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Photoferrotrophs Produce a PioAB Electron Conduit for Extracellular Electron Uptake
Photoferrotrophy is a form of anoxygenic photosynthesis whereby bacteria utilize soluble or insoluble forms of ferrous iron as an electron donor to fix carbon dioxide using light energy. They can also use poised electrodes as their electron donor via phototrophic extracellular electron uptake (photo...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6831781/ https://www.ncbi.nlm.nih.gov/pubmed/31690680 http://dx.doi.org/10.1128/mBio.02668-19 |
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author | Gupta, Dinesh Sutherland, Molly C. Rengasamy, Karthikeyan Meacham, J. Mark Kranz, Robert G. Bose, Arpita |
author_facet | Gupta, Dinesh Sutherland, Molly C. Rengasamy, Karthikeyan Meacham, J. Mark Kranz, Robert G. Bose, Arpita |
author_sort | Gupta, Dinesh |
collection | PubMed |
description | Photoferrotrophy is a form of anoxygenic photosynthesis whereby bacteria utilize soluble or insoluble forms of ferrous iron as an electron donor to fix carbon dioxide using light energy. They can also use poised electrodes as their electron donor via phototrophic extracellular electron uptake (phototrophic EEU). The electron uptake mechanisms underlying these processes are not well understood. Using Rhodopseudomonas palustris TIE-1 as a model, we show that a single periplasmic decaheme cytochrome c, PioA, and an outer membrane porin, PioB, form a complex allowing extracellular electron uptake across the outer membrane from both soluble iron and poised electrodes. We observe that PioA undergoes postsecretory proteolysis of its N terminus to produce a shorter heme-attached PioA (holo-PioA(C), where PioA(C) represents the C terminus of PioA), which can exist both freely in the periplasm and in a complex with PioB. The extended N-terminal peptide controls heme attachment, and its processing is required to produce wild-type levels of holo-PioA(C) and holo-PioA(C)B complex. It is also conserved in PioA homologs from other phototrophs. The presence of PioAB in these organisms correlate with their ability to perform photoferrotrophy and phototrophic EEU. |
format | Online Article Text |
id | pubmed-6831781 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-68317812019-11-08 Photoferrotrophs Produce a PioAB Electron Conduit for Extracellular Electron Uptake Gupta, Dinesh Sutherland, Molly C. Rengasamy, Karthikeyan Meacham, J. Mark Kranz, Robert G. Bose, Arpita mBio Research Article Photoferrotrophy is a form of anoxygenic photosynthesis whereby bacteria utilize soluble or insoluble forms of ferrous iron as an electron donor to fix carbon dioxide using light energy. They can also use poised electrodes as their electron donor via phototrophic extracellular electron uptake (phototrophic EEU). The electron uptake mechanisms underlying these processes are not well understood. Using Rhodopseudomonas palustris TIE-1 as a model, we show that a single periplasmic decaheme cytochrome c, PioA, and an outer membrane porin, PioB, form a complex allowing extracellular electron uptake across the outer membrane from both soluble iron and poised electrodes. We observe that PioA undergoes postsecretory proteolysis of its N terminus to produce a shorter heme-attached PioA (holo-PioA(C), where PioA(C) represents the C terminus of PioA), which can exist both freely in the periplasm and in a complex with PioB. The extended N-terminal peptide controls heme attachment, and its processing is required to produce wild-type levels of holo-PioA(C) and holo-PioA(C)B complex. It is also conserved in PioA homologs from other phototrophs. The presence of PioAB in these organisms correlate with their ability to perform photoferrotrophy and phototrophic EEU. American Society for Microbiology 2019-11-05 /pmc/articles/PMC6831781/ /pubmed/31690680 http://dx.doi.org/10.1128/mBio.02668-19 Text en Copyright © 2019 Gupta 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 Gupta, Dinesh Sutherland, Molly C. Rengasamy, Karthikeyan Meacham, J. Mark Kranz, Robert G. Bose, Arpita Photoferrotrophs Produce a PioAB Electron Conduit for Extracellular Electron Uptake |
title | Photoferrotrophs Produce a PioAB Electron Conduit for Extracellular Electron Uptake |
title_full | Photoferrotrophs Produce a PioAB Electron Conduit for Extracellular Electron Uptake |
title_fullStr | Photoferrotrophs Produce a PioAB Electron Conduit for Extracellular Electron Uptake |
title_full_unstemmed | Photoferrotrophs Produce a PioAB Electron Conduit for Extracellular Electron Uptake |
title_short | Photoferrotrophs Produce a PioAB Electron Conduit for Extracellular Electron Uptake |
title_sort | photoferrotrophs produce a pioab electron conduit for extracellular electron uptake |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6831781/ https://www.ncbi.nlm.nih.gov/pubmed/31690680 http://dx.doi.org/10.1128/mBio.02668-19 |
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