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首页> 外文期刊>The Indian Journal of Agricultural Sciences >In vitro isolation, regeneration and purification of yellow mutant in chrysanthemum (Chrysanthemum morifolium) cv. Lalit through ray floret regeneration
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In vitro isolation, regeneration and purification of yellow mutant in chrysanthemum (Chrysanthemum morifolium) cv. Lalit through ray floret regeneration

机译:菊花(Chrysanthemum)CV中黄突变体的体外分离,再生和纯化。 Lalit通过Ray Floret再生

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摘要

Mutations, induced or spontaneous, play an important role in inducing genetic variations in chrysanthemum (Chrysanthemum morifolium Ramat.). Isolation and purification of mutated tissue is impossible through conventional methods that results complete loss of the precious mutants due to lack of suitable techniques to isolate them through conventional methods. In the present investigation, an effort was made to develop efficient ray floret regeneration protocols to isolate, purify and establish a novel mutant which spontaneously appeared as chimera in the form of yellow flowers in chrysanthemum (Chrysanthemum morifolium) cv. Lalit (white). Maximum survival (82.0%) and callus formation (90.28%) in minimum duration (6.6 days) were recorded when the ray florets were pre-treated with mancozeb-45 (0.2%) + carbendazim (0.2%) + 8-HQC (200 mg/l) for 3 h followed by surface sterilized with HgCl2 (0.1%) for a duration of four minutes and cultured on Murashige and Skoog (MS) medium supplemented with 6-Benzylaminopurine (BAP) (4.0 mg/l) and NAA (1.0 mg/l). The maximum regeneration of micro-shoots (80%) from the ray floret induced callus was recorded on MS medium fortified with BAP (4.0 mg/l), NAA (0.5 mg/l) and gibberellic acid (GA3) (0.1 mg/l). MS medium supplemented with BAP (4.0 mg/l) + NAA (0.05 mg/l) + GA3 (0.1 mg/l) was found to be best for highest micro-shoot proliferation (92.0%). Highest rooting (86.0%) was induced after culturing the micro-shoots individually on half-strength MS medium fortified with 0.5 mg/l NAA and 50 g/l sucrose. Successful acclimatization of in vitro raised plantlets was done in glass jar with polypropylene cap filled with a mixture of sterilized coco-peat, soilrite and perlite (1:1:1) supplemented with half-strength MS inorganic salts. After 3-4 weeks of acclimatization, the plantlets were successfully transferred to ambient conditions and compared with the parent variety Lalit. The in vitro raised plants produced all bright yellow flowers as compared to the original variety Lalit with white flowers.
机译:突变,诱导或自发,在诱导菊花遗传变异(菊花Morifolium Ramat)中起着重要作用。通过常规方法可以通过缺乏合适的技术通过常规方法分离出来的常规技术来分离突变组织的分离和纯化是不可能的。在本调查中,努力开发有效的射线小花再生方案,以分离,纯化和建立一种新的突变体,其在菊花(菊花莫利夫菊酯)CV中的黄色花朵形式自发地出现嵌合体。 Lalit(白色)。当用ManCozeb-45(0.2%)+碳氮氮珠(0.2%)+ 8-HQC(200 Mg / L)3小时,然后用HgCl 2(0.1%)进行表面灭菌4分钟,并在弥补含有6-苄氨基嘌呤(BAP)(4.0mg / L)和NAA(4.0mg / L)和NAA( 1.0 mg / l)。从雷小花诱导的愈伤组织的微芽(80%)的最大再生被记录在用BAP(4.0mg / L),NAA(0.5mg / L)和赤霉酸(GA3)(0.1mg / L. )。介于补充有烤盘(4.0mg / L)+ Naa(0.05mg / L)+ Ga 3(0.1mg / L)的MS培养基最适合最高微芽增殖(92.0%)。在用0.5mg / L Naa和50g / L蔗糖的半强度MS培养物上单独培养微芽后诱导最高生根(86.0%)。体外升高的小植物的成功适应于玻璃罐中用聚丙烯帽进行,其中包含灭菌的可可 - 泥炭,土渣和珍珠岩(1:1:1)的混合物,补充有半强度MS无机盐。在适应3-4周后,将植物成功转移到环境条件下并与母体品种Lalit进行比较。与原始品种Lalit与白花相比,体外升高的植物产生了所有亮黄色的花朵。

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