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嗜麦芽窄食单胞菌L2丝氨酸β-内酰胺酶的序列分析与酶动力学

Sequence analysis and enzyme kinetics of the L2 serine beta-lactamase from Stenotrophomonas maltophilia.

作者信息

Walsh T R, MacGowan A P, Bennett P M

机构信息

Bristol Centre for Antimicrobial Research and Evaluation, Department of Microbiology and Pathology, Medical School, University of Bristol, United Kingdom.

出版信息

Antimicrob Agents Chemother. 1997 Jul;41(7):1460-4. doi: 10.1128/AAC.41.7.1460.

Abstract

The L2 serine active-site beta-lactamase from Stenotrophomonas maltophilia has been classified as a clavulanic acid-sensitive cephalosporinase. The gene encoding this enzyme from S. maltophilia 1275 IID has been cloned on a 3.3-kb fragment into pK18 under the control of a Ptac promoter to generate recombinant plasmid pUB5840; when expressed in Escherichia coli, this gene confers resistance to cephalosporins and penicillins. Sequence analysis has revealed an open reading frame (ORF) of 909 bp with a GC content of 71.6%, comparable to that of the L1 metallo-beta-lactamase gene (68.4%) from the same bacterium. The ORF encodes an unmodified protein of 303 amino acids with a predicted molecular mass of 31.5 kDa, accommodating a putative leader peptide of 27 amino acids. Comparison of the amino acid sequence with those of other beta-lactamases showed it to be most closely related (54% identity) to the BLA-A beta-lactamase from Yersinia enterocolitica. Sequence identity is most obvious near the STXK active-site motif and the SDN loop motif common to all serine active-site penicillinases. Sequences outside the conserved regions display low homology with comparable regions of other class A penicillinases. Kinetics of the enzyme from the cloned gene demonstrated an increase in activity with cefotaxime but markedly less activity with imipenem than previously reported. Hence, the S. maltophilia L2 beta-lactamase is an inducible Ambler class A beta-lactamase which would account for the sensitivity to clavulanic acid.

摘要

嗜麦芽窄食单胞菌的L2丝氨酸活性位点β-内酰胺酶已被归类为对克拉维酸敏感的头孢菌素酶。来自嗜麦芽窄食单胞菌1275 IID的编码该酶的基因已被克隆到一个3.3 kb的片段上,并在Ptac启动子的控制下插入到pK18中,以产生重组质粒pUB5840;当在大肠杆菌中表达时,该基因赋予对头孢菌素和青霉素的抗性。序列分析揭示了一个909 bp的开放阅读框(ORF),其GC含量为71.6%,与来自同一细菌的L1金属β-内酰胺酶基因(68.4%)相当。该ORF编码一个由303个氨基酸组成的未修饰蛋白质,预测分子量为31.5 kDa,包含一个27个氨基酸的推定前导肽。将该氨基酸序列与其他β-内酰胺酶的序列进行比较,发现它与小肠结肠炎耶尔森菌的BLA-Aβ-内酰胺酶关系最为密切(同一性为54%)。序列同一性在所有丝氨酸活性位点青霉素酶共有的STXK活性位点基序和SDN环基序附近最为明显。保守区域外的序列与其他A类青霉素酶的可比区域显示出低同源性。来自克隆基因的酶的动力学表明,其对头孢噻肟的活性增加,但对亚胺培南的活性明显低于先前报道。因此,嗜麦芽窄食单胞菌L2β-内酰胺酶是一种可诱导的安布勒A类β-内酰胺酶,这可以解释其对克拉维酸的敏感性。

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