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Efficient Biolistic Transformation and Regeneration Capacity of an EgTCTP Transgene in Protocorm-like Bodies of Phalaenopsis Orchid

机译:蝴蝶兰原球茎样体中EgTCTP转基因的高效基因枪转换和再生能力。

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An efficient genetic transformation system using the biolistic method and protocorm-like bodies (PLBs) of Phalaenopsis orchidwas established for introducing the EgTCTP gene obtained from oil palm leaves. A pCAMBIA 1302 vector containing the greenfluorescent protein (mgfp5) as reporter gene and the selectable marker hygromycin phosphotransferase (hpt) gene under the cauliflowermosaic virus (CaMV) 35S promoter were used in this experiment. The transformed PLBs were cultured on MS medium containing 20mg/L hygromycin for 2 months. The surviving PLBs with green fluorescence spots were used to calculate a transformation frequency(93.34%). PLBs containing the transformed EgTCTP gene had the highest percentage of regeneration frequency (95.66%) and numbersof regenerated shoots per explant (3.78?±1.89 shoots) compared to the control. The time required for initiation of primordial shoots inthe transformed PLBs (55.22?±26.56 days) was much shorter than for the control. Evaluation of the regeneration efficiency, determinedthat the status of the EgTCTP transformants was above average: score=4.04?±0.88. The EgTCTP gene was detected in the PLBs overa period of at least 6 months with subculturing every 4 weeks. The stability of the transgenes within the PLBs was confirmed by PCRand this indicated that the transgenes had been integrated into the genome of the transformants. This is the first successful report tointroduce EgTCTP gene into PLBs of Phalaenopsis orchid.
机译:建立了利用生物枪法和蝴蝶兰原球茎样体(PLBs)的有效遗传转化系统,用于导入从油棕叶中获得的EgTCTP基因。在该实验中,使用了以绿色荧光蛋白(mgfp5)为报告基因的pCAMBIA 1302载体和花椰菜花叶病毒(CaMV)35S启动子下的选择标记潮霉素磷酸转移酶(hpt)基因。将转化的PLB在含有20mg / L潮霉素的MS培养基上培养2个月。存活的带有绿色荧光斑点的PLB用于计算转化频率(93.34%)。与对照相比,含有转化的EgTCTP基因的PLB具有最高的再生频率百分比(95.66%)和每个植株的再生芽数(3.78?±1.89个芽)。在转化的PLBs中初生芽萌发所需的时间(55.22±26.56天)比对照的要短得多。评估再生效率,确定EgTCTP转化体的状态高于平均水平:得分=4.04≤±0.88。每4周传代培养至少6个月,在PLB中检测到EgTCTP基因。通过PCR证实了转基因在PLBs内的稳定性,这表明转基因已经整合到转化体的基因组中。这是将EgTCTP基因导入蝴蝶兰PLBs的第一个成功报告。

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