Kalousek S, Schrot G, Lubitz W, Bläsi U
Institute of Microbiology and Genetics, University of Vienna, Austria.
J Biotechnol. 1994 Mar 15;33(1):15-9. doi: 10.1016/0168-1656(94)90094-9.
A new positive selection vector, pGS23, based on the Lambda lysis cassette has been designed for efficient expression of homologous and heterologous genes in Escherichia coli. The plasmid permits controlled expression of a gene of interest under transcriptional control of the lac promoter with translation initiation of coding sequences directed by the phage T7 gene 10 ribosome binding site. The application of the vector system was tested for high level expression of the heterologous phbA gene of Alcaligenes eutrophus in E. coli.
一种基于λ裂解盒的新型阳性选择载体pGS23已被设计用于在大肠杆菌中高效表达同源和异源基因。该质粒允许在乳糖启动子的转录控制下对目的基因进行可控表达,其编码序列的翻译起始由噬菌体T7基因10核糖体结合位点引导。测试了该载体系统在大肠杆菌中高水平表达产碱杆菌异源phbA基因的应用。