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长柄双花木愈伤组织诱导及植株再生
引用本文:曾建军,肖宜安,孙敏,.长柄双花木愈伤组织诱导及植株再生[J].广西植物,2006,26(6):628-630,601.
作者姓名:曾建军  肖宜安  孙敏  
作者单位:1. 井冈山学院,生命科学学院,江西,吉安,343009
2. 西南师范大学,生命科学学院,重庆,400715
基金项目:江西省教育厅科研基金 , 国家自然科学基金
摘    要:以长柄双花木当年生嫩梢上的叶柄、嫩茎、嫩叶为外植体,对影响长柄双花木愈伤组织诱导和继代、分化主要因素进行研究。结果表明:在培养基MS+NAA0.5mg/L+2,4-D2.0mg/L上,三种外植体均可诱导出愈伤组织,其中叶片愈伤组织诱导率最高。该培养基还可作为愈伤组织继代培养基,但继代培养周期不超过2周。愈伤组织接种在MS+BA2mg/L上分化不定芽,根的诱导在1/2MS+IBA0.5mg/L培养基上进行。

关 键 词:长柄双花木  愈伤组织  诱导  继代培养
文章编号:1000-3142(2006)06-0628-03
收稿时间:2005-03-14
修稿时间:2005-03-142005-10-20

Callus induction and plant regeneration of Disanthus cercidifolius var.longipes
ZENG Jian-jun,XIAO Yian,SUN Min.Callus induction and plant regeneration of Disanthus cercidifolius var.longipes[J].Guihaia,2006,26(6):628-630,601.
Authors:ZENG Jian-jun  XIAO Yian  SUN Min
Abstract:The stems,leaves and petioles explants from Disanthus cercidifolius Maxim.var.longipes H.T.Chang were cultured on MS medium with BA,NAA,2,4-D,IBA of different concentration to induce regeneration plant. The results indicated that leaf was the best explant for callus induction,and the best suitable medium was MS NAA 0.5 mg/L 2,4-D 2.0 mg/L,it also could be used as the medium for callus subculture. MS medium only supplemented with BA mg/L could obtain higher frequency of differentiation. When studying root regeneration culture,1/2MS medium supplemented with IBA 0.5 mg/L had better root regeneration.
Keywords:Disanthus cercidifolius var  longipes  callus  induction  subculture
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