赵龙;周贤轩;

• 1:合肥工业大学生物与食品工程学院

摘要(Abstract)：

[目的]获得大肠杆菌的Ⅱ型丙酮酸激酶。[方法]首先用MEGA7软件对不同生物丙酮酸激酶的编码基因进行聚类分析;通过聚合酶链式反应(PCR)扩增了大肠杆菌的Ⅱ型丙酮酸激酶基因pykA,将其克隆到pET_28a载体中,构建了重组质粒载体pET_28a-pyk A并在大肠杆菌BL21中实现了Ⅱ型丙酮酸激酶(PykA)的高效表达;利用镍柱亲和层析系统纯化了PykA蛋白,并进行了高效液相色谱(HPLC)检测。[结果]聚类分析结果表明,大肠杆菌Ⅱ型丙酮酸激酶与其他原核生物的丙酮酸激酶氨基酸序列具有高度同源性。HPLC检测发现Ⅱ型丙酮酸激酶Pyk A在体外可以高效地将ADP转化为ATP。[结论]该研究获得了Ⅱ型丙酮酸激酶,为ATP的合成以及Ⅱ型丙酮酸激酶为基础的ATP再生系统的研究提供了参考。

关键词(KeyWords)： Ⅱ型丙酮酸激酶;蛋白表达;高效液相色谱;大肠杆菌;ATP再生系统

Abstract:

Keywords:

基金项目(Foundation):

作者(Author): 赵龙;周贤轩;

Email:

DOI: 10.13989/j.cnki.0517-6611.2017.25.045

参考文献(References)：

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