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Indole modulates cooperative protein–protein interactions in the flagellar motor
Indole is a major component of the bacterial exometabolome, and the mechanisms for its wide-ranging effects on bacterial physiology are biomedically significant, although they remain poorly understood. Here, we determined how indole modulates the functions of a widely conserved motility apparatus, t...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9205328/ https://www.ncbi.nlm.nih.gov/pubmed/35719892 http://dx.doi.org/10.1093/pnasnexus/pgac035 |
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author | Gupta, Rachit Rhee, Kathy Y Beagle, Sarah D Chawla, Ravi Perdomo, Nicolas Lockless, Steve W Lele, Pushkar P |
author_facet | Gupta, Rachit Rhee, Kathy Y Beagle, Sarah D Chawla, Ravi Perdomo, Nicolas Lockless, Steve W Lele, Pushkar P |
author_sort | Gupta, Rachit |
collection | PubMed |
description | Indole is a major component of the bacterial exometabolome, and the mechanisms for its wide-ranging effects on bacterial physiology are biomedically significant, although they remain poorly understood. Here, we determined how indole modulates the functions of a widely conserved motility apparatus, the bacterial flagellum. Our experiments in Escherichia coli revealed that indole influences the rotation rates and reversals in the flagellum's direction of rotation via multiple mechanisms. At concentrations higher than 1 mM, indole decreased the membrane potential to dissipate the power available for the rotation of the motor that operates the flagellum. Below 1 mM, indole did not dissipate the membrane potential. Instead, experiments and modeling indicated that indole weakens cooperative protein interactions within the flagellar complexes to inhibit motility. The metabolite also induced reversals in the rotational direction of the motor to promote a weak chemotactic response, even when the chemotaxis response regulator, CheY, was lacking. Experiments further revealed that indole does not require the transporter Mtr to cross the membrane and influence motor functions. Based on these findings, we propose that indole modulates intra- and inter-protein interactions in the cell to influence several physiological functions. |
format | Online Article Text |
id | pubmed-9205328 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-92053282022-06-17 Indole modulates cooperative protein–protein interactions in the flagellar motor Gupta, Rachit Rhee, Kathy Y Beagle, Sarah D Chawla, Ravi Perdomo, Nicolas Lockless, Steve W Lele, Pushkar P PNAS Nexus Physical Sciences and Engineering Indole is a major component of the bacterial exometabolome, and the mechanisms for its wide-ranging effects on bacterial physiology are biomedically significant, although they remain poorly understood. Here, we determined how indole modulates the functions of a widely conserved motility apparatus, the bacterial flagellum. Our experiments in Escherichia coli revealed that indole influences the rotation rates and reversals in the flagellum's direction of rotation via multiple mechanisms. At concentrations higher than 1 mM, indole decreased the membrane potential to dissipate the power available for the rotation of the motor that operates the flagellum. Below 1 mM, indole did not dissipate the membrane potential. Instead, experiments and modeling indicated that indole weakens cooperative protein interactions within the flagellar complexes to inhibit motility. The metabolite also induced reversals in the rotational direction of the motor to promote a weak chemotactic response, even when the chemotaxis response regulator, CheY, was lacking. Experiments further revealed that indole does not require the transporter Mtr to cross the membrane and influence motor functions. Based on these findings, we propose that indole modulates intra- and inter-protein interactions in the cell to influence several physiological functions. Oxford University Press 2022-05-13 /pmc/articles/PMC9205328/ /pubmed/35719892 http://dx.doi.org/10.1093/pnasnexus/pgac035 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of the National Academy of Sciences. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Physical Sciences and Engineering Gupta, Rachit Rhee, Kathy Y Beagle, Sarah D Chawla, Ravi Perdomo, Nicolas Lockless, Steve W Lele, Pushkar P Indole modulates cooperative protein–protein interactions in the flagellar motor |
title | Indole modulates cooperative protein–protein interactions in the flagellar motor |
title_full | Indole modulates cooperative protein–protein interactions in the flagellar motor |
title_fullStr | Indole modulates cooperative protein–protein interactions in the flagellar motor |
title_full_unstemmed | Indole modulates cooperative protein–protein interactions in the flagellar motor |
title_short | Indole modulates cooperative protein–protein interactions in the flagellar motor |
title_sort | indole modulates cooperative protein–protein interactions in the flagellar motor |
topic | Physical Sciences and Engineering |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9205328/ https://www.ncbi.nlm.nih.gov/pubmed/35719892 http://dx.doi.org/10.1093/pnasnexus/pgac035 |
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