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本文引用的文献

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Biochemical characterization of the carbapenem-hydrolyzing beta-lactamase AsbM1 from Aeromonas sobria AER 14M: a member of a novel subgroup of metallo-beta-lactamases.嗜水气单胞菌AER 14M中碳青霉烯水解β-内酰胺酶AsbM1的生化特性:金属β-内酰胺酶新亚组的一员
FEMS Microbiol Lett. 1996 Apr 1;137(2-3):193-200. doi: 10.1111/j.1574-6968.1996.tb08105.x.
2
AmpG, a signal transducer in chromosomal beta-lactamase induction.AmpG,一种参与染色体β-内酰胺酶诱导的信号转导蛋白。
Mol Microbiol. 1993 Aug;9(4):703-15. doi: 10.1111/j.1365-2958.1993.tb01731.x.
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Structural conservation in the CheY superfamily.CheY超家族中的结构保守性。
Biochemistry. 1993 Nov 9;32(44):11741-53. doi: 10.1021/bi00095a001.
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A common system controls the induction of very different genes. The class-A beta-lactamase of Proteus vulgaris and the enterobacterial class-C beta-lactamase.一个共同的系统控制着非常不同基因的诱导。普通变形杆菌的A类β-内酰胺酶和肠杆菌科的C类β-内酰胺酶。
Eur J Biochem. 1994 Nov 15;226(1):149-57. doi: 10.1111/j.1432-1033.1994.tb20036.x.
5
Pharmacodynamics of piperacillin alone and in combination with tazobactam against piperacillin-resistant and -susceptible organisms in an in vitro model of infection.在体外感染模型中,哌拉西林单独及与他唑巴坦联合应用对耐哌拉西林和哌拉西林敏感菌的药效学研究。
Antimicrob Agents Chemother. 1994 Oct;38(10):2351-6. doi: 10.1128/AAC.38.10.2351.
6
Cloning and expression of a cloxacillin-hydrolyzing enzyme and a cephalosporinase from Aeromonas sobria AER 14M in Escherichia coli: requirement for an E. coli chromosomal mutation for efficient expression of the class D enzyme.嗜水气单胞菌AER 14M中一种氯唑西林水解酶和一种头孢菌素酶在大肠杆菌中的克隆与表达:D类酶高效表达对大肠杆菌染色体突变的需求
Antimicrob Agents Chemother. 1994 Sep;38(9):2078-85. doi: 10.1128/AAC.38.9.2078.
7
A functional classification scheme for beta-lactamases and its correlation with molecular structure.β-内酰胺酶的功能分类方案及其与分子结构的相关性。
Antimicrob Agents Chemother. 1995 Jun;39(6):1211-33. doi: 10.1128/AAC.39.6.1211.
8
Analysis of gene control signals by DNA fusion and cloning in Escherichia coli.通过在大肠杆菌中进行DNA融合和克隆分析基因控制信号。
J Mol Biol. 1980 Apr;138(2):179-207. doi: 10.1016/0022-2836(80)90283-1.
9
Determination of plasmid copy number by fluorescence densitometry.通过荧光密度测定法测定质粒拷贝数。
Plasmid. 1983 Mar;9(2):182-90. doi: 10.1016/0147-619x(83)90019-7.
10
Rapid method for screening large numbers of Escherichia coli colonies for production of plasmid-mediated beta-lactamases.快速筛选大量产质粒介导β-内酰胺酶大肠杆菌菌落的方法。
Antimicrob Agents Chemother. 1983 Feb;23(2):308-12. doi: 10.1128/AAC.23.2.308.

詹氏气单胞菌AER 14中AsbA1、OXA - 12和AsbM1β-内酰胺酶的表达由一个双组分调节子调控。

Expression of the AsbA1, OXA-12, and AsbM1 beta-lactamases in Aeromonas jandaei AER 14 is coordinated by a two-component regulon.

作者信息

Alksne L E, Rasmussen B A

机构信息

Infectious Disease Section, Wyeth-Ayerst Research, Pearl River, New York 10965, USA.

出版信息

J Bacteriol. 1997 Mar;179(6):2006-13. doi: 10.1128/jb.179.6.2006-2013.1997.

DOI:10.1128/jb.179.6.2006-2013.1997
PMID:9068648
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC178926/
Abstract

Aeromonas jandaei AER 14 (formerly Aeromonas sobria AER 14) expresses three inducible beta-lactamases, AsbA1, OXA-12 (AsbB1), and AsbM1. Mutant strains that constitutively overexpress all three enzyme simultaneously, suggesting that they share a common regulatory pathway, have been isolated. Detectable expression of the cloned genes of AsbA1 and OXA-12 in some Escherichia coli K-12 laboratory strains is achieved only in the presence of a blp mutation. These mutations map to the cre operon at 0 min, which encodes a classical two-component regulatory system of unknown function. Two regulatory elements from A. jandaei which permit high-level constitutive expression of OXA-12 in E. coli were cloned. Both loci encode proteins with characteristics of response regulator proteins of two-component regulatory systems. One of these loci, designated blrA, bestowed constitutive expression of all three beta-lactamases in A. jandaei AER 14 when present on a multicopy plasmid, confirming its role in the regulatory pathway of beta-lactamase production in this organism.

摘要

詹氏气单胞菌AER 14(以前称为温和气单胞菌AER 14)表达三种诱导型β-内酰胺酶,即AsbA1、OXA-12(AsbB1)和AsbM1。已分离出同时组成型过表达这三种酶的突变菌株,这表明它们共享一条共同的调控途径。只有在存在blp突变的情况下,才能在一些大肠杆菌K-12实验室菌株中检测到AsbA1和OXA-12克隆基因的表达。这些突变定位于0分钟处的cre操纵子,该操纵子编码一个功能未知的经典双组分调控系统。克隆了来自詹氏气单胞菌的两个调控元件,它们可使大肠杆菌中OXA-12实现高水平组成型表达。这两个位点都编码具有双组分调控系统应答调节蛋白特征的蛋白质。其中一个位点命名为blrA,当它存在于多拷贝质粒上时,能使詹氏气单胞菌AER 14中所有三种β-内酰胺酶组成型表达,证实了其在该生物体β-内酰胺酶产生调控途径中的作用。