STUDIES ON THE BIOSYNTHESIS OF BIALAPHOS (SF-1293) .12. C-P BOND FORMATION MECHANISM OF BIALAPHOS - DISCOVERY OF A P-METHYLATION ENZYME

被引:50
作者
KAMIGIRI, K
HIDAKA, T
IMAI, S
MURAKAMI, T
SETO, H
机构
[1] MEIJI SEIKA KAISHA LTD,PHARMACEUT RES CTR,KOHOKU KU,YOKOHAMA,KANAGAWA 222,JAPAN
[2] MEIJI SEIKA KAISHA LTD,PHARMACEUT TECHNOL LABS,ODAWARA,KANAGAWA 25001,JAPAN
关键词
D O I
10.7164/antibiotics.45.781
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
An enzymatic activity catalyzing P-methylation of N-acetyldemethylphosphinothricin, a biosynthetic intermediate of the herbicide bialaphos, was detected in a cell extract of Streptomyces hygroscopicus SF-1293, a bialaphos producing organism. The gene coding for this P-methylation enzyme in the bialaphos biosynthetic gene cluster was also expressed in Streptomyces lividans. The methyl donor of the reaction was determined to be methylcobalamin. The P-methylation enzyme utilized both N-acetyldemethylbialaphos and N-acetyldemethylphosphinothricin as substrates.
引用
收藏
页码:781 / 787
页数:7
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