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Two-step computational redesign of Bacillus subtilis cellulase and β-glucanase for enhanced thermostability and activity.

Huan Zhang,Tong Zhu,Qinglin Zhai,Qiansi Chen,Xuanshuo Zhang,Yiqiang Chen,Wei He,Jingjing Li,Jianqiang Fan,Jiemeng Tao,Xingchuan Hu,Lingfeng Qi,Chaochao Wang,Kuanqi Liao,Yanchun Chen,Yinglu Cui,Shanyi Chen,Bian Wu

Published 2024 in International Journal of Biological Macromolecules

ABSTRACT

The growing demand for biocatalysts in biomass processing highlights the necessity of enhancing the thermostability of glycoside hydrolases. However, improving both thermostability and activity is often hindered by trade-offs between backbone rigidity and the flexibility of substrate-binding regions. In this study, Bacillus subtilis cellulase and β-glucanase were engineered using a two-step process incorporating the computational tools Pythia and ESM-2, which were found complementary in improving stability and activity. The engineered cellulase and β-glucanase exhibited increases in their apparent melting temperatures (5.8 °C and 8.4 °C), accompanied by up to a 1.5-fold increase in initial activities. At 50 °C, while the wild-type cellulase lost 60% of its activity after 24 h and wild-type β-glucanase lost activity completely in 2 h, the engineered cellulase-M5 retained its initial activity, and β-glucanase-M7 displayed a 2.2-fold increase in its half-life. Structural analysis indicated that Pythia-identified mutations likely enhanced backbone robustness through refined polar and hydrophobic interactions, while beneficial mutations from ESM-2 appeared to affect polysaccharide-binding regions. This two-step computational redesign offers a promising approach for optimizing both thermostability and activity in glycoside hydrolases and other enzyme families with extensive sequence diversity.

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