Cargando…
Regulation of peptidoglycan synthesis by outer membrane proteins
Growth of the meshlike peptidoglycan (PG) sacculus located between the bacterial inner and outer membranes (OM) is tightly regulated to ensure cellular integrity, maintain cell shape and orchestrate division. Cytoskeletal elements direct placement and activity of PG synthases from inside the cell bu...
Autores principales: | , , , , , , , , , , , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
2010
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3060616/ https://www.ncbi.nlm.nih.gov/pubmed/21183073 http://dx.doi.org/10.1016/j.cell.2010.11.038 |
_version_ | 1782200523892457472 |
---|---|
author | Typas, Athanasios Banzhaf, Manuel van den Berg van Saparoea, Bart Verheul, Jolanda Biboy, Jacob Nichols, Robert J. Zietek, Matylda Beilharz, Katrin Kannenberg, Kai von Rechenberg, Moritz Breukink, Eefjan den Blaauwen, Tanneke Gross, Carol A. Vollmer, Waldemar |
author_facet | Typas, Athanasios Banzhaf, Manuel van den Berg van Saparoea, Bart Verheul, Jolanda Biboy, Jacob Nichols, Robert J. Zietek, Matylda Beilharz, Katrin Kannenberg, Kai von Rechenberg, Moritz Breukink, Eefjan den Blaauwen, Tanneke Gross, Carol A. Vollmer, Waldemar |
author_sort | Typas, Athanasios |
collection | PubMed |
description | Growth of the meshlike peptidoglycan (PG) sacculus located between the bacterial inner and outer membranes (OM) is tightly regulated to ensure cellular integrity, maintain cell shape and orchestrate division. Cytoskeletal elements direct placement and activity of PG synthases from inside the cell but precise spatiotemporal control over this process is poorly understood. We demonstrate that PG synthases are also controlled from outside the sacculus. Two OM lipoproteins, LpoA and LpoB, are essential for the function respectively of PBP1A and PBP1B, the major E. coli bifunctional PG synthases. Each Lpo protein binds specifically to its cognate PBP and stimulates its transpeptidase activity, thereby facilitating attachment of new PG to the sacculus. LpoB shows partial septal localization and our data suggest that the LpoB-PBP1B complex contributes to OM constriction during cell division. LpoA/ LpoB and their PBP docking regions are restricted to γ-proteobacteria, providing models for niche-specific regulation of sacculus growth. |
format | Text |
id | pubmed-3060616 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
record_format | MEDLINE/PubMed |
spelling | pubmed-30606162011-12-23 Regulation of peptidoglycan synthesis by outer membrane proteins Typas, Athanasios Banzhaf, Manuel van den Berg van Saparoea, Bart Verheul, Jolanda Biboy, Jacob Nichols, Robert J. Zietek, Matylda Beilharz, Katrin Kannenberg, Kai von Rechenberg, Moritz Breukink, Eefjan den Blaauwen, Tanneke Gross, Carol A. Vollmer, Waldemar Cell Article Growth of the meshlike peptidoglycan (PG) sacculus located between the bacterial inner and outer membranes (OM) is tightly regulated to ensure cellular integrity, maintain cell shape and orchestrate division. Cytoskeletal elements direct placement and activity of PG synthases from inside the cell but precise spatiotemporal control over this process is poorly understood. We demonstrate that PG synthases are also controlled from outside the sacculus. Two OM lipoproteins, LpoA and LpoB, are essential for the function respectively of PBP1A and PBP1B, the major E. coli bifunctional PG synthases. Each Lpo protein binds specifically to its cognate PBP and stimulates its transpeptidase activity, thereby facilitating attachment of new PG to the sacculus. LpoB shows partial septal localization and our data suggest that the LpoB-PBP1B complex contributes to OM constriction during cell division. LpoA/ LpoB and their PBP docking regions are restricted to γ-proteobacteria, providing models for niche-specific regulation of sacculus growth. 2010-12-23 /pmc/articles/PMC3060616/ /pubmed/21183073 http://dx.doi.org/10.1016/j.cell.2010.11.038 Text en https://creativecommons.org/licenses/by/3.0/ Open Access under CC BY 3.0 (https://creativecommons.org/licenses/by/3.0/) license. |
spellingShingle | Article Typas, Athanasios Banzhaf, Manuel van den Berg van Saparoea, Bart Verheul, Jolanda Biboy, Jacob Nichols, Robert J. Zietek, Matylda Beilharz, Katrin Kannenberg, Kai von Rechenberg, Moritz Breukink, Eefjan den Blaauwen, Tanneke Gross, Carol A. Vollmer, Waldemar Regulation of peptidoglycan synthesis by outer membrane proteins |
title | Regulation of peptidoglycan synthesis by outer membrane
proteins |
title_full | Regulation of peptidoglycan synthesis by outer membrane
proteins |
title_fullStr | Regulation of peptidoglycan synthesis by outer membrane
proteins |
title_full_unstemmed | Regulation of peptidoglycan synthesis by outer membrane
proteins |
title_short | Regulation of peptidoglycan synthesis by outer membrane
proteins |
title_sort | regulation of peptidoglycan synthesis by outer membrane
proteins |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3060616/ https://www.ncbi.nlm.nih.gov/pubmed/21183073 http://dx.doi.org/10.1016/j.cell.2010.11.038 |
work_keys_str_mv | AT typasathanasios regulationofpeptidoglycansynthesisbyoutermembraneproteins AT banzhafmanuel regulationofpeptidoglycansynthesisbyoutermembraneproteins AT vandenbergvansaparoeabart regulationofpeptidoglycansynthesisbyoutermembraneproteins AT verheuljolanda regulationofpeptidoglycansynthesisbyoutermembraneproteins AT biboyjacob regulationofpeptidoglycansynthesisbyoutermembraneproteins AT nicholsrobertj regulationofpeptidoglycansynthesisbyoutermembraneproteins AT zietekmatylda regulationofpeptidoglycansynthesisbyoutermembraneproteins AT beilharzkatrin regulationofpeptidoglycansynthesisbyoutermembraneproteins AT kannenbergkai regulationofpeptidoglycansynthesisbyoutermembraneproteins AT vonrechenbergmoritz regulationofpeptidoglycansynthesisbyoutermembraneproteins AT breukinkeefjan regulationofpeptidoglycansynthesisbyoutermembraneproteins AT denblaauwentanneke regulationofpeptidoglycansynthesisbyoutermembraneproteins AT grosscarola regulationofpeptidoglycansynthesisbyoutermembraneproteins AT vollmerwaldemar regulationofpeptidoglycansynthesisbyoutermembraneproteins |