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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group
2015
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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. |
format | Online Article Text |
id | pubmed-4525482 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
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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