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Adaptation in bacterial flagellar and motility systems: from regulon members to ‘foraging’-like behavior in E. coli
Bacterial flagellar motility and chemotaxis help cells to reach the most favorable environments and to successfully compete with other micro-organisms in response to external stimuli. Escherichia coli is a motile gram-negative bacterium, and the flagellar regulon in E. coli is controlled by a master...
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Formato: | Texto |
Lenguaje: | English |
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Oxford University Press
2007
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1935009/ https://www.ncbi.nlm.nih.gov/pubmed/17576668 http://dx.doi.org/10.1093/nar/gkm456 |
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author | Zhao, Kai Liu, Mingzhu Burgess, Richard R. |
author_facet | Zhao, Kai Liu, Mingzhu Burgess, Richard R. |
author_sort | Zhao, Kai |
collection | PubMed |
description | Bacterial flagellar motility and chemotaxis help cells to reach the most favorable environments and to successfully compete with other micro-organisms in response to external stimuli. Escherichia coli is a motile gram-negative bacterium, and the flagellar regulon in E. coli is controlled by a master regulator FlhDC as well as a second regulator, flagellum-specific sigma factor, σ(F). To define the physiological role of these two regulators, we carried out transcription profiling experiments to identify, on a genome-wide basis, genes under the control of these two regulators. In addition, the synchronized pattern of increasing CRP activity causing increasing FlhDC expression with decreasing carbon source quality, together with the apparent coupling of motility activity with the activation of motility and chemotaxis genes in poor quality carbon sources, highlights the importance of CRP activation in allowing E. coli to devote progressively more of its limited reserves to search out better conditions. In adaptation to a variety of carbon sources, the motile bacteria carry out tactical responses by increasing flagellar operation but restricting costly flagellar synthesis, indicating its capability of strategically using the precious energy in nutrient-poor environments for maximizing survival. |
format | Text |
id | pubmed-1935009 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-19350092007-08-07 Adaptation in bacterial flagellar and motility systems: from regulon members to ‘foraging’-like behavior in E. coli Zhao, Kai Liu, Mingzhu Burgess, Richard R. Nucleic Acids Res Genomics Bacterial flagellar motility and chemotaxis help cells to reach the most favorable environments and to successfully compete with other micro-organisms in response to external stimuli. Escherichia coli is a motile gram-negative bacterium, and the flagellar regulon in E. coli is controlled by a master regulator FlhDC as well as a second regulator, flagellum-specific sigma factor, σ(F). To define the physiological role of these two regulators, we carried out transcription profiling experiments to identify, on a genome-wide basis, genes under the control of these two regulators. In addition, the synchronized pattern of increasing CRP activity causing increasing FlhDC expression with decreasing carbon source quality, together with the apparent coupling of motility activity with the activation of motility and chemotaxis genes in poor quality carbon sources, highlights the importance of CRP activation in allowing E. coli to devote progressively more of its limited reserves to search out better conditions. In adaptation to a variety of carbon sources, the motile bacteria carry out tactical responses by increasing flagellar operation but restricting costly flagellar synthesis, indicating its capability of strategically using the precious energy in nutrient-poor environments for maximizing survival. Oxford University Press 2007-07 2007-06-18 /pmc/articles/PMC1935009/ /pubmed/17576668 http://dx.doi.org/10.1093/nar/gkm456 Text en © 2007 The Author(s) http://creativecommons.org/licenses/by-nc/2.0/uk/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Genomics Zhao, Kai Liu, Mingzhu Burgess, Richard R. Adaptation in bacterial flagellar and motility systems: from regulon members to ‘foraging’-like behavior in E. coli |
title | Adaptation in bacterial flagellar and motility systems: from regulon members to ‘foraging’-like behavior in E. coli |
title_full | Adaptation in bacterial flagellar and motility systems: from regulon members to ‘foraging’-like behavior in E. coli |
title_fullStr | Adaptation in bacterial flagellar and motility systems: from regulon members to ‘foraging’-like behavior in E. coli |
title_full_unstemmed | Adaptation in bacterial flagellar and motility systems: from regulon members to ‘foraging’-like behavior in E. coli |
title_short | Adaptation in bacterial flagellar and motility systems: from regulon members to ‘foraging’-like behavior in E. coli |
title_sort | adaptation in bacterial flagellar and motility systems: from regulon members to ‘foraging’-like behavior in e. coli |
topic | Genomics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1935009/ https://www.ncbi.nlm.nih.gov/pubmed/17576668 http://dx.doi.org/10.1093/nar/gkm456 |
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