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首页> 外文期刊>Applied Microbiology and Biotechnology >Characterization of a negative regulator AveI for avermectin biosynthesis in Streptomyces avermitilis NRRL8165
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Characterization of a negative regulator AveI for avermectin biosynthesis in Streptomyces avermitilis NRRL8165

机译:阿维链霉菌NRRL8165中阿维菌素生物合成负调节剂AveI的表征

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摘要

A transcriptional activator for actinorhodin biosynthesis, AtrA, was previously characterized in Streptomyces coelicolor A3(2), and an orthologue of atrA, named aveI, is identified in the Streptomyces avermitilis NRRL8165 genome (Uguru et al., Mol Microbiol, 58:131-150, 2005). In this study, genetic and functional characterization of aveI gene was reported. Deletion of aveI gene led to increased biosynthesis of avermectin B1a by about 16-fold. The increased synthesis of avermectin B1a was suppressed by complementation with either aveI gene or its orthologue gene atrA from S. coelicolor, suggesting AveI and AtrA shared the similar functionality and were negative regulators for avermectin biosynthesis in S. avermitilis. However, when aveI was introduced into S. coelicolor on a multi-copy plasmid, the production of actinorhodin was significantly increased, indicating that aveI had a positive effect on actinorhodin biosynthesis in S. coelicolor, the same as its orthologue atrA. Electrophoretic mobility shift assays revealed AveI can bind specifically to the promoter region of actII-ORF4 in vitro but not that of aveR. Although its mechanism still needs to be defined, the species-differential regulation by the same regulator may represent an example of the evolutional strategy that enables bacteria to adapt the existing molecular machinery to a variety of functionalities for growth and survival.
机译:放线菌素生物合成的转录激活因子AtrA先前已在coelicolor链霉菌A3(2)中进行了表征,而atverA的直向同源物ave1在阿维链霉菌NRRL8165基因组中得到鉴定(Uguru等人,Mol Microbiol,58:131- 150,2005)。在这项研究中,报告了aveI基因的遗传和功能表征。 aveI基因的缺失导致阿维菌素B1a的生物合成增加了约16倍。阿维菌素B1a合成的增加被来自食管链球菌的aveI基因或其直向同源基因atrA的互补所抑制,这表明AveI和AtrA具有相似的功能,并且是阿维链霉菌中阿维菌素生物合成的负调节剂。但是,当在多拷贝质粒上将aveI引入天蓝色链霉菌时,放线菌丝蛋白的产量显着增加,这表明aveI对天蓝色链霉菌中放线菌丝素的生物合成具有积极作用,与其直系同源物atrA相同。电泳迁移率变动分析表明,AveI可以在体外特异性结合actII-ORF4的启动子区域,但不能与aveR的启动子区域结合。尽管仍然需要定义其机制,但同一调节器对物种的差异性调节可能代表了进化策略的一个例子,该策略使细菌能够使现有分子机制适应多种功能,以实现生长和生存。

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