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Influence of PGRS for the in vitro Plant Regeneration and Flowering in Portulaca oleracea (L.): A Medicinal and Ornamental Plant

机译:PGRS对马齿Port(Portulaca oleracea(L.))的体外植物再生和开花的影响:药用和观赏植物

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摘要

In vitro flowering system was developed to conquer the setback associated with flower development in in vivo condition. For this, an efficient, reliable and quick regeneration protocol has been developed for Portulaca oleracea L. using nodes of similar to 1.0-1.5 cm size. Each node procured from young, healthy shoots from garden raised plants. Multiple shoot formation (5.13 +/- 0.34) was recorded within two weeks on MS nutrient medium fortified with kinetin (0.5 mg L-1). Shoots were multiplied by subculturing on the same medium after 21 days. On first subculture, in vitro flower buds developed, when the developed shoots were maintained for another two weeks on the same medium along with gibberellic acid (0.2 mg L-1). When these flower bud containing shoots were transferred to MS medium containing Indole-3-butyric acid (0.25 mg (L-1)), in vitro roots emerged and the flower buds underwent anthesis. The rooted plantlets were hardened and successfully established in earthen pots with 70% success rate. The present research illustrates in vitro flowering system to get rid off problems associated with flower growth and development.
机译:开发了体外开花系统以克服体内条件下与花卉发育相关的挫折。为此,已经针对马齿Port(Portulaca oleracea L.)开发了一种有效,可靠和快速的再生方案,其使用类似1.0-1.5cm大小的节。每个节点都是从花园种植的植物的年轻健康芽中采购的。在两周内用动蛋白(0.5 mg L-1)强化的MS营养培养基上记录了多次芽形成(5.13 +/- 0.34)。 21天后通过在相同培养基上亚培养来繁殖芽。第一次传代培养时,会产生体外花芽,此时将已发育的芽与赤霉素(0.2 mg L-1)一起在同一培养基上再维持两周。当将这些含有花蕾的芽转移到含有吲哚-3-丁酸(0.25 mg(L-1))的MS培养基中时,就会出现离体根,并对花蕾进行开花。将生根的小苗硬化,并在土盆中成功建立,成功率为70%。本研究说明了体外开花系统,以摆脱与花卉生长发育相关的问题。

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