| 产品名称： | Cunninghamella echinulata (Thaxter) Thaxter var. echinulata |
|---|---|
| 商品货号： | TS206062 |
| Deposited As： | Cunninghamella echinulata (Thaxter) Thaxter var. echinulata, teleomorph |
| Strain Designations： | NRRL 3655 NRRL 11498, NRRL A-11498 |
| Application： | produces carbomycin derivatives magnamycin derivatives produces leucomycin derivatives produces niddamycin derivatives transforms antineoplastic agents transforms sesquiterpene lactone costunolide converts: antitumor alkaloid acronycine to 9-hydroxyacronycine |
| 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： | frozen |
| Storage Conditions： | Frozen: -80°C or colder Freeze-Dried: 2°C to 8°C Live Culture: See Propagation Section |
| Type Strain： | no |
| Preceptrol®： | no |
| Medium： | ATCC® Medium 336: Potato dextrose agar (PDA) |
| Growth Conditions： | Temperature: 24.0°C |
| Name of Depositor： | NRRL |
| Cross References： | Nucleotide (GenBank) : AF043517 Cunninghamella echinulata var. echinulata major nuclease C1A Nucleotide (GenBank) : AF109676 Cunninghamella echinulata var. echinulata minor nuclease C1B |
| References： | Theriault RJ. Mycarosyl macrolide antibiotics. US Patent 3,784,447 dated Jan 8 1974 Betts RE, et al. Microbial transformations of antitumor compounds. I. Conversion of acronycine to 9-hydroxyacronycine by Cunninghamella echinulata. J. Med. Chem. 17: 599-602, 1974. PubMed: 4829940 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 |
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| 产品名称： | Cunninghamella echinulata (Thaxter) Thaxter var. echinulata |
|---|---|
| 商品货号： | TS206062 |
| Deposited As： | Cunninghamella echinulata (Thaxter) Thaxter var. echinulata, teleomorph |
| Strain Designations： | NRRL 3655 NRRL 11498, NRRL A-11498 |
| Application： | produces carbomycin derivatives magnamycin derivatives produces leucomycin derivatives produces niddamycin derivatives transforms antineoplastic agents transforms sesquiterpene lactone costunolide converts: antitumor alkaloid acronycine to 9-hydroxyacronycine |
| 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： | frozen |
| Storage Conditions： | Frozen: -80°C or colder Freeze-Dried: 2°C to 8°C Live Culture: See Propagation Section |
| Type Strain： | no |
| Preceptrol®： | no |
| Medium： | ATCC® Medium 336: Potato dextrose agar (PDA) |
| Growth Conditions： | Temperature: 24.0°C |
| Name of Depositor： | NRRL |
| Cross References： | Nucleotide (GenBank) : AF043517 Cunninghamella echinulata var. echinulata major nuclease C1A Nucleotide (GenBank) : AF109676 Cunninghamella echinulata var. echinulata minor nuclease C1B |
| References： | Theriault RJ. Mycarosyl macrolide antibiotics. US Patent 3,784,447 dated Jan 8 1974 Betts RE, et al. Microbial transformations of antitumor compounds. I. Conversion of acronycine to 9-hydroxyacronycine by Cunninghamella echinulata. J. Med. Chem. 17: 599-602, 1974. PubMed: 4829940 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 |
