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<em>Umbelopsis isabellina</em> (Oudemans) Gams
<em>Umbelopsis isabellina</em> (Oudemans) Gams
規(guī)格:
貨期:
編號(hào):B193858
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(chēng) Umbelopsis isabellina (Oudemans) Gams
商品貨號(hào) B193858
Deposited As Mortierella isabellina Oudemans
Strain Designations NRRL 1757
Application
Hydroxylates ethylbenzene
Hydroxylates progesterone
Oxidizes alkyl benzyl sulfide
Oxidizes bibenzyl
Oxidizes organic sulphides
Produces (+)-(3R)-ethyl 3-hydroxy-3-(3,4-dimethoxyphenyl) propionate
Produces (S)-4-hydroxy-alpha-lapachone
Produces benzylic hydroxylase
Produces chiral isothiocyanate sulfoxides
Produces chroman-4-ol
Produces thiochroman-4-ol
Reduces chromanone
Reduces thiochromanone
Sulfoxidates methylphenylsulfide thioanisole
Transforms organophosphines
Conversion of olefins to vicinal diols
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
Morphology
Medium ATCC® Medium 336: Potato dextrose agar (PDA)
ATCC® Medium 325: Malt extract agar (Blakeslee's formula)
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

AAGGATCATTACCAAAAGATAATCTTTCAAATCGAAAGATCTTTTCCTTTGTGCTGGCTTTGACCGTATGTAATTTTGGGACTTAAACATGGTAGCTTTTTTGTTACCGGTCCCAAAAACAATTATATCATCCTTATGAAAAACTTACTGAACAACTAAACAATGATTTTAATAATCTGTTTAAAACAACTTTCAACAACGGATCTCTTGGTTCTCGCATCGATGAAGAACGCAGCGAAATGCGATACGTAATGTGAATTGCAGAATTCAGTGAATCATCGAATCTTTGAACGCACATTGCACTCCTTGGTATTCCGAGGAGTATGCCTGTTTCAGTATCATGAGCACTCTCACACCTAACCTTTGGGTTTTGTTGTGGAATTGGGATGCGCCGATTTTAATAGTCGGCACTCCTAAAATGTAGTTCTTGGCTGTTTCCTACTACAGCAGTTTGGCCTAATAGTTTTGACTTTTGTCAAATCTTTGGCTACATTTGCTTCTGGAAATCAGTYTTGATAATACAGAAAACTCATTCAAACTTTGATCTGAAATCAGGTAGGGCTACCCGCTGAACTTAAG


D1D2 region of the 28S ribosomal RNA gene

CATATCAATAAGCGGAGGAAAAGAAACTAACAAGGATTCCCCTAGTAACGGCGAGTGAAGCGGGAAGAGCTCAAATTTAAAATCTGGCTTGCTTGCAAGTCCGAGTTGTAGTCTGAAGAAGCGTTTTCCATGAAAGCTGAGGCACAAGTCCTTTGGAACAGGGCATCATAGAGGGTGAGAATCCCGTCCATGGTCTCATGCATTTCATTTTGTGATACGTTTTCTAAGAGTCAGGTTGTTTGGGAATGCAGCCTAAAATGGGTGGTAAATTTCATCTAAAGCTAAATATTGGCGAGAGACCGATAGCGAACAAGTACCGTGAGGGAAAGATGAAAAGAACTTTGAAAAGAGAGTTAAAAAGTACGTGAAATTGTTGAAAGGGAACCGTTTGAAGCCAGTCTTGCTTACTTGTGATCAATCTTAGCTTCGGCTTGGATGCACTCTCAAGTTATGCAGGTCAACGTCAGTTTGAGAGGTGGGAAAAAAGTTTGAGGAATGTGGCCTTCGGGTGTTATAGCCTCTTACTAAATACCATCTCCTGGACTGAGGCTCGCAGCAAAAATGTGGGCTGGTTTGCTCCTGAGGTGAATCATTATTAAGACAGCTTGCTGACTTAGTTTTGTGGATCTTCACGGTAGGCTAGCTTCTAATTTGCTTAGGTCGTTGACATAATGGCTTTAAATGA

Name of Depositor NRRL
References

. . Biocatalysis 10: 65-76, 1994.

Holland HL, et al. Preparation of homochiral chroman-4-ols and thiochroman-4-ols by microbial biotransformation. Tetrahedron Asymmetry 2: 335-338, 1991.

Holland HL, et al. Biotransformation of organic sulfides. Part 7. Formation of chiral isothiocyanate sulfoxides and related compounds by microbial biotransformation. Tetrahedron Asymmetry 6: 1569-1574, 1995.

Bardot V, et al. Microbial synthesis of (+)-(3R)-ethyl 3-hydroxy-3-(3,4-dimethoxyphenyl)propionate. Tetrahedron Asymmetry 7: 1077-1088, 1996.

Holland HL, et al. Microbial oxidation of benzyl sulfides and bibenzyl by Mortierella isabellina and Helminthosporium species. Can. J. Chem. 69: 1989-1993, 1991.

. . Can. J. Chem. 73: 1399-1405, 1995.

O'Donnell KL. Zygomycetes in culture. Athens, GA: Univ. Georgia; 1979

Holland HL, et al. Fungal hydroxylation of ethyl benzene and derivatives. Tetrahedron Lett. 26: 6409-6412, 1985.

Holland HL, et al. The oxidation of organic sulphides by Mortierella isabellina. 2. Effects of substituents on the stereochemistry of sulphoxide formation. Can. J. Chem. 63: 1118-1120, 1985.

Holland HL, et al. Fungal biotransformation of organophosphines. Xenobiotica 23: 519-524, 1993. PubMed: 8342299

Holland HL, et al. Side chain hydroxylation of aromatic compounds by fungi. Part 5. Exploring the benzylic hydroxylase of Mortierella isabellina. Tetrahedron Asymmetry 4: 1353-1364, 1993.

Holland HL, et al. Effect of cell immobilization and organic solvents on sulfoxidation and steroid hydroxylation by Mortierella isabellina. J. Ind. Microbiol. 10: 195-197, 1992. PubMed: 1368869

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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