Eniwa RBP, Research Development Corporation of Japan, Megumino Kita 3-1-1, Eniwa-Shi, 061-13, Hokkaido, Japan.
J Chem Ecol. 1992 Oct;18(10):1819-32. doi: 10.1007/BF02751106.
Bioassay-guided isolation of bioactive natural substances requires monitoring of all fractionation and purification steps using a bioassay system. This is often a long and tedious process, especially with insect feeding bioassays. We report here a new method, based on the principle of bioautography, for a quick isolation of insect antifeedant compounds. TLC plates, after development, are coated with a thin layer of artificial diet and fed toSpodoptera litura larvae. The location of uneaten areas is then compared with theR fvalues of the TLC spots, in order to determine rapidly the active fractions. This methods allows for a very fast determination of the most active antifeedant compounds in a complex mixture and considerably speeds up the isolation process. This new method was successfully applied in the study of antifeedant activity of several plant samples, and results are presented here for a model plant,Skimmia japonica (Rutaceae). Using this new method, the compounds responsible for the feeding-deterrent activity, three furanocoumarins (bergapten, xanthotoxin, and oxypeucedanin), were quickly and efficiently identified.
生物测定指导的生物活性天然物质的分离需要使用生物测定系统监测所有分馏和纯化步骤。这通常是一个漫长而乏味的过程,特别是对于昆虫饲养生物测定。我们在这里报告了一种新的方法,该方法基于生物自显影的原理,用于快速分离昆虫拒食化合物。在开发后,TLC 板用薄层人工饲料覆盖,并喂食小菜蛾幼虫。然后将未食用区域的位置与 TLC 斑点的 R f 值进行比较,以便快速确定活性馏分。该方法允许在复杂混合物中非常快速地确定最有效的拒食化合物,并大大加快了分离过程。该新方法已成功应用于几种植物样品的拒食活性研究,这里呈现了一种模式植物,山矾(芸香科)的结果。使用这种新方法,能够快速有效地鉴定出负责拒食活性的三种呋喃香豆素(补骨脂素、花椒毒素和氧化前胡素)。