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新型含查尔酮部分的 α-氨基膦酸酯衍生物的设计、合成与抗 TM V 活性,诱导植物疾病抗性并针对 TM V 外壳蛋白。

Design, synthesis and anti-TMV activity of novel α-aminophosphonate derivatives containing a chalcone moiety that induce resistance against plant disease and target the TMV coat protein.

机构信息

State Key Laboratory Breeding Base of Green Pesticide and Agricultural Bioengineering, Key Laboratory of Green Pesticide and Agricultural Bioengineering, Ministry of Education, Center for R & D of Fine Chemicals of Guizhou University, Guiyang 550025, China.

Guizhou University Medical college, Guiyang 550025, China.

出版信息

Pestic Biochem Physiol. 2021 Feb;172:104749. doi: 10.1016/j.pestbp.2020.104749. Epub 2020 Nov 14.

DOI:10.1016/j.pestbp.2020.104749
PMID:33518042
Abstract

Plant viral diseases, known as "plant cancer", with high contagiosity can substantially reduce crop quality and yield. To identify potential anti-tobacco mosaic virus (TMV) agents with different mechanisms, a series of novel α-aminophosphonate derivatives containing a chalcone moiety were designed and synthesized. Bioassay results revealed that some target compounds exhibited improved curative activity against TMV in vivo, and the EC value of compound B was 356.7 mg L. The activities of the defensive enzymes POD and CAT from tobacco leaves treated with B and B showed that these target compounds could improve the photosynthetic ability of the leaves and activate plant host resistance against TMV infection. The binding constant between B and TMV Coat Protein (CP) (2.51 × 10 M), calculated by the fluorescence titration experiment and docking results, revealed that B has a strong interaction with TMV CP. Further docking analysis revealed that B was embedded between two layers of the TMV CP, which was consistent with the 2:1 binding mode of TMV CP and B determined by the binding affinity experiment. The TEM morphological study of TMV treated with B and B indicated that this series of target compounds may trigger the disassembly of TMV by interacting directly with TMV CP. This study provides new insight for the discovery of antiviral compounds with two different mechanisms of action.

摘要

植物病毒病,又称“植物癌症”,传染性强,可大幅降低作物的质量和产量。为了寻找具有不同作用机制的潜在抗烟草花叶病毒(TMV)药剂,设计并合成了一系列含有查尔酮结构的新型α-氨基膦酸酯衍生物。生物测定结果表明,部分目标化合物在体内对 TMV 具有更好的治疗活性,化合物 B 的 EC 值为 356.7 mg/L。B 和 B 处理的烟草叶片防御酶 POD 和 CAT 的活性表明,这些目标化合物可以提高叶片的光合作用能力,并激活植物对 TMV 感染的抗性。荧光滴定实验和对接结果计算得出 B 与 TMV 外壳蛋白(CP)的结合常数(2.51×10 M)表明,B 与 TMV CP 具有很强的相互作用。进一步的对接分析表明,B 嵌入在 TMV CP 的两层之间,与结合亲和力实验确定的 TMV CP 和 B 的 2:1 结合模式一致。B 和 B 处理的 TMV 的 TEM 形态研究表明,该系列目标化合物可能通过与 TMV CP 直接相互作用触发 TMV 的解体。该研究为发现具有两种不同作用机制的抗病毒化合物提供了新的思路。

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