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Production of a Trichoderma reesei QM9414 xylanase in Pichia pastoris and its application in biobleaching of wheat straw pulp

机译:毕赤酵母中里氏木霉QM9414木聚糖酶的生产及其在麦草浆生物漂白中的应用

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The purpose of this study was to produce a Trichoderma reesei xylanase (XYN2) in Pichia pastoris and to test its potential application for pulp bleaching. The recombinant xylanase was purified by a two-step process of ultrafiltration and gel filtration chromatography. The molecular mass of the recombinant enzyme was 21 and 25 kDa by SDS–PAGE analysis, due to different glycosylation of the native protein. The optimum pH and temperature of the recombinant XYN2 was 5.0 and 50 °C. Enzyme activity was stable at 50 °C and at pH 5.0–7.0. The bleaching ability of the recombinant xylanase was also studied at 50 °C and pH 6.0, using wheat straw pulp. Biobleaching of the xylanase produced chlorine dioxide savings of up to 60%, while retaining brightness at the control level and led to a lower kappa number and small enhancements in tensile, burst and tear strength of pulp fibers.
机译:这项研究的目的是在巴斯德毕赤酵母中生产里氏木霉木聚糖酶(XYN2),并测试其在纸浆漂白中的潜在应用。通过两步超滤和凝胶过滤色谱法纯化重组木聚糖酶。通过SDS-PAGE分析,由于天然蛋白的糖基化程度不同,重组酶的分子量分别为21和25 kDa。重组XYN2的最佳pH和温度为5.0和50°C。酶的活性在50°C和pH 5.0-7.0下稳定。还使用小麦草浆在50°C和pH 6.0下研究了重组木聚糖酶的漂白能力。木聚糖酶的生物漂白可节省高达60%的二氧化氯,同时将亮度保持在控制水平,并导致较低的卡伯值和纸浆纤维的拉伸,破裂和撕裂强度的小幅提高。

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