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Improvement of caproic acid production in a Clostridium kluyveri H068 and Methanogen 166 co-culture fermentation system
The aim of this study was to develop a bioprocess capable of producing caproic acid using a binary fermentation system consisting of Clostridium kluyveri H068 and Methanogen 166 which could then be applied to the brewing of Chinese strong flavor liquor. We initially explored the mechanism by which t...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6202304/ https://www.ncbi.nlm.nih.gov/pubmed/30361817 http://dx.doi.org/10.1186/s13568-018-0705-1 |
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author | Yan, Shoubao Dong, Dong |
author_facet | Yan, Shoubao Dong, Dong |
author_sort | Yan, Shoubao |
collection | PubMed |
description | The aim of this study was to develop a bioprocess capable of producing caproic acid using a binary fermentation system consisting of Clostridium kluyveri H068 and Methanogen 166 which could then be applied to the brewing of Chinese strong flavor liquor. We initially explored the mechanism by which the Methanogen 166 strain facilitates caproic acid accumulation, revealing its ability to convert accumulated H(2) that is produced by C. kluyveri H068 into methane, thereby eliminating the hydrogen-mediated feedback inhibition that normally constrains C. kluyveri H068 and thus enhancing caproic acid production. In addition, laboratory experiments were conducted to optimize this binary fermentation system, allowing us to determine that the optimum conditions for caproic acid production are a mixed inoculum size of 10% with a C. kluyveri H588/Methanogen 166 inoculation ratio of 2:1 (v/v), a sodium acetate concentration of 20 g/L, a 4% ethanol content (v/v), and a yeast extract concentration of 10 g/L. We further scaled this optimized condition up to use in a 1000 L fermenter and the obtained caproic acid broth was subjected to pit-entry fermentation. Our results demonstrated that this pit-entry fermentation approach was an efficient means of improving the quality of Chinese strong flavor liquor. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13568-018-0705-1) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6202304 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-62023042018-11-06 Improvement of caproic acid production in a Clostridium kluyveri H068 and Methanogen 166 co-culture fermentation system Yan, Shoubao Dong, Dong AMB Express Original Article The aim of this study was to develop a bioprocess capable of producing caproic acid using a binary fermentation system consisting of Clostridium kluyveri H068 and Methanogen 166 which could then be applied to the brewing of Chinese strong flavor liquor. We initially explored the mechanism by which the Methanogen 166 strain facilitates caproic acid accumulation, revealing its ability to convert accumulated H(2) that is produced by C. kluyveri H068 into methane, thereby eliminating the hydrogen-mediated feedback inhibition that normally constrains C. kluyveri H068 and thus enhancing caproic acid production. In addition, laboratory experiments were conducted to optimize this binary fermentation system, allowing us to determine that the optimum conditions for caproic acid production are a mixed inoculum size of 10% with a C. kluyveri H588/Methanogen 166 inoculation ratio of 2:1 (v/v), a sodium acetate concentration of 20 g/L, a 4% ethanol content (v/v), and a yeast extract concentration of 10 g/L. We further scaled this optimized condition up to use in a 1000 L fermenter and the obtained caproic acid broth was subjected to pit-entry fermentation. Our results demonstrated that this pit-entry fermentation approach was an efficient means of improving the quality of Chinese strong flavor liquor. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13568-018-0705-1) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2018-10-25 /pmc/articles/PMC6202304/ /pubmed/30361817 http://dx.doi.org/10.1186/s13568-018-0705-1 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. |
spellingShingle | Original Article Yan, Shoubao Dong, Dong Improvement of caproic acid production in a Clostridium kluyveri H068 and Methanogen 166 co-culture fermentation system |
title | Improvement of caproic acid production in a Clostridium kluyveri H068 and Methanogen 166 co-culture fermentation system |
title_full | Improvement of caproic acid production in a Clostridium kluyveri H068 and Methanogen 166 co-culture fermentation system |
title_fullStr | Improvement of caproic acid production in a Clostridium kluyveri H068 and Methanogen 166 co-culture fermentation system |
title_full_unstemmed | Improvement of caproic acid production in a Clostridium kluyveri H068 and Methanogen 166 co-culture fermentation system |
title_short | Improvement of caproic acid production in a Clostridium kluyveri H068 and Methanogen 166 co-culture fermentation system |
title_sort | improvement of caproic acid production in a clostridium kluyveri h068 and methanogen 166 co-culture fermentation system |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6202304/ https://www.ncbi.nlm.nih.gov/pubmed/30361817 http://dx.doi.org/10.1186/s13568-018-0705-1 |
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