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Metabolic changes of the acetogen Clostridium sp. AWRP through adaptation to acetate challenge

In this study, we report the phenotypic changes that occurred in the acetogenic bacterium Clostridium sp. AWRP as a result of an adaptive laboratory evolution (ALE) under the acetate challenge. Acetate-adapted strain 46 T-a displayed acetate tolerance to acetate up to 10 g L(−1) and increased ethano...

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Autores principales: Kwon, Soo Jae, Lee, Joungmin, Lee, Hyun Sook
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9768041/
https://www.ncbi.nlm.nih.gov/pubmed/36569090
http://dx.doi.org/10.3389/fmicb.2022.982442
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author Kwon, Soo Jae
Lee, Joungmin
Lee, Hyun Sook
author_facet Kwon, Soo Jae
Lee, Joungmin
Lee, Hyun Sook
author_sort Kwon, Soo Jae
collection PubMed
description In this study, we report the phenotypic changes that occurred in the acetogenic bacterium Clostridium sp. AWRP as a result of an adaptive laboratory evolution (ALE) under the acetate challenge. Acetate-adapted strain 46 T-a displayed acetate tolerance to acetate up to 10 g L(−1) and increased ethanol production in small-scale cultures. The adapted strain showed a higher cell density than AWRP even without exogenous acetate supplementation. 46 T-a was shown to have reduced gas consumption rate and metabolite production. It was intriguing to note that 46 T-a, unlike AWRP, continued to consume H(2) at low CO(2) levels. Genome sequencing revealed that the adapted strain harbored three point mutations in the genes encoding an electron-bifurcating hydrogenase (Hyt) crucial for autotrophic growth in CO(2) + H(2), in addition to one in the dnaK gene. Transcriptome analysis revealed that most genes involved in the CO(2)-fixation Wood-Ljungdahl pathway and auxiliary pathways for energy conservation (e.g., Rnf complex, Nfn, etc.) were significantly down-regulated in 46 T-a. Several metabolic pathways involved in dissimilation of nucleosides and carbohydrates were significantly up-regulated in 46 T-a, indicating that 46 T-a evolved to utilize organic substrates rather than CO(2) + H(2). Further investigation into degeneration in carbon fixation of the acetate-adapted strain will provide practical implications for CO(2) + H(2) fermentation using acetogenic bacteria for long-term continuous fermentation.
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spelling pubmed-97680412022-12-22 Metabolic changes of the acetogen Clostridium sp. AWRP through adaptation to acetate challenge Kwon, Soo Jae Lee, Joungmin Lee, Hyun Sook Front Microbiol Microbiology In this study, we report the phenotypic changes that occurred in the acetogenic bacterium Clostridium sp. AWRP as a result of an adaptive laboratory evolution (ALE) under the acetate challenge. Acetate-adapted strain 46 T-a displayed acetate tolerance to acetate up to 10 g L(−1) and increased ethanol production in small-scale cultures. The adapted strain showed a higher cell density than AWRP even without exogenous acetate supplementation. 46 T-a was shown to have reduced gas consumption rate and metabolite production. It was intriguing to note that 46 T-a, unlike AWRP, continued to consume H(2) at low CO(2) levels. Genome sequencing revealed that the adapted strain harbored three point mutations in the genes encoding an electron-bifurcating hydrogenase (Hyt) crucial for autotrophic growth in CO(2) + H(2), in addition to one in the dnaK gene. Transcriptome analysis revealed that most genes involved in the CO(2)-fixation Wood-Ljungdahl pathway and auxiliary pathways for energy conservation (e.g., Rnf complex, Nfn, etc.) were significantly down-regulated in 46 T-a. Several metabolic pathways involved in dissimilation of nucleosides and carbohydrates were significantly up-regulated in 46 T-a, indicating that 46 T-a evolved to utilize organic substrates rather than CO(2) + H(2). Further investigation into degeneration in carbon fixation of the acetate-adapted strain will provide practical implications for CO(2) + H(2) fermentation using acetogenic bacteria for long-term continuous fermentation. Frontiers Media S.A. 2022-12-07 /pmc/articles/PMC9768041/ /pubmed/36569090 http://dx.doi.org/10.3389/fmicb.2022.982442 Text en Copyright © 2022 Kwon, Lee and Lee. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Kwon, Soo Jae
Lee, Joungmin
Lee, Hyun Sook
Metabolic changes of the acetogen Clostridium sp. AWRP through adaptation to acetate challenge
title Metabolic changes of the acetogen Clostridium sp. AWRP through adaptation to acetate challenge
title_full Metabolic changes of the acetogen Clostridium sp. AWRP through adaptation to acetate challenge
title_fullStr Metabolic changes of the acetogen Clostridium sp. AWRP through adaptation to acetate challenge
title_full_unstemmed Metabolic changes of the acetogen Clostridium sp. AWRP through adaptation to acetate challenge
title_short Metabolic changes of the acetogen Clostridium sp. AWRP through adaptation to acetate challenge
title_sort metabolic changes of the acetogen clostridium sp. awrp through adaptation to acetate challenge
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9768041/
https://www.ncbi.nlm.nih.gov/pubmed/36569090
http://dx.doi.org/10.3389/fmicb.2022.982442
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