Please use this identifier to cite or link to this item: http://buratest.brunel.ac.uk/handle/2438/7720
Title: Characterisation of ATP-dependent Mur Ligases involved in the biogenesis of cell wall Peptidoglycan in Mycobacterium tuberculosis
Authors: Munshi, T
Gupta, A
Evangelopoulos, D
Guzman, JD
Keep, NH
Bhakta, S
Gibbons, S
Issue Date: 2013
Publisher: Public Library of Science
Citation: PLoS one, 8(3), e60143, 2013
Abstract: ATP-dependent Mur ligases (Mur synthetases) play essential roles in the biosynthesis of cell wall peptidoglycan (PG) as they catalyze the ligation of key amino acid residues to the stem peptide at the expense of ATP hydrolysis, thus representing potential targets for antibacterial drug discovery. In this study we characterized the division/cell wall (dcw) operon and identified a promoter driving the co-transcription of mur synthetases along with key cell division genes such as ftsQ and ftsW. Furthermore, we have extended our previous investigations of MurE to MurC, MurD and MurF synthetases from Mycobacterium tuberculosis. Functional analyses of the pure recombinant enzymes revealed that the presence of divalent cations is an absolute requirement for their activities. We also observed that higher concentrations of ATP and UDP-sugar substrates were inhibitory for the activities of all Mur synthetases suggesting stringent control of the cytoplasmic steps of the peptidoglycan biosynthetic pathway. In line with the previous findings on the regulation of mycobacterial MurD and corynebacterial MurC synthetases via phosphorylation, we found that all of the Mur synthetases interacted with the Ser/Thr protein kinases, PknA and PknB. In addition, we critically analyzed the interaction network of all of the Mur synthetases with proteins involved in cell division and cell wall PG biosynthesis to re-evaluate the importance of these key enzymes as novel therapeutic targets in anti-tubercular drug discovery. © 2013 Munshi et al.
Description: © 2013 Munshi et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
URI: http://bura.brunel.ac.uk/handle/2438/7720
DOI: http://dx.doi.org/10.1371/journal.pone.0060143
ISSN: 1932-6203
Appears in Collections:Biological Sciences
Publications
Dept of Life Sciences Research Papers

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