
Genetic Modification of Carbon Catabolite Repression in Trichoderma reesei for Improved Protein Production
Author(s) -
Tiikari-Setälä,
Marja Paloheimo,
Jarno Kallio,
Jari Vehmaanperä,
Merja Penttilä,
Markku Saloheimo
Publication year - 2009
Publication title -
applied and environmental microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.552
H-Index - 324
eISSN - 1070-6291
pISSN - 0099-2240
DOI - 10.1128/aem.00282-09
Subject(s) - trichoderma reesei , catabolite repression , cellulase , mutant , microbiology and biotechnology , biology , gene , enzyme , biochemistry
The cellulase and hemicellulase genes of the filamentous fungusTrichoderma reesei have been shown to be under carbon catabolite repression mediated by the regulatory genecre1 . In this study, strains were constructed in which thecre1 gene was either completely removed or replaced by a truncated mutant variant,cre1 -1 , found previously in the Rut-C30 mutant strain with enhanced enzyme production capability. TheT .reesei transformants with either deletion or truncation ofcre1 had clearly altered colony morphology compared with the parental strains, forming smaller colonies and fewer aerial hyphae and spores. Liquid cultures in a medium with glucose as a carbon source showed that the transformants were derepressed in cellulase and hemicellulase production. Interestingly, they also produced significantly elevated levels of these hydrolytic enzymes in fermentations carried out in a medium inducing the hydrolase genes. This suggests thatcre1 acts as a modulator of cellulase and hemicellulase gene expression under both noninducing and inducing conditions. There was no phenotypic difference between the Δcre1 andcre1 -1 mutant strains in any of the experiments done, indicating that thecre1 -1 gene is practically a null allele. The results of this work indicate thatcre1 is a valid target gene in strain engineering for improved enzyme production inT .reesei .