Improvement of alkaliphily of thermostable GH family 10 xylanase from Thermotoga maritima by directed evolution

Wataru Tsukimura, K. Watanabe, C. Morokuma, R. Yatsunami, T. Fukui, Satoshi Nakamura
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引用次数: 1

Abstract

Xylanase B (XynTB) from hyperthermophilic bacterium Thermotoga maritima MSB8 is a thermostable xylanase classified into glycoside hydrolase family 10. XynTB is most active at pH 6.0, and shows lower activity at alkaline pHs. Improvement of alkaliphily of XynTB was attempted by directed evolution. One mutant enzyme that showed slightly higher activity under high temperature and alkaline pH conditions was acquired from a newly constructed random mutant library. Protein engineering study of this mutant revealed that the amino acid substitution N92D (Asn92 was substituted by Asp) could contribute to the improvement of alkaliphily.
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定向进化改良海洋热藓耐热GH家族10木聚糖酶的嗜碱性
木聚糖酶B (xyyntb)是一种耐热木聚糖酶,属于糖苷水解酶家族10。XynTB在pH 6.0时活性最强,在碱性pH下活性较低。通过定向进化的方法,尝试改善XynTB的碱度。从新构建的随机突变体文库中获得了一个在高温和碱性条件下表现出较高活性的突变体酶。对该突变体的蛋白质工程研究表明,氨基酸取代N92D (Asn92被Asp取代)有助于改善其碱性。
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