纤维素酶
定点突变
大草莺属
突变
毕赤酵母
突变体
酶动力学
蛋白质工程
酶
化学
生物化学
纤维素
纤维素乙醇
基质(水族馆)
微生物学
生物
活动站点
重组DNA
基因
生态学
作者
Haiyan Zhou,Xiao-Nan Yi,Qi Chen,Jian-Bao Zhou,Shufang Li,Xue Cai,De-Shui Chen,Xin‐Ping Cheng,Mian Li,Hongyan Wang,Kai-Qian Chen,Zhi‐Qiang Liu,Yu‐Guo Zheng
标识
DOI:10.1016/j.enzmictec.2021.109963
摘要
In order to improve the catalytic efficiency of cellulase for more effective utilization of lignocellulose, a novel endoglucanase (CgEndo) from Colletotrichum graminicola was expressed by Pichia pastoris X33 and modified by site-directed mutagenesis. Two mutants, Y63S and N20D/S113T, with 62.31% and 57.14% increased enzyme activities were obtained, respectively. On this basis, their biochemical properties, kinetic parameters, structural information as well as the application in biomass degradation were investigated and compared with the wild-type CgEngo. The results indicated that the mutation Y63S and N20D/S113T resulted in an improvement of proximity between enzyme and substrate through conformational changes of the catalytic region, which might contribute to the higher enzyme activities and catalysis efficiency (Kcat/Km) of Y63S and N20D/S113T. These findings laid important foundation for the further engineering of this endoglucanase and practical application in efficient degradation of cellulosic biomass in nature.
科研通智能强力驱动
Strongly Powered by AbleSci AI