| 黄蔷薇的组织培养 |
| |
| 引用本文： | 张继东.黄蔷薇的组织培养[J].甘肃林业职业技术学院学报,2006(1). |
| |
| 作者姓名： | 张继东 |
| |
| 作者单位： | 甘肃省林业职业技术学院 |
| |
| 基金项目： | 甘肃林业职业技术学院中青年教师专项科技基金资助项目。 |
| |
| 摘 要： | 黄蔷薇采用不同发育期的当年生嫩枝,在无菌条件下处理后作为诱导培养的外植体,进行组织培养。经试验表明,适宜的诱导腋芽培养基为1/3MS BA0.3mg/L NAA0.1mg/L,继代培养基为1/2MS BA0.1mg/L IBAA0.2mg/L,生根培养基为1/2MS IAA0.5mg/L。试管苗在适宜的环境条件下培养后,可实现黄蔷薇的快速繁育。
|
| 关 键 词： | 黄蔷薇 组织培养 |
Tissue Culture of Rosa hugonis Hemsl |
| |
| ZHANG Ji-dong.Tissue Culture of Rosa hugonis Hemsl[J].Journal of Gansu Forestry Technological College(Comprehensive),2006(1). |
| |
| Authors: | ZHANG Ji-dong |
| |
| Institution: | Gansu Forestry Technology college |
| |
| Abstract: | The Rosa hugonis Hemsl took fresh layer of the different development period the same year , processed after the aseptic condition, as the induction raise outside planted body, carried on the tissue culture. Indicated after the experiment, is suitable induction yeya culture medium 1/3MS BA0.3mg/L NAA0.1mg/Lcontinues generation of culture medium 1/2MS BA0.1mg/L IBAA0.2mg/L, takes root culture medium 1/2MS IAA0.5mg/L. The test tube seedling after is suitable under the environmental condition raises, may realize the Rosa hugonis Hemsl 's fast breeding |
| |
| Keywords: | Rosa hugonis Hemsl tissue culture |
| 本文献已被 CNKI 等数据库收录！ |
|
