宁波泰斯拓生物

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浙江省宁波市镇海区庄市街道兴庄路9号创e慧谷42号楼B幢401室
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Aspergillus alliaceus Thom et Church, anamorph

货号 TS140633
中文名称 null
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产品简介
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产品名称: Aspergillus alliaceus Thom et Church, anamorph
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.
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.