Direct fermentation of cellulose to ethanol by Saccharomyces cerevisiae displaying a bifunctional cellobiohydrolase gene from Orpinomyces sp. Y102
A cellobiohydrolase gene, cbhC16, isolated from the cDNA library of a rumen fungus. The recombinant CbhC16 demonstrated a specific activity of 7.0 U mg−1 protein against phosphoric acid-swollen avicel, and cellobiose was the main product in the reaction mixture. Glucose was further released from cel...
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Published in | Renewable energy Vol. 159; pp. 1029 - 1035 |
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Format | Journal Article |
Language | English |
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01.10.2020
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Abstract | A cellobiohydrolase gene, cbhC16, isolated from the cDNA library of a rumen fungus. The recombinant CbhC16 demonstrated a specific activity of 7.0 U mg−1 protein against phosphoric acid-swollen avicel, and cellobiose was the main product in the reaction mixture. Glucose was further released from cellobiose by the action of CbhC16 and fermented to ethanol by Saccharomyces cerevisiae. This phenomenon, possessing activities of both cellobiohydrolase and β-glucosidase, is rarely observed in the hydrolysis by typical cellobiohydrolases. Yeast cells displaying CbhC16 were inoculated into YNB–CAA broth containing carboxymethyl cellulose, β-glucan, ammonia fibre explosion-treated rice straw, or wheat bran, and incubated at 30 °C for 3 d. Under the same conditions, 0.20, 0.61, 0.15, and 0.61 g/L of ethanol were detected in the culture supernatant of the strain with the recombinant plasmid containing cbhC16, whereas wild-type yeasts without the recombinant plasmid containing cbhC16 did not produce detectable ethanol levels. The results indicated that yeast strains with cbhC16 could directly saccharify and ferment cellulose to produce ethanol in singular step. This gene encoding both cellobiohydrolase and β-glucosidase activities will enable developing a simple approach for producing a consolidated microorganism that will directly convert cellulosic feedstocks to ethanol.
•A novel cellobiohydrolase cbhC16 gene was cloned from an rumen fungus.•The expressed CbhC16 possesses both cellobiohydrolase and β-glucosidase activities.•The CbhC16 degrades cellulose to glucose without the synergism of β-glucosidase.•The yeast displaying sole CbhC16 directly converts cellulosic substrates to ethanol. |
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AbstractList | A cellobiohydrolase gene, cbhC16, isolated from the cDNA library of a rumen fungus. The recombinant CbhC16 demonstrated a specific activity of 7.0 U mg−1 protein against phosphoric acid-swollen avicel, and cellobiose was the main product in the reaction mixture. Glucose was further released from cellobiose by the action of CbhC16 and fermented to ethanol by Saccharomyces cerevisiae. This phenomenon, possessing activities of both cellobiohydrolase and β-glucosidase, is rarely observed in the hydrolysis by typical cellobiohydrolases. Yeast cells displaying CbhC16 were inoculated into YNB–CAA broth containing carboxymethyl cellulose, β-glucan, ammonia fibre explosion-treated rice straw, or wheat bran, and incubated at 30 °C for 3 d. Under the same conditions, 0.20, 0.61, 0.15, and 0.61 g/L of ethanol were detected in the culture supernatant of the strain with the recombinant plasmid containing cbhC16, whereas wild-type yeasts without the recombinant plasmid containing cbhC16 did not produce detectable ethanol levels. The results indicated that yeast strains with cbhC16 could directly saccharify and ferment cellulose to produce ethanol in singular step. This gene encoding both cellobiohydrolase and β-glucosidase activities will enable developing a simple approach for producing a consolidated microorganism that will directly convert cellulosic feedstocks to ethanol.
•A novel cellobiohydrolase cbhC16 gene was cloned from an rumen fungus.•The expressed CbhC16 possesses both cellobiohydrolase and β-glucosidase activities.•The CbhC16 degrades cellulose to glucose without the synergism of β-glucosidase.•The yeast displaying sole CbhC16 directly converts cellulosic substrates to ethanol. |
Author | Chang, Wan-Jhu Chen, Yo-Chia Hsu, Teng-Chieh Liu, Jeng-Chen Chen, Hui-Jye |
Author_xml | – sequence: 1 givenname: Jeng-Chen surname: Liu fullname: Liu, Jeng-Chen organization: Department of Biological Science and Technology, National Pingtung University of Science and Technology, Pingtung, Taiwan, ROC – sequence: 2 givenname: Wan-Jhu surname: Chang fullname: Chang, Wan-Jhu organization: Department of Biological Science and Technology, National Pingtung University of Science and Technology, Pingtung, Taiwan, ROC – sequence: 3 givenname: Teng-Chieh surname: Hsu fullname: Hsu, Teng-Chieh organization: Institute of Nuclear Energy Research, Taiwan, ROC – sequence: 4 givenname: Hui-Jye surname: Chen fullname: Chen, Hui-Jye organization: Graduate Institute of Biomedical Sciences, China Medical University, Taichung, Taiwan, ROC – sequence: 5 givenname: Yo-Chia surname: Chen fullname: Chen, Yo-Chia email: yochia.chen@gmail.com organization: Department of Biological Science and Technology, National Pingtung University of Science and Technology, Pingtung, Taiwan, ROC |
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CitedBy_id | crossref_primary_10_1007_s12155_023_10607_5 crossref_primary_10_1016_j_renene_2022_01_047 crossref_primary_10_1007_s13399_020_00891_y crossref_primary_10_1016_j_nbt_2023_10_011 crossref_primary_10_1016_j_molstruc_2023_137254 |
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Keywords | Bioethanol Orpinomyces β-glucosidase Anaerobic rumen fungus Cellobiohydrolase |
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Title | Direct fermentation of cellulose to ethanol by Saccharomyces cerevisiae displaying a bifunctional cellobiohydrolase gene from Orpinomyces sp. Y102 |
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