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ATCC18500

ZKCC-44606

ATCC18500

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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,主要用于羟基化物11,13-脱氢糖苷,氧化菊花醇,产生11-α-羟基孕酮,产生L-苹果酸,生产德国国会大厦,产生琥珀酸,转化类黄酮,将菊花氧化成菊花酸,倍半萜内酯-科斯图内酯的转化
培养基ATCC® Medium 312: Czapek's agar
存储人NRRL
出品公司ATCC
分离来源rubber sheet
参考文献Singh K, et al. Large-scale transformation of steroids by fungal spores. Appl. Microbiol. 16: 393-400, 1968. PubMed: 5645421 Sehgal SN, et al. 11 alpha-hydroxylation of steroids by spores of Aspergillus ochraceus. Can. J. Microbiol. 14: 529-532, 1968. PubMed: 5665975 Miski M, Davis PJ. Microbiologically catalyzed enantio- and diastereoselective oxidation of chrysanthemol stereoisomers to chrysanthemic acids. Appl. Environ. Microbiol. 54: 2268-2272, 1988. Bercovitz A, et al. Localization of pyruvate carboxylase in organic acid-producing Aspergillus strains. Appl. Environ. Microbiol. 56: 1594-1597, 1990. PubMed: 2383004 Iida M, et al. Microbial hydroxylation of 11,13-dehydrosantonin by Aspergillus niger. J. Ferment. Bioeng. 76: 296-299, 1993. Ibrahim AR, Abul-Hajj YJ. Microbiological transformation of flavone and isoflavone. Xenobiotica 20: 363-373, 1990. PubMed: 2346033 Clark AM, Hufford CD. Microbial transformations of the sesquiterpene lactone costunolide. J. Chem. Soc. Perkin Trans. 1979: 3022-3028, 1979. Madyastha KM, et al. Studies on the microsomal 11alpha-hydroxylation of progesterone in Aspergillus ochraceus: isolation, characterization, and solubilization of the hydroxylase system. Can. J. Biochem. Cell Biol. 62: 100-107, 1984.
模式菌株否
生长条件24 ℃
菌株特点ATCC 18500是赭曲霉,Aspergillus ochraceus 。
菌株类型赭曲霉,Aspergillus ochraceus
菌种又名NRRL 405 [4718]
菌种名称ATCC18500, ATCC 18500
产品目录号18500
生物安全等级1
其他保藏库编号BCRC32098,ATCC 18500 ;NRRL 405
ATCC18500标准菌株基本信息ATCC
ATCC18500, ATCC 18500
NRRL 405 [4718]
赭曲霉,Aspergillus ochraceus
NRRL
rubber sheet
18500
BCRC32098,ATCC 18500 ;NRRL 405
ATCC® Medium 312: Czapek's agar
24 ℃
1
否
科研,生产,主要用于羟基化物11,13-脱氢糖苷,氧化菊花醇,产生11-α-羟基孕酮,产生L-苹果酸,生产德国国会大厦,产生琥珀酸,转化类黄酮,将菊花氧化成菊花酸,倍半萜内酯-科斯图内酯的转化
ATCC 18500是赭曲霉,Aspergillus ochraceus 。
Singh K, et al. Large-scale transformation of steroids by fungal spores. Appl. Microbiol. 16: 393-400, 1968. PubMed: 5645421
Sehgal SN, et al. 11 alpha-hydroxylation of steroids by spores of Aspergillus ochraceus. Can. J. Microbiol. 14: 529-532, 1968. PubMed: 5665975
Miski M, Davis PJ. Microbiologically catalyzed enantio- and diastereoselective oxidation of chrysanthemol stereoisomers to chrysanthemic acids. Appl. Environ. Microbiol. 54: 2268-2272, 1988.
Bercovitz A, et al. Localization of pyruvate carboxylase in organic acid-producing Aspergillus strains. Appl. Environ. Microbiol. 56: 1594-1597, 1990. PubMed: 2383004
Iida M, et al. Microbial hydroxylation of 11,13-dehydrosantonin by Aspergillus niger. J. Ferment. Bioeng. 76: 296-299, 1993.
Ibrahim AR, Abul-Hajj YJ. Microbiological transformation of flavone and isoflavone. Xenobiotica 20: 363-373, 1990. PubMed: 2346033
Clark AM, Hufford CD. Microbial transformations of the sesquiterpene lactone costunolide. J. Chem. Soc. Perkin Trans. 1979: 3022-3028, 1979.
Madyastha KM, et al. Studies on the microsomal 11alpha-hydroxylation of progesterone in Aspergillus ochraceus: isolation, characterization, and solubilization of the hydroxylase system. Can. J. Biochem. Cell Biol. 62: 100-107, 1984.

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