Description
产品说明
| 所属分类 | 微生物 > 模式菌株 |
|---|---|
| 品牌 / 来源 | CS-BIC | 中科生信 |
| 应用 | 科研，生产，主要用于氧化阿扑啡，氧化菊花醇，生产双氢月桂碱，生产丙咪嗪，倍半萜内酯-科斯图内酯的转化，将菊花氧化成菊花酸 |
| 培养基 | ATCC® Medium 313: Czapek's agar |
| 存储人 | NRRL |
| 出品公司 | ATCC |
| 参考文献 | Davis PJ, Talaat RE. Microbiological systems in organic synthesis: preparative-scale resolution of (R,S)-glaucine by Fusarium solani and stereospecific oxidation of (R)-(-)-glaucine by Aspergillus flavipes. Appl. Environ. Microbiol. 41: 1243-1247, 1981. Kerr KM, Davis PJ. Microbial transformations in organic synthesis. 3. Synthesis, characterization and fungal metabolism of cis- and trans-7-methylglaucine. J. Org. Chem. 48: 928-932, 1983. Miski M, Davis PJ. Microbiologically catalyzed enantio- and diastereoselective oxidation of chrysanthemol stereoisomers to chrysanthemic acids. Appl. Environ. Microbiol. 54: 2268-2272, 1988. 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 |
| 模式菌株 | 否 |
| 生长条件 | 26 ℃ |
| 菌株特点 | ATCC 1030是黄曲霉,Aspergillus flavipes 。 |
| 菌株类型 | 黄曲霉,黄柄曲霉;黄柄曲霉菌;菌黄柄曲霉;黄炳曲霉属Aspergillus flavipes |
| 菌种又名 | NRRL 286 [114, QM 1993] |
| 菌种名称 | ATCC1030, ATCC 1030 |
| 产品目录号 | 1030 |
| 生物安全等级 | 1 |
| 其他保藏库编号 | BCRC33709，ATCC 1030; NRRL 286; QM 1993 |
| ATCC1030标准菌株基本信息 | ATCC ATCC1030, ATCC 1030 NRRL 286 [114, QM 1993] 黄曲霉,黄柄曲霉;黄柄曲霉菌;菌黄柄曲霉;黄炳曲霉属Aspergillus flavipes NRRL 1030 BCRC33709，ATCC 1030; NRRL 286; QM 1993 ATCC® Medium 313: Czapek's agar 26 ℃ 1 否 科研，生产，主要用于氧化阿扑啡，氧化菊花醇，生产双氢月桂碱，生产丙咪嗪，倍半萜内酯-科斯图内酯的转化，将菊花氧化成菊花酸 ATCC 1030是黄曲霉,Aspergillus flavipes 。 Davis PJ, Talaat RE. Microbiological systems in organic synthesis: preparative-scale resolution of (R,S)-glaucine by Fusarium solani and stereospecific oxidation of (R)-(-)-glaucine by Aspergillus flavipes. Appl. Environ. Microbiol. 41: 1243-1247, 1981. Kerr KM, Davis PJ. Microbial transformations in organic synthesis. 3. Synthesis, characterization and fungal metabolism of cis- and trans-7-methylglaucine. J. Org. Chem. 48: 928-932, 1983. Miski M, Davis PJ. Microbiologically catalyzed enantio- and diastereoselective oxidation of chrysanthemol stereoisomers to chrysanthemic acids. Appl. Environ. Microbiol. 54: 2268-2272, 1988. 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 |
Related
