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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...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2021
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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. |
format | Online Article Text |
id | pubmed-7936347 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
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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