Genzentrum der Universität München und Institut für Pharmazeutische Biologie der Universität München, Karlstr. 29, D-8000 München 2, Federal Republic of Germany.
Planta Med. 1987 Oct;53(5):465-9. doi: 10.1055/s-2006-962774.
Epidermis of steins and petioles of LUPINUS POLYPHYLLUS accumulates quinolizidine alkaloids at a concentration of about 30 mM. Since lupanine is synthesized mainly in green mesophyll tissue and not in the epidermis, the alkaloids have to be transported into the epidermal cells. Uptake of [ (3)H]-lupanine into isolated epidermis was 3 to 20 times higher in epidermal cells as compared to the corresponding mesophyll cells. Uptake of lupanine is time dependent and proceeds against a concentration gradient. The uptake depends on temperature and can be characterized by an activation energy of 34 kJ/mol. The process shows multiphasic uptake kinetics and is reduced by SH-group inhibitors (NEM, PHMB) and inhibitors of the energy metabolism (cyanide, antimycine, DNP, CCCP). All these data provide first evidence that simple diffusion cannot be the mechanism for the uptake of lupanine into epidermal cells. The uptake is probably catalyzed by transport proteins.
羽扇豆的茎表皮和叶柄积累了约 30mM 的喹诺里西啶生物碱。由于羽扇豆碱主要在绿色的叶肉组织中合成,而不是在表皮中,因此生物碱必须被运输到表皮细胞中。与相应的叶肉细胞相比,[(3)H] -羽扇豆碱进入分离的表皮中的摄取量高 3 至 20 倍。羽扇豆碱的摄取是时间依赖性的,并逆浓度梯度进行。摄取取决于温度,可以用 34kJ/mol 的活化能来描述。该过程显示出多相摄取动力学,并被 SH 基团抑制剂(NEM、PHMB)和能量代谢抑制剂(氰化物、抗霉素、DNP、CCCP)所抑制。所有这些数据首次提供了证据,证明简单扩散不可能是羽扇豆碱进入表皮细胞的摄取机制。摄取可能是由转运蛋白催化的。