| Literature DB >> 30372528 |
Xiaodong Chi1, Yunqing Chang2,3, Mengmiao Li1, Jin Lin1, Yi Liu2, Chuanyou Li2, Shenjie Tang3, Junjie Zhang1.
Abstract
Toxin-antitoxin (TA) systems are regarded as genetic modules that facilitate bacterial survival under stress conditions. In this study, a novel TA system in Mycobacterium tuberculosis H37Rv chromosome was identified, termed as mt-PemIK, which consists of antitoxin mt-PemI and toxin mt-PemK (Rv3098A). Induction of mt-PemK leads to growth arrest in Mycobacterium smegmatis, while the toxic effect of mt-PemK is eliminated by co-expression of mt-PemI. mt-PemK is characterized as an endoribonuclease whose activity is pH-dependent. mt-PemK, as well as some other M. tuberculosis toxin/antitoxin proteins, can be modified by pupylation, suggesting that the Pup-proteasome system is involved in the regulation of TA systems. These results are helpful to understand the mechanisms of M. tuberculosis growth regulation under stress conditions.Entities:
Keywords: zzm321990Mycobacterium tuberculosiszzm321990; mt-PemK (Rv3098A); pupylation; toxin-antitoxin system
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Year: 2018 PMID: 30372528 DOI: 10.1002/1873-3468.13280
Source DB: PubMed Journal: FEBS Lett ISSN: 0014-5793 Impact factor: 4.124