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Developing a mesophilic co-culture for direct conversion of cellulose to butanol in consolidated bioprocess
BACKGROUND: Consolidated bioprocessing (CBP) of butanol production from cellulosic biomass is a promising strategy for cost saving compared to other processes featuring dedicated cellulase production. CBP requires microbial strains capable of hydrolyzing biomass with enzymes produced on its own with...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4471926/ https://www.ncbi.nlm.nih.gov/pubmed/26089984 http://dx.doi.org/10.1186/s13068-015-0266-3 |
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author | Wang, Zhenyu Cao, Guangli Zheng, Ju Fu, Defeng Song, Jinzhu Zhang, Junzheng Zhao, Lei Yang, Qian |
author_facet | Wang, Zhenyu Cao, Guangli Zheng, Ju Fu, Defeng Song, Jinzhu Zhang, Junzheng Zhao, Lei Yang, Qian |
author_sort | Wang, Zhenyu |
collection | PubMed |
description | BACKGROUND: Consolidated bioprocessing (CBP) of butanol production from cellulosic biomass is a promising strategy for cost saving compared to other processes featuring dedicated cellulase production. CBP requires microbial strains capable of hydrolyzing biomass with enzymes produced on its own with high rate and high conversion and simultaneously produce a desired product at high yield. However, current reported butanol-producing candidates are unable to utilize cellulose as a sole carbon source and energy source. Consequently, developing a co-culture system using different microorganisms by taking advantage of their specific metabolic capacities to produce butanol directly from cellulose in consolidated bioprocess is of great interest. RESULTS: This study was mainly undertaken to find complementary organisms to the butanol producer that allow simultaneous saccharification and fermentation of cellulose to butanol in their co-culture under mesophilic condition. Accordingly, a highly efficient and stable consortium N3 on cellulose degradation was first developed by multiple subcultures. Subsequently, the functional microorganisms with 16S rRNA sequences identical to the denaturing gradient gel electrophoresis (DGGE) profile were isolated from consortium N3. The isolate Clostridium celevecrescens N3-2 exhibited higher cellulose-degrading capability was thus chosen as the partner strain for butanol production with Clostridium acetobutylicum ATCC824. Meanwhile, the established stable consortium N3 was also investigated to produce butanol by co-culturing with C. acetobutylicum ATCC824. Butanol was produced from cellulose when C. acetobutylicum ATCC824 was co-cultured with either consortium N3 or C. celevecrescens N3-2. Co-culturing C. acetobutylicum ATCC824 with the stable consortium N3 resulted in a relatively higher butanol concentration, 3.73 g/L, and higher production yield, 0.145 g/g of glucose equivalent. CONCLUSIONS: The newly isolated microbial consortium N3 and strain C. celevecrescens N3-2 displayed effective degradation of cellulose and produced considerable amounts of butanol when they were co-cultured with C. acetobutylicum ATCC824. This is the first report of application of co-culture to produce butanol directly from cellulose under mesophilic condition. Our results indicated that co-culture of mesophilic cellulolytic microbe and butanol-producing clostridia provides a technically feasible and more simplified way for producing butanol directly from cellulose. |
format | Online Article Text |
id | pubmed-4471926 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-44719262015-06-19 Developing a mesophilic co-culture for direct conversion of cellulose to butanol in consolidated bioprocess Wang, Zhenyu Cao, Guangli Zheng, Ju Fu, Defeng Song, Jinzhu Zhang, Junzheng Zhao, Lei Yang, Qian Biotechnol Biofuels Research BACKGROUND: Consolidated bioprocessing (CBP) of butanol production from cellulosic biomass is a promising strategy for cost saving compared to other processes featuring dedicated cellulase production. CBP requires microbial strains capable of hydrolyzing biomass with enzymes produced on its own with high rate and high conversion and simultaneously produce a desired product at high yield. However, current reported butanol-producing candidates are unable to utilize cellulose as a sole carbon source and energy source. Consequently, developing a co-culture system using different microorganisms by taking advantage of their specific metabolic capacities to produce butanol directly from cellulose in consolidated bioprocess is of great interest. RESULTS: This study was mainly undertaken to find complementary organisms to the butanol producer that allow simultaneous saccharification and fermentation of cellulose to butanol in their co-culture under mesophilic condition. Accordingly, a highly efficient and stable consortium N3 on cellulose degradation was first developed by multiple subcultures. Subsequently, the functional microorganisms with 16S rRNA sequences identical to the denaturing gradient gel electrophoresis (DGGE) profile were isolated from consortium N3. The isolate Clostridium celevecrescens N3-2 exhibited higher cellulose-degrading capability was thus chosen as the partner strain for butanol production with Clostridium acetobutylicum ATCC824. Meanwhile, the established stable consortium N3 was also investigated to produce butanol by co-culturing with C. acetobutylicum ATCC824. Butanol was produced from cellulose when C. acetobutylicum ATCC824 was co-cultured with either consortium N3 or C. celevecrescens N3-2. Co-culturing C. acetobutylicum ATCC824 with the stable consortium N3 resulted in a relatively higher butanol concentration, 3.73 g/L, and higher production yield, 0.145 g/g of glucose equivalent. CONCLUSIONS: The newly isolated microbial consortium N3 and strain C. celevecrescens N3-2 displayed effective degradation of cellulose and produced considerable amounts of butanol when they were co-cultured with C. acetobutylicum ATCC824. This is the first report of application of co-culture to produce butanol directly from cellulose under mesophilic condition. Our results indicated that co-culture of mesophilic cellulolytic microbe and butanol-producing clostridia provides a technically feasible and more simplified way for producing butanol directly from cellulose. BioMed Central 2015-06-12 /pmc/articles/PMC4471926/ /pubmed/26089984 http://dx.doi.org/10.1186/s13068-015-0266-3 Text en © Wang et al. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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 Wang, Zhenyu Cao, Guangli Zheng, Ju Fu, Defeng Song, Jinzhu Zhang, Junzheng Zhao, Lei Yang, Qian Developing a mesophilic co-culture for direct conversion of cellulose to butanol in consolidated bioprocess |
title | Developing a mesophilic co-culture for direct conversion of cellulose to butanol in consolidated bioprocess |
title_full | Developing a mesophilic co-culture for direct conversion of cellulose to butanol in consolidated bioprocess |
title_fullStr | Developing a mesophilic co-culture for direct conversion of cellulose to butanol in consolidated bioprocess |
title_full_unstemmed | Developing a mesophilic co-culture for direct conversion of cellulose to butanol in consolidated bioprocess |
title_short | Developing a mesophilic co-culture for direct conversion of cellulose to butanol in consolidated bioprocess |
title_sort | developing a mesophilic co-culture for direct conversion of cellulose to butanol in consolidated bioprocess |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4471926/ https://www.ncbi.nlm.nih.gov/pubmed/26089984 http://dx.doi.org/10.1186/s13068-015-0266-3 |
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