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MamA as a Model Protein for Structure-Based Insight into the Evolutionary Origins of Magnetotactic Bacteria
MamA is a highly conserved protein found in magnetotactic bacteria (MTB), a diverse group of prokaryotes capable of navigating according to magnetic fields – an ability known as magnetotaxis. Questions surround the acquisition of this magnetic navigation ability; namely, whether it arose through hor...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4482739/ https://www.ncbi.nlm.nih.gov/pubmed/26114501 http://dx.doi.org/10.1371/journal.pone.0130394 |
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author | Zeytuni, Natalie Cronin, Samuel Lefèvre, Christopher T. Arnoux, Pascal Baran, Dror Shtein, Zvi Davidov, Geula Zarivach, Raz |
author_facet | Zeytuni, Natalie Cronin, Samuel Lefèvre, Christopher T. Arnoux, Pascal Baran, Dror Shtein, Zvi Davidov, Geula Zarivach, Raz |
author_sort | Zeytuni, Natalie |
collection | PubMed |
description | MamA is a highly conserved protein found in magnetotactic bacteria (MTB), a diverse group of prokaryotes capable of navigating according to magnetic fields – an ability known as magnetotaxis. Questions surround the acquisition of this magnetic navigation ability; namely, whether it arose through horizontal or vertical gene transfer. Though its exact function is unknown, MamA surrounds the magnetosome, the magnetic organelle embedding a biomineralised nanoparticle and responsible for magnetotaxis. Several structures for MamA from a variety of species have been determined and show a high degree of structural similarity. By determining the structure of MamA from Desulfovibrio magneticus RS-1 using X-ray crystallography, we have opened up the structure-sequence landscape. As such, this allows us to perform structural- and phylogenetic-based analyses using a variety of previously determined MamA from a diverse range of MTB species across various phylogenetic groups. We found that MamA has remained remarkably constant throughout evolution with minimal change between different taxa despite sequence variations. These findings, coupled with the generation of phylogenetic trees using both amino acid sequences and 16S rRNA, indicate that magnetotaxis likely did not spread via horizontal gene transfer and instead has a significantly earlier, primordial origin. |
format | Online Article Text |
id | pubmed-4482739 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-44827392015-06-29 MamA as a Model Protein for Structure-Based Insight into the Evolutionary Origins of Magnetotactic Bacteria Zeytuni, Natalie Cronin, Samuel Lefèvre, Christopher T. Arnoux, Pascal Baran, Dror Shtein, Zvi Davidov, Geula Zarivach, Raz PLoS One Research Article MamA is a highly conserved protein found in magnetotactic bacteria (MTB), a diverse group of prokaryotes capable of navigating according to magnetic fields – an ability known as magnetotaxis. Questions surround the acquisition of this magnetic navigation ability; namely, whether it arose through horizontal or vertical gene transfer. Though its exact function is unknown, MamA surrounds the magnetosome, the magnetic organelle embedding a biomineralised nanoparticle and responsible for magnetotaxis. Several structures for MamA from a variety of species have been determined and show a high degree of structural similarity. By determining the structure of MamA from Desulfovibrio magneticus RS-1 using X-ray crystallography, we have opened up the structure-sequence landscape. As such, this allows us to perform structural- and phylogenetic-based analyses using a variety of previously determined MamA from a diverse range of MTB species across various phylogenetic groups. We found that MamA has remained remarkably constant throughout evolution with minimal change between different taxa despite sequence variations. These findings, coupled with the generation of phylogenetic trees using both amino acid sequences and 16S rRNA, indicate that magnetotaxis likely did not spread via horizontal gene transfer and instead has a significantly earlier, primordial origin. Public Library of Science 2015-06-26 /pmc/articles/PMC4482739/ /pubmed/26114501 http://dx.doi.org/10.1371/journal.pone.0130394 Text en © 2015 Zeytuni et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Zeytuni, Natalie Cronin, Samuel Lefèvre, Christopher T. Arnoux, Pascal Baran, Dror Shtein, Zvi Davidov, Geula Zarivach, Raz MamA as a Model Protein for Structure-Based Insight into the Evolutionary Origins of Magnetotactic Bacteria |
title | MamA as a Model Protein for Structure-Based Insight into the Evolutionary Origins of Magnetotactic Bacteria |
title_full | MamA as a Model Protein for Structure-Based Insight into the Evolutionary Origins of Magnetotactic Bacteria |
title_fullStr | MamA as a Model Protein for Structure-Based Insight into the Evolutionary Origins of Magnetotactic Bacteria |
title_full_unstemmed | MamA as a Model Protein for Structure-Based Insight into the Evolutionary Origins of Magnetotactic Bacteria |
title_short | MamA as a Model Protein for Structure-Based Insight into the Evolutionary Origins of Magnetotactic Bacteria |
title_sort | mama as a model protein for structure-based insight into the evolutionary origins of magnetotactic bacteria |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4482739/ https://www.ncbi.nlm.nih.gov/pubmed/26114501 http://dx.doi.org/10.1371/journal.pone.0130394 |
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