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Acetogenic bacteria utilize light-driven electrons as an energy source for autotrophic growth

Acetogenic bacteria use cellular redox energy to convert CO(2) to acetate using the Wood–Ljungdahl (WL) pathway. Such redox energy can be derived from electrons generated from H(2) as well as from inorganic materials, such as photoresponsive semiconductors. We have developed a nanoparticle-microbe h...

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Autores principales: Jin, Sangrak, Jeon, Yale, Jeon, Min Soo, Shin, Jongoh, Song, Yoseb, Kang, Seulgi, Bae, Jiyun, Cho, Suhyung, Lee, Jung-Kul, Kim, Dong Rip, Cho, Byung-Kwan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7936347/
https://www.ncbi.nlm.nih.gov/pubmed/33619098
http://dx.doi.org/10.1073/pnas.2020552118
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author Jin, Sangrak
Jeon, Yale
Jeon, Min Soo
Shin, Jongoh
Song, Yoseb
Kang, Seulgi
Bae, Jiyun
Cho, Suhyung
Lee, Jung-Kul
Kim, Dong Rip
Cho, Byung-Kwan
author_facet Jin, Sangrak
Jeon, Yale
Jeon, Min Soo
Shin, Jongoh
Song, Yoseb
Kang, Seulgi
Bae, Jiyun
Cho, Suhyung
Lee, Jung-Kul
Kim, Dong Rip
Cho, Byung-Kwan
author_sort Jin, Sangrak
collection PubMed
description Acetogenic bacteria use cellular redox energy to convert CO(2) to acetate using the Wood–Ljungdahl (WL) pathway. Such redox energy can be derived from electrons generated from H(2) as well as from inorganic materials, such as photoresponsive semiconductors. We have developed a nanoparticle-microbe hybrid system in which chemically synthesized cadmium sulfide nanoparticles (CdS-NPs) are displayed on the cell surface of the industrial acetogen Clostridium autoethanogenum. The hybrid system converts CO(2) into acetate without the need for additional energy sources, such as H(2), and uses only light-induced electrons from CdS-NPs. To elucidate the underlying mechanism by which C. autoethanogenum uses electrons generated from external energy sources to reduce CO(2), we performed transcriptional analysis. Our results indicate that genes encoding the metal ion or flavin-binding proteins were highly up-regulated under CdS-driven autotrophic conditions along with the activation of genes associated with the WL pathway and energy conservation system. Furthermore, the addition of these cofactors increased the CO(2) fixation rate under light-exposure conditions. Our results demonstrate the potential to improve the efficiency of artificial photosynthesis systems based on acetogenic bacteria integrated with photoresponsive nanoparticles.
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spelling pubmed-79363472021-03-11 Acetogenic bacteria utilize light-driven electrons as an energy source for autotrophic growth Jin, Sangrak Jeon, Yale Jeon, Min Soo Shin, Jongoh Song, Yoseb Kang, Seulgi Bae, Jiyun Cho, Suhyung Lee, Jung-Kul Kim, Dong Rip Cho, Byung-Kwan Proc Natl Acad Sci U S A Biological Sciences Acetogenic bacteria use cellular redox energy to convert CO(2) to acetate using the Wood–Ljungdahl (WL) pathway. Such redox energy can be derived from electrons generated from H(2) as well as from inorganic materials, such as photoresponsive semiconductors. We have developed a nanoparticle-microbe hybrid system in which chemically synthesized cadmium sulfide nanoparticles (CdS-NPs) are displayed on the cell surface of the industrial acetogen Clostridium autoethanogenum. The hybrid system converts CO(2) into acetate without the need for additional energy sources, such as H(2), and uses only light-induced electrons from CdS-NPs. To elucidate the underlying mechanism by which C. autoethanogenum uses electrons generated from external energy sources to reduce CO(2), we performed transcriptional analysis. Our results indicate that genes encoding the metal ion or flavin-binding proteins were highly up-regulated under CdS-driven autotrophic conditions along with the activation of genes associated with the WL pathway and energy conservation system. Furthermore, the addition of these cofactors increased the CO(2) fixation rate under light-exposure conditions. Our results demonstrate the potential to improve the efficiency of artificial photosynthesis systems based on acetogenic bacteria integrated with photoresponsive nanoparticles. National Academy of Sciences 2021-03-02 2021-02-22 /pmc/articles/PMC7936347/ /pubmed/33619098 http://dx.doi.org/10.1073/pnas.2020552118 Text en Copyright © 2021 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/ https://creativecommons.org/licenses/by-nc-nd/4.0/This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Biological Sciences
Jin, Sangrak
Jeon, Yale
Jeon, Min Soo
Shin, Jongoh
Song, Yoseb
Kang, Seulgi
Bae, Jiyun
Cho, Suhyung
Lee, Jung-Kul
Kim, Dong Rip
Cho, Byung-Kwan
Acetogenic bacteria utilize light-driven electrons as an energy source for autotrophic growth
title Acetogenic bacteria utilize light-driven electrons as an energy source for autotrophic growth
title_full Acetogenic bacteria utilize light-driven electrons as an energy source for autotrophic growth
title_fullStr Acetogenic bacteria utilize light-driven electrons as an energy source for autotrophic growth
title_full_unstemmed Acetogenic bacteria utilize light-driven electrons as an energy source for autotrophic growth
title_short Acetogenic bacteria utilize light-driven electrons as an energy source for autotrophic growth
title_sort acetogenic bacteria utilize light-driven electrons as an energy source for autotrophic growth
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7936347/
https://www.ncbi.nlm.nih.gov/pubmed/33619098
http://dx.doi.org/10.1073/pnas.2020552118
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