Pedras M Soledade C, Hossain Mohammad
University of Saskatchewan, Department of Chemistry, Saskatoon, Canada.
Org Biomol Chem. 2006 Jul 7;4(13):2581-90. doi: 10.1039/b604400j. Epub 2006 May 30.
The strongly antifungal phytoalexins brassilexin and sinalexin were metabolized by the stem rot fungus Sclerotinia sclerotiorum to glucosyl derivatives, whereas the phytoalexins brassicanal A, spirobrassinin and 1-methoxyspirobrassinin, displaying lower antifungal activity, were transformed via non-glucosylating pathways. Significantly, these transformations led to metabolites displaying no detectable antifungal activity. The chemical characterization of all new metabolites as well as the chemistry of these processes and a facile chemical synthesis of 1-beta-D-glucopyranosylbrassilexin are reported. Overall, our results indicate that phytoalexins, strongly antifungal against S. sclerotiorum, are detoxified via glucosylation, which in turn suggests that S. sclerotiorum has acquired efficient glucosyltransferase(s) that can disarm some of the most active plant chemical defenses. Consequently, we suggest that these glucosylation reactions are potential metabolic targets to control S. sclerotiorum.
具有强抗真菌活性的植物抗毒素油菜抗毒素和芥子抗毒素被菌核病菌代谢为葡萄糖基衍生物,而抗真菌活性较低的植物抗毒素芸苔醛A、螺旋油菜素和1-甲氧基螺旋油菜素则通过非糖基化途径进行转化。值得注意的是,这些转化产生的代谢产物没有可检测到的抗真菌活性。本文报道了所有新代谢产物的化学表征、这些过程的化学性质以及1-β-D-吡喃葡萄糖基油菜抗毒素的简便化学合成方法。总体而言,我们的结果表明,对菌核病菌具有强抗真菌活性的植物抗毒素通过糖基化作用被解毒,这反过来表明菌核病菌已经获得了能够解除一些最活跃的植物化学防御的高效葡萄糖基转移酶。因此,我们认为这些糖基化反应是控制菌核病菌的潜在代谢靶点。