The Journal of Antibiotics
Online ISSN : 1881-1469
Print ISSN : 0021-8820
ISSN-L : 0021-8820
STUDIES ON THE BIOSYNTHESIS OF BIALAPHOS (SF-1293) 12.
C-P BOND FORMATION MECHANISM OF BIALAPHOS: DISCOVERY OF A P-METHYLATION ENZYME
KAZUMA KAMIGIRITOMOMI HIDAKASATOSHI IMAITAKESHI MURAKAMHARUO SETO
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1992 Volume 45 Issue 5 Pages 781-787

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Abstract

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.

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© Japan Antibiotics Research Association
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