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Enhanced Production of Trichoderma reesei Endoglucanases and Use of the New Cellulase Preparations in Producing the Stonewashed Effect on Denim Fabric

机译:里氏木霉内切葡聚糖酶的产量提高以及新纤维素酶制剂在牛仔布上的水洗效果

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摘要

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.
机译:构建里氏木霉菌株以产生具有或不具有纤维二糖水解酶I(CBHI)的升高量的内切葡聚糖酶II(EGII)。 EGII转化子产生的内切葡聚糖酶活性与egl2表达盒的拷贝数相关。 egl2表达盒的一个拷贝(其中egl2在cbh1启动子之下)使内切葡聚糖酶活性的产生增加了2.3倍,而两个拷贝使产生的产量比亲本菌株高了约3倍。当使用具有升高的EGII含量的酶时,获得了对牛仔布的改善的石洗效果。通过用过量产生EGI的CBHI阴性菌株中的egl2基因编码区代替cbh2基因座,可以构建产生大量EGI和-II活性而没有CBHI和-II的里氏木霉菌株。 EG-转化菌株产生的内切葡聚糖酶活性比宿主菌株增加了四倍。产生内切葡聚糖酶的菌株的滤纸降解活性降低到检测以下,这可能是由于缺乏纤维二糖水解酶。

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