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Atomic-level architecture of Caulobacter crescentus flagellar filaments provide evidence for multi-flagellin filament stabilization
Flagella are dynamic, ion-powered machines with assembly pathways that are optimized for efficient flagella production. In bacteria, dozens of genes are coordinated at specific times in the cell lifecycle to generate each component of the flagellum. This is the case for Caulobacter crescentus, but l...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10369909/ https://www.ncbi.nlm.nih.gov/pubmed/37503001 http://dx.doi.org/10.1101/2023.07.10.548443 |
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author | Sanchez, Juan C. Montemayor, Eric J. Ploscariu, Nicoleta T. Parrell, Daniel Baumgardt, Joseph K. Yang, Jie E. Sibert, Bryan Cai, Kai Wright, Elizabeth R. |
author_facet | Sanchez, Juan C. Montemayor, Eric J. Ploscariu, Nicoleta T. Parrell, Daniel Baumgardt, Joseph K. Yang, Jie E. Sibert, Bryan Cai, Kai Wright, Elizabeth R. |
author_sort | Sanchez, Juan C. |
collection | PubMed |
description | Flagella are dynamic, ion-powered machines with assembly pathways that are optimized for efficient flagella production. In bacteria, dozens of genes are coordinated at specific times in the cell lifecycle to generate each component of the flagellum. This is the case for Caulobacter crescentus, but little is known about why this species encodes six different flagellin genes. Furthermore, little is known about the benefits multi-flagellin species possess over single flagellin species, if any, or what molecular properties allow for multi-flagellin filaments to assemble. Here we present an in-depth analysis of several single flagellin filaments from C. crescentus, including an extremely well-resolved structure of a bacterial flagellar filament. We highlight key molecular interactions that differ between each bacterial strain and speculate how these interactions may alleviate or impose helical strain on the overall architecture of the filament. We detail conserved residues within the flagellin subunit that allow for the synthesis of multi-flagellin filaments. We further comment on how these molecular differences impact bacterial motility and highlight how no single flagellin filament achieves wild-type levels of motility, suggesting C. crescentus has evolved to produce a filament optimized for motility comprised of six flagellins. Finally, we highlight an ordered arrangement of glycosylation sites on the surface of the filaments and speculate how these sites may protect the β-hairpin located on the surface exposed domain of the flagellin subunit. |
format | Online Article Text |
id | pubmed-10369909 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-103699092023-07-27 Atomic-level architecture of Caulobacter crescentus flagellar filaments provide evidence for multi-flagellin filament stabilization Sanchez, Juan C. Montemayor, Eric J. Ploscariu, Nicoleta T. Parrell, Daniel Baumgardt, Joseph K. Yang, Jie E. Sibert, Bryan Cai, Kai Wright, Elizabeth R. bioRxiv Article Flagella are dynamic, ion-powered machines with assembly pathways that are optimized for efficient flagella production. In bacteria, dozens of genes are coordinated at specific times in the cell lifecycle to generate each component of the flagellum. This is the case for Caulobacter crescentus, but little is known about why this species encodes six different flagellin genes. Furthermore, little is known about the benefits multi-flagellin species possess over single flagellin species, if any, or what molecular properties allow for multi-flagellin filaments to assemble. Here we present an in-depth analysis of several single flagellin filaments from C. crescentus, including an extremely well-resolved structure of a bacterial flagellar filament. We highlight key molecular interactions that differ between each bacterial strain and speculate how these interactions may alleviate or impose helical strain on the overall architecture of the filament. We detail conserved residues within the flagellin subunit that allow for the synthesis of multi-flagellin filaments. We further comment on how these molecular differences impact bacterial motility and highlight how no single flagellin filament achieves wild-type levels of motility, suggesting C. crescentus has evolved to produce a filament optimized for motility comprised of six flagellins. Finally, we highlight an ordered arrangement of glycosylation sites on the surface of the filaments and speculate how these sites may protect the β-hairpin located on the surface exposed domain of the flagellin subunit. Cold Spring Harbor Laboratory 2023-07-10 /pmc/articles/PMC10369909/ /pubmed/37503001 http://dx.doi.org/10.1101/2023.07.10.548443 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Sanchez, Juan C. Montemayor, Eric J. Ploscariu, Nicoleta T. Parrell, Daniel Baumgardt, Joseph K. Yang, Jie E. Sibert, Bryan Cai, Kai Wright, Elizabeth R. Atomic-level architecture of Caulobacter crescentus flagellar filaments provide evidence for multi-flagellin filament stabilization |
title | Atomic-level architecture of Caulobacter crescentus flagellar filaments provide evidence for multi-flagellin filament stabilization |
title_full | Atomic-level architecture of Caulobacter crescentus flagellar filaments provide evidence for multi-flagellin filament stabilization |
title_fullStr | Atomic-level architecture of Caulobacter crescentus flagellar filaments provide evidence for multi-flagellin filament stabilization |
title_full_unstemmed | Atomic-level architecture of Caulobacter crescentus flagellar filaments provide evidence for multi-flagellin filament stabilization |
title_short | Atomic-level architecture of Caulobacter crescentus flagellar filaments provide evidence for multi-flagellin filament stabilization |
title_sort | atomic-level architecture of caulobacter crescentus flagellar filaments provide evidence for multi-flagellin filament stabilization |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10369909/ https://www.ncbi.nlm.nih.gov/pubmed/37503001 http://dx.doi.org/10.1101/2023.07.10.548443 |
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