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Coupling Novel Probes with Molecular Localization Microscopy Reveals Cell Wall Homeostatic Mechanisms in Staphylococcus aureus
[Image: see text] Bacterial cell wall peptidoglycan is essential for viability, and its synthesis is targeted by antibiotics, including penicillin. To determine how peptidoglycan homeostasis controls cell architecture, growth, and division, we have developed novel labeling approaches. These are comp...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9764285/ https://www.ncbi.nlm.nih.gov/pubmed/36414253 http://dx.doi.org/10.1021/acschembio.2c00741 |
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author | Lund, Victoria A. Gangotra, Haneesh Zhao, Zhen Sutton, Joshua A. F. Wacnik, Katarzyna DeMeester, Kristen Liang, Hai Santiago, Cintia Leimkuhler Grimes, Catherine Jones, Simon Foster, Simon J. |
author_facet | Lund, Victoria A. Gangotra, Haneesh Zhao, Zhen Sutton, Joshua A. F. Wacnik, Katarzyna DeMeester, Kristen Liang, Hai Santiago, Cintia Leimkuhler Grimes, Catherine Jones, Simon Foster, Simon J. |
author_sort | Lund, Victoria A. |
collection | PubMed |
description | [Image: see text] Bacterial cell wall peptidoglycan is essential for viability, and its synthesis is targeted by antibiotics, including penicillin. To determine how peptidoglycan homeostasis controls cell architecture, growth, and division, we have developed novel labeling approaches. These are compatible with super-resolution fluorescence microscopy to examine peptidoglycan synthesis, hydrolysis, and the localization of the enzymes required for its biosynthesis (penicillin binding proteins (PBPs)). Synthesis of a cephalosporin-based fluorescent probe revealed a pattern of PBPs at the septum during division, supporting a model of dispersed peptidoglycan synthesis. Metabolic and hydroxylamine-based probes respectively enabled the synthesis of glycan strands and associated reducing termini of the peptidoglycan to be mapped. Foci and arcs of reducing termini appear as a result of both synthesis of glycan strands and glucosaminidase activity of the major peptidoglycan hydrolase, SagB. Our studies provide molecular level details of how essential peptidoglycan dynamics are controlled during growth and division. |
format | Online Article Text |
id | pubmed-9764285 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-97642852022-12-21 Coupling Novel Probes with Molecular Localization Microscopy Reveals Cell Wall Homeostatic Mechanisms in Staphylococcus aureus Lund, Victoria A. Gangotra, Haneesh Zhao, Zhen Sutton, Joshua A. F. Wacnik, Katarzyna DeMeester, Kristen Liang, Hai Santiago, Cintia Leimkuhler Grimes, Catherine Jones, Simon Foster, Simon J. ACS Chem Biol [Image: see text] Bacterial cell wall peptidoglycan is essential for viability, and its synthesis is targeted by antibiotics, including penicillin. To determine how peptidoglycan homeostasis controls cell architecture, growth, and division, we have developed novel labeling approaches. These are compatible with super-resolution fluorescence microscopy to examine peptidoglycan synthesis, hydrolysis, and the localization of the enzymes required for its biosynthesis (penicillin binding proteins (PBPs)). Synthesis of a cephalosporin-based fluorescent probe revealed a pattern of PBPs at the septum during division, supporting a model of dispersed peptidoglycan synthesis. Metabolic and hydroxylamine-based probes respectively enabled the synthesis of glycan strands and associated reducing termini of the peptidoglycan to be mapped. Foci and arcs of reducing termini appear as a result of both synthesis of glycan strands and glucosaminidase activity of the major peptidoglycan hydrolase, SagB. Our studies provide molecular level details of how essential peptidoglycan dynamics are controlled during growth and division. American Chemical Society 2022-11-22 2022-12-16 /pmc/articles/PMC9764285/ /pubmed/36414253 http://dx.doi.org/10.1021/acschembio.2c00741 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Lund, Victoria A. Gangotra, Haneesh Zhao, Zhen Sutton, Joshua A. F. Wacnik, Katarzyna DeMeester, Kristen Liang, Hai Santiago, Cintia Leimkuhler Grimes, Catherine Jones, Simon Foster, Simon J. Coupling Novel Probes with Molecular Localization Microscopy Reveals Cell Wall Homeostatic Mechanisms in Staphylococcus aureus |
title | Coupling Novel
Probes with Molecular Localization
Microscopy Reveals Cell Wall Homeostatic Mechanisms in Staphylococcus
aureus |
title_full | Coupling Novel
Probes with Molecular Localization
Microscopy Reveals Cell Wall Homeostatic Mechanisms in Staphylococcus
aureus |
title_fullStr | Coupling Novel
Probes with Molecular Localization
Microscopy Reveals Cell Wall Homeostatic Mechanisms in Staphylococcus
aureus |
title_full_unstemmed | Coupling Novel
Probes with Molecular Localization
Microscopy Reveals Cell Wall Homeostatic Mechanisms in Staphylococcus
aureus |
title_short | Coupling Novel
Probes with Molecular Localization
Microscopy Reveals Cell Wall Homeostatic Mechanisms in Staphylococcus
aureus |
title_sort | coupling novel
probes with molecular localization
microscopy reveals cell wall homeostatic mechanisms in staphylococcus
aureus |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9764285/ https://www.ncbi.nlm.nih.gov/pubmed/36414253 http://dx.doi.org/10.1021/acschembio.2c00741 |
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