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Management of enzyme diversity in high-performance cellulolytic cocktails
BACKGROUND: Modern biorefineries require enzymatic cocktails of improved efficiency to generate fermentable sugars from lignocellulosic biomass. Cellulolytic fungi, among other microorganisms, have demonstrated the highest potential in terms of enzymatic productivity, complexity and efficiency. On t...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5477296/ https://www.ncbi.nlm.nih.gov/pubmed/28649275 http://dx.doi.org/10.1186/s13068-017-0845-6 |
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author | Reyes-Sosa, Francisco Manuel López Morales, Macarena Platero Gómez, Ana Isabel Valbuena Crespo, Noelia Sánchez Zamorano, Laura Rocha-Martín, Javier Molina-Heredia, Fernando P. Díez García, Bruno |
author_facet | Reyes-Sosa, Francisco Manuel López Morales, Macarena Platero Gómez, Ana Isabel Valbuena Crespo, Noelia Sánchez Zamorano, Laura Rocha-Martín, Javier Molina-Heredia, Fernando P. Díez García, Bruno |
author_sort | Reyes-Sosa, Francisco Manuel |
collection | PubMed |
description | BACKGROUND: Modern biorefineries require enzymatic cocktails of improved efficiency to generate fermentable sugars from lignocellulosic biomass. Cellulolytic fungi, among other microorganisms, have demonstrated the highest potential in terms of enzymatic productivity, complexity and efficiency. On the other hand, under cellulolytic-inducing conditions, they often produce a considerable diversity of carbohydrate-active enzymes which allow them to adapt to changing environmental conditions. However, industrial conditions are fixed and adjusted to the optimum of the whole cocktail, resulting in underperformance of individual enzymes. RESULTS: One of these cellulolytic cocktails from Myceliophthora thermophila has been analyzed here by means of LC–MS/MS. Pure GH6 family members detected have been characterized, confirming previous studies, and added to whole cocktails to compare their contribution in the hydrolysis of industrial substrates. Finally, independent deletions of two GH6 family members, as an example of the enzymatic diversity management, led to the development of a strain producing a more efficient cellulolytic cocktail. CONCLUSIONS: These data indicate that the deletion of noncontributive cellulases (here EG VI) can increase the cellulolytic efficiency of the cocktail, validating the management of cellulase diversity as a strategy to obtain improved fungal cellulolytic cocktails. |
format | Online Article Text |
id | pubmed-5477296 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-54772962017-06-23 Management of enzyme diversity in high-performance cellulolytic cocktails Reyes-Sosa, Francisco Manuel López Morales, Macarena Platero Gómez, Ana Isabel Valbuena Crespo, Noelia Sánchez Zamorano, Laura Rocha-Martín, Javier Molina-Heredia, Fernando P. Díez García, Bruno Biotechnol Biofuels Research BACKGROUND: Modern biorefineries require enzymatic cocktails of improved efficiency to generate fermentable sugars from lignocellulosic biomass. Cellulolytic fungi, among other microorganisms, have demonstrated the highest potential in terms of enzymatic productivity, complexity and efficiency. On the other hand, under cellulolytic-inducing conditions, they often produce a considerable diversity of carbohydrate-active enzymes which allow them to adapt to changing environmental conditions. However, industrial conditions are fixed and adjusted to the optimum of the whole cocktail, resulting in underperformance of individual enzymes. RESULTS: One of these cellulolytic cocktails from Myceliophthora thermophila has been analyzed here by means of LC–MS/MS. Pure GH6 family members detected have been characterized, confirming previous studies, and added to whole cocktails to compare their contribution in the hydrolysis of industrial substrates. Finally, independent deletions of two GH6 family members, as an example of the enzymatic diversity management, led to the development of a strain producing a more efficient cellulolytic cocktail. CONCLUSIONS: These data indicate that the deletion of noncontributive cellulases (here EG VI) can increase the cellulolytic efficiency of the cocktail, validating the management of cellulase diversity as a strategy to obtain improved fungal cellulolytic cocktails. BioMed Central 2017-06-19 /pmc/articles/PMC5477296/ /pubmed/28649275 http://dx.doi.org/10.1186/s13068-017-0845-6 Text en © The Author(s) 2017 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 Reyes-Sosa, Francisco Manuel López Morales, Macarena Platero Gómez, Ana Isabel Valbuena Crespo, Noelia Sánchez Zamorano, Laura Rocha-Martín, Javier Molina-Heredia, Fernando P. Díez García, Bruno Management of enzyme diversity in high-performance cellulolytic cocktails |
title | Management of enzyme diversity in high-performance cellulolytic cocktails |
title_full | Management of enzyme diversity in high-performance cellulolytic cocktails |
title_fullStr | Management of enzyme diversity in high-performance cellulolytic cocktails |
title_full_unstemmed | Management of enzyme diversity in high-performance cellulolytic cocktails |
title_short | Management of enzyme diversity in high-performance cellulolytic cocktails |
title_sort | management of enzyme diversity in high-performance cellulolytic cocktails |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5477296/ https://www.ncbi.nlm.nih.gov/pubmed/28649275 http://dx.doi.org/10.1186/s13068-017-0845-6 |
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