Department of Medicinal Chemistry and Pharmacognosy, University of Minnesota, Minneapolis, MN 55455, U.S.A.
Planta Med. 1989 Oct;55(5):446-51. doi: 10.1055/s-2006-962061.
AMMI VISNAGA (L.) Lam. globular, heart, and torpedo shaped embryos were induced from the calli of sterile seedling hypocotyls in Murashige and Skoog's medium with or without either 0.5 ppm benzyladenine or 1.0 ppm 2,4-D. After transfer of the calli into liquid media supplemented with 10 mM L-glutamine, all three embryo stages were observed after eight weeks. Liquid media lacking growth regulators appeared to enhance the development into torpedo stage embryos, especially at four weeks. Eight weeks after the transfer of the callus into liquid media, flasks containing predominately one microscopic stage were pooled, transferred into fresh liquid media, and the production of the furanochromones, khellin and visnagin, in the embryos were determined by a normal phase HPLC method. All three embryo stages produced similar amounts of khellin and visagin. Maximum production was reached at six weeks. The six-week-old torpedo shaped embryos produced 0.57% khellin and 0.72% visnagin on a dry weight basis. The embryo cultures produced significantly higher concentrations of the furanochromones than A. VISNAGA cell suspensions (reported previously) that produced approximately 0.1-0.3% visnagin and no detectable khellin. In addition, the production of khellin and visnagin in the fruits, seedlings, young plants, and flowering or fruiting AMMI VISNAGA (L.) Lam plants was determined. Upon germination of the fruits, a rapid decline in the content of the furanochromones was observed. Subsequent experiments showed that the majority of the furanochromone content in fruits was released into the media within one to two days. Total visnagin content (media + seedlings) was unchanged, however, a loss of 40% of the khellin content was found after 2-4 weeks. When media containing seedlings was spiked with exogenous khellin and visnagin, the concentrations of both furanochromones declined, apparently due to uptake by the roots and subsequent catabolism in the plant. No evidence for degradative enzymes in media exposed to seedlings was observed. During vegetative growth of the plants, relatively low levels of furanochromones were found. High concentrations were observed at early flowering, followed by a decline, and a gradual rise at fruiting as was previously reported by other investigators. In the vegetative stages, visnagin concentrations were higher than those for khellin, whereas in fruiting plants and fruits, the ratio was reversed.
阿玛米·维萨尼亚(L.)拉姆。从无菌幼苗下胚轴愈伤组织中诱导出球形、心形和鱼雷形胚胎,在添加或不添加 0.5 ppm 苄基腺嘌呤或 1.0 ppm 2,4-D 的 Murashige 和 Skoog 培养基中进行。将愈伤组织转移到补充有 10 mM L-谷氨酰胺的液体培养基中后,在八周后观察到所有三个胚胎阶段。缺乏生长调节剂的液体培养基似乎增强了向鱼雷形胚胎的发育,特别是在四周时。将愈伤组织转移到液体培养基中八周后,将主要含有一个微观阶段的培养瓶汇集在一起,转移到新鲜的液体培养基中,并通过正相 HPLC 方法确定胚胎中呋喃并色酮类化合物,即黄葵素和维萨宁的产生。所有三个胚胎阶段都产生了类似量的黄葵素和维萨宁。最大产量在六周时达到。六周大的鱼雷形胚胎在干重基础上产生 0.57%的黄葵素和 0.72%的维萨宁。胚胎培养物产生的呋喃并色酮浓度明显高于先前报道的 A. VISNAGA 细胞悬浮液(约 0.1-0.3%的维萨宁和无法检测到的黄葵素)。此外,还测定了果实、幼苗、幼株、开花或结果的 AMMI VISNAGA(L.)Lam 植物以及果实、幼苗、幼株、开花或结果的 AMMI VISNAGA(L.)Lam 植物中呋喃并色酮的含量。果实发芽后,观察到呋喃并色酮含量迅速下降。随后的实验表明,果实中大部分呋喃并色酮含量在一到两天内释放到培养基中。然而,总维萨宁含量(培养基+幼苗)保持不变,但在 2-4 周后发现黄葵素含量损失了 40%。当含有幼苗的培养基中加入外源黄葵素和维萨宁时,两种呋喃并色酮的浓度均下降,显然是由于根部吸收和随后在植物中的代谢。在暴露于幼苗的培养基中未观察到降解酶的证据。在植物的营养生长过程中,发现呋喃并色酮含量较低。在早期开花时观察到高浓度,随后下降,并在结果时逐渐升高,这与其他研究人员之前的报道一致。在营养阶段,维萨宁的浓度高于黄葵素,而在结果植物和果实中,比例则相反。