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首页> 外文期刊>Plant Cell, Tissue and Organ Culture: An International Journal on in Vitro Culture of Higher Plants >Production of herbicide-resistant transgenic sweet potato plants through Agrobacterium tumefaciens method
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Production of herbicide-resistant transgenic sweet potato plants through Agrobacterium tumefaciens method

机译:通过根癌农杆菌法生产抗除草剂的转基因甘薯植物

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Transgenic herbicide-resistant sweet potato plants [Ipomoea batatas (L.) Lam.] were produced through Agrobacterium-mediated transformation system. Embryogenic calli derived from shoot apical meristems were infected with Agrobacterium tumefaciens strain EHA105 harboring the pCAMBIA3301 vector containing the bar gene encoding phosphinothricin N-acetyltransferase (PAT) and the gusA gene encoding (l-glucuronidase (GUS). The PPT-resistant calli and plants were selected with 5 and 2.5 mg 1(-1) PPT, respectively. Soil-grown plants were obtained 28-36 weeks after Agrobacterium-mediated transformation. Genetic transformation of the regenerated plants growing under selection was demonstrated by PCR, and Southern blot analysis revealed that one to three copies of the transgene were integrated into the plant genome of each transgenic plant. Expression of the bar gene in transgenic plants was confirmed by RT-PCR and application of herbicide. Transgenic plants sprayed with Basta containing 900 mg 1(-1) of glufosinate ammonium remained green and healthy. The transformation frequency was 2.8% determined by herbicide application which was high when compared to our previous biolistic method. In addition, possible problems with multiple copies of transgene were also discussed. We therefore report here a successful and reliable Agrobacterium-mediated transformation of the bar gene conferring herbicide-resistance and this method may be useful for routine transformation and has the potential to develop new varieties of sweet potato with several important genes for value-added traits such as enhanced tolerance to the herbicide Basta.
机译:通过农杆菌介导的转化系统生产了抗转基因除草剂的甘薯植物[Ipomoea batatas(L.)Lam。]。用根癌农杆菌菌株EHA105感染源自芽顶分生组织的胚性愈伤组织,该菌株带有pCAMBIA3301载体,该载体包含编码草丁膦N-乙酰基转移酶(PAT)的bar基因和编码(1-葡糖醛酸糖苷酶(GUS)的gusA基因。分别用5 mg和2.5 mg 1(-1)PPT选择土壤,在土壤杆菌介导的转化后28-36周获得土壤生长的植物,通过PCR和Southern blot分析证明了选择生长的再生植物的遗传转化结果表明,每株转基因植物的基因组中已整合了1-3个转基因,通过RT-PCR和除草剂的应用证实了bar基因在转基因植物中的表达,喷洒了含900 mg 1(-)的Basta的转基因植物。 1)草铵膦铵盐保持绿色,健康,经除草剂施用后转化率高达2.8%。与我们以前的射弹方法相比。另外,还讨论了转基因多拷贝的可能问题。因此,我们在这里报告成功而可靠的农杆菌介导的bar基因赋予除草剂抗性的转化,该方法可能对常规转化有用,并且具有开发甘薯新品种的潜力,该品种具有几个重要的增值性状基因增强了对除草剂Basta的耐受性。

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