Cargando…

Anode Biofilm Transcriptomics Reveals Outer Surface Components Essential for High Density Current Production in Geobacter sulfurreducens Fuel Cells

The mechanisms by which Geobacter sulfurreducens transfers electrons through relatively thick (>50 µm) biofilms to electrodes acting as a sole electron acceptor were investigated. Biofilms of Geobacter sulfurreducens were grown either in flow-through systems with graphite anodes as the electron a...

Descripción completa

Detalles Bibliográficos
Autores principales: Nevin, Kelly P., Kim, Byoung-Chan, Glaven, Richard H., Johnson, Jessica P., Woodard, Trevor L., Methé, Barbara A., DiDonato, Raymond J., Covalla, Sean F., Franks, Ashley E., Liu, Anna, Lovley, Derek R.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2680965/
https://www.ncbi.nlm.nih.gov/pubmed/19461962
http://dx.doi.org/10.1371/journal.pone.0005628
_version_ 1782166993493819392
author Nevin, Kelly P.
Kim, Byoung-Chan
Glaven, Richard H.
Johnson, Jessica P.
Woodard, Trevor L.
Methé, Barbara A.
DiDonato, Raymond J.
Covalla, Sean F.
Franks, Ashley E.
Liu, Anna
Lovley, Derek R.
author_facet Nevin, Kelly P.
Kim, Byoung-Chan
Glaven, Richard H.
Johnson, Jessica P.
Woodard, Trevor L.
Methé, Barbara A.
DiDonato, Raymond J.
Covalla, Sean F.
Franks, Ashley E.
Liu, Anna
Lovley, Derek R.
author_sort Nevin, Kelly P.
collection PubMed
description The mechanisms by which Geobacter sulfurreducens transfers electrons through relatively thick (>50 µm) biofilms to electrodes acting as a sole electron acceptor were investigated. Biofilms of Geobacter sulfurreducens were grown either in flow-through systems with graphite anodes as the electron acceptor or on the same graphite surface, but with fumarate as the sole electron acceptor. Fumarate-grown biofilms were not immediately capable of significant current production, suggesting substantial physiological differences from current-producing biofilms. Microarray analysis revealed 13 genes in current-harvesting biofilms that had significantly higher transcript levels. The greatest increases were for pilA, the gene immediately downstream of pilA, and the genes for two outer c-type membrane cytochromes, OmcB and OmcZ. Down-regulated genes included the genes for the outer-membrane c-type cytochromes, OmcS and OmcT. Results of quantitative RT-PCR of gene transcript levels during biofilm growth were consistent with microarray results. OmcZ and the outer-surface c-type cytochrome, OmcE, were more abundant and OmcS was less abundant in current-harvesting cells. Strains in which pilA, the gene immediately downstream from pilA, omcB, omcS, omcE, or omcZ was deleted demonstrated that only deletion of pilA or omcZ severely inhibited current production and biofilm formation in current-harvesting mode. In contrast, these gene deletions had no impact on biofilm formation on graphite surfaces when fumarate served as the electron acceptor. These results suggest that biofilms grown harvesting current are specifically poised for electron transfer to electrodes and that, in addition to pili, OmcZ is a key component in electron transfer through differentiated G. sulfurreducens biofilms to electrodes.
format Text
id pubmed-2680965
institution National Center for Biotechnology Information
language English
publishDate 2009
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-26809652009-05-20 Anode Biofilm Transcriptomics Reveals Outer Surface Components Essential for High Density Current Production in Geobacter sulfurreducens Fuel Cells Nevin, Kelly P. Kim, Byoung-Chan Glaven, Richard H. Johnson, Jessica P. Woodard, Trevor L. Methé, Barbara A. DiDonato, Raymond J. Covalla, Sean F. Franks, Ashley E. Liu, Anna Lovley, Derek R. PLoS One Research Article The mechanisms by which Geobacter sulfurreducens transfers electrons through relatively thick (>50 µm) biofilms to electrodes acting as a sole electron acceptor were investigated. Biofilms of Geobacter sulfurreducens were grown either in flow-through systems with graphite anodes as the electron acceptor or on the same graphite surface, but with fumarate as the sole electron acceptor. Fumarate-grown biofilms were not immediately capable of significant current production, suggesting substantial physiological differences from current-producing biofilms. Microarray analysis revealed 13 genes in current-harvesting biofilms that had significantly higher transcript levels. The greatest increases were for pilA, the gene immediately downstream of pilA, and the genes for two outer c-type membrane cytochromes, OmcB and OmcZ. Down-regulated genes included the genes for the outer-membrane c-type cytochromes, OmcS and OmcT. Results of quantitative RT-PCR of gene transcript levels during biofilm growth were consistent with microarray results. OmcZ and the outer-surface c-type cytochrome, OmcE, were more abundant and OmcS was less abundant in current-harvesting cells. Strains in which pilA, the gene immediately downstream from pilA, omcB, omcS, omcE, or omcZ was deleted demonstrated that only deletion of pilA or omcZ severely inhibited current production and biofilm formation in current-harvesting mode. In contrast, these gene deletions had no impact on biofilm formation on graphite surfaces when fumarate served as the electron acceptor. These results suggest that biofilms grown harvesting current are specifically poised for electron transfer to electrodes and that, in addition to pili, OmcZ is a key component in electron transfer through differentiated G. sulfurreducens biofilms to electrodes. Public Library of Science 2009-05-20 /pmc/articles/PMC2680965/ /pubmed/19461962 http://dx.doi.org/10.1371/journal.pone.0005628 Text en Nevin 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
Nevin, Kelly P.
Kim, Byoung-Chan
Glaven, Richard H.
Johnson, Jessica P.
Woodard, Trevor L.
Methé, Barbara A.
DiDonato, Raymond J.
Covalla, Sean F.
Franks, Ashley E.
Liu, Anna
Lovley, Derek R.
Anode Biofilm Transcriptomics Reveals Outer Surface Components Essential for High Density Current Production in Geobacter sulfurreducens Fuel Cells
title Anode Biofilm Transcriptomics Reveals Outer Surface Components Essential for High Density Current Production in Geobacter sulfurreducens Fuel Cells
title_full Anode Biofilm Transcriptomics Reveals Outer Surface Components Essential for High Density Current Production in Geobacter sulfurreducens Fuel Cells
title_fullStr Anode Biofilm Transcriptomics Reveals Outer Surface Components Essential for High Density Current Production in Geobacter sulfurreducens Fuel Cells
title_full_unstemmed Anode Biofilm Transcriptomics Reveals Outer Surface Components Essential for High Density Current Production in Geobacter sulfurreducens Fuel Cells
title_short Anode Biofilm Transcriptomics Reveals Outer Surface Components Essential for High Density Current Production in Geobacter sulfurreducens Fuel Cells
title_sort anode biofilm transcriptomics reveals outer surface components essential for high density current production in geobacter sulfurreducens fuel cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2680965/
https://www.ncbi.nlm.nih.gov/pubmed/19461962
http://dx.doi.org/10.1371/journal.pone.0005628
work_keys_str_mv AT nevinkellyp anodebiofilmtranscriptomicsrevealsoutersurfacecomponentsessentialforhighdensitycurrentproductioningeobactersulfurreducensfuelcells
AT kimbyoungchan anodebiofilmtranscriptomicsrevealsoutersurfacecomponentsessentialforhighdensitycurrentproductioningeobactersulfurreducensfuelcells
AT glavenrichardh anodebiofilmtranscriptomicsrevealsoutersurfacecomponentsessentialforhighdensitycurrentproductioningeobactersulfurreducensfuelcells
AT johnsonjessicap anodebiofilmtranscriptomicsrevealsoutersurfacecomponentsessentialforhighdensitycurrentproductioningeobactersulfurreducensfuelcells
AT woodardtrevorl anodebiofilmtranscriptomicsrevealsoutersurfacecomponentsessentialforhighdensitycurrentproductioningeobactersulfurreducensfuelcells
AT methebarbaraa anodebiofilmtranscriptomicsrevealsoutersurfacecomponentsessentialforhighdensitycurrentproductioningeobactersulfurreducensfuelcells
AT didonatoraymondj anodebiofilmtranscriptomicsrevealsoutersurfacecomponentsessentialforhighdensitycurrentproductioningeobactersulfurreducensfuelcells
AT covallaseanf anodebiofilmtranscriptomicsrevealsoutersurfacecomponentsessentialforhighdensitycurrentproductioningeobactersulfurreducensfuelcells
AT franksashleye anodebiofilmtranscriptomicsrevealsoutersurfacecomponentsessentialforhighdensitycurrentproductioningeobactersulfurreducensfuelcells
AT liuanna anodebiofilmtranscriptomicsrevealsoutersurfacecomponentsessentialforhighdensitycurrentproductioningeobactersulfurreducensfuelcells
AT lovleyderekr anodebiofilmtranscriptomicsrevealsoutersurfacecomponentsessentialforhighdensitycurrentproductioningeobactersulfurreducensfuelcells