Abstract

BackgroundThe soft rot ascomycetal fungus Trichoderma reesei is utilized for industrial production of secreted enzymes, especially lignocellulose degrading enzymes. T. reesei uses several different enzymes for the degradation of plant cell wall-derived material, including 9 characterized cellulases, 15 characterized hemicellulases and at least 42 genes predicted to encode cellulolytic or hemicellulolytic activities. Production of cellulases and hemicellulases is modulated by environmental and physiological conditions. Several regulators affecting the expression of cellulase and hemicellulase genes have been identified but more factors still unknown are believed to be present in the genome of T. reesei.ResultsWe have used transcriptional profiling data from T. reesei cultures in which cellulase/hemicellulase production was induced by the addition of different lignocellulose-derived materials to identify putative novel regulators for cellulase and hemicellulase genes. Based on this induction data, supplemented with other published genome-wide data on different protein production conditions, 28 candidate regulatory genes were selected for further studies and they were overexpressed in T. reesei. Overexpression of seven genes led to at least 1.5-fold increased production of cellulase and/or xylanase activity in the modified strains as compared to the parental strain. Deletion of gene 77513, here designated as ace3, was found to be detrimental for cellulase production and for the expression of several cellulase genes studied. This deletion also significantly reduced xylanase activity and expression of xylan-degrading enzyme genes. Furthermore, our data revealed the presence of co-regulated chromosomal regions containing carbohydrate-active enzyme genes and candidate regulatory genes.ConclusionsTranscriptional profiling results from glycoside hydrolase induction experiments combined with a previous study of specific protein production conditions was shown to be an effective method for finding novel candidate regulatory genes affecting the production of cellulases and hemicellulases. Recombinant strains with improved cellulase and/or xylanase production properties were constructed, and a gene essential for cellulase gene expression was found. In addition, more evidence was gained on the chromatin level regional regulation of carbohydrate-active enzyme gene expression.

Highlights

  • The soft rot ascomycetal fungus Trichoderma reesei is utilized for industrial production of secreted enzymes, especially lignocellulose degrading enzymes

  • Analysis of transcriptome data to identify candidates for regulators of cellulase and hemicellulase genes Transcriptome analysis has previously been carried out to study the expression of carbohydrate-active enzymes (CAZy) genes in T. reesei cultures that were induced by the addition of different types of lignocellulose material, purified carbohydrate polymers or disaccharides (Avicel cellulose, pretreated wheat straw, pretreated spruce or sophorose) [8]

  • Combining genome-wide data on cultures with different protein production properties is a useful method for identifying novel regulatory genes relevant for cellulase and xylanase production in T. reesei

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Summary

Introduction

The soft rot ascomycetal fungus Trichoderma reesei is utilized for industrial production of secreted enzymes, especially lignocellulose degrading enzymes. T. reesei uses several different enzymes for the degradation of plant cell wall-derived material, including 9 characterized cellulases, 15 characterized hemicellulases and at least 42 genes predicted to encode cellulolytic or hemicellulolytic activities. Trichoderma reesei (an anamorph of Hypocrea jecorina) is an extremely efficient producer of cellulose- and hemicellulose-degrading enzymes, and is widely employed by the enzyme industry for the production of its own enzymes as well as for producing proteins from other sources [2,3]. The genome of T. reesei encodes nine characterized cellulase enzymes and 15 characterized hemicellulase enzymes. A large number of genes encoding candidate carbohydrate-active enzymes (CAZy) [4,5] have been identified from the genome [6,7]. According to an updated annotation, the genome encodes 201 glycoside hydrolase genes, 22 carbohydrate esterase genes and 5 polysaccharide lyase genes, of which at least 66 are known or predicted to encode cellulolytic and hemicellulolytic activities [8]

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