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首页> 外文期刊>Molecular biology reports >Molecular cloning and characterization of a mannose-binding lectin gene from Pinellia cordata
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Molecular cloning and characterization of a mannose-binding lectin gene from Pinellia cordata

机译:半夏甘露糖结合凝集素基因的分子克隆与鉴定

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Using RNA extracted from Pinellia cordata young leaves and primers designed according to the conserved regions of Araceae lectins, the full-length cDNA of Pinellia cordata agglutinin (PCL) was cloned by rapid amplification of cDNA ends (RACE). The full-length cDNA of pcl was 1,182 bp and contained a 768 bp open reading frame (ORF) encoding a lectin precursor of 256 amino acids. Through comparative analysis of pcl gene and its deduced amino acid sequence with those of other Araceae species, it was found that pcl encoded a precursor lectin with signal peptide. PCL is a mannose-binding lectin with three mannose-binding sites. Semi-quantitative RT-PCR analysis revealed that pcl is expressed in all tested tissues including leaf, stem and bulbil, but with the highest expression in bulbil. PCL protein was successfully expressed in Escherichia coli with the molecular weight expected.
机译:使用从半夏幼叶中提取的RNA和根据天南星凝集素保守区设计的引物,通过快速扩增cDNA末端(RACE)克隆半夏凝集素(PCL)的全长cDNA。 pc1的全长cDNA为1182 bp,包含一个768 bp的开放阅读框(ORF),编码256个氨基酸的凝集素前体。通过对pcl基因及其推导的氨基酸序列与其他天南星科物种的比较,发现pcl编码带有信号肽的前体凝集素。 PCL是具有三个甘露糖结合位点的甘露糖结合凝集素。半定量RT-PCR分析显示pcl在所有测试的组织中都表达,包括叶,茎和球茎,但在球茎中表达最高。 PCL蛋白已在大肠杆菌中成功表达,具有预期的分子量。

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