DIRECT SEQUENCING OF THE AMPLIFIED STRUCTURAL GENE AND PROMOTER FOR THE EXTENDED-BROAD-SPECTRUM BETA-LACTAMASE TEM-9 (RHH-1) OF KLEBSIELLA-PNEUMONIAE

被引:103
作者
MABILAT, C [1 ]
GOUSSARD, S [1 ]
SOUGAKOFF, W [1 ]
SPENCER, RC [1 ]
COURVALIN, P [1 ]
机构
[1] ROYAL HALLAMSHIRE HOSP, DEPT BACTERIOL, SHEFFIELD S10 2JF, S YORKSHIRE, ENGLAND
关键词
D O I
10.1016/0147-619X(90)90041-A
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Extended-broad-spectrum β-lactamase TEM-9, detected in a clinical isolate of Klebsiella pneumoniae, confers high-level resistance to recent cephalosporins, in particular ceftazidime, and to the monobactam aztreonam. Using oligonucleotide probes, we found that the plasmid gene blaT-9 encoding TEM-9 differs from characterized blaT genes by a new combination of already known mutations. Gene blaT-9 was further studied by direct sequencing of an amplified 1.1-kb DNA fragment which contained the open reading frame and its promoter. Analysis of the nucleotide and of the deduced amino acid sequence confirmed the hybridization results and indicated that TEM-9 differs from TEM-1 by four amino acid substitutions: Phe at position 19 and Met at position 261, which have been found in TEM-4 and are known not to expand the enzyme substrate range; Lys 102, detected in TEM-3 and TEM-4, and Ser 162, present in TEM-5 and TEM-7. Each of the latter substitutions enlarges the substrate spectrum of the enzymes and they are found associated for the first time in TEM-9. © 1990.
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页码:27 / 34
页数:8
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