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

Authors :
Toshiaki Fukui
Rie Yatsunami
K Watanabe
Satoshi Nakamura
C Morokuma
Wataru Tsukimura
Source :
Journal of Japanese Society for Extremophiles. 9:15-18
Publication Year :
2010
Publisher :
Japanese Society for Extremophiles, 2010.

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.

Details

ISSN :
21869936
Volume :
9
Database :
OpenAIRE
Journal :
Journal of Japanese Society for Extremophiles
Accession number :
edsair.doi.dedup.....b3f3bf8365e35904a9324f85a7ae718a
Full Text :
https://doi.org/10.3118/jjse.9.15