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首页> 外文期刊>HortScience >Combined in vitro and in vivo propagation for rapid multiplication ofgrapevine cv. Arka Neelamani
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Combined in vitro and in vivo propagation for rapid multiplication ofgrapevine cv. Arka Neelamani

机译:结合体外和体内繁殖快速繁殖葡萄树简历。 Arka Neelamani

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摘要

A novel combination of in vitro and in vivo approaches was employed to generate sufficient stock of an introduced grape (Vitis vinifera L.) ev. Arka Neelamani which significantly accelerated the multiplication rate. The in vitro part included induction of root and shoot growth in shoot tip and nodal microcuttings in MS medium containing 1 muM IAA, sequential pruning of shoots at 1, 1.5, and 2 months, leaving the basal one to two nodes, resulting in fresh sprouts on the stump, and use of remaining stumps for in vivo establishment. The in vivo part included acclimatization of in vitro rooted plantlets and stumps, use of single node cuttings from 1.5- to 2-month-old in vivo shoots for the subsequent propagation, and utilizing the fresh sprout growth from these cuttings and in vivo stumps for further propagation. Employing both in vitro and in vivo approaches, we achieved a multiplication rate unparalleled to the general micropropagation or conventional propagation and significant stock was obtained within 6 months of introducing the material. The in vivo plants exhibited adult characters like distichous phyllotaxy, three lobed leaves and normal pattern of tendril development within 2 months from planting.
机译:采用体外和体内方法的新颖组合以产生足够量的引入的葡萄(Vitis vinifera L.)ev。 Arka Neelamani大大加快了繁殖速度。体外部分包括在含有1μMIAA的MS培养基中诱导芽尖和根尖生长以及节点微切屑的萌发,在1,1.5和2个月时依次修剪芽,使基部一到两个结节,从而产生新芽在树桩上,以及将剩余的树桩用于体内建立。体内部分包括使体外生根的小苗和树桩适应环境,将1.5个月至2个月大的体内枝条单节插条用于随后的繁殖,并利用这些插条和体内树桩的新鲜芽苗生长来进一步传播。利用体外和体内方法,我们获得了与普通微繁或常规繁殖无可比拟的繁殖率,并且在引入该材料后的6个月内获得了大量存货。体内植物在种植后的两个月内表现出成年特征,如叶状叶状叶序,三叶状叶和卷须发育的正常模式。

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