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.
Original language | English |
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Pages (from-to) | 3956-3964 |
Journal | Applied and Environmental Microbiology |
Volume | 68 |
Issue number | 8 |
DOIs | |
Publication status | Published - 2002 |
MoE publication type | A1 Journal article-refereed |
Keywords
- Trichoderma reesei
- endoglucanase
- cellobiohydrolase
- cellulase
- stonewashing
- denim fabric
- denims
- clothes