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Iron Corrosion via Direct Metal-Microbe Electron Transfer

The concept that anaerobic microorganisms can directly accept electrons from Fe(0) has been controversial because direct metal-microbe electron transfer has previously only been indirectly inferred. Fe(0) oxidation was studied with Geobacter sulfurreducens strain ACL, an autotrophic strain that was...

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Autores principales: Tang, Hai-Yan, Holmes, Dawn E., Ueki, Toshiyuki, Palacios, Paola A., Lovley, Derek R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6520446/
https://www.ncbi.nlm.nih.gov/pubmed/31088920
http://dx.doi.org/10.1128/mBio.00303-19
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author Tang, Hai-Yan
Holmes, Dawn E.
Ueki, Toshiyuki
Palacios, Paola A.
Lovley, Derek R.
author_facet Tang, Hai-Yan
Holmes, Dawn E.
Ueki, Toshiyuki
Palacios, Paola A.
Lovley, Derek R.
author_sort Tang, Hai-Yan
collection PubMed
description The concept that anaerobic microorganisms can directly accept electrons from Fe(0) has been controversial because direct metal-microbe electron transfer has previously only been indirectly inferred. Fe(0) oxidation was studied with Geobacter sulfurreducens strain ACL, an autotrophic strain that was previously shown to grow with electrons derived from a graphite cathode as the sole electron donor. Strain ACL grew with Fe(0) as the sole electron donor and fumarate as the electron acceptor. However, it appeared that at least a portion of the electron transfer was via H(2) produced nonenzymatically from the oxidation of Fe(0) to Fe(II). H(2), which accumulated in abiotic controls, was consumed during the growth of strain ACL, the cells were predominately planktonic, and genes for the uptake hydrogenase were highly expressed. Strain ACL(HF) was constructed to prevent growth on H(2) or formate by deleting the genes for the uptake of hydrogenase and formate dehydrogenases from strain ACL. Strain ACL(HF) also grew with Fe(0) as the sole electron donor, but H(2) accumulated in the culture, and cells heavily colonized Fe(0) surfaces with no visible planktonic growth. Transcriptomics suggested that the outer surface c-type cytochromes OmcS and OmcZ were important during growth of strain ACL(HF) on Fe(0). Strain ACL(HF) did not grow on Fe(0) if the gene for either of these cytochromes was deleted. The specific attachment of strain ACL(HF) to Fe(0), coupled with requirements for known extracellular electrical contacts, suggest that direct metal-microbe electron transfer is the most likely option for Fe(0) serving as an electron donor.
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spelling pubmed-65204462019-05-16 Iron Corrosion via Direct Metal-Microbe Electron Transfer Tang, Hai-Yan Holmes, Dawn E. Ueki, Toshiyuki Palacios, Paola A. Lovley, Derek R. mBio Research Article The concept that anaerobic microorganisms can directly accept electrons from Fe(0) has been controversial because direct metal-microbe electron transfer has previously only been indirectly inferred. Fe(0) oxidation was studied with Geobacter sulfurreducens strain ACL, an autotrophic strain that was previously shown to grow with electrons derived from a graphite cathode as the sole electron donor. Strain ACL grew with Fe(0) as the sole electron donor and fumarate as the electron acceptor. However, it appeared that at least a portion of the electron transfer was via H(2) produced nonenzymatically from the oxidation of Fe(0) to Fe(II). H(2), which accumulated in abiotic controls, was consumed during the growth of strain ACL, the cells were predominately planktonic, and genes for the uptake hydrogenase were highly expressed. Strain ACL(HF) was constructed to prevent growth on H(2) or formate by deleting the genes for the uptake of hydrogenase and formate dehydrogenases from strain ACL. Strain ACL(HF) also grew with Fe(0) as the sole electron donor, but H(2) accumulated in the culture, and cells heavily colonized Fe(0) surfaces with no visible planktonic growth. Transcriptomics suggested that the outer surface c-type cytochromes OmcS and OmcZ were important during growth of strain ACL(HF) on Fe(0). Strain ACL(HF) did not grow on Fe(0) if the gene for either of these cytochromes was deleted. The specific attachment of strain ACL(HF) to Fe(0), coupled with requirements for known extracellular electrical contacts, suggest that direct metal-microbe electron transfer is the most likely option for Fe(0) serving as an electron donor. American Society for Microbiology 2019-05-14 /pmc/articles/PMC6520446/ /pubmed/31088920 http://dx.doi.org/10.1128/mBio.00303-19 Text en Copyright © 2019 Tang et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Tang, Hai-Yan
Holmes, Dawn E.
Ueki, Toshiyuki
Palacios, Paola A.
Lovley, Derek R.
Iron Corrosion via Direct Metal-Microbe Electron Transfer
title Iron Corrosion via Direct Metal-Microbe Electron Transfer
title_full Iron Corrosion via Direct Metal-Microbe Electron Transfer
title_fullStr Iron Corrosion via Direct Metal-Microbe Electron Transfer
title_full_unstemmed Iron Corrosion via Direct Metal-Microbe Electron Transfer
title_short Iron Corrosion via Direct Metal-Microbe Electron Transfer
title_sort iron corrosion via direct metal-microbe electron transfer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6520446/
https://www.ncbi.nlm.nih.gov/pubmed/31088920
http://dx.doi.org/10.1128/mBio.00303-19
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