摘要:本实验克隆了来源于大肠杆菌JM109的细胞周质空间中表达的磷酸盐结合蛋白(Phosphate binding protein, PBP)编码基因phos。通过重组、转化、酶切、酶连等一系列操作,将phos基因替换重组质粒pTrcHisC-(inpN)3-gfp中的绿色荧光蛋白编码基因gfp,构建了能够展示磷酸盐吸附蛋白的3拷贝InpN串联重复大肠杆菌细胞表面展示体系。最后用磷钼酸比色法测定磷酸盐含量,从而检测构建的重组菌的磷酸盐吸附能力。从检测结果可知,构建的重组菌与对照大肠杆菌JM109相比,有显著的磷酸盐吸附能力。4518
关键词: 磷酸盐吸附蛋白,大肠杆菌,PCR,重组菌
Cell surface display of phosphate binding protein utilizing tandem repeats of ice nucleation protein
Abstract:In this study, a gene encoding phosphate binding protein (phos) which was expressed in the periplasm was cloned from Escherichia coli JM109. The recombinant plasmid pTrcHisC-(inpN)3-phos was constructed by replacing gene gfp (coding the green fluorescent protein) from the recombinant plasmid pTrcHisC-(inpN)3-gfp using restriction enzyme digestion, ligation and transfomation methods. The phosphate binding protein can be displayed on the bacterial surface utilizing tandem repeats of N-domain of ice nucleation protein. Then, phosphomolybdate colorimetry was used to determine the phosphate binding ability of recombinant strain. According to the results, compared with E. coli JM109, the recombinant strain showed high efficiency of phosphate binding ability.