首页 | 本学科首页   官方微博 | 高级检索  
     

夏蜡梅组织培养试验初报
引用本文:邵果园,蔡荣荣,王力超,梁国鲁. 夏蜡梅组织培养试验初报[J]. 浙江林业科技, 2006, 26(5): 28-30
作者姓名:邵果园  蔡荣荣  王力超  梁国鲁
作者单位:1. 浙江林学院,林业与生物技术学院,浙江,临安,311300;西南大学,园艺园林学院,重庆,400716
2. 浙江林学院,林业与生物技术学院,浙江,临安,311300
3. 西南大学,园艺园林学院,重庆,400716
摘    要:以夏蜡梅茎段为外植体,进行夏蜡梅组培试验,结果表明:外植体茎段的最佳消毒方式是先用70%酒精消毒10—15s,再用0.1%HgCl溶液浸泡3—5min;继代增殖培养的最佳培养基为MS+6-BA2.0mg/L+NAA0.1mg/L+蔗糖30g/L,增殖系数4.03,茎芽生长粗壮;最佳生根培养基为I/2MS+IBA0.4mg/L。

关 键 词:夏蜡梅  组织培养  增殖  生根
文章编号:1001-3776(2006)05-0028-03
收稿时间:2006-08-20
修稿时间:2006-08-20

Study on Tissue Culture of Calycanthus chinensis
SHAO Guo-yuan,CAI Rong-rong,WANG Li-chao,LIANG Guo-lu. Study on Tissue Culture of Calycanthus chinensis[J]. Journal of Zhejiang Forestry Science and Technology, 2006, 26(5): 28-30
Authors:SHAO Guo-yuan  CAI Rong-rong  WANG Li-chao  LIANG Guo-lu
Abstract:Experiment on tissue culture of Calycanthus chinensis by using stems as explant showed that the optimal sterilizing method was dipping the stems in 70% alcohol for 10 - 15 seconds and 0.1% Hgcl for 3 - 4 minutes. The optimum medium for multiplication was MS + 6-BA2.0mg/L + NAA0.1mg/L + sugar 30 g/L, and the rate of regeneration reached 4.03 with the IBA concentration of 0.4 mg/L in 1/2MS.
Keywords:Calycanthus chinensis   tissue culture   multiplication   rooting
本文献已被 CNKI 维普 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号