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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.

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。

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