Affiliation:
1. Primalco Ltd. Biotec, Rajamäki, Finland
Abstract
ABSTRACT
Trichoderma reesei
strains were constructed for production of elevated amounts of endoglucanase II (EGII) with or without cellobiohydrolase I (CBHI). The endoglucanase activity produced by the EGII transformants correlated with the copy number of the
egl2
expression cassette. One copy of the
egl2
expression cassette in which the
egl2
was under the
cbh1
promoter increased production of endoglucanase activity 2.3-fold, and two copies increased production about 3-fold above that of the parent strain. When the enzyme with elevated EGII content was used, an improved stonewashing effect on denim fabric was achieved. A
T. reesei
strain producing high amounts of EGI and -II activities without CBHI and -II was constructed by replacing the
cbh2
locus with the coding region of the
egl2
gene in the EGI-overproducing CBHI-negative strain. Production of endoglucanase activity by the EG-transformant strain was increased fourfold above that of the host strain. The filter paper-degrading activity of the endoglucanase-overproducing strain was lowered to below detection, presumably because of the lack of cellobiohydrolases.
Publisher
American Society for Microbiology
Subject
Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology
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