Cunninghamella echinulata (Thaxter) Thaxter var. echinulata
商品貨號(hào)
B166628
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
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
