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质粒介导的β-内酰胺酶基因的分子克隆及DNA同源性

Molecular cloning and DNA homology of plasmid-mediated beta-lactamase genes.

作者信息

Levesque R C, Medeiros A A, Jacoby G A

出版信息

Mol Gen Genet. 1987 Feb;206(2):252-8. doi: 10.1007/BF00333581.

Abstract

Molecular cloning of DNA fragments between 1.5 and 8 kb from BamHI, EcoRI, HindIII, SalI, or Sau3A digests permitted the isolation of structural genes coding for TEM-1, ROB-1, OXA-1, OXA-3, OXA-4, OXA-5, PSE-1, PSE-2, PSE-3, PSE-4, CARB-3, CARB-4, AER-1, and LCR-1 beta-lactamases. Ampicillin-resistant clones were selected and it was confirmed that they contained the respective beta-lactamase genes by isoelectric focusing. Detailed physical maps of 14 different recombinant plasmids were constructed using 8 restriction endonucleases. Plasmid deletions and lacZ fusions were used to localize the beta-lactamase structural genes. DNA probes were constructed for the TEM-1, ROB-1, OXA-1, and PSE-1 genes. Under conditions of high stringency, hybridization was observed between the genes for TEM-1 and TEM-2 or TLE-1, OXA-1 and OXA-4, and PSE-1 and PSE-4 or CARB-3, while the ROB-1 gene probe showed no cross-hybridization. Such bla gene probes should facilitate studies of beta-lactamase molecular epidemiology.

摘要

从BamHI、EcoRI、HindIII、SalI或Sau3A酶切片段中克隆1.5至8 kb之间的DNA片段,使得编码TEM-1、ROB-1、OXA-1、OXA-3、OXA-4、OXA-5、PSE-1、PSE-2、PSE-3、PSE-4、CARB-3、CARB-4、AER-1和LCR-1β-内酰胺酶的结构基因得以分离。挑选出对氨苄青霉素耐药的克隆,并通过等电聚焦证实它们含有各自的β-内酰胺酶基因。使用8种限制性内切酶构建了14种不同重组质粒的详细物理图谱。利用质粒缺失和lacZ融合来定位β-内酰胺酶结构基因。构建了针对TEM-1、ROB-1、OXA-1和PSE-1基因的DNA探针。在高严谨度条件下,观察到TEM-1基因与TEM-2或TLE-1基因、OXA-1基因与OXA-4基因、PSE-1基因与PSE-4或CARB-3基因之间发生杂交,而ROB-1基因探针未显示交叉杂交。此类bla基因探针应有助于β-内酰胺酶分子流行病学研究。

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