Manipulation of metabolic pathways controlled by signaling molecules, inducers of antibiotic production, for genome mining in Streptomyces spp.

被引:23
作者
Arakawa, Kenji [1 ]
机构
[1] Hiroshima Univ, Grad Sch Adv Sci Matter, Dept Mol Biotechnol, 1-3-1 Kagamiyama, Hiroshima 7398530, Japan
来源
ANTONIE VAN LEEUWENHOEK INTERNATIONAL JOURNAL OF GENERAL AND MOLECULAR MICROBIOLOGY | 2018年 / 111卷 / 05期
关键词
Streptomyces; Signaling molecule; Regulatory cascade; Secondary metabolites; Biosynthesis; BIOSYNTHETIC GENE CLUSTERS; FACTOR REGULATORY CASCADE; A-FACTOR RECEPTOR; SECONDARY METABOLISM; BUTYROLACTONE AUTOREGULATOR; COELICOLOR A3(2); MORPHOLOGICAL DEVELOPMENT; VIRGINIAMYCIN BIOSYNTHESIS; TRANSCRIPTIONAL REGULATOR; LANKAMYCIN PRODUCTION;
D O I
10.1007/s10482-018-1052-6
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Streptomyces is well characterized by an ability to produce a wide variety of secondary metabolites including antibiotics, whose expression is strictly controlled by small diffusible signaling molecules at nano-molar concentrations. The signaling molecules identified to date are classified into three skeletons; gamma-butyrolactones, furans, and gamma-butenolides. Accumulated data suggest the structural diversity of the signaling molecules in Streptomyces species and their potential in activating cryptic secondary metabolite biosynthetic pathways. Several genome mining approaches to activate silent biosynthetic gene clusters have been reported for natural product discovery. This review updates recent examples on genetic manipulation including blockage of metabolic pathways together with inactivation of transcriptional repressor genes.
引用
收藏
页码:743 / 751
页数:9
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