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Multifunctional cellulase catalysis targeted by fusion to different carbohydrate-binding modules
BACKGROUND: Carbohydrate binding modules (CBMs) bind polysaccharides and help target glycoside hydrolases catalytic domains to their appropriate carbohydrate substrates. To better understand how CBMs can improve cellulolytic enzyme reactivity, representatives from each of the 18 families of CBM foun...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4687162/ https://www.ncbi.nlm.nih.gov/pubmed/26697109 http://dx.doi.org/10.1186/s13068-015-0402-0 |
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author | Walker, Johnnie A. Takasuka, Taichi E. Deng, Kai Bianchetti, Christopher M. Udell, Hannah S. Prom, Ben M. Kim, Hyunkee Adams, Paul D. Northen, Trent R. Fox, Brian G. |
author_facet | Walker, Johnnie A. Takasuka, Taichi E. Deng, Kai Bianchetti, Christopher M. Udell, Hannah S. Prom, Ben M. Kim, Hyunkee Adams, Paul D. Northen, Trent R. Fox, Brian G. |
author_sort | Walker, Johnnie A. |
collection | PubMed |
description | BACKGROUND: Carbohydrate binding modules (CBMs) bind polysaccharides and help target glycoside hydrolases catalytic domains to their appropriate carbohydrate substrates. To better understand how CBMs can improve cellulolytic enzyme reactivity, representatives from each of the 18 families of CBM found in Ruminoclostridiumthermocellum were fused to the multifunctional GH5 catalytic domain of CelE (Cthe_0797, CelEcc), which can hydrolyze numerous types of polysaccharides including cellulose, mannan, and xylan. Since CelE is a cellulosomal enzyme, none of these fusions to a CBM previously existed. RESULTS: CelEcc_CBM fusions were assayed for their ability to hydrolyze cellulose, lichenan, xylan, and mannan. Several CelEcc_CBM fusions showed enhanced hydrolytic activity with different substrates relative to the fusion to CBM3a from the cellulosome scaffoldin, which has high affinity for binding to crystalline cellulose. Additional binding studies and quantitative catalysis studies using nanostructure-initiator mass spectrometry (NIMS) were carried out with the CBM3a, CBM6, CBM30, and CBM44 fusion enzymes. In general, and consistent with observations of others, enhanced enzyme reactivity was correlated with moderate binding affinity of the CBM. Numerical analysis of reaction time courses showed that CelEcc_CBM44, a combination of a multifunctional enzyme domain with a CBM having broad binding specificity, gave the fastest rates for hydrolysis of both the hexose and pentose fractions of ionic-liquid pretreated switchgrass. CONCLUSION: We have shown that fusions of different CBMs to a single multifunctional GH5 catalytic domain can increase its rate of reaction with different pure polysaccharides and with pretreated biomass. This fusion approach, incorporating domains with broad specificity for binding and catalysis, provides a new avenue to improve reactivity of simple combinations of enzymes within the complexity of plant biomass. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13068-015-0402-0) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4687162 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-46871622015-12-23 Multifunctional cellulase catalysis targeted by fusion to different carbohydrate-binding modules Walker, Johnnie A. Takasuka, Taichi E. Deng, Kai Bianchetti, Christopher M. Udell, Hannah S. Prom, Ben M. Kim, Hyunkee Adams, Paul D. Northen, Trent R. Fox, Brian G. Biotechnol Biofuels Research BACKGROUND: Carbohydrate binding modules (CBMs) bind polysaccharides and help target glycoside hydrolases catalytic domains to their appropriate carbohydrate substrates. To better understand how CBMs can improve cellulolytic enzyme reactivity, representatives from each of the 18 families of CBM found in Ruminoclostridiumthermocellum were fused to the multifunctional GH5 catalytic domain of CelE (Cthe_0797, CelEcc), which can hydrolyze numerous types of polysaccharides including cellulose, mannan, and xylan. Since CelE is a cellulosomal enzyme, none of these fusions to a CBM previously existed. RESULTS: CelEcc_CBM fusions were assayed for their ability to hydrolyze cellulose, lichenan, xylan, and mannan. Several CelEcc_CBM fusions showed enhanced hydrolytic activity with different substrates relative to the fusion to CBM3a from the cellulosome scaffoldin, which has high affinity for binding to crystalline cellulose. Additional binding studies and quantitative catalysis studies using nanostructure-initiator mass spectrometry (NIMS) were carried out with the CBM3a, CBM6, CBM30, and CBM44 fusion enzymes. In general, and consistent with observations of others, enhanced enzyme reactivity was correlated with moderate binding affinity of the CBM. Numerical analysis of reaction time courses showed that CelEcc_CBM44, a combination of a multifunctional enzyme domain with a CBM having broad binding specificity, gave the fastest rates for hydrolysis of both the hexose and pentose fractions of ionic-liquid pretreated switchgrass. CONCLUSION: We have shown that fusions of different CBMs to a single multifunctional GH5 catalytic domain can increase its rate of reaction with different pure polysaccharides and with pretreated biomass. This fusion approach, incorporating domains with broad specificity for binding and catalysis, provides a new avenue to improve reactivity of simple combinations of enzymes within the complexity of plant biomass. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13068-015-0402-0) contains supplementary material, which is available to authorized users. BioMed Central 2015-12-21 /pmc/articles/PMC4687162/ /pubmed/26697109 http://dx.doi.org/10.1186/s13068-015-0402-0 Text en © Walker et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Walker, Johnnie A. Takasuka, Taichi E. Deng, Kai Bianchetti, Christopher M. Udell, Hannah S. Prom, Ben M. Kim, Hyunkee Adams, Paul D. Northen, Trent R. Fox, Brian G. Multifunctional cellulase catalysis targeted by fusion to different carbohydrate-binding modules |
title | Multifunctional cellulase catalysis targeted by fusion to different carbohydrate-binding modules |
title_full | Multifunctional cellulase catalysis targeted by fusion to different carbohydrate-binding modules |
title_fullStr | Multifunctional cellulase catalysis targeted by fusion to different carbohydrate-binding modules |
title_full_unstemmed | Multifunctional cellulase catalysis targeted by fusion to different carbohydrate-binding modules |
title_short | Multifunctional cellulase catalysis targeted by fusion to different carbohydrate-binding modules |
title_sort | multifunctional cellulase catalysis targeted by fusion to different carbohydrate-binding modules |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4687162/ https://www.ncbi.nlm.nih.gov/pubmed/26697109 http://dx.doi.org/10.1186/s13068-015-0402-0 |
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