摘要
探索以包涵体形式表达的重组蛋氨酸裂解酶的纯化、复性方法,并对其活性进行检测。将阴道毛滴虫蛋氨酸裂解酶重组表达载体PET-15b-mgl1转化大肠杆菌BL21,经异丙基-β-D-硫代半乳糖苷(IPTG)诱导,并对表达条件进行优化,获得大量表达。通过对包涵体的纯化及复性研究,检测重组蛋氨酸裂解酶的免疫活性及酶活性。Western blotting结果表明,重组蛋氨酸裂解酶免疫小鼠制备的多抗可以和从阴道毛滴虫中提取的天然蛋氨酸裂解酶发生特异性反应。活性检测结果显示复性蛋氨酸裂解酶有活性,复性效率达到25%左右。以包涵体形式表达的蛋氨酸裂解酶经变性、纯化及复性后,获得大量有活性的酶,为深入了解其结构、功能及酶学性质,开展其在临床检测中的应用研究奠定基础。
It was to study the purification,renaturation and activity of recombinant Methionine γ-Lyase expressed as inclusion body in E.coli.The E.coli BL21 transformed with PET-15b-mgl1 was cultured and induced by IPTG.The best expression condition of recombinant Methionine γ-Lyase was decided by screening.The purification and renaturation of recombinant Methionine γ-Lyase were explored and the activity was tested. It was proved by Western blotting that the antiserum of Mice immunized with purified Methionine γ-Lyase could specially bind to wild Methionine γ-Lyase purified from Trichomonas vaginalis.Renatured Methionine γ-Lyase with 25% biological activity was prepared after being dissolved,purified and renatured.The results indicate that recombinant MGL expressed as inclusion body retained satisfactory activity after renaturation,suggesting potential efficacy in the research on structure,function,character and clinical trials.
出处
《生物技术通报》
CAS
CSCD
北大核心
2010年第4期189-193,共5页
Biotechnology Bulletin
关键词
蛋氨酸裂解酶
同型半胱氨酸
基因表达
包涵体
复性
Methionine γ-Lyase Homocysteine Gene expression Inclusion body Renaturation