Fujiwara S, Tsubokura N, Kurusu Y, Minami K, Kobayashi Y
Department of Applied Biochemistry, Faculty of Applied Biological Sciences, Hiroshima University, Japan.
Nucleic Acids Res. 1990 Feb 25;18(4):739-44. doi: 10.1093/nar/18.4.739.
Bacillus subtilis plasmid pGR71 is a promoter-probe shuttle vector derived from pUB110. The expression of the cat gene on pGR71 in B. subtilis requires the insertion of a Bacillus promoter and a ribosomal binding site (RBS) into the HindIII cloning site immediately upstream from the cat gene. A recombinant plasmid of pGR71, named pGR71-369, was obtained by a spontaneous deletion of a fragment containing most of the inserted HindIII fragment and the replication origin necessary for multiplication in Escherichia coli. The expression of the cat gene in B. subtilis cells carrying this plasmid was inducible by heat. Nucleotide sequence analysis of the upstream region of the cat gene, deletion analysis, and dot blot hybridization analysis of mRNA in various conditions revealed that the cat gene was expressed by heat-inducible translational coupling and that the regulatory region of heat inducibility was present in the upstream region of the cat gene.
枯草芽孢杆菌质粒pGR71是一种源自pUB110的启动子探针穿梭载体。pGR71上cat基因在枯草芽孢杆菌中的表达需要将一个芽孢杆菌启动子和一个核糖体结合位点(RBS)插入到cat基因上游紧邻的HindIII克隆位点。通过自发缺失包含大部分插入的HindIII片段和在大肠杆菌中增殖所必需的复制起点的片段,获得了一种名为pGR71 - 369的pGR71重组质粒。携带该质粒的枯草芽孢杆菌细胞中cat基因的表达可受热诱导。对cat基因上游区域的核苷酸序列分析、缺失分析以及在各种条件下对mRNA的斑点杂交分析表明,cat基因通过热诱导翻译偶联表达,并且热诱导的调控区域存在于cat基因的上游区域。