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Practical screening of purified cellobiohydrolases and endoglucanases with α-cellulose and specification of hydrodynamics
BACKGROUND: It is important to generate biofuels and society must be weaned from its dependency on fossil fuels. In order to produce biofuels, lignocellulose is pretreated and the resulting cellulose is hydrolyzed by cellulases such as cellobiohydrolases (CBH) and endoglucanases (EG). Until now, the...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2936879/ https://www.ncbi.nlm.nih.gov/pubmed/20718965 http://dx.doi.org/10.1186/1754-6834-3-18 |
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author | Jäger, Gernot Wu, Zhuojun Garschhammer, Kerstin Engel, Philip Klement, Tobias Rinaldi, Roberto Spiess, Antje C Büchs, Jochen |
author_facet | Jäger, Gernot Wu, Zhuojun Garschhammer, Kerstin Engel, Philip Klement, Tobias Rinaldi, Roberto Spiess, Antje C Büchs, Jochen |
author_sort | Jäger, Gernot |
collection | PubMed |
description | BACKGROUND: It is important to generate biofuels and society must be weaned from its dependency on fossil fuels. In order to produce biofuels, lignocellulose is pretreated and the resulting cellulose is hydrolyzed by cellulases such as cellobiohydrolases (CBH) and endoglucanases (EG). Until now, the biofuel industry has usually applied impractical celluloses to screen for cellulases capable of degrading naturally occurring, insoluble cellulose. This study investigates how these cellulases adsorb and hydrolyze insoluble α-cellulose − considered to be a more practical substrate which mimics the alkaline-pretreated biomass used in biorefineries. Moreover, this study investigates how hydrodynamics affects cellulase adsorption and activity onto α-cellulose. RESULTS: First, the cellulases CBH I, CBH II, EG I and EG II were purified from Trichoderma reesei and CBH I and EG I were utilized in order to study and model the adsorption isotherms (Langmuir) and kinetics (pseudo-first-order). Second, the adsorption kinetics and cellulase activities were studied under different hydrodynamic conditions, including liquid mixing and particle suspension. Third, in order to compare α-cellulose with three typically used celluloses, the exact cellulase activities towards all four substrates were measured. It was found that, using α-cellulose, the adsorption models fitted to the experimental data and yielded parameters comparable to those for filter paper. Moreover, it was determined that higher shaking frequencies clearly improved the adsorption of cellulases onto α-cellulose and thus bolstered their activity. Complete suspension of α-cellulose particles was the optimal operating condition in order to ensure efficient cellulase adsorption and activity. Finally, all four purified cellulases displayed comparable activities only on insoluble α-cellulose. CONCLUSIONS: α-Cellulose is an excellent substrate to screen for CBHs and EGs. This current investigation shows in detail, for the first time, the adsorption of purified cellulases onto α-cellulose, the effect of hydrodynamics on cellulase adsorption and the correlation between the adsorption and the activity of cellulases at different hydrodynamic conditions. Complete suspension of the substrate has to be ensured in order to optimize the cellulase attack. In the future, screenings should be conducted with α-cellulose so that proper cellulases are selected to best hydrolyze the real alkaline-pretreated biomass used in biorefineries. |
format | Text |
id | pubmed-2936879 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-29368792010-09-13 Practical screening of purified cellobiohydrolases and endoglucanases with α-cellulose and specification of hydrodynamics Jäger, Gernot Wu, Zhuojun Garschhammer, Kerstin Engel, Philip Klement, Tobias Rinaldi, Roberto Spiess, Antje C Büchs, Jochen Biotechnol Biofuels Research BACKGROUND: It is important to generate biofuels and society must be weaned from its dependency on fossil fuels. In order to produce biofuels, lignocellulose is pretreated and the resulting cellulose is hydrolyzed by cellulases such as cellobiohydrolases (CBH) and endoglucanases (EG). Until now, the biofuel industry has usually applied impractical celluloses to screen for cellulases capable of degrading naturally occurring, insoluble cellulose. This study investigates how these cellulases adsorb and hydrolyze insoluble α-cellulose − considered to be a more practical substrate which mimics the alkaline-pretreated biomass used in biorefineries. Moreover, this study investigates how hydrodynamics affects cellulase adsorption and activity onto α-cellulose. RESULTS: First, the cellulases CBH I, CBH II, EG I and EG II were purified from Trichoderma reesei and CBH I and EG I were utilized in order to study and model the adsorption isotherms (Langmuir) and kinetics (pseudo-first-order). Second, the adsorption kinetics and cellulase activities were studied under different hydrodynamic conditions, including liquid mixing and particle suspension. Third, in order to compare α-cellulose with three typically used celluloses, the exact cellulase activities towards all four substrates were measured. It was found that, using α-cellulose, the adsorption models fitted to the experimental data and yielded parameters comparable to those for filter paper. Moreover, it was determined that higher shaking frequencies clearly improved the adsorption of cellulases onto α-cellulose and thus bolstered their activity. Complete suspension of α-cellulose particles was the optimal operating condition in order to ensure efficient cellulase adsorption and activity. Finally, all four purified cellulases displayed comparable activities only on insoluble α-cellulose. CONCLUSIONS: α-Cellulose is an excellent substrate to screen for CBHs and EGs. This current investigation shows in detail, for the first time, the adsorption of purified cellulases onto α-cellulose, the effect of hydrodynamics on cellulase adsorption and the correlation between the adsorption and the activity of cellulases at different hydrodynamic conditions. Complete suspension of the substrate has to be ensured in order to optimize the cellulase attack. In the future, screenings should be conducted with α-cellulose so that proper cellulases are selected to best hydrolyze the real alkaline-pretreated biomass used in biorefineries. BioMed Central 2010-08-18 /pmc/articles/PMC2936879/ /pubmed/20718965 http://dx.doi.org/10.1186/1754-6834-3-18 Text en Copyright © 2010 Jäger et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Jäger, Gernot Wu, Zhuojun Garschhammer, Kerstin Engel, Philip Klement, Tobias Rinaldi, Roberto Spiess, Antje C Büchs, Jochen Practical screening of purified cellobiohydrolases and endoglucanases with α-cellulose and specification of hydrodynamics |
title | Practical screening of purified cellobiohydrolases and endoglucanases with α-cellulose and specification of hydrodynamics |
title_full | Practical screening of purified cellobiohydrolases and endoglucanases with α-cellulose and specification of hydrodynamics |
title_fullStr | Practical screening of purified cellobiohydrolases and endoglucanases with α-cellulose and specification of hydrodynamics |
title_full_unstemmed | Practical screening of purified cellobiohydrolases and endoglucanases with α-cellulose and specification of hydrodynamics |
title_short | Practical screening of purified cellobiohydrolases and endoglucanases with α-cellulose and specification of hydrodynamics |
title_sort | practical screening of purified cellobiohydrolases and endoglucanases with α-cellulose and specification of hydrodynamics |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2936879/ https://www.ncbi.nlm.nih.gov/pubmed/20718965 http://dx.doi.org/10.1186/1754-6834-3-18 |
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