) | 1988-09-07 | 1992-07-14 | Phycotech, Inc. | Process for the heterotrophic production of microbial products with high concentrations of omega-3 highly unsaturated fatty acids |
US5173409A (en) | 1989-12-08 | 1992-12-22 | Ecogen Inc. | Recovery of bt endotoxin protein from lysed cell mixtures |
US5288619A (en) | 1989-12-18 | 1994-02-22 | Kraft General Foods, Inc. | Enzymatic method for preparing transesterified oils |
FR2656874B1 (fr) | 1990-01-11 | 1992-04-03 | Commissariat Energie Atomique | Procede de production et d'extraction d'anti-oxydants a partir d'une culture de micro-organismes et photobioreacteur pour la mise en óoeuvre de ce procede. |
US5407957A (en) | 1990-02-13 | 1995-04-18 | Martek Corporation | Production of docosahexaenoic acid by dinoflagellates |
US5133963A (en) | 1990-12-21 | 1992-07-28 | Shuntaro Ise | Method of producing commercially useful poultry products with increased concentrations of Omega-3 polyunsaturated fatty acids |
US5658767A (en) | 1991-01-24 | 1997-08-19 | Martek Corporation | Arachidonic acid and methods for the production and use thereof |
US6270828B1 (en) | 1993-11-12 | 2001-08-07 | Cargrill Incorporated | Canola variety producing a seed with reduced glucosinolates and linolenic acid yielding an oil with low sulfur, improved sensory characteristics and increased oxidative stability |
FR2686619B1 (fr) | 1992-01-28 | 1995-07-13 | Commissariat Energie Atomique | Procede de production selective de lipides poly-insatures a partir d'une culture de micro-algues du type porphyridium et cuve utilisee dans ce procede. |
US5476787A (en) | 1992-04-24 | 1995-12-19 | Director-General Of Agency Of Industrial Science And Technology | Method of removing nitrogen impurities from water using hydrocarbon-producing microalga |
DE4219360C2 (de) | 1992-06-12 | 1994-07-28 | Milupa Ag | Verfahren zur Gewinnung von Lipiden mit einem hohen Anteil von langkettig-hochungesättigten Fettsäuren |
AU695940B2 (en) | 1993-04-27 | 1998-08-27 | Cargill Incorporated | Non-hydrogenated canola oil for food applications |
FR2719222B1 (fr) | 1994-05-02 | 1996-06-21 | Rocher Yves Biolog Vegetale | Vésicules lipidiques, leur procédé de fabrication et leurs applications. |
WO1996005278A1 (de) | 1994-08-16 | 1996-02-22 | Dr. Frische Gmbh | Verfahren zur gewinnung von nicht wasserlöslichen, nativen produkten aus nativen stoffgemengen mit hilfe der zentrifugalkraft |
US5583019A (en) | 1995-01-24 | 1996-12-10 | Omegatech Inc. | Method for production of arachidonic acid |
DE69637953D1 (de) | 1995-04-17 | 2009-07-30 | Nat Inst Of Advanced Ind Scien | Hoch ungesättigte fettsäurenproduzierende mikroorganismen und verfahren zur herstellung von hoch ungesättigten fettsäuren durch verwendung dieser mikroorganismen |
DE69508558T2 (de) | 1995-05-04 | 1999-08-26 | Nestle Sa | Verfahren zur Fraktionierung von Fettsäuren |
JPH099981A (ja) | 1995-06-28 | 1997-01-14 | Sekiyu Sangyo Kasseika Center | 油水二相系微生物反応における油水分離方法 |
GB9514649D0 (en) | 1995-07-18 | 1995-09-13 | Zeneca Ltd | Extraction of triglycerides from microorganisms |
JP3985035B2 (ja) | 1995-09-14 | 2007-10-03 | 独立行政法人産業技術総合研究所 | (n−6)系ドコサペンタエン酸含有油脂ならびに該油脂の製造方法および用途 |
CA2627832C (en) | 1996-03-28 | 2012-12-11 | Dsm Ip Assets B.V. | Preparation of microbial polyunsaturated fatty acid containing oil from pasteurised biomass |
CN1715394A (zh) | 1996-03-28 | 2006-01-04 | 吉斯特-布罗卡迪斯股份有限公司 | 粒状微生物生物质的制备及其有价值的化合物的分离方法 |
US6255505B1 (en) | 1996-03-28 | 2001-07-03 | Gist-Brocades, B.V. | Microbial polyunsaturated fatty acid containing oil from pasteurised biomass |
ATE215120T1 (de) | 1996-05-15 | 2002-04-15 | Dsm Nv | Verfahren zum extrahieren von sterol mit einem polaren lösungsmittel zur herstellung eines mikrobiellen öles mit niedrigem sterolgehalt |
EP0969086A1 (en) | 1996-07-03 | 2000-01-05 | Sagami Chemical Research Center | Microorganisms producing docosahexaenoic acid and process for the production of docosahexaenoic acid |
EP0935667B1 (en) | 1996-07-23 | 2006-12-06 | Nagase Chemtex Corporation | Process for preparing docosahexaenoic acid and docosapentaenoic acid |
US5951875A (en) | 1996-12-20 | 1999-09-14 | Eastman Chemical Company | Adsorptive bubble separation methods and systems for dewatering suspensions of microalgae and extracting components therefrom |
GB9701705D0 (en) | 1997-01-28 | 1997-03-19 | Norsk Hydro As | Purifying polyunsatured fatty acid glycerides |
DE69840022D1 (de) | 1997-03-04 | 2008-10-30 | Suntory Ltd | Verfahren zur herstellung von hochungesättigten fettsäuren und hochungesättigte fettsäuren enthaltendes lipid |
ES2337530T3 (es) | 1997-05-02 | 2010-04-26 | Dsm Ip Assets B.V. | Aislamiento de cristales de carotenoide a partir de biomasa microbiana. |
EP1905309A1 (en) | 1997-05-27 | 2008-04-02 | SemBioSys Genetics Inc. | Uses of oil bodies |
US7585645B2 (en) | 1997-05-27 | 2009-09-08 | Sembiosys Genetics Inc. | Thioredoxin and thioredoxin reductase containing oil body based products |
US6566583B1 (en) | 1997-06-04 | 2003-05-20 | Daniel Facciotti | Schizochytrium PKS genes |
JP3836231B2 (ja) | 1997-10-17 | 2006-10-25 | 日本化学飼料株式会社 | ホタテガイ中腸腺から得られる高度不飽和脂肪酸含有油及びその製造方法 |
EP0987926B1 (en) | 1997-11-12 | 2004-04-28 | Mitsubishi Denki Kabushiki Kaisha | An electroluminescent light |
JP2002508929A (ja) | 1997-12-23 | 2002-03-26 | ディーシーブイ・インコーポレイテッド・ドゥーイング・ビジネス・アズ・バイオ−テクニカル・リソーシィズ | リノール酸イソメラーゼ |
AU3786799A (en) | 1998-05-05 | 1999-11-23 | University Of Tennessee Research Corporation, The | An instrument and method for measurement of stability of oils |
JP2000041684A (ja) | 1998-07-29 | 2000-02-15 | Daicel Chem Ind Ltd | 新規なd−アミノアシラーゼおよびその製造方法、並びに該d−アミノアシラーゼを利用したd−アミノ酸の製造方法 |
JP2000135096A (ja) | 1998-08-28 | 2000-05-16 | Tadayuki Imanaka | 界面活性剤、その生産方法およびその利用方法 |
FR2782921B1 (fr) | 1998-09-09 | 2002-09-20 | Dior Christian Parfums | Extrait lipidique de l'algue skeletonema, procede de preparation et utilisation dans des domaines cosmetique et pharmaceutique, notamment dermatologique |
US6166231A (en) | 1998-12-15 | 2000-12-26 | Martek Biosciences Corporation | Two phase extraction of oil from biomass |
CA2260397A1 (en) | 1999-01-29 | 2000-07-29 | Atlantis Marine Inc. | Method of converting rendered triglyceride oil from marine sources into bland, stable food oil |
JP2000245492A (ja) | 1999-03-02 | 2000-09-12 | Kyowa Hakko Kogyo Co Ltd | 微生物抽出脂質 |
KR19990046733A (ko) | 1999-04-20 | 1999-07-05 | 류성구 | 미생물슈도모나스에의한도코사핵사노인산(dha)의제조방법 |
US6344349B1 (en) | 1999-12-06 | 2002-02-05 | Decant Technologies Llc | Process and system for electrical extraction of intracellular matter from biological matter |
EP2295595B1 (en) | 2000-01-19 | 2019-05-01 | DSM IP Assets B.V. | Solventless extraction process |
DE60130737T3 (de) | 2000-01-28 | 2016-01-14 | Dsm Ip Assets B.V. | Verstärkte Produktion von Lipiden enthaltend mehrfachungesättigte Fettsäuren durch hochdichte Kulturen von eukariotischen Mikroben in Gärvorrichtungen |
JP5461750B2 (ja) | 2000-04-12 | 2014-04-02 | ウエストファリア セパレーター アーゲー | 油と極性脂質を含有する天然物質の分画方法 |
DE10018213A1 (de) | 2000-04-12 | 2001-10-25 | Westfalia Separator Ind Gmbh | Verfahren zur Fraktionierung von öl-und lecithinhaltigen nativen Rohstoffen |
EP1178103A1 (en) | 2000-08-02 | 2002-02-06 | Dsm N.V. | Purifying crude pufa oils |
US20060060520A1 (en) | 2001-06-25 | 2006-03-23 | Bomberger David C | Systems and methods using a solvent for the removal of lipids from fluids |
US20030060509A1 (en) | 2001-08-24 | 2003-03-27 | Elswyk Mary Van | Products containing highly unsaturated fatty acids for use by women and their children during stages of preconception, pregnancy and lactation/post-partum |
EP2261312A1 (en) | 2001-12-12 | 2010-12-15 | Martek Biosciences Corporation | Extraction and Winterization of Lipids from Oilseed and Microbial Sources |
CN1177024C (zh) | 2002-03-27 | 2004-11-24 | 西南农业大学 | 水剂法生产食用菜籽蛋白和油脂的方法 |
CA2484334C (en) | 2002-05-03 | 2013-01-22 | Martek Biosciences Corporation | High-quality lipids and methods for producing by enzymatic liberation from biomass |
JP2005529621A (ja) | 2002-06-19 | 2005-10-06 | デーエスエム イーペー アセッツ ベスローテン フェンノートシャップ | 微生物細胞及び微生物油の低温殺菌方法 |
MX338455B (es) | 2003-10-02 | 2016-04-18 | Dsm Ip Assets Bv | Produccion de altos niveles de dha en microalgas usando cantidades modificadas de cloruro y potasio. |
BRPI0418239B1 (pt) | 2003-12-30 | 2013-10-01 | processo de desaeraÇço | |
US7038559B2 (en) | 2004-02-23 | 2006-05-02 | Ruby Richard C | Vertically separated acoustic filters and resonators |
CA2558255C (en) | 2004-03-01 | 2014-01-14 | Suntory Limited | Process for producing phospholipid containing long chain polyunsaturated fatty acid as constituent thereof and utilization of the same |
CN1946835A (zh) | 2004-04-27 | 2007-04-11 | 巴克斯特国际公司 | 搅拌罐反应器系统 |
EP1597976B1 (en) * | 2004-05-21 | 2013-01-30 | Nestec S.A. | Use of polyol esters of fatty acids in aerated frozen confection with improved nutritional attributes |
DE102004062141A1 (de) | 2004-12-23 | 2006-07-06 | Nutrinova Nutrition Specialties & Food Ingredients Gmbh | Verfahren zur Herstellung eines Rohöls aus Gemischen von Mikroorganismen und Pflanzen, das so hergestellte Öl sowie die spezifischen Verwendungen des so hergestellten und gegebenenfalls zusätzlich raffinierten Öls |
DE102005003624A1 (de) | 2005-01-26 | 2006-07-27 | Nutrinova Nutrition Specialties & Food Ingredients Gmbh | Herstellung und Anwendung eines antioxidativ wirksamen Extraktes aus Crypthecodinium sp. |
WO2006128244A1 (en) | 2005-06-03 | 2006-12-07 | Mc Farlane Marketing (Aust.) Pty. Ltd. | Lipid extract of mussels and method for preparation thereof |
ES2909600T3 (es) | 2005-06-07 | 2022-05-09 | Dsm Nutritional Products Ag | Microorganismos eucarióticos para producir lípidos y antioxidantes |
EP1903883A4 (en) | 2005-07-01 | 2010-06-23 | Martek Biosciences Corp | OIL PRODUCT CONTAINING MULTIPLE UNSATURATED FATTY ACIDS AND ITS USES AND MANUFACTURING |
US7527734B1 (en) | 2005-11-15 | 2009-05-05 | Shepherd Samuel L | Rapid non-equilibrium decompression of microorganism-containing waste streams |
AU2007213506A1 (en) | 2006-02-07 | 2007-08-16 | Universitetet I Oslo | Omega 3 |
NZ573719A (en) | 2006-07-05 | 2011-08-26 | Photonz Corp Ltd | Production of ultrapure eicosapentaenoic acid and polar lipids from largely heterotrophic culture of nitzschia laevis |
EP1887011A1 (en) | 2006-08-09 | 2008-02-13 | Thermphos Trading GmbH | Alpha amino acid phosphonic acid compounds, method of preparation and use thereof |
WO2008130372A2 (en) | 2006-09-28 | 2008-10-30 | Microbia, Inc. | Production of sterols in oleaginous yeast and fungi |
KR100810314B1 (ko) | 2006-10-11 | 2008-03-04 | 삼성전자주식회사 | 휴대 단말기의 키 입력 장치 |
CN101610824A (zh) * | 2006-12-22 | 2009-12-23 | 丹尼斯科美国公司 | 酶辅助的水性脂类提取物的脱乳化作用 |
CN101224022B (zh) | 2007-01-15 | 2012-10-31 | 天津科技大学 | 水酶法同时制备芝麻油和蛋白质的工艺方法 |
CA2702247A1 (en) | 2007-06-14 | 2008-12-18 | Nickolaos Mitropoulos | Algae growth for biofuels |
CA2697730C (en) | 2007-08-29 | 2014-04-08 | Aker Biomarine Asa | A new method for making krill meal |
US20100226977A1 (en) | 2007-08-29 | 2010-09-09 | Aker Biomarine Asa | Low viscosity phospholipid compositions |
JP5244966B2 (ja) | 2008-03-26 | 2013-07-24 | ビーワイディー カンパニー リミテッド | リチウム電池用正極材料 |
ITMI20081203A1 (it) | 2008-06-30 | 2010-01-01 | Eni Spa | Procedimento per l'estrazione di acidi grassi da biomassa algale |
EP2145942A1 (de) | 2008-07-15 | 2010-01-20 | Lonza Ltd. | Verfahren zur Isolierung von Ölen aus Zellen und Biomasse |
US20120036767A1 (en) | 2008-08-04 | 2012-02-16 | Larach Mario C | Continuous cultivation, harvesting, and extraction of photosynthetic cultures |
ES2625483T3 (es) | 2008-10-02 | 2017-07-19 | Nieves Gonzalez Ramon | Extracto de microalgas que contiene ácidos grasos omega 3-poliinsaturados y método para extraer aceite de microorganismos |
US9896642B2 (en) | 2008-10-14 | 2018-02-20 | Corbion Biotech, Inc. | Methods of microbial oil extraction and separation |
MX339664B (es) | 2008-10-14 | 2016-06-03 | Solazyme Inc | Composiciones alimenticias a partir de biomasa de microalgas. |
CN101447860B (zh) | 2008-11-28 | 2010-12-22 | 清华大学 | 任意位高速滑动相关器及其应用 |
CN101455240B (zh) | 2008-12-29 | 2011-04-06 | 东北农业大学 | 水酶法提取南瓜籽油的方法 |
SE534278C2 (sv) | 2009-02-17 | 2011-06-28 | Alfa Laval Corp Ab | Ett kontinuerligt förfarande för isolering av oljor från alger eller mikroorganismer |
EP2406370A4 (en) | 2009-03-10 | 2013-08-14 | Srs Energy | FRACTIONATION OF ALGAE BIOMASS |
US9296985B2 (en) | 2009-03-10 | 2016-03-29 | Valicor, Inc. | Algae biomass fractionation |
CN109609562A (zh) | 2009-03-19 | 2019-04-12 | 帝斯曼知识产权资产管理有限公司 | 破囊壶菌、脂肪酸组合物和其制备方法及用途 |
US8207363B2 (en) | 2009-03-19 | 2012-06-26 | Martek Biosciences Corporation | Thraustochytrids, fatty acid compositions, and methods of making and uses thereof |
US8476060B2 (en) | 2009-04-13 | 2013-07-02 | Board Of Regents, The University Of Texas System | Process for separating lipids from a biomass |
CN106367198A (zh) | 2009-04-14 | 2017-02-01 | 泰拉瑞亚控股公司 | 微生物油提取和分离方法 |
CN101531690B (zh) | 2009-04-28 | 2011-09-14 | 浙江神茗山茶业科技有限公司 | 一种用水作溶剂直接从茶叶籽仁中提取茶皂素和茶叶籽油的工艺 |
AU2010254104A1 (en) | 2009-05-26 | 2011-12-15 | Solazyme, Inc. | Fractionation of oil-bearing microbial biomass |
KR101659765B1 (ko) | 2009-09-28 | 2016-09-27 | 삼성전자주식회사 | 다중 모드 휴대용 단말기에서 전력 소모를 줄이기 위한 장치 및 방법 |
WO2011059745A1 (en) | 2009-10-28 | 2011-05-19 | The Arizona Board Of Regents For And On Behalf Of Arizona State University | Bacterium for production of fatty acids |
CA2787344C (en) | 2010-01-19 | 2018-03-20 | Dsm Ip Assets B.V. | Eicosapentaenoic acid-producing microorganisms, fatty acid compositions, and methods of making and uses thereof |
WO2011130573A1 (en) | 2010-04-14 | 2011-10-20 | Solazyme, Inc. | Fuel and chemical production from oleaginous yeast |
WO2011130576A1 (en) | 2010-04-14 | 2011-10-20 | Solazyme, Inc. | Oleaginous yeast food compositions |
US20110263709A1 (en) * | 2010-04-22 | 2011-10-27 | E. I. Du Pont De Nemours And Company | Method for obtaining polyunsaturated fatty acid-containing compositions from microbial biomass |
US9023625B2 (en) | 2010-06-14 | 2015-05-05 | Io-Mega Holding Corporation | Methods for production of algae derived oils |
US9028696B2 (en) | 2010-07-26 | 2015-05-12 | Sapphire Energy, Inc. | Process for the recovery of oleaginous compounds from biomass |
CN103080325B (zh) | 2010-07-26 | 2014-08-06 | 蓝宝石能源公司 | 用于从生物质回收油质化合物的方法 |
US8192627B2 (en) | 2010-08-06 | 2012-06-05 | Icm, Inc. | Bio-oil recovery methods |
US20120040428A1 (en) | 2010-08-13 | 2012-02-16 | Paul Reep | Procedure for extracting of lipids from algae without cell sacrifice |
US20120129244A1 (en) | 2010-10-17 | 2012-05-24 | Michael Phillip Green | Systems, methods and apparatuses for dewatering, flocculating and harvesting algae cells |
MX2012012250A (es) | 2010-10-18 | 2013-03-05 | Originoil Inc | Sistemas, aparatos, y metodos para extraer lipidos no polares de una lechada acuosa de algas y lipidos producidos de la misma. |
CN101985637B (zh) | 2010-11-02 | 2014-05-07 | 嘉必优生物工程(武汉)有限公司 | 一种微生物油脂的提取方法 |
CN108823254A (zh) | 2010-11-03 | 2018-11-16 | 柯碧恩生物技术公司 | 具有降低倾点的微生物油、从其中产生的介电流体、以及相关方法 |
ES2490619T3 (es) | 2010-11-08 | 2014-09-04 | Neste Oil Oyj | Método de extracción de lípidos a partir de biomasa |
WO2012109642A1 (en) | 2011-02-12 | 2012-08-16 | Phycal, Inc. | Aqueous extraction methods for high lipid microorganisms |
CN103649313B (zh) | 2011-03-07 | 2017-10-24 | Dsm营养产品股份公司 | 工程化破囊壶菌属微生物 |
WO2012125611A2 (en) | 2011-03-15 | 2012-09-20 | Iowa State University Research Foundation | Oil extraction from microalgae |
FR2975705B1 (fr) | 2011-05-27 | 2014-12-26 | Roquette Freres | Procede d'extraction du squalene a partir de microalgues |
CN102433215A (zh) | 2011-09-22 | 2012-05-02 | 厦门汇盛生物有限公司 | 一种从真菌或藻类中物理破壁提取油脂的方法 |
CN102388988B (zh) * | 2011-11-08 | 2013-01-23 | 中国农业科学院油料作物研究所 | 一种微生物油的分提方法 |
US9200236B2 (en) | 2011-11-17 | 2015-12-01 | Heliae Development, Llc | Omega 7 rich compositions and methods of isolating omega 7 fatty acids |
WO2013156720A2 (fr) | 2012-04-16 | 2013-10-24 | Roquette Freres | Procédé de raffinage du squalène produit par microalgues |
CN104508113A (zh) | 2012-06-29 | 2015-04-08 | Bp生物燃料英国有限公司 | 从微生物中分离可再生物质的方法 |
WO2015095462A1 (en) | 2013-12-20 | 2015-06-25 | BP Biofuels UK Limited | Process for extracting lipids for use in production of biofuels |
CA2934491C (en) | 2013-12-20 | 2023-09-26 | Dsm Ip Assets B.V. | Processes for obtaining microbial oil from microbial cells |
SG11201605066WA (en) | 2013-12-20 | 2016-07-28 | Dsm Ip Assets Bv | Processes for obtaining microbial oil from microbial cells |
KR20240001258A (ko) | 2013-12-20 | 2024-01-03 | 마라 리뉴어블즈 코퍼레이션 | 미생물로부터 오일을 회수하는 방법 |
KR102435268B1 (ko) | 2013-12-20 | 2022-08-22 | 디에스엠 뉴트리셔널 프라덕츠 아게 | 미생물로부터 오일을 회수하는 방법 |
US11124736B2 (en) | 2013-12-20 | 2021-09-21 | Dsm Ip Assets B.V. | Processes for obtaining microbial oil from microbial cells |
JP2017504318A (ja) | 2013-12-20 | 2017-02-09 | ディーエスエム アイピー アセッツ ビー.ブイ. | 微生物細胞から微生物油を入手するための方法 |
CN105960235B (zh) | 2013-12-20 | 2021-01-08 | 帝斯曼知识产权资产管理有限公司 | 用于从微生物细胞获得微生物油的方法 |
JP6882160B2 (ja) | 2014-07-07 | 2021-06-02 | コモンウェルス サイエンティフィック アンド インダストリアル リサーチ オーガナイゼーション | 植物脂質から工業製品を製造する工程 |
-
2014
- 2014-12-19 CA CA2934491A patent/CA2934491C/en active Active
- 2014-12-19 AU AU2014369042A patent/AU2014369042B2/en active Active
- 2014-12-19 MX MX2016008213A patent/MX370606B/es active IP Right Grant
- 2014-12-19 KR KR1020167019570A patent/KR102552228B1/ko active IP Right Grant
- 2014-12-19 CN CN201480074727.2A patent/CN105939710B/zh active Active
- 2014-12-19 SG SG11201605033UA patent/SG11201605033UA/en unknown
- 2014-12-19 IL IL278961A patent/IL278961B2/en unknown
- 2014-12-19 TW TW103144475A patent/TWI708836B/zh active
- 2014-12-19 WO PCT/US2014/071461 patent/WO2015095690A2/en active Application Filing
- 2014-12-19 US US15/106,368 patent/US10472316B2/en active Active
- 2014-12-19 EP EP14870820.9A patent/EP3082792A4/en active Pending
- 2014-12-19 AR ARP140104837A patent/AR098896A1/es unknown
- 2014-12-19 JP JP2016541284A patent/JP2017501709A/ja active Pending
-
2016
- 2016-06-20 IL IL246341A patent/IL246341A0/en unknown
-
2019
- 2019-11-25 JP JP2019212553A patent/JP6989094B2/ja active Active
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2004504849A (ja) * | 2000-08-02 | 2004-02-19 | デーエスエム・ナムローゼ・フェンノートシャップ | 微生物由来の油の単離方法 |
WO2006046943A2 (en) * | 2004-10-22 | 2006-05-04 | Martek Biosciences Corporation | Methods for producing lipids by liberation from biomass |
JP2013532964A (ja) * | 2010-06-01 | 2013-08-22 | ディーエスエム アイピー アセッツ ビー.ブイ. | 細胞からの脂質の抽出およびそれに由来する生産物 |
Also Published As
Publication number | Publication date |
---|---|
AU2014369042A1 (en) | 2016-07-07 |
SG11201605033UA (en) | 2016-07-28 |
AR098896A1 (es) | 2016-06-22 |
WO2015095690A2 (en) | 2015-06-25 |
CA2934491C (en) | 2023-09-26 |
IL278961B1 (en) | 2023-09-01 |
CN105939710B (zh) | 2020-05-08 |
IL278961A (en) | 2021-01-31 |
CN105939710A (zh) | 2016-09-14 |
JP2020054349A (ja) | 2020-04-09 |
EP3082792A2 (en) | 2016-10-26 |
KR20160102008A (ko) | 2016-08-26 |
JP6989094B2 (ja) | 2022-01-05 |
AU2014369042B2 (en) | 2020-04-30 |
US10472316B2 (en) | 2019-11-12 |
TWI708836B (zh) | 2020-11-01 |
TW201529831A (zh) | 2015-08-01 |
CA2934491A1 (en) | 2015-06-25 |
KR102552228B1 (ko) | 2023-07-05 |
BR112016014514A2 (pt) | 2017-09-19 |
WO2015095690A3 (en) | 2015-12-23 |
EP3082792A4 (en) | 2017-08-16 |
MX370606B (es) | 2019-12-18 |
US20160340287A1 (en) | 2016-11-24 |
MX2016008213A (es) | 2016-11-09 |
IL278961B2 (en) | 2024-01-01 |
IL246341A0 (en) | 2016-08-31 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP6989094B2 (ja) | 微生物細胞から微生物油を入手する方法 | |
JP7164265B2 (ja) | 微生物細胞から微生物油を入手する方法 | |
JP7487961B2 (ja) | 微生物細胞から微生物油を入手するための方法 | |
JP7381649B2 (ja) | 微生物細胞から微生物油を入手するための方法 | |
JP6705581B2 (ja) | 微生物細胞から微生物油を入手するための方法 | |
BR112016014514B1 (pt) | Processo para a obtenção de um óleo microbiano que compreende um ou mais ácidos graxos poli-insaturados a partir de uma ou mais células microbianas e óleo |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20171219 |
|
A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20171219 |
|
A977 | Report on retrieval |
Free format text: JAPANESE INTERMEDIATE CODE: A971007 Effective date: 20181024 |
|
A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20181106 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20190206 |
|
A02 | Decision of refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A02 Effective date: 20190723 |