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A NOVEL METHOD FOR RAPID MICROPROPAGATION OF PINEAPPLE

机译:菠萝快速微繁殖的新方法

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摘要

A novel micropropagation method for pineapple (Ananas comosus L.), based on shoot elongation induced in vitro, was demonstrated for two cultivars. Decapitated in vitro plantlets were used as explants. Shoot etiolation was induced by placing explants in a Murashige and Skoog (MS) medium containing NAA (10 mu M) and incubating in darkness at 28C for30 to 40 days. The mean number of the regenerated etiolated shoots per explant was 2.6+/-0.29. The etiolated shoots were placed into N6 medium supplemented with kinetin or BA (25 or 20 mu M, respectively). After 4 to 6 weeks, shoots regenerated along the nodes. The highest regeneration rate was 15 and 13 plantlets per node with 25 mu M kinetin and 20 mu M BA, respectively. Regenerated plantlets were rooted on a growth-regulator-free MS medium. Residual shoots of the initial explants could be recycled by rooting on a growth-regulator-free MS medium. This procedure enables the regeneration of several thousand plantlets per year. Chemical names used: naphthaleneacetic acid (NAA); benzyladenine (BA).
机译:在两个品种上,基于体外诱导的枝条伸长率,提出了一种新的菠萝微繁殖方法(Ananas comosus L.)。脱去胚的小苗用作外植体。通过将外植体置于含有NAA(10μM)的Murashige and Skoog(MS)培养基中,并在黑暗中于28°C孵育30至40天,来诱导嫩芽黄化。每个外植体的再生黄化芽的平均数为2.6 +/- 0.29。将黄化的芽置于补充了激动素或BA(分别为25或20μM)的N6培养基中。 4至6周后,新芽沿着结节再生。最高再生速率为每节分别有25μM激动素和20μM BA的15和13株小植株。再生的小植株植于无生长调节剂的MS培养基上。可以通过在无生长调节剂的MS培养基上生根来回收原始外植体的残留芽。该程序每年可再生数千株小苗。使用的化学名称:萘乙酸(NAA);苄腺嘌呤(BA)。

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