2. Academic Validation
  3. Novel Thiazole Phenoxypyridine Derivatives Protect Maize from Residual Pesticide Injury Caused by PPO-Inhibitor Fomesafen

Novel Thiazole Phenoxypyridine Derivatives Protect Maize from Residual Pesticide Injury Caused by PPO-Inhibitor Fomesafen

  • Biomolecules. 2019 Sep 20;9(10):514. doi: 10.3390/biom9100514.
Li-Xia Zhao 1,  Min-Lei Yin 2,  Qing-Rui Wang 3,  Yue-Li Zou 4,  Tao Ren 5,  Shuang Gao 6,  Ying Fu 7,  Fei Ye 8
Affiliations

Affiliations

  • 1 Department of Applied Chemistry, College of Science, Northeast Agricultural University, Harbin 150030, China. zhaolixia@neau.edu.cn.
  • 2 Department of Applied Chemistry, College of Science, Northeast Agricultural University, Harbin 150030, China. minlei@aliyun.com.
  • 3 Department of Applied Chemistry, College of Science, Northeast Agricultural University, Harbin 150030, China. qingruiwang@hotmail.com.
  • 4 Department of Applied Chemistry, College of Science, Northeast Agricultural University, Harbin 150030, China. zouyuelineau@hotmail.com.
  • 5 Department of Applied Chemistry, College of Science, Northeast Agricultural University, Harbin 150030, China. woshibanye@gmail.com.
  • 6 Department of Applied Chemistry, College of Science, Northeast Agricultural University, Harbin 150030, China. gaoshuang@neau.edu.cn.
  • 7 Department of Applied Chemistry, College of Science, Northeast Agricultural University, Harbin 150030, China. fuying@neau.edu.cn.
  • 8 Department of Applied Chemistry, College of Science, Northeast Agricultural University, Harbin 150030, China. yefei@neau.edu.cn.
PMID: 31547161 DOI: 10.3390/biom9100514
Abstract

The herbicide fomesafen has the advantages of low toxicity and high selectivity, and the target of this compound is Protoporphyrinogen IX oxidase (PPO, EC 1.3.3.4). However, this herbicide has a long residual period and can have phytotoxic effects on succeeding crops. To protect maize from fomesafen, a series of thiazole phenoxypyridines were designed based on structure-activity relationships, active substructure combinations, and bioisosterism. Bioassays showed that thiazole phenoxypyridines could improve maize tolerance under fomesafen toxicity stress to varying degrees at a dose of 10 mg·kg-1. Compound 4i exhibited the best effects. After being treated by compound 4i, average recovery rates of growth index exceeded 72%, glutathione content markedly increased by 167% and Glutathione S-transferase activity was almost 163% of fomesafen-treated group. More importantly, after being treated by compound 4i, the activity of PPO, the main target Enzyme of fomesafen, recovered to 93% of the control level. The molecular docking result exhibited that the compound 4i could compete with fomesafen to bind with the herbicide target Enzyme, which consequently attained the herbicide detoxification. The present work suggests that compound 4i could be developed as a potential safener to protect maize from fomesafen.

Keywords

PPO; molecular docking; safener activity; synthesis; thiazole phenoxypyridines.

Figures
Products