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Functional characterization of HigBA toxin-antitoxin system in an Arctic bacterium, Bosea sp. PAMC 26642
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Functional characterization of HigBA toxin-antitoxin system in an Arctic bacterium, Bosea sp. PAMC 26642
Eunsil Choi 1,2, Ahhyun Huh 1, Changmin Oh 1, Jeong-Il Oh 1,2, Ho Young Kang 1,2, Jihwan Hwang 1,2
Journal of Microbiology 2022;60(2):192-206
DOI: https://doi.org/10.1007/s12275-022-1619-9
Published online: February 1, 2022
1Department of Microbiology, Pusan National University, Busan 46241, Republic of Korea, 2Microbiological Resource Research Institute, Pusan National University, Busan 46241, Republic of Korea1Department of Microbiology, Pusan National University, Busan 46241, Republic of Korea, 2Microbiological Resource Research Institute, Pusan National University, Busan 46241, Republic of Korea
Corresponding author:  Jihwan Hwang , Tel: +82-51-510-2194;, 
Received: 29 November 2021   • Revised: 15 December 2021   • Accepted: 20 December 2021
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Toxin-antitoxin (TA) systems are growth-controlling genetic elements consisting of an intracellular toxin protein and its cognate antitoxin. TA systems have been spread among microbial genomes through horizontal gene transfer and are now prevalent in most bacterial and archaeal genomes. Under normal growth conditions, antitoxins tightly counteract the activity of the toxins. Upon stresses, antitoxins are inactivated, releasing activated toxins, which induce growth arrest or cell death. In this study, among nine functional TA modules in Bosea sp. PAMC 26642 living in Arctic lichen, we investigated the functionality of BoHigBA2. BohigBA2 is located close to a genomic island and adjacent to flagellar gene clusters. The expression of BohigB2 induced the inhibition of E. coli growth at 37°C, which was more manifest at 18°C, and this growth defect was reversed when BohigA2 was co-expressed, suggesting that this BoHigBA2 module might be an active TA module in Bosea sp. PAMC 26642. Live/dead staining and viable count analyses revealed that the BoHigB2 toxin had a bactericidal effect, causing cell death. Furthermore, we demonstrated that BoHigB2 possessed mRNA-specific ribonuclease activity on various mRNAs and cleaved only mRNAs being translated, which might impede overall translation and consequently lead to cell death. Our study provides the insight to understand the cold adaptation of Bosea sp. PAMC 26642 living in the Arctic.

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    Functional characterization of HigBA toxin-antitoxin system in an Arctic bacterium, Bosea sp. PAMC 26642
    J. Microbiol. 2022;60(2):192-206.   Published online February 1, 2022
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