Disciplines
Biology (60%); Industrial Biotechnology (10%); Computer Sciences (30%)
Keywords
Long Non-Coding Rna,
Trichoderma reesei,
Cellulase Expression,
Chromatin Accesibility,
DNA methylation,
Filamentous Fungi
Abstract
Fungi are a relatively understudied and incredibly versatile group of organisms with
enormous value and potential for covering the rising human demands. The filamentous
fungus Trichoderma reesei is used for the biotechnical production of carbohydrate-active
enzymes, in particular cellulases. These enzymes are essential for many other
manufacturing industries, for example the food, feed, textile and paper industry. Through a
process of random mutagenesis and following screening, researchers have generated
strains of T. reesei, which have enhanced cellulase production capacities. However,
spontaneous strain degeneration, a phenomenon during which an organism progressively
and irreversibly loses its production capacity, does negatively influence cellulase production
by T. reesei. It was reported that also other biotechnological production organisms are
affected by this phenomenon. This means that this phenomenon can at least result in
economic losses or - in worse case - it poses a threat for the secure availability of certain
products.
On the one hand, the project leader and her co-workers have recently identified the
contribution of epigenetic regulatory mechanisms playing a role in this phenomenon, and
also the involvement of long non-coding RNAs in the regulation of cellulase expression. On
the other hand, technological breakthroughs, notably long-read sequencing techniques, have
revolutionized the fields of epigenomics and transcriptomics and opened new research
avenues in non-model organisms like T. reesei.
Therefore, the current research study will i) investigate the changes in the epigenetic
landscape associated with loss of cellulase expression in T. reesei and ii) reveal the long
non-coding RNA repertoire and its putative role in cellulase expression in T. reesei using
long-read sequencing techniques for both purposes. Third, the modification of the cellulase
expression capacities by a combination of genetic and epigenetic strain engineering
strategies is planned.