风信子离体快繁体系的建立  

Rapid Micropropagation System Via in Vitro Culture in Hyacinthus orientalis L.

作　　者：孙晓梅[1] 李妍[1] 杨宏光[1] 崔文山[1] 王亚斌[1] 

机构地区：[1]沈阳农业大学林学院,沈阳110866

出　　处：《沈阳农业大学学报》2010年第1期33-36,共4页Journal of Shenyang Agricultural University

基　　金：沈阳市科技攻关项目(1071146-3-00)

摘　　要：研究以风信子Gipsy queen的鳞片及幼叶为外植体直接诱导不定芽生成,结果表明:Gipsy queen单鳞片、双鳞片的初代最佳诱导培养基为:MS+6-BA5.0mg·L-1+NAA0.1mg·L-1,且双鳞片诱导效果好于单鳞片,诱导率达100%,增殖系数达10;幼叶外植体初代最佳诱导培养基为:MS+6-BA3.0mg·L-1+NAA0.2mg·L-1,幼叶作为外植体比鳞片诱导效果好,诱导率达100%,增殖系数达26.27;最佳继代培养基为:MS+6-BA2.0mg·L-1+NAA0.5mg·L-1+KT0.2mg·L-1,增殖系数达2.91;生根诱导最佳培养基为:1/2MS+NAA0.2mg·L-1,生根率可达93.33%。Adventitious shoots were induced from scale segments and tender leafs of Hyacinthus orientalis L.cv.Gipsy Queen.As the result of this experiment： the appropriate medium for initial culture of single-scale and twin-scale of Gipsy Queen was： MS＋6-BA5.0mg·L^-1＋NAA0.1mg·L^-1,and twin-scale was better than single-scale.The induction rate was 100%,the proliferation multiple was 10.The appropriate medium for tender leafs was： MS＋6-BA3.0mg·L^-1＋ NAA0.2mg.L^-1,and the effect was better than that of scale segments.The induction rate was 100%,the proliferation multiple was 26.27.The best medium on subculture multiplication was MS ＋6-BA2.0mg·L^-1 ＋NAA0.5mg·L^-1 ＋KT0.2mg·L^-1.The proliferation multiple was 2.91.The ratio of root induction for the bulblets was 93.33% on the medium of 1/2MS＋NAA0.2mg·L^-1.

关 键 词：风信子 离体快繁 鳞片 幼叶 

分 类 号：Q949.718.23[生物学—植物学]