Abant Izzet Baysal University, Department of Biology, 14280 Bolu, Turkey.
Plant Physiol Biochem. 2013 Dec;73:139-43. doi: 10.1016/j.plaphy.2013.09.007. Epub 2013 Sep 24.
Elimination of calcium (Ca), magnesium (Mg) or both from the medium of callus cultures of Digitalis davisiana Heywood, Digitalis lamarckii Ivanina, Digitalis trojana Ivanina and Digitalis cariensis Boiss. ex Jaub. et Spach increased cardenolides production. Callus was induced from hypocotyl segments from one-month old seedlings were cultured on MS medium containing 0.5 μg ml(-1) thidiazuron (TDZ) and 0.25 μg ml(-1) indole acetic acid (IAA). After 30 days of culture, callus was transferred in hormone-free MS medium (MSO) as well as Ca or Mg or both were completely eliminated from same medium. The amount of five cardenolides from D. davisiana Heywood, D. lamarckii Ivanina, D. trojana Ivanina and D. cariensis Boiss. ex Jaub. et Spach were compared. Higher amounts of five cardenolides and total cardenolides were obtained when callus of four Digitalis species were incubated on MS medium lacking both Ca and Mg. The mean contents of total cardenolides obtained were in the order of D. lamarckii (2017.97 μg g(-1))>D. trojana (1385.75 μg g(-1))>D. cariensis (1038.65 μg g(-1))>D. davisiana (899.86 μg g(-1)) when both Ca and Mg were eliminated from the medium, respectively. This protocol is useful for development of new strategies for the large-scale production of cardenolides.
从毛地黄属的 Digitalis davisiana Heywood、Digitalis lamarckii Ivanina、Digitalis trojana Ivanina 和 Digitalis cariensis Boiss. ex Jaub. et Spach 的愈伤组织培养基中去除钙 (Ca)、镁 (Mg) 或两者都可增加强心苷的产量。将来自一个月大幼苗下胚轴段的愈伤组织诱导在含有 0.5 μg ml(-1) 噻二唑脲 (TDZ) 和 0.25 μg ml(-1) 吲哚乙酸 (IAA) 的 MS 培养基上进行培养。培养 30 天后,将愈伤组织转移到不含激素的 MS 培养基 (MSO) 中,同时从相同培养基中完全去除 Ca 或 Mg 或两者。比较了来自 D. davisiana Heywood、D. lamarckii Ivanina、D. trojana Ivanina 和 D. cariensis Boiss. ex Jaub. et Spach 的五种强心苷的含量。当四种毛地黄属植物的愈伤组织在缺乏 Ca 和 Mg 的 MS 培养基上孵育时,获得了更高量的五种强心苷和总强心苷。当从培养基中去除 Ca 和 Mg 时,总强心苷的平均含量顺序为 D. lamarckii(2017.97 μg g(-1))>D. trojana(1385.75 μg g(-1))>D. cariensis(1038.65 μg g(-1))>D. davisiana(899.86 μg g(-1))。该方案可用于开发大规模生产强心苷的新策略。