Inicio  /  Applied Sciences  /  Vol: 12 Par: 11 (2022)  /  Artículo
ARTÍCULO
TITULO

A Highly Glyphosate-Resistant EPSPS Mutant from Laboratory Evolution

Yuan Yuan    
Zhengfu Zhou    
Yuhua Zhan    
Xiubin Ke    
Yongliang Yan    
Min Lin    
Pengcheng Li    
Shijie Jiang    
Jin Wang and Wei Lu    

Resumen

EPSP synthase is the target enzyme of glyphosate herbicides. Due to the extensive use of glyphosate, it is very important to obtain EPSPS genes with high glyphosate resistance for the development of transgenic crops. GR79-EPSPS is a class I EPSP synthase with certain glyphosate resistance isolated from glyphosate-contaminated soil. After more than 1000 generations, a Y40I substitution was identified, and the enzyme had a nearly 1.8-fold decrease in Km [PEP] and a 1.7-fold increase in Ki[glyphosate] compared to the wild-type enzyme. Enzyme dynamics and molecular dynamics analysis showed that the substitution was near the hinge region of EPSPS, and the affinity of glyphosate binding to amino acid residues of the active site decreased due to Y40I substitution, resulting in an increase in glyphosate resistance. These results provide more evidence for the combination of directed evolution and rational design of protein engineering.