Cyclic heptapeptide microcystin biosynthesis requires the glutamate racemase gene

被引:30
|
作者
Nishizawa, T
Asayama, M
Shirai, M [1 ]
机构
[1] Ibaraki Univ, Sch Agr, Genet Mol Lab, Ami, Ibaraki 3000393, Japan
[2] Ibaraki Univ, Ctr Gene Res, Ami, Ibaraki 3000393, Japan
[3] Tokyo Univ Agr & Technol, United Grad Sch, Tokyo 1838509, Japan
来源
MICROBIOLOGY-SGM | 2001年 / 147卷
关键词
amino acid racemase; cyanobacteria; Microcystis; peptide synthetase gene; microcystin biosynthesis;
D O I
10.1099/00221287-147-5-1235
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
It was demonstrated previously that the operon consisting of the nonribosomal peptide synthetase (NRPS) gene coupled with the polyketide synthase (PKS) gene involved in cyclic heptapeptide microcystin synthesis includes two different D-amino acid synthetase genes, an epimerization domain at the 3' end of module 2, and the racemase gene mcyF, To determine the role of mcyF in microcystin synthesis, gene-disruption and complementation analyses were carried out. Insertional mutagenesis in the mcyF gene, generated by homologous recombination, abolished only microcystin synthesis, but did not influence cell growth, Furthermore, McyF supported D-Glu-independent growth of a strain of Escherichia coli defective in D-Glu synthesis, It is concluded that mcyF is the glutamic acid racemase gene involved in the synthesis of D-Glu residues in the microcystin molecule. This is the first report of the racemase in prokaryotic NRPS.
引用
收藏
页码:1235 / 1241
页数:7
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