Takeuchi Haruka, Nomura Masahiro, Horikoshi Ryo, Aasano Shu, Miyake Takaaki, Kobayashi Takeru, Murai Masatoshi, Chen Ying-Ju, Earley Fergus, Mina John, Crossthwaite Andrew
Research & Development Division, Mitsui Chemicals Crop & Life Solutions, Inc.
Agrochemicals Laboratories, Nippon Kayaku Co., Ltd.
J Pestic Sci. 2024 Nov 20;49(4):203-209. doi: 10.1584/jpestics.D24-008.
Flometoquin (FLO) is a novel quinoline-type insecticide that elicits a quick knock-down effect against target pests; however, its mode of action (MoA) remains unknown. In this study, we investigated its MoA systematically, using varying biochemical techniques. Since FLO-treated insects exhibited symptoms similar to those induced by respiratory inhibitors, we examined the effect of FLO on respiratory enzyme complexes using mitochondria isolated from different insects (housefly, diamondback moth, and western flower thrips). We found that FLO itself is not active; however, its deacylated metabolite, FloMet, specifically inhibits the activity of ubiquinol-cytochrome oxidoreductase (complex III) in mitochondria at the nM level. Ligand binding assays and monitoring the reduction kinetics of cytochrome hemes and clearly revealed that FloMet inhibits complex III by binding to the Q site.
氟甲喹(FLO)是一种新型喹啉类杀虫剂,对目标害虫具有快速击倒作用;然而,其作用模式(MoA)尚不清楚。在本研究中,我们使用各种生化技术系统地研究了其作用模式。由于经FLO处理的昆虫表现出与呼吸抑制剂诱导的症状相似的症状,我们使用从不同昆虫(家蝇、小菜蛾和西花蓟马)分离的线粒体研究了FLO对呼吸酶复合物的影响。我们发现FLO本身没有活性;然而,其脱酰基代谢产物FloMet在纳摩尔水平上特异性抑制线粒体中泛醇-细胞色素氧化还原酶(复合物III)的活性。配体结合试验以及对细胞色素血红素 和 的还原动力学监测清楚地表明,FloMet通过与Q位点结合来抑制复合物III。