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首页> 外文期刊>Plant Cell, Tissue and Organ Culture (PCTOC) >Agrobacterium-mediated transformation of alfalfa (Medicago sativa) using a synthetic cry3a gene to enhance resistance against alfalfa weevil
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Agrobacterium-mediated transformation of alfalfa (Medicago sativa) using a synthetic cry3a gene to enhance resistance against alfalfa weevil

机译:农杆菌介导的苜蓿(苜蓿(Medicago sativa))转化利用合成的cry3a基因增强了对苜蓿象鼻虫的抗性

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摘要

To introduce genetic resistance against alfalfa weevil (Hypera postica), leaves and petiole explants of three commercial alfalfa genotypes, including Km-27, Kk-14 and Syn-18 were transformed with Agrobacterium tumefaciens strains GV101, LBA4404 and AGL01. All the Agrobacterium strains used harbored the recombinant binary vector pBI121 containing a synthetic cry3a gene under the control of CaMV35S promoter as well as the nptII gene as selectable marker. Transformed explants were cultured on callus-induction medium, and the germinated somatic embryos were then transferred to the regeneration medium. The primary transformants were evaluated by PCR and Southern blot analysis. The results indicated successful integration of the target gene into the genomes of primary transgenic lines. Moreover, the expression of Cry3a protein in the transgenic plants was confirmed by ELISA method. Three transgenic lines, including TL6, TL8 and TL11 showed significantly higher levels of insect resistance against H. postica larvae (mortality rate of 73–90 % after infestation), in comparison with the control plants during the two-year bioassays. All transgenic plants were fertile and no irregular behavior in terms of growth and the morphological traits were observed. Transgenic plants developed during the course of this study are currently being grown in greenhouse and will be crossed with each other for seed production.
机译:为了引入对苜蓿象鼻虫(Hypera postica)的遗传抗性,用根癌土壤杆菌菌株GV101,LBA4404和AGL01转化了包括Km-27,Kk-14和Syn-18在内的三种商业苜蓿基因型的叶和叶柄外植体。所有使用的农杆菌菌株都含有重组二元载体pBI121,其包含在CaMV35S启动子控制下的合成cry3a基因以及作为选择标记的nptII基因。将转化的外植体培养在愈伤组织诱导培养基上,然后将发芽的体细胞胚转移到再生培养基上。通过PCR和Southern印迹分析评估初级转化体。结果表明靶基因成功整合到初级转基因品系的基因组中。此外,通过ELISA方法证实了Cry3a蛋白在转基因植物中的表达。与两年生化分析中的对照植物相比,包括TL6,TL8和TL11在内的三个转基因品系显示出对Post.H.postica幼虫的昆虫抗性水平显着更高(侵染后死亡率为73-90%)。所有转基因植物都是可育的,并且在生长方面没有观察到不规则行为,并且没有观察到形态特征。在这项研究过程中开发的转基因植物目前正在温室中生长,并将彼此杂交以产生种子。

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