Królicka A, Staniszewska I, Maliński E, Szafranek J, Lojkowska E
Faculty of Biotechnology, University of Gdańsk, Poland.
Pharmazie. 2003 Aug;58(8):590-2.
In order to check the possibility of producing secondary metabolites, in vitro cultures of A. visnaga callus were established. The best growth of A. visnaga callus was obtained on Murashige and Skoog medium (MS) containing 6-benzyladenine (BA) and alpha-naphtaleneacetic acid (NAA). The study was concentrated on the induction of production of secondary metabolites by exposing callus to abiotic elicitors: benzo(1,2,3)-thiadiazole-7-carbothionic acid S-methyl ester (BION) and a suspension of silica (SiO2) and biotic elicitors: autoclaved lysates of Enterobacter sakazaki and scleroglucan. GC analysis indicated that not-elicited callus of A. visnaga grown in darkness accumulated 2 times more visnagin than the one which was grown under a 16-h photoperiod. The highest accumulation of visnagin was observed in the callus culture elicited with scleroglucan or BION. Scleroglucan induced also the accumulation of khellin in A. visnaga callus. The presented work shows that biosynthesis of pharmacologically important secondary metabolites in A. visnaga cultures could be stimulated by application of elicitors.
为了检验产生次生代谢产物的可能性,建立了紫花前胡愈伤组织的体外培养体系。紫花前胡愈伤组织在含有6-苄基腺嘌呤(BA)和α-萘乙酸(NAA)的Murashige和Skoog培养基(MS)上生长最佳。该研究集中于通过将愈伤组织暴露于非生物诱导剂:苯并(1,2,3)-噻二唑-7-硫代羧酸S-甲酯(BION)和二氧化硅(SiO₂)悬浮液以及生物诱导剂:阪崎肠杆菌的高压灭菌裂解物和硬葡聚糖,来诱导次生代谢产物的产生。气相色谱分析表明,在黑暗中生长的未诱导的紫花前胡愈伤组织积累的紫花前胡内酯比在16小时光周期下生长的愈伤组织多2倍。在用硬葡聚糖或BION诱导的愈伤组织培养物中观察到紫花前胡内酯的最高积累量。硬葡聚糖还诱导了紫花前胡愈伤组织中凯林的积累。目前的工作表明,应用诱导剂可以刺激紫花前胡培养物中具有药理重要性的次生代谢产物的生物合成。