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The Fe(II)-oxidizing Zetaproteobacteria: historical, ecological and genomic perspectives

The Zetaproteobacteria are a class of bacteria typically associated with marine Fe(II)-oxidizing environments. First discovered in the hydrothermal vents at Loihi Seamount, Hawaii, they have become model organisms for marine microbial Fe(II) oxidation. In addition to deep sea and shallow hydrotherma...

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Autores principales: McAllister, Sean M, Moore, Ryan M, Gartman, Amy, Luther, George W, Emerson, David, Chan, Clara S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6443915/
https://www.ncbi.nlm.nih.gov/pubmed/30715272
http://dx.doi.org/10.1093/femsec/fiz015
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author McAllister, Sean M
Moore, Ryan M
Gartman, Amy
Luther, George W
Emerson, David
Chan, Clara S
author_facet McAllister, Sean M
Moore, Ryan M
Gartman, Amy
Luther, George W
Emerson, David
Chan, Clara S
author_sort McAllister, Sean M
collection PubMed
description The Zetaproteobacteria are a class of bacteria typically associated with marine Fe(II)-oxidizing environments. First discovered in the hydrothermal vents at Loihi Seamount, Hawaii, they have become model organisms for marine microbial Fe(II) oxidation. In addition to deep sea and shallow hydrothermal vents, Zetaproteobacteria are found in coastal sediments, other marine subsurface environments, steel corrosion biofilms and saline terrestrial springs. Isolates from a range of environments all grow by autotrophic Fe(II) oxidation. Their success lies partly in their microaerophily, which enables them to compete with abiotic Fe(II) oxidation at Fe(II)-rich oxic/anoxic transition zones. To determine the known diversity of the Zetaproteobacteria, we have used 16S rRNA gene sequences to define 59 operational taxonomic units (OTUs), at 97% similarity. While some Zetaproteobacteria taxa appear to be cosmopolitan, others are enriched by specific habitats. OTU networks show that certain Zetaproteobacteria co-exist, sharing compatible niches. These niches may correspond with adaptations to O(2), H(2) and nitrate availability, based on genomic analyses of metabolic potential. Also, a putative Fe(II) oxidation gene has been found in diverse Zetaproteobacteria taxa, suggesting that the Zetaproteobacteria evolved as Fe(II) oxidation specialists. In all, studies suggest that Zetaproteobacteria are widespread, and therefore may have a broad influence on marine and saline terrestrial Fe cycling.
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spelling pubmed-64439152019-04-08 The Fe(II)-oxidizing Zetaproteobacteria: historical, ecological and genomic perspectives McAllister, Sean M Moore, Ryan M Gartman, Amy Luther, George W Emerson, David Chan, Clara S FEMS Microbiol Ecol Minireview The Zetaproteobacteria are a class of bacteria typically associated with marine Fe(II)-oxidizing environments. First discovered in the hydrothermal vents at Loihi Seamount, Hawaii, they have become model organisms for marine microbial Fe(II) oxidation. In addition to deep sea and shallow hydrothermal vents, Zetaproteobacteria are found in coastal sediments, other marine subsurface environments, steel corrosion biofilms and saline terrestrial springs. Isolates from a range of environments all grow by autotrophic Fe(II) oxidation. Their success lies partly in their microaerophily, which enables them to compete with abiotic Fe(II) oxidation at Fe(II)-rich oxic/anoxic transition zones. To determine the known diversity of the Zetaproteobacteria, we have used 16S rRNA gene sequences to define 59 operational taxonomic units (OTUs), at 97% similarity. While some Zetaproteobacteria taxa appear to be cosmopolitan, others are enriched by specific habitats. OTU networks show that certain Zetaproteobacteria co-exist, sharing compatible niches. These niches may correspond with adaptations to O(2), H(2) and nitrate availability, based on genomic analyses of metabolic potential. Also, a putative Fe(II) oxidation gene has been found in diverse Zetaproteobacteria taxa, suggesting that the Zetaproteobacteria evolved as Fe(II) oxidation specialists. In all, studies suggest that Zetaproteobacteria are widespread, and therefore may have a broad influence on marine and saline terrestrial Fe cycling. Oxford University Press 2019-01-30 /pmc/articles/PMC6443915/ /pubmed/30715272 http://dx.doi.org/10.1093/femsec/fiz015 Text en © FEMS 2019. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Minireview
McAllister, Sean M
Moore, Ryan M
Gartman, Amy
Luther, George W
Emerson, David
Chan, Clara S
The Fe(II)-oxidizing Zetaproteobacteria: historical, ecological and genomic perspectives
title The Fe(II)-oxidizing Zetaproteobacteria: historical, ecological and genomic perspectives
title_full The Fe(II)-oxidizing Zetaproteobacteria: historical, ecological and genomic perspectives
title_fullStr The Fe(II)-oxidizing Zetaproteobacteria: historical, ecological and genomic perspectives
title_full_unstemmed The Fe(II)-oxidizing Zetaproteobacteria: historical, ecological and genomic perspectives
title_short The Fe(II)-oxidizing Zetaproteobacteria: historical, ecological and genomic perspectives
title_sort fe(ii)-oxidizing zetaproteobacteria: historical, ecological and genomic perspectives
topic Minireview
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6443915/
https://www.ncbi.nlm.nih.gov/pubmed/30715272
http://dx.doi.org/10.1093/femsec/fiz015
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