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Mucor circinelloides f. griseocyanus Schipper, teleomorph
Mucor circinelloides f. griseocyanus Schipper, teleomorph
規(guī)格:
貨期:
編號:B166843
品牌:Mingzhoubio

標(biāo)準(zhǔn)菌株
定量菌液
DNA
RNA

規(guī)格:
凍干粉
斜面
甘油
平板


產(chǎn)品名稱 Mucor circinelloides f. griseocyanus Schipper, teleomorph
商品貨號 B166843
Deposited As Mucor griseocyanus Hagem, teleomorph
Strain Designations [CBS 223.56, FHP 753, IMI 116946]
Application
produces imipramine
produces oxoalkylxanthines oxoalkylxanthine
transformation of sesquiterpene lactone costunolide
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 mating type plus
Comments
steroid conversions
Medium ATCC® Medium 336: Potato dextrose agar (PDA)
Growth Conditions
Temperature: 26.0°C
Name of Depositor AF Blakeslee
References

Eppstein SH, et al. Microbiological transformation of steroids. XV. Tertiary hydroxylation of steroids by fungi of the order Mucorales. J. Am. Chem. Soc. 80: 3382-3389, 1958.

Nesemann G, et al. Microbiological process for the preparation of oxoalkylxanthines. Canadian Patent 1,022,867

Nesemann G, et al. Mikrobiologisches Verfahren zur Herstellung von Oxoalkylxanthinen. German Federal Republic Patent 2,302,772

Singh K, et al. Transformation of steroids by Mucor griseo-cyanus. Can. J. Microbiol. 13: 1271-1281, 1967. PubMed: 6054683

Clark AM, Hufford CD. Microbial transformations of the sesquiterpene lactone costunolide. J. Chem. Soc. Perkin Trans. 1979: 3022-3028, 1979.

Hufford CD, et al. Metabolism of imipramine by microorganisms. J. Pharm. Sci. 70: 151-155, 1981. PubMed: 7205217

梅經(jīng)理 17280875617 1438578920
胡經(jīng)理 13345964880 2438244627
周經(jīng)理 17757487661 1296385441
于經(jīng)理 18067160830 2088210172
沈經(jīng)理 19548299266 2662369050
李經(jīng)理 13626845108 972239479
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