JPS623791A - カビ類または藻類による脂質の製造法 - Google Patents
カビ類または藻類による脂質の製造法Info
- Publication number
- JPS623791A JPS623791A JP60144371A JP14437185A JPS623791A JP S623791 A JPS623791 A JP S623791A JP 60144371 A JP60144371 A JP 60144371A JP 14437185 A JP14437185 A JP 14437185A JP S623791 A JPS623791 A JP S623791A
- Authority
- JP
- Japan
- Prior art keywords
- genus
- surfactant
- algae
- lipid
- lipids
- 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.)
- Granted
Links
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- 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 claims abstract description 9
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- 240000002900 Arthrospira platensis Species 0.000 claims description 5
- 235000016425 Arthrospira platensis Nutrition 0.000 claims description 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 5
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- UHVMMEOXYDMDKI-JKYCWFKZSA-L zinc;1-(5-cyanopyridin-2-yl)-3-[(1s,2s)-2-(6-fluoro-2-hydroxy-3-propanoylphenyl)cyclopropyl]urea;diacetate Chemical compound [Zn+2].CC([O-])=O.CC([O-])=O.CCC(=O)C1=CC=C(F)C([C@H]2[C@H](C2)NC(=O)NC=2N=CC(=CC=2)C#N)=C1O UHVMMEOXYDMDKI-JKYCWFKZSA-L 0.000 claims description 4
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- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical class OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 claims description 3
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- 150000004781 alginic acids Chemical class 0.000 claims description 3
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- 102000008186 Collagen Human genes 0.000 claims description 2
- 108010035532 Collagen Proteins 0.000 claims description 2
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims description 2
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- 239000011148 porous material Substances 0.000 claims description 2
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- 241001450909 Gongronella Species 0.000 claims 2
- 241001450823 Helicostylum Species 0.000 claims 2
- 150000001735 carboxylic acids Chemical class 0.000 claims 2
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- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims 1
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- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 abstract 1
- 239000000243 solution Substances 0.000 description 32
- 239000002609 medium Substances 0.000 description 25
- 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 description 24
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- 230000001580 bacterial effect Effects 0.000 description 4
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- 150000004665 fatty acids Chemical class 0.000 description 4
- 239000008103 glucose Substances 0.000 description 4
- FGIUAXJPYTZDNR-UHFFFAOYSA-N potassium nitrate Chemical compound [K+].[O-][N+]([O-])=O FGIUAXJPYTZDNR-UHFFFAOYSA-N 0.000 description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 3
- 229930182558 Sterol Natural products 0.000 description 3
- 238000012136 culture method Methods 0.000 description 3
- 238000000605 extraction Methods 0.000 description 3
- 239000000499 gel Substances 0.000 description 3
- 230000014759 maintenance of location Effects 0.000 description 3
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- 235000003702 sterols Nutrition 0.000 description 3
- 238000012546 transfer Methods 0.000 description 3
- 239000011800 void material Substances 0.000 description 3
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- 244000249214 Chlorella pyrenoidosa Species 0.000 description 2
- 235000007091 Chlorella pyrenoidosa Nutrition 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 2
- 241000233866 Fungi Species 0.000 description 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
- 241000235575 Mortierella Species 0.000 description 2
- 241000047703 Nonion Species 0.000 description 2
- RVGRUAULSDPKGF-UHFFFAOYSA-N Poloxamer Chemical compound C1CO1.CC1CO1 RVGRUAULSDPKGF-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
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- RWSXRVCMGQZWBV-WDSKDSINSA-N glutathione Chemical compound OC(=O)[C@@H](N)CCC(=O)N[C@@H](CS)C(=O)NCC(O)=O RWSXRVCMGQZWBV-WDSKDSINSA-N 0.000 description 2
- 239000001963 growth medium Substances 0.000 description 2
- NDJKXXJCMXVBJW-UHFFFAOYSA-N heptadecane Chemical compound CCCCCCCCCCCCCCCCC NDJKXXJCMXVBJW-UHFFFAOYSA-N 0.000 description 2
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- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 235000010482 polyoxyethylene sorbitan monooleate Nutrition 0.000 description 2
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- 230000035484 reaction time Effects 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 238000000638 solvent extraction Methods 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- 239000012138 yeast extract Substances 0.000 description 2
- IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical compound CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- 241000131314 Aspergillus candidus Species 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- 241001450911 Circinella Species 0.000 description 1
- 241000221760 Claviceps Species 0.000 description 1
- 244000205754 Colocasia esculenta Species 0.000 description 1
- 235000006481 Colocasia esculenta Nutrition 0.000 description 1
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 1
- 241001450825 Fennellomyces Species 0.000 description 1
- 108010024636 Glutathione Proteins 0.000 description 1
- 241001450899 Gongronella butleri Species 0.000 description 1
- 241000223199 Humicola grisea Species 0.000 description 1
- 239000007836 KH2PO4 Substances 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 229920002292 Nylon 6 Polymers 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 241000684698 Paecilomyces sp. (in: Hypocreales) Species 0.000 description 1
- 241000282320 Panthera leo Species 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
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- 229920001213 Polysorbate 20 Polymers 0.000 description 1
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- 241001494715 Porphyridium purpureum Species 0.000 description 1
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- 235000013752 Rhizopus oryzae Nutrition 0.000 description 1
- 239000004147 Sorbitan trioleate Substances 0.000 description 1
- PRXRUNOAOLTIEF-ADSICKODSA-N Sorbitan trioleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC[C@@H](OC(=O)CCCCCCC\C=C/CCCCCCCC)[C@H]1OC[C@H](O)[C@H]1OC(=O)CCCCCCC\C=C/CCCCCCCC PRXRUNOAOLTIEF-ADSICKODSA-N 0.000 description 1
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- 241000096008 Thamnostylum nigricans Species 0.000 description 1
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- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 238000010306 acid treatment Methods 0.000 description 1
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- 238000005273 aeration Methods 0.000 description 1
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- 150000003973 alkyl amines Chemical class 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 1
- 235000014121 butter Nutrition 0.000 description 1
- 235000001046 cacaotero Nutrition 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
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- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 239000003093 cationic surfactant Substances 0.000 description 1
- 238000005119 centrifugation Methods 0.000 description 1
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- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- NVVZQXQBYZPMLJ-UHFFFAOYSA-N formaldehyde;naphthalene-1-sulfonic acid Chemical compound O=C.C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 NVVZQXQBYZPMLJ-UHFFFAOYSA-N 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 229960003180 glutathione Drugs 0.000 description 1
- RNQBLUNNAYFBIW-NPULLEENSA-M hexadecyl(trimethyl)azanium (2S)-2-(6-methoxynaphthalen-2-yl)propanoate Chemical compound COc1ccc2cc(ccc2c1)[C@H](C)C([O-])=O.CCCCCCCCCCCCCCCC[N+](C)(C)C RNQBLUNNAYFBIW-NPULLEENSA-M 0.000 description 1
- 238000000265 homogenisation Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 238000009776 industrial production Methods 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000011147 inorganic material Substances 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
- 229910000359 iron(II) sulfate Inorganic materials 0.000 description 1
- 239000012533 medium component Substances 0.000 description 1
- 229910000372 mercury(II) sulfate Inorganic materials 0.000 description 1
- 238000005555 metalworking Methods 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 229910000402 monopotassium phosphate Inorganic materials 0.000 description 1
- 235000019796 monopotassium phosphate Nutrition 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
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- 235000021317 phosphate Nutrition 0.000 description 1
- 230000001766 physiological effect Effects 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
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- 239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 description 1
- 235000010486 polyoxyethylene sorbitan monolaurate Nutrition 0.000 description 1
- 239000000244 polyoxyethylene sorbitan monooleate Substances 0.000 description 1
- 239000000249 polyoxyethylene sorbitan monopalmitate Substances 0.000 description 1
- 235000010483 polyoxyethylene sorbitan monopalmitate Nutrition 0.000 description 1
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- GNSKLFRGEWLPPA-UHFFFAOYSA-M potassium dihydrogen phosphate Chemical compound [K+].OP(O)([O-])=O GNSKLFRGEWLPPA-UHFFFAOYSA-M 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000012827 research and development Methods 0.000 description 1
- 235000010413 sodium alginate Nutrition 0.000 description 1
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- 235000017550 sodium carbonate Nutrition 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000001509 sodium citrate Substances 0.000 description 1
- NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 235000019337 sorbitan trioleate Nutrition 0.000 description 1
- 229960000391 sorbitan trioleate Drugs 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- 239000003981 vehicle Substances 0.000 description 1
- 238000009423 ventilation Methods 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
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- 239000008207 working material Substances 0.000 description 1
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- NWONKYPBYAMBJT-UHFFFAOYSA-L zinc sulfate Chemical compound [Zn+2].[O-]S([O-])(=O)=O NWONKYPBYAMBJT-UHFFFAOYSA-L 0.000 description 1
- 229910000368 zinc sulfate Inorganic materials 0.000 description 1
- 239000011686 zinc sulphate Substances 0.000 description 1
- 235000009529 zinc sulphate Nutrition 0.000 description 1
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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
- C12P7/6463—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
- 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
- C12N1/38—Chemical stimulation of growth or activity by addition of chemical compounds which are not essential growth factors; Stimulation of growth by removal of a chemical compound
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Health & Medical Sciences (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Biotechnology (AREA)
- Genetics & Genomics (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Health & Medical Sciences (AREA)
- Biochemistry (AREA)
- General Chemical & Material Sciences (AREA)
- General Engineering & Computer Science (AREA)
- Microbiology (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Cell Biology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Tropical Medicine & Parasitology (AREA)
- Virology (AREA)
- Biomedical Technology (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP60144371A JPS623791A (ja) | 1985-07-01 | 1985-07-01 | カビ類または藻類による脂質の製造法 |
DE19863686788 DE3686788T2 (de) | 1985-07-01 | 1986-06-28 | Verfahren zur sekretiven fermentation von lipiden mit pilzen oder algen. |
EP19860108818 EP0207475B1 (en) | 1985-07-01 | 1986-06-28 | Process for secretive fermentation of lipids by fungi or algae |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP60144371A JPS623791A (ja) | 1985-07-01 | 1985-07-01 | カビ類または藻類による脂質の製造法 |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS623791A true JPS623791A (ja) | 1987-01-09 |
JPH0412714B2 JPH0412714B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1992-03-05 |
Family
ID=15360559
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP60144371A Granted JPS623791A (ja) | 1985-07-01 | 1985-07-01 | カビ類または藻類による脂質の製造法 |
Country Status (3)
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS626694A (ja) * | 1985-07-02 | 1987-01-13 | Kanegafuchi Chem Ind Co Ltd | カビ類または藻類による脂質製造方法 |
WO1990007283A1 (en) * | 1988-12-23 | 1990-07-12 | Suntory Limited | Feed for fish and shellfish |
JP2007510436A (ja) * | 2003-11-12 | 2007-04-26 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | 油性酵母中において多価不飽和脂肪酸レベルを変更するのに適したδ12デサチュラーゼ |
US20110124544A1 (en) * | 2008-08-08 | 2011-05-26 | The Dial Corporation | Consumer products comprising algae derived ingredients |
US7972855B2 (en) | 1999-08-13 | 2011-07-05 | Suntory Holdings Limited | Microorganisms that extracellularly secrete lipids and methods of producing lipid and lipid vesicles encapsulating lipids using said microorganisms |
JP2012504967A (ja) * | 2008-10-09 | 2012-03-01 | メノン アンド アソシエイツ,インコーポレイテッド | 燃料用セルロース系原料の微生物処理方法 |
JP2015104381A (ja) * | 2013-12-03 | 2015-06-08 | 花王株式会社 | ソフォロリピッドの製造方法 |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5204250A (en) * | 1986-03-31 | 1993-04-20 | Suntory Limited | Process for production of arachidonic acid |
JPS63133994A (ja) * | 1986-11-21 | 1988-06-06 | Lion Corp | γ−リノレン酸を含有する脂質の製造方法 |
JPS63185389A (ja) * | 1987-01-27 | 1988-07-30 | Suntory Ltd | 微生物変換による高度不飽和脂肪酸の製造方法 |
ES2039451T5 (es) * | 1987-01-28 | 1998-10-16 | Suntory Ltd | Procedimiento para la produccion de acido araquidonico. |
EP1276891B1 (en) * | 2000-03-29 | 2005-05-18 | Council of Scientific and Industrial Research | A method for enhancing levels of polyunsaturated fatty acids in thraustochytrids |
WO2010009348A2 (en) * | 2008-07-16 | 2010-01-21 | The Texas A&M University System | Transformation of glycerol and cellulosic materials into high energy fuels |
WO2011140520A2 (en) | 2010-05-07 | 2011-11-10 | Menon & Associates | Bioreactors comprising fungal strains |
US8932602B2 (en) | 2010-08-11 | 2015-01-13 | Menon Renewable Products, Inc. | Pharmaceutical products from fungal strains |
WO2012021735A2 (en) | 2010-08-11 | 2012-02-16 | Menon & Associates, Inc. | Pharmaceutical products from gungal strains |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS57144987A (en) * | 1981-01-19 | 1982-09-07 | Cpc International Inc | Production of oil or fat |
JPS57198798A (en) * | 1981-06-01 | 1982-12-06 | Asahi Denka Kogyo Kk | Ester exchange of oils and fats |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2697061A (en) * | 1950-08-17 | 1954-12-14 | Texaco Development Corp | Processing of hydrocarbons |
US2697062A (en) * | 1951-03-30 | 1954-12-14 | Texaco Development Corp | Processing of hydrocarbons |
GB1141940A (en) * | 1966-10-28 | 1969-02-05 | Kyowa Hakko Kogyo Kk | Process for producing proteins by fermentation |
NZ199244A (en) * | 1981-01-19 | 1985-03-20 | Cpc International Inc | Production of fats and oils by cultivation of yeast cells |
-
1985
- 1985-07-01 JP JP60144371A patent/JPS623791A/ja active Granted
-
1986
- 1986-06-28 EP EP19860108818 patent/EP0207475B1/en not_active Expired
- 1986-06-28 DE DE19863686788 patent/DE3686788T2/de not_active Expired - Fee Related
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS57144987A (en) * | 1981-01-19 | 1982-09-07 | Cpc International Inc | Production of oil or fat |
JPS57198798A (en) * | 1981-06-01 | 1982-12-06 | Asahi Denka Kogyo Kk | Ester exchange of oils and fats |
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS626694A (ja) * | 1985-07-02 | 1987-01-13 | Kanegafuchi Chem Ind Co Ltd | カビ類または藻類による脂質製造方法 |
WO1990007283A1 (en) * | 1988-12-23 | 1990-07-12 | Suntory Limited | Feed for fish and shellfish |
US7972855B2 (en) | 1999-08-13 | 2011-07-05 | Suntory Holdings Limited | Microorganisms that extracellularly secrete lipids and methods of producing lipid and lipid vesicles encapsulating lipids using said microorganisms |
JP4748907B2 (ja) * | 1999-08-13 | 2011-08-17 | サントリーホールディングス株式会社 | 脂質を菌体外に分泌する微生物ならびに当該微生物を用いた脂質および脂質を内包する油滴小胞の製造方法 |
US10201514B2 (en) | 1999-08-13 | 2019-02-12 | Suntory Holdings Limited | Microorganisms that extracellularly secrete lipids and methods of producing lipid and lipid particles encapsulating lipids using said microorganisms |
JP2007510436A (ja) * | 2003-11-12 | 2007-04-26 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | 油性酵母中において多価不飽和脂肪酸レベルを変更するのに適したδ12デサチュラーゼ |
US20110124544A1 (en) * | 2008-08-08 | 2011-05-26 | The Dial Corporation | Consumer products comprising algae derived ingredients |
US8927475B2 (en) * | 2008-08-08 | 2015-01-06 | The Dial Corporation | Consumer products comprising algae derived ingredients |
JP2012504967A (ja) * | 2008-10-09 | 2012-03-01 | メノン アンド アソシエイツ,インコーポレイテッド | 燃料用セルロース系原料の微生物処理方法 |
JP2015104381A (ja) * | 2013-12-03 | 2015-06-08 | 花王株式会社 | ソフォロリピッドの製造方法 |
Also Published As
Publication number | Publication date |
---|---|
JPH0412714B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1992-03-05 |
EP0207475B1 (en) | 1992-09-23 |
EP0207475A3 (en) | 1988-10-05 |
DE3686788D1 (de) | 1992-10-29 |
EP0207475A2 (en) | 1987-01-07 |
DE3686788T2 (de) | 1993-04-08 |
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