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甜叶菊叶片离体培养及试管无性系的建立
引用本文:娄玉霞,,宋磊 等. 甜叶菊叶片离体培养及试管无性系的建立[J]. 上海师范大学学报(自然科学版), 2000, 29(4): 74-77
作者姓名:娄玉霞    宋磊 等
作者单位:上海师范大学,生物与化学工程学院,上海奉贤,201418
摘    要:研究了离体条件下甜叶菊(Stiuia rebaudiana Bertoni)叶片愈伤组织诱导和植株再生技术,离体培养以MS为基本培养基并附加300mg/L水解酪蛋白,离体叶片在BA 0.5mg/L和NAA 0.5mg/L的培养基上诱导形成愈伤组织,在BA 0.5mg/L和NAA0.05mg/L的培养基上可诱导愈伤组织分化不定芽,分化频率为100%,不定芽在White基本培养基并附 加NAA0.01mg/L的培养基上诱导生根,生根率可达100%,炼苗后移栽,成活率达95%以上。

关 键 词:甜叶菊 叶片 愈伤组织 再生植株 离体培养 试管无性系
文章编号:1000-5137(2000)04-0074-04
修稿时间:2000-07-03

The Tissue Culture and Plantlet Regeneration in Vitro of Stevia Rebaudiana Bertoni
LOU Yu-xia,SONG Lei,LI Xin-guo,CHENG Guo-fu. The Tissue Culture and Plantlet Regeneration in Vitro of Stevia Rebaudiana Bertoni[J]. Journal of Shanghai Normal University(Natural Sciences), 2000, 29(4): 74-77
Authors:LOU Yu-xia  SONG Lei  LI Xin-guo  CHENG Guo-fu
Abstract:The research of callus induction and plantlet regeneration in vitro of Stevia rebaudiana Bertoni was carried out using the tender leaves and MS medium as the basic medium. The effects of plant growth regulators on the plantlet regeneration were compared. Callus can be induced from the excised leaves that were cultured on the basic medium supplemented with 0.5 mg/L BA and 0.5 mg/L NAA. For the adventitious bud regeneration of the callus, supplement with 0.5 mg/L BA and 0.05 mg/L NAA was appropriate, giving a regeneration frequency of 100%. Rooting occurred on the White medium supplemented with 0.01 mg/L NAA. The rooting rate could reach up to 100%. The technique of somatic cell cloning of Stevia rebaudiana Bertoni was established in vitro.
Keywords:Stevia rebaudiana Bertoni  leaves  callus  plantlet regeneration in vitro
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