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Torque, but not FliL, regulates mechanosensitive flagellar motor-function
The stator-complex in the bacterial flagellar motor is responsible for surface-sensing. It remodels in response to perturbations in viscous loads, recruiting additional stator-units as the load increases. Here, we tested a hypothesis that the amount of torque generated by each stator-unit modulates...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5514156/ https://www.ncbi.nlm.nih.gov/pubmed/28717192 http://dx.doi.org/10.1038/s41598-017-05521-8 |
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author | Chawla, Ravi Ford, Katie M. Lele, Pushkar P. |
author_facet | Chawla, Ravi Ford, Katie M. Lele, Pushkar P. |
author_sort | Chawla, Ravi |
collection | PubMed |
description | The stator-complex in the bacterial flagellar motor is responsible for surface-sensing. It remodels in response to perturbations in viscous loads, recruiting additional stator-units as the load increases. Here, we tested a hypothesis that the amount of torque generated by each stator-unit modulates its association with the rotor. To do this, we measured stator-binding to the rotor in mutants in which motors reportedly develop lower torque compared to wildtype motors. First, we employed a strain lacking fliL. Contrary to earlier reports, measurements indicated that the torque generated by motors in the fliL strain was similar to that in the wildtype, at high loads. In these motors, stator-binding was unchanged. Next, experiments with a paralyzed strain indicated that the stator-binding was measurably weaker when motors were unable to generate torque. An analytical model was developed that incorporated an exponential dependence of the unit’s dissociation rate on the force delivered to the rotor. The model provided accurate fits to measurements of stator-rotor binding over a wide range of loads. Based on these results, we propose that the binding of each stator-unit is enhanced by the force it develops. Furthermore, FliL does not play a significant role in motor function in E. coli. |
format | Online Article Text |
id | pubmed-5514156 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55141562017-07-19 Torque, but not FliL, regulates mechanosensitive flagellar motor-function Chawla, Ravi Ford, Katie M. Lele, Pushkar P. Sci Rep Article The stator-complex in the bacterial flagellar motor is responsible for surface-sensing. It remodels in response to perturbations in viscous loads, recruiting additional stator-units as the load increases. Here, we tested a hypothesis that the amount of torque generated by each stator-unit modulates its association with the rotor. To do this, we measured stator-binding to the rotor in mutants in which motors reportedly develop lower torque compared to wildtype motors. First, we employed a strain lacking fliL. Contrary to earlier reports, measurements indicated that the torque generated by motors in the fliL strain was similar to that in the wildtype, at high loads. In these motors, stator-binding was unchanged. Next, experiments with a paralyzed strain indicated that the stator-binding was measurably weaker when motors were unable to generate torque. An analytical model was developed that incorporated an exponential dependence of the unit’s dissociation rate on the force delivered to the rotor. The model provided accurate fits to measurements of stator-rotor binding over a wide range of loads. Based on these results, we propose that the binding of each stator-unit is enhanced by the force it develops. Furthermore, FliL does not play a significant role in motor function in E. coli. Nature Publishing Group UK 2017-07-17 /pmc/articles/PMC5514156/ /pubmed/28717192 http://dx.doi.org/10.1038/s41598-017-05521-8 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Chawla, Ravi Ford, Katie M. Lele, Pushkar P. Torque, but not FliL, regulates mechanosensitive flagellar motor-function |
title | Torque, but not FliL, regulates mechanosensitive flagellar motor-function |
title_full | Torque, but not FliL, regulates mechanosensitive flagellar motor-function |
title_fullStr | Torque, but not FliL, regulates mechanosensitive flagellar motor-function |
title_full_unstemmed | Torque, but not FliL, regulates mechanosensitive flagellar motor-function |
title_short | Torque, but not FliL, regulates mechanosensitive flagellar motor-function |
title_sort | torque, but not flil, regulates mechanosensitive flagellar motor-function |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5514156/ https://www.ncbi.nlm.nih.gov/pubmed/28717192 http://dx.doi.org/10.1038/s41598-017-05521-8 |
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