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首页> 外文期刊>Current Journal of Applied Science and Technology >Recombinant Coat Protein of Banana Bract Mosaic Virus as a Potential Antigen for Serological Detection of the Virus
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Recombinant Coat Protein of Banana Bract Mosaic Virus as a Potential Antigen for Serological Detection of the Virus

机译:香蕉苞片镶嵌病毒的重组涂层蛋白作为病毒血清学检测的潜在抗原

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摘要

Banana bract mosaic disease caused by Banana bract mosaic potyvirus (BBrMV) is reported to instigate heavy loss in banana and plantain across Asia. Almost all the cultivars of banana succumb to the disease resulting in malformed bunches weighing less than half of normal ones. In the current study the coat protein (CP) gene segment present at the 3’ terminal region of the viral genome amplified by RT-PCR was cloned into expression vectors, pRSET-C and pGEX-4T-2 to use it for raising polyclonal antiserum which in turn will aid in developing assays to detect the virus. Recombinant BBrMV CP (rCP) in pRSET-C when expressed was insoluble whereas, it was in the soluble fraction when expressed from pGEX-4T-2. The GST-fusion protein was purified by GSH sepharose affinity column chromatography and western blot analysis was performed using anti GST antibodies. 360 μg/ml of protein was purified from 1 l of culture. The GST tag was cleaved from the purified protein by incubation with thrombin at 25°C overnight.? The rCP was characterized using ultracentrifugation, fluorescence spectroscopy and electron microscopy. The tagless monomer failed to assemble to virus like particles (VLPs) in vitro which was substantiated by fluorescence spectroscopy. This study will be first step towards deciphering structure and functions of Banana bract mosaic virus coat protein.
机译:据报道,香蕉苞片卷曲卷虫菌(BBRMV)引起的香蕉苞片褪色疾病,以在亚洲的香蕉和植物群中煽动重型损失。几乎所有的香蕉品种都屈服于疾病,导致畸形的串,重量不到正常的一半。在目前研究中,将存在于将RT-PCR扩增的病毒基因组的3'末端区域的涂层蛋白(CP)基因片段克隆到表达载体中,PRSET-C和PGEX-4T-2以使用它来延长多克隆抗血清这反过来将有助于开发测定以检测病毒。当表达时,在Putsex-C的重组BBRMV CP(RCP)在从PGEX-4T-2表达时在可溶性级分中。通过GSH Sepharose亲和柱色谱法纯化GST-融合蛋白,使用抗GST抗体进行蛋白质印迹分析。从1L培养物中纯化360μg/ ml蛋白质。通过在25℃下与凝血酶孵育过夜,通过与凝血酶孵育来从纯化的蛋白质中切割GST标签。使用超速离心,荧光光谱和电子显微镜表征RCP。标签单体未能组装到体外颗粒(VLP)等病毒,其通过荧光光谱证实。本研究将迈出朝向香蕉苞片镶嵌病毒外套蛋白的破译结构和功能的第一步。

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