Distinct Spatiotemporal Dynamics of Peptidoglycan Synthesis between Mycobacterium smegmatis and Mycobacterium tuberculosis

Peptidoglycan (PG), a polymer cross-linked by d-amino acid-containing peptides, is an essential component of the bacterial cell wall. We found that a fluorescent d-alanine analog (FDAA) incorporates chiefly at one of the two poles in Mycobacterium smegmatis but that polar dominance varies as a funct...

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Main Authors: Helene Botella, Guangli Yang, Ouathek Ouerfelli, Sabine Ehrt, Carl F. Nathan, Julien Vaubourgeix, Christina L. Stallings
Format: Article
Language:English
Published: American Society for Microbiology 2017-09-01
Series:mBio
Online Access:http://mbio.asm.org/cgi/content/full/8/5/e01183-17
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spelling doaj-de4915c0aecf4598b70aa31443a9ba9a2021-07-02T07:27:12ZengAmerican Society for MicrobiologymBio2150-75112017-09-0185e01183-1710.1128/mBio.01183-17Distinct Spatiotemporal Dynamics of Peptidoglycan Synthesis between Mycobacterium smegmatis and Mycobacterium tuberculosisHelene BotellaGuangli YangOuathek OuerfelliSabine EhrtCarl F. NathanJulien VaubourgeixChristina L. StallingsPeptidoglycan (PG), a polymer cross-linked by d-amino acid-containing peptides, is an essential component of the bacterial cell wall. We found that a fluorescent d-alanine analog (FDAA) incorporates chiefly at one of the two poles in Mycobacterium smegmatis but that polar dominance varies as a function of the cell cycle in Mycobacterium tuberculosis: immediately after cytokinesis, FDAAs are incorporated chiefly at one of the two poles, but just before cytokinesis, FDAAs are incorporated comparably at both. These observations suggest that mycobacterial PG-synthesizing enzymes are localized in functional compartments at the poles and septum and that the capacity for PG synthesis matures at the new pole in M. tuberculosis. Deeper knowledge of the biology of mycobacterial PG synthesis may help in discovering drugs that disable previously unappreciated steps in the process.http://mbio.asm.org/cgi/content/full/8/5/e01183-17
collection DOAJ
language English
format Article
sources DOAJ
author Helene Botella
Guangli Yang
Ouathek Ouerfelli
Sabine Ehrt
Carl F. Nathan
Julien Vaubourgeix
Christina L. Stallings
spellingShingle Helene Botella
Guangli Yang
Ouathek Ouerfelli
Sabine Ehrt
Carl F. Nathan
Julien Vaubourgeix
Christina L. Stallings
Distinct Spatiotemporal Dynamics of Peptidoglycan Synthesis between Mycobacterium smegmatis and Mycobacterium tuberculosis
mBio
author_facet Helene Botella
Guangli Yang
Ouathek Ouerfelli
Sabine Ehrt
Carl F. Nathan
Julien Vaubourgeix
Christina L. Stallings
author_sort Helene Botella
title Distinct Spatiotemporal Dynamics of Peptidoglycan Synthesis between Mycobacterium smegmatis and Mycobacterium tuberculosis
title_short Distinct Spatiotemporal Dynamics of Peptidoglycan Synthesis between Mycobacterium smegmatis and Mycobacterium tuberculosis
title_full Distinct Spatiotemporal Dynamics of Peptidoglycan Synthesis between Mycobacterium smegmatis and Mycobacterium tuberculosis
title_fullStr Distinct Spatiotemporal Dynamics of Peptidoglycan Synthesis between Mycobacterium smegmatis and Mycobacterium tuberculosis
title_full_unstemmed Distinct Spatiotemporal Dynamics of Peptidoglycan Synthesis between Mycobacterium smegmatis and Mycobacterium tuberculosis
title_sort distinct spatiotemporal dynamics of peptidoglycan synthesis between mycobacterium smegmatis and mycobacterium tuberculosis
publisher American Society for Microbiology
series mBio
issn 2150-7511
publishDate 2017-09-01
description Peptidoglycan (PG), a polymer cross-linked by d-amino acid-containing peptides, is an essential component of the bacterial cell wall. We found that a fluorescent d-alanine analog (FDAA) incorporates chiefly at one of the two poles in Mycobacterium smegmatis but that polar dominance varies as a function of the cell cycle in Mycobacterium tuberculosis: immediately after cytokinesis, FDAAs are incorporated chiefly at one of the two poles, but just before cytokinesis, FDAAs are incorporated comparably at both. These observations suggest that mycobacterial PG-synthesizing enzymes are localized in functional compartments at the poles and septum and that the capacity for PG synthesis matures at the new pole in M. tuberculosis. Deeper knowledge of the biology of mycobacterial PG synthesis may help in discovering drugs that disable previously unappreciated steps in the process.
url http://mbio.asm.org/cgi/content/full/8/5/e01183-17
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