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Phototrophic extracellular electron uptake is linked to carbon dioxide fixation in the bacterium Rhodopseudomonas palustris
Extracellular electron uptake (EEU) is the ability of microbes to take up electrons from solid-phase conductive substances such as metal oxides. EEU is performed by prevalent phototrophic bacterial genera, but the electron transfer pathways and the physiological electron sinks are poorly understood....
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6430793/ https://www.ncbi.nlm.nih.gov/pubmed/30902976 http://dx.doi.org/10.1038/s41467-019-09377-6 |
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author | Guzman, Michael S. Rengasamy, Karthikeyan Binkley, Michael M. Jones, Clive Ranaivoarisoa, Tahina Onina Singh, Rajesh Fike, David A. Meacham, J. Mark Bose, Arpita |
author_facet | Guzman, Michael S. Rengasamy, Karthikeyan Binkley, Michael M. Jones, Clive Ranaivoarisoa, Tahina Onina Singh, Rajesh Fike, David A. Meacham, J. Mark Bose, Arpita |
author_sort | Guzman, Michael S. |
collection | PubMed |
description | Extracellular electron uptake (EEU) is the ability of microbes to take up electrons from solid-phase conductive substances such as metal oxides. EEU is performed by prevalent phototrophic bacterial genera, but the electron transfer pathways and the physiological electron sinks are poorly understood. Here we show that electrons enter the photosynthetic electron transport chain during EEU in the phototrophic bacterium Rhodopseudomonas palustris TIE-1. Cathodic electron flow is also correlated with a highly reducing intracellular redox environment. We show that reducing equivalents are used for carbon dioxide (CO(2)) fixation, which is the primary electron sink. Deletion of the genes encoding ruBisCO (the CO(2)-fixing enzyme of the Calvin-Benson-Bassham cycle) leads to a 90% reduction in EEU. This work shows that phototrophs can directly use solid-phase conductive substances for electron transfer, energy transduction, and CO(2) fixation. |
format | Online Article Text |
id | pubmed-6430793 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-64307932019-03-25 Phototrophic extracellular electron uptake is linked to carbon dioxide fixation in the bacterium Rhodopseudomonas palustris Guzman, Michael S. Rengasamy, Karthikeyan Binkley, Michael M. Jones, Clive Ranaivoarisoa, Tahina Onina Singh, Rajesh Fike, David A. Meacham, J. Mark Bose, Arpita Nat Commun Article Extracellular electron uptake (EEU) is the ability of microbes to take up electrons from solid-phase conductive substances such as metal oxides. EEU is performed by prevalent phototrophic bacterial genera, but the electron transfer pathways and the physiological electron sinks are poorly understood. Here we show that electrons enter the photosynthetic electron transport chain during EEU in the phototrophic bacterium Rhodopseudomonas palustris TIE-1. Cathodic electron flow is also correlated with a highly reducing intracellular redox environment. We show that reducing equivalents are used for carbon dioxide (CO(2)) fixation, which is the primary electron sink. Deletion of the genes encoding ruBisCO (the CO(2)-fixing enzyme of the Calvin-Benson-Bassham cycle) leads to a 90% reduction in EEU. This work shows that phototrophs can directly use solid-phase conductive substances for electron transfer, energy transduction, and CO(2) fixation. Nature Publishing Group UK 2019-03-22 /pmc/articles/PMC6430793/ /pubmed/30902976 http://dx.doi.org/10.1038/s41467-019-09377-6 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Guzman, Michael S. Rengasamy, Karthikeyan Binkley, Michael M. Jones, Clive Ranaivoarisoa, Tahina Onina Singh, Rajesh Fike, David A. Meacham, J. Mark Bose, Arpita Phototrophic extracellular electron uptake is linked to carbon dioxide fixation in the bacterium Rhodopseudomonas palustris |
title | Phototrophic extracellular electron uptake is linked to carbon dioxide fixation in the bacterium Rhodopseudomonas palustris |
title_full | Phototrophic extracellular electron uptake is linked to carbon dioxide fixation in the bacterium Rhodopseudomonas palustris |
title_fullStr | Phototrophic extracellular electron uptake is linked to carbon dioxide fixation in the bacterium Rhodopseudomonas palustris |
title_full_unstemmed | Phototrophic extracellular electron uptake is linked to carbon dioxide fixation in the bacterium Rhodopseudomonas palustris |
title_short | Phototrophic extracellular electron uptake is linked to carbon dioxide fixation in the bacterium Rhodopseudomonas palustris |
title_sort | phototrophic extracellular electron uptake is linked to carbon dioxide fixation in the bacterium rhodopseudomonas palustris |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6430793/ https://www.ncbi.nlm.nih.gov/pubmed/30902976 http://dx.doi.org/10.1038/s41467-019-09377-6 |
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