Cargando…

A cellular automaton model of crystalline cellulose hydrolysis by cellulases

BACKGROUND: Cellulose from plant biomass is an abundant, renewable material which could be a major feedstock for low emissions transport fuels such as cellulosic ethanol. Cellulase enzymes that break down cellulose into fermentable sugars are composed of different types - cellobiohydrolases I and II...

Descripción completa

Detalles Bibliográficos
Autores principales: Warden, Andrew C, Little, Bryce A, Haritos, Victoria S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3214134/
https://www.ncbi.nlm.nih.gov/pubmed/22005054
http://dx.doi.org/10.1186/1754-6834-4-39
_version_ 1782216206488436736
author Warden, Andrew C
Little, Bryce A
Haritos, Victoria S
author_facet Warden, Andrew C
Little, Bryce A
Haritos, Victoria S
author_sort Warden, Andrew C
collection PubMed
description BACKGROUND: Cellulose from plant biomass is an abundant, renewable material which could be a major feedstock for low emissions transport fuels such as cellulosic ethanol. Cellulase enzymes that break down cellulose into fermentable sugars are composed of different types - cellobiohydrolases I and II, endoglucanase and β-glucosidase - with separate functions. They form a complex interacting network between themselves, soluble hydrolysis product molecules, solution and solid phase substrates and inhibitors. There have been many models proposed for enzymatic saccharification however none have yet employed a cellular automaton approach, which allows important phenomena, such as enzyme crowding on the surface of solid substrates, denaturation and substrate inhibition, to be considered in the model. RESULTS: The Cellulase 4D model was developed de novo taking into account the size and composition of the substrate and surface-acting enzymes were ascribed behaviors based on their movements, catalytic activities and rates, affinity for, and potential for crowding of, the cellulose surface, substrates and inhibitors, and denaturation rates. A basic case modeled on literature-derived parameters obtained from Trichoderma reesei cellulases resulted in cellulose hydrolysis curves that closely matched curves obtained from published experimental data. Scenarios were tested in the model, which included variation of enzyme loadings, adsorption strengths of surface acting enzymes and reaction periods, and the effect on saccharide production over time was assessed. The model simulations indicated an optimal enzyme loading of between 0.5 and 2 of the base case concentrations where a balance was obtained between enzyme crowding on the cellulose crystal, and that the affinities of enzymes for the cellulose surface had a large effect on cellulose hydrolysis. In addition, improvements to the cellobiohydrolase I activity period substantially improved overall glucose production. CONCLUSIONS: Cellulase 4D simulates the enzymatic hydrolysis of cellulose to glucose by surface and solution phase-acting enzymes and accounts for complex phenomena that have previously not been included in cellulose hydrolysis models. The model is intended as a tool for industry, researchers and educators alike to explore options for enzyme engineering and process development and to test hypotheses regarding cellulase mechanisms.
format Online
Article
Text
id pubmed-3214134
institution National Center for Biotechnology Information
language English
publishDate 2011
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-32141342011-11-14 A cellular automaton model of crystalline cellulose hydrolysis by cellulases Warden, Andrew C Little, Bryce A Haritos, Victoria S Biotechnol Biofuels Research BACKGROUND: Cellulose from plant biomass is an abundant, renewable material which could be a major feedstock for low emissions transport fuels such as cellulosic ethanol. Cellulase enzymes that break down cellulose into fermentable sugars are composed of different types - cellobiohydrolases I and II, endoglucanase and β-glucosidase - with separate functions. They form a complex interacting network between themselves, soluble hydrolysis product molecules, solution and solid phase substrates and inhibitors. There have been many models proposed for enzymatic saccharification however none have yet employed a cellular automaton approach, which allows important phenomena, such as enzyme crowding on the surface of solid substrates, denaturation and substrate inhibition, to be considered in the model. RESULTS: The Cellulase 4D model was developed de novo taking into account the size and composition of the substrate and surface-acting enzymes were ascribed behaviors based on their movements, catalytic activities and rates, affinity for, and potential for crowding of, the cellulose surface, substrates and inhibitors, and denaturation rates. A basic case modeled on literature-derived parameters obtained from Trichoderma reesei cellulases resulted in cellulose hydrolysis curves that closely matched curves obtained from published experimental data. Scenarios were tested in the model, which included variation of enzyme loadings, adsorption strengths of surface acting enzymes and reaction periods, and the effect on saccharide production over time was assessed. The model simulations indicated an optimal enzyme loading of between 0.5 and 2 of the base case concentrations where a balance was obtained between enzyme crowding on the cellulose crystal, and that the affinities of enzymes for the cellulose surface had a large effect on cellulose hydrolysis. In addition, improvements to the cellobiohydrolase I activity period substantially improved overall glucose production. CONCLUSIONS: Cellulase 4D simulates the enzymatic hydrolysis of cellulose to glucose by surface and solution phase-acting enzymes and accounts for complex phenomena that have previously not been included in cellulose hydrolysis models. The model is intended as a tool for industry, researchers and educators alike to explore options for enzyme engineering and process development and to test hypotheses regarding cellulase mechanisms. BioMed Central 2011-10-17 /pmc/articles/PMC3214134/ /pubmed/22005054 http://dx.doi.org/10.1186/1754-6834-4-39 Text en Copyright ©2011 Warden 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
Warden, Andrew C
Little, Bryce A
Haritos, Victoria S
A cellular automaton model of crystalline cellulose hydrolysis by cellulases
title A cellular automaton model of crystalline cellulose hydrolysis by cellulases
title_full A cellular automaton model of crystalline cellulose hydrolysis by cellulases
title_fullStr A cellular automaton model of crystalline cellulose hydrolysis by cellulases
title_full_unstemmed A cellular automaton model of crystalline cellulose hydrolysis by cellulases
title_short A cellular automaton model of crystalline cellulose hydrolysis by cellulases
title_sort cellular automaton model of crystalline cellulose hydrolysis by cellulases
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3214134/
https://www.ncbi.nlm.nih.gov/pubmed/22005054
http://dx.doi.org/10.1186/1754-6834-4-39
work_keys_str_mv AT wardenandrewc acellularautomatonmodelofcrystallinecellulosehydrolysisbycellulases
AT littlebrycea acellularautomatonmodelofcrystallinecellulosehydrolysisbycellulases
AT haritosvictorias acellularautomatonmodelofcrystallinecellulosehydrolysisbycellulases
AT wardenandrewc cellularautomatonmodelofcrystallinecellulosehydrolysisbycellulases
AT littlebrycea cellularautomatonmodelofcrystallinecellulosehydrolysisbycellulases
AT haritosvictorias cellularautomatonmodelofcrystallinecellulosehydrolysisbycellulases