Mandal N, RajBhandary U L
Department of Biology, Massachusetts Institute of Technology, Cambridge 02139.
J Bacteriol. 1992 Dec;174(23):7827-30. doi: 10.1128/jb.174.23.7827-7830.1992.
We show that the metY locus which specifies tRNA(2fMet) in Escherichia coli K-12 specifies tRNA(1fMet) in E. coli B. This conclusion is based on results of Southern blot analysis of E. coli B and K-12 DNAs and on polymerase chain reaction amplification, cloning, and sequencing of an approximately 200-bp region of DNA corresponding to the metY loci of E. coli B and E. coli K-12. We also show that the metY locus of E. coli B is transcriptionally active. E. coli strains transformed with the multicopy plasmid vector pUC19 carrying the metY locus of E. coli B overproduce tRNA(1fMet) in E. coli B and E. coli K-12 in contrast to strains transformed with pUC19 carrying the corresponding locus from E. coli K-12, which overproduce tRNA(2fMet).
我们发现,在大肠杆菌K-12中指定tRNA(2fMet)的metY基因座在大肠杆菌B中指定tRNA(1fMet)。这一结论基于对大肠杆菌B和K-12 DNA的Southern印迹分析结果,以及对与大肠杆菌B和大肠杆菌K-12的metY基因座相对应的约200 bp DNA区域进行的聚合酶链反应扩增、克隆和测序结果。我们还表明,大肠杆菌B的metY基因座具有转录活性。与用携带大肠杆菌K-12相应基因座的pUC19转化的菌株相比,用携带大肠杆菌B的metY基因座的多拷贝质粒载体pUC19转化的大肠杆菌菌株在大肠杆菌B和大肠杆菌K-12中过量产生tRNA(1fMet),而携带大肠杆菌K-12相应基因座的pUC19转化的菌株则过量产生tRNA(2fMet)。