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    ‘京枣39’离体叶片高效再生体系的建立

    Establishment of high-efficiency regeneration system from in vitro leaves of ‘Jingzao 39’

    • 摘要:
        目的  ‘京枣39’是一种优质的枣鲜食新品种,目前尚无有效的离体再生体系,影响了自根苗的培育和苗木纯度。为了解决枣遗传转化效率低等问题,本研究探究了枣叶片再生的不同影响因素,以期建立高效的叶片再生体系。
        方法  以‘京枣39’组培苗叶片为试材,研究了不同接种方式、基本培养基种类、植物生长调节剂种类和浓度配比对离体叶片直接诱导不定芽再生的影响。
        结果  正交试验结果表明:叶片正放的接种方式再生率远高于叶片反放,是‘京枣39’叶片再生不定芽的最佳放置方式;基本培养基对‘京枣39’叶片再生的影响要大于植物生长调节剂,且最优培养基为1/2 MS,最佳植物生长调节剂为细胞分裂素6-BA,本研究确立的‘京枣39’组培苗叶片再生的最优体系为1/2 MS + 1 mg/L噻苯隆 + 0.5 mg/L 6-BA + 0.2 mg/L NAA + 30 g/L麦芽糖 + 6 g/L琼脂,再生率可达79.17%,平均每叶片再生不定芽能达到4.67个。进而初探并建立了‘京枣39’组培苗的最佳扩繁体系为:MS + 20 g/L麦芽糖 + 6 g/L琼脂 + 3 mg/L 6-BA + 0.1 mg/L NAA,分枝率高达88%,平均分枝数达2.76枝;以及最适生根体系为:1/2MS + 20 g/L蔗糖 + 8 g/L琼脂 + 1.5 mg/L IBA + 0.3 mg/L NAA,生根率达90.91%,平均根长达4.08 cm。
        结论  ‘京枣39’叶片再生效率受外界影响因素很大,尤其是基本培养基种类和接种方式,且每个因素都不是独立起作用的。本研究为之后以‘京枣39’叶片为转基因材料进行枣相关基因功能验证建立了完整的培育体系,同时为加快枣的相关研究进程奠定基础。

       

      Abstract:
        Objective   ‘Jingzao 39’ is a new high-quality jujube variety. There is no effective regeneration system in vitro at present, which affects the cultivation of self-rooted seedlings and the purity of seedlings. In order to solve the problems of low genetic transformation efficiency of jujube, different influencing factors of jujube leaf regeneration were explored in this study, in order to establish an efficient leaf regeneration system.
        Method   Using the leaves of tissue cultured seedlings of ‘Jingzao 39’ as experimental materials, the effects of different inoculation methods, types of basic culture medium, types and concentration ratio of plant growth regulators on the direct induction of adventitious bud regeneration from detached leaves were studied.
        Result   The results showed that the regeneration rate of the inoculation method with the leaves being placed upward was much higher than that of back up, which was the best placement method for the regeneration of adventitious buds from leaves of ‘Jingzao 39’. The effect of basic culture medium on leaf regeneration of ‘Jingzao 39’ was greater than that of plant growth regulator, and the optimal basic medium and plant growth regulator were 1/2 MS and cytokinin 6-BA, respectively. The optimal regeneration system for leaves of ‘Jingzao 39’ tissue cultured seedlings established in this study was 1/2 MS medium + 1.0 mg/L thiabenduron + 0.5 mg/L 6-BA + 0.2 mg/L NAA + 30 g/L maltose + 6 g/L agar, an average of 4.67 adventitious buds could be regenerated for each leaf. Then, the optimal propagation system of ‘Jingzao 39’ tissue culture seedlings was initially explored and established: MS + 20 g/L maltose + 6 g/L agar + 3.00 mg/L 6-BA + 0.10 mg/L NAA, with the branching rate up to 88%, and the average branch number of 2.76; the most suitable rooting medium was: 1/2MS + 20 g/L sucrose + 8 g/L agar + 1.50 mg/L IBA + 0.30 mg/L NAA, with rooting rate of 90.91%, and the average root length up to 4.08 cm.
        Conclusion   The leaf regeneration efficiency of ‘Jingzao 39’ is greatly influenced by external factors, especially the basic medium type and inoculation method, and each factor does not play an independent role. This study establishes a complete cultivation system for the functional verification of interested gene with the leaves of ‘Jingzao 39’ as transgenic materials, and lays a foundation for accelerating the jujube research process.

       

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