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Genome-Scale Analysis of Acetobacterium woodii Identifies Translational Regulation of Acetogenesis

Acetogens synthesize acetyl-CoA via the CO(2)-fixing Wood-Ljungdahl pathway. Despite their ecological and biotechnological importance, their translational regulation of carbon and energy metabolisms remains unclear. Here, we report how carbon and energy metabolisms in the model acetogen Acetobacteri...

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Autores principales: Shin, Jongoh, Song, Yoseb, Kang, Seulgi, Jin, Sangrak, Lee, Jung-Kul, Kim, Dong Rip, Cho, Suhyung, Müller, Volker, Cho, Byung-Kwan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8407422/
https://www.ncbi.nlm.nih.gov/pubmed/34313456
http://dx.doi.org/10.1128/mSystems.00696-21
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author Shin, Jongoh
Song, Yoseb
Kang, Seulgi
Jin, Sangrak
Lee, Jung-Kul
Kim, Dong Rip
Cho, Suhyung
Müller, Volker
Cho, Byung-Kwan
author_facet Shin, Jongoh
Song, Yoseb
Kang, Seulgi
Jin, Sangrak
Lee, Jung-Kul
Kim, Dong Rip
Cho, Suhyung
Müller, Volker
Cho, Byung-Kwan
author_sort Shin, Jongoh
collection PubMed
description Acetogens synthesize acetyl-CoA via the CO(2)-fixing Wood-Ljungdahl pathway. Despite their ecological and biotechnological importance, their translational regulation of carbon and energy metabolisms remains unclear. Here, we report how carbon and energy metabolisms in the model acetogen Acetobacterium woodii are translationally controlled under different growth conditions. Data integration of genome-scale transcriptomic and translatomic analyses revealed that the acetogenesis genes, including those of the Wood-Ljungdahl pathway and energy metabolism, showed changes in translational efficiency under autotrophic growth conditions. In particular, genes encoding the Wood-Ljungdahl pathway are translated at similar levels to achieve efficient acetogenesis activity under autotrophic growth conditions, whereas genes encoding the carbonyl branch present increased translation levels in comparison to those for the methyl branch under heterotrophic growth conditions. The translation efficiency of genes in the pathways is differentially regulated by 5′ untranslated regions and ribosome-binding sequences under different growth conditions. Our findings provide potential strategies to optimize the metabolism of syngas-fermenting acetogenic bacteria for better productivity. IMPORTANCE Acetogens are capable of reducing CO(2) to multicarbon compounds (e.g., ethanol or 2,3-butanediol) via the Wood-Ljungdahl pathway. Given that protein synthesis in bacteria is highly energy consuming, acetogens living at the thermodynamic limit of life are inevitably under translation control. Here, we dissect the translational regulation of carbon and energy metabolisms in the model acetogen Acetobacterium woodii under heterotrophic and autotrophic growth conditions. The latter may be experienced when acetogen is used as a cell factory that synthesizes products from CO(2) during the gas fermentation process. We found that the methyl and carbonyl branches of the Wood-Ljungdahl pathway are activated at similar translation levels during autotrophic growth. Translation is mainly regulated by the 5′-untranslated-region structure and ribosome-binding-site sequence. This work reveals novel translational regulation for coping with autotrophic growth conditions and provides the systematic data set, including the transcriptome, translatome, and promoter/5′-untranslated-region bioparts.
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spelling pubmed-84074222021-09-09 Genome-Scale Analysis of Acetobacterium woodii Identifies Translational Regulation of Acetogenesis Shin, Jongoh Song, Yoseb Kang, Seulgi Jin, Sangrak Lee, Jung-Kul Kim, Dong Rip Cho, Suhyung Müller, Volker Cho, Byung-Kwan mSystems Research Article Acetogens synthesize acetyl-CoA via the CO(2)-fixing Wood-Ljungdahl pathway. Despite their ecological and biotechnological importance, their translational regulation of carbon and energy metabolisms remains unclear. Here, we report how carbon and energy metabolisms in the model acetogen Acetobacterium woodii are translationally controlled under different growth conditions. Data integration of genome-scale transcriptomic and translatomic analyses revealed that the acetogenesis genes, including those of the Wood-Ljungdahl pathway and energy metabolism, showed changes in translational efficiency under autotrophic growth conditions. In particular, genes encoding the Wood-Ljungdahl pathway are translated at similar levels to achieve efficient acetogenesis activity under autotrophic growth conditions, whereas genes encoding the carbonyl branch present increased translation levels in comparison to those for the methyl branch under heterotrophic growth conditions. The translation efficiency of genes in the pathways is differentially regulated by 5′ untranslated regions and ribosome-binding sequences under different growth conditions. Our findings provide potential strategies to optimize the metabolism of syngas-fermenting acetogenic bacteria for better productivity. IMPORTANCE Acetogens are capable of reducing CO(2) to multicarbon compounds (e.g., ethanol or 2,3-butanediol) via the Wood-Ljungdahl pathway. Given that protein synthesis in bacteria is highly energy consuming, acetogens living at the thermodynamic limit of life are inevitably under translation control. Here, we dissect the translational regulation of carbon and energy metabolisms in the model acetogen Acetobacterium woodii under heterotrophic and autotrophic growth conditions. The latter may be experienced when acetogen is used as a cell factory that synthesizes products from CO(2) during the gas fermentation process. We found that the methyl and carbonyl branches of the Wood-Ljungdahl pathway are activated at similar translation levels during autotrophic growth. Translation is mainly regulated by the 5′-untranslated-region structure and ribosome-binding-site sequence. This work reveals novel translational regulation for coping with autotrophic growth conditions and provides the systematic data set, including the transcriptome, translatome, and promoter/5′-untranslated-region bioparts. American Society for Microbiology 2021-07-27 /pmc/articles/PMC8407422/ /pubmed/34313456 http://dx.doi.org/10.1128/mSystems.00696-21 Text en Copyright © 2021 Shin et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Shin, Jongoh
Song, Yoseb
Kang, Seulgi
Jin, Sangrak
Lee, Jung-Kul
Kim, Dong Rip
Cho, Suhyung
Müller, Volker
Cho, Byung-Kwan
Genome-Scale Analysis of Acetobacterium woodii Identifies Translational Regulation of Acetogenesis
title Genome-Scale Analysis of Acetobacterium woodii Identifies Translational Regulation of Acetogenesis
title_full Genome-Scale Analysis of Acetobacterium woodii Identifies Translational Regulation of Acetogenesis
title_fullStr Genome-Scale Analysis of Acetobacterium woodii Identifies Translational Regulation of Acetogenesis
title_full_unstemmed Genome-Scale Analysis of Acetobacterium woodii Identifies Translational Regulation of Acetogenesis
title_short Genome-Scale Analysis of Acetobacterium woodii Identifies Translational Regulation of Acetogenesis
title_sort genome-scale analysis of acetobacterium woodii identifies translational regulation of acetogenesis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8407422/
https://www.ncbi.nlm.nih.gov/pubmed/34313456
http://dx.doi.org/10.1128/mSystems.00696-21
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