Department of Botany and Ecology, University of Zielona Góra, Szafrana 1, 65-516 Zielona Góra, Poland.
Department of Chemistry, Wrocław University of Environmental and Life Sciences, Norwida 25, 50-375 Wrocław, Poland.
Molecules. 2018 Sep 15;23(9):2362. doi: 10.3390/molecules23092362.
Jasmonates show great potential in sustainable agriculture due to their various roles in natural mechanisms of plant defense, and because they are non-toxic, non-mutagenic, and easily metabolized. The aim of the study was to explore structure⁻activity relationships of dihydrojasmone, -jasmone, and their derivatives at the plant⁻aphid interface. We focused on the behavioral responses of aphids, following the exogenous application of natural jasmonates and their derivatives to the host plants. Aphid probing behavior was examined using an electrical penetration graph technique (EPG). The chemoenzymatic transformation of -jasmone and the activity of two new derivatives are described. The application of jasmone, dihydrojasmone, the hydroxyderivatives, epoxyderivatives, and alkyl-substituted δ-lactones hindered the foraging activity of (Sulz.) (Hemiptera: Aphididae) during early stages of probing at the level of non-phloem tissues. The application of saturated bicyclic epoxy-δ-lactone enhanced plant acceptance by . Jasmonate derivatives containing a hydroxy group, especially in correlation with a lactone ring, were more active than natural compounds and other derivatives studied. Jasmonates of the present study are worth considering as elements of sustainable aphid control as components of the "push⁻pull" strategy.
茉莉酮酸酯因其在植物防御天然机制中的多种作用,以及其无毒、非诱变和易代谢的特点,在可持续农业中具有巨大的潜力。本研究旨在探索二氢茉莉酮酸酯、茉莉酮酸及其衍生物在植物-蚜虫界面的结构-活性关系。我们专注于蚜虫的行为反应,研究了天然茉莉酮酸及其衍生物在宿主植物上的外源应用。采用电穿透图技术(EPG)检测蚜虫的探测行为。描述了 -jasmone 的化学酶转化和两种新衍生物的活性。茉莉酮酸、二氢茉莉酮酸、羟基衍生物、环氧化物衍生物和烷基取代的 δ-内脂的应用,在非韧皮部组织探测的早期阶段,阻碍了 (Sulz.)(半翅目:蚜科)的觅食活动。饱和双环环氧-δ-内脂的应用增强了 对植物的接受性。含有羟基的茉莉酮酸衍生物,特别是与内酯环相关的衍生物,比天然化合物和其他研究的衍生物更具活性。本研究中的茉莉酮酸酯作为“推-拉”策略的组成部分,值得考虑作为可持续控制蚜虫的要素。