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The effects of CO(2) and H(2) on CO metabolism by pure and mixed microbial cultures
BACKGROUND: Syngas fermentation, the bioconversion of CO, CO(2), and H(2) to biofuels and chemicals, has undergone considerable optimization for industrial applications. Even more, full-scale plants for ethanol production from syngas fermentation by pure cultures are being built worldwide. The compo...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5603099/ https://www.ncbi.nlm.nih.gov/pubmed/28936234 http://dx.doi.org/10.1186/s13068-017-0910-1 |
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author | Esquivel-Elizondo, Sofia Delgado, Anca G. Rittmann, Bruce E. Krajmalnik-Brown, Rosa |
author_facet | Esquivel-Elizondo, Sofia Delgado, Anca G. Rittmann, Bruce E. Krajmalnik-Brown, Rosa |
author_sort | Esquivel-Elizondo, Sofia |
collection | PubMed |
description | BACKGROUND: Syngas fermentation, the bioconversion of CO, CO(2), and H(2) to biofuels and chemicals, has undergone considerable optimization for industrial applications. Even more, full-scale plants for ethanol production from syngas fermentation by pure cultures are being built worldwide. The composition of syngas depends on the feedstock gasified and the gasification conditions. However, it remains unclear how different syngas mixtures affect the metabolism of carboxidotrophs, including the ethanol/acetate ratios. In addition, the potential application of mixed cultures in syngas fermentation and their advantages over pure cultures have not been deeply explored. In this work, the effects of CO(2) and H(2) on the CO metabolism by pure and mixed cultures were studied and compared. For this, a CO-enriched mixed culture and two isolated carboxidotrophs were grown with different combinations of syngas components (CO, CO:H(2), CO:CO(2), or CO:CO(2):H(2)). RESULTS: The CO metabolism of the mixed culture was somehow affected by the addition of CO(2) and/or H(2), but the pure cultures were more sensitive to changes in gas composition than the mixed culture. CO(2) inhibited CO oxidation by the Pleomorphomonas-like isolate and decreased the ethanol/acetate ratio by the Acetobacterium-like isolate. H(2) did not inhibit ethanol or H(2) production by the Acetobacterium and Pleomorphomonas isolates, respectively, but decreased their CO consumption rates. As part of the mixed culture, these isolates, together with other microorganisms, consumed H(2) and CO(2) (along with CO) for all conditions tested and at similar CO consumption rates (2.6 ± 0.6 mmol CO L(−1) day(−1)), while maintaining overall function (acetate production). Providing a continuous supply of CO by membrane diffusion caused the mixed culture to switch from acetate to ethanol production, presumably due to the increased supply of electron donor. In parallel with this change in metabolic function, the structure of the microbial community became dominated by Geosporobacter phylotypes, instead of Acetobacterium and Pleomorphomonas phylotypes. CONCLUSIONS: These results provide evidence for the potential of mixed-culture syngas fermentation, since the CO-enriched mixed culture showed high functional redundancy, was resilient to changes in syngas composition, and was capable of producing acetate or ethanol as main products of CO metabolism. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13068-017-0910-1) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5603099 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-56030992017-09-21 The effects of CO(2) and H(2) on CO metabolism by pure and mixed microbial cultures Esquivel-Elizondo, Sofia Delgado, Anca G. Rittmann, Bruce E. Krajmalnik-Brown, Rosa Biotechnol Biofuels Research BACKGROUND: Syngas fermentation, the bioconversion of CO, CO(2), and H(2) to biofuels and chemicals, has undergone considerable optimization for industrial applications. Even more, full-scale plants for ethanol production from syngas fermentation by pure cultures are being built worldwide. The composition of syngas depends on the feedstock gasified and the gasification conditions. However, it remains unclear how different syngas mixtures affect the metabolism of carboxidotrophs, including the ethanol/acetate ratios. In addition, the potential application of mixed cultures in syngas fermentation and their advantages over pure cultures have not been deeply explored. In this work, the effects of CO(2) and H(2) on the CO metabolism by pure and mixed cultures were studied and compared. For this, a CO-enriched mixed culture and two isolated carboxidotrophs were grown with different combinations of syngas components (CO, CO:H(2), CO:CO(2), or CO:CO(2):H(2)). RESULTS: The CO metabolism of the mixed culture was somehow affected by the addition of CO(2) and/or H(2), but the pure cultures were more sensitive to changes in gas composition than the mixed culture. CO(2) inhibited CO oxidation by the Pleomorphomonas-like isolate and decreased the ethanol/acetate ratio by the Acetobacterium-like isolate. H(2) did not inhibit ethanol or H(2) production by the Acetobacterium and Pleomorphomonas isolates, respectively, but decreased their CO consumption rates. As part of the mixed culture, these isolates, together with other microorganisms, consumed H(2) and CO(2) (along with CO) for all conditions tested and at similar CO consumption rates (2.6 ± 0.6 mmol CO L(−1) day(−1)), while maintaining overall function (acetate production). Providing a continuous supply of CO by membrane diffusion caused the mixed culture to switch from acetate to ethanol production, presumably due to the increased supply of electron donor. In parallel with this change in metabolic function, the structure of the microbial community became dominated by Geosporobacter phylotypes, instead of Acetobacterium and Pleomorphomonas phylotypes. CONCLUSIONS: These results provide evidence for the potential of mixed-culture syngas fermentation, since the CO-enriched mixed culture showed high functional redundancy, was resilient to changes in syngas composition, and was capable of producing acetate or ethanol as main products of CO metabolism. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13068-017-0910-1) contains supplementary material, which is available to authorized users. BioMed Central 2017-09-16 /pmc/articles/PMC5603099/ /pubmed/28936234 http://dx.doi.org/10.1186/s13068-017-0910-1 Text en © The Author(s) 2017 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 Esquivel-Elizondo, Sofia Delgado, Anca G. Rittmann, Bruce E. Krajmalnik-Brown, Rosa The effects of CO(2) and H(2) on CO metabolism by pure and mixed microbial cultures |
title | The effects of CO(2) and H(2) on CO metabolism by pure and mixed microbial cultures |
title_full | The effects of CO(2) and H(2) on CO metabolism by pure and mixed microbial cultures |
title_fullStr | The effects of CO(2) and H(2) on CO metabolism by pure and mixed microbial cultures |
title_full_unstemmed | The effects of CO(2) and H(2) on CO metabolism by pure and mixed microbial cultures |
title_short | The effects of CO(2) and H(2) on CO metabolism by pure and mixed microbial cultures |
title_sort | effects of co(2) and h(2) on co metabolism by pure and mixed microbial cultures |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5603099/ https://www.ncbi.nlm.nih.gov/pubmed/28936234 http://dx.doi.org/10.1186/s13068-017-0910-1 |
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