Biosynthesis of desosamine: Construction of a new macrolide carrying a genetically designed sugar moiety

被引:89
作者
Borisova, SA
Zhao, LS
Sherman, DH
Liu, HW
机构
[1] Univ Minnesota, Dept Chem, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Dept Microbiol & Biol Proc, Inst Technol, Minneapolis, MN 55455 USA
关键词
D O I
10.1021/ol9906007
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
[GRAPHICS] The appended sugars in macrolide antibiotics are indispensable to the biological activities of these important drugs. In an effort to generate a set of novel macrolide derivatives, we have created a new analogue of methymycin and neomethymycin, antibiotics produced by Streptomyces venezuelae, This analogue 15 carrying a different sugar, D-quinovose, instead of D-desosamine, was constructed by taking advantage of targeted gene deletion combined with a specific pathway-independent C-3 reduction capability of the wild type S. venezuelae.
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页码:133 / 136
页数:4
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