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An efficient micropropagation protocol for Stevia rebaudiana

机译:一种有效的甜叶菊微繁殖方案

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The present study was conducted to develop an efficient and reproducible mass multiplication protocol in stevia. The shoot-tip and nodal segments were used as explants. The survival percentage of nodal explants was 100%, when explants were treated with HgCl2 (0.1%) for 3 minutes along with bavistin (0.2%) and streptocyclin (0.2%) for 45 minutes. The nodal and shoot-tip explants were best responded to MS medium supplemented with 2.0 mg/1 BAP. Among the different media used, MS medium supplemented with2.0 mg/1 BAP showed the maximum shoot induction (98.0%) in 4.7 days and (74.0%) in 7.1 days using nodal and shoot tip explants, respectively. BAP alone was found to be better for establishment of aseptic culture of stevia instead of combinations of different cytokinins and auxins. MS basal medium supplemented with 0.3 mg/1 BAP + 0.3 mg/1 Kin + 0.1 mg/1 NAA was proved to be the best with 34.9 shoots/explant developed from nodal and shoot-tip explants after 30 days on culture medium. Maximum rooting (90±7.75%) was observed on the half MS medium supplemented with 0.5 mg/1 NAA with 21.2 roots per shoot in 7.4 days. The roots formed in medium without hormone were not healthy. Rooted shoots were separated individually and transferred to plastic bag containing sand, soil and vermi compost in ratio of 1:1:1 with 100% survival. The hardened plants were transferred to field using recommended agronomic practices.
机译:进行本研究以开发一种在甜叶菊中有效且可重复的大量繁殖方案。芽尖和节段用作外植体。用HgCl2(0.1%),巴维斯汀(0.2%)和链霉素(0.2%)处理45分钟后,外植体的存活百分比为100%。节点和芽尖外植体对补充了2.0 mg / 1 BAP的MS培养基反应最好。在使用的不同培养基中,分别使用结节和芽尖外植体,补充有2.0 mg / 1 BAP的MS培养基分别在4.7天和7.1天显示出最大的芽诱导(98.0%)和(7.1%)(74.0%)。发现单独的BAP比建立不同细胞分裂素和生长素的组合更适合建立甜菊的无菌培养。补充0.3 mg / 1 BAP + 0.3 mg / 1 Kin + 0.1 mg / 1 NAA的MS基础培养基被证明是最好的,在培养基上培养30天后,从结节和梢尖外植体发育出34.9枝/植株。在7.4天内,在补充有0.5 mg / 1 NAA和每枝21.2个根的半MS培养基上观察到最大的生根(90±7.75%)。在没有激素的培养基中形成的根不健康。将生根的芽单独分离,并转移到装有沙,土壤和朱砂堆肥的塑料袋中,塑料袋的比例为1:1:1:1,存活率为100%。使用推荐的农艺方法将已硬化的植物转移到田间。

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