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非典型独脚金内酯类似物对两种种群中刺激萌发的选择性。

Noncanonical Strigolactone Analogues Highlight Selectivity for Stimulating Germination in Two Populations.

机构信息

Université Paris-Saclay, CNRS, Institut de Chimie des Substances Naturelles, UPR 2301, 91198, Gif-sur-Yvette, France.

Université Paris-Saclay, INRAE, AgroParisTech, Institut Jean-Pierre Bourgin (IJPB), 78000, Versailles, France.

出版信息

J Nat Prod. 2022 Aug 26;85(8):1976-1992. doi: 10.1021/acs.jnatprod.2c00282. Epub 2022 Jul 1.

Abstract

Strigolactones (SLs) are plant hormones exuded in the rhizosphere with a signaling role for the development of arbuscular mycorrhizal (AM) fungi and as stimulants of seed germination of the parasitic weeds , , and , the most threatening weeds of major crops worldwide. is present mainly on rape, hemp, and tobacco in France. 2a preferentially attacks hemp, while 1 attacks rapeseed. The recently isolated cannalactone () from hemp root exudates has been characterized as a noncanonical SL that selectively stimulates the germination of 2a seeds in comparison with 1. In the present work, (-)-solanacol (), a canonical orobanchol-type SL exuded by tobacco and tomato, was established to possess a remarkable selective germination stimulant activity for 2a seeds. Two cannalactone analogues, named (±)-SdL19 and (±)-SdL118, have been synthesized. They have an unsaturated acyclic carbon chain with a tertiary hydroxy group and a methyl or a cyclopropyl group instead of a cyclohexane A-ring, respectively. (±)-SdL analogues are able to selectively stimulate 2a, revealing that these minimal structural elements are key for this selective bioactivity. In addition, (±)-SdL19 is able to inhibit shoot branching in and and induces hyphal branching in the AM fungus , like SLs.

摘要

独脚金内酯(SLs)是一种在根际分泌的植物激素,具有刺激丛枝菌根真菌发育和刺激寄生杂草种子萌发的信号作用,其中 、 和 是全球主要作物最具威胁性的杂草。法国的油菜、大麻和烟草中主要存在 。2a 优先攻击大麻,而 1 则攻击油菜。最近从大麻根渗出物中分离出的 cannalactone() 被表征为一种非典型的 SL,与 1 相比,它选择性地刺激 2a 种子的萌发。在本工作中,(-)-solanacol(),一种由烟草和番茄分泌的典型或根壳烷型 SL,被证明对 2a 种子具有显著的选择性萌发刺激活性。合成了两种 cannalactone 类似物,分别命名为(±)-SdL19 和 (±)-SdL118。它们具有不饱和的无环碳链,带有一个叔羟基和一个甲基或环丙基,分别取代环己烷 A 环。(±)-SdL 类似物能够选择性地刺激 2a,表明这些最小的结构元素是这种选择性生物活性的关键。此外,(±)-SdL19 能够抑制 和 中的分枝,并诱导丛枝菌根真菌中的菌丝分枝,就像 SLs 一样。

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