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在天蓝色链霉菌中,麦角硫因受硫醇特异性抗西格玛因子RsrA和西格玛(R)调节,并对其产生调控作用。

Mycothiol regulates and is regulated by a thiol-specific antisigma factor RsrA and sigma(R) in Streptomyces coelicolor.

作者信息

Park Joo-Hong, Roe Jung-Hye

机构信息

School of Biological Sciences and Institute of Microbiology, Seoul National University, Seoul 151-742, Korea.

出版信息

Mol Microbiol. 2008 May;68(4):861-70. doi: 10.1111/j.1365-2958.2008.06191.x.

Abstract

Mycothiol (MSH) is a small thiol molecule with a cysteine-ligated disaccharide structure found in actinomycetes that include streptomycetes and mycobacteria. In Streptomyces coelicolor, a model organism for antibiotic production and differentiation, the amount of MSH is under the control of a sigma factor sigma(R), which is regulated by an antisigma factor RsrA with a thiol-disulphide redox switch. We found that the first gene (mshA) in the biosynthetic pathway for MSH and the gene for amidase (mca) that participates in detoxifying mycothiol-reactive drugs are under direct control of sigma(R). The sigma(R) target genes are induced not only by a thiol oxidant diamide, but also by alkylating agents that cause a rapid decrease in MSH. Expression of the sigma(R) regulon was also elevated in MSH-deficient mutants, suggesting that a decrease in the level of MSH is a natural intracellular trigger for sigma(R) activation. We found that MSH was capable of reducing RsrA to bind sigma(R), whereas glutathione was not. These results support a proposal that the RsrA-sigma(R) system senses the intracellular level of reduced MSH, and that MSH serves as a natural modulator of the transcription system for its own replenishment in addition to being a redox buffer and drug detoxifier.

摘要

巯基乙醇(MSH)是一种具有半胱氨酸连接二糖结构的小分子硫醇,存在于包括链霉菌和分枝杆菌在内的放线菌中。在作为抗生素生产和分化模式生物的天蓝色链霉菌中,MSH的含量受σ因子σ(R)的控制,而σ(R)由具有硫醇-二硫键氧化还原开关的抗σ因子RsrA调节。我们发现,MSH生物合成途径中的第一个基因(mshA)和参与解毒与巯基乙醇反应性药物的酰胺酶基因(mca)直接受σ(R)的控制。σ(R)靶基因不仅由硫醇氧化剂二酰胺诱导,还由导致MSH迅速减少的烷基化剂诱导。在MSH缺陷型突变体中,σ(R)调控子的表达也升高,这表明MSH水平的降低是σ(R)激活的天然细胞内触发因素。我们发现,MSH能够还原RsrA以结合σ(R),而谷胱甘肽则不能。这些结果支持了一种观点,即RsrA-σ(R)系统感知细胞内还原型MSH的水平,并且MSH除了作为氧化还原缓冲剂和药物解毒剂外,还作为其自身补充的转录系统的天然调节剂。

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