Functional analysis of the validamycin biosynthetic gene cluster and engineered production of validoxylamine A

被引:112
作者
Bai, L
Li, L
Xu, H
Minagawa, K
Yu, Y
Zhang, YR
Zhou, XF
Fioss, HG
Mahmud, T
Deng, ZX [1 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Life Sci & Biotechnol, Lab Microbial Metab, Shanghai 200030, Peoples R China
[2] Univ Washington, Dept Chem, Seattle, WA 98195 USA
[3] Oregon State Univ, Dept Pharmaceut Sci, Corvallis, OR 97331 USA
来源
CHEMISTRY & BIOLOGY | 2006年 / 13卷 / 04期
关键词
D O I
10.1016/j.chembiol.2006.02.002
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 45 kb DNA sequencing analysis from Streptomyces hygroscopicus 5008 involved in validamycin A (VALA) biosynthesis revealed 16 structural genes, 2 regulatory genes, 5 genes related transport, transposition/integration or tellurium resistance; another 4 genes had no obvious identity. The VAL-A biosynthetic pathway was proposed, with assignment of the required genetic functions confined to the sequenced region. A cluster of eight reassembled genes was found to support VAL-A synthesis in a heterologous host, S. lividans 1326. In vivo inactivation of the putative glycosyltransferase gene (valG) abolished the final attachment of glucose for VAL production and resulted in accumulation of the VAL-A precursor, validoxylamine, while the normal production of VAL-A could be restored by complementation with valG. The role of valG in the glycosylation of validoxylamine to VAL-A was demonstrated in vitro by enzymatic assay.
引用
收藏
页码:387 / 397
页数:11
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