| 产品名称： | Aspergillus flavipes (Bainier et Sartory) Thom et Church, anamorph |
|---|---|
| 商品货号： | TS206467 |
| Strain Designations： | NRRL 286 114, QM 1993 |
| Alternate State： | Fennellia flavipes Wiley et Simmons, teleomorph |
| Application： | oxidizes aporphine oxidizes chrysanthemol produces didehydroglaucine produces imipramine transformation of sesquiterpene lactone costunolide oxidizes chrysanthemols to chrysanthemic acids |
| Biosafety Level： | 1
Biosafety classification is based on U.S. Public Health Service Guidelines, it is the responsibility of the customer to ensure that their facilities comply with biosafety regulations for their own country. |
| Product Format： | freeze-dried |
| Type Strain： | no |
| Preceptrol®： | no |
| Medium： | ATCC® Medium 313: Czapeks agar |
| Growth Conditions： | Temperature: 26.0°C |
| Name of Depositor： | NRRL |
| Chain of Custody： | ATCC < |
| References： | Davis PJ, Talaat RE. Microbiological systems in organic synthesis: preparative-scale resolution of (R,S)-glaucine by Fusarium solani and stereospecific oxidation of (R)-(-)-glaucine by Aspergillus flavipes. Appl. Environ. Microbiol. 41: 1243-1247, 1981. Kerr KM, Davis PJ. Microbial transformations in organic synthesis. 3. Synthesis, characterization and fungal metabolism of cis- and trans-7-methylglaucine. J. Org. Chem. 48: 928-932, 1983. Miski M, Davis PJ. Microbiologically catalyzed enantio- and diastereoselective oxidation of chrysanthemol stereoisomers to chrysanthemic acids. Appl. Environ. Microbiol. 54: 2268-2272, 1988. Clark AM, Hufford CD. Microbial transformations of the sesquiterpene lactone costunolide. J. Chem. Soc. Perkin Trans. 1979: 3022-3028, 1979. Hufford CD, et al. Metabolism of imipramine by microorganisms. J. Pharm. Sci. 70: 151-155, 1981. PubMed: 7205217 |
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| 产品名称： | Aspergillus flavipes (Bainier et Sartory) Thom et Church, anamorph |
|---|---|
| 商品货号： | TS206467 |
| Strain Designations： | NRRL 286 114, QM 1993 |
| Alternate State： | Fennellia flavipes Wiley et Simmons, teleomorph |
| Application： | oxidizes aporphine oxidizes chrysanthemol produces didehydroglaucine produces imipramine transformation of sesquiterpene lactone costunolide oxidizes chrysanthemols to chrysanthemic acids |
| Biosafety Level： | 1
Biosafety classification is based on U.S. Public Health Service Guidelines, it is the responsibility of the customer to ensure that their facilities comply with biosafety regulations for their own country. |
| Product Format： | freeze-dried |
| Type Strain： | no |
| Preceptrol®： | no |
| Medium： | ATCC® Medium 313: Czapeks agar |
| Growth Conditions： | Temperature: 26.0°C |
| Name of Depositor： | NRRL |
| Chain of Custody： | ATCC < |
| References： | Davis PJ, Talaat RE. Microbiological systems in organic synthesis: preparative-scale resolution of (R,S)-glaucine by Fusarium solani and stereospecific oxidation of (R)-(-)-glaucine by Aspergillus flavipes. Appl. Environ. Microbiol. 41: 1243-1247, 1981. Kerr KM, Davis PJ. Microbial transformations in organic synthesis. 3. Synthesis, characterization and fungal metabolism of cis- and trans-7-methylglaucine. J. Org. Chem. 48: 928-932, 1983. Miski M, Davis PJ. Microbiologically catalyzed enantio- and diastereoselective oxidation of chrysanthemol stereoisomers to chrysanthemic acids. Appl. Environ. Microbiol. 54: 2268-2272, 1988. Clark AM, Hufford CD. Microbial transformations of the sesquiterpene lactone costunolide. J. Chem. Soc. Perkin Trans. 1979: 3022-3028, 1979. Hufford CD, et al. Metabolism of imipramine by microorganisms. J. Pharm. Sci. 70: 151-155, 1981. PubMed: 7205217 |
