Optimization of in vitro Propagation of Purple Passion Fruit (Passiflora edulis), an Important Medicinal and Ornamental Plant

Mostafa Eshghi Khas, A. Abbasifar, Babak ValizadehKaji
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引用次数: 5

Abstract

Tissue culture techniques can be beneficial for quick clonal propagation and production of disease-free plants of purple passion fruit as one of the most important medicinal and ornamental plants. These techniques are essential tools for the production of transgenic plants and high-value phytochemicals. The present study was planned to introduce an efficient in vitro propagation for purple passion fruit(Passiflora edulis Sims.). To do so, the effect of different plant growth regulators was investigated on micropropagation medium of purple passion fruit. For proliferation stage, nodal segments were cultured in media supplemented with various combinations of different plant growth regulators including: BA (0, 2.2, 4.4 and 8.9 μM), TDZ (2.3, 4.5 and 9.1 μM), GA3 (0 and 2.9 μM) and IBA (0 and 0.5 μM).  For rooting, shoots with about 1.5 cm long originating from explants were removed and cultured in half-strength MS medium containing different concentrations of auxin-based plant growth regulators including: IAA (0, 1.1, 2.9, 5.7 and 11.4 μM), IBA (1, 2.5, 4.9 and 8.9 μM), and NAA (1.1, 2.7, 5.4, 10.7 μM). For the proliferation stage, the best plant growth regulator combination was 8.9 μM BA+2.9 μM GA3+0.5 μM IBA, resulting in the maximum shoot proliferation, number of shoots per explants, and shoot length. Half-strength MS medium supplemented with 5.4 μM NAA or 8.9 μM IBA was the most effective treatment for the rooting of shoots. Gradual acclimatization of the rooted plantlets was performed and the plantlets were established in the soil successfully. The micropropagated plants did not exhibit any visually detectable variation to their mother plants.
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药用和观赏植物紫西番莲离体繁殖的优化
紫百香果是一种重要的药用和观赏植物,其组织培养技术有利于快速克隆繁殖和无害化植株的生产。这些技术是生产转基因植物和高价值植物化学物质的重要工具。本研究旨在为紫百香果(Passiflora edulis Sims.)提供一种高效的离体繁殖方法。为此,研究了不同植物生长调节剂对紫百香果微繁培养基的影响。在增殖阶段,在添加不同植物生长调节剂组合的培养基中培养节段,这些调节剂组合包括:BA(0、2.2、4.4和8.9 μM)、TDZ(2.3、4.5和9.1 μM)、GA3(0和2.9 μM)和IBA(0和0.5 μM)。为了生根,将外植体产生的1.5 cm左右的芽拔出,在含有不同浓度生长素植物生长调节剂IAA(0、1.1、2.9、5.7和11.4 μM)、IBA(1、2.5、4.9和8.9 μM)和NAA(1.1、2.7、5.4、10.7 μM)的半强MS培养基中培养。在增殖阶段,生长调节剂组合为8.9 μM BA+2.9 μM GA3+0.5 μM IBA时,芽增殖量、单外植体芽数和芽长均达到最大值。半强MS培养基中添加5.4 μM NAA或8.9 μM IBA的处理对生根效果最好。对生根苗进行逐步驯化,成功地在土壤中生根。微繁殖植株没有表现出任何目测到的变异。
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