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粉色马蹄莲组织培养研究
引用本文:王进忠,高文,高遐虹,冯强,孙淑玲,张民照,于同泉. 粉色马蹄莲组织培养研究[J]. 北京农学院学报, 2005, 20(2): 10-13
作者姓名:王进忠  高文  高遐虹  冯强  孙淑玲  张民照  于同泉
作者单位:北京农学院;北京农学院;北京农学院;北京农学院;北京农学院;北京农学院
基金项目:北京市自然科学基金 , 北京市重点实验室基金
摘    要:以粉色马蹄莲块茎芽、叶和植株为外植体,MS为基本培养基,在加NAA0.2mg/L+BA1~3mg/L时,有利于丛芽和愈伤组织的诱导。在加NAA0.2~0.5mg/L+BA0.5~1mg/L时,既有利于不定丛芽的分化诱导,又利于不定芽的生长。在BA为0.2mg/L时,有利于不定芽的生长,但对愈伤组织及不定芽的诱导不利,增殖系数低。高浓度BA有利于愈伤组织和芽的分化,低浓度则对芽的生长有利。外植体叶和植株在各处理中无显著差异,特别是生长后期。叶组织在培养中大部分死亡,只有极少部分产生愈伤组织。植株在培养过程中叶片逐渐变黄、枯死。

关 键 词:彩色马蹄莲  组织培养  愈伤组织
文章编号:1002-3186(2005)02-0010-04
修稿时间:2004-11-12

Tissue Culture of Coloured Common Callalily (Zantedeschla)
WANG Jin-zhong,GAO Wen,GAO Xia-hong,FENG Qiang,SUN Shu-ling,ZHANG Min-Zhao,YU Tang-quan. Tissue Culture of Coloured Common Callalily (Zantedeschla)[J]. Journal of Beijing Agricultural College, 2005, 20(2): 10-13
Authors:WANG Jin-zhong  GAO Wen  GAO Xia-hong  FENG Qiang  SUN Shu-ling  ZHANG Min-Zhao  YU Tang-quan
Abstract:Leaf ,plant and tuber of coloured common callalily ( Zantedeschia antedschina Spreng ) as explants were cultured on MS medium supplemented with different combinationns of plant regulators. The addition of BA 1~3 mg/L and NAA 0.2~0.5 mg/L to MS medium was favorable to the induction of shoots and calli. Enrichment of the basic medium with NAA 0.2~0.5 mg/L and BA 0.5~1.0 mg/L promoted the induction of adventitious shoots and their growth. BA concentrations for 0.2 mg/L were favourable for the growth of adventitious shoots but unfavorabla for the induction of calli and adventitious shoots, resulting in low proliferation coefficients. Higher concentrations of BA were favorable for the differentiation of calli and shoots where as lower concentrations favorable for the growth of shoots. For explant of leaf and small plant,there is no significant different among each treatment of different concentrations of NAA and BA,especially among those in later period of growth.Most of the leaves was died in growth and only a few shoots addition was produced.Plants were weaken as time prolonged.
Keywords:coloured common callalily  tissue culture  calli
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