Consolidated bioprocessing for bioethanol production by metabolically engineered Bacillus subtilis strains

Abstract 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 (C...

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Main Authors: Fatemeh Maleki, Mohammad Changizian, Narges Zolfaghari, Sarah Rajaei, Kambiz Akbari Noghabi, Hossein Shahbani Zahiri
Format: Article
Language:English
Published: Nature Publishing Group 2021-07-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-021-92627-9
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spelling doaj-68ff566b6f8d4cc7bd13ce35d77b17832021-07-04T11:30:57ZengNature Publishing GroupScientific Reports2045-23222021-07-0111111310.1038/s41598-021-92627-9Consolidated bioprocessing for bioethanol production by metabolically engineered Bacillus subtilis strainsFatemeh Maleki0Mohammad Changizian1Narges Zolfaghari2Sarah Rajaei3Kambiz Akbari Noghabi4Hossein Shahbani Zahiri5Department of Energy and Environmental Biotechnology, National Institute of Genetic Engineering and Biotechnology (NIGEB)Department of Energy and Environmental Biotechnology, National Institute of Genetic Engineering and Biotechnology (NIGEB)Department of Energy and Environmental Biotechnology, National Institute of Genetic Engineering and Biotechnology (NIGEB)Department of Energy and Environmental Biotechnology, National Institute of Genetic Engineering and Biotechnology (NIGEB)Department of Energy and Environmental Biotechnology, National Institute of Genetic Engineering and Biotechnology (NIGEB)Department of Energy and Environmental Biotechnology, National Institute of Genetic Engineering and Biotechnology (NIGEB)Abstract 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.https://doi.org/10.1038/s41598-021-92627-9
collection DOAJ
language English
format Article
sources DOAJ
author Fatemeh Maleki
Mohammad Changizian
Narges Zolfaghari
Sarah Rajaei
Kambiz Akbari Noghabi
Hossein Shahbani Zahiri
spellingShingle Fatemeh Maleki
Mohammad Changizian
Narges Zolfaghari
Sarah Rajaei
Kambiz Akbari Noghabi
Hossein Shahbani Zahiri
Consolidated bioprocessing for bioethanol production by metabolically engineered Bacillus subtilis strains
Scientific Reports
author_facet Fatemeh Maleki
Mohammad Changizian
Narges Zolfaghari
Sarah Rajaei
Kambiz Akbari Noghabi
Hossein Shahbani Zahiri
author_sort Fatemeh Maleki
title 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_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_sort consolidated bioprocessing for bioethanol production by metabolically engineered bacillus subtilis strains
publisher Nature Publishing Group
series Scientific Reports
issn 2045-2322
publishDate 2021-07-01
description Abstract 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.
url https://doi.org/10.1038/s41598-021-92627-9
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