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Rational engineering of the Trichoderma reesei RUT-C30 strain into an industrially relevant platform for cellulase production

BACKGROUND: The path for the development of hypersecreting strains of Trichoderma reesei capable of producing industrially relevant enzyme titers remains elusive despite over 70 years of research and industrial utilization. Herein, we describe the rational engineering of the publicly available T. re...

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Autores principales: Fonseca, Lucas Miranda, Parreiras, Lucas Salera, Murakami, Mario Tyago
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7243233/
https://www.ncbi.nlm.nih.gov/pubmed/32461765
http://dx.doi.org/10.1186/s13068-020-01732-w
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author Fonseca, Lucas Miranda
Parreiras, Lucas Salera
Murakami, Mario Tyago
author_facet Fonseca, Lucas Miranda
Parreiras, Lucas Salera
Murakami, Mario Tyago
author_sort Fonseca, Lucas Miranda
collection PubMed
description BACKGROUND: The path for the development of hypersecreting strains of Trichoderma reesei capable of producing industrially relevant enzyme titers remains elusive despite over 70 years of research and industrial utilization. Herein, we describe the rational engineering of the publicly available T. reesei RUT-C30 strain and a customized process for cellulase production based on agroindustrial by-products. RESULTS: A CRISPR/Cas9 system was used to introduce six genetic modifications in RUT-C30. Implemented changes included the constitutive expression of a mutated allele of the cellulase master regulator XYR1, the expression of two heterologous enzymes, the β-glucosidase CEL3A from Talaromyces emersonii and the invertase SUC1 from Aspergillus niger, and the deletion of genes encoding the cellulase repressor ACE1 and the extracellular proteases SLP1 and PEP1. These alterations resulted in a remarkable increase of protein secretion rates by RUT-C30 and amended its well described β-glucosidase deficiency while enabling the utilization of sucrose and eliminating the requirement of inducing sugars for enzyme production. With a developed sugarcane molasses-based bioprocess, the engineered strain reached an extracellular protein titer of 80.6 g L(−1) (0.24 g L(−1) h(−1)), which is the highest experimentally supported titer so far reported for T. reesei. The produced enzyme cocktail displayed increased levels of cellulase and hemicellulase activities, with particularly large increments being observed for the specific activities of β-glucosidase (72-fold) and xylanase (42-fold). Notably, it also exhibited a saccharification efficiency similar to that of a commercially available cellulase preparation in the deconstruction of industrially pretreated sugarcane straw. CONCLUSION: This work demonstrates the rational steps for the development of a cellulase hyperproducing strain from a well-characterized genetic background available in the public domain, the RUT-C30, associated with an industrially relevant bioprocess, paving new perspectives for Trichoderma research on cellulase production.
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spelling pubmed-72432332020-05-22 Rational engineering of the Trichoderma reesei RUT-C30 strain into an industrially relevant platform for cellulase production Fonseca, Lucas Miranda Parreiras, Lucas Salera Murakami, Mario Tyago Biotechnol Biofuels Research BACKGROUND: The path for the development of hypersecreting strains of Trichoderma reesei capable of producing industrially relevant enzyme titers remains elusive despite over 70 years of research and industrial utilization. Herein, we describe the rational engineering of the publicly available T. reesei RUT-C30 strain and a customized process for cellulase production based on agroindustrial by-products. RESULTS: A CRISPR/Cas9 system was used to introduce six genetic modifications in RUT-C30. Implemented changes included the constitutive expression of a mutated allele of the cellulase master regulator XYR1, the expression of two heterologous enzymes, the β-glucosidase CEL3A from Talaromyces emersonii and the invertase SUC1 from Aspergillus niger, and the deletion of genes encoding the cellulase repressor ACE1 and the extracellular proteases SLP1 and PEP1. These alterations resulted in a remarkable increase of protein secretion rates by RUT-C30 and amended its well described β-glucosidase deficiency while enabling the utilization of sucrose and eliminating the requirement of inducing sugars for enzyme production. With a developed sugarcane molasses-based bioprocess, the engineered strain reached an extracellular protein titer of 80.6 g L(−1) (0.24 g L(−1) h(−1)), which is the highest experimentally supported titer so far reported for T. reesei. The produced enzyme cocktail displayed increased levels of cellulase and hemicellulase activities, with particularly large increments being observed for the specific activities of β-glucosidase (72-fold) and xylanase (42-fold). Notably, it also exhibited a saccharification efficiency similar to that of a commercially available cellulase preparation in the deconstruction of industrially pretreated sugarcane straw. CONCLUSION: This work demonstrates the rational steps for the development of a cellulase hyperproducing strain from a well-characterized genetic background available in the public domain, the RUT-C30, associated with an industrially relevant bioprocess, paving new perspectives for Trichoderma research on cellulase production. BioMed Central 2020-05-22 /pmc/articles/PMC7243233/ /pubmed/32461765 http://dx.doi.org/10.1186/s13068-020-01732-w Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data.
spellingShingle Research
Fonseca, Lucas Miranda
Parreiras, Lucas Salera
Murakami, Mario Tyago
Rational engineering of the Trichoderma reesei RUT-C30 strain into an industrially relevant platform for cellulase production
title Rational engineering of the Trichoderma reesei RUT-C30 strain into an industrially relevant platform for cellulase production
title_full Rational engineering of the Trichoderma reesei RUT-C30 strain into an industrially relevant platform for cellulase production
title_fullStr Rational engineering of the Trichoderma reesei RUT-C30 strain into an industrially relevant platform for cellulase production
title_full_unstemmed Rational engineering of the Trichoderma reesei RUT-C30 strain into an industrially relevant platform for cellulase production
title_short Rational engineering of the Trichoderma reesei RUT-C30 strain into an industrially relevant platform for cellulase production
title_sort rational engineering of the trichoderma reesei rut-c30 strain into an industrially relevant platform for cellulase production
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7243233/
https://www.ncbi.nlm.nih.gov/pubmed/32461765
http://dx.doi.org/10.1186/s13068-020-01732-w
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