Toxin–antitoxin (TA) systems are genetic modules composed of a toxin interfering with cellular processes and its cognate antitoxin, which counteracts the activity of the toxin. TA modules are widespread in bacterial and archaeal genomes. It has been suggested that TA modules participate in the adaptation of prokaryotes to unfavorable conditions. The Bosea sp. PAMC 26642 used in this study was isolated from the Arctic lichen Stereocaulon sp. There are 12 putative type II TA loci in the genome of Bosea sp. PAMC 26642. Of these, nine functional TA systems have been shown to be toxic in Escherichia coli. The toxin inhibits growth, but this inhibition is reversed when the cognate antitoxin genes are coexpressed, indicating that these putative TA loci were bona fide TA modules. Only the BoVapC1 (AXW83_01405) toxin, a homolog of VapC, showed growth inhibition specific to low temperatures, which was recovered by the coexpression of BoVapB1 (AXW83_01400). Microscopic observation and growth monitoring revealed that the BoVapC1 toxin had bacteriostatic effects on the growth of E. coli and induced morphological changes. Quantitative real time polymerase chain reaction and northern blotting analyses showed that the BoVapC1 toxin had a ribonuclease activity on the initiator tRNAfMet, implying that degradation of tRNAfMet might trigger growth arrest in E. coli. Furthermore, the BoVapBC1 system was found to contribute to survival against prolonged exposure at 4°C. This is the first study to identify the function of TA systems in cold adaptation.
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机译:毒素-抗毒素 (TA) 系统是由干扰细胞过程的毒素及其同源抗毒素组成的遗传模块,后者抵消毒素的活性。TA 模块广泛存在于细菌和古细菌基因组中。有人提出 TA 模块参与原核生物对不利条件的适应。本研究中使用的 Bosea sp. PAMC 26642 是从北极地衣 Stereocaulon sp. 中分离出来的。Bosea sp. PAMC 26642 的基因组中有 12 个推定的 II 型 TA 位点。其中,9 个功能性 TA 系统已被证明在大肠杆菌中具有毒性。毒素抑制生长,但当同源抗毒素基因共表达时,这种抑制会逆转,表明这些推定的 TA 基因座是真正的 TA 模块。只有 BoVapC1 (AXW83_01405) 毒素(VapC 的同源物)显示出低温特异性的生长抑制,可通过 BoVapB1 (AXW83_01400) 的共表达恢复。显微镜观察和生长监测显示,BoVapC1 毒素对大肠杆菌的生长具有抑菌作用,并诱导形态变化。定量实时聚合酶链反应和 Northern 印迹分析显示,BoVapC1 毒素对起始体 tRNAfMet 具有核糖核酸酶活性,这意味着 tRNAfMet 的降解可能触发大肠杆菌的生长停滞。此外,发现 BoVapBC1 系统有助于在 4°C 下长时间暴露的存活率。这是第一项确定 TA 系统在冷适应中功能的研究。
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