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https://doi.org/10.7554/eLife.37516
Title: | Maturing Mycobacterium smegmatis peptidoglycan requires non-canonical crosslinks to maintain shape | Authors: | Baranowski, C Welsh, M.A Sham, L.-T Eskandarian, H.A Lim, H.C Kieser, K.J Wagner, J.C McKinney, J.D Fantner, G.E Ioerger, T.R Walker, S Bernhardt, T.G Rubin, E.J Rego, E.H |
Keywords: | amoxicillin amoxicillin plus clavulanic acid beta lactam binding protein carbapenem carboxypeptidase D carboxypeptidase transpeptidase hygromycin meropenem peptidoglycan amino acid aminoacyltransferase amoxicillin cross linking reagent meropenem penicillin binding protein peptidoglycan peptidoglycan transpeptidase Agrobacterium tumefaciens Article atomic force microscopy bacterial strain bacterium culture canonical analysis cell division controlled study CRISPR Cas system cross linking daughter cell Escherichia coli fluorescence fluorescence activated cell sorting fractional anisotropy genetic analysis genetic linkage genetic manipulation MIC50 microscopy minimum inhibitory concentration morphological trait Mycobacterium smegmatis nonhuman organelle shape osmolarity polymerization population protein expression real time polymerase chain reaction sequence analysis single cell analysis sputum analysis time-lapse microscopy tuberculosis Bacillus biological model cell wall chemistry drug effect kinetics metabolism microbial viability Mycobacterium smegmatis Amino Acids Aminoacyltransferases Amoxicillin Bacillus Cell Wall Cross-Linking Reagents Escherichia coli Fluorescence Kinetics Meropenem Microbial Viability Models, Biological Mycobacterium smegmatis Penicillin-Binding Proteins Peptidoglycan |
Issue Date: | 2018 | Citation: | Baranowski, C, Welsh, M.A, Sham, L.-T, Eskandarian, H.A, Lim, H.C, Kieser, K.J, Wagner, J.C, McKinney, J.D, Fantner, G.E, Ioerger, T.R, Walker, S, Bernhardt, T.G, Rubin, E.J, Rego, E.H (2018). Maturing Mycobacterium smegmatis peptidoglycan requires non-canonical crosslinks to maintain shape. eLife 7 : e37516. ScholarBank@NUS Repository. https://doi.org/10.7554/eLife.37516 | Rights: | Attribution 4.0 International | Abstract: | In most well-studied rod-shaped bacteria, peptidoglycan is primarily crosslinked by penicillin-binding proteins (PBPs). However, in mycobacteria, crosslinks formed by L,D-transpeptidases (LDTs) are highly abundant. To elucidate the role of these unusual crosslinks, we characterized Mycobacterium smegmatis cells lacking all LDTs. We find that crosslinks generate by LDTs are required for rod shape maintenance specifically at sites of aging cell wall, a byproduct of polar elongation. Asymmetric polar growth leads to a non-uniform distribution of these two types of crosslinks in a single cell. Consequently, in the absence of LDT-mediated crosslinks, PBP-catalyzed crosslinks become more important. Because of this, Mycobacterium tuberculosis (Mtb) is more rapidly killed using a combination of drugs capable of PBP-and LDT-inhibition. Thus, knowledge about the spatial and genetic relationship between drug targets can be exploited to more effectively treat this pathogen. © Baranowski et al. | Source Title: | eLife | URI: | https://scholarbank.nus.edu.sg/handle/10635/177836 | ISSN: | 2050084X | DOI: | 10.7554/eLife.37516 | Rights: | Attribution 4.0 International |
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