Ouellette M, Bissonnette L, Roy P H
Département de Biochimie, Faculté des Sciences et Génie, Université Laval, Québec, Canada.
Proc Natl Acad Sci U S A. 1987 Nov;84(21):7378-82. doi: 10.1073/pnas.84.21.7378.
Several plasmid-encoded beta-lactamases are on multiresistance transposable elements. The OXA-1 beta-lactamase gene is part of Tn2603, which is borne on the R plasmid RGN238. We report here the complete nucleotide sequence of the OXA-1 beta-lactamase gene and flanking sequences. The OXA-1 gene shows a greater than 50% sequence divergence from the OXA-2 gene, yet there is significant functional similarity at the peptide level. Analysis of 5' and 3' flanking sequences shows that Tn2603 differs from its probable precursor, Tn21, by a precise 1004-base-pair insertion, containing the OXA-1 structural gene, at the target sequence AAAGTT, which is located between the Tn21 streptomycin/spectinomycin (aadA) promoter and its structural gene. A 5- for 6-base repeat of the target sequence is found at the end of the insertion. The same precise insertion and repeat of the target sequence are found for the OXA-2 gene from R46. The 5' flanking regions of two other genes, the trimethoprim-resistance gene from R388 and the gentamicin resistance (aadB) gene from pDGO100, are greater than 98% homologous to the 5' flanking sequences of the OXA-1, OXA-2, and aadA genes until they diverge at the target sequence. From the available sequence data a recombinational hot spot is defined at the nucleotide level 5' of the aadA gene of Tn21, and a second potential hot spot is proposed 3' of this gene.
几种质粒编码的β-内酰胺酶存在于多抗性转座元件上。OXA-1β-内酰胺酶基因是Tn2603的一部分,Tn2603携带在R质粒RGN238上。我们在此报告OXA-1β-内酰胺酶基因及其侧翼序列的完整核苷酸序列。OXA-1基因与OXA-2基因的序列差异大于50%,但在肽水平上存在显著的功能相似性。对5'和3'侧翼序列的分析表明,Tn2603与其可能的前体Tn21的不同之处在于,在位于Tn21链霉素/壮观霉素(aadA)启动子及其结构基因之间的靶序列AAAGTT处精确插入了1004个碱基对,其中包含OXA-1结构基因。在插入末端发现了靶序列的5个碱基对到6个碱基对的重复。在R46的OXA-2基因中也发现了相同的精确插入和靶序列重复。另外两个基因,R388的甲氧苄啶抗性基因和pDGO100的庆大霉素抗性(aadB)基因的5'侧翼区域,与OXA-1、OXA-2和aadA基因的5'侧翼序列的同源性大于98%,直到它们在靶序列处发生分歧。根据现有的序列数据,在Tn21的aadA基因5'端的核苷酸水平上定义了一个重组热点,并在该基因3'端提出了第二个潜在热点。