风铃玉的组织培养与快速繁殖

吴正景1,*, 黄雪娇1, 王柏1, 彭涛2, 马文瑶1
1河南科技大学林学院, 河南洛阳471003; 2卢氏县中药材生产管理办公室, 河南卢氏472200

通信作者:吴正景;E-mail: wzj135@sohu.com;Tel: 0379-64282669

摘 要:

以风铃玉叶片为外植体诱导愈伤组织并分化出不定芽发生, 经生根得到再生植株, 建立风铃玉离体再生体系。风铃玉愈伤组织诱导的较好培养基为MS+NAA 0.2 mg∙L-1+6-BA 0.2 mg∙L-1, 诱导率为85.7%; 最佳诱芽培养基是MS+IBA 0.02 mg∙L-1+6-BA 0.2 mg∙L-1, 能直接诱导出生长健壮的丛生芽; 最佳生根培养基是1/2MS+IBA 0.1 mg∙L-1, 生根率高达83.3%。

关键词:风铃玉; 叶片; 组织培养; 快速繁殖

收稿:2015-09-09   修定:2015-09-25

资助:河南科技大学博士科研基金(09001216)。

Tissue Culture and Rapid Propagation of Ophthalmophyllum friedrichiae

WU Zheng-Jing1,*, HUANG Xue-Jiao1, WANG Bai1, PENG Tao2, MA Wen-Yao1
1forestery College, Henan University of Science and Technology, Luoyang, Henan 471003, China; 2Lushi County Management Office of Herbal Medicine, Lushi, Henan 472200, China

Corresponding author: WU Zheng-Jing; E-mail: wzj135@sohu.com; Tel: 0379-64282669

Abstract:

In this paper we studied in vitro culture of Ophthalmophyllum friedrichiae by using leaf as explants, including callus induction, adventitious shoot differentiation and rooting. The results indicated that MS+NAA 0.2 mg∙L-1+6-BA 0.2 mg∙L-1 was the suitable medium for callus induction, with an induction rate of 85.7%. The best medium for adventitious bud differentiation was MS+IBA 0.02 mg∙L-1+6-BA 0.2 mg∙L-1, and the shoots induced were strong. 1/2MS+IBA 0.02 mg∙L-1+6-BA 0.2 mg∙L-1 was the optimum medium for rooting, and the rooting rate reached 83.3%.

Key words: Ophthalmophyllum friedrichiae; leaf; tissue culture; rapid propagation

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