An iterative type I polyketide synthase PKSN catalyzes synthesis of the decaketide alternapyrone with regio-specific octa-methylation

被引:87
作者
Fujii, I
Yoshida, N
Shimomaki, S
Oikawa, H
Ebizuka, Y
机构
[1] Univ Tokyo, Grad Sch Pharmaceut Sci, Bunkyo Ku, Tokyo 113033, Japan
[2] Hokkaido Univ, Grad Sch Sci, Sapporo, Hokkaido 0600810, Japan
来源
CHEMISTRY & BIOLOGY | 2005年 / 12卷 / 12期
基金
日本学术振兴会;
关键词
D O I
10.1016/j.chembiol.2005.09.015
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A biosynthetic gene cluster containing five genes, alt1-5, was cloned from Alternaria solani, a causal fungus of early blight disease to tomato and potato. Homology searching indicated that the altl, 2, and 3 genes code for cytochrome P450s and the alt4 gene for a FAD-dependent oxygenase/oxidase. The alt5 gene encodes a polyketide synthase (PKS), named PKSN, that was found to be an iterative type I complex reduced-type PKS with a C-methyltransferase domain. To identify the PKSN function, the alt5 gene was introduced into the fungal host Aspergillus oryzae under an alpha-amylase promoter. The transformant produced a polyketide compound, named alternapyrone, whose structure is shown to be 3,5-dimethyl-4-hydroxy6-(1,3,5,7,11,13-hexamethyl-3,5,1 1-pentadecatrienyl)pyran-2-one. Labeling experiments confirmed that alternapyrone is a decalketide with octa-methylation from methionine on every C-2 unit except the third unit.
引用
收藏
页码:1301 / 1309
页数:9
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