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Cunninghamella echinulata (Thaxter) Thaxter var. <em>echinulata</em>
Cunninghamella echinulata (Thaxter) Thaxter var. <em>echinulata</em>
規格:
貨期:
編號:B205831
品牌:Mingzhoubio

標準菌株
定量菌液
DNA
RNA

規格:
凍干粉
斜面
甘油
平板


產品名稱 Cunninghamella echinulata (Thaxter) Thaxter var. echinulata
商品貨號 B205831
Deposited As Cunninghamella bainieri Naumov
Strain Designations 29 [CBS 596.68, IMI 199844]
Application
Assay of papaverine
Metabolizes (+/-)N-(n-propyl)amphetamine
Metabolizes pargyline
Metabolizes phencyclidine
Metabolizes selegeline deprenyl
Produces 10-fluro-19-norpredinsolone
Produces 4-phenylphenol 4-hydroxybiphenyl
Produces 9-hydroxyacronycine
Produces imipramine
Transforms N-methylcarbazole
Transforms methoxyamphetamines
Transforms phenazopyridine
Transforms propranolol
Transforms sesquiterpene lactone costunolide
Transforms stemodin
Transforms tranylcypromine
Conversion of acronycine to 9-hydroxy-acronycine
Conversion of biphenyl to 4-hydroxybiphenyl
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
Storage Conditions Frozen: -80°C or colder
Freeze-Dried: 2°C to 8°C
Live Culture: See Propagation Section
Type Strain no
Preceptrol&reg; no
Comments
Monooxygenase activity
Morphology After 7 days on Cornmeal agar at 25°C, colonies off-white, tan or grey, densely floccose. Sporophores erect, branched, terminating in a vesicle; vesicles globose or subglobose. Sporangiola hyaline to orange, evidently echinulate. Zygospores not observed.
Medium ATCC® Medium 307: Cornmeal agar
ATCC® Medium 325: Malt extract agar (Blakeslee's formula)
ATCC® Medium 336: Potato dextrose agar (PDA)
Growth Conditions
Temperature: 24°C to 26°C
Atmosphere: Typical aerobic
Sequenced Data
18S ribosomal RNA gene, partial sequence; internal transcribed spacer 1, 5.8S ribosomal RNA gene, and internal transcribed spacer 2, complete sequence; and 28S ribosomal RNA gene, partial sequence

GGTTTCCGTAGGTGAACCTGCGGAAGGATCATTAACTATTGTGGGAAAAGACGTAAAACATCTTTGACCATTAAATCATCCATAATGTGGGTCAAACCACATGCGCAATGTATTATAAGGTGTTATTTAGTTAGCATCTTTTTATTTGTAATATGGCCTTAAAAAAGCCACATTACTAATTTTTTTATACTAAATTAACTGAAAAAACGATTGACCATAATTTATGGTTGTTTAAACAATATATTAACTTATATAAAAACAACTTTCAGCAATGGATCTCTCGGCTTTCGTATCGATGAAGAACGCAGCAAATCGCGATATTTAATGTGATCTGCCTATAGTGAATCATCAAATCTTTGAACGCATCTTGCACCCTATGGTATTCCGTAGGGTACATCTGTTTCAGTACCATTCAAACATCTCCCTCACTCCTTTTTTTACTAAGAGAGAATGAGATCAGAGATAAATTATAAATGGTCCTGGGTAAGCTGTGTATCAAGTCTTTTGACTTTTTACCTGACGGAATTTTATCACTACCCGCCCTTATATCTTAGCGTATAAGCTCGGTGCTAGGAGTTAAAAGCATAGTAAAGAACCTAACTTGCCTTTGTCAGCCTCCTTCCTTTTAGGTTGGAGGACATGATGCGACTGTGGGACGCCCGATTACCCTCGACTTAAATATCTGTTAAGGTAAATTCTTGACTTATCTTTGCAAAAAGGTATGATAGAATTGGCTTTAATGTTTTTACATCTAGAGTTATTCTTTTAGCTCCTGATGGGAGAAAAAAGCACTAGGAATTCTTTGGAAGTCTTTTTGCCTATTTTTCCATTTTTTTGGCCTGAAATCAGATGGGACTACCCGCTGAACTTAAGCATATCATAA


D1D2 region of the 28S ribosomal RNA gene

ATATCAATAAGCGGAGGAAAAGAAAATAACAATGATTCCCTCAGTAACGGCGAGTGAACAGGGAAAAGCTCAAAGTTGGAACCTGGTGGGCCTAGCCTACCCGGATTGTAAACTAAAGTTTTTGGGTCGTTTAGTCAGCCAGATAAATAAGTCCTCTGGAAAGGGGCGACATAGAGGGTGAAATCCCCGTCTTTGGTCTGAGCATGATTAGGCGTTTGGCCTGGAAACGAAGAGTCAGGTTGTTTGGGAATGCAGCCTAAAATGGGAGGTAAATCTCTCCTAAAGCTAAATATTGACGAAAGACCGATAGCGAACAAGTACCGTGAGGGAAAGATGAAAAGCACTTTGAAAAGAGGGTCAAAAAGTACGTGAAATTGCTGAAAGGGAACCGTATAAAATCAGACTTACTGATAGGTAATCAACCTTCCTCTTGGGGAGGGTGCACTTGCCTGTTATTGTATGCCAGCAATACTTTGGTTGGGAGGAAAAAAGTAGGAGAAATGTAGCCTAGGCTTCGGTTTAGGTGTTATAGTCTTTTGCAAAATACTCTCGGCTGGAGTAAGGAACGCAGCAAACCGTAAGGCGAAGATTTTGGGCGCTTGGAATTAATAGTTGGAGAATTTCTGCTTCGGGTGGTGCTTTAGCTATTAGTTTTAACCCGCTTAAAGTTCTTTTAATTTGCTTAGGTTGTTGGCTTAATGATTTTATATGAC

Name of Depositor VM Cutter
Isolation
Hibiscus flowers, Ann Arbor, MI
References

Coutts RT, et al. Metabolism of (+ or - )-N-(n-propyl) amphetamine by Cunninghamella echinulata. Appl. Environ. Microbiol. 37: 429-432, 1979. PubMed: 453824

Smith RV, et al. Mechanism of hydroxylation of biphenyl by Cunninghamella echinulata. Biochem. J. 196: 369-371, 1981. PubMed: 7306077

Mills JS. 10-Fluoro-19-nor steroids. US Patent 3,053,858 dated Sep 11 1962

Badria FA, Hufford CD. Microbial transformations of stemodin, a Stemodia diterpene. Phytochemistry 30: 2265-2268, 1991.

Yang W, Davis PJ. Microbial models of mammalian metabolism. Biotransformations of N-methylcarbazole using the fungus Cunninghamella echinulata. Drug Metab. Dispos. 20: 38-46, 1992. PubMed: 1346994

Davila JC, et al. Cytotoxicity induced by papaverine hydrochloride in fungal cell systems. Toxicol. Lett. 54: 23-31, 1990. PubMed: 2244336

Foster BC, et al. Aromatic hydroxylation and sulfation of phenazopyridine by Cunninghamella echinulata. Can. J. Microbiol. 37: 504-508, 1991.

Foster BC, et al. The biotransformation of tranylcypromine by Cunninghamella echinulata. Can. J. Microbiol. 37: 791-795, 1991. PubMed: 1777857

Ferris JP, et al. Monooxygenase activity in Cunninghamella bainieri: evidence for a fungal system similar to liver microsomes. Arch. Biochem. Biophys. 156: 97-103, 1973. PubMed: 4730481

Hufford CD, et al. Metabolism of phencyclidine by microorganisms. J. Pharm. Sci. 70: 155-158, 1981. PubMed: 7205218

Ferris JP, et al. Aryl hydrocarbon hydroxylase activity in the fungus Cunninghamella bainieri: evidence for the presence of cytochrome P-450. Arch. Biochem. Biophys. 175: 443-452, 1976. PubMed: 8708

Coutts RT, et al. Fungal metabolism of (-)-deprenyl and pargyline. Life Sci. 29: 1951-1958, 1981. PubMed: 6796795

Foster BC, et al. Biotransformation of 2-, 3-, and 4-methoxy-amphetamines by Cunninghamella echinulata. Xenobiotica 21: 1337-1346, 1991. PubMed: 1796610

Foster BC, et al. In vitro assessment of cytotoxicity and biotransformation of propranolol in Cunninghamella echinulata. Xenobiotica 22: 1221-1228, 1992. PubMed: 1492414

Foster BC, et al. Biotransformation of tri-substituted methoxyamphetamines by Cunninghamella echinulata. Xenobiotica 22: 1383-1394, 1992. PubMed: 1494884

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.

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

梅經理 17280875617 1438578920
胡經理 13345964880 2438244627
周經理 17757487661 1296385441
于經理 18067160830 2088210172
沈經理 19548299266 2662369050
李經理 13626845108 972239479
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