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Sodium-driven energy conversion for flagellar rotation of the earliest divergent hyperthermophilic bacterium

Aquifex aeolicus is a hyperthermophilic, hydrogen-oxidizing and carbon-fixing bacterium that can grow at temperatures up to 95 °C. A. aeolicus has an almost complete set of flagellar genes that are conserved in bacteria. Here we observed that A. aeolicus has polar flagellum and can swim with a speed...

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Autores principales: Takekawa, Norihiro, Nishiyama, Masayoshi, Kaneseki, Tsuyoshi, Kanai, Tamotsu, Atomi, Haruyuki, Kojima, Seiji, Homma, Michio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4525482/
https://www.ncbi.nlm.nih.gov/pubmed/26244427
http://dx.doi.org/10.1038/srep12711
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author Takekawa, Norihiro
Nishiyama, Masayoshi
Kaneseki, Tsuyoshi
Kanai, Tamotsu
Atomi, Haruyuki
Kojima, Seiji
Homma, Michio
author_facet Takekawa, Norihiro
Nishiyama, Masayoshi
Kaneseki, Tsuyoshi
Kanai, Tamotsu
Atomi, Haruyuki
Kojima, Seiji
Homma, Michio
author_sort Takekawa, Norihiro
collection PubMed
description Aquifex aeolicus is a hyperthermophilic, hydrogen-oxidizing and carbon-fixing bacterium that can grow at temperatures up to 95 °C. A. aeolicus has an almost complete set of flagellar genes that are conserved in bacteria. Here we observed that A. aeolicus has polar flagellum and can swim with a speed of 90 μm s(−1) at 85 °C. We expressed the A. aeolicus mot genes (motA and motB), which encode the torque generating stator proteins of the flagellar motor, in a corresponding mot nonmotile mutant of Escherichia coli. Its motility was slightly recovered by expression of A. aeolicus MotA and chimeric MotB whose periplasmic region was replaced with that of E. coli. A point mutation in the A. aeolicus MotA cytoplasmic region remarkably enhanced the motility. Using this system in E. coli, we demonstrate that the A. aeolicus motor is driven by Na(+). As motor proteins from hyperthermophilic bacteria represent the earliest motor proteins in evolution, this study strongly suggests that ancient bacteria used Na(+) for energy coupling of the flagellar motor. The Na(+)-driven flagellar genes might have been laterally transferred from early-branched bacteria into late-branched bacteria and the interaction surfaces of the stator and rotor seem not to change in evolution.
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spelling pubmed-45254822015-08-06 Sodium-driven energy conversion for flagellar rotation of the earliest divergent hyperthermophilic bacterium Takekawa, Norihiro Nishiyama, Masayoshi Kaneseki, Tsuyoshi Kanai, Tamotsu Atomi, Haruyuki Kojima, Seiji Homma, Michio Sci Rep Article Aquifex aeolicus is a hyperthermophilic, hydrogen-oxidizing and carbon-fixing bacterium that can grow at temperatures up to 95 °C. A. aeolicus has an almost complete set of flagellar genes that are conserved in bacteria. Here we observed that A. aeolicus has polar flagellum and can swim with a speed of 90 μm s(−1) at 85 °C. We expressed the A. aeolicus mot genes (motA and motB), which encode the torque generating stator proteins of the flagellar motor, in a corresponding mot nonmotile mutant of Escherichia coli. Its motility was slightly recovered by expression of A. aeolicus MotA and chimeric MotB whose periplasmic region was replaced with that of E. coli. A point mutation in the A. aeolicus MotA cytoplasmic region remarkably enhanced the motility. Using this system in E. coli, we demonstrate that the A. aeolicus motor is driven by Na(+). As motor proteins from hyperthermophilic bacteria represent the earliest motor proteins in evolution, this study strongly suggests that ancient bacteria used Na(+) for energy coupling of the flagellar motor. The Na(+)-driven flagellar genes might have been laterally transferred from early-branched bacteria into late-branched bacteria and the interaction surfaces of the stator and rotor seem not to change in evolution. Nature Publishing Group 2015-08-05 /pmc/articles/PMC4525482/ /pubmed/26244427 http://dx.doi.org/10.1038/srep12711 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Takekawa, Norihiro
Nishiyama, Masayoshi
Kaneseki, Tsuyoshi
Kanai, Tamotsu
Atomi, Haruyuki
Kojima, Seiji
Homma, Michio
Sodium-driven energy conversion for flagellar rotation of the earliest divergent hyperthermophilic bacterium
title Sodium-driven energy conversion for flagellar rotation of the earliest divergent hyperthermophilic bacterium
title_full Sodium-driven energy conversion for flagellar rotation of the earliest divergent hyperthermophilic bacterium
title_fullStr Sodium-driven energy conversion for flagellar rotation of the earliest divergent hyperthermophilic bacterium
title_full_unstemmed Sodium-driven energy conversion for flagellar rotation of the earliest divergent hyperthermophilic bacterium
title_short Sodium-driven energy conversion for flagellar rotation of the earliest divergent hyperthermophilic bacterium
title_sort sodium-driven energy conversion for flagellar rotation of the earliest divergent hyperthermophilic bacterium
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4525482/
https://www.ncbi.nlm.nih.gov/pubmed/26244427
http://dx.doi.org/10.1038/srep12711
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