《植物生理学报》 2015, 51(10): 1729-1734
通信作者:云;E-mail: yyong3819@163.com;Tel: 189075903361
摘 要:
本文对黄花马铃苣苔进行离体培养与快速繁殖技术研究。结果表明, 黄花马铃苣苔叶片外植体的最适初代诱导培养基为MS+0.5 mg•L-1 6-BA+0.1 mg•L-1 NAA, pH值为6.5。最适继代增殖培养基为MS+0.1 mg•L-1 6-BA+0.1 mg•L-1 NAA, 培养30 d的增殖系数为7.30。最适生根培养基为MS+0.5 mg•L-1 IBA, 生根率100%。对生根组培苗进行移栽, 成活率最高达91.43%。关键词:黄花马铃苣苔; 叶片; 离体培养
收稿:2015-05-12 修定:2015-08-25
资助:海南省科学事业费项目(kyys-2013-12)。
Corresponding author: YUN Yong; E-mail: yyong3819@163.com; Tel: 189075903361
Abstract:
We investigated in vitro culture and rapid propagation of Oreocharis flavida. The optimal medium for bud induction from leaves was MS+0.5 mg•L-1 6-BA+0.1 mg•L-1 NAA (pH 6.5). The optimal medium for subculture of bud multiplication was MS+0.1 mg•L-1 6-BA+0.1 mg•L-1 NAA, and the proliferation coefficient was 7.30 at 30 d. The optimal rooting medium was MS+NAA 0.5 mg•L-1, the rooting rate was 100%. The rooting plantlets were transplanted in the matix and the highest survival rate was 91.43%.Key words: Oreocharis flavida; leaf; in vitro culture
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