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Consolidated bioprocessing for bioethanol production by metabolically engineered Bacillus subtilis strains
Bioethanol produced by fermentative microorganisms is regarded as an alternative to fossil fuel. Bioethanol to be used as a viable energy source must be produced cost-effectively by removing expense-intensive steps such as the enzymatic hydrolysis of substrate. Consolidated bioprocessing (CBP) is be...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8253836/ https://www.ncbi.nlm.nih.gov/pubmed/34215768 http://dx.doi.org/10.1038/s41598-021-92627-9 |
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author | Maleki, Fatemeh Changizian, Mohammad Zolfaghari, Narges Rajaei, Sarah Noghabi, Kambiz Akbari Zahiri, Hossein Shahbani |
author_facet | Maleki, Fatemeh Changizian, Mohammad Zolfaghari, Narges Rajaei, Sarah Noghabi, Kambiz Akbari Zahiri, Hossein Shahbani |
author_sort | Maleki, Fatemeh |
collection | PubMed |
description | Bioethanol produced by fermentative microorganisms is regarded as an alternative to fossil fuel. Bioethanol to be used as a viable energy source must be produced cost-effectively by removing expense-intensive steps such as the enzymatic hydrolysis of substrate. Consolidated bioprocessing (CBP) is believed to be a practical solution combining saccharification and fermentation in a single step catalyzed by a microorganism. Bacillus subtills with innate ability to grow on a diversity of carbohydrates seems promising for affordable CBP bioethanol production using renewable plant biomass and wastes. In this study, the genes encoding alcohol dehydrogenase from Z. mobilis (adh(Z)) and S. cerevisiae (adh(S)) were each used with Z. mobilis pyruvate decarboxylase gene (pdc(Z)) to create ethanologenic operons in a lactate-deficient (Δldh) B. subtilis resulting in NZ and NZS strains, respectively. The S. cerevisiae adh(S) caused significantly more ethanol production by NZS and therefore was used to make two other operons including one with double copies of both pdc(Z) and adh(S) and the other with a single pdc(Z) but double adh(S) genes expressed in N(ZS)2 and NZS2 strains, respectively. In addition, two fusion genes were constructed with pdc(Z) and adh(S) in alternate orientations and used for ethanol production by the harboring strains namely NZ:S and NS:Z, respectively. While the increase of gene dosage was not associated with elevated carbon flow for ethanol production, the fusion gene adh(S):pdc(Z) resulted in a more than two times increase of productivity by strain NS:Z as compared with NZS during 48 h fermentation. The CBP ethanol production by NZS and NS:Z using potatoes resulted in 16.3 g/L and 21.5 g/L ethanol during 96 h fermentation, respectively. For the first time in this study, B. subtilis was successfully used for CBP ethanol production with S. cerevisiae alcohol dehydrogenase. The results of the study provide insights on the potentials of B. subtilis for affordable bioethanol production from inexpensive plant biomass and wastes. However, the potentials need to be improved by metabolic and process engineering for higher yields of ethanol production and plant biomass utilization. |
format | Online Article Text |
id | pubmed-8253836 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-82538362021-07-06 Consolidated bioprocessing for bioethanol production by metabolically engineered Bacillus subtilis strains Maleki, Fatemeh Changizian, Mohammad Zolfaghari, Narges Rajaei, Sarah Noghabi, Kambiz Akbari Zahiri, Hossein Shahbani Sci Rep Article Bioethanol produced by fermentative microorganisms is regarded as an alternative to fossil fuel. Bioethanol to be used as a viable energy source must be produced cost-effectively by removing expense-intensive steps such as the enzymatic hydrolysis of substrate. Consolidated bioprocessing (CBP) is believed to be a practical solution combining saccharification and fermentation in a single step catalyzed by a microorganism. Bacillus subtills with innate ability to grow on a diversity of carbohydrates seems promising for affordable CBP bioethanol production using renewable plant biomass and wastes. In this study, the genes encoding alcohol dehydrogenase from Z. mobilis (adh(Z)) and S. cerevisiae (adh(S)) were each used with Z. mobilis pyruvate decarboxylase gene (pdc(Z)) to create ethanologenic operons in a lactate-deficient (Δldh) B. subtilis resulting in NZ and NZS strains, respectively. The S. cerevisiae adh(S) caused significantly more ethanol production by NZS and therefore was used to make two other operons including one with double copies of both pdc(Z) and adh(S) and the other with a single pdc(Z) but double adh(S) genes expressed in N(ZS)2 and NZS2 strains, respectively. In addition, two fusion genes were constructed with pdc(Z) and adh(S) in alternate orientations and used for ethanol production by the harboring strains namely NZ:S and NS:Z, respectively. While the increase of gene dosage was not associated with elevated carbon flow for ethanol production, the fusion gene adh(S):pdc(Z) resulted in a more than two times increase of productivity by strain NS:Z as compared with NZS during 48 h fermentation. The CBP ethanol production by NZS and NS:Z using potatoes resulted in 16.3 g/L and 21.5 g/L ethanol during 96 h fermentation, respectively. For the first time in this study, B. subtilis was successfully used for CBP ethanol production with S. cerevisiae alcohol dehydrogenase. The results of the study provide insights on the potentials of B. subtilis for affordable bioethanol production from inexpensive plant biomass and wastes. However, the potentials need to be improved by metabolic and process engineering for higher yields of ethanol production and plant biomass utilization. Nature Publishing Group UK 2021-07-02 /pmc/articles/PMC8253836/ /pubmed/34215768 http://dx.doi.org/10.1038/s41598-021-92627-9 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Maleki, Fatemeh Changizian, Mohammad Zolfaghari, Narges Rajaei, Sarah Noghabi, Kambiz Akbari Zahiri, Hossein Shahbani Consolidated bioprocessing for bioethanol production by metabolically engineered Bacillus subtilis strains |
title | Consolidated bioprocessing for bioethanol production by metabolically engineered Bacillus subtilis strains |
title_full | Consolidated bioprocessing for bioethanol production by metabolically engineered Bacillus subtilis strains |
title_fullStr | Consolidated bioprocessing for bioethanol production by metabolically engineered Bacillus subtilis strains |
title_full_unstemmed | Consolidated bioprocessing for bioethanol production by metabolically engineered Bacillus subtilis strains |
title_short | Consolidated bioprocessing for bioethanol production by metabolically engineered Bacillus subtilis strains |
title_sort | consolidated bioprocessing for bioethanol production by metabolically engineered bacillus subtilis strains |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8253836/ https://www.ncbi.nlm.nih.gov/pubmed/34215768 http://dx.doi.org/10.1038/s41598-021-92627-9 |
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