Loop optimization of <i>Trichoderma reesei</i> endoglucanases for balancing the activity–stability trade‐off through cross‐strategy between machine learning and the B‐factor analysis
Le Gao, Qi Guo, Ruinan Xu, Haofan Dong, Chi-Chun Zhou, Zhuohang Yu, Zhaokun Zhang, Lixian Wang, Xiaoyi Chen, Xin Wu
Abstract
Abstract Trichoderma reesei endoglucanases (EGs) have limited industrial applications due to its low thermostability and activity. Here, we aimed to improve the thermostability of EGs from T. reesei without reducing its activity counteracting the activity–stability trade‐off. A cross‐strategy combination of machine learning and B‐factor analysis was used to predict beneficial amino acid substitution in EG loop optimization. Experimental validation showed single‐site mutated EG concomitantly improved enzymatic activity and thermal properties by 17.21%–18.06% and 49.85%–62.90%, respectively, compared with wild‐type EGs. Furthermore, the mechanism explained mutant variants had lower root mean square deviation values and a more stable overall structure than the wild type. According to this study, EGs loop optimization is crucial for balancing the activity–stability trade‐off, which may provide new insights into how loop region function interacts with enzymatic characteristics. Moreover, the cross‐strategy between machine learning and B‐factor analysis improved superior enzyme activity–stability performance, which integrated structure‐dependent and sequence‐dependent information.