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Thermoascus aurantiacus is a promising source of enzymes for biomass deconstruction under thermophilic conditions

BACKGROUND: Thermophilic fungi have attracted increased interest for their ability to secrete enzymes that deconstruct biomass at high temperatures. However, development of thermophilic fungi as enzyme producers for biomass deconstruction has not been thoroughly investigated. Comparing the enzymatic...

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Autores principales: McClendon, Shara D, Batth, Tanveer, Petzold, Christopher J, Adams, Paul D, Simmons, Blake A, Singer, Steven W
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3507748/
https://www.ncbi.nlm.nih.gov/pubmed/22839529
http://dx.doi.org/10.1186/1754-6834-5-54
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author McClendon, Shara D
Batth, Tanveer
Petzold, Christopher J
Adams, Paul D
Simmons, Blake A
Singer, Steven W
author_facet McClendon, Shara D
Batth, Tanveer
Petzold, Christopher J
Adams, Paul D
Simmons, Blake A
Singer, Steven W
author_sort McClendon, Shara D
collection PubMed
description BACKGROUND: Thermophilic fungi have attracted increased interest for their ability to secrete enzymes that deconstruct biomass at high temperatures. However, development of thermophilic fungi as enzyme producers for biomass deconstruction has not been thoroughly investigated. Comparing the enzymatic activities of thermophilic fungal strains that grow on targeted biomass feedstocks has the potential to identify promising candidates for strain development. Thielavia terrestris and Thermoascus aurantiacus were chosen for characterization based on literature precedents. RESULTS: Thermoascus aurantiacus and Thielavia terrestris were cultivated on various biomass substrates and culture supernatants assayed for glycoside hydrolase activities. Supernatants from both cultures possessed comparable glycoside hydrolase activities when incubated with artificial biomass substrates. In contrast, saccharifications of ionic liquid pretreated switchgrass (Panicum virgatum) revealed that T. aurantiacus enzymes released more glucose than T. terrestris enzymes over a range of protein mass loadings and temperatures. Temperature-dependent saccharifications demonstrated that the T. aurantiacus proteins retained higher levels of activity compared to a commercial enzyme mixture sold by Novozymes, Cellic CTec2, at elevated temperatures. Enzymes secreted by T. aurantiacus released glucose at similar protein loadings to CTec2 on dilute acid, ammonia fiber expansion, or ionic liquid pretreated switchgrass. Proteomic analysis of the T. aurantiacus culture supernatant revealed dominant glycoside hydrolases from families 5, 7, 10, and 61, proteins that are key enzymes in commercial cocktails. CONCLUSIONS: T. aurantiacus produces a complement of secreted proteins capable of higher levels of saccharification of pretreated switchgrass than T. terrestris enzymes. The T. aurantiacus enzymatic cocktail performs at the same level as commercially available enzymatic cocktail for biomass deconstruction, without strain development or genetic modifications. Therefore, T. aurantiacus provides an excellent platform to develop a thermophilic fungal system for enzyme production for the conversion of biomass to biofuels.
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spelling pubmed-35077482012-11-28 Thermoascus aurantiacus is a promising source of enzymes for biomass deconstruction under thermophilic conditions McClendon, Shara D Batth, Tanveer Petzold, Christopher J Adams, Paul D Simmons, Blake A Singer, Steven W Biotechnol Biofuels Research BACKGROUND: Thermophilic fungi have attracted increased interest for their ability to secrete enzymes that deconstruct biomass at high temperatures. However, development of thermophilic fungi as enzyme producers for biomass deconstruction has not been thoroughly investigated. Comparing the enzymatic activities of thermophilic fungal strains that grow on targeted biomass feedstocks has the potential to identify promising candidates for strain development. Thielavia terrestris and Thermoascus aurantiacus were chosen for characterization based on literature precedents. RESULTS: Thermoascus aurantiacus and Thielavia terrestris were cultivated on various biomass substrates and culture supernatants assayed for glycoside hydrolase activities. Supernatants from both cultures possessed comparable glycoside hydrolase activities when incubated with artificial biomass substrates. In contrast, saccharifications of ionic liquid pretreated switchgrass (Panicum virgatum) revealed that T. aurantiacus enzymes released more glucose than T. terrestris enzymes over a range of protein mass loadings and temperatures. Temperature-dependent saccharifications demonstrated that the T. aurantiacus proteins retained higher levels of activity compared to a commercial enzyme mixture sold by Novozymes, Cellic CTec2, at elevated temperatures. Enzymes secreted by T. aurantiacus released glucose at similar protein loadings to CTec2 on dilute acid, ammonia fiber expansion, or ionic liquid pretreated switchgrass. Proteomic analysis of the T. aurantiacus culture supernatant revealed dominant glycoside hydrolases from families 5, 7, 10, and 61, proteins that are key enzymes in commercial cocktails. CONCLUSIONS: T. aurantiacus produces a complement of secreted proteins capable of higher levels of saccharification of pretreated switchgrass than T. terrestris enzymes. The T. aurantiacus enzymatic cocktail performs at the same level as commercially available enzymatic cocktail for biomass deconstruction, without strain development or genetic modifications. Therefore, T. aurantiacus provides an excellent platform to develop a thermophilic fungal system for enzyme production for the conversion of biomass to biofuels. BioMed Central 2012-07-28 /pmc/articles/PMC3507748/ /pubmed/22839529 http://dx.doi.org/10.1186/1754-6834-5-54 Text en Copyright ©2012 McClendon 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
McClendon, Shara D
Batth, Tanveer
Petzold, Christopher J
Adams, Paul D
Simmons, Blake A
Singer, Steven W
Thermoascus aurantiacus is a promising source of enzymes for biomass deconstruction under thermophilic conditions
title Thermoascus aurantiacus is a promising source of enzymes for biomass deconstruction under thermophilic conditions
title_full Thermoascus aurantiacus is a promising source of enzymes for biomass deconstruction under thermophilic conditions
title_fullStr Thermoascus aurantiacus is a promising source of enzymes for biomass deconstruction under thermophilic conditions
title_full_unstemmed Thermoascus aurantiacus is a promising source of enzymes for biomass deconstruction under thermophilic conditions
title_short Thermoascus aurantiacus is a promising source of enzymes for biomass deconstruction under thermophilic conditions
title_sort thermoascus aurantiacus is a promising source of enzymes for biomass deconstruction under thermophilic conditions
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3507748/
https://www.ncbi.nlm.nih.gov/pubmed/22839529
http://dx.doi.org/10.1186/1754-6834-5-54
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