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Glycoside Hydrolases from a targeted Compost Metagenome, activity-screening and functional characterization

BACKGROUND: Metagenomics approaches provide access to environmental genetic diversity for biotechnology applications, enabling the discovery of new enzymes and pathways for numerous catalytic processes. Discovery of new glycoside hydrolases with improved biocatalytic properties for the efficient con...

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Autores principales: Dougherty, Michael J, D’haeseleer, Patrik, Hazen, Terry C, Simmons, Blake A, Adams, Paul D, Hadi, Masood Z
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3477009/
https://www.ncbi.nlm.nih.gov/pubmed/22759983
http://dx.doi.org/10.1186/1472-6750-12-38
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author Dougherty, Michael J
D’haeseleer, Patrik
Hazen, Terry C
Simmons, Blake A
Adams, Paul D
Hadi, Masood Z
author_facet Dougherty, Michael J
D’haeseleer, Patrik
Hazen, Terry C
Simmons, Blake A
Adams, Paul D
Hadi, Masood Z
author_sort Dougherty, Michael J
collection PubMed
description BACKGROUND: Metagenomics approaches provide access to environmental genetic diversity for biotechnology applications, enabling the discovery of new enzymes and pathways for numerous catalytic processes. Discovery of new glycoside hydrolases with improved biocatalytic properties for the efficient conversion of lignocellulosic material to biofuels is a critical challenge in the development of economically viable routes from biomass to fuels and chemicals. RESULTS: Twenty-two putative ORFs (open reading frames) were identified from a switchgrass-adapted compost community based on sequence homology to related gene families. These ORFs were expressed in E. coli and assayed for predicted activities. Seven of the ORFs were demonstrated to encode active enzymes, encompassing five classes of hemicellulases. Four enzymes were over expressed in vivo, purified to homogeneity and subjected to detailed biochemical characterization. Their pH optima ranged between 5.5 - 7.5 and they exhibit moderate thermostability up to ~60-70°C. CONCLUSIONS: Seven active enzymes were identified from this set of ORFs comprising five different hemicellulose activities. These enzymes have been shown to have useful properties, such as moderate thermal stability and broad pH optima, and may serve as the starting points for future protein engineering towards the goal of developing efficient enzyme cocktails for biomass degradation under diverse process conditions.
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spelling pubmed-34770092012-10-20 Glycoside Hydrolases from a targeted Compost Metagenome, activity-screening and functional characterization Dougherty, Michael J D’haeseleer, Patrik Hazen, Terry C Simmons, Blake A Adams, Paul D Hadi, Masood Z BMC Biotechnol Research Article BACKGROUND: Metagenomics approaches provide access to environmental genetic diversity for biotechnology applications, enabling the discovery of new enzymes and pathways for numerous catalytic processes. Discovery of new glycoside hydrolases with improved biocatalytic properties for the efficient conversion of lignocellulosic material to biofuels is a critical challenge in the development of economically viable routes from biomass to fuels and chemicals. RESULTS: Twenty-two putative ORFs (open reading frames) were identified from a switchgrass-adapted compost community based on sequence homology to related gene families. These ORFs were expressed in E. coli and assayed for predicted activities. Seven of the ORFs were demonstrated to encode active enzymes, encompassing five classes of hemicellulases. Four enzymes were over expressed in vivo, purified to homogeneity and subjected to detailed biochemical characterization. Their pH optima ranged between 5.5 - 7.5 and they exhibit moderate thermostability up to ~60-70°C. CONCLUSIONS: Seven active enzymes were identified from this set of ORFs comprising five different hemicellulose activities. These enzymes have been shown to have useful properties, such as moderate thermal stability and broad pH optima, and may serve as the starting points for future protein engineering towards the goal of developing efficient enzyme cocktails for biomass degradation under diverse process conditions. BioMed Central 2012-07-03 /pmc/articles/PMC3477009/ /pubmed/22759983 http://dx.doi.org/10.1186/1472-6750-12-38 Text en Copyright ©2012 Dougherty 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 Article
Dougherty, Michael J
D’haeseleer, Patrik
Hazen, Terry C
Simmons, Blake A
Adams, Paul D
Hadi, Masood Z
Glycoside Hydrolases from a targeted Compost Metagenome, activity-screening and functional characterization
title Glycoside Hydrolases from a targeted Compost Metagenome, activity-screening and functional characterization
title_full Glycoside Hydrolases from a targeted Compost Metagenome, activity-screening and functional characterization
title_fullStr Glycoside Hydrolases from a targeted Compost Metagenome, activity-screening and functional characterization
title_full_unstemmed Glycoside Hydrolases from a targeted Compost Metagenome, activity-screening and functional characterization
title_short Glycoside Hydrolases from a targeted Compost Metagenome, activity-screening and functional characterization
title_sort glycoside hydrolases from a targeted compost metagenome, activity-screening and functional characterization
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3477009/
https://www.ncbi.nlm.nih.gov/pubmed/22759983
http://dx.doi.org/10.1186/1472-6750-12-38
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