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首页> 外文期刊>Euphytica >Plant recovery of cryopreserved apical meristem-tips of Melia azedarach L. using encapsulation/dehydration and assessment of their genetic stability
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Plant recovery of cryopreserved apical meristem-tips of Melia azedarach L. using encapsulation/dehydration and assessment of their genetic stability

机译:利用包封/脱水法及其低温稳定性评估苦ia种子低温保存的顶端分生组织尖端的植物恢复性

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摘要

A cryopreservation process usingencapsulation/dehydration technique was setup for apical meristem-tips of invitro plantlets of `paradise tree' (Melia azedarach L. var. gigantea,clone `El dorado'). Apical meristem-tipswere cultured for one day on MS basalmedium with 2 μM BA and 0.5 μM IBAand encapsulated with 3% sodium alginate.The highest shoot proliferation rate aftercryopreservation was obtained whenencapsulated apical meristem-tips werepregrown for 3 days in liquid medium with0.5, 0.75 and 1 M of sucrose for 24 hoursprogressively, desiccated for 5 hours withsilicagel followed by rapid or slowcooling. Survival after freezing in liquidnitrogen ranged between 67–83% andshoot proliferation ranged between 43–60%. This cryopreservation treatmentpreserved genetic stability, when it wasevaluated using the electrophoreticpatterns of nine isozyme systems and RAPDprofiles.
机译:针对“天堂树”(Melia azedarach L. var。gigantea,克隆“ El dorado”)的离体小植株的顶端分生组织尖端,建立了使用包封/脱水技术的低温保存过程。在含有2μMBA和0.5μMIBA的MS basalmedium上培养顶生分生组织尖端,并用3%海藻酸钠封装。在0.5, 0.75和1 M的蔗糖逐渐进行24小时,用硅胶干燥5小时,然后快速或缓慢冷却。在液氮中冷冻后的存活率在67%至83%之间,而芽期增殖在43%至60%之间。当使用9种同工酶系统的电泳图谱和RAPD图谱对其进行评估时,这种低温保存处理可以保持遗传稳定性。

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