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d-amino acids signal a stress-dependent run-away response in Vibrio cholerae
To explore favourable niches while avoiding threats, many bacteria use a chemotaxis navigation system. Despite decades of studies on chemotaxis, most signals and sensory proteins are still unknown. Many bacterial species release d-amino acids to the environment; however, their function remains large...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10390336/ https://www.ncbi.nlm.nih.gov/pubmed/37365341 http://dx.doi.org/10.1038/s41564-023-01419-6 |
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author | Irazoki, Oihane ter Beek, Josy Alvarez, Laura Mateus, André Colin, Remy Typas, Athanasios Savitski, Mikhail M. Sourjik, Victor Berntsson, Ronnie P.-A. Cava, Felipe |
author_facet | Irazoki, Oihane ter Beek, Josy Alvarez, Laura Mateus, André Colin, Remy Typas, Athanasios Savitski, Mikhail M. Sourjik, Victor Berntsson, Ronnie P.-A. Cava, Felipe |
author_sort | Irazoki, Oihane |
collection | PubMed |
description | To explore favourable niches while avoiding threats, many bacteria use a chemotaxis navigation system. Despite decades of studies on chemotaxis, most signals and sensory proteins are still unknown. Many bacterial species release d-amino acids to the environment; however, their function remains largely unrecognized. Here we reveal that d-arginine and d-lysine are chemotactic repellent signals for the cholera pathogen Vibrio cholerae. These d-amino acids are sensed by a single chemoreceptor MCP(DRK) co-transcribed with the racemase enzyme that synthesizes them under the control of the stress-response sigma factor RpoS. Structural characterization of this chemoreceptor bound to either d-arginine or d-lysine allowed us to pinpoint the residues defining its specificity. Interestingly, the specificity for these d-amino acids appears to be restricted to those MCP(DRK) orthologues transcriptionally linked to the racemase. Our results suggest that d-amino acids can shape the biodiversity and structure of complex microbial communities under adverse conditions. |
format | Online Article Text |
id | pubmed-10390336 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-103903362023-08-02 d-amino acids signal a stress-dependent run-away response in Vibrio cholerae Irazoki, Oihane ter Beek, Josy Alvarez, Laura Mateus, André Colin, Remy Typas, Athanasios Savitski, Mikhail M. Sourjik, Victor Berntsson, Ronnie P.-A. Cava, Felipe Nat Microbiol Article To explore favourable niches while avoiding threats, many bacteria use a chemotaxis navigation system. Despite decades of studies on chemotaxis, most signals and sensory proteins are still unknown. Many bacterial species release d-amino acids to the environment; however, their function remains largely unrecognized. Here we reveal that d-arginine and d-lysine are chemotactic repellent signals for the cholera pathogen Vibrio cholerae. These d-amino acids are sensed by a single chemoreceptor MCP(DRK) co-transcribed with the racemase enzyme that synthesizes them under the control of the stress-response sigma factor RpoS. Structural characterization of this chemoreceptor bound to either d-arginine or d-lysine allowed us to pinpoint the residues defining its specificity. Interestingly, the specificity for these d-amino acids appears to be restricted to those MCP(DRK) orthologues transcriptionally linked to the racemase. Our results suggest that d-amino acids can shape the biodiversity and structure of complex microbial communities under adverse conditions. Nature Publishing Group UK 2023-06-26 2023 /pmc/articles/PMC10390336/ /pubmed/37365341 http://dx.doi.org/10.1038/s41564-023-01419-6 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Irazoki, Oihane ter Beek, Josy Alvarez, Laura Mateus, André Colin, Remy Typas, Athanasios Savitski, Mikhail M. Sourjik, Victor Berntsson, Ronnie P.-A. Cava, Felipe d-amino acids signal a stress-dependent run-away response in Vibrio cholerae |
title | d-amino acids signal a stress-dependent run-away response in Vibrio cholerae |
title_full | d-amino acids signal a stress-dependent run-away response in Vibrio cholerae |
title_fullStr | d-amino acids signal a stress-dependent run-away response in Vibrio cholerae |
title_full_unstemmed | d-amino acids signal a stress-dependent run-away response in Vibrio cholerae |
title_short | d-amino acids signal a stress-dependent run-away response in Vibrio cholerae |
title_sort | d-amino acids signal a stress-dependent run-away response in vibrio cholerae |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10390336/ https://www.ncbi.nlm.nih.gov/pubmed/37365341 http://dx.doi.org/10.1038/s41564-023-01419-6 |
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