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驱蚊草组培快繁技术研究
引用本文:郝会军,刘英,王洪波,丁世民.驱蚊草组培快繁技术研究[J].山东林业科技,2006(5):25-25,51.
作者姓名:郝会军  刘英  王洪波  丁世民
作者单位:潍坊职业学院,潍坊,261041
摘    要:以驱蚊草幼嫩茎段为外植体,将其接种在MS BA2.0mg/L 2,4-D0.2mg/L培养基上进行培养,15~20天嫩茎诱导形成愈伤组织,诱导率达90%,然后将愈伤组织接种于MS BA1.0mg/L 2,4-D0.5mg/L的培养基中进行培养,15天左右开始形成丛生芽,最后将成苗接种于1/2MS NAA0.5 mg/L培养基中,7~10天生根率可达100%。

关 键 词:驱蚊草  组织培养  快速繁殖
文章编号:1002-2724(2006)05-0025-02
收稿时间:2006-08-04
修稿时间:2006-08-04

Study on the tissure culture and fast reproduction of Pelargonium graueolens
Hao Huijun et al..Study on the tissure culture and fast reproduction of Pelargonium graueolens[J].Journal of Shandong Forestry Science and Technology,2006(5):25-25,51.
Authors:Hao Huijun
Institution:Weifang Vocational College, Weifang 261041
Abstract:This experiment take Pelargonium graueolens's young tender stem as to explant, has studied the influence of different phytohormone combination multiplying to the bud, the effect of different type auxins taking root. The result indicated that, induction effect2 is best in MS BA2.0mg/L 2,4-D0.2mg/L, which inductivity might achieve 90%, moreover the quality of callus to be better; The best culture medium of inducing the bud which grows thickly is MS BA1.0mg/L 2,4-D0.5mg/L; The best culture medium of taking root is 1/2MS NAA0.5mg/L.
Keywords:Pelargonium graueolens  Tissue culture  Fast reproduction
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