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β-内酰胺酶的功能分类更新。

Updated functional classification of beta-lactamases.

机构信息

Department of Biology, Indiana University, Bloomington, IN 47401, USA.

出版信息

Antimicrob Agents Chemother. 2010 Mar;54(3):969-76. doi: 10.1128/AAC.01009-09. Epub 2009 Dec 7.

Abstract

Two classification schemes for beta-lactamases are currently in use. The molecular classification is based on the amino acid sequence and divides beta-lactamases into class A, C, and D enzymes which utilize serine for beta-lactam hydrolysis and class B metalloenzymes which require divalent zinc ions for substrate hydrolysis. The functional classification scheme updated herein is based on the 1995 proposal by Bush et al. (K. Bush, G. A. Jacoby, and A. A. Medeiros, Antimicrob. Agents Chemother. 39:1211-1233, 1995). It takes into account substrate and inhibitor profiles in an attempt to group the enzymes in ways that can be correlated with their phenotype in clinical isolates. Major groupings generally correlate with the more broadly based molecular classification. The updated system includes group 1 (class C) cephalosporinases; group 2 (classes A and D) broad-spectrum, inhibitor-resistant, and extended-spectrum beta-lactamases and serine carbapenemases; and group 3 metallo-beta-lactamases. Several new subgroups of each of the major groups are described, based on specific attributes of individual enzymes. A list of attributes is also suggested for the description of a new beta-lactamase, including the requisite microbiological properties, substrate and inhibitor profiles, and molecular sequence data that provide an adequate characterization for a new beta-lactam-hydrolyzing enzyme.

摘要

目前有两种β-内酰胺酶分类方案在使用。分子分类基于氨基酸序列,将β-内酰胺酶分为 A、C 和 D 类酶,它们利用丝氨酸进行β-内酰胺水解,以及 B 类金属酶,它们需要二价锌离子进行底物水解。本文更新的功能分类方案基于 Bush 等人(K. Bush、G. A. Jacoby 和 A. A. Medeiros,Antimicrob. Agents Chemother. 39:1211-1233, 1995)的 1995 年提案。它考虑了底物和抑制剂谱,试图以能够与临床分离物中的表型相关联的方式对酶进行分组。主要分组通常与更广泛的分子分类相关。更新的系统包括第 1 组(C 类)头孢菌素酶;第 2 组(A 类和 D 类)广谱、抑制剂耐药和扩展谱β-内酰胺酶和丝氨酸碳青霉烯酶;以及第 3 组金属β-内酰胺酶。根据个别酶的特定属性,对每个主要组的几个新亚组进行了描述。还建议了一个属性列表,用于描述新的β-内酰胺酶,包括必要的微生物学特性、底物和抑制剂谱以及分子序列数据,这些数据为新的β-内酰胺水解酶提供了充分的特征描述。

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本文引用的文献

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Antimicrob Agents Chemother. 2009 Jul;53(7):3159-61. doi: 10.1128/AAC.00133-09. Epub 2009 May 4.
2
Genetic and biochemical characterization of the first extended-spectrum CARB-type beta-lactamase, RTG-4, from Acinetobacter baumannii.
Antimicrob Agents Chemother. 2009 Jul;53(7):3010-6. doi: 10.1128/AAC.01164-08. Epub 2009 Apr 20.
3
Extended-spectrum cephalosporinases in Pseudomonas aeruginosa.
Antimicrob Agents Chemother. 2009 May;53(5):1766-71. doi: 10.1128/AAC.01410-08. Epub 2009 Mar 2.
4
AmpC beta-lactamases.
Clin Microbiol Rev. 2009 Jan;22(1):161-82, Table of Contents. doi: 10.1128/CMR.00036-08.
5
Emergence of a cefepime- and cefpirome-resistant Citrobacter freundii clinical isolate harbouring a novel chromosomally encoded AmpC beta-lactamase, CMY-37.
Int J Antimicrob Agents. 2008 Sep;32(3):256-61. doi: 10.1016/j.ijantimicag.2008.04.019. Epub 2008 Jul 10.
7
Institutional spread of clonally related Serratia marcescens isolates with a novel AmpC cephalosporinase (S4): a 4-year experience in Taiwan.
Diagn Microbiol Infect Dis. 2008 Aug;61(4):460-7. doi: 10.1016/j.diagmicrobio.2008.03.010. Epub 2008 May 2.
8
Contribution of extended-spectrum AmpC (ESAC) beta-lactamases to carbapenem resistance in Escherichia coli.
FEMS Microbiol Lett. 2008 May;282(2):238-40. doi: 10.1111/j.1574-6968.2008.01126.x. Epub 2008 Mar 27.
9
Extended-spectrum cephalosporinases: structure, detection and epidemiology.
Future Microbiol. 2007 Jun;2(3):297-307. doi: 10.2217/17460913.2.3.297.
10
Carbapenemases: the versatile beta-lactamases.
Clin Microbiol Rev. 2007 Jul;20(3):440-58, table of contents. doi: 10.1128/CMR.00001-07.

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