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谷胱甘肽S-转移酶可能通过直接代谢作用参与(L.)中(S)-(-)-帕拉索宁的解毒过程。

Glutathione S-Transferase May Contribute to the Detoxification of (S)-(-)-Palasonin in (L.) via Direct Metabolism.

作者信息

Fan Qiqi, Liu Jiyuan, Li Yifan, Zhang Yalin

机构信息

Key Laboratory of Plant Protection Resources and Pest Management, Ministry of Education, Entomological Museum, College of Plant Protection, Northwest A&F University, Yangling, Xianyang 712100, China.

出版信息

Insects. 2022 Oct 28;13(11):989. doi: 10.3390/insects13110989.

Abstract

The control of primarily involves chemical insecticides, but overuse has brought about many negative effects. Our previous study reported that (S)-(-)-palasonin (PLN) is a plant-derived active substance with significant insecticidal activity against . However, we noticed a possible cross-resistance between (S)-(-)-palasonin and other insecticides which may be related to metabolic detoxification. In order to further explore the detoxification effect of detoxification enzymes on (S)-(-)-palasonin in , the effects of (S)-(-)-palasonin on enzyme activity and transcription level were determined, and the detoxification and metabolism of GSTs on (S)-(-)-palasonin were studied by in vitro inhibition and metabolism experiments. During this study, GST enzyme activity was significantly increased in after (S)-(-)-palasonin treatment. The expression levels of 19 GSTs genes were significantly increased whereas the expression levels of 1 gene decreased. Furthermore, (S)-(-)-palasonin is shown to be stabilized with GSTs and metabolized GSTs (GSTd1, GSTd2, GSTs1 and GSTs2) in vitro, with the highest metabolic rate of 80.59% for GSTs1. This study advances the beneficial utilization of (S)-(-)-palasonin as a botanical pesticide to control in the field.

摘要

对[害虫名称未给出]的防治主要涉及化学杀虫剂,但过度使用已带来许多负面影响。我们之前的研究报告称,(S)-(-)-帕拉索宁(PLN)是一种植物源活性物质,对[害虫名称未给出]具有显著的杀虫活性。然而,我们注意到(S)-(-)-帕拉索宁与其他杀虫剂之间可能存在交叉抗性,这可能与代谢解毒有关。为了进一步探究解毒酶对[害虫名称未给出]体内(S)-(-)-帕拉索宁的解毒作用,测定了(S)-(-)-帕拉索宁对酶活性和转录水平的影响,并通过体外抑制和代谢实验研究了谷胱甘肽S-转移酶(GSTs)对(S)-(-)-帕拉索宁的解毒和代谢作用。在这项研究中,经(S)-(-)-帕拉索宁处理后,[害虫名称未给出]体内的GST酶活性显著增加。19个GSTs基因的表达水平显著升高,而1个基因的表达水平下降。此外,(S)-(-)-帕拉索宁在体外与GSTs结合并被GSTs(GSTd1、GSTd2、GSTs1和GSTs2)代谢,其中GSTs1的最高代谢率为80.59%。本研究推动了(S)-(-)-帕拉索宁作为一种植物源杀虫剂在田间防治[害虫名称未给出]的有益利用。

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