Xiang H, Wei W, Zhang Y, Tan H
Institute of Microbiology, Chinese Academy of Sciences, Beijing, PR China.
Biomol Eng. 2000 Jun;16(6):207-9. doi: 10.1016/s1389-0344(99)00055-6.
The glutathione-S-transferase A1 cDNA was amplified from the total RNAs of human liver by RT-PCR, and inserted into plasmid pMG36e. The hGSTA1 was expressed in Lactococcus lactis MG1363 and verified by SDS-PAGE and Western blot, purified by affinity chromatography and showed enzymatic activity.
通过逆转录聚合酶链反应(RT-PCR)从人肝脏的总RNA中扩增出谷胱甘肽-S-转移酶A1(glutathione-S-transferase A1)的互补DNA(cDNA),并将其插入质粒pMG36e中。人谷胱甘肽-S-转移酶A1(hGSTA1)在乳酸乳球菌MG1363中表达,并通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)和蛋白质免疫印迹法(Western blot)进行验证,通过亲和层析法进行纯化并显示出酶活性。