| 非洲菊的组培快繁 |
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| 引用本文： | 陈晓静,李梅婷,林馨.非洲菊的组培快繁[J].福建农林大学学报(自然科学版),2006,35(2):169-172. |
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| 作者姓名： | 陈晓静 李梅婷 林馨 |
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| 作者单位： | 福建农林大学园艺学院,福建农林大学园艺植物遗传育种研究所,福建,福州,350002 |
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| 摘 要： | 以非洲菊红花黄芯品系F1幼苗的带芽短缩茎、无芽短缩茎、叶片和盆花的花托作外植体,进行组培快繁研究.结果表明:诱导愈伤组织及芽的增殖培养基均以MS+3.0 mg.L-1BA+0.1 mg.L-1NAA为佳,生根培养基以1/2 MS+0.2 mg.L-12,4-D为好;带芽短缩茎作外植体与无芽短缩茎、嫩叶和花托相比,明显缩短了愈伤组织诱导期和芽苗的诱导分化期.
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| 关 键 词： | 非洲菊 组织培养 快速繁殖 |
| 文章编号： | 1671-5470(2006)02-0169-04 |
| 收稿时间： | 2005-11-21 |
| 修稿时间： | 2006-02-22 |
In vitro propagation of Gerbera jamesonii |
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| CHEN Xiao-jing,LI Mei-ting,LIN Xin.In vitro propagation of Gerbera jamesonii[J].Journal of Fujian Agricultural and Forestry University,2006,35(2):169-172. |
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| Authors: | CHEN Xiao-jing LI Mei-ting LIN Xin |
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| Abstract: | The tissue culture and rapid propagation of Gerbera jamesonii was mainly studied from the explants of stem nodes with buds.Compared with the explants of receptacles and tender leaves, it significantly shortened the inducing and differentiating period of the shoots,as well as the inducing period of callus.The solid MS medium with 3.0 mg·L~(-1) BA and 0.1 mg·L~(-1) NAA was suitable for both the inducement of callus and the multiplacation of shoots;then the solid 1/2 MS medium supplemented with 0.2 mg·L~(-1)2,4-D was suitable for the induction of roots. |
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| Keywords: | Gerbera jamesonii in vitro culture rapid propagation |
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