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吊钟花的组织培养技术研究
Tissue Culture of Enkianthus quinqueflorus Lour.

作  者: ; ; ; ;

机构地区: 深圳市仙湖植物园

出  处: 《热带亚热带植物学报》 2009年第4期383-387,共5页

摘  要: 以吊钟花(Enkianthus quinqueflorus Lour.)茎尖及带腋芽的茎段为外植体进行组织培养。结果表明,改良B5培养基(B5大量元素和钙盐+MS有机物、铁盐、微量元素)最有利于吊钟花的培养,外植体在改良B5+2,4-D1mgL^-1的培养基中,愈伤组织诱导率可达100%。在含BA1~2mgL^-1+NAA0.1~0.5mgL^-1培养基中,可诱导产生不定芽。继代培养以改良毯+BA1mgL^-1+NAA0.5mgL^-1培养基的增殖系数最高。生根培养基以1/2MS+IBA2mg L^-1为最佳,生根率可达80%以上。试管苗移栽成活率为90%以上。 The rapid propagation of Enkianthus quinqueflouus Lour. had been established by using shoot-tip or stem with auxiliary buds as explants. The modified B5 medium as basal medium was optimum for callus induction. The callus induction rate was up to 100% cultured on Bsmedium with 1 mg L^-1 2,4-D. The adventitious buds were induced on 135 medium supplemented with 1- 2 mg L^-1BA + 0.1 -0.5 mg L^-1 NAA. Propagation coefficient was the highest when adventitious buds were subcultured on modified 135 + 1 mg L^-1 BA + 0.5 mg L^-1 NAA. The rooting could reach 80% when adventitious buds cultured on 1/2MS +2 mg L^-1 IBA, and the survival of plantlet could reach 90% after transferred into perlite bed.

关 键 词: 吊钟花 组织培养

领  域: [生物学]

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