Characterization, Structural Analysis, and Thermal Stability Mutation of a New Zearalenone-Degrading Enzyme Mined from Bacillus subtilis
["Shi, Jinghao","Mwabulili, Fred","Xie, Yanli","Yang, Yuhui","Sun, Shumin","Li, Qian","Ma, Weibin","Jia, Hang"]
2024-02-01
期刊论文
(6)
Zearalenone (ZEN) is a widespread mycotoxin that causes serious damage to animal husbandry and poses a threat to human health. A screen of ZEN-degrading soil bacteria yielded Bacillus subtilis YT-4, which yielded 80% ZEN degradation after 6 h and 95% after 36 h. The gene sequence encoding the degradative enzyme ZENY was mined from the genome of YT-4 and expressed in yeast. ZENY is an alpha/beta-hydrolase with an optimal enzyme activity at 37 degrees C and pH 8. By breaking the lactone ring of ZEN, it produces ZENY-C18H24O5 with a molecular weight of 320.16 g/mol. Sequence comparison and molecular docking analyses identified the catalytic ZENY triad 99S-245H-123E and the primary ZEN-binding mode within the hydrophobic pocket of the enzyme. To improve the thermal stability of the enzyme for industrial applications, we introduced a mutation at the N-terminus, specifically replacing the fifth residue N with V, and achieved a 25% improvement in stability at 45 degrees C. These findings aim to achieve ZEN biodegradation and provide insight into the structure and function of ZEN hydrolases.
来源平台:JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY