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OxyR is a key regulator in response to oxidative stress in Streptomyces avermitilis
Author(s) -
Xingchao Liu,
Meng Sun,
Yaqing Cheng,
Renjun Yang,
Ying Wen,
Zhi Chen,
Jilun Li
Publication year - 2016
Publication title -
microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.352
H-Index - 35
eISSN - 1465-2080
pISSN - 1350-0872
DOI - 10.1099/mic.0.000251
Subject(s) - oxidative stress , streptomyces avermitilis , transcription (linguistics) , regulator , transcriptional regulation , transcription factor , biochemistry , mutant , regulation of gene expression , biology , microbiology and biotechnology , oxidative phosphorylation , chemistry , gene , streptomyces , genetics , bacteria , linguistics , philosophy
The role of the H 2 O 2 -sensing transcriptional regulator OxyR in oxidative stress responses in Streptomyces avermitilis was investigated. An oxyR deletion mutant was more sensitive to H 2 O 2 and er -butyl hydroperoxide than was the WT strain, indicating that OxyR mediates the defensive system against H 2 O 2 and organic peroxide. Evidence presented herein suggests that in cells treated with exogenous H 2 O 2 , the oxidized form of OxyR activated expression of ahpCD by binding to a palindromic sequence of the promoter region. Oxidized OxyR also induced expression of other antioxidant enzymes (KatA1, KatA2, KatA3 and OhrB1) and oxidative stress regulators (CatR, OhrR and σ R ). The thiol-oxidative stress regulator gene sigR was regulated at the transcription level by OxyR. We conclude that OxyR is necessary to activate transcription of sigR from the σ R -dependent promoter to express an unstable larger isoform of σ R during oxidative stress. In response to oxidative stress, OxyR facilitates rapid production of H 2 O 2 -scavenging enzymes to repair oxidative damage through direct regulation and cascaded regulation of CatR, OhrR and σ R .

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