›› 2010, Vol. 18 ›› Issue (2): 286-290.DOI: 10.11733/j.issn.1007-0435.2010.02.027

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Establishment of micropropagation system of Ligularia jaluensis Kom.

DONG Ran1, PAN Yan-yan1, WANG Li-qing2, GU De-feng1, LIU Hong-zhang1   

  1. 1. Jilin Agricultural University, College of Horticulture, Changchun 130118, China;
    2. Panshi Horticultural Specialty Technical Popularization Station of Jilin Province, Panshi 132300, China
  • Received:2009-11-10 Revised:2010-01-16 Online:2010-04-15 Published:2010-04-15

复序橐吾组培再生体系研究

董然1, 潘艳艳1, 王丽清2, 顾德峰1, 刘洪章1   

  1. 1. 吉林农业大学园艺学院, 吉林, 长春, 130118;
    2. 吉林省磐石市园艺特产技术推广站, 吉林, 磐石, 132300
  • 通讯作者: 刘洪章,E-mail:lhz999@126.com
  • 作者简介:董然(1966- ),女,吉林敦化人,教授,博士,主要从事长白山观赏植物资源驯化及开发领域研究,E-mail:Dongr999@163.com
  • 基金资助:
    吉林省科技厅支撑项目(20060222)资助

Abstract: The experiment was based on MS culture media and Ligularia jaluensis Kom.Used explants were from aseptic leavses of the germination seeds in vitro.An appropriate culture medium was obtained via regulating the concentrations of cytokinin and auxin.The optimal sterilization method for seeds of Ligularia jaluensis Kom.was 75% ethanol 30 s+1‰ HgCl2 4 min.MS+ 6-BA 0.5 mg/L+2,4-D 1.0 mg/L was the best culture medium for the first generation callus,the induced ratio of green compact callus reached 90% with this culture medium.The Propagation Coefficient of 3.9 times indicated that MS+6-BA1.0 mg/L+NAA0.1mg/L was the optimal culture medium for subculture proliferation.The best rooting medium was 1/2MS+NAA0.5 mg/L,the survival rate of the plantlets was shown to be up to 100%.

Key words: Ligularia jaluensis Kom., leaf, tissue culture

摘要: 用复序橐吾(Ligularia jaluensis Kom.)种子获得无菌苗,取其叶片为外植体,以MS培养基为基础,通过添加不同浓度和种类的细胞分裂素及生长素,目的是筛选出叶片组织培养的最适培养基。结果表明:种子较好的灭菌时间为75%酒精30 s+1‰升汞4min;初代培养基为MS+6-BA0.5mg/L+2,4-D1.0mg/L,由此获得的愈伤组织致密、颜色绿,具有很好的诱导效果,其诱导率达到90%;继代增殖的最适培养基为MS+6-BA1.0mg/L+NAA0.1mg/L,其增殖倍数高达3.9,并且苗生长状况良好;生根最适培养基为:1/2MS+NAA 0.5mg/L,生根率达100%。

关键词: 复序橐吾, 叶片, 组织培养

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