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[利用杆状病毒表达系统直接表达猪睾丸3α/β(20β)-羟基类固醇脱氢酶cDNA]

[Direct expression of the pig testicular 3 alpha/beta(20 beta)- hydroxysteroid dehydrogenase cDNA using baculovirus expression system].

作者信息

Nakajin S, Nakajima T, Uchida M, Shinoda M

机构信息

Faculty of Pharmaceutical Sciences, Hoshi University, Tokyo, Japan.

出版信息

Yakugaku Zasshi. 1995 Apr;115(4):344-50. doi: 10.1248/yakushi1947.115.4_344.

Abstract

The direct expression of the pig testicular 3 alpha/beta(20 beta)- hydroxysteroid dehydrogenase (HSD) cDNA using a baculovirus expression system was investigated. A minimum essential cDNA containing the coding region of 3 alpha/beta(20 beta)-HSD was amplified by polymerase chain reaction (PCR) to extend the DNA linker including the Bam HI restriction site in the both ends of the cDNA. As the template, 3 alpha/beta(20 beta)-HSD cDNA, pBS 52, which was subcloned to Bluescript II was used. The PCR fragment was ligated to Bam HI-cut transfer plasmid (pBlueBac III). Recombinant transfer plasmid (pBlueBac-20 beta) constructed was cotransfected into Spodoptera frugiperda Sf-9 cells with the baculovirus. After transfection, the recombinant virus was detected by the plaque assay with color selection. The expression of 3 alpha/beta(20 beta)-HSD cDNA was detected by Western blotting and enzyme assay. The expressed protein showed the same molecular weight and immunochemical cross-reaction to the native enzyme. Furthermore, it had 3-keto reductase activity of 3 alpha/beta(20 beta)-HSD for 5 alpha-dihydrotestosterone and 20-keto reductase activity for 17 alpha-hydroxyprogesterone in the presence of NADPH.

摘要

利用杆状病毒表达系统对猪睾丸3α/β(20β)-羟基类固醇脱氢酶(HSD) cDNA的直接表达进行了研究。通过聚合酶链反应(PCR)扩增包含3α/β(20β)-HSD编码区的最小必需cDNA,以延伸cDNA两端包含Bam HI限制性位点的DNA接头。以亚克隆到pBS 52的3α/β(20β)-HSD cDNA为模板,将其亚克隆到Bluescript II中。将PCR片段连接到经Bam HI酶切的转移质粒(pBlueBac III)上。构建的重组转移质粒(pBlueBac-20β)与杆状病毒共转染到草地贪夜蛾Sf-9细胞中。转染后,通过带有颜色选择的噬斑测定法检测重组病毒。通过蛋白质印迹法和酶活性测定法检测3α/β(20β)-HSD cDNA的表达。表达的蛋白与天然酶具有相同的分子量和免疫化学交叉反应。此外,在NADPH存在的情况下,它对5α-二氢睾酮具有3α/β(20β)-HSD的3-酮还原酶活性,对17α-羟基孕酮具有20-酮还原酶活性。

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