Please use this identifier to cite or link to this item: 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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