Santos P M, Di Bartolo I, Blatny J M, Zennaro E, Valla S
Department of Biology, Third University of Rome, Italy.
FEMS Microbiol Lett. 2001 Feb 5;195(1):91-6. doi: 10.1111/j.1574-6968.2001.tb10503.x.
Broad-host-range plasmid RK2-based promoter probe vectors with a known nucleotide sequence were constructed. In the absence of an upstream promoter, the expression of two tested reporter genes (luc and lacZ) in Escherichia coli was virtually zero, while insertion of the Ptrc promoter resulted in strong inducer-dependent expression. The lacZ-based vectors were mobilized into Pseudomonas fluorescens ST, Pseudomonas putida KT2442, Sphingomonas spp. and Burkholderia spp. LB400, and expression analyses indicated that the properties observed in E. coli are maintained across the species barriers. In addition, the previously established knowledge of RK2 molecular biology allows easy manipulations of features such as plasmid copy number, further extending the application potential of the vectors.
构建了基于广宿主范围质粒RK2且具有已知核苷酸序列的启动子探针载体。在没有上游启动子的情况下,两种测试报告基因(luc和lacZ)在大肠杆菌中的表达几乎为零,而Ptrc启动子的插入导致了强烈的诱导物依赖性表达。基于lacZ的载体被转移到荧光假单胞菌ST、恶臭假单胞菌KT2442、鞘氨醇单胞菌属和伯克霍尔德菌属LB400中,表达分析表明在大肠杆菌中观察到的特性在物种屏障之间得以保留。此外,先前建立的RK2分子生物学知识使得对诸如质粒拷贝数等特征的操作变得容易,进一步扩展了载体的应用潜力。