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非洲紫罗兰叶片体细胞胚培养及快繁技术研究
引用本文:师嘉临,师桂英,任治斌,汉梅兰,师春娟.非洲紫罗兰叶片体细胞胚培养及快繁技术研究[J].植物遗传资源学报,2005,6(4):453-456.
作者姓名:师嘉临  师桂英  任治斌  汉梅兰  师春娟
作者单位:1. 全国贫困地区干部培训中心,兰州,730070
2. 甘肃农业大学园艺系,兰州,730070
3. 兰州市南北两山环境绿化工程指挥部,兰州,730000
4. 兰州市园林科学研究所,兰州,730070
5. 甘肃省小陇山林业科学研究所,天水,741026
摘    要:以非洲紫罗兰叶片为材料进行胚状体诱导及快繁技术研究.结果表明:.在MS NAA0.1mg/L BA0.1 mg/L 2,4-D1.0 mg/L的培养基上培养15d利于诱导胚性细胞分化,起始黑暗培养5~10d可提高胚性细胞分化率;在MS BA0.05~1mg/L的培养基上可诱导胚状体大量发生;在MS NAA0.1mg/L十BA0.1 mg/L的培养基上能够获得茎芽快速增殖;在1/2MS NAA0.01mg/L的培养基上可以生根.

关 键 词:非洲紫罗兰  胚状体  快繁
收稿时间:2004-10-27
修稿时间:2005-09-05

Somatic Embryogenic Culture and Rapid Prpagation in vitro of Saintpaulia ionantha from Leaf
SHI Jia-lin,SHI Gui-ying,REN Zhi-bin,HAN Mei-lan,SHI Chun-juan.Somatic Embryogenic Culture and Rapid Prpagation in vitro of Saintpaulia ionantha from Leaf[J].Journal of Plant Genetic Resources,2005,6(4):453-456.
Authors:SHI Jia-lin  SHI Gui-ying  REN Zhi-bin  HAN Mei-lan  SHI Chun-juan
Abstract:Somatic embryoid of Saintpaulia ionantha was obtained from the leaf explants thought rapid propagation.Embryonic cells were preliminary induced on MS+BA0.1mg/L+NAA0.1mg/L+2,4-D1.0mg/L for 15 days,and their regeneration could be increased by 5-10 d initial dark culture.Embryoid could be easily induced on MS+BA0.05-1mg/L.Rapid propagation medium was MS+NAA0.1mg/L +BA0.1 mg/L.Roots could be easily induced on 1/2 MS+NAA0.01mg/L.
Keywords:Saintpaulia ionantha  Embryoid  Rapid propagation
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