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Tailoring the Hinge Residue at the Substrate Access Tunnel Entrance Improves the Catalytic Performance of Industrialized Nitrile Hydratase Toward 3-Cyanopyridine
ChemistrySelect ( IF 1.9 ) Pub Date : 2022-09-09 , DOI: 10.1002/slct.202201941 Yuanyuan Xia 1 , Meng Yin 1 , Lukasz Peplowski 2 , Zhongyi Cheng 1 , Zhemin Zhou 1, 3
ChemistrySelect ( IF 1.9 ) Pub Date : 2022-09-09 , DOI: 10.1002/slct.202201941 Yuanyuan Xia 1 , Meng Yin 1 , Lukasz Peplowski 2 , Zhongyi Cheng 1 , Zhemin Zhou 1, 3
Affiliation
A hinge residue at the entrance of the substrate access tunnel of H-NHase was identified through substrate access tunnel calculations, site-saturation mutagenesis, molecular docking and molecular dynamics simulations. The mutant showed higher specific activity towards 3-cyanopyridine and better thermostability.
中文翻译:
调整底物通道入口处的铰链残渣提高工业化腈水合酶对 3-氰基吡啶的催化性能
通过底物通道计算、位点饱和诱变、分子对接和分子动力学模拟,确定了 H-NHase 底物通道入口处的铰链残基。该突变体对3-氰基吡啶表现出更高的比活性和更好的热稳定性。
更新日期:2022-09-11
中文翻译:
调整底物通道入口处的铰链残渣提高工业化腈水合酶对 3-氰基吡啶的催化性能
通过底物通道计算、位点饱和诱变、分子对接和分子动力学模拟,确定了 H-NHase 底物通道入口处的铰链残基。该突变体对3-氰基吡啶表现出更高的比活性和更好的热稳定性。