NO744417L - - Google Patents
Info
- Publication number
- NO744417L NO744417L NO744417A NO744417A NO744417L NO 744417 L NO744417 L NO 744417L NO 744417 A NO744417 A NO 744417A NO 744417 A NO744417 A NO 744417A NO 744417 L NO744417 L NO 744417L
- Authority
- NO
- Norway
- Prior art keywords
- medium
- substrate
- microorganism
- cyclopentane
- maintained
- Prior art date
Links
- 239000000758 substrate Substances 0.000 claims description 33
- 238000000034 method Methods 0.000 claims description 29
- 244000005700 microbiome Species 0.000 claims description 24
- 238000006243 chemical reaction Methods 0.000 claims description 16
- 150000001720 carbohydrates Chemical class 0.000 claims description 13
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 claims description 12
- 239000008103 glucose Substances 0.000 claims description 12
- -1 2-substituted-cyclopentane-1,3,4-trione Chemical class 0.000 claims description 9
- 241001123635 Dipodascus Species 0.000 claims description 6
- IYVJDJXPPVXUBA-UHFFFAOYSA-N methyl 7-(2,3,5-trioxocyclopentyl)heptanoate Chemical compound COC(=O)CCCCCCC1C(=O)CC(=O)C1=O IYVJDJXPPVXUBA-UHFFFAOYSA-N 0.000 claims description 6
- 241000235349 Ascomycota Species 0.000 claims description 5
- CMNLEGQFTCUTAD-UHFFFAOYSA-N methyl 7-(2-methoxy-3,5-dioxocyclopenten-1-yl)heptanoate Chemical compound COC(=O)CCCCCCC1=C(OC)C(=O)CC1=O CMNLEGQFTCUTAD-UHFFFAOYSA-N 0.000 claims description 5
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 230000008569 process Effects 0.000 claims description 4
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 3
- 239000005977 Ethylene Substances 0.000 claims description 3
- 239000002253 acid Substances 0.000 claims description 3
- 125000000217 alkyl group Chemical group 0.000 claims description 3
- 229940041514 candida albicans extract Drugs 0.000 claims description 3
- 150000001875 compounds Chemical class 0.000 claims description 3
- GNSKLFRGEWLPPA-UHFFFAOYSA-M potassium dihydrogen phosphate Chemical compound [K+].OP(O)([O-])=O GNSKLFRGEWLPPA-UHFFFAOYSA-M 0.000 claims description 3
- 239000001509 sodium citrate Substances 0.000 claims description 3
- 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 claims description 3
- 239000012138 yeast extract Substances 0.000 claims description 3
- 150000007513 acids Chemical class 0.000 claims description 2
- LLSDKQJKOVVTOJ-UHFFFAOYSA-L calcium chloride dihydrate Chemical compound O.O.[Cl-].[Cl-].[Ca+2] LLSDKQJKOVVTOJ-UHFFFAOYSA-L 0.000 claims description 2
- 229940052299 calcium chloride dihydrate Drugs 0.000 claims description 2
- 230000002906 microbiologic effect Effects 0.000 claims description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 2
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 claims 1
- 229910052921 ammonium sulfate Inorganic materials 0.000 claims 1
- 235000011130 ammonium sulphate Nutrition 0.000 claims 1
- 125000005678 ethenylene group Chemical group [H]C([*:1])=C([H])[*:2] 0.000 claims 1
- 125000002791 glucosyl group Chemical group C1([C@H](O)[C@@H](O)[C@H](O)[C@H](O1)CO)* 0.000 claims 1
- CKAODHQJQJOTCB-UHFFFAOYSA-L magnesium;dichloride;heptahydrate Chemical compound O.O.O.O.O.O.O.[Mg+2].[Cl-].[Cl-] CKAODHQJQJOTCB-UHFFFAOYSA-L 0.000 claims 1
- 229910000402 monopotassium phosphate Inorganic materials 0.000 claims 1
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 18
- 238000011534 incubation Methods 0.000 description 12
- 239000000047 product Substances 0.000 description 11
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 7
- 240000004808 Saccharomyces cerevisiae Species 0.000 description 5
- 241000228427 Eurotiales Species 0.000 description 4
- 241000235388 Mucorales Species 0.000 description 4
- 235000014680 Saccharomyces cerevisiae Nutrition 0.000 description 4
- 241000235343 Saccharomycetales Species 0.000 description 4
- 241000235346 Schizosaccharomyces Species 0.000 description 4
- 238000000855 fermentation Methods 0.000 description 4
- 230000004151 fermentation Effects 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 230000006872 improvement Effects 0.000 description 3
- 238000012423 maintenance Methods 0.000 description 3
- PAWQVTBBRAZDMG-UHFFFAOYSA-N 2-(3-bromo-2-fluorophenyl)acetic acid Chemical compound OC(=O)CC1=CC=CC(Br)=C1F PAWQVTBBRAZDMG-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- HSFWRNGVRCDJHI-UHFFFAOYSA-N Acetylene Chemical compound C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 241000896533 Gliocladium Species 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
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 241000235017 Zygosaccharomyces Species 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 150000001940 cyclopentanes Chemical class 0.000 description 2
- 238000000605 extraction Methods 0.000 description 2
- 235000015097 nutrients Nutrition 0.000 description 2
- 125000004430 oxygen atom Chemical group O* 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 241000235389 Absidia Species 0.000 description 1
- 229920001817 Agar Polymers 0.000 description 1
- 241000223602 Alternaria alternata Species 0.000 description 1
- 241000228254 Aspergillus restrictus Species 0.000 description 1
- 241001465318 Aspergillus terreus Species 0.000 description 1
- 241000122818 Aspergillus ustus Species 0.000 description 1
- 241000308595 Buckleyzyma aurantiaca Species 0.000 description 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- 241000222120 Candida <Saccharomycetales> Species 0.000 description 1
- 241001149472 Clonostachys rosea Species 0.000 description 1
- 241000896542 Clonostachys rosea f. catenulata Species 0.000 description 1
- 241001514654 Cystobasidium pallidum Species 0.000 description 1
- 241000178262 Dipodascus aggregatus Species 0.000 description 1
- 241001123634 Dipodascus albidus Species 0.000 description 1
- 241001465321 Eremothecium Species 0.000 description 1
- 241000577870 Fusarium decemcellulare Species 0.000 description 1
- 244000168141 Geotrichum candidum Species 0.000 description 1
- 235000017388 Geotrichum candidum Nutrition 0.000 description 1
- 241001634870 Hamigera striata Species 0.000 description 1
- 244000286779 Hansenula anomala Species 0.000 description 1
- 235000014683 Hansenula anomala Nutrition 0.000 description 1
- NHTMVDHEPJAVLT-UHFFFAOYSA-N Isooctane Chemical compound CC(C)CC(C)(C)C NHTMVDHEPJAVLT-UHFFFAOYSA-N 0.000 description 1
- 241001459306 Lichtheimia blakesleeana Species 0.000 description 1
- 241001598067 Memnoniella echinata Species 0.000 description 1
- 241000235395 Mucor Species 0.000 description 1
- 241001450846 Mucor heterogamus Species 0.000 description 1
- 241001236817 Paecilomyces <Clavicipitaceae> Species 0.000 description 1
- 241000228147 Penicillium camemberti Species 0.000 description 1
- 241000985530 Penicillium glabrum Species 0.000 description 1
- 241000898625 Penicillium granulatum Species 0.000 description 1
- 241000122123 Penicillium italicum Species 0.000 description 1
- 241000095431 Penicillium multicolor Species 0.000 description 1
- 241001149509 Penicillium vulpinum Species 0.000 description 1
- 241000235401 Phycomyces blakesleeanus Species 0.000 description 1
- 241000235645 Pichia kudriavzevii Species 0.000 description 1
- 241000133646 Sclerocleista ornata Species 0.000 description 1
- 241000221696 Sclerotinia sclerotiorum Species 0.000 description 1
- 241001279364 Stachybotrys chartarum Species 0.000 description 1
- 241000764290 Talaromyces pseudostromaticus Species 0.000 description 1
- 241001540751 Talaromyces ruber Species 0.000 description 1
- 239000004809 Teflon Substances 0.000 description 1
- 229920006362 Teflon® Polymers 0.000 description 1
- 241000223261 Trichoderma viride Species 0.000 description 1
- 239000008272 agar Substances 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229960002713 calcium chloride Drugs 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- HGAZMNJKRQFZKS-UHFFFAOYSA-N chloroethene;ethenyl acetate Chemical compound ClC=C.CC(=O)OC=C HGAZMNJKRQFZKS-UHFFFAOYSA-N 0.000 description 1
- 239000008121 dextrose Substances 0.000 description 1
- JVSWJIKNEAIKJW-UHFFFAOYSA-N dimethyl-hexane Natural products CCCCCC(C)C JVSWJIKNEAIKJW-UHFFFAOYSA-N 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 229950011333 edamine Drugs 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 235000021321 essential mineral Nutrition 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 230000002045 lasting effect Effects 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- WRUGWIBCXHJTDG-UHFFFAOYSA-L magnesium sulfate heptahydrate Chemical compound O.O.O.O.O.O.O.[Mg+2].[O-]S([O-])(=O)=O WRUGWIBCXHJTDG-UHFFFAOYSA-L 0.000 description 1
- 229940061634 magnesium sulfate heptahydrate Drugs 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- OIMNNAXGHPCXMA-HCCKASOXSA-N methyl 7-[(3r)-3-hydroxy-2,5-dioxocyclopentyl]heptanoate Chemical compound COC(=O)CCCCCCC1C(=O)C[C@@H](O)C1=O OIMNNAXGHPCXMA-HCCKASOXSA-N 0.000 description 1
- 238000013048 microbiological method Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229940094443 oxytocics prostaglandins Drugs 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 150000003180 prostaglandins Chemical class 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 238000004809 thin layer chromatography Methods 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- 238000009423 ventilation Methods 0.000 description 1
Classifications
-
- 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
- C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S435/00—Chemistry: molecular biology and microbiology
- Y10S435/8215—Microorganisms
- Y10S435/911—Microorganisms using fungi
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Molecular Biology (AREA)
- Microbiology (AREA)
- Biotechnology (AREA)
- Biomedical Technology (AREA)
- Biochemistry (AREA)
- General Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US423257A US3925156A (en) | 1973-12-10 | 1973-12-10 | Microbiological process for preparing 2-substituted-4-(r)-hydroxy-cyclopentane-1,3-diones |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO744417L true NO744417L (fr) | 1975-07-07 |
Family
ID=23678213
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO744417A NO744417L (fr) | 1973-12-10 | 1974-12-06 |
Country Status (23)
| Country | Link |
|---|---|
| US (1) | US3925156A (fr) |
| AR (1) | AR207967A1 (fr) |
| AT (1) | AT333690B (fr) |
| BE (1) | BE823174A (fr) |
| BG (1) | BG27094A3 (fr) |
| CA (1) | CA1038785A (fr) |
| CS (1) | CS177040B2 (fr) |
| DD (1) | DD114397A5 (fr) |
| DE (1) | DE2458121C3 (fr) |
| ES (1) | ES432718A1 (fr) |
| FI (1) | FI346874A (fr) |
| FR (1) | FR2253827B1 (fr) |
| GB (1) | GB1442553A (fr) |
| HU (1) | HU168825B (fr) |
| IL (1) | IL46103A (fr) |
| NL (1) | NL7415982A (fr) |
| NO (1) | NO744417L (fr) |
| PH (1) | PH11007A (fr) |
| PL (1) | PL92530B1 (fr) |
| RO (1) | RO63720A (fr) |
| SE (1) | SE7415405L (fr) |
| SU (1) | SU520926A3 (fr) |
| ZA (1) | ZA747392B (fr) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4642290A (en) * | 1982-12-06 | 1987-02-10 | Sih Charles J | Process for preparing a compound for use in the production of L-carnitine |
| US4710468A (en) * | 1983-10-24 | 1987-12-01 | Sigma-Tau Industrie Pharmaceutiche Riunite S.P.A. | Process for preparing L-carnitine and chemical intermediates employed therein |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3773622A (en) * | 1972-09-29 | 1973-11-20 | Wisconsin Alumni Res Found | Method for preparing 2-substituted-4-hydroxy-cyclopentane-1,3-diones |
-
1973
- 1973-12-10 US US423257A patent/US3925156A/en not_active Expired - Lifetime
-
1974
- 1974-01-01 AR AR256757A patent/AR207967A1/es active
- 1974-11-19 ZA ZA00747392A patent/ZA747392B/xx unknown
- 1974-11-19 CA CA214,057A patent/CA1038785A/fr not_active Expired
- 1974-11-21 IL IL46103A patent/IL46103A/xx unknown
- 1974-11-29 FI FI3468/74A patent/FI346874A/fi unknown
- 1974-12-02 PH PH16585A patent/PH11007A/en unknown
- 1974-12-03 GB GB5226274A patent/GB1442553A/en not_active Expired
- 1974-12-05 CS CS8323A patent/CS177040B2/cs unknown
- 1974-12-05 BG BG028372A patent/BG27094A3/xx unknown
- 1974-12-06 NO NO744417A patent/NO744417L/no unknown
- 1974-12-06 DD DD182837A patent/DD114397A5/xx unknown
- 1974-12-09 PL PL1974176287A patent/PL92530B1/pl unknown
- 1974-12-09 SE SE7415405A patent/SE7415405L/xx unknown
- 1974-12-09 SU SU2085735A patent/SU520926A3/ru active
- 1974-12-09 NL NL7415982A patent/NL7415982A/xx not_active Application Discontinuation
- 1974-12-09 HU HUMI569A patent/HU168825B/hu unknown
- 1974-12-09 DE DE2458121A patent/DE2458121C3/de not_active Expired
- 1974-12-09 RO RO7400080736A patent/RO63720A/fr unknown
- 1974-12-09 ES ES432718A patent/ES432718A1/es not_active Expired
- 1974-12-09 AT AT981074A patent/AT333690B/de not_active IP Right Cessation
- 1974-12-10 FR FR7440487A patent/FR2253827B1/fr not_active Expired
- 1974-12-10 BE BE151350A patent/BE823174A/fr unknown
Also Published As
| Publication number | Publication date |
|---|---|
| ATA981074A (de) | 1976-04-15 |
| DE2458121B2 (de) | 1977-08-04 |
| HU168825B (fr) | 1976-07-28 |
| PL92530B1 (fr) | 1977-04-30 |
| US3925156A (en) | 1975-12-09 |
| BG27094A3 (bg) | 1979-08-15 |
| IL46103A (en) | 1978-07-31 |
| SE7415405L (fr) | 1975-06-11 |
| BE823174A (fr) | 1975-04-01 |
| AR207967A1 (es) | 1976-11-22 |
| DD114397A5 (fr) | 1975-08-05 |
| GB1442553A (en) | 1976-07-14 |
| AT333690B (de) | 1976-12-10 |
| CA1038785A (fr) | 1978-09-19 |
| FR2253827B1 (fr) | 1977-11-10 |
| NL7415982A (nl) | 1975-06-12 |
| CS177040B2 (fr) | 1977-07-29 |
| AU7561674A (en) | 1976-05-27 |
| ES432718A1 (es) | 1977-03-01 |
| FR2253827A1 (fr) | 1975-07-04 |
| DE2458121C3 (de) | 1978-04-13 |
| PH11007A (en) | 1977-10-20 |
| DE2458121A1 (de) | 1975-06-12 |
| RO63720A (fr) | 1978-10-15 |
| SU520926A3 (ru) | 1976-07-05 |
| ZA747392B (en) | 1975-12-31 |
| IL46103A0 (en) | 1975-02-10 |
| FI346874A (fr) | 1975-06-11 |
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