Dayan Franck E, Owens Daniel K, Watson Susan B, Asolkar Ratnakar N, Boddy Louis G
Natural Products Utilization Research Unit, US Department of Agriculture-Agricultural Research Service, Thad Cochran Center, University of Mississippi MS, USA.
Marrone Bio Innovations Davis, CA, USA.
Front Plant Sci. 2015 Apr 8;6:222. doi: 10.3389/fpls.2015.00222. eCollection 2015.
Sarmentine, 1-(1-pyrrolidinyl)-(2E,4E)-2,4-decadien-1-one, is a natural amide isolated from the fruits of Piper species. The compound has a number of interesting biological properties, including its broad-spectrum activity on weeds as a contact herbicide. Initial studies highlighted a similarity in response between plants treated with sarmentine and herbicidal soaps such as pelargonic acid (nonanoic acid). However, little was known about the mechanism of action leading to the rapid desiccation of foliage treated by sarmentine. In cucumber cotyledon disc-assays, sarmentine induced rapid light-independent loss of membrane integrity at 100 μM or higher concentration, whereas 3 mM pelargonic acid was required for a similar effect. Sarmentine was between 10 and 30 times more active than pelargonic acid on wild mustard, velvetleaf, redroot pigweed and crabgrass. Additionally, the potency of 30 μM sarmentine was greatly stimulated by light, suggesting that this natural product may also interfere with photosynthetic processes. This was confirmed by observing a complete inhibition of photosynthetic electron transport at that concentration. Sarmentine also acted as an inhibitor of photosystem II (PSII) on isolated thylakoid membranes by competing for the binding site of plastoquinone. This can be attributed in part to structural similarities between herbicides like sarmentine and diuron. While this mechanism of action accounts for the light stimulation of the activity of sarmentine, it does not account for its ability to destabilize membranes in darkness. In this respect, sarmentine has some structural similarity to crotonoyl-CoA, the substrate of enoyl-ACP reductase, a key enzyme in the early steps of fatty acid synthesis. Inhibitors of this enzyme, such as triclosan, cause rapid loss of membrane integrity in the dark. Sarmentine inhibited the activity of enoyl-ACP reductase, with an I 50app of 18.3 μM. Therefore, the herbicidal activity of sarmentine appears to be a complex process associated with multiple mechanisms of action.
沙门汀,即1-(1-吡咯烷基)-(2E,4E)-2,4-癸二烯-1-酮,是一种从胡椒属植物果实中分离出的天然酰胺。该化合物具有许多有趣的生物学特性,包括作为接触性除草剂对杂草的广谱活性。初步研究强调了用沙门汀处理的植物与除草皂(如壬酸)之间反应的相似性。然而,对于导致沙门汀处理的叶片快速干燥的作用机制知之甚少。在黄瓜子叶圆盘试验中,沙门汀在100μM或更高浓度下诱导膜完整性的快速非光依赖性丧失,而类似效果则需要3mM壬酸。沙门汀对野芥菜、苘麻、红根苋和马唐的活性比壬酸高10至30倍。此外,30μM沙门汀的效力受到光的极大刺激,这表明这种天然产物也可能干扰光合作用过程。在该浓度下观察到光合电子传递完全受到抑制,证实了这一点。沙门汀还通过竞争质体醌的结合位点,作为分离类囊体膜上光系统II(PSII)的抑制剂。这部分可归因于沙门汀和敌草隆等除草剂之间的结构相似性。虽然这种作用机制解释了沙门汀活性的光刺激,但它无法解释其在黑暗中破坏膜稳定性的能力。在这方面,沙门汀与巴豆酰辅酶A有一些结构相似性,巴豆酰辅酶A是脂肪酸合成早期步骤中的关键酶烯酰-ACP还原酶 的底物。该酶的抑制剂,如三氯生,会在黑暗中导致膜完整性的快速丧失。沙门汀抑制烯酰-ACP还原酶的活性,其半数抑制浓度(I50app)为18.3μM。因此,沙门汀的除草活性似乎是一个与多种作用机制相关的复杂过程。