Hopkins J D, O'Brien T F, Syvanen M
Department of Medical Microbiology and Immunology, School of Medicine, University of California, Davis 95616.
Plasmid. 1988 Sep;20(2):163-6. doi: 10.1016/0147-619x(88)90021-2.
pLST1000, an 80-kb plasmid found in Enterobacteriaceae in North and South America, harbors the aadB and several other resistance genes. We suggested earlier that, because of its widespread distribution, pLST1000 could act as a carrier plasmid, bringing the aadB gene to new locations. This paper presents the restriction enzyme recognition site and functional map of the plasmid. The resistance genes lie in a discreet region. The aadB and aadA genes form an operon with the aadB gene promoter proximal. This operon is flanked by bla-TEM and bla-OXA2 genes, the former located in a functional Tn3-like transposon. This arrangement is similar to that of relatives of the transposon TN21, where additional resistance genes are precisely inserted in recombinational "hot spot" sequences that flank the aadA gene. We were not able to demonstrate transposition of the aadB gene in Escherichia coli. A sul gene and mer operon lie beyond the bla-OXA2 gene. The transfer genes form a single region, defined by insertions of Tn5-132 that give the Tra- phenotype.
pLST1000是一种在北美洲和南美洲的肠杆菌科细菌中发现的80千碱基对的质粒,携带aadB和其他几个抗性基因。我们之前曾提出,由于其广泛分布,pLST1000可能作为一种载体质粒,将aadB基因带到新的位置。本文介绍了该质粒的限制酶识别位点和功能图谱。抗性基因位于一个离散区域。aadB和aadA基因形成一个操纵子,aadB基因启动子位于近端。这个操纵子两侧是bla-TEM和bla-OXA2基因,前者位于一个功能性的Tn3样转座子中。这种排列与转座子TN21的亲属相似,其中额外的抗性基因精确插入到aadA基因两侧的重组“热点”序列中。我们未能在大肠杆菌中证明aadB基因的转座。一个sul基因和mer操纵子位于bla-OXA2基因之外。转移基因形成一个单一区域,由赋予Tra-表型的Tn5-132插入所定义。