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大花萱草组织培养研究
引用本文:刘志洋,李海涛,朱祥春,孟婧,高继国.大花萱草组织培养研究[J].东北农业大学学报,2008,39(1):43-45.
作者姓名:刘志洋  李海涛  朱祥春  孟婧  高继国
作者单位:1. 哈尔滨市农业科学院,哈尔滨,150070
2. 东北农业大学生命科学学院,哈尔滨,150030
基金项目:东北农业大学开放实验室基金
摘    要:采取大花萱草茎尖为外植体接种在不同培养基上,研究了不同浓度的NAA和6-BA对于外植体生长的影响,并探索了最适于产生愈伤组织和生根的培养基配方。结果表明,有利于外植体产生愈伤组织的培养基配方是MS+6-BA1.0mg·L-1+NAA0.05mg·L-1+30g糖+8g琼脂;适合愈伤组织诱导生芽培养基配方是MS+6-BA1.0mg·L-1+30g糖+8g琼脂;适合幼苗生根的培养基配方是1/2MS+NAA0.5mg·L-1+30g糖+8g琼脂。

关 键 词:大花萱草  组织培养  愈伤组织
文章编号:1005-9369(2008)01-0043-03
收稿时间:2006-12-21
修稿时间:2006年12月21

Study on tissue culture of Hemerocallis fulva
LIU Zhiyang,LI Haitao,ZHU Xiangchun,MENG Jing,GAO Jiguo.Study on tissue culture of Hemerocallis fulva[J].Journal of Northeast Agricultural University,2008,39(1):43-45.
Authors:LIU Zhiyang  LI Haitao  ZHU Xiangchun  MENG Jing  GAO Jiguo
Abstract:The stem apex of Hemerocallis fulva was taken as explant cultured in vitro to induce callus with different culture medium. The effects of different concentration 6-BA and NAA culture medium on explant growth was studied. The results showed that MS+6-BA 1.0 mg·L-1+NAA 0.05 mg·L-1+30 g sugar+8 g agaragar solid culture medium was advantageous to induce callus;after cultured in MS+6-BA 1.0 mg·L-1+30 g sugar+8 g agar-agar, the compact construction callus was formed and differentiation, the clamp seedling was formed;and 1/2 MS+NAA 0.5 mg·L-1+30 g sugar+8 g agaragar solid culture medium was the best medium to induce root.
Keywords:Hemerocallis fulva  tissue culture  callus tissue
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