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Bespoke Biomolecular Wires for Transmembrane Electron Transfer: Spontaneous Assembly of a Functionalized Multiheme Electron Conduit
Shewanella oneidensis exchanges electrons between cellular metabolism and external redox partners in a process that attracts much attention for production of green electricity (microbial fuel cells) and chemicals (microbial electrosynthesis). A critical component of this pathway is the outer membran...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8415449/ https://www.ncbi.nlm.nih.gov/pubmed/34484155 http://dx.doi.org/10.3389/fmicb.2021.714508 |
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author | Piper, Samuel E. H. Edwards, Marcus J. van Wonderen, Jessica H. Casadevall, Carla Martel, Anne Jeuken, Lars J. C. Reisner, Erwin Clarke, Thomas A. Butt, Julea N. |
author_facet | Piper, Samuel E. H. Edwards, Marcus J. van Wonderen, Jessica H. Casadevall, Carla Martel, Anne Jeuken, Lars J. C. Reisner, Erwin Clarke, Thomas A. Butt, Julea N. |
author_sort | Piper, Samuel E. H. |
collection | PubMed |
description | Shewanella oneidensis exchanges electrons between cellular metabolism and external redox partners in a process that attracts much attention for production of green electricity (microbial fuel cells) and chemicals (microbial electrosynthesis). A critical component of this pathway is the outer membrane spanning MTR complex, a biomolecular wire formed of the MtrA, MtrB, and MtrC proteins. MtrA and MtrC are decaheme cytochromes that form a chain of close-packed hemes to define an electron transfer pathway of 185 Å. MtrA is wrapped inside MtrB for solubility across the outer membrane lipid bilayer; MtrC sits outside the cell for electron exchange with external redox partners. Here, we demonstrate tight and spontaneous in vitro association of MtrAB with separately purified MtrC. The resulting complex is comparable with the MTR complex naturally assembled by Shewanella in terms of both its structure and rates of electron transfer across a lipid bilayer. Our findings reveal the potential for building bespoke electron conduits where MtrAB combines with chemically modified MtrC, in this case, labeled with a Ru-dye that enables light-triggered electron injection into the MtrC heme chain. |
format | Online Article Text |
id | pubmed-8415449 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-84154492021-09-04 Bespoke Biomolecular Wires for Transmembrane Electron Transfer: Spontaneous Assembly of a Functionalized Multiheme Electron Conduit Piper, Samuel E. H. Edwards, Marcus J. van Wonderen, Jessica H. Casadevall, Carla Martel, Anne Jeuken, Lars J. C. Reisner, Erwin Clarke, Thomas A. Butt, Julea N. Front Microbiol Microbiology Shewanella oneidensis exchanges electrons between cellular metabolism and external redox partners in a process that attracts much attention for production of green electricity (microbial fuel cells) and chemicals (microbial electrosynthesis). A critical component of this pathway is the outer membrane spanning MTR complex, a biomolecular wire formed of the MtrA, MtrB, and MtrC proteins. MtrA and MtrC are decaheme cytochromes that form a chain of close-packed hemes to define an electron transfer pathway of 185 Å. MtrA is wrapped inside MtrB for solubility across the outer membrane lipid bilayer; MtrC sits outside the cell for electron exchange with external redox partners. Here, we demonstrate tight and spontaneous in vitro association of MtrAB with separately purified MtrC. The resulting complex is comparable with the MTR complex naturally assembled by Shewanella in terms of both its structure and rates of electron transfer across a lipid bilayer. Our findings reveal the potential for building bespoke electron conduits where MtrAB combines with chemically modified MtrC, in this case, labeled with a Ru-dye that enables light-triggered electron injection into the MtrC heme chain. Frontiers Media S.A. 2021-08-16 /pmc/articles/PMC8415449/ /pubmed/34484155 http://dx.doi.org/10.3389/fmicb.2021.714508 Text en Copyright © 2021 Piper, Edwards, van Wonderen, Casadevall, Martel, Jeuken, Reisner, Clarke and Butt. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Piper, Samuel E. H. Edwards, Marcus J. van Wonderen, Jessica H. Casadevall, Carla Martel, Anne Jeuken, Lars J. C. Reisner, Erwin Clarke, Thomas A. Butt, Julea N. Bespoke Biomolecular Wires for Transmembrane Electron Transfer: Spontaneous Assembly of a Functionalized Multiheme Electron Conduit |
title | Bespoke Biomolecular Wires for Transmembrane Electron Transfer: Spontaneous Assembly of a Functionalized Multiheme Electron Conduit |
title_full | Bespoke Biomolecular Wires for Transmembrane Electron Transfer: Spontaneous Assembly of a Functionalized Multiheme Electron Conduit |
title_fullStr | Bespoke Biomolecular Wires for Transmembrane Electron Transfer: Spontaneous Assembly of a Functionalized Multiheme Electron Conduit |
title_full_unstemmed | Bespoke Biomolecular Wires for Transmembrane Electron Transfer: Spontaneous Assembly of a Functionalized Multiheme Electron Conduit |
title_short | Bespoke Biomolecular Wires for Transmembrane Electron Transfer: Spontaneous Assembly of a Functionalized Multiheme Electron Conduit |
title_sort | bespoke biomolecular wires for transmembrane electron transfer: spontaneous assembly of a functionalized multiheme electron conduit |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8415449/ https://www.ncbi.nlm.nih.gov/pubmed/34484155 http://dx.doi.org/10.3389/fmicb.2021.714508 |
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