2011
DOI: 10.18388/abp.2011_2278
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Prokaryotic toxin-antitoxin systems--the role in bacterial physiology and application in molecular biology.

Abstract: Bacteria have developed multiple complex mechanisms ensuring an adequate response to environmental changes. In this context, bacterial cell division and growth are subject to strict control to ensure metabolic balance and cell survival. A plethora of studies cast light on toxin-antitoxin (TA) systems as metabolism regulators acting in response to environmental stress conditions. Many of those studies suggest direct relations between the TA systems and the pathogenic potential or antibiotic resistance of releva… Show more

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Cited by 48 publications
(40 citation statements)
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“…A putative toxin-antitoxin cassette was found. These cassettes can play a role in the stabilization of foreign DNA, such as plasmids [40]. They have also been shown to contribute to stress resistance and the persister phenotype [41].…”
Section: Resultsmentioning
confidence: 99%
“…A putative toxin-antitoxin cassette was found. These cassettes can play a role in the stabilization of foreign DNA, such as plasmids [40]. They have also been shown to contribute to stress resistance and the persister phenotype [41].…”
Section: Resultsmentioning
confidence: 99%
“…There are many excellent reviews covering the physiological functions of TA systems [7,8,27-30], their role in stress response [31,32], their mechanism of action [33], their structures [34,35], their involvement in multicellular bacterial behavior [36], their induction by antibiotics [37], their applications in biotechnology [38,39], or some combination thereof [40-43]; these aspects of TA systems will not be discussed here. This review will focus on recent experiments aimed at exploitation of TA systems as an antibacterial strategy and challenges therein.…”
Section: Toxin-antitoxin Systems and The Induction Of Bacterial Cell mentioning
confidence: 99%
“…Herein, we report a novel screening method for protein‐splicing activity in cis and in trans , in which productive protein splicing is selected by cell growth. In this system, we exploit the CcdA/CcdB type II toxin/antitoxin system from Escherichia coli , which has been used for the selection of positive clones during gene cloning (Figure A) . The toxic effect of CcdB, a potent poison of the A subunit of topoisomerase II gyrase A, can be neutralized by complexation with the antitoxin CcdA; this rejuvenates CcdB‐gyrase A complexes through allosteric regulation .…”
Section: Figurementioning
confidence: 99%