The Chair and Department of Pharmacognosy, Faculty of Pharmacy, Medical University of Gdansk, al. gen. J. Hallera 107, 80-416 Gdansk, Poland.
Z Naturforsch C J Biosci. 2012 Jan-Feb;67(1-2):65-76. doi: 10.1515/znc-2012-1-209.
An efficient micropropagation protocol of Cyclopia genistoides (L.) Vent., an indigenous South African shrub of economic importance, was established. In vitro shoot cultures were obtained from shoot tip fragments of sterile seedlings cultured on solid Schenk and Hildebrandt (SH) medium supplemented with 9.84 microM 6-(gamma,gamma-dimethylallylamino)purine (2iP) and 1.0 microM thidiazuron (TDZ). Maximum shoot multiplication rate [(8.2 +/- 1.3) microshoots/explant)] was observed on this medium composition. Prior to rooting, the multiplied shoots were elongated for 60 days (two 30-days passages) on SH medium with one-half sucrose concentration, supplemented with 4.92 microM indole-3-butyric acid (IBA). The rooting of explants was only possible in the case of the elongated shoots. The highest root induction rate (54.8%) was achieved on solid SH medium with one-half sucrose and one-half potassium nitrate and ammonium nitrate concentration, respectively, supplemented with 28.54 microM indole-3-acetic acid (IAA) and 260.25 microM citric acid. The plantlets were acclimatized for 30 days in the glasshouse, with the use of peat/gravel/perlite substrate (1:1:1). The highest acclimatization rate (80%) was obtained for explants rooted with the use of IAA-supplemented medium. The phytochemical profile of the regenerated plants was similar to that of the reference intact plant material. HPLC analyses showed that C. genistoides plantlets obtained by the micropropagation procedure kept the ability to produce xanthones (mangiferin and isomangiferin) and the flavanone hesperidin, characteristic of wild-growing shrubs.
建立了一种高效的 Cyclopia genistoides(L.)Vent.(南非本土具有经济重要性的灌木)微繁殖协议。通过在固体 Schenk 和 Hildebrandt(SH)培养基上培养无菌幼苗的茎尖片段获得离体芽培养物,该培养基补充有 9.84µM 6-(γ,γ-二甲基烯丙基氨基)嘌呤(2iP)和 1.0µM 噻二唑隆(TDZ)。在这种培养基组成上观察到最大的芽增殖率[(8.2±1.3)微芽/外植体)]。在生根之前,将增殖的芽在半蔗糖浓度的 SH 培养基上伸长 60 天(两次 30 天的传代),补充有 4.92µM 吲哚-3-丁酸(IBA)。只有伸长的芽才能生根。在半蔗糖和半硝酸钾和硝酸铵浓度的固体 SH 培养基上,分别补充有 28.54µM 吲哚-3-乙酸(IAA)和 260.25µM 柠檬酸,获得了最高的生根诱导率(54.8%)。将幼苗在温室中适应 30 天,使用泥炭/砾石/珍珠岩基质(1:1:1)。在使用补充有 IAA 的培养基进行生根的外植体中获得了最高的适应率(80%)。再生植物的植物化学特征与参考完整植物材料相似。HPLC 分析表明,通过微繁殖程序获得的 C. genistoides 植物保持了产生黄烷酮(芒果苷和异芒果苷)和类黄酮橙皮苷的能力,这是野生生长灌木的特征。