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甜叶菊叶片离体培养及试管无性系的建立 被引量:13

The Tissue Culture and Plantlet Regeneration in Vitro of Stevia Rebaudiana Bertoni
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摘要 研究了离体条件下甜叶菊 (Stivia 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 30 0 mg/L水解酪蛋白 .离体叶片在 BA0 .5mg/L和NAA0 .5mg/L的培养基上诱导形成愈伤组织 .在 BA0 .5mg/L和 NAA0 .0 5mg/L的培养基上可诱导愈伤组织分化不定芽 ,分化频率为 1 0 0 % .不定芽在 White基本培养基并附加 NAA0 .0 1 mg/L的培养基上诱导生根 ,生根率可达 1 0 0 % .炼苗后移栽 ,成活率达 95%以上 . 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.
出处 《上海师范大学学报(自然科学版)》 2000年第4期74-77,共4页 Journal of Shanghai Normal University(Natural Sciences)
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 Stevia rebaudiana Bertoni leaves callus plantlet regeneration in vitro
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参考文献5

  • 1徐沛楷.日本等国对甜叶菊的研究[J].国外抖技,10:31-34.
  • 2吴国柱.甜叶菊主要生物学特性的初步观察[J].江西农业科技,1984,7:22-26.
  • 3王凯基.甜叶菊离体茎诱导完整植株初报[J].植物生理学通讯,1980,(3):32-33.
  • 4樊映汉.甜叶菊(Stevia rebaudiana Beroni)的茎尖培养[J].植物生理学通讯,1981,(3):28-31.
  • 5DOLEV E. Control of vitrification in proliferating shoots of M26. in: Somers DA (ed). The Intrnarional Association for Pant Tissue Culture. 6th Inter . Cong . Plant Tissue Cell Culture Minneapolis, 1986. Minnesota : University of Minnesota, 1986, 242.

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