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Engineering a Rhodopsin-Based Photo-Electrosynthetic System in Bacteria for CO(2) Fixation

[Image: see text] A key goal of synthetic biology is to engineer organisms that can use solar energy to convert CO(2) to biomass, chemicals, and fuels. We engineered a light-dependent electron transfer chain by integrating rhodopsin and an electron donor to form a closed redox loop, which drives rho...

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Autores principales: Davison, Paul A., Tu, Weiming, Xu, Jiabao, Della Valle, Simona, Thompson, Ian P., Hunter, C. Neil, Huang, Wei E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9680020/
https://www.ncbi.nlm.nih.gov/pubmed/36264158
http://dx.doi.org/10.1021/acssynbio.2c00397
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author Davison, Paul A.
Tu, Weiming
Xu, Jiabao
Della Valle, Simona
Thompson, Ian P.
Hunter, C. Neil
Huang, Wei E.
author_facet Davison, Paul A.
Tu, Weiming
Xu, Jiabao
Della Valle, Simona
Thompson, Ian P.
Hunter, C. Neil
Huang, Wei E.
author_sort Davison, Paul A.
collection PubMed
description [Image: see text] A key goal of synthetic biology is to engineer organisms that can use solar energy to convert CO(2) to biomass, chemicals, and fuels. We engineered a light-dependent electron transfer chain by integrating rhodopsin and an electron donor to form a closed redox loop, which drives rhodopsin-dependent CO(2) fixation. A light-driven proton pump comprising Gloeobacter rhodopsin (GR) and its cofactor retinal have been assembled in Ralstonia eutropha (Cupriavidus necator) H16. In the presence of light, this strain fixed inorganic carbon (or bicarbonate) leading to 20% growth enhancement, when formate was used as an electron donor. We found that an electrode from a solar panel can replace organic compounds to serve as the electron donor, mediated by the electron shuttle molecule riboflavin. In this new autotrophic and photo-electrosynthetic system, GR is augmented by an external photocell for reductive CO(2) fixation. We demonstrated that this hybrid photo-electrosynthetic pathway can drive the engineered R. eutropha strain to grow using CO(2) as the sole carbon source. In this system, a bioreactor with only two inputs, light and CO(2), enables the R. eutropha strain to perform a rhodopsin-dependent autotrophic growth. Light energy alone, supplied by a solar panel, can drive the conversion of CO(2) into biomass with a maximum electron transfer efficiency of 20%.
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spelling pubmed-96800202022-11-23 Engineering a Rhodopsin-Based Photo-Electrosynthetic System in Bacteria for CO(2) Fixation Davison, Paul A. Tu, Weiming Xu, Jiabao Della Valle, Simona Thompson, Ian P. Hunter, C. Neil Huang, Wei E. ACS Synth Biol [Image: see text] A key goal of synthetic biology is to engineer organisms that can use solar energy to convert CO(2) to biomass, chemicals, and fuels. We engineered a light-dependent electron transfer chain by integrating rhodopsin and an electron donor to form a closed redox loop, which drives rhodopsin-dependent CO(2) fixation. A light-driven proton pump comprising Gloeobacter rhodopsin (GR) and its cofactor retinal have been assembled in Ralstonia eutropha (Cupriavidus necator) H16. In the presence of light, this strain fixed inorganic carbon (or bicarbonate) leading to 20% growth enhancement, when formate was used as an electron donor. We found that an electrode from a solar panel can replace organic compounds to serve as the electron donor, mediated by the electron shuttle molecule riboflavin. In this new autotrophic and photo-electrosynthetic system, GR is augmented by an external photocell for reductive CO(2) fixation. We demonstrated that this hybrid photo-electrosynthetic pathway can drive the engineered R. eutropha strain to grow using CO(2) as the sole carbon source. In this system, a bioreactor with only two inputs, light and CO(2), enables the R. eutropha strain to perform a rhodopsin-dependent autotrophic growth. Light energy alone, supplied by a solar panel, can drive the conversion of CO(2) into biomass with a maximum electron transfer efficiency of 20%. American Chemical Society 2022-10-20 2022-11-18 /pmc/articles/PMC9680020/ /pubmed/36264158 http://dx.doi.org/10.1021/acssynbio.2c00397 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Davison, Paul A.
Tu, Weiming
Xu, Jiabao
Della Valle, Simona
Thompson, Ian P.
Hunter, C. Neil
Huang, Wei E.
Engineering a Rhodopsin-Based Photo-Electrosynthetic System in Bacteria for CO(2) Fixation
title Engineering a Rhodopsin-Based Photo-Electrosynthetic System in Bacteria for CO(2) Fixation
title_full Engineering a Rhodopsin-Based Photo-Electrosynthetic System in Bacteria for CO(2) Fixation
title_fullStr Engineering a Rhodopsin-Based Photo-Electrosynthetic System in Bacteria for CO(2) Fixation
title_full_unstemmed Engineering a Rhodopsin-Based Photo-Electrosynthetic System in Bacteria for CO(2) Fixation
title_short Engineering a Rhodopsin-Based Photo-Electrosynthetic System in Bacteria for CO(2) Fixation
title_sort engineering a rhodopsin-based photo-electrosynthetic system in bacteria for co(2) fixation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9680020/
https://www.ncbi.nlm.nih.gov/pubmed/36264158
http://dx.doi.org/10.1021/acssynbio.2c00397
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