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出 处:《安徽农业科学》2009年第17期7854-7854,7874,共2页Journal of Anhui Agricultural Sciences
基 金:江西省教育厅科技项目(GJJ09603)
摘 要:[目的]建立虎舌红的高频再生体系,为利用转基因技术改良其品质奠定基础。[方法]以虎舌红试管苗顶端叶片为试材进行组织培养和不定梢诱导试验。[结果]外植体在9种培养基上均能诱导出愈伤组织,4号培养基的不定芽再生率最高,为45.80%,植株生长健壮;其次是7号培养基,其不定芽再生率为39.76%。从整体上看,不定芽的再生率都不高,最高的也未超过50.00%。综合考虑愈伤组织诱导和不定芽再生,适合虎舌红叶片不定芽再生的培养基为:1/2 MS+TDZ 2.0mg/L+IAA0.2~0.4mg/L+AgNO3 3.0~5.0mg/L。选健壮苗接种于1/2MS+IBA 0.3mg/L+NAA 0.5mg/L培养基上,20d后生根率可达90%,炼苗后再生植株的移栽成活率达80%以上。[结论]该研究成功建立了虎舌红叶片的离体再生体系。The aim of the study was to establish the high-frequency regeneration system of Ardisia mamillata and lay a basis for improving its quality by transgenic technology. [ Method] With the apical leaves of tube A. mamillata seedlings as tested materials, its tissue culture and induction experiment of adventitious shoots were performed. [Result] The ealli could be induced from all the explants growing on the 9 media. On Medium 4, the regeneration rate of adventitious buds was highest, being 45.80% and the plantlets grew mbnstly. On Medium 7, the regeneration rate of adventitious buds was secondary, being 39.76%. Totally, the regeneration rate of adventitious buds was not high and the highest did not exceed 50.00%. Considering callns induction and the regeneration of adventitious buds comprehensively, the suitable medium for the regeneration of adventitious buds from A. mamiliata leaves was 1/2 MS + TDZ 2.0 mg/L + IAA 0.2-0.4 mg/L + AgNO3 3.0- 5.0 mg/L. The strong cultured seedlings were selected and inoculated onto the medium 1/2 MS + IBA 0.3 mg/L + NAA 0.5 mg/L, their rooting rate could reach 90% after 20 d and the transplanting survival rate of hardened regenerated plants was higher than 80%. [ Conclusion] The in vitro regeneration system of A. mamillata leaves was estabished successfully in this study.
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