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美国红栌的组织培养与快速繁殖技术研究
引用本文:胡相伟,张守琪,李毅.美国红栌的组织培养与快速繁殖技术研究[J].甘肃农业大学学报,2006,41(2):59-61.
作者姓名:胡相伟  张守琪  李毅
作者单位:1. 兰州市林木繁育中心,甘肃,兰州,730085
2. 甘肃农业大学,甘肃,兰州,730070
基金项目:兰州市科学技术局科技发展规划项目(04-2-16)
摘    要:以美国红栌叶片为外植体材料,筛选各个培养阶段的最适培养基配方,结果表明:MS+6-BA 1.5 mg/L+NAA 0.5 mg/L对叶片诱导愈伤组织效果最好;MS+6-BA 1.0 mg/L为分化培养基的适宜配方;1/2 MS+IBA 1.0mg/L+蔗糖15 mg/L+琼脂5 g/L生根效果良好;采用平茬复壮技术可以达到越冬的良好效果.

关 键 词:美国红栌  组织培养  快速繁殖
文章编号:1003-4315(2006)02-0059-03
收稿时间:2005-08-29
修稿时间:2005-08-29

Tissue culture and rapid propagation of Continus coggygria
HU Xiang-wei,ZHANG Shou-qi,LI Yi.Tissue culture and rapid propagation of Continus coggygria[J].Journal of Gansu Agricultural University,2006,41(2):59-61.
Authors:HU Xiang-wei  ZHANG Shou-qi  LI Yi
Institution:1.Lanzhou Forest Tree Breeding, Honggu 730085 ; 2. Gansu Agricultural University,Lanzhou 730070,China
Abstract:The leaves of Continus coggygria were taken as explant,and the optimum media for each culture stage were selected out.The results showed that the medium MS 6-BA 1.5 mg/L NAA 0.5 mg/L was the best for inducing callus from leaf;medium MS 6-BA 1.0 mg/L was the most suitable for propagation;medium 1/2 MS IBA 1.0 mg/L surcrose 15g/L agar 5g/L was the optimum for rooting.
Keywords:Continus coggyria  tissue culture  rapid propagation  
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