| 产品名称： | Rhizopus oryzae Went et Prinsen Geerligs |
|---|---|
| 商品货号： | TS168204 |
| Deposited As： | Rhizopus arrhizus Fischer |
| Strain Designations： | RH 176 CBS 381.52, IFO 5780, IFO 6155, IMI 90340 |
| Application： | Produces 16-hydroxyverrucarin A and B
Produces 3-hydroxyverrucarin A
Produces hydroxylated steroids steroids, hydroxylated
Produces imipramine
Degrades: insect molting hormones
Transformation of sesquiterpene lactone costunolide
Transformation of prostanoids
Transformation of verrucarins A and B
Transformation of stemodin
Transformation of isopinocampheol
Produces: 16-hydroxyverrucarin A and B and 3-hydroxyverrucarin A by transformation of verrucarins A and B |
| 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®： | no |
| Comments： | Reduction of 2-cyano-1-tetralones to cyanalcohols |
| Medium： | ATCC® Medium 336: Potato dextrose agar (PDA) ATCC® Medium 307: Cornmeal agar ATCC® Medium 28: Emmons modification of Sabourauds agar |
| Growth Conditions： | Temperature: 25°C
Atmosphere: Typical aerobic |
| Sequenced Data： |
No DNA sequencing was performed in house on this product.
|
| Name of Depositor： | Upjohn Co. |
| References： | Z. Naturforsch. Sect. C Biosci. 49: 553-560, 1994. Peppler HJ. Microbial technology. New York: Reinhold; 1967. Nelson E. Method of making low-temperature meteorological balloons. US Patent 2,646,370 dated Jul 21 1953 . . Can. J. Chem. 68: 282-293, 1990. . . Can. J. Chem. 59: 1651-1655, 1981. . . Can. J. Chem. 63: 1127-1131, 1985. . . Tetrahedron Lett. 36: 6461-6462, 1995. 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 Holland HL, Diakow PR. Microbial hydroxylation of steroids. 5. Metabolism of androst-5-ene-3, 17-dione and related compounds by Rhizopus arrhizus TS168204. Can. J. Chem. 57: 436-440, 1979. Holland HL, Diakow PR. Microbial hydroxylation of steroids. 6. Hydroxylation of C-6-substituted androst-4-ene-3, 17-diones by Rhizopus arrhizus TS168204. Can. J. Chem. 57: 1585-1587, 1979. Canonica L, et al. The microbiological oxidation of insect moulting hormones. J. Chem. Soc. Chem. Commun. 1974: 656-657, 1974. Hufford CD, et al. Preparation, characterization, and antiviral activity of microbial metabolites of stemodin. J. Nat. Prod. 54: 1543-1552, 1991. PubMed: 1667410 Pavanasasivam G, Jarvis BB. Microbial transformation of macrocyclic trichothecenes. Appl. Environ. Microbiol. 46: 480-483, 1983. |
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| 产品名称： | Rhizopus oryzae Went et Prinsen Geerligs |
|---|---|
| 商品货号： | TS168204 |
| Deposited As： | Rhizopus arrhizus Fischer |
| Strain Designations： | RH 176 CBS 381.52, IFO 5780, IFO 6155, IMI 90340 |
| Application： | Produces 16-hydroxyverrucarin A and B
Produces 3-hydroxyverrucarin A
Produces hydroxylated steroids steroids, hydroxylated
Produces imipramine
Degrades: insect molting hormones
Transformation of sesquiterpene lactone costunolide
Transformation of prostanoids
Transformation of verrucarins A and B
Transformation of stemodin
Transformation of isopinocampheol
Produces: 16-hydroxyverrucarin A and B and 3-hydroxyverrucarin A by transformation of verrucarins A and B |
| 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®： | no |
| Comments： | Reduction of 2-cyano-1-tetralones to cyanalcohols |
| Medium： | ATCC® Medium 336: Potato dextrose agar (PDA) ATCC® Medium 307: Cornmeal agar ATCC® Medium 28: Emmons modification of Sabourauds agar |
| Growth Conditions： | Temperature: 25°C
Atmosphere: Typical aerobic |
| Sequenced Data： |
No DNA sequencing was performed in house on this product.
|
| Name of Depositor： | Upjohn Co. |
| References： | Z. Naturforsch. Sect. C Biosci. 49: 553-560, 1994. Peppler HJ. Microbial technology. New York: Reinhold; 1967. Nelson E. Method of making low-temperature meteorological balloons. US Patent 2,646,370 dated Jul 21 1953 . . Can. J. Chem. 68: 282-293, 1990. . . Can. J. Chem. 59: 1651-1655, 1981. . . Can. J. Chem. 63: 1127-1131, 1985. . . Tetrahedron Lett. 36: 6461-6462, 1995. 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 Holland HL, Diakow PR. Microbial hydroxylation of steroids. 5. Metabolism of androst-5-ene-3, 17-dione and related compounds by Rhizopus arrhizus TS168204. Can. J. Chem. 57: 436-440, 1979. Holland HL, Diakow PR. Microbial hydroxylation of steroids. 6. Hydroxylation of C-6-substituted androst-4-ene-3, 17-diones by Rhizopus arrhizus TS168204. Can. J. Chem. 57: 1585-1587, 1979. Canonica L, et al. The microbiological oxidation of insect moulting hormones. J. Chem. Soc. Chem. Commun. 1974: 656-657, 1974. Hufford CD, et al. Preparation, characterization, and antiviral activity of microbial metabolites of stemodin. J. Nat. Prod. 54: 1543-1552, 1991. PubMed: 1667410 Pavanasasivam G, Jarvis BB. Microbial transformation of macrocyclic trichothecenes. Appl. Environ. Microbiol. 46: 480-483, 1983. |
