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傅萼辉, 徐惠珠, 陈建国. 红糖槭(Acer rubrum L.)茎段离体培养研究[J]. 植物科学学报, 1989, 7(2): 173-178.
引用本文: 傅萼辉, 徐惠珠, 陈建国. 红糖槭(Acer rubrum L.)茎段离体培养研究[J]. 植物科学学报, 1989, 7(2): 173-178.
Fu Ehui, Xu Huizhu, Chen Jianguo. IN VITRO CULTURE OF RED MAPLE STEM SEGMENTS[J]. Plant Science Journal, 1989, 7(2): 173-178.
Citation: Fu Ehui, Xu Huizhu, Chen Jianguo. IN VITRO CULTURE OF RED MAPLE STEM SEGMENTS[J]. Plant Science Journal, 1989, 7(2): 173-178.

红糖槭(Acer rubrum L.)茎段离体培养研究

IN VITRO CULTURE OF RED MAPLE STEM SEGMENTS

  • 摘要: 红糖槭(Acer rubrum L.)原产北美洲,近年引入我国。关于它的离体培养研究尚未见报道。我们采用自配的基本培养基与不同种类的植物激素及其不同配比组成试验组合对红糖械茎段进行离体培养试验,获得完整植株并移栽成活。

     

    Abstract: The red maple (Acer rubrum L.), one of the sugar-producing maple species is native to North America. The species has been introduced into China in recent years, but the quantity of introduced trees is too small to meet the needs of normal experiments for the study of its introduction and acclimatization. That is why we have been engaging in the culture of stem segments in vitro.Stem segments, 1-1.5 cm in length, were surface-sterilized in 70% alcohol and in 0.10% HgCl2 water solution and cultured on newly formulated agar-sugar basal medium supplemented with NAA 2mg/l, ZE 2mg/l and GA 5mg/l. The culture was conducted under controlled temperature (25±3℃) and light (1,000-2,000 lux, 12 hours a day) in the culture room. On the 15th day of the culture, white calluses formed on the stem nodes. When the calluses were subcultured on the basal medium supplemented with NAA 0.5 mg/l, KT 2 mg/l, ZE 2 mg/l, and GA 3 mg/l for 20 days, they developed into dark green spheriods or ovoids. In another 20 days 20% of these sphriods and ovoids produced ab- normal shoots. When the shoots were transferred to the basal medium modified by addition of IBA 0.1 mg/l, BA 2 mg/l, ZE 0.5 mg/l and GA 0.3 mg/l, the normal shoot growth occurred satisfactorily. Another way for successful shoot induction and growth was to transfer the calluses straight to this medium for subclture. shoots sprouted from the lower part of the calluses near the medium surface. Roots were induced successfully in the basal medium supplemented with IBA 0.5 mg/l. The rooted plantlets began their normal growth two weeks after being transplanted in the culture soil (pH 6).

     

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