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首页> 外文期刊>Medicinal Plants >In vitro propagation studies in Amaryllis belladonna L.
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In vitro propagation studies in Amaryllis belladonna L.

机译:在Amaryllis Belladonna L.的体外繁殖研究。

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Three explants viz. bulb scale, leaf disc and mature embryos were cultured on different modifications of MS medium to achieve the best in vitro response. For bulb scale culture, nutrient medium MS2N.5B proved better for callus initiation. Culture medium MS.4Td exhibited higher shoot proliferating efficiency, while number of shoot (s) per explants and shoot of higher length were documented on media MS2N.5B/ MS3N.5B. For cultured leaf disc, inoculation medium MS2D.5B/ MS3D.5B promoted higher degree ofcallus induction. Higher morphogenic calli formation was exhibited by culture medium MS2N.5B/MSN.5B. However, plantlets in higher number was recovered from regeneration medium MS.5Td/MSB. For mature embryo culture, culture medium MS2D.5B proved well forcallus initiation. Inoculation medium MSN.5B exhibited higher number of shoot proliferating explants. Number of shoots per explant in higher frequencies were obtained on medium MSN.5B/MSB. However, shoot of higher length was recorded on medium MSB. Higher in vitro rooting response (root proliferating efficiency, number of roots and mean root length) was exhibited by culture medium MS2IB. The plantlets were transferred to pots and hardened in Environmental Growth Cabinet and Net House during preliminaryweaning period and transferred to field successfully. Phenotypic normal plants were recovered.
机译:三个外在植物viz。在MS培养基的不同修饰上培养灯泡量表,叶片和成熟胚,以达到最佳的体外反应。对于灯泡规模培养,营养培养基MS2N.5b对愈伤组织开始证明了。培养基MS.4TD表现出较高的抗噬菌体增殖效率,而在媒体MS2N.5B / MS3N.5B上记录了每次外植体的芽数量和更高长度的芽。对于培养的叶片,接种培养基MS2D.5B / MS3D.5B促进了较高程度的Callus诱导。通过培养基MS2N.5B / MSN.5B表现出较高的形态发生愈伤组织。然而,从再生培养基MS.5TD / MSB中回收较高数量的植株。对于成熟的胚胎培养,培养基MS2D.5B证明了FORCALLUS启动。接种培养基MSN.5B表现出更多数量的枝叶增殖外植体。在Media MSN.5b / MSB上获得了较高频率下每个探测器的芽数。然而,在媒体MSB上记录更高长度的拍摄。通过培养基MS2表现出培养基的体外生根响应(根系增殖效率,根数和平均根长)。将植物转移到盆栽上并在预先加换期间在环境生长柜和网屋中硬化,并成功转移到现场。回收表型正常植物。

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