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Transgenic tomato line expressing modified Bacillus thuringiensis cry1Ab gene showing complete resistance to two lepidopteran pests

机译:表达改良的苏云金芽孢杆菌cry1Ab基因的转基因番茄品系对两种鳞翅目害虫具有完全抗性

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摘要

The modified truncated Bt-cry1Ab gene of Bacillus thuringiensis has been used for the development and selection of over expressing transgenic events in a commercially important variety of tomato (Solanum lycopersicum L.) by Agrobacterium-mediated leaf-disc transformation procedure. The integration and inheritance of cry1Ab gene in T0 transgenic plants and their progenies were determined by PCR, RT-PCR and Southern blot hybridization analysis. The toxin expression was monitored by double antibody sandwich enzyme-linked immunosorbent assay (DAS-ELISA). The transgenic line Ab25 E, expressing 0.47 ± 0.01% Cry1Ab toxin of total soluble protein (TSP) was finally selected in the T4 generation from the segregating population, showing 100% mortality to the second instar larvae of H. armigera and S. litura and minimal damages to leaves and fruits. Southern blot analysis data revealed single copy introgression of cry1Ab gene in highly-expressing Ab25 E transgenic line and expression of Cry1Ab toxin of molecular mass ~65 kDa was evident in Western blot analyses in transgenic plants of T4, T5 and T6 generation. Receptor binding assay performed with partially purified Cry1Ab protein from Ab25 E transgenic tomato line, confirmed efficient protein-protein interaction of Cry1Ab toxin with receptor(s) of both the insects. The higher level of Cry1Ab toxin (≈ 0.47 ± 0.01% TSP) did not affect the normal in vitro regeneration, plant development and fruit yield in this transgenic line. This high expressing Cry1Ab homozygous transgenic line can be a useful candidate in tomato breeding programmes for introgression of important agronomical traits.Electronic supplementary materialThe online version of this article (doi:10.1186/2193-1801-3-84) contains supplementary material, which is available to authorized users.
机译:苏云金芽孢杆菌的修饰的截短的Bt-cry1Ab基因已被用于通过农杆菌介导的叶盘转化程序开发和选择商业上重要的番茄品种(Solanum lycopersicum L.)中过表达的转基因事件。通过PCR,RT-PCR和Southern blot杂交分析确定cry1Ab基因在T0转基因植物及其后代中的整合和遗传。通过双抗体夹心酶联免疫吸附测定(DAS-ELISA)监测毒素表达。最终从分离群体的T4代中选择了表达总可溶性蛋白(TSP)的0.47%±0.01%Cry1Ab毒素的转基因Ab25 E,显示其对棉铃虫和斜纹夜蛾第二龄幼虫的死亡率为100%。对叶子和果实的损害最小。 Southern印迹分析数据显示,在高表达Ab25 E转基因株系中cry1Ab基因的单拷贝渗入,在T4,T5和T6代转基因植物的Western印迹分析中,分子质量约为65kDa的Cry1Ab毒素表达明显。用来自Ab25 E转基因番茄品系的部分纯化的Cry1Ab蛋白进行的受体结合测定,证实了Cry1Ab毒素与两种昆虫的受体的有效蛋白-蛋白相互作用。较高水平的Cry1Ab毒素(≈0.47±±0.01%TSP)不影响该转基因品系的正常体外再生,植物发育和果实产量。这种高表达的Cry1Ab纯合转基因品系可能是重要育种性状渗入番茄育种计划的有用候选物。电子补充材料本文的在线版本(doi:10.1186 / 2193-1801-3-84)包含补充材料,该材料是可供授权用户使用。

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