Characterisation of recombinant Trichoderma reesei cellobiohydrolase and the potential of cellulase mixture in hydrolyzing oil palm empty fruit bunches

The potential for recombinant cellulases from fungi to hydrolyze oil palm empty fruit bunches (OPEFB) into simple sugars was investigated. A mixture of two recombinant enzymes consisting of a cellobiohydrolase from Trichoderma reesei and an endoglucanase from Aspergillus niger, was evaluated for OPE...

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Main Authors: Xia, D. Q. H., Yee, Y. H., Illias, R. M., Mahadi, N. M., Bakar, F. D. A., Murad, A .M. A.
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Published: Malaysian Society of Applied Biology 2017
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Online Access:http://eprints.utm.my/id/eprint/76796/
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spelling my.utm.767962018-04-30T14:07:35Z http://eprints.utm.my/id/eprint/76796/ Characterisation of recombinant Trichoderma reesei cellobiohydrolase and the potential of cellulase mixture in hydrolyzing oil palm empty fruit bunches Xia, D. Q. H. Yee, Y. H. Illias, R. M. Mahadi, N. M. Bakar, F. D. A. Murad, A .M. A. TP Chemical technology The potential for recombinant cellulases from fungi to hydrolyze oil palm empty fruit bunches (OPEFB) into simple sugars was investigated. A mixture of two recombinant enzymes consisting of a cellobiohydrolase from Trichoderma reesei and an endoglucanase from Aspergillus niger, was evaluated for OPEFB hydrolysis. The development of A. niger endoglucanase has been described previously. In this work, the development of a recombinant cellobiohydrolase and the activity of this enzyme mixture towards OPEFB hydrolysis were described. To obtain recombinant cellobiohydrolase, the cDNA encoding for cellobiohydrolase, cbhII, was isolated from the T. reesei strain M5, and the gene was expressed in the methylotrophic yeast, Pichia pastoris. Partially purified CbhII demonstrated optimum activity at 50°C and pH 5.0. This enzyme was shown to hydrolyze Avicel at a concentration of 0.486 U/mg under optimum conditions. Hydrolysis of pretreated OPEFB using CbhII and endoglucanase EglA showed that the total reducing sugar produced was higher in the enzyme mixture reaction than were produced in an individual enzyme reaction. Addition of β-glucosidase and an enzyme cofactor significantly increased enzyme activity and OPEFB cellulose hydrolysis. This study demonstrated the capability of an enzyme mixture to produce sugars from oil palm lignocellulosic waste. Malaysian Society of Applied Biology 2017 Article PeerReviewed Xia, D. Q. H. and Yee, Y. H. and Illias, R. M. and Mahadi, N. M. and Bakar, F. D. A. and Murad, A .M. A. (2017) Characterisation of recombinant Trichoderma reesei cellobiohydrolase and the potential of cellulase mixture in hydrolyzing oil palm empty fruit bunches. Malaysian Applied Biology, 46 (2). pp. 11-19. ISSN 0126-8643 https://www.scopus.com/inward/record.uri?eid=2-s2.0-85021765350&partnerID=40&md5=d4806cd6bf57e2578456cddbfee0af40
institution Universiti Teknologi Malaysia
building UTM Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Teknologi Malaysia
content_source UTM Institutional Repository
url_provider http://eprints.utm.my/
topic TP Chemical technology
spellingShingle TP Chemical technology
Xia, D. Q. H.
Yee, Y. H.
Illias, R. M.
Mahadi, N. M.
Bakar, F. D. A.
Murad, A .M. A.
Characterisation of recombinant Trichoderma reesei cellobiohydrolase and the potential of cellulase mixture in hydrolyzing oil palm empty fruit bunches
description The potential for recombinant cellulases from fungi to hydrolyze oil palm empty fruit bunches (OPEFB) into simple sugars was investigated. A mixture of two recombinant enzymes consisting of a cellobiohydrolase from Trichoderma reesei and an endoglucanase from Aspergillus niger, was evaluated for OPEFB hydrolysis. The development of A. niger endoglucanase has been described previously. In this work, the development of a recombinant cellobiohydrolase and the activity of this enzyme mixture towards OPEFB hydrolysis were described. To obtain recombinant cellobiohydrolase, the cDNA encoding for cellobiohydrolase, cbhII, was isolated from the T. reesei strain M5, and the gene was expressed in the methylotrophic yeast, Pichia pastoris. Partially purified CbhII demonstrated optimum activity at 50°C and pH 5.0. This enzyme was shown to hydrolyze Avicel at a concentration of 0.486 U/mg under optimum conditions. Hydrolysis of pretreated OPEFB using CbhII and endoglucanase EglA showed that the total reducing sugar produced was higher in the enzyme mixture reaction than were produced in an individual enzyme reaction. Addition of β-glucosidase and an enzyme cofactor significantly increased enzyme activity and OPEFB cellulose hydrolysis. This study demonstrated the capability of an enzyme mixture to produce sugars from oil palm lignocellulosic waste.
format Article
author Xia, D. Q. H.
Yee, Y. H.
Illias, R. M.
Mahadi, N. M.
Bakar, F. D. A.
Murad, A .M. A.
author_facet Xia, D. Q. H.
Yee, Y. H.
Illias, R. M.
Mahadi, N. M.
Bakar, F. D. A.
Murad, A .M. A.
author_sort Xia, D. Q. H.
title Characterisation of recombinant Trichoderma reesei cellobiohydrolase and the potential of cellulase mixture in hydrolyzing oil palm empty fruit bunches
title_short Characterisation of recombinant Trichoderma reesei cellobiohydrolase and the potential of cellulase mixture in hydrolyzing oil palm empty fruit bunches
title_full Characterisation of recombinant Trichoderma reesei cellobiohydrolase and the potential of cellulase mixture in hydrolyzing oil palm empty fruit bunches
title_fullStr Characterisation of recombinant Trichoderma reesei cellobiohydrolase and the potential of cellulase mixture in hydrolyzing oil palm empty fruit bunches
title_full_unstemmed Characterisation of recombinant Trichoderma reesei cellobiohydrolase and the potential of cellulase mixture in hydrolyzing oil palm empty fruit bunches
title_sort characterisation of recombinant trichoderma reesei cellobiohydrolase and the potential of cellulase mixture in hydrolyzing oil palm empty fruit bunches
publisher Malaysian Society of Applied Biology
publishDate 2017
url http://eprints.utm.my/id/eprint/76796/
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85021765350&partnerID=40&md5=d4806cd6bf57e2578456cddbfee0af40
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score 13.209306