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在呼吸抑制条件下,主要的环磷酸腺苷受体蛋白MSMEG_6189在结核分枝杆菌中诱导编码喹啉氧化酶的操纵子。

Induction of the Operon Encoding the Quinol Oxidase Under Respiration-Inhibitory Conditions by the Major cAMP Receptor Protein MSMEG_6189 in .

作者信息

Ko Eon-Min, Oh Jeong-Il

机构信息

Department of Integrated Biological Science, Pusan National University, Busan, South Korea.

出版信息

Front Microbiol. 2020 Nov 30;11:608624. doi: 10.3389/fmicb.2020.608624. eCollection 2020.

Abstract

The respiratory electron transport chain (ETC) of is terminated with two terminal oxidases, the cytochrome oxidase and the cytochrome quinol oxidase. The quinol oxidase with a higher binding affinity for O than the oxidase is known to play an important role in aerobic respiration under oxygen-limiting conditions. Using relevant () and () mutant strains of , we demonstrated that Crp1 plays a predominant role in induction of the operon under ETC-inhibitory conditions. Two Crp-binding sequences were identified upstream of the gene, both of which are necessary for induction of expression under ETC-inhibitory conditions. The intracellular level of cAMP in was found to be increased under ETC-inhibitory conditions. The gene was found to be negatively regulated by Crp1 and Crp2, which appears to lead to significantly low cellular abundance of Crp2 relative to Crp1 in . Our RNA sequencing analyses suggest that in addition to the SigF partner switching system, Crp1 is involved in induction of gene expression in exposed to ETC-inhibitory conditions.

摘要

的呼吸电子传递链(ETC)由两种末端氧化酶终止,即细胞色素氧化酶和细胞色素喹啉氧化酶。已知对O的结合亲和力高于氧化酶的喹啉氧化酶在氧气限制条件下的有氧呼吸中起重要作用。使用相关的()和()突变菌株,我们证明Crp1在ETC抑制条件下的操纵子诱导中起主要作用。在基因上游鉴定出两个Crp结合序列,这两个序列对于ETC抑制条件下的表达诱导都是必需的。发现在ETC抑制条件下细胞内cAMP水平升高。发现基因受Crp1和Crp2负调控,这似乎导致相对于中的Crp1,Crp2的细胞丰度显著降低。我们的RNA测序分析表明,除了SigF伴侣切换系统外,Crp1还参与了暴露于ETC抑制条件下的基因表达诱导。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/226b/7739888/d442a193a9ce/fmicb-11-608624-g0001.jpg

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