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首页> 外文期刊>The Indian Journal of Agricultural Sciences >Cloning and heterologous expression of Os-AP2/ERF-N22 drought inducible rice transcription factor in E-coli
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Cloning and heterologous expression of Os-AP2/ERF-N22 drought inducible rice transcription factor in E-coli

机译:O-AP2 / ERF-N22干旱诱导型诱导型 - COLI诱导水稻转录因子的克隆与异源表达

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摘要

AP2/ERF a plant specific transcription factor plays a crucial role in the expression and regulation of abiotic stress related genes. In this study, we have characterized a rice transcription factor named Os-AP2/ERF-N22. It contains single AP2 domain which spans from 5th to 70th amino acid residue in the protein which is 243 amino acid residue long. The partial sequence of the gene encoding Os-AP2/ERF transcription factor was amplified and cloned into pET29a bacterial expression vector. The histidine-tagged truncated Os-AP2/ERF-N22 protein was expressed in BL21(DE3) strain of E. coli after induction with 0.5mM IPTG. A time course induction study was used to optimize the protein expression and the recombinant Os-AP2/ERF-N22 was purified using Ni-NIA agarose column chromatography. The 26.74 kDa recombinant Os-AP2/ERF-N22 was visualized using SDS-PAGE analysis and its expression was further confirmed by western blot analysis using anti-his primary antibody and alkaline phosphatase conjugated secondary antibody. Antibody against the purified truncated AP2/ERF-N22 was custom synthesized and it was used to quantitate the expression of Os-AP2/ERF-N22 transcription factor in rice at the protein level.
机译:AP2 / ERF植物特异性转录因子在非生物应激相关基因的表达和调节中起着至关重要的作用。在这项研究中,我们表征了名为OS-AP2 / ERF-N22的水稻转录因子。它含有单个AP2结构域,其在蛋白质中的第5至第70氨基酸残基跨越243氨基酸残基。扩增编码OS-AP2 / ERF转录因子的基因的部分序列并克隆到PET29A细菌表达载体中。组氨酸标记的截短的OS-AP2 / ERF-N22蛋白在用0.5mM IPTG诱导后在大肠​​杆菌的BL21(DE3)菌株中表达。使用时间过程诱导研究优化蛋白质表达,并使用Ni-NiA琼脂糖柱色谱法纯化重组OS-AP2 / ERF-N22。使用SDS-PAGE分析可视化26.74kDA重组OS-AP2 / ERF-N22,并使用抗他的原发性抗体和碱性磷酸酶共轭二抗进一步证实其表达。纯化截短的AP2 / ERF-N22的抗体是定制的合成,它用于定量蛋白质水平在水稻中的OS-AP2 / ERF-N22转录因子的表达。

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