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H(2) drives metabolic rearrangements in gas-fermenting Clostridium autoethanogenum

BACKGROUND: The global demand for affordable carbon has never been stronger, and there is an imperative in many industrial processes to use waste streams to make products. Gas-fermenting acetogens offer a potential solution and several commercial gas fermentation plants are currently under construct...

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Autores principales: Valgepea, Kaspar, de Souza Pinto Lemgruber, Renato, Abdalla, Tanus, Binos, Steve, Takemori, Nobuaki, Takemori, Ayako, Tanaka, Yuki, Tappel, Ryan, Köpke, Michael, Simpson, Séan Dennis, Nielsen, Lars Keld, Marcellin, Esteban
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5831606/
https://www.ncbi.nlm.nih.gov/pubmed/29507607
http://dx.doi.org/10.1186/s13068-018-1052-9
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author Valgepea, Kaspar
de Souza Pinto Lemgruber, Renato
Abdalla, Tanus
Binos, Steve
Takemori, Nobuaki
Takemori, Ayako
Tanaka, Yuki
Tappel, Ryan
Köpke, Michael
Simpson, Séan Dennis
Nielsen, Lars Keld
Marcellin, Esteban
author_facet Valgepea, Kaspar
de Souza Pinto Lemgruber, Renato
Abdalla, Tanus
Binos, Steve
Takemori, Nobuaki
Takemori, Ayako
Tanaka, Yuki
Tappel, Ryan
Köpke, Michael
Simpson, Séan Dennis
Nielsen, Lars Keld
Marcellin, Esteban
author_sort Valgepea, Kaspar
collection PubMed
description BACKGROUND: The global demand for affordable carbon has never been stronger, and there is an imperative in many industrial processes to use waste streams to make products. Gas-fermenting acetogens offer a potential solution and several commercial gas fermentation plants are currently under construction. As energy limits acetogen metabolism, supply of H(2) should diminish substrate loss to CO(2) and facilitate production of reduced and energy-intensive products. However, the effects of H(2) supply on CO-grown acetogens have yet to be experimentally quantified under controlled growth conditions. RESULTS: Here, we quantify the effects of H(2) supplementation by comparing growth on CO, syngas, and a high-H(2) CO gas mix using chemostat cultures of Clostridium autoethanogenum. Cultures were characterised at the molecular level using metabolomics, proteomics, gas analysis, and a genome-scale metabolic model. CO-limited chemostats operated at two steady-state biomass concentrations facilitated co-utilisation of CO and H(2). We show that H(2) supply strongly impacts carbon distribution with a fourfold reduction in substrate loss as CO(2) (61% vs. 17%) and a proportional increase of flux to ethanol (15% vs. 61%). Notably, H(2) supplementation lowers the molar acetate/ethanol ratio by fivefold. At the molecular level, quantitative proteome analysis showed no obvious changes leading to these metabolic rearrangements suggesting the involvement of post-translational regulation. Metabolic modelling showed that H(2) availability provided reducing power via H(2) oxidation and saved redox as cells reduced all the CO(2) to formate directly using H(2) in the Wood–Ljungdahl pathway. Modelling further indicated that the methylene-THF reductase reaction was ferredoxin reducing under all conditions. In combination with proteomics, modelling also showed that ethanol was synthesised through the acetaldehyde:ferredoxin oxidoreductase (AOR) activity. CONCLUSIONS: Our quantitative molecular analysis revealed that H(2) drives rearrangements at several layers of metabolism and provides novel links between carbon, energy, and redox metabolism advancing our understanding of energy conservation in acetogens. We conclude that H(2) supply can substantially increase the efficiency of gas fermentation and thus the feed gas composition can be considered an important factor in developing gas fermentation-based bioprocesses. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13068-018-1052-9) contains supplementary material, which is available to authorized users.
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spelling pubmed-58316062018-03-05 H(2) drives metabolic rearrangements in gas-fermenting Clostridium autoethanogenum Valgepea, Kaspar de Souza Pinto Lemgruber, Renato Abdalla, Tanus Binos, Steve Takemori, Nobuaki Takemori, Ayako Tanaka, Yuki Tappel, Ryan Köpke, Michael Simpson, Séan Dennis Nielsen, Lars Keld Marcellin, Esteban Biotechnol Biofuels Research BACKGROUND: The global demand for affordable carbon has never been stronger, and there is an imperative in many industrial processes to use waste streams to make products. Gas-fermenting acetogens offer a potential solution and several commercial gas fermentation plants are currently under construction. As energy limits acetogen metabolism, supply of H(2) should diminish substrate loss to CO(2) and facilitate production of reduced and energy-intensive products. However, the effects of H(2) supply on CO-grown acetogens have yet to be experimentally quantified under controlled growth conditions. RESULTS: Here, we quantify the effects of H(2) supplementation by comparing growth on CO, syngas, and a high-H(2) CO gas mix using chemostat cultures of Clostridium autoethanogenum. Cultures were characterised at the molecular level using metabolomics, proteomics, gas analysis, and a genome-scale metabolic model. CO-limited chemostats operated at two steady-state biomass concentrations facilitated co-utilisation of CO and H(2). We show that H(2) supply strongly impacts carbon distribution with a fourfold reduction in substrate loss as CO(2) (61% vs. 17%) and a proportional increase of flux to ethanol (15% vs. 61%). Notably, H(2) supplementation lowers the molar acetate/ethanol ratio by fivefold. At the molecular level, quantitative proteome analysis showed no obvious changes leading to these metabolic rearrangements suggesting the involvement of post-translational regulation. Metabolic modelling showed that H(2) availability provided reducing power via H(2) oxidation and saved redox as cells reduced all the CO(2) to formate directly using H(2) in the Wood–Ljungdahl pathway. Modelling further indicated that the methylene-THF reductase reaction was ferredoxin reducing under all conditions. In combination with proteomics, modelling also showed that ethanol was synthesised through the acetaldehyde:ferredoxin oxidoreductase (AOR) activity. CONCLUSIONS: Our quantitative molecular analysis revealed that H(2) drives rearrangements at several layers of metabolism and provides novel links between carbon, energy, and redox metabolism advancing our understanding of energy conservation in acetogens. We conclude that H(2) supply can substantially increase the efficiency of gas fermentation and thus the feed gas composition can be considered an important factor in developing gas fermentation-based bioprocesses. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13068-018-1052-9) contains supplementary material, which is available to authorized users. BioMed Central 2018-03-01 /pmc/articles/PMC5831606/ /pubmed/29507607 http://dx.doi.org/10.1186/s13068-018-1052-9 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Valgepea, Kaspar
de Souza Pinto Lemgruber, Renato
Abdalla, Tanus
Binos, Steve
Takemori, Nobuaki
Takemori, Ayako
Tanaka, Yuki
Tappel, Ryan
Köpke, Michael
Simpson, Séan Dennis
Nielsen, Lars Keld
Marcellin, Esteban
H(2) drives metabolic rearrangements in gas-fermenting Clostridium autoethanogenum
title H(2) drives metabolic rearrangements in gas-fermenting Clostridium autoethanogenum
title_full H(2) drives metabolic rearrangements in gas-fermenting Clostridium autoethanogenum
title_fullStr H(2) drives metabolic rearrangements in gas-fermenting Clostridium autoethanogenum
title_full_unstemmed H(2) drives metabolic rearrangements in gas-fermenting Clostridium autoethanogenum
title_short H(2) drives metabolic rearrangements in gas-fermenting Clostridium autoethanogenum
title_sort h(2) drives metabolic rearrangements in gas-fermenting clostridium autoethanogenum
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5831606/
https://www.ncbi.nlm.nih.gov/pubmed/29507607
http://dx.doi.org/10.1186/s13068-018-1052-9
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