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A Cell Cycle and Nutritional Checkpoint Controlling Bacterial Surface Adhesion

In natural environments, bacteria often adhere to surfaces where they form complex multicellular communities. Surface adherence is determined by the biochemical composition of the cell envelope. We describe a novel regulatory mechanism by which the bacterium, Caulobacter crescentus, integrates cell...

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Autores principales: Fiebig, Aretha, Herrou, Julien, Fumeaux, Coralie, Radhakrishnan, Sunish K., Viollier, Patrick H., Crosson, Sean
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3900383/
https://www.ncbi.nlm.nih.gov/pubmed/24465221
http://dx.doi.org/10.1371/journal.pgen.1004101
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author Fiebig, Aretha
Herrou, Julien
Fumeaux, Coralie
Radhakrishnan, Sunish K.
Viollier, Patrick H.
Crosson, Sean
author_facet Fiebig, Aretha
Herrou, Julien
Fumeaux, Coralie
Radhakrishnan, Sunish K.
Viollier, Patrick H.
Crosson, Sean
author_sort Fiebig, Aretha
collection PubMed
description In natural environments, bacteria often adhere to surfaces where they form complex multicellular communities. Surface adherence is determined by the biochemical composition of the cell envelope. We describe a novel regulatory mechanism by which the bacterium, Caulobacter crescentus, integrates cell cycle and nutritional signals to control development of an adhesive envelope structure known as the holdfast. Specifically, we have discovered a 68-residue protein inhibitor of holdfast development (HfiA) that directly targets a conserved glycolipid glycosyltransferase required for holdfast production (HfsJ). Multiple cell cycle regulators associate with the hfiA and hfsJ promoters and control their expression, temporally constraining holdfast development to the late stages of G1. HfiA further functions as part of a ‘nutritional override’ system that decouples holdfast development from the cell cycle in response to nutritional cues. This control mechanism can limit surface adhesion in nutritionally sub-optimal environments without affecting cell cycle progression. We conclude that post-translational regulation of cell envelope enzymes by small proteins like HfiA may provide a general means to modulate the surface properties of bacterial cells.
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spelling pubmed-39003832014-01-24 A Cell Cycle and Nutritional Checkpoint Controlling Bacterial Surface Adhesion Fiebig, Aretha Herrou, Julien Fumeaux, Coralie Radhakrishnan, Sunish K. Viollier, Patrick H. Crosson, Sean PLoS Genet Research Article In natural environments, bacteria often adhere to surfaces where they form complex multicellular communities. Surface adherence is determined by the biochemical composition of the cell envelope. We describe a novel regulatory mechanism by which the bacterium, Caulobacter crescentus, integrates cell cycle and nutritional signals to control development of an adhesive envelope structure known as the holdfast. Specifically, we have discovered a 68-residue protein inhibitor of holdfast development (HfiA) that directly targets a conserved glycolipid glycosyltransferase required for holdfast production (HfsJ). Multiple cell cycle regulators associate with the hfiA and hfsJ promoters and control their expression, temporally constraining holdfast development to the late stages of G1. HfiA further functions as part of a ‘nutritional override’ system that decouples holdfast development from the cell cycle in response to nutritional cues. This control mechanism can limit surface adhesion in nutritionally sub-optimal environments without affecting cell cycle progression. We conclude that post-translational regulation of cell envelope enzymes by small proteins like HfiA may provide a general means to modulate the surface properties of bacterial cells. Public Library of Science 2014-01-23 /pmc/articles/PMC3900383/ /pubmed/24465221 http://dx.doi.org/10.1371/journal.pgen.1004101 Text en © 2014 Fiebig et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Fiebig, Aretha
Herrou, Julien
Fumeaux, Coralie
Radhakrishnan, Sunish K.
Viollier, Patrick H.
Crosson, Sean
A Cell Cycle and Nutritional Checkpoint Controlling Bacterial Surface Adhesion
title A Cell Cycle and Nutritional Checkpoint Controlling Bacterial Surface Adhesion
title_full A Cell Cycle and Nutritional Checkpoint Controlling Bacterial Surface Adhesion
title_fullStr A Cell Cycle and Nutritional Checkpoint Controlling Bacterial Surface Adhesion
title_full_unstemmed A Cell Cycle and Nutritional Checkpoint Controlling Bacterial Surface Adhesion
title_short A Cell Cycle and Nutritional Checkpoint Controlling Bacterial Surface Adhesion
title_sort cell cycle and nutritional checkpoint controlling bacterial surface adhesion
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3900383/
https://www.ncbi.nlm.nih.gov/pubmed/24465221
http://dx.doi.org/10.1371/journal.pgen.1004101
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