Departamento de Tecnología Farmacéutica, Biotecnología y Microbiología Industrial, Junín 956, 1113, Buenos Aires, Argentina.
Plant Cell Rep. 1987 Apr;6(2):135-7. doi: 10.1007/BF00276671.
Callus tissues from different explants (hypocotyl, cotyledon, root, leaf and fruit) of Solanum eleagnifolium Cav. were cultured on a modified Murashige-Skoog medium, with 1 mg.1(-1) 2,4-D as the sole growth regulator. The presence of the alkaloid solasodine was determined by spectrophotometric and TLC methods. Its concentration ranged from 1.00 to 2.15 mg.g(-1) DW. The calli from different explants showed a direct association between the solasodine production and their growth, although they have a different production rate. It was also observed that about the seventh week of culture the metabolite concentration decreased in all cases.
不同外植体(下胚轴、子叶、根、叶和果实)的银莲花组织在改良的 Murashige-Skoog 培养基上培养,以 1 mg.1(-1) 2,4-D 作为唯一的生长调节剂。通过分光光度法和 TLC 方法确定生物碱澳洲茄碱的存在。其浓度范围为 1.00 至 2.15 mg.g(-1) DW。不同外植体的愈伤组织的澳洲茄碱产量与其生长呈直接相关,尽管它们的产量不同。还观察到在所有情况下,培养的第七周左右,代谢物浓度下降。