| Literature DB >> 27875313 |
Juan-Mei He1,2, Hong Zhu1, Guo-Song Zheng1, Pan-Pan Liu1, Jin Wang1, Guo-Ping Zhao1, Guo-Qiang Zhu3, Wei-Hong Jiang4,5, Yin-Hua Lu6,7.
Abstract
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.Entities:
Keywords: actinobacteria; gene regulation; nitrogen metabolism; secondary metabolism; transcription regulation
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Year: 2016 PMID: 27875313 PMCID: PMC5159505 DOI: 10.1074/jbc.M116.762476
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157