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Engineering artificial photosynthesis based on rhodopsin for CO(2) fixation

Microbial rhodopsin, a significant contributor to sustaining life through light harvesting, holds untapped potential for carbon fixation. Here, we construct an artificial photosynthesis system which combines the proton-pumping ability of rhodopsin with an extracellular electron uptake mechanism, est...

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Autores principales: Tu, Weiming, Xu, Jiabao, Thompson, Ian P., Huang, Wei E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10696030/
https://www.ncbi.nlm.nih.gov/pubmed/38049399
http://dx.doi.org/10.1038/s41467-023-43524-4
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author Tu, Weiming
Xu, Jiabao
Thompson, Ian P.
Huang, Wei E.
author_facet Tu, Weiming
Xu, Jiabao
Thompson, Ian P.
Huang, Wei E.
author_sort Tu, Weiming
collection PubMed
description Microbial rhodopsin, a significant contributor to sustaining life through light harvesting, holds untapped potential for carbon fixation. Here, we construct an artificial photosynthesis system which combines the proton-pumping ability of rhodopsin with an extracellular electron uptake mechanism, establishing a pathway to drive photoelectrosynthetic CO(2) fixation by Ralstonia eutropha (also known as Cupriavidus necator) H16, a facultatively chemolithoautotrophic soil bacterium. R. eutropha is engineered to heterologously express an extracellular electron transfer pathway of Shewanella oneidensis MR-1 and Gloeobacter rhodopsin (GR). Employing GR and the outer-membrane conduit MtrCAB from S. oneidensis, extracellular electrons and GR-driven proton motive force are integrated into R. eutropha’s native electron transport chain (ETC). Inspired by natural photosynthesis, the photoelectrochemical system splits water to supply electrons to R. eutropha via the Mtr outer-membrane route. The light-activated proton pump - GR, supported by canthaxanthin as an antenna, powers ATP synthesis and reverses the ETC to regenerate NADH/NADPH, facilitating R. eutropha’s biomass synthesis from CO(2). Overexpression of a carbonic anhydrase further enhances CO(2) fixation. This artificial photosynthesis system has the potential to advance the development of efficient photosynthesis, redefining our understanding of the ecological role of microbial rhodopsins in nature.
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spelling pubmed-106960302023-12-06 Engineering artificial photosynthesis based on rhodopsin for CO(2) fixation Tu, Weiming Xu, Jiabao Thompson, Ian P. Huang, Wei E. Nat Commun Article Microbial rhodopsin, a significant contributor to sustaining life through light harvesting, holds untapped potential for carbon fixation. Here, we construct an artificial photosynthesis system which combines the proton-pumping ability of rhodopsin with an extracellular electron uptake mechanism, establishing a pathway to drive photoelectrosynthetic CO(2) fixation by Ralstonia eutropha (also known as Cupriavidus necator) H16, a facultatively chemolithoautotrophic soil bacterium. R. eutropha is engineered to heterologously express an extracellular electron transfer pathway of Shewanella oneidensis MR-1 and Gloeobacter rhodopsin (GR). Employing GR and the outer-membrane conduit MtrCAB from S. oneidensis, extracellular electrons and GR-driven proton motive force are integrated into R. eutropha’s native electron transport chain (ETC). Inspired by natural photosynthesis, the photoelectrochemical system splits water to supply electrons to R. eutropha via the Mtr outer-membrane route. The light-activated proton pump - GR, supported by canthaxanthin as an antenna, powers ATP synthesis and reverses the ETC to regenerate NADH/NADPH, facilitating R. eutropha’s biomass synthesis from CO(2). Overexpression of a carbonic anhydrase further enhances CO(2) fixation. This artificial photosynthesis system has the potential to advance the development of efficient photosynthesis, redefining our understanding of the ecological role of microbial rhodopsins in nature. Nature Publishing Group UK 2023-12-04 /pmc/articles/PMC10696030/ /pubmed/38049399 http://dx.doi.org/10.1038/s41467-023-43524-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Tu, Weiming
Xu, Jiabao
Thompson, Ian P.
Huang, Wei E.
Engineering artificial photosynthesis based on rhodopsin for CO(2) fixation
title Engineering artificial photosynthesis based on rhodopsin for CO(2) fixation
title_full Engineering artificial photosynthesis based on rhodopsin for CO(2) fixation
title_fullStr Engineering artificial photosynthesis based on rhodopsin for CO(2) fixation
title_full_unstemmed Engineering artificial photosynthesis based on rhodopsin for CO(2) fixation
title_short Engineering artificial photosynthesis based on rhodopsin for CO(2) fixation
title_sort engineering artificial photosynthesis based on rhodopsin for co(2) fixation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10696030/
https://www.ncbi.nlm.nih.gov/pubmed/38049399
http://dx.doi.org/10.1038/s41467-023-43524-4
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