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微信小章| 产品名称： | Rhizoctonia leguminicola Gough et Elliott, anamorph |
|---|---|
| 商品货号： | TS191903 |
| Application： | produces slaframine produces swainsonine produces alpha-mannosidase inhibitor swainsonine |
| 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： | frozen |
| Storage Conditions： | Frozen: -80°C or colder Freeze-Dried: 2°C to 8°C Live Culture: See Propagation Section |
| Type Strain： | no |
| Preceptrol®： | no |
| Medium： | ATCC® Medium 336: Potato dextrose agar (PDA) |
| Growth Conditions： | Temperature: 24.0°C |
| Name of Depositor： | HP Broquist |
| Chain of Custody： | ATCC < |
| Isolation： | red clover |
| References： | Gardiner RA, et al. Slaframine. Absolute stereochemistry and a revised structure. J. Am. Chem. Soc. 90: 5639-5640, 1968. PubMed: 5679170 Aust SD, et al. Slaframine: a parasympathomimetic from Rhizoctonia leguminicola. Biotechnol. Bioeng. 10: 403-412, 1968. Clevenstine EC, et al. Biosynthesis of slaframine, (1S, 6S, 8aS)-1-acetoxy-6-aminooctahydroindolizine, a parasympathomimetic alkaloid of fungal origin. 3. Origin of the pyrrolidine ring. Biochemistry 18: 3658-3663, 1979. PubMed: 476077 Clevenstine EC, et al. Biosynthesis of slaframine, (1S,6S,8aS)-1-acetoxy-6-aminooctahydroindolizine, a parasympathomimetic alkaloid of fungal origin. 4. Metabolic fate of ethyl pipecolylacetate, 1,3-dioxooctahydroindolizine, and 1-hydroxyoctahydroindolizine in Rhizoctonia leguminicola. Biochemistry 18: 3663-3667, 1979. PubMed: 476078 Broquist HP, Snyder JJ. Rhizoctonia toxin. Microb. Toxins 7: 319-333, 1971. Schneider MJ, et al. (1S, 2R, 8R, 8aR)-1,2,8-trihydroxyocta-hydroindolizine (swainsonine), an alpha-mannosidase inhibitor from Rhizoctonia leguminicola. Tetrahedron 39: 29-32, 1983. |