GB1461841A - Method for carrying out enzymic reactions by means of the use of biphasic aqueous-organic systems - Google Patents
Method for carrying out enzymic reactions by means of the use of biphasic aqueous-organic systemsInfo
- Publication number
- GB1461841A GB1461841A GB50274A GB50274A GB1461841A GB 1461841 A GB1461841 A GB 1461841A GB 50274 A GB50274 A GB 50274A GB 50274 A GB50274 A GB 50274A GB 1461841 A GB1461841 A GB 1461841A
- Authority
- GB
- United Kingdom
- Prior art keywords
- giving
- water
- enzymic reactions
- jan
- substrate
- 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.)
- Expired
Links
- 238000006243 chemical reaction Methods 0.000 title abstract 3
- 230000002051 biphasic effect Effects 0.000 title abstract 2
- 238000000034 method Methods 0.000 title 1
- 239000000758 substrate Substances 0.000 abstract 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 3
- ZTQSAGDEMFDKMZ-UHFFFAOYSA-N Butyraldehyde Chemical compound CCCC=O ZTQSAGDEMFDKMZ-UHFFFAOYSA-N 0.000 abstract 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 abstract 2
- MUMGGOZAMZWBJJ-DYKIIFRCSA-N Testostosterone Chemical compound O=C1CC[C@]2(C)[C@H]3CC[C@](C)([C@H](CC4)O)[C@@H]4[C@@H]3CCC2=C1 MUMGGOZAMZWBJJ-DYKIIFRCSA-N 0.000 abstract 2
- DNXHEGUUPJUMQT-UHFFFAOYSA-N (+)-estrone Natural products OC1=CC=C2C3CCC(C)(C(CC4)=O)C4C3CCC2=C1 DNXHEGUUPJUMQT-UHFFFAOYSA-N 0.000 abstract 1
- PROQIPRRNZUXQM-UHFFFAOYSA-N (16alpha,17betaOH)-Estra-1,3,5(10)-triene-3,16,17-triol Natural products OC1=CC=C2C3CCC(C)(C(C(O)C4)O)C4C3CCC2=C1 PROQIPRRNZUXQM-UHFFFAOYSA-N 0.000 abstract 1
- VOXZDWNPVJITMN-ZBRFXRBCSA-N 17β-estradiol Chemical compound OC1=CC=C2[C@H]3CC[C@](C)([C@H](CC4)O)[C@@H]4[C@@H]3CCC2=C1 VOXZDWNPVJITMN-ZBRFXRBCSA-N 0.000 abstract 1
- 102000007698 Alcohol dehydrogenase Human genes 0.000 abstract 1
- 108010021809 Alcohol dehydrogenase Proteins 0.000 abstract 1
- WKRLQDKEXYKHJB-UHFFFAOYSA-N Equilin Natural products OC1=CC=C2C3CCC(C)(C(CC4)=O)C4C3=CCC2=C1 WKRLQDKEXYKHJB-UHFFFAOYSA-N 0.000 abstract 1
- DNXHEGUUPJUMQT-CBZIJGRNSA-N Estrone Chemical compound OC1=CC=C2[C@H]3CC[C@](C)(C(CC4)=O)[C@@H]4[C@@H]3CCC2=C1 DNXHEGUUPJUMQT-CBZIJGRNSA-N 0.000 abstract 1
- 102000011145 Hydroxysteroid Dehydrogenases Human genes 0.000 abstract 1
- 108010062875 Hydroxysteroid Dehydrogenases Proteins 0.000 abstract 1
- 102000003855 L-lactate dehydrogenase Human genes 0.000 abstract 1
- 108700023483 L-lactate dehydrogenases Proteins 0.000 abstract 1
- 108010029541 Laccase Proteins 0.000 abstract 1
- 102000004882 Lipase Human genes 0.000 abstract 1
- 108090001060 Lipase Proteins 0.000 abstract 1
- 239000004367 Lipase Substances 0.000 abstract 1
- 150000001298 alcohols Chemical class 0.000 abstract 1
- 125000001931 aliphatic group Chemical group 0.000 abstract 1
- 150000005215 alkyl ethers Chemical class 0.000 abstract 1
- AEMFNILZOJDQLW-QAGGRKNESA-N androst-4-ene-3,17-dione Chemical compound O=C1CC[C@]2(C)[C@H]3CC[C@](C)(C(CC4)=O)[C@@H]4[C@@H]3CCC2=C1 AEMFNILZOJDQLW-QAGGRKNESA-N 0.000 abstract 1
- 229960005471 androstenedione Drugs 0.000 abstract 1
- AEMFNILZOJDQLW-UHFFFAOYSA-N androstenedione Natural products O=C1CCC2(C)C3CCC(C)(C(CC4)=O)C4C3CCC2=C1 AEMFNILZOJDQLW-UHFFFAOYSA-N 0.000 abstract 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 abstract 1
- 150000001735 carboxylic acids Chemical class 0.000 abstract 1
- PDRGHUMCVRDZLQ-UHFFFAOYSA-N d-equilenin Natural products OC1=CC=C2C(CCC3(C4CCC3=O)C)=C4C=CC2=C1 PDRGHUMCVRDZLQ-UHFFFAOYSA-N 0.000 abstract 1
- 235000014113 dietary fatty acids Nutrition 0.000 abstract 1
- RGLYKWWBQGJZGM-ISLYRVAYSA-N diethylstilbestrol Chemical compound C=1C=C(O)C=CC=1C(/CC)=C(\CC)C1=CC=C(O)C=C1 RGLYKWWBQGJZGM-ISLYRVAYSA-N 0.000 abstract 1
- 229960000452 diethylstilbestrol Drugs 0.000 abstract 1
- PDRGHUMCVRDZLQ-WMZOPIPTSA-N equilenin Chemical compound OC1=CC=C2C(CC[C@]3([C@H]4CCC3=O)C)=C4C=CC2=C1 PDRGHUMCVRDZLQ-WMZOPIPTSA-N 0.000 abstract 1
- WKRLQDKEXYKHJB-HFTRVMKXSA-N equilin Chemical compound OC1=CC=C2[C@H]3CC[C@](C)(C(CC4)=O)[C@@H]4C3=CCC2=C1 WKRLQDKEXYKHJB-HFTRVMKXSA-N 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- 229960005309 estradiol Drugs 0.000 abstract 1
- 229930182833 estradiol Natural products 0.000 abstract 1
- PROQIPRRNZUXQM-ZXXIGWHRSA-N estriol Chemical compound OC1=CC=C2[C@H]3CC[C@](C)([C@H]([C@H](O)C4)O)[C@@H]4[C@@H]3CCC2=C1 PROQIPRRNZUXQM-ZXXIGWHRSA-N 0.000 abstract 1
- 229960001348 estriol Drugs 0.000 abstract 1
- 229960003399 estrone Drugs 0.000 abstract 1
- 229930195729 fatty acid Natural products 0.000 abstract 1
- 239000000194 fatty acid Substances 0.000 abstract 1
- 150000004665 fatty acids Chemical class 0.000 abstract 1
- 150000008282 halocarbons Chemical class 0.000 abstract 1
- 235000019421 lipase Nutrition 0.000 abstract 1
- 239000004006 olive oil Substances 0.000 abstract 1
- 235000008390 olive oil Nutrition 0.000 abstract 1
- 239000003960 organic solvent Substances 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
- 229960003604 testosterone Drugs 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P1/00—Preparation of compounds or compositions, not provided for in groups C12P3/00 - C12P39/00, by using microorganisms or enzymes
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Zoology (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Chemical & Material Sciences (AREA)
- Biotechnology (AREA)
- Mycology (AREA)
- Health & Medical Sciences (AREA)
- Biochemistry (AREA)
- Microbiology (AREA)
- General Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Steroid Compounds (AREA)
- Enzymes And Modification Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IT19642/73A IT978495B (it) | 1973-01-26 | 1973-01-26 | Procedimento per condurre reazio ni enzimatiche mediante l uso di sistemi bifasici acquoso organici |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1461841A true GB1461841A (en) | 1977-01-19 |
Family
ID=11160009
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB50274A Expired GB1461841A (en) | 1973-01-26 | 1974-01-04 | Method for carrying out enzymic reactions by means of the use of biphasic aqueous-organic systems |
Country Status (16)
Families Citing this family (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4102744A (en) * | 1976-12-20 | 1978-07-25 | Exxon Research & Engineering Co. | Two phase fermentation |
| DE2927535A1 (de) * | 1979-07-07 | 1981-01-08 | Bayer Ag | Stereoselektive spaltung von phenylglycinderivaten mit enzymharzen |
| DE3105556A1 (de) * | 1981-02-16 | 1982-09-02 | Henkel KGaA, 4000 Düsseldorf | "verbessertes verfahren zur herstellung von xanthomonas-biopolymeren" |
| US4352882A (en) * | 1981-09-08 | 1982-10-05 | Kelco Biospecialties Limited | Production of xanthan gum by emulsion fermentation |
| EP0089126B1 (en) * | 1982-03-15 | 1986-07-30 | Imperial Chemical Industries Plc | Process of oxidising hydrocarbons |
| JPH0724587B2 (ja) * | 1982-07-08 | 1995-03-22 | 三井東圧化学株式会社 | 酵素を利用した反応方法 |
| DE3461105D1 (en) * | 1983-02-03 | 1986-12-04 | Duphar Int Res | Method for the enzymatic conversion of a water-insoluble or substantially water-insoluble organic substrate |
| US4636470A (en) * | 1984-08-17 | 1987-01-13 | Stauffer Chemical Company | Resolution of racemates of amino acids |
| FR2588272B1 (fr) * | 1985-10-07 | 1988-12-02 | Gattefosse Ets Sa | Procede de synthese d'esters d'acides organiques et d'alcools en phase heterogene par catalyse enzymatique |
| JPS63133989A (ja) * | 1986-11-26 | 1988-06-06 | Agency Of Ind Science & Technol | 酵素反応方法 |
| EP0333877B1 (en) * | 1987-09-25 | 1994-11-09 | MITSUI TOATSU CHEMICALS, Inc. | Process for preparing purified aqueous indole solution |
| DD282822A7 (de) * | 1988-05-06 | 1990-09-26 | Univ Halle Wittenberg | Verfahren zur biokatalytischen umsetzung schlecht wasserloeslicher substanzen |
| US5288619A (en) * | 1989-12-18 | 1994-02-22 | Kraft General Foods, Inc. | Enzymatic method for preparing transesterified oils |
| KR100585471B1 (ko) * | 1998-03-31 | 2006-06-02 | 다카라 바이오 가부시키가이샤 | 리소스핑고리피드의 제조 방법 |
| DE10029671A1 (de) * | 2000-06-23 | 2002-01-10 | Frieder Schauer | Biotransformation von biologisch aktiven Verindungen aus verschiedenen chemischen Stoffklassen mittels der Enzyme Laccase und Manganperoxidase |
| DE10161274A1 (de) * | 2001-12-13 | 2003-06-26 | Cognis Deutschland Gmbh | Verfahren zur Herstellung von C4-C12-Fettsäuren |
| DE10208007A1 (de) * | 2002-02-26 | 2003-09-18 | Forschungszentrum Juelich Gmbh | Verfahren zur Herstellung von Alkoholen aus Substraten mittels Oxidoreduktasen, Zweiphasensystem umfassend eine wässrige Phase und eine organische Phase sowie Vorrichtung zur Durchführung des Verfahrens |
| JP2019024038A (ja) * | 2017-07-24 | 2019-02-14 | 株式会社ディスコ | ウェーハの加工方法 |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2053770A (en) * | 1933-08-15 | 1936-09-08 | Dreyfus Henry | Removal from a fermenting medium of organic compounds produced by the fermentation |
| US2676181A (en) * | 1951-11-13 | 1954-04-20 | Upjohn Co | Oxidation of steroids |
| US3060100A (en) * | 1954-02-05 | 1962-10-23 | Ciba Geigy Corp | Manufacture of new products of enzymatic oxidation |
| US3804714A (en) * | 1972-06-23 | 1974-04-16 | British Petroleum Co | Enzymic oxidation process |
-
1973
- 1973-01-26 IT IT19642/73A patent/IT978495B/it active
-
1974
- 1974-01-04 GB GB50274A patent/GB1461841A/en not_active Expired
- 1974-01-08 ZA ZA740150A patent/ZA74150B/xx unknown
- 1974-01-09 CA CA189,786A patent/CA1005771A/en not_active Expired
- 1974-01-11 US US432564A patent/US3926726A/en not_active Expired - Lifetime
- 1974-01-18 DE DE2402452A patent/DE2402452C2/de not_active Expired
- 1974-01-21 CH CH77074A patent/CH606431A5/xx not_active IP Right Cessation
- 1974-01-22 NL NLAANVRAGE7400882,A patent/NL175436C/xx not_active IP Right Cessation
- 1974-01-23 JP JP1086274A patent/JPS5645593B2/ja not_active Expired
- 1974-01-23 SE SE7400872A patent/SE404184B/xx unknown
- 1974-01-23 LU LU69227A patent/LU69227A1/xx unknown
- 1974-01-24 FR FR7402434A patent/FR2215465B1/fr not_active Expired
- 1974-01-25 SU SU1992113A patent/SU504503A3/ru active
- 1974-01-25 AT AT63374*#A patent/AT330120B/de not_active IP Right Cessation
- 1974-01-25 HU HU74SA00002586A patent/HU172074B/hu unknown
- 1974-01-25 BE BE140186A patent/BE810170A/xx not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| SU504503A3 (ru) | 1976-02-25 |
| ATA63374A (de) | 1975-09-15 |
| JPS49108286A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1974-10-15 |
| FR2215465A1 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1974-08-23 |
| IT978495B (it) | 1974-09-20 |
| AU6442674A (en) | 1975-07-17 |
| NL175436B (nl) | 1984-06-01 |
| US3926726A (en) | 1975-12-16 |
| ZA74150B (en) | 1974-11-27 |
| BE810170A (fr) | 1974-05-16 |
| CH606431A5 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1978-10-31 |
| JPS5645593B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1981-10-27 |
| NL7400882A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1974-07-30 |
| NL175436C (nl) | 1984-11-01 |
| AT330120B (de) | 1976-06-10 |
| DE2402452C2 (de) | 1983-05-11 |
| CA1005771A (en) | 1977-02-22 |
| HU172074B (hu) | 1978-05-28 |
| SE404184B (sv) | 1978-09-25 |
| DE2402452A1 (de) | 1974-08-01 |
| LU69227A1 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1974-04-08 |
| FR2215465B1 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1976-10-08 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed [section 19, patents act 1949] | ||
| 732 | Registration of transactions, instruments or events in the register (sect. 32/1977) | ||
| PCNP | Patent ceased through non-payment of renewal fee |