Journal of Capital Medical University ›› 2001, Vol. 22 ›› Issue (1): 1-5.

• 论著 • Previous Articles     Next Articles

Construction of pBV-BPI600 Recombinant Expression Vector and its Expression in E. coli

An Yunqing, Liu Qing, Ke Yan, Shen Haizhong   

  1. Department of Microbiology and Immunology, Capital University of Medical Sciences
  • Received:2000-04-17 Revised:1900-01-01 Online:2001-01-15 Published:2001-01-15

Abstract: BPI 600 bp gene which encode 193 amino acid fragments(rBPI21)BPI N-terminal was amplified by RT-PCR from mRNA that were extracted from qHL-60; It was digested by EcoRI and BamHI to obtain BPI 400 bp and BPI 200 bp fragments.②PUC18-BPI200 and PUC18-BPI400 recombinant cloning vector were successfully constructed, and sequences were identical with those of the report. ③pBV-BPI600 recombinant expression vector was successfully constructed, It was transformated into the competent E. coli DH5α and BPI21 recombinant protein was expressed by temperature induced method. The results of SDS-PAGE and Western blot has proved that the expressed recombinant protein is rBPI21 which is encoded by BPI600 gene.

Key words: recombinant bactericidal/permeability increasing protein, pBV220 expression vector, PUC18 cloning vector

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