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青稞类钙调素蛋白基因 CML19的克隆、序列分析及原核表达
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引用本文:韦泽秀,原红军,扎 桑,王玉林,徐齐君,曾兴权,尼玛扎西.青稞类钙调素蛋白基因 CML19的克隆、序列分析及原核表达[J].西北农业学报,2018,27(7):963~969
DOI:10.7606/j.issn.1004-1389.2018.07.006
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作者单位
韦泽秀,原红军,扎 桑,王玉林,徐齐君,曾兴权,尼玛扎西 (1.西藏自治区农牧科学院 农业资源与环境研究所拉萨 8500022.省部共建青稞和牦牛种质资源与遗传改良国家重点实验室拉萨 8500023.西藏自治区农牧科学院 农业研究所拉萨 8500024. 西藏自治区农牧科学院拉萨 850002) 
基金项目:西藏财政专项(2017CZZX001/2);西藏科技重大专项(Z2016B01N01)。
中文摘要:根据鉴定得到青稞类钙调素蛋白基因 CML19的序列设计引物,以青稞叶片的cDNA为模板,扩增得到目的片段,对目的基因序列进行鉴定和分析,进一步构建该基因的原核表达载体pET28a- CML19,转入大肠杆菌BL21(DE3),利用IPTG 诱导外源蛋白质表达并检测。结果表明,扩增得到 CML19的CDS序列全长为447 bp,编码的蛋白质含有148个氨基酸,分子质量为16.46 ku,理论等电点(pI)为4.40,总平均亲水性(GRAVY)为-0.176,不稳定系数为49.59,存在典型的EF手结构域;系统进化分析表明,青稞 CML19与山羊草具有较近的亲缘关系;原核表达蛋白结果显示,重组蛋白主要以包涵体形式存在于沉淀中。初步阐明青稞 CML19基因的序列特征,为进一步制备抗体、探讨 CML19基因的功能奠定基础。
中文关键词:青稞  类钙调素蛋白   CML19  序列分析  原核表达
 
Cloning, Sequence Analysis and Prokaryotic Expression of CaM-like Protein Gene CML19 from Tibetan Hulless Barley (Hordeum vulgare L.var.nudum HK.f.)
Abstract:The primers were designed according to the sequence of the identified Tibetan Hulless barley CaM-like protein gene CML19, and target fragment was amplified from the cDNA of the barley leaf. After that, target sequence was sequenced and analysed. Prokaryotic expression vector pET28a-CML19 was constructed and transformed into E. coli BL21(DE3). At the same time, positive bacteria was induced by IPTG to express and detect foreign proteins. The results showed that, the full CDS of CML19 was amplified and the size was 447 bp. According to the results of bioinformatics analysis, CML19 encodes a protein containing 148 amino acids with a relative molecular mass of 16.46 ku, a theoretical isoelectric point (pI) of 4.40, a total average hydrophilicity (GRAVY) of -0.176, an unstable coefficient of 49.59, aEF-hand domain. Phylogenetic analysis showed that the CML19 had a close genetic relationship with Aegilops tauschii. The results of protein expression showed that the recombinant protein was mainly precipitated in the form of inclusion bodies. In this study, we first elucidated the sequence characteristics of CML19 gene in Tibetan Hulless Barley, laying a foundation for further preparation of antibody and exploring the function of CML19 gene.
keywords:Tibetan Hulless barley  CaM-like protein   CML19  Sequence analysis  Prokaryotic expression
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