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Direct and highly productive conversion of cyanobacteria Arthrospira platensis to ethanol with CaCl(2) addition
BACKGROUND: The cyanobacterium Arthrospira platensis shows promise as a carbohydrate feedstock for biofuel production. The glycogen accumulated in A. platensis can be extracted by lysozyme-degrading the peptidoglycan layer of the bacterial cell walls. The extracted glycogen can be converted to ethan...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5828149/ https://www.ncbi.nlm.nih.gov/pubmed/29492105 http://dx.doi.org/10.1186/s13068-018-1050-y |
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author | Aikawa, Shimpei Inokuma, Kentaro Wakai, Satoshi Sasaki, Kengo Ogino, Chiaki Chang, Jo-Shu Hasunuma, Tomohisa Kondo, Akihiko |
author_facet | Aikawa, Shimpei Inokuma, Kentaro Wakai, Satoshi Sasaki, Kengo Ogino, Chiaki Chang, Jo-Shu Hasunuma, Tomohisa Kondo, Akihiko |
author_sort | Aikawa, Shimpei |
collection | PubMed |
description | BACKGROUND: The cyanobacterium Arthrospira platensis shows promise as a carbohydrate feedstock for biofuel production. The glycogen accumulated in A. platensis can be extracted by lysozyme-degrading the peptidoglycan layer of the bacterial cell walls. The extracted glycogen can be converted to ethanol through hydrolysis by amylolytic enzymes and fermentation by the yeast Saccharomyces cerevisiae. Thus, in the presence of lysozyme, a recombinant yeast expressing α-amylase and glucoamylase can convert A. platensis directly to ethanol, which would simplify the procedure for ethanol production. However, the ethanol titer and productivity in this process are lower than in ethanol production from cyanobacteria and green algae in previous reports. RESULTS: To increase the ethanol titer, a high concentration of A. platensis biomass was employed as the carbon source for the ethanol production using a recombinant amylase-expressing yeast. The addition of lysozyme to the fermentation medium increased the ethanol titer, but not the ethanol productivity. The addition of CaCl(2) increased both the ethanol titer and productivity by causing the delamination of polysaccharide layer on the cell surface of A. platensis. In the presence of lysozyme and CaCl(2), ethanol titer, yield, and productivity improved to 48 g L(−1), 93% of theoretical yield, and 1.0 g L(−1) h(−1) from A. platensis, corresponding to 90 g L(−1) of glycogen. CONCLUSIONS: We developed an ethanol conversion process using a recombinant amylase-expressing yeast from A. platensis with a high titer, yield, and productivity by adding both lysozyme and CaCl(2). The direct and highly productive conversion process from A. platensis via yeast fermentation could be applied to multiple industrial bulk chemicals. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13068-018-1050-y) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5828149 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-58281492018-02-28 Direct and highly productive conversion of cyanobacteria Arthrospira platensis to ethanol with CaCl(2) addition Aikawa, Shimpei Inokuma, Kentaro Wakai, Satoshi Sasaki, Kengo Ogino, Chiaki Chang, Jo-Shu Hasunuma, Tomohisa Kondo, Akihiko Biotechnol Biofuels Research BACKGROUND: The cyanobacterium Arthrospira platensis shows promise as a carbohydrate feedstock for biofuel production. The glycogen accumulated in A. platensis can be extracted by lysozyme-degrading the peptidoglycan layer of the bacterial cell walls. The extracted glycogen can be converted to ethanol through hydrolysis by amylolytic enzymes and fermentation by the yeast Saccharomyces cerevisiae. Thus, in the presence of lysozyme, a recombinant yeast expressing α-amylase and glucoamylase can convert A. platensis directly to ethanol, which would simplify the procedure for ethanol production. However, the ethanol titer and productivity in this process are lower than in ethanol production from cyanobacteria and green algae in previous reports. RESULTS: To increase the ethanol titer, a high concentration of A. platensis biomass was employed as the carbon source for the ethanol production using a recombinant amylase-expressing yeast. The addition of lysozyme to the fermentation medium increased the ethanol titer, but not the ethanol productivity. The addition of CaCl(2) increased both the ethanol titer and productivity by causing the delamination of polysaccharide layer on the cell surface of A. platensis. In the presence of lysozyme and CaCl(2), ethanol titer, yield, and productivity improved to 48 g L(−1), 93% of theoretical yield, and 1.0 g L(−1) h(−1) from A. platensis, corresponding to 90 g L(−1) of glycogen. CONCLUSIONS: We developed an ethanol conversion process using a recombinant amylase-expressing yeast from A. platensis with a high titer, yield, and productivity by adding both lysozyme and CaCl(2). The direct and highly productive conversion process from A. platensis via yeast fermentation could be applied to multiple industrial bulk chemicals. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13068-018-1050-y) contains supplementary material, which is available to authorized users. BioMed Central 2018-02-27 /pmc/articles/PMC5828149/ /pubmed/29492105 http://dx.doi.org/10.1186/s13068-018-1050-y 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. 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 Aikawa, Shimpei Inokuma, Kentaro Wakai, Satoshi Sasaki, Kengo Ogino, Chiaki Chang, Jo-Shu Hasunuma, Tomohisa Kondo, Akihiko Direct and highly productive conversion of cyanobacteria Arthrospira platensis to ethanol with CaCl(2) addition |
title | Direct and highly productive conversion of cyanobacteria Arthrospira platensis to ethanol with CaCl(2) addition |
title_full | Direct and highly productive conversion of cyanobacteria Arthrospira platensis to ethanol with CaCl(2) addition |
title_fullStr | Direct and highly productive conversion of cyanobacteria Arthrospira platensis to ethanol with CaCl(2) addition |
title_full_unstemmed | Direct and highly productive conversion of cyanobacteria Arthrospira platensis to ethanol with CaCl(2) addition |
title_short | Direct and highly productive conversion of cyanobacteria Arthrospira platensis to ethanol with CaCl(2) addition |
title_sort | direct and highly productive conversion of cyanobacteria arthrospira platensis to ethanol with cacl(2) addition |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5828149/ https://www.ncbi.nlm.nih.gov/pubmed/29492105 http://dx.doi.org/10.1186/s13068-018-1050-y |
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