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      Cloning, expression and purification of the methionine-S-sulfoxide reductase gene of Giardia lamblia

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          Abstract

          Objective To clone and express the methionine-S-sulfoxide reductase gene of the Giardia lamblia ( GLMSR), and obtain the recombinant GlMSR protein.

          Methods According to the GLMSR gene homologous sequences in GenBank, the specific primers were designed. Using the genomic DNA of Giardia lamblia Chinese C2 as template, the MSR gene was amplified by PCR and was inserted into the expression vector pET28a to generate pET28a-Glmsr. The pET28a-Glmsr was transformed into E. coli JM109. The positive clone was selected and identified by sequencing. The expression vector pET28a-Glmsr was transformed into E. coli BL21 (DE3) by chemical method. The expression of Glmsr was induced by isopropyl thiogalactoside (IPTG). The expression of the recombinant protein was analyzed by SDS-PAGE. Recombinant proteinin the sediment was collected and purified by Ni 2+ affinity chromatography and verified by Western blotting.

          Results The electrophoresis result showed that there was a DNA band of approximately 624 bp, meant that the GLMSR gene sequences were obtained. The recombinant expression vector was constructed and identified by PCR, enzyme digestion and sequencing. The above results were all consistent with expectation. The recombinant protein’s molecular mass (Mr) is approximately 25 000, which was consistent with expectation (22 800). The results of SDS-PAGE showed that the recombinant protein was expressed in the sediment. The result of Western blotting showed that the recombinant protein can be recognized by anti-His-tag antibody.

          Conclusion In this study, we successfully cloned the GLMSR gene coding sequence of Giardia lamblia and obtained the purified recombinant protein.

          Abstract

          摘要: 目的 蓝氏贾第鞭毛虫 (简称为贾第虫) 甲硫氨酸硫氧化物还原酶基因 ( GlMSR), 进行原核表达获得其重组 蛋白。 方法 依据GenBank中 GlMSR 序列设计引物, 以贾第虫中国C2 克隆株基因组DNA 为模板, 通过PCR扩增编码 序列, 将所得片段连接至质粒pET28a 以构建原核表达载体pET28a-GlMSR, 将pET28a-GlMSR 导入大肠杆菌 E.coli JM109并挑取阳性克隆进行基因测序和鉴定。用化学方法将经测序验证的重组质粒pET28a-GlMSR转化至 E.coli BL21 (DE3) 。经异丙基硫代半乳糖苷 (Isopropyl β-D-Thiogalactoside, IPTG) 诱导表达后, 聚丙烯酰胺凝胶电泳检测重组蛋白 表达结果。收集沉淀中的重组表达产物, 镍柱亲和层析纯化带组氨酸标签的重组蛋白, 并通过免疫印迹鉴定纯化结 果。 结果电泳结果显示在约624 bp处出现目的DNA条带, 表明成功得到 GlMSR 编码序列; PCR 鉴定、酶切鉴定以及 基因测序结果表明成功构建重组表达载体pET28a- GlMSR, 经IPTG诱导后在沉淀中获得目的蛋白, 目的蛋白分子量 (Mr) 约为25 000, 与预期分子量 (Mr) 22 800基本相符。经Western blot分析显示该重组蛋白含有His6标签。 结论本 研究克隆、表达了蓝氏贾第虫GlMSR基因, 并纯化获得重组蛋白, 为进一步探索该酶的功能奠定了基础。

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          Author and article information

          Journal
          CTM
          China Tropical Medicine
          China Tropical Medicine (China )
          1009-9727
          01 November 2019
          01 January 2020
          : 19
          : 11
          : 1014-1017
          Affiliations
          1Medical School of Dalian University, Dalian, Liaoning 116622, China
          Author notes
          *Corresponding author: WANG Yunhua, E-mail: yunhua1977@ 123456126.com
          Article
          j.cnki.46-1064/r.2019.11.02
          10.13604/j.cnki.46-1064/r.2019.11.02
          © 2019 Editorial Department of China Tropical Medicine

          This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 Unported License (CC BY-NC 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. See https://creativecommons.org/licenses/by-nc/4.0/.

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