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Evolution of higher torque in Campylobacter-type bacterial flagellar motors

Understanding the evolution of molecular machines underpins our understanding of the development of life on earth. A well-studied case are bacterial flagellar motors that spin helical propellers for bacterial motility. Diverse motors produce different torques, but how this diversity evolved remains...

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Autores principales: Chaban, Bonnie, Coleman, Izaak, Beeby, Morgan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5758724/
https://www.ncbi.nlm.nih.gov/pubmed/29311627
http://dx.doi.org/10.1038/s41598-017-18115-1
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author Chaban, Bonnie
Coleman, Izaak
Beeby, Morgan
author_facet Chaban, Bonnie
Coleman, Izaak
Beeby, Morgan
author_sort Chaban, Bonnie
collection PubMed
description Understanding the evolution of molecular machines underpins our understanding of the development of life on earth. A well-studied case are bacterial flagellar motors that spin helical propellers for bacterial motility. Diverse motors produce different torques, but how this diversity evolved remains unknown. To gain insights into evolution of the high-torque ε-proteobacterial motor exemplified by the Campylobacter jejuni motor, we inferred ancestral states by combining phylogenetics, electron cryotomography, and motility assays to characterize motors from Wolinella succinogenes, Arcobacter butzleri and Bdellovibrio bacteriovorus. Observation of ~12 stator complexes in many proteobacteria, yet ~17 in ε-proteobacteria suggest a “quantum leap” evolutionary event. Campylobacter-type motors have high stator occupancy in wider rings of additional stator complexes that are scaffolded by large proteinaceous periplasmic rings. We propose a model for motor evolution wherein independent inner- and outer-membrane structures fused to form a scaffold for additional stator complexes. Significantly, inner- and outer-membrane associated structures have evolved independently multiple times, suggesting that evolution of such structures is facile and poised the ε-proteobacteria to fuse them to form the high-torque Campylobacter-type motor.
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spelling pubmed-57587242018-01-10 Evolution of higher torque in Campylobacter-type bacterial flagellar motors Chaban, Bonnie Coleman, Izaak Beeby, Morgan Sci Rep Article Understanding the evolution of molecular machines underpins our understanding of the development of life on earth. A well-studied case are bacterial flagellar motors that spin helical propellers for bacterial motility. Diverse motors produce different torques, but how this diversity evolved remains unknown. To gain insights into evolution of the high-torque ε-proteobacterial motor exemplified by the Campylobacter jejuni motor, we inferred ancestral states by combining phylogenetics, electron cryotomography, and motility assays to characterize motors from Wolinella succinogenes, Arcobacter butzleri and Bdellovibrio bacteriovorus. Observation of ~12 stator complexes in many proteobacteria, yet ~17 in ε-proteobacteria suggest a “quantum leap” evolutionary event. Campylobacter-type motors have high stator occupancy in wider rings of additional stator complexes that are scaffolded by large proteinaceous periplasmic rings. We propose a model for motor evolution wherein independent inner- and outer-membrane structures fused to form a scaffold for additional stator complexes. Significantly, inner- and outer-membrane associated structures have evolved independently multiple times, suggesting that evolution of such structures is facile and poised the ε-proteobacteria to fuse them to form the high-torque Campylobacter-type motor. Nature Publishing Group UK 2018-01-08 /pmc/articles/PMC5758724/ /pubmed/29311627 http://dx.doi.org/10.1038/s41598-017-18115-1 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
Chaban, Bonnie
Coleman, Izaak
Beeby, Morgan
Evolution of higher torque in Campylobacter-type bacterial flagellar motors
title Evolution of higher torque in Campylobacter-type bacterial flagellar motors
title_full Evolution of higher torque in Campylobacter-type bacterial flagellar motors
title_fullStr Evolution of higher torque in Campylobacter-type bacterial flagellar motors
title_full_unstemmed Evolution of higher torque in Campylobacter-type bacterial flagellar motors
title_short Evolution of higher torque in Campylobacter-type bacterial flagellar motors
title_sort evolution of higher torque in campylobacter-type bacterial flagellar motors
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5758724/
https://www.ncbi.nlm.nih.gov/pubmed/29311627
http://dx.doi.org/10.1038/s41598-017-18115-1
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