| 产品名称： | Cunninghamella echinulata (Thaxter) Thaxter var. echinulata |
|---|---|
| 商品货号： | TS209990 |
| Deposited As： | Cunninghamella echinulata (Thaxter) Thaxter var. echinulata, teleomorph |
| Strain Designations： | NRRL 1386 C885, CBS 156.28 |
| Application： | produces hydroxylated biphenyl compounds produces imipramine transformation of antitumor agents transformation of sesquiterpene lactone costunolide transformation of: pergolide to pergolide sulfoxide and pergolide sulfone |
| 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 |
| Mating Type： | mates with ATCC 11585b mating type plus mates with ATCC 11585b |
| Medium： | ATCC® Medium 307: Cornmeal agar |
| Growth Conditions： | Temperature: 24.0°C |
| Name of Depositor： | NRRL |
| Chain of Custody： | ATCC < |
| References： | Schwartz RD. Microbial production of hydroxylated biphenyl compounds. US Patent 4,153,509 dated May 8 1979 Clark AM, Hufford CD. Microbial transformations of the sesquiterpene lactone costunolide. J. Chem. Soc. Perkin Trans. 1979: 3022-3028, 1979. Chien MM, Rosazza JP. Microbial transformations of natural antitumor agents. 9. O-Demethylation of 9-methoxyellipticine. J. Nat. Prod. 42: 643-647, 1979. PubMed: 575547 Hufford CD, et al. Metabolism of imipramine by microorganisms. J. Pharm. Sci. 70: 151-155, 1981. PubMed: 7205217 Smith RV, et al. Microbial transformations of pergolide to pergolide sulfoxide and pergolide sulfone. J. Pharm. Sci. 72: 733-736, 1983. PubMed: 6684155 |
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| 产品名称： | Cunninghamella echinulata (Thaxter) Thaxter var. echinulata |
|---|---|
| 商品货号： | TS209990 |
| Deposited As： | Cunninghamella echinulata (Thaxter) Thaxter var. echinulata, teleomorph |
| Strain Designations： | NRRL 1386 C885, CBS 156.28 |
| Application： | produces hydroxylated biphenyl compounds produces imipramine transformation of antitumor agents transformation of sesquiterpene lactone costunolide transformation of: pergolide to pergolide sulfoxide and pergolide sulfone |
| 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 |
| Mating Type： | mates with ATCC 11585b mating type plus mates with ATCC 11585b |
| Medium： | ATCC® Medium 307: Cornmeal agar |
| Growth Conditions： | Temperature: 24.0°C |
| Name of Depositor： | NRRL |
| Chain of Custody： | ATCC < |
| References： | Schwartz RD. Microbial production of hydroxylated biphenyl compounds. US Patent 4,153,509 dated May 8 1979 Clark AM, Hufford CD. Microbial transformations of the sesquiterpene lactone costunolide. J. Chem. Soc. Perkin Trans. 1979: 3022-3028, 1979. Chien MM, Rosazza JP. Microbial transformations of natural antitumor agents. 9. O-Demethylation of 9-methoxyellipticine. J. Nat. Prod. 42: 643-647, 1979. PubMed: 575547 Hufford CD, et al. Metabolism of imipramine by microorganisms. J. Pharm. Sci. 70: 151-155, 1981. PubMed: 7205217 Smith RV, et al. Microbial transformations of pergolide to pergolide sulfoxide and pergolide sulfone. J. Pharm. Sci. 72: 733-736, 1983. PubMed: 6684155 |
