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l-Methionine repressible promoters for tuneable gene expression in Trichoderma reesei
BACKGROUND: Trichoderma reesei is the main producer of lignocellulolytic enzymes that are required for plant biomass hydrolysis in the biorefinery industry. Although the molecular toolbox for T. reesei is already well developed, repressible promoters for strain engineering and functional genomics st...
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/PMC4536894/ https://www.ncbi.nlm.nih.gov/pubmed/26271614 http://dx.doi.org/10.1186/s12934-015-0308-3 |
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author | Bischof, Robert H. Horejs, Jennifer Metz, Benjamin Gamauf, Christian Kubicek, Christian P Seiboth, Bernhard |
author_facet | Bischof, Robert H. Horejs, Jennifer Metz, Benjamin Gamauf, Christian Kubicek, Christian P Seiboth, Bernhard |
author_sort | Bischof, Robert H. |
collection | PubMed |
description | BACKGROUND: Trichoderma reesei is the main producer of lignocellulolytic enzymes that are required for plant biomass hydrolysis in the biorefinery industry. Although the molecular toolbox for T. reesei is already well developed, repressible promoters for strain engineering and functional genomics studies are still lacking. One such promoter that is widely employed for yeasts is that of the l-methionine repressible MET3 gene, encoding ATP sulphurylase. RESULTS: We show that the MET3 system can only be applied for T. reesei when the cellulase inducing carbon source lactose is used but not when wheat straw, a relevant lignocellulosic substrate for enzyme production, is employed. We therefore performed a transcriptomic screen for genes that are l-methionine repressible in a wheat straw culture. This analysis retrieved 50 differentially regulated genes of which 33 were downregulated. Among these, genes encoding transport proteins as well as iron containing DszA like monooxygenases and TauD like dioxygenases were strongly overrepresented. We show that the promoter region of one of these dioxygenases can be used for the strongly repressible expression of the Aspergillus niger sucA encoded extracellular invertase in T. reesei wheat straw cultures. This system is also portable to other carbon sources including d-glucose and glycerol as demonstrated by the repressible expression of the Escherichia coli lacZ encoded ß-galactosidase in T. reesei. CONCLUSION: We describe a novel, versatile set of promoters for T. reesei that can be used to drive recombinant gene expression in wheat straw cultures at different expression strengths and in an l-methionine repressible manner. The dioxygenase promoter that we studied in detail is furthermore compatible with different carbon sources and therefore applicable for manipulating protein production as well as functional genomics with T. reesei. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12934-015-0308-3) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4536894 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-45368942015-08-15 l-Methionine repressible promoters for tuneable gene expression in Trichoderma reesei Bischof, Robert H. Horejs, Jennifer Metz, Benjamin Gamauf, Christian Kubicek, Christian P Seiboth, Bernhard Microb Cell Fact Research BACKGROUND: Trichoderma reesei is the main producer of lignocellulolytic enzymes that are required for plant biomass hydrolysis in the biorefinery industry. Although the molecular toolbox for T. reesei is already well developed, repressible promoters for strain engineering and functional genomics studies are still lacking. One such promoter that is widely employed for yeasts is that of the l-methionine repressible MET3 gene, encoding ATP sulphurylase. RESULTS: We show that the MET3 system can only be applied for T. reesei when the cellulase inducing carbon source lactose is used but not when wheat straw, a relevant lignocellulosic substrate for enzyme production, is employed. We therefore performed a transcriptomic screen for genes that are l-methionine repressible in a wheat straw culture. This analysis retrieved 50 differentially regulated genes of which 33 were downregulated. Among these, genes encoding transport proteins as well as iron containing DszA like monooxygenases and TauD like dioxygenases were strongly overrepresented. We show that the promoter region of one of these dioxygenases can be used for the strongly repressible expression of the Aspergillus niger sucA encoded extracellular invertase in T. reesei wheat straw cultures. This system is also portable to other carbon sources including d-glucose and glycerol as demonstrated by the repressible expression of the Escherichia coli lacZ encoded ß-galactosidase in T. reesei. CONCLUSION: We describe a novel, versatile set of promoters for T. reesei that can be used to drive recombinant gene expression in wheat straw cultures at different expression strengths and in an l-methionine repressible manner. The dioxygenase promoter that we studied in detail is furthermore compatible with different carbon sources and therefore applicable for manipulating protein production as well as functional genomics with T. reesei. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12934-015-0308-3) contains supplementary material, which is available to authorized users. BioMed Central 2015-08-14 /pmc/articles/PMC4536894/ /pubmed/26271614 http://dx.doi.org/10.1186/s12934-015-0308-3 Text en © Bischof 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 Bischof, Robert H. Horejs, Jennifer Metz, Benjamin Gamauf, Christian Kubicek, Christian P Seiboth, Bernhard l-Methionine repressible promoters for tuneable gene expression in Trichoderma reesei |
title | l-Methionine repressible promoters for tuneable gene expression in Trichoderma reesei |
title_full | l-Methionine repressible promoters for tuneable gene expression in Trichoderma reesei |
title_fullStr | l-Methionine repressible promoters for tuneable gene expression in Trichoderma reesei |
title_full_unstemmed | l-Methionine repressible promoters for tuneable gene expression in Trichoderma reesei |
title_short | l-Methionine repressible promoters for tuneable gene expression in Trichoderma reesei |
title_sort | l-methionine repressible promoters for tuneable gene expression in trichoderma reesei |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4536894/ https://www.ncbi.nlm.nih.gov/pubmed/26271614 http://dx.doi.org/10.1186/s12934-015-0308-3 |
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