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[大车前体外再生体系的建立与优化]

[Establishment and optimization of in vitro regeneration system for Plantago major L].

作者信息

Li Ping, Chen Hua, Li Yin-Xin

机构信息

Key Laboratory of Photosynthesis and Environmental Molecular Physiology, Institute of Botany, The Chinese Academy of Sciences, Beijing, 100093.

出版信息

Sheng Wu Gong Cheng Xue Bao. 2005 Nov;21(6):916-22.

PMID:16468346
Abstract

Plantago major is not only used as medicinal herb but also an important model plant of ecology. Little work has been reported on the tissue culture of P. major. A reproducible system for direct shoot morphogenesis and callus induction of Plantago major L. 'Giant Turkish' was described. Using seed as explants, the adventitious buds were obtained 4 to 5 weeks following incubation on MS medium supplemented with 0.2 mg/L IAA and 1.0 mg/L TDZ. The frequency of adventitious buds was as high as 100%. The average number of buds per explant was 14.6. Random amplified polymorphic DNA analysis on 9 regenerants indicated that somaclonal variation occurred at DNA level. Using leaves as explants, calli were easily induced on MS medium supplemented with 1.0 mg/L NAA 3 weeks following inoculation. The frequency of callus induction can be as high as 98%. On MS medium containing 4.0 mg/L 6-BA, 25% of calli differentiated and the mean number of buds per piece of callus was 2.8. The buds developed roots on 11/2 MS medium and formed plantlets, 90% of which survived when transplanted to greenhouse.

摘要

大车前不仅被用作草药,也是一种重要的生态模式植物。关于大车前组织培养的报道较少。本文描述了一种可重复的大车前‘巨型土耳其’直接芽形态发生和愈伤组织诱导体系。以种子为外植体,在添加0.2 mg/L IAA和1.0 mg/L TDZ的MS培养基上培养4至5周后获得不定芽。不定芽发生率高达100%。每个外植体平均芽数为14.6。对9个再生植株进行随机扩增多态性DNA分析表明,在DNA水平上发生了体细胞克隆变异。以叶片为外植体,接种3周后在添加1.0 mg/L NAA的MS培养基上很容易诱导出愈伤组织。愈伤组织诱导率可高达98%。在含有4.0 mg/L 6 - BA的MS培养基上,25%的愈伤组织分化,每块愈伤组织平均芽数为2.8。芽在1/2MS培养基上生根并形成植株,其中90%移栽到温室后存活。

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