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Citation:

Study on Culture Media for Micropropagation of Oplopanax elatus Nakai

  • Received Date: 2007-09-15
  • Taking the tender leaves ofOplopanax elatus as exp lants for the experiment, Uniform Design were used totest the most suitable media for callus induction, differentiation of shoot and rooting. The results showed thatN6 +6-BA 0. 5 mg·L-1 + 2, 4-D 0. 2 mg·L-1 +Vc 10 mg·L-1 was fitted for callus induction, the medium fordifferentiation of shootwas N6 + 6-BA 4. 5 mg·L-1 +NAA 0. 1 mg·L-1 +Vc 20 mg·L-1 , the medium forrooting was 1 /4MS + IBA 0. 1mg·L-1 +NAA 0. 1 mg·L-1. Tissue culture required different kinds of culturemedia in different phases.
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  • [1] 张俊兰,赵占英,王殿芝. 长白山五加科药用植物[J]. 北方园艺, 1996 (6) : 46

    [2] 张宏桂, 刘松艳, 付爱华. 野生东北刺人参茎挥发油成分及其抗皮肤癣菌作用[J]. 中国药学杂志, 1999, 34 (6) : 369 - 371

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    [5] 刘继生, 张 鹏, 孙静刚. 外源赤霉素对东北刺人参种子萌发的影响[J]. 林业科技, 2005, 30 (2) : 45 - 47

    [6] 张 鹏,刘继生,潘宜才,等. 东北刺人参人工扩繁研究技术现状[J]. 延边大学农学学报, 2003, 25 (1) : 65 - 68

    [7] 贺善安. 中国珍稀植物[M]. 上海: 上海科学技术出版社,1998: 38

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    [9] 朴炫春,廉美兰,刘继生,等.东北刺人参组培快繁的可行性研究[J]. 延边大学农学报, 2006, 28 (1) : 10 - 13

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    Moon H K, Kim J A, Park S Y, et al.Somatic embryogenesis andp lantlet formation from a rare and endangered tree species, Oplopanax elatus [J]. [Monograph] Dongguk University, Seoul, Republic of Korea, 2006, 49 (4) : 320 - 325
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    Cho H J, YangW Y, Yun DW, et al1Somatic embryogenesis frominflorescences derived callus of Oplopanax elatus Nakai. [J]. Research Reports of the Rural Development Administration, Biotechnology, 1991, 33 (3) : 1 - 6
    [12] 金英善,曹后男,刘继生,等. 东北刺人参愈伤组织的诱导[J].延边大学农学学报, 2003, 25 (1) : 16 - 19

    [13] 顾地周,何晓燕,朱俊义,等. 细叶杜香的组织培养和快速繁殖[J]. 植物生理学通讯, 2007, 43 (5) : 898

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Study on Culture Media for Micropropagation of Oplopanax elatus Nakai

  • 1. Department of Biology, Tonghua Normal University, Tonghua 134002, Jilin, China

Abstract: Taking the tender leaves ofOplopanax elatus as exp lants for the experiment, Uniform Design were used totest the most suitable media for callus induction, differentiation of shoot and rooting. The results showed thatN6 +6-BA 0. 5 mg·L-1 + 2, 4-D 0. 2 mg·L-1 +Vc 10 mg·L-1 was fitted for callus induction, the medium fordifferentiation of shootwas N6 + 6-BA 4. 5 mg·L-1 +NAA 0. 1 mg·L-1 +Vc 20 mg·L-1 , the medium forrooting was 1 /4MS + IBA 0. 1mg·L-1 +NAA 0. 1 mg·L-1. Tissue culture required different kinds of culturemedia in different phases.

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