›› 2009, Vol. 52 ›› Issue (5): 514-521.

• 研究论文 • 上一篇    下一篇

豆薯种子中的杀虫成分及其毒力测定

李有志,魏孝义,徐汉虹,黄小清,姚振威   

  • 出版日期:2009-05-20 发布日期:2009-05-20
  • 通讯作者: 徐汉虹

Insecticidal ingredients from yam bean (Pachyrrhizus erosus) seeds and their insecticidal toxicity

  • Online:2009-05-20 Published:2009-05-20

摘要: 为明确豆薯Pachyrrhizus erosus (L.) Urban种子中的杀虫成分及其杀虫毒力,以白纹伊蚊Aedes albopictus 4龄幼虫为目标昆虫,在活性跟踪的基础上,通过多种色谱技术和核磁共振技术分离鉴定其化学成分结构,并通过浸渍法、点滴、夹毒叶碟法等测定各化合物对白纹伊蚊幼虫、棉蚜Aphis gossypii无翅成蚜、甘薯天蛾Herse convolvuli幼虫和小菜蛾Plutella xylostella幼虫的杀虫活性和作用方式。结果表明,从豆薯种子中共分离、鉴定了14个化合物,即12a-hydoxyrotenone,pachyrrhizine,12a-hydoxypachyrrhizone,12α-dehydropachyrrizone,α-naphthoflavone,7-methoxyflavanone,12α-hydroxydolineone,6-methoxyflavone,4′-hydoxyflavanone,quercetin dihydate,5-methoxyflavone,7-hydroxyflavone,3′-hydoxyflavanone和3-hydroxyflavone。上述化合物中的前7个化合物对白纹伊蚊4龄幼虫具有毒杀活性, 处理24 h的LC50分别是25.0,51.1,196.2,48.4,98.9,107.2 和15.6 mg/L;前6个化合物对棉蚜成虫24 h 的毒力分别为1.5,10.9,80.7,8,32.1和112.8 mg/L;前5个化合物以及12α-hydroxydolineone对甘薯天蛾3龄幼虫有毒杀活性;12α-hydoxyrotenone对3龄小菜蛾幼虫24 h的胃毒毒力LD50为17.3 μg/头,7-methoxyflavanone对该虫仅表现出较弱的生长发育抑制活性。首次从豆薯种子中分离得9个化合物,即6-methoxyflavone,4′-hydoxyflavanone,quercetin dihydate,α-naphthoflavone,7-methoxyflavanone,5-methoxyflavone,7-hydroxyflavone,3′-hydoxyflavanone和3-hydroxyflavone;豆薯种子含有7个活性成分,其作用方式因目标昆虫不同而不同,其主要杀虫成分不是鱼藤酮而是12α-羟基鱼藤酮。

关键词: 豆薯种子, 杀虫成分, 化合物结构, 毒力, 12α-羟基鱼藤酮

Abstract: Insecticidal compounds from seeds of yam bean Pachyrrhizus erosus (L.) Urban were studied in order to determine their insecticidal toxicity. Using the 4th instar larvae of Aedes albopictus as target insect pest, the active ingredients were isolated from the methanol extracts of the seeds by activity-directed fractionation with column chromatography and thin layer chromatography (TLC), and identified predominantly on the basis of NMR data. Insecticidal activities and action mode of these compounds were determined against the 4th instar larvae of A. albopictus, Aphis gossypii apterae, the 3rd instar larvae of both Herse convolvuli and Plutella xylostella by leaf dip method, topical application and leaf disk method, respectively. Fourteen compounds were isolated and identified, which were 12α-hydoxyrotenone, pachyrrhizine, 12α-hydoxypachyrrhizone, 12α-dehydropachyrrizone, α-naphthoflavone, 7-methoxyflavanone, 12a-hydroxydolineone, 6-methoxyflavone, 4′-hydoxyflavanone, quercetin dehydrate, 5-methoxyflavone, 7-hydroxyflavone, 3′-hydoxyflavanone and 3-hydroxyflavone. The results of bioassay showed that among the 14 compounds, the former seven possessed insecticidal activity against A. albopictus larvae, with corresponding LC50 values at 24 h after treatment being 25.0, 51.1, 196.2, 48.4, 98.9, 107.2 and 15.6 mg/L, respectively; the former six exhibited insecticidal activity against A. gossypii apterae, with the LC50 values at 24 h after treatment being 1.5, 10.9, 80.7, 66.8, 32.1 and 112.8 mg/L, respectively; the former five and 12α-hydroxydolineone had insecticidal activities against H. convolvuli larvae; 12α-hydoxyrotenone exhibited stomach toxicity to the 3rd instar larvae of P. xylostella, with the LD50 values being 17.3 μg/individual at 24 h after treatment, while 7-methoxyflavone only possessed weak growth inhibition activity to the insect pest. Nine-compounds (6-methoxyflavone, 4′-hydoxyflavanone, quercetin dehydrate, α-naphthoflavone, 7-methoxyflavanone, 5-methoxyflavone, 7-hydroxyflavone, 3′-hydoxyflavanone and 3-hydroxyflavone) were isolated from the seeds of P. erosus for the first time. There were seven insecticidal compounds altogether from the seeds, whose action modes to the different tested insects were different. The main insecticidal ingredient was not rotenone but 12a-hydoxyrotenone.

Key words: Pachyrrhizus erosus seeds, insecticidal ingredients, chemical structure, toxicity, 12α-hydoxyrotenone