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作 者:许耀祖[1] 韦彦余[1] 王晓军[1] 赵民安[1] 赵海清[1]
机构地区:[1]中国科学院新疆理化技术研究所
出 处:《园艺学报》2006年第1期182-185,共4页Acta Horticulturae Sinica
基 金:中国科学院西部行动高新技术资助项目(KGCX2-SW-506)
摘 要:以薰衣草叶片为外植体进行了离体再生研究。结果表明:叶片愈伤组织诱导最佳的培养基是MS+2,4-D 0.1 mg/L+6-BA 0.5 mg/L,诱导率高达100%;液体悬浮—固体培养芽分化率达92.5%,芽数/愈伤组织达6.6;正交试验筛选出芽增殖最佳培养基为MS+NAA 2.0 mg/L+6-BA 0.5 mg/L+IAA 1.0mg/L,其增殖系数高达8.7;在芽增殖培养基上可直接生根,生根率达100%。The regeneration system of Lavandula angustifolia ‘Munstead' in vitro was studied with leaves as explants, and the results showed the optimal medium for callus induction was MS + 2, 4-D 0. 1 mg/ L + 6-BA 0. 5 mg/L with the induction frequency of 100%. Liquid suspension-solid culture can achieve adventitious bud differentiation rate of 92.5% and 6. 6 bud per callus. Best bud multiplying medium which was MS medium supplemented with NAA 2. 0 mg/L and 6-BA 0. 5 mg/L and IAA 1.0 mg/L was sifted through orthogonal experiment with multiplying coefficient of 8.7. The rooting of rootless bud could be accomplished directly in the bud multiplying medium with rooting frequency of 100%.
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