Veiga Thiago A M, González-Vázquez Raquel, Neto João Oiano, Silva Maria F G F, King-Díaz Beatriz, Lotina-Hennsen Blas
Departamento de Química, Universidade Federal de São Carlos (UFSCar), 13565-905, São Carlos, S.P., Brazil.
Arch Biochem Biophys. 2007 Sep 1;465(1):38-43. doi: 10.1016/j.abb.2007.05.002. Epub 2007 May 24.
Four natural products were isolated from plants of the Rutaceae and Meliaceae families and their effect on photosynthesis was tested. Siderin (1) inhibited both ATP synthesis and electron flow (basal, phosphorylating, and uncoupled) from water to methylviologen (MV); therefore, it acts as Hill reaction inhibitor in freshly lysed spinach thylakoids. Natural products 2-4 were inactive. Secondary metabolite 1 did not inhibit PSI electron transport. It inhibits partial reactions of PSII electron flow from water to 2,6-dichlorophenol indophenol (DCPIP), from water to sodium silicomolybdate, and partially inhibits electron flow from diphenylcarbazid (DPC) to DCPIP. These results established that the site of inhibition of 1 was at the donor and acceptor sides of PSII, between P(680) and Q(A). Chlorophyll a fluorescence measurements confirmed the behavior of the Toona ciliate coumarin 1 as P(680) to Q(A) inhibitor by the creation of silent centers. May be this is the mechanisms of action of 1 and is the way in which it develops a phytotoxic activity against photosynthesis.
从芸香科和楝科植物中分离出四种天然产物,并测试了它们对光合作用的影响。西地林(1)抑制ATP合成以及从水到甲基紫精(MV)的电子流动(基础、磷酸化和解偶联状态);因此,它在新鲜裂解的菠菜类囊体中作为希尔反应抑制剂起作用。天然产物2 - 4没有活性。次生代谢产物1不抑制PSI电子传递。它抑制PSII电子从水到2,6 - 二氯酚靛酚(DCPIP)、从水到硅钼酸钠的部分反应,并部分抑制从二苯基卡巴肼(DPC)到DCPIP的电子流动。这些结果表明,1的抑制位点在PSII的供体侧和受体侧,位于P(680)和Q(A)之间。叶绿素a荧光测量通过产生沉默中心证实了香椿香豆素1作为P(680)到Q(A)抑制剂的行为。也许这就是1的作用机制,也是它对光合作用产生植物毒性活性的方式。