产品名称: | Aspergillus alliaceus Thom et Church, anamorph |
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商品货号: | TS140633 |
Strain Designations: | NRRL 315 4656, CBS 536.65, IFO 7538, IMI 51982, QM 1885, WB 315 |
Alternate State: | Petromyces alliaceus Malloch et Cain, teleomorph |
Application: | transformation of flavonoids |
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 |
Intended Use: | |
Preceptrol®: | no |
Comments: | with teleomorph |
Medium: | ATCC® Medium 325: Malt extract agar (Blakeslees formula) |
Growth Conditions: | Temperature: 24.0°C |
Sequenced Data: | No DNA sequencing was performed in house on this product.
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Name of Depositor: | NRRL |
Chain of Custody: | ATCC < |
Isolation: | dead blister beetle, Macrobasis albida, Washington, DC |
References: | Goetz MA, et al. Asperlicin, a novel non-peptidal cholecystokinin antagonist from Aspergillus alliaceus. Fermentation, isolation and biological properties. J. Antibiot. 38: 1633-1637, 1985. PubMed: 3005212 Ibrahim AR, Abul-Hajj YJ. Microbiological transformation of flavone and isoflavone. Xenobiotica 20: 363-373, 1990. PubMed: 2346033 Formisyn P, et al. Biotransformation by fungi: oxidation of ellipticine into 9-hydroxy-ellipticine by an Aspergillus alliaceus strain CBS 536.65. Lett. Appl. Microbiol. 19: 244-246, 1994. Laakso JA, et al. Isokotanins A-C: new bicoumarins from the sclerotia of Aspergillus alliaceus. J. Nat. Prod. 57: 128-133, 1994. PubMed: 8158157 Chien MM, Rosazza JP. Microbial transformations of natural antitumor agents. VIII. Formation of 8- and 9-hydroxy-ellipticines. Drug Metab. Dispos. 7: 211-214, 1979. PubMed: 39722 Burkhead KD, et al. I. Hydroxylation of aniline by Aspergillus alliaceus, A. albertensis and A. terreus. J. Ind. Microbiol. 13: 233-237, 1994. |