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Adsorption of β-glucosidases in two commercial preparations onto pretreated biomass and lignin

BACKGROUND: Enzyme recycling is a method to reduce the production costs for advanced bioethanol by lowering the overall use of enzymes. Commercial cellulase preparations consist of many different enzymes that are important for efficient and complete cellulose (and hemicellulose) hydrolysis. This abu...

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Autores principales: Haven, Mai Østergaard, Jørgensen, Henning
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4176991/
https://www.ncbi.nlm.nih.gov/pubmed/24274678
http://dx.doi.org/10.1186/1754-6834-6-165
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author Haven, Mai Østergaard
Jørgensen, Henning
author_facet Haven, Mai Østergaard
Jørgensen, Henning
author_sort Haven, Mai Østergaard
collection PubMed
description BACKGROUND: Enzyme recycling is a method to reduce the production costs for advanced bioethanol by lowering the overall use of enzymes. Commercial cellulase preparations consist of many different enzymes that are important for efficient and complete cellulose (and hemicellulose) hydrolysis. This abundance of different activities complicates enzyme recycling since the individual enzymes behave differently in the process. Previously, the general perception was that β-glucosidases could easily be recycled via the liquid phase, as they have mostly been observed not to adsorb to pretreated biomass or only adsorb to a minor extent. RESULTS: The results from this study with Cellic® CTec2 revealed that the vast majority of the β-glucosidase activity was lost from the liquid phase and was adsorbed to the residual biomass during hydrolysis and fermentation. Adsorption studies with β-glucosidases in two commercial preparations (Novozym 188 and Cellic® CTec2) to substrates mimicking the components in pretreated wheat straw revealed that the Aspergillus niger β-glucosidase in Novozym 188 did not adsorb significantly to any of the components in pretreated wheat straw, whereas the β-glucosidase in Cellic® CTec2 adsorbed strongly to lignin. The extent of adsorption of β-glucosidase from Cellic® CTec2 was affected by both type of biomass and pretreatment method. With approximately 65% of the β-glucosidases from Cellic® CTec2 adsorbed onto lignin from pretreated wheat straw, the activity of the β-glucosidases in the slurry decreased by only 15%. This demonstrated that some enzyme remained active despite being bound. It was possible to reduce the adsorption of Cellic® CTec2 β-glucosidase to lignin from pretreated wheat straw by addition of bovine serum albumin or poly(ethylene glycol). CONCLUSIONS: Contrary to the β-glucosidases in Novozym 188, the β-glucosidases in Cellic® CTec2 adsorb significantly to lignin. The lignin adsorption observed for Cellic® CTec2 is usually not a problem during hydrolysis and fermentation since most of the catalytic activity is retained. However, adsorption of β-glucosidases to lignin may prove to be a problem when trying to recycle enzymes in the production of advanced bioethanol.
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spelling pubmed-41769912014-09-28 Adsorption of β-glucosidases in two commercial preparations onto pretreated biomass and lignin Haven, Mai Østergaard Jørgensen, Henning Biotechnol Biofuels Research BACKGROUND: Enzyme recycling is a method to reduce the production costs for advanced bioethanol by lowering the overall use of enzymes. Commercial cellulase preparations consist of many different enzymes that are important for efficient and complete cellulose (and hemicellulose) hydrolysis. This abundance of different activities complicates enzyme recycling since the individual enzymes behave differently in the process. Previously, the general perception was that β-glucosidases could easily be recycled via the liquid phase, as they have mostly been observed not to adsorb to pretreated biomass or only adsorb to a minor extent. RESULTS: The results from this study with Cellic® CTec2 revealed that the vast majority of the β-glucosidase activity was lost from the liquid phase and was adsorbed to the residual biomass during hydrolysis and fermentation. Adsorption studies with β-glucosidases in two commercial preparations (Novozym 188 and Cellic® CTec2) to substrates mimicking the components in pretreated wheat straw revealed that the Aspergillus niger β-glucosidase in Novozym 188 did not adsorb significantly to any of the components in pretreated wheat straw, whereas the β-glucosidase in Cellic® CTec2 adsorbed strongly to lignin. The extent of adsorption of β-glucosidase from Cellic® CTec2 was affected by both type of biomass and pretreatment method. With approximately 65% of the β-glucosidases from Cellic® CTec2 adsorbed onto lignin from pretreated wheat straw, the activity of the β-glucosidases in the slurry decreased by only 15%. This demonstrated that some enzyme remained active despite being bound. It was possible to reduce the adsorption of Cellic® CTec2 β-glucosidase to lignin from pretreated wheat straw by addition of bovine serum albumin or poly(ethylene glycol). CONCLUSIONS: Contrary to the β-glucosidases in Novozym 188, the β-glucosidases in Cellic® CTec2 adsorb significantly to lignin. The lignin adsorption observed for Cellic® CTec2 is usually not a problem during hydrolysis and fermentation since most of the catalytic activity is retained. However, adsorption of β-glucosidases to lignin may prove to be a problem when trying to recycle enzymes in the production of advanced bioethanol. BioMed Central 2013-11-25 /pmc/articles/PMC4176991/ /pubmed/24274678 http://dx.doi.org/10.1186/1754-6834-6-165 Text en Copyright © 2013 Haven and Jørgensen; 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
Haven, Mai Østergaard
Jørgensen, Henning
Adsorption of β-glucosidases in two commercial preparations onto pretreated biomass and lignin
title Adsorption of β-glucosidases in two commercial preparations onto pretreated biomass and lignin
title_full Adsorption of β-glucosidases in two commercial preparations onto pretreated biomass and lignin
title_fullStr Adsorption of β-glucosidases in two commercial preparations onto pretreated biomass and lignin
title_full_unstemmed Adsorption of β-glucosidases in two commercial preparations onto pretreated biomass and lignin
title_short Adsorption of β-glucosidases in two commercial preparations onto pretreated biomass and lignin
title_sort adsorption of β-glucosidases in two commercial preparations onto pretreated biomass and lignin
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4176991/
https://www.ncbi.nlm.nih.gov/pubmed/24274678
http://dx.doi.org/10.1186/1754-6834-6-165
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