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Comparative genomics of freshwater Fe-oxidizing bacteria: implications for physiology, ecology, and systematics
The two microaerophilic, Fe-oxidizing bacteria (FeOB) Sideroxydans ES-1 and Gallionella ES-2 have single circular chromosomes of 3.00 and 3.16 Mb that encode 3049 and 3006 genes, respectively. Multi-locus sequence analysis (MLSA) confirmed the relationship of these two organisms to one another, and...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2013
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3770913/ https://www.ncbi.nlm.nih.gov/pubmed/24062729 http://dx.doi.org/10.3389/fmicb.2013.00254 |
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author | Emerson, David Field, Erin K. Chertkov, Olga Davenport, Karen W. Goodwin, Lynne Munk, Christine Nolan, Matt Woyke, Tanja |
author_facet | Emerson, David Field, Erin K. Chertkov, Olga Davenport, Karen W. Goodwin, Lynne Munk, Christine Nolan, Matt Woyke, Tanja |
author_sort | Emerson, David |
collection | PubMed |
description | The two microaerophilic, Fe-oxidizing bacteria (FeOB) Sideroxydans ES-1 and Gallionella ES-2 have single circular chromosomes of 3.00 and 3.16 Mb that encode 3049 and 3006 genes, respectively. Multi-locus sequence analysis (MLSA) confirmed the relationship of these two organisms to one another, and indicated they may form a novel order, the Gallionellalaes, within the Betaproteobacteria. Both are adapted for chemolithoautotropy, including pathways for CO(2)-fixation, and electron transport pathways adapted for growth at low O(2)-levels, an important adaptation for growing on Fe(II). Both genomes contain Mto-genes implicated in iron-oxidation, as well as other genes that could be involved in Fe-oxidation. Nearly 10% of their genomes are devoted to environmental sensing, signal transduction, and chemotaxis, consistent with their requirement for growing in narrow redox gradients of Fe(II) and O(2). There are important differences as well. Sideroxydans ES-1 is more metabolically flexible, and can utilize reduced S-compounds, including thiosulfate, for lithotrophic growth. It has a suite of genes for nitrogen fixation. Gallionella ES-2 contains additional gene clusters for exopolysaccharide production, and has more capacity to resist heavy metals. Both strains contain genes for hemerythrins and globins, but ES-1 has an especially high numbers of these genes that may be involved in oxygen homeostasis, or storage. The two strains share homology with the marine FeOB Mariprofundus ferrooxydans PV-1 in CO(2) fixation genes, and respiratory genes. In addition, ES-1 shares a suite of 20 potentially redox active genes with PV-1, as well as a large prophage. Combined these genetic, morphological, and physiological differences indicate that these are two novel species, Sideroxydans lithotrophicus ES-1(T) (ATCC 700298(T); JCM 14762; DSMZ 22444; NCMA B100), and Gallionella capsiferriformans ES-2(T) (ATCC 700299(T); JCM 14763; DSMZ 22445; NCMA B101). |
format | Online Article Text |
id | pubmed-3770913 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-37709132013-09-23 Comparative genomics of freshwater Fe-oxidizing bacteria: implications for physiology, ecology, and systematics Emerson, David Field, Erin K. Chertkov, Olga Davenport, Karen W. Goodwin, Lynne Munk, Christine Nolan, Matt Woyke, Tanja Front Microbiol Microbiology The two microaerophilic, Fe-oxidizing bacteria (FeOB) Sideroxydans ES-1 and Gallionella ES-2 have single circular chromosomes of 3.00 and 3.16 Mb that encode 3049 and 3006 genes, respectively. Multi-locus sequence analysis (MLSA) confirmed the relationship of these two organisms to one another, and indicated they may form a novel order, the Gallionellalaes, within the Betaproteobacteria. Both are adapted for chemolithoautotropy, including pathways for CO(2)-fixation, and electron transport pathways adapted for growth at low O(2)-levels, an important adaptation for growing on Fe(II). Both genomes contain Mto-genes implicated in iron-oxidation, as well as other genes that could be involved in Fe-oxidation. Nearly 10% of their genomes are devoted to environmental sensing, signal transduction, and chemotaxis, consistent with their requirement for growing in narrow redox gradients of Fe(II) and O(2). There are important differences as well. Sideroxydans ES-1 is more metabolically flexible, and can utilize reduced S-compounds, including thiosulfate, for lithotrophic growth. It has a suite of genes for nitrogen fixation. Gallionella ES-2 contains additional gene clusters for exopolysaccharide production, and has more capacity to resist heavy metals. Both strains contain genes for hemerythrins and globins, but ES-1 has an especially high numbers of these genes that may be involved in oxygen homeostasis, or storage. The two strains share homology with the marine FeOB Mariprofundus ferrooxydans PV-1 in CO(2) fixation genes, and respiratory genes. In addition, ES-1 shares a suite of 20 potentially redox active genes with PV-1, as well as a large prophage. Combined these genetic, morphological, and physiological differences indicate that these are two novel species, Sideroxydans lithotrophicus ES-1(T) (ATCC 700298(T); JCM 14762; DSMZ 22444; NCMA B100), and Gallionella capsiferriformans ES-2(T) (ATCC 700299(T); JCM 14763; DSMZ 22445; NCMA B101). Frontiers Media S.A. 2013-09-12 /pmc/articles/PMC3770913/ /pubmed/24062729 http://dx.doi.org/10.3389/fmicb.2013.00254 Text en Copyright © 2013 Emerson, Field, Chertkov, Davenport, Goodwin, Munk, Nolan and Woyke. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Emerson, David Field, Erin K. Chertkov, Olga Davenport, Karen W. Goodwin, Lynne Munk, Christine Nolan, Matt Woyke, Tanja Comparative genomics of freshwater Fe-oxidizing bacteria: implications for physiology, ecology, and systematics |
title | Comparative genomics of freshwater Fe-oxidizing bacteria: implications for physiology, ecology, and systematics |
title_full | Comparative genomics of freshwater Fe-oxidizing bacteria: implications for physiology, ecology, and systematics |
title_fullStr | Comparative genomics of freshwater Fe-oxidizing bacteria: implications for physiology, ecology, and systematics |
title_full_unstemmed | Comparative genomics of freshwater Fe-oxidizing bacteria: implications for physiology, ecology, and systematics |
title_short | Comparative genomics of freshwater Fe-oxidizing bacteria: implications for physiology, ecology, and systematics |
title_sort | comparative genomics of freshwater fe-oxidizing bacteria: implications for physiology, ecology, and systematics |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3770913/ https://www.ncbi.nlm.nih.gov/pubmed/24062729 http://dx.doi.org/10.3389/fmicb.2013.00254 |
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