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本文引用的文献

1
The ability of beta-lactam antibiotics to select mutants with derepressed beta-lactamase synthesis from Citrobacter freundii.
J Antimicrob Chemother. 1995 Sep;36(3):483-96. doi: 10.1093/jac/36.3.483.
2
Sequences of wild-type and mutant ampD genes of Citrobacter freundii and Enterobacter cloacae.弗氏柠檬酸杆菌和阴沟肠杆菌野生型及突变型ampD基因序列。
Antimicrob Agents Chemother. 1993 Feb;37(2):224-8. doi: 10.1128/AAC.37.2.224.
3
The negative regulator of beta-lactamase induction AmpD is a N-acetyl-anhydromuramyl-L-alanine amidase.β-内酰胺酶诱导的负调节因子AmpD是一种N-乙酰脱氨胞壁酰-L-丙氨酸酰胺酶。
FEMS Microbiol Lett. 1994 Sep 15;122(1-2):159-64. doi: 10.1111/j.1574-6968.1994.tb07159.x.
4
Bacterial cell wall recycling provides cytosolic muropeptides as effectors for beta-lactamase induction.细菌细胞壁循环利用可提供胞质内的胞壁肽作为诱导β-内酰胺酶的效应物。
EMBO J. 1994 Oct 3;13(19):4684-94. doi: 10.1002/j.1460-2075.1994.tb06792.x.
5
Common evolutionary origin of chromosomal beta-lactamase genes in enterobacteria.肠道细菌中染色体β-内酰胺酶基因的共同进化起源
J Bacteriol. 1982 May;150(2):528-34. doi: 10.1128/jb.150.2.528-534.1982.
6
Inducible type I beta-lactamases of gram-negative bacteria and resistance to beta-lactam antibiotics.革兰氏阴性菌的诱导型I类β-内酰胺酶与对β-内酰胺抗生素的耐药性
J Antimicrob Chemother. 1986 Jan;17(1):51-61. doi: 10.1093/jac/17.1.51.
7
Cloning, sequencing and expression of a Bacillus bacteriolytic enzyme in Escherichia coli.一种芽孢杆菌溶菌酶在大肠杆菌中的克隆、测序及表达
Mol Gen Genet. 1988 Oct;214(2):241-8. doi: 10.1007/BF00337717.
8
Regulatory components in Citrobacter freundii ampC beta-lactamase induction.弗氏柠檬酸杆菌ampCβ-内酰胺酶诱导中的调控成分。
Proc Natl Acad Sci U S A. 1985 Jul;82(14):4620-4. doi: 10.1073/pnas.82.14.4620.
9
ampG is essential for high-level expression of AmpC beta-lactamase in Enterobacter cloacae.ampG基因对于阴沟肠杆菌中AmpCβ-内酰胺酶的高水平表达至关重要。
Antimicrob Agents Chemother. 1989 Nov;33(11):1946-51. doi: 10.1128/AAC.33.11.1946.
10
Signalling proteins in enterobacterial AmpC beta-lactamase regulation.肠杆菌AmpCβ-内酰胺酶调控中的信号蛋白
Mol Microbiol. 1989 Aug;3(8):1091-102. doi: 10.1111/j.1365-2958.1989.tb00259.x.

弗氏柠檬酸杆菌ampD突变体的DNA序列差异

DNA sequence differences of ampD mutants of Citrobacter freundii.

作者信息

Stapleton P, Shannon K, Phillips I

机构信息

Department of Microbiology, United Medical and Dental School, London, United Kingdom.

出版信息

Antimicrob Agents Chemother. 1995 Nov;39(11):2494-8. doi: 10.1128/AAC.39.11.2494.

DOI:10.1128/AAC.39.11.2494
PMID:8585732
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC162971/
Abstract

Three groups of mutants with increased levels of beta-lactamase synthesis were selected from Citrobacter freundii 382010 by beta-lactam antibiotics at concentrations just above the MIC. Uninduced cultures of the hyperinducible group had 3- to 5-fold more beta-lactamase activity than the parent strain, with one mutant (termed type b) expressing 19 times the activity of the parent strain; the partially derepressed group had a relative 55-fold increase, while fully derepressed strains exhibited a 460-fold increase. Upon induction by growth in the presence of cefoxitin (32 micrograms/ml) for 2 h, the hyperinducible and derepressed groups had similar relative beta-lactamase activities of 650 and 725, respectively. Induction of beta-lactamase activity from partially derepressed mutants resulted in a relative activity of only 240. The ampD gene including its promoter region was amplified from the parent strain and the mutant strains by PCR. The sequence of ampD from the parent strain showed only three nucleotide changes from a previously published sequence, none of which resulted in a change to the deduced amino acid sequence. Hyperinducible mutant strains of type a had an amino acid change of either a tryptophan in codon 95 to an arginine (Trp-95-->Arg) (three mutants) or Ala-158-->Asp (one mutant). The hyperinducible type b strain had the change Tyr-102-->Asp. The derepressed strains had the following changes: Val-33-->Gly (one mutant), Asp-164-->Glu (one mutant), and Trp-95-->termination codon (two mutants). We infer that the amino acid changes in the hyperinducible mutants result in altered AmpD activity, whereas, in contrast, they lead to an inactive protein in derepressed mutants. No nucleotide differences were found in the ampD gene from partially derepressed strains.

摘要

通过高于最低抑菌浓度(MIC)的β-内酰胺类抗生素从弗氏柠檬酸杆菌382010中筛选出三组β-内酰胺酶合成水平升高的突变体。超诱导组的未诱导培养物的β-内酰胺酶活性比亲本菌株高3至5倍,其中一个突变体(称为b型)的活性是亲本菌株的19倍;部分去阻遏组相对增加了55倍,而完全去阻遏菌株则增加了460倍。在头孢西丁(32微克/毫升)存在下生长2小时进行诱导后,超诱导组和去阻遏组的相对β-内酰胺酶活性分别为650和725,相似。部分去阻遏突变体诱导β-内酰胺酶活性后,相对活性仅为240。通过聚合酶链反应(PCR)从亲本菌株和突变菌株中扩增出包括其启动子区域的ampD基因。亲本菌株的ampD序列与先前发表的序列相比仅显示三个核苷酸变化,均未导致推导的氨基酸序列发生变化。a型超诱导突变菌株的氨基酸变化为密码子95处的色氨酸变为精氨酸(Trp-95→Arg)(三个突变体)或Ala-158→Asp(一个突变体)。超诱导b型菌株的变化为Tyr-102→Asp。去阻遏菌株有以下变化:Val-33→Gly(一个突变体)、Asp-164→Glu(一个突变体)和Trp-95→终止密码子(两个突变体)。我们推断,超诱导突变体中的氨基酸变化导致AmpD活性改变,而相比之下,它们导致去阻遏突变体中的蛋白质无活性。在部分去阻遏菌株的ampD基因中未发现核苷酸差异。