| 出品公司: | ATCC |
|---|---|
| 菌种名称: | ATCC7159, ATCC 7159 |
| 菌种又名: | CBS 209.27 [DSM 1344] |
| 菌株类型: | 白僵菌Beauveria bassiana |
| 存储人: | CBS |
| 分离来源: | 实验室污染物 |
| 产品目录号: | 7159 |
| 培养基: |
ATCC®培养基200:YM琼脂或YM肉汤
ATCC®培养基324：麦芽提取物琼脂
ATCC®培养基336：马铃薯葡萄糖琼脂（PDA）
|
| 生长条件: |
温度：24°C至26°C
大气：典型有氧
|
| 生物安全等级: | 1 |
| 模式菌株: | 是（硫孢子丝菌型菌株） |
| 应用: |
科研，生产，主要用于水解1,2-二氢萘
水解1,2-环氧茚
水解氧化苯乙烯
羟基多环烯酮
代谢苯环利定
氧化蒿醚
氧化羟基二烷基苯甲酸酯
产生2-氘环烷酮
产生3-氘环烷酮
生产卡霉素衍生物-麦格纳霉素衍生物
产生羟甲基吡啶（异构体）
产生白霉素衍生物
产生奈达霉素衍生物
7-氮杂布伦丹和6-氮杂戊烷衍生物的羟基化反应
合成多环烯酮的羟基化反应
α，β-不饱和酮的还原
将硝酸异山梨酯转化为5-单硝酸异山梨酯
培高利特向培高利特亚砜的转化
2,2,5,7,8-五甲基-6-羟基铬的糖基化
|
| 菌株特点: |
ATCC7159 白僵菌Beauveria bassiana |
| 参考文献: |
Ropenga JS, et al. Isosorbide dinitrate bioconversion by Beauveria strains: implication of glutathione transferase levels. Appl. Microbiol. Biotechnol. 31: 176-178, 1989.
Pedragosa-Moreau S, et al. Microbiological transformations. 28. Enantiocomplementary epoxide hydrolyses as a preparative access to both enantiomers of styrene oxide. J. Org. Chem. 58: 5533-5536, 1993.
Theriault RJ. Mycarosyl macrolide antibiotics. US Patent 3,784,447 dated Jan 8 1974
Taylor JJ. Further clarification of Sporotrichum species. Mycologia 62: 823, 1970.
Johnson RA, et al. Microbial oxygenation of dialkylbenzenes. Bioorg Chem 2: 99-110, 1973.
Kergomard A, et al. Microbiological reduction of alpha,beta-unsaturated ketones by Beauveria sulfurescens. J. Org. Chem. 47: 792-798, 1982.
Hu Y, et al. Microbial oxidataion of the antimalarial drug arteether. Bioorg. Chem. 20: 148-154, 1992.
Hufford CD, et al. Metabolism of phencyclidine by microorganisms. J. Pharm. Sci. 70: 155-158, 1981. PubMed: 7205218
Furstoss R, et al. Microbiological transformations 2. Hydroxylations of non activated carbons in globular type amides. Tetrahedron Lett 22: 445-448, 1981.
Dauphin G, et al. Microbiological synthesis and circular dichroism of optically active 2-deuterio-cycloalkanones. Tetrahedron Lett 21: 4275-4278, 1980.
Pedragosa-Moreau S, et al. Microbiological transformations. 31: Synthesis of enantiopure epoxides and vicinal diols using fungal epoxide hydrolase mediated hydrolysis. Tetrahedron Lett. 37: 3319-3322, 1996.
Dauphin G, et al. Microbial glycosylation of 2, 2, 5, 7, 8-pentamethyl- 6-hydroxychroman. Agric Biol Chem 53: 1433-1435, 1989.
Dauphin G, et al. Microbiological synthesis of optically active 3-deuterio-cycloalkanones. J. Chem. Soc. Chem. Commun. 1980: 318-319, 1980.
Smith RV, et al. Microbial transformations of pergolide to pergolide sulfoxide and pergolide sulfone. J. Pharm. Sci. 72: 733-736, 1983. PubMed: 6684155
Modyanova LV, et al. Microbial transformation of nitrogen-containing heterocyclic compounds. I. Hydroxylation of isomeric monomethylpyridines and dimethylpyridines by microscopic fungi. Biotekhnologiya 3: 24-27, 1990.
Hammoumi A, et al. Microbial hydroxylation and functionalization of synthetic polycyclic enones. Tetrahedron Asymmetry 4: 1295-1306, 1993.
Xu Y, et al. Biosynthesis of the cyclooligomer depsipeptide bassianolide, an insecticidal virulence factor of Beauveria bassiana. Fungal Genet. Biol. 46: 353-364, 2009. PubMed: 19285149
Xu Y, et al. Biosynthesis of the cyclooligomer depsipeptide beauvericin, a virulence factor of the entomopathogenic fungus Beauveria bassiana. Chem. Biol. 15: 898-907, 2008. PubMed: 18804027
type strain of Sporotrichum sulfurescens
|
买家导航
