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Goethite Reduction by a Neutrophilic Member of the Alphaproteobacterial Genus Telmatospirillum

In tropical iron ore regions, biologically mediated reduction of crystalline iron oxides drives ongoing iron cycling that contributes to the stability of surface duricrusts. This represents a biotechnological opportunity with respect to post-mining rehabilitation attempts, requiring re-formation of...

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Autores principales: Gagen, Emma J., Zaugg, Julian, Tyson, Gene W., Southam, Gordon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6933298/
https://www.ncbi.nlm.nih.gov/pubmed/31921089
http://dx.doi.org/10.3389/fmicb.2019.02938
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author Gagen, Emma J.
Zaugg, Julian
Tyson, Gene W.
Southam, Gordon
author_facet Gagen, Emma J.
Zaugg, Julian
Tyson, Gene W.
Southam, Gordon
author_sort Gagen, Emma J.
collection PubMed
description In tropical iron ore regions, biologically mediated reduction of crystalline iron oxides drives ongoing iron cycling that contributes to the stability of surface duricrusts. This represents a biotechnological opportunity with respect to post-mining rehabilitation attempts, requiring re-formation of these duricrusts. However, cultivated dissimilatory iron reducing bacteria typically reduce crystalline iron oxides quite poorly. A glucose-fermenting microbial consortium capable of reducing at least 27 mmol/L goethite was enriched from an iron duricrust region. Metagenome analysis led to the recovery of a metagenome assembled genome (MAG) of an iron reducer belonging to the alphaproteobacterial genus Telmatospirillum. This is the first report of iron reduction within the Telmatospirillum and the first reported genome of an iron-reducing, neutrophilic member of the Alphaproteobacteria. The Telmatospirillum MAG encodes putative metal transfer reductases (MtrA, MtrB) and a novel, multi-heme outer membrane cytochrome for extracellular electron transfer. In the presence of goethite, short chain fatty acid production shifted significantly in favor of acetate rather than propionate, indicating goethite is a hydrogen sink in the culture. Therefore, the presence of fermentative bacteria likely promotes iron reduction via hydrogen production. Stimulating microbial fermentation has potential to drive reduction of crystalline iron oxides, the rate limiting step for iron duricrust re-formation.
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spelling pubmed-69332982020-01-09 Goethite Reduction by a Neutrophilic Member of the Alphaproteobacterial Genus Telmatospirillum Gagen, Emma J. Zaugg, Julian Tyson, Gene W. Southam, Gordon Front Microbiol Microbiology In tropical iron ore regions, biologically mediated reduction of crystalline iron oxides drives ongoing iron cycling that contributes to the stability of surface duricrusts. This represents a biotechnological opportunity with respect to post-mining rehabilitation attempts, requiring re-formation of these duricrusts. However, cultivated dissimilatory iron reducing bacteria typically reduce crystalline iron oxides quite poorly. A glucose-fermenting microbial consortium capable of reducing at least 27 mmol/L goethite was enriched from an iron duricrust region. Metagenome analysis led to the recovery of a metagenome assembled genome (MAG) of an iron reducer belonging to the alphaproteobacterial genus Telmatospirillum. This is the first report of iron reduction within the Telmatospirillum and the first reported genome of an iron-reducing, neutrophilic member of the Alphaproteobacteria. The Telmatospirillum MAG encodes putative metal transfer reductases (MtrA, MtrB) and a novel, multi-heme outer membrane cytochrome for extracellular electron transfer. In the presence of goethite, short chain fatty acid production shifted significantly in favor of acetate rather than propionate, indicating goethite is a hydrogen sink in the culture. Therefore, the presence of fermentative bacteria likely promotes iron reduction via hydrogen production. Stimulating microbial fermentation has potential to drive reduction of crystalline iron oxides, the rate limiting step for iron duricrust re-formation. Frontiers Media S.A. 2019-12-20 /pmc/articles/PMC6933298/ /pubmed/31921089 http://dx.doi.org/10.3389/fmicb.2019.02938 Text en Copyright © 2019 Gagen, Zaugg, Tyson and Southam. http://creativecommons.org/licenses/by/4.0/ 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) and the copyright owner(s) 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
Gagen, Emma J.
Zaugg, Julian
Tyson, Gene W.
Southam, Gordon
Goethite Reduction by a Neutrophilic Member of the Alphaproteobacterial Genus Telmatospirillum
title Goethite Reduction by a Neutrophilic Member of the Alphaproteobacterial Genus Telmatospirillum
title_full Goethite Reduction by a Neutrophilic Member of the Alphaproteobacterial Genus Telmatospirillum
title_fullStr Goethite Reduction by a Neutrophilic Member of the Alphaproteobacterial Genus Telmatospirillum
title_full_unstemmed Goethite Reduction by a Neutrophilic Member of the Alphaproteobacterial Genus Telmatospirillum
title_short Goethite Reduction by a Neutrophilic Member of the Alphaproteobacterial Genus Telmatospirillum
title_sort goethite reduction by a neutrophilic member of the alphaproteobacterial genus telmatospirillum
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6933298/
https://www.ncbi.nlm.nih.gov/pubmed/31921089
http://dx.doi.org/10.3389/fmicb.2019.02938
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