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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...

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Autores principales: Gupta, Dinesh, Sutherland, Molly C., Rengasamy, Karthikeyan, Meacham, J. Mark, Kranz, Robert G., Bose, Arpita
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2019
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.
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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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