益达胺
生物
异源表达
基因
异源的
谷胱甘肽转移酶
谷胱甘肽
生物化学
遗传学
分子生物学
酶
杀虫剂
生态学
重组DNA
作者
Qiuyang Pang,Wen-Jie He,Minggao Li,Sheng Wang,Xue-Yao Zhang,Qian Zhang,Rui-Yan Ma,Rui-Yan Ma,Yan‐Qiong Guo,Rui-Yan Ma
出处
期刊:Chemosphere
[Elsevier]
日期:2024-08-01
卷期号:362: 142722-142722
标识
DOI:10.1016/j.chemosphere.2024.142722
摘要
Glutathione S-transferases (GSTs) are multifunctional enzymes, and insect GSTs play a pivotal role in the metabolism of insecticides. Grapholita molesta is a worldwide pest that causes substantial economic losses to the fruit industry. However, it remains unclear how imidacloprid, a commonly used insecticide in orchards, is metabolized by G. molesta. In the present study, the synergist diethyl maleate (DEM), which inhibits the GST activity, exhibited a 22-fold synergistic ratio against imidacloprid. Two new GST genes, GmGSTD2 (OR096251) and GmGSTD3 (OR096252), were identified and successfully cloned, showing the highest expression in the Malpighian tubes. Knockdown of GmGSTD2 and GmGSTD3 by RNA interference, increased the mortality of G. molesta from 28% to 47% following imidacloprid treatment. Both recombinant GmGSTD2 and GmGSTD3 proteins exhibited 1-chloro-2,4-dinitrobenzene (CDNB) activity and could be inhibited by imidacloprid in vitro, with maximum inhibition was 60% for GmGSTD2 and 80% for GmGSTD3. These results suggested that GSTs participate in the metabolism of imidacloprid with GmGSTD2 and GmGSTD3 playing key roles in this process.
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