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Microbiology 154 (2008), 2776-2785; DOI  10.1099/mic.0.2008/019638-0
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Microbiology 154 (2008), 2776-2785; DOI  10.1099/mic.0.2008/019638-0
© 2008 Society for General Microbiology

Important role of the nucleotide excision repair pathway in Mycobacterium smegmatis in conferring protection against commonly encountered DNA-damaging agents

Krishna Kurthkoti, Pradeep Kumar, Ruchi Jain and Umesh Varshney

Department of Microbiology and Cell Biology, Indian Institute of Science, Bangalore 560012, India

Correspondence
Umesh Varshney
varshney{at}mcbl.iisc.ernet.in
or
uvarshney{at}gmail.com

Mycobacteria are an important group of human pathogens. Although the DNA repair mechanisms in mycobacteria are not well understood, these are vital for the pathogen's persistence in the host macrophages. In this study, we generated a null mutation in the uvrB gene of Mycobacterium smegmatis to allow us to compare the significance of the nucleotide excision repair (NER) pathway with two important base excision repair pathways, initiated by uracil DNA glycosylase (Ung) and formamidopyrimidine DNA glycosylase (Fpg or MutM), in an isogenic strain background. The strain deficient in NER was the most sensitive to commonly encountered DNA-damaging agents such as UV, low pH, reactive oxygen species, hypoxia, and was also sensitive to acidified nitrite. Taken together with previous observations on NER-deficient M. tuberculosis, these results suggest that NER is an important DNA repair pathway in mycobacteria.


Abbreviations: BER, base excision repair; NER, nucleotide excision repair; RNI, reactive nitrogen intermediates; ROS, reactive oxygen species







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