Waking up Streptomyces Secondary Metabolism by Constitutive Expression of Activators or Genetic Disruption of Repressors

被引:29
作者
Aigle, Bertrand [1 ]
Corre, Christophe [2 ]
机构
[1] Univ Lorraine, UMR UL INRA 1128, EFABA IFR110, Vandoeuvre Les Nancy, France
[2] Univ Warwick, Dept Chem, Coventry CV4 7AL, W Midlands, England
来源
NATURAL PRODUCT BIOSYNTHESIS BY MICROORGANISMS AND PLANTS, PT C | 2012年 / 517卷
关键词
MACROLIDE ANTIBIOTIC SPIRAMYCIN; TRANSCRIPTIONAL REGULATORY GENE; COMPLETE GENOME SEQUENCE; COELICOLOR A3(2); POLYKETIDE SYNTHASE; TYLOSIN BIOSYNTHESIS; LINEAR CHROMOSOME; AMBOFACIENS; CLUSTER; PROTEIN;
D O I
10.1016/B978-0-12-404634-4.00017-6
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Streptomycete bacteria are renowned as a prolific source of natural products with diverse biological activities. Production of these metabolites is often subject to transcriptional regulation: the biosynthetic genes remain silent until the required environmental and/or physiological signals occur. Consequently, in the laboratory environment, many gene clusters that direct the biosynthesis of natural products with clinical potential are not expressed or at very low level preventing the production/detection of the associated metabolite. Genetic engineering of streptomycetes can unleash the production of many new natural products. This chapter describes the overexpression of pathway-specific activators, the genetic disruption of pathway-specific repressors, and the main strategy used to identify and characterize new natural products from these engineered Streptomyces strains.
引用
收藏
页码:343 / 366
页数:24
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