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PMID: 22861048 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Biosynthetic pathway for high structural diversity of a common dilactone core in antimycin production.

Organic letters ·Vol. 14 ·No. 16 ·2012-08-17 ·Pages 4142-5

Yan Y, Zhang L, Ito T, Qu X, Asakawa Y, Awakawa T, Abe I, Liu W

Abstract

We herein report comparative analysis of two versions of the biosynthetic gene clusters of antimycins, a natural product family possessing up to 44 distinct entities. The biosynthetic pathway of antimycins is amenable to the high structural variation of the substrates, supported by successes in heterologous expression of the ant cluster and in fluorine incorporation. The latter facilitated the investigation of the structure-activity relationship into the usually invariable 3-formamidosalicylic acid moiety of the molecules.

MeSH Terms
Anti-Bacterial Agents/biosynthesis,chemistry Antimycin A/analogs & derivatives,biosynthesis,chemistry Biosynthetic Pathways/genetics Genes, Bacterial Molecular Structure Streptomyces/chemistry,genetics,metabolism Structure-Activity Relationship
Chemicals
Anti-Bacterial Agents antimycin Antimycin A
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Yan Yan
State Key Laboratory of Bioorganic and Natural Products Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Road, Shanghai 200032, China.
Zhang Lihan
Ito Takuya
Qu Xudong
Asakawa Yoshinori
Awakawa Takayoshi
Abe Ikuro
Liu Wen
Article Info
Journal
Organic letters
Abbr.
Org Lett
ISSN
1523-7052
Published
2012-08-17
Epub
2012-00-03
Pages
4142-5
Language
English
Region
United States
NLM ID
100890393
Subset
IM
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