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Super-Agrobacterium ver. 4: Improving the Transformation Frequencies and Genetic Engineering Possibilities for Crop Plants

机译:超级农杆菌ver。 4:提高农作物的转化频率和基因工程可能性

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摘要

Agrobacterium tumefaciens has been utilized for both transient and stable transformations of plants. These transformation methods have been used in fields such as breeding GM crops, protein production in plant cells, and the functional analysis of genes. However, some plants have significantly lower transient gene transfer and stable transformation rates, creating a technical barrier that needs to be resolved. In this study, Super-Agrobacterium was updated to ver. 4 by introducing both the ACC deaminase (acdS) and GABA transaminase (gabT) genes, whose resultant enzymes degrade ACC, the ethylene precursor, and GABA, respectively. A. tumefaciens strain GV2260, which is similar to other major strains (EHA105, GV3101, LBA4404, and MP90), was used in this study. The abilities of the Super-Agrobacterium ver. 4 were evaluated in Erianthus ravennae, Solanum lycopersicum “Micro-Tom,” Nicotiana benthamiana, and S. torvum. Super-Agrobacterium ver. 4 showed the highest T-DNA transfer (transient transformation) frequencies in E. ravennae and S. lycopersicum, but not in N. benthamiana and S. torvum. In tomato, Super-Agrobacterium ver. 4 increased the stable transformation rate by 3.6-fold compared to the original GV2260 strain. Super-Agrobacterium ver. 4 enables reduction of the amount of time and labor required for transformations by approximately 72%, and is therefore a more effective and powerful tool for plant genetic engineering and functional analysis, than the previously developed strains. As our system has a plasmid containing the acdS and gabT genes, it could be used in combination with other major strains such as EHA105, EHA101, LBA4404, MP90, and AGL1. Super-Agrobacterium ver. 4, could thus possibly be a breakthrough application for improving basic plant science research methods.
机译:根癌农杆菌已用于植物的瞬时和稳定转化。这些转化方法已用于诸如转基因作物的育种,植物细胞中蛋白质的生产以及基因的功能分析等领域。但是,某些植物的瞬时基因转移和稳定的转化率显着降低,从而产生了需要解决的技术障碍。在这项研究中,将超级农杆菌更新为ver.。通过引入ACC脱氨酶(acdS)和GABA转氨酶(gabT)基因,可将其分解为ACC,乙烯前体和GABA,从而分别引入图4所示的基因。本研究使用了与其他主要菌株(EHA105,GV3101,LBA4404和MP90)相似的根癌农杆菌GV2260。超级农杆菌ver。在Erianthus ravennae,Solanum lycopersicum“ Micro-Tom”,Nicotiana benthamiana和S. torvum中评估了4种。超级农杆菌ver。图4显示了在R. ravennae和S. lycopersicum中最高的T-DNA转移(瞬时转化)频率,但在N. benthamiana和S. torvum中没有。在番茄中,超级农杆菌ver。与原始GV2260菌株相比,图4的稳定转化率提高了3.6倍。超级农杆菌 ver。 4使转化所需的时间和劳动力减少了约72%,因此,与以前开发的菌株相比,它是用于植物基因工程和功能分析的更有效和强大的工具。由于我们的系统有一个包含 acdS gabT 基因的质粒,因此可以与其他主要菌株(例如EHA105,EHA101,LBA4404,MP90和AGL1)结合使用。超级农杆菌 ver。因此,图4可能是改进基础植物科学研究方法的突破性应用。

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