The Effect of Single Co-expression of The DnaK-DnaJ-GrpE and GroEL/ES Chaperones and Their Combination on Expression Intein-pretrombin-2 in Escherichia coli ER2566

I. Maksum, D Agus Yusuf Wildan, Khomaini Hasan, T. Subroto
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Abstract

The use of recombinant thrombin in the manufacture of fibrin glue allows diseases contamination to be avoided. However, the expression of recombinant protein in E. coli still has a disadvantage of the formation of inclusion bodies, so it needs to be minimized by co-expression of chaperones. Therefore, the aim of this study was to determine the effect of single DnaK-DnaJ-GrpE and GroEL/ES chaperone expression and their combination on the expression of intein-pretrombin-2Ti,pH on E. coli ER2566. The method started with isolation of pTWIN1-prethrombin-2Ti,pH and pG-KJE8 from E. coli TOP10F' and DH5α respectively, the co-transformation of the expression host E. coli ER2566 using pG-KJE8 and pTWIN1-prethrombin-2Ti,pHvectors, the chaperone co-expression was induced using L-Arabinosa before IPTG induction and cell culture growth was incubated at 22 oC. The expression products were characterized by using Sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS-PAGE) analysis. The results of the co-expression of chaperone showed that the number of soluble fraction was higher than the one without co-expression of chaperone. In addition, the co-expression of chaperone using pG-KJE8 in intein-prothrombin-2Ti,pH expression was sufficient using tetracycline as an inducer.
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dna - dnaj - grpe和GroEL/ES伴侣蛋白单共表达及其联合表达对大肠埃希菌ER2566中蛋白原-2表达的影响
重组凝血酶在纤维蛋白胶生产中的应用可以避免疾病污染。然而,重组蛋白在大肠杆菌中的表达仍然存在形成包涵体的缺点,因此需要通过伴侣蛋白的共表达来将其最小化。因此,本研究的目的是确定单个dna - dnaj - grpe和GroEL/ES伴侣蛋白表达及其联合表达对大肠杆菌ER2566上interin -pretrombin- 2ti、pH表达的影响。方法首先分别从大肠杆菌TOP10F′和DH5α中分离pTWIN1-prethrombin-2Ti、pH和pG-KJE8,用pG-KJE8和pTWIN1-prethrombin-2Ti、pHvectors共转化表达宿主大肠杆菌ER2566,在IPTG诱导前用L-Arabinosa诱导伴侣共表达,22℃培养细胞生长。表达产物采用十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)分析。伴蛋白共表达的结果表明,可溶性分数的数量高于未伴蛋白共表达的分数。此外,以四环素为诱导剂,pG-KJE8在凝血素- 2ti、pH中共表达伴侣蛋白是足够的。
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CiteScore
0.80
自引率
0.00%
发文量
15
审稿时长
24 weeks
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