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Direct Involvement of the Master Nitrogen Metabolism Regulator GlnR in Antibiotic Biosynthesis in Streptomyces

机译:主氮代谢调节剂GlnR直接参与链霉菌类抗生素的生物合成

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摘要

GlnR, an OmpR-like orphan two-component system response regulator, is a master regulator of nitrogen metabolism in the genus Streptomyces. In this work, evidence that GlnR is also directly involved in the regulation of antibiotic biosynthesis is provided. In the model strain Streptomyces coelicolor M145, an in-frame deletion of glnR resulted in markedly increased actinorhodin (ACT) production but reduced undecylprodigiosin (RED) biosynthesis when exposed to R2YE culture medium. Transcriptional analysis coupled with DNA binding studies revealed that GlnR represses ACT but activates RED production directly via the pathway-specific activator genes actII-ORF4 and redZ, respectively. The precise GlnR-binding sites upstream of these two target genes were defined. In addition, the direct involvement of GlnR in antibiotic biosynthesis was further identified in Streptomyces avermitilis, which produces the important anthelmintic agent avermectin. We found that S. avermitilis GlnR (GlnRsav) could stimulate avermectin but repress oligomycin production directly through the respective pathway-specific activator genes, aveR and olmRI/RII. To the best of our knowledge, this report describes the first experimental evidence demonstrating that GlnR regulates antibiotic biosynthesis directly through pathway-specific regulators in Streptomyces. Our results suggest that GlnR-mediated regulation of antibiotic biosynthesis is likely to be universal in streptomycetes. These findings also indicate that GlnR is not only a master nitrogen regulator but also an important controller of secondary metabolism, which may help to balance nitrogen metabolism and antibiotic biosynthesis in streptomycetes.
机译:GlnR是类OmpR的孤儿两组分系统响应调节剂,是链霉菌属中氮代谢的主要调节剂。在这项工作中,提供了GlnR也直接参与抗生素生物合成调节的证据。在模型菌株coelicolor M145链霉菌中,在框架内缺失glnR会导致放线菌丝蛋白(ACT)产量显着增加,但暴露于R2YE培养基时十一碳黄酮素(RED)的生物合成减少。转录分析与DNA结合研究表明,GlnR分别通过途径特异性激活基因actII-ORF4和redZ直接抑制ACT,但直接激活RED的产生。定义了这两个靶基因上游的精确GlnR结合位点。另外,在阿维链霉菌中进一步鉴定出GlnR直接参与抗生素的生物合成,这产生了重要的驱虫剂阿维菌素。我们发现阿维链霉菌GlnR(GlnRsav)可以刺激阿维菌素,但直接通过各自的途径特异性激活基因aveR和olmRI / RII抑制寡霉素的产生。据我们所知,本报告描述了第一个实验证据,表明GlnR通过链霉菌中的途径特异性调节剂直接调节抗生素的生物合成。我们的结果表明,GlnR介导的抗生素生物合成调控可能在链霉菌中普遍存在。这些发现还表明,GlnR不仅是氮的主要调节剂,而且还是次级代谢的重要控制器,这可能有助于平衡链霉菌中的氮代谢和抗生素的生物合成。

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