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Feasibility study of on-site solid-state enzyme production by Aspergillus oryzae

BACKGROUND: The development of biorefinery systems that use lignocellulosic biomass as a renewable carbon source to produce fuels and chemicals is attracting increasing attention. The process cost of enzymatic saccharification of biomass is a major challenge for commercialization. To decrease this c...

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Autores principales: Shinkawa, Satoru, Mitsuzawa, Shigenobu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7045521/
https://www.ncbi.nlm.nih.gov/pubmed/32127918
http://dx.doi.org/10.1186/s13068-020-1669-3
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author Shinkawa, Satoru
Mitsuzawa, Shigenobu
author_facet Shinkawa, Satoru
Mitsuzawa, Shigenobu
author_sort Shinkawa, Satoru
collection PubMed
description BACKGROUND: The development of biorefinery systems that use lignocellulosic biomass as a renewable carbon source to produce fuels and chemicals is attracting increasing attention. The process cost of enzymatic saccharification of biomass is a major challenge for commercialization. To decrease this cost, researchers have proposed on-site solid-state fermentation (SSF). This study investigated the feasibility of using Aspergillus oryzae as a host microorganism for SSF recombinant enzyme production with ammonia-treated rice straw as model biomass. Eight A. oryzae strains were tested, all of which are used in the food industry. We evaluated the effects of acetic acid, a fermentation inhibitor. We also developed a platform strain for targeted recombinant enzyme production by gene engineering technologies. RESULTS: The SSF validation test showed variation in the visibility of mycelium growth and secreted protein in all eight A. oryzae strains. The strains used to produce shoyu and miso grew better under test conditions. The ammonia-treated rice straw contained noticeable amounts of acetic acid. This acetic acid enhanced the protein production by A. oryzae in a liquid-state fermentation test. The newly developed platform strain successfully secreted three foreign saccharifying enzymes. CONCLUSIONS: A. oryzae is a promising candidate as a host microorganism for on-site SSF recombinant enzyme production, which bodes well for the future development of a more cost-efficient saccharifying enzyme production system.
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spelling pubmed-70455212020-03-03 Feasibility study of on-site solid-state enzyme production by Aspergillus oryzae Shinkawa, Satoru Mitsuzawa, Shigenobu Biotechnol Biofuels Research BACKGROUND: The development of biorefinery systems that use lignocellulosic biomass as a renewable carbon source to produce fuels and chemicals is attracting increasing attention. The process cost of enzymatic saccharification of biomass is a major challenge for commercialization. To decrease this cost, researchers have proposed on-site solid-state fermentation (SSF). This study investigated the feasibility of using Aspergillus oryzae as a host microorganism for SSF recombinant enzyme production with ammonia-treated rice straw as model biomass. Eight A. oryzae strains were tested, all of which are used in the food industry. We evaluated the effects of acetic acid, a fermentation inhibitor. We also developed a platform strain for targeted recombinant enzyme production by gene engineering technologies. RESULTS: The SSF validation test showed variation in the visibility of mycelium growth and secreted protein in all eight A. oryzae strains. The strains used to produce shoyu and miso grew better under test conditions. The ammonia-treated rice straw contained noticeable amounts of acetic acid. This acetic acid enhanced the protein production by A. oryzae in a liquid-state fermentation test. The newly developed platform strain successfully secreted three foreign saccharifying enzymes. CONCLUSIONS: A. oryzae is a promising candidate as a host microorganism for on-site SSF recombinant enzyme production, which bodes well for the future development of a more cost-efficient saccharifying enzyme production system. BioMed Central 2020-02-26 /pmc/articles/PMC7045521/ /pubmed/32127918 http://dx.doi.org/10.1186/s13068-020-1669-3 Text en © The Author(s) 2020 Open AccessThis 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/. 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 in a credit line to the data.
spellingShingle Research
Shinkawa, Satoru
Mitsuzawa, Shigenobu
Feasibility study of on-site solid-state enzyme production by Aspergillus oryzae
title Feasibility study of on-site solid-state enzyme production by Aspergillus oryzae
title_full Feasibility study of on-site solid-state enzyme production by Aspergillus oryzae
title_fullStr Feasibility study of on-site solid-state enzyme production by Aspergillus oryzae
title_full_unstemmed Feasibility study of on-site solid-state enzyme production by Aspergillus oryzae
title_short Feasibility study of on-site solid-state enzyme production by Aspergillus oryzae
title_sort feasibility study of on-site solid-state enzyme production by aspergillus oryzae
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7045521/
https://www.ncbi.nlm.nih.gov/pubmed/32127918
http://dx.doi.org/10.1186/s13068-020-1669-3
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