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ampR Gene Mutations That Greatly Increase Class C β-Lactamase Activity in Enterobacter cloacae

机译:ampR基因突变可大大增加阴沟肠杆菌中的C类β-内酰胺酶活性

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摘要

The ampC and ampR genes of Enterobacter cloacae GN7471 were cloned into pMW218 to yield pKU403. Four mutant plasmids derived from pKU403 (pKU404, pKU405, pKU406, and pKU407) were isolated in an AmpD mutant of Escherichia coli ML4953 by selection with ceftazidime or aztreonam. The β-lactamase activities expressed by pKU404, pKU405, pKU406, and pKU407 were about 450, 75, 160, and 160 times higher, respectively, than that expressed by the original plasmid, pKU403. These mutant plasmids all carried point mutations in the ampR gene. In pKU404 and pKU405, Asp-135 was changed to Asn and Val, respectively. In both pKU406 and pKU407, Arg-86 was changed to Cys. The ease of selection of AmpR mutations at a frequency of about 10−6 in this study strongly suggests that derepressed strains, such as AmpD or AmpR mutants, could frequently emerge in the clinical setting.
机译:将阴沟肠杆菌GN7471的ampC和ampR基因克隆到pMW218中,得到pKU403。通过用头孢他啶或氨曲南选择,在大肠杆菌ML4953的AmpD突变体中分离了衍生自pKU403的四种突变质粒(pKU404,pKU405,pKU406和pKU407)。 pKU404,pKU405,pKU406和pKU407所表达的β-内酰胺酶活性分别比原始质粒pKU403所表达的β-内酰胺酶活性高约450、75、160和160倍。这些突变质粒均在ampR基因中带有点突变。在pKU404和pKU405中,Asp-135分别更改为Asn和Val。在pKU406和pKU407中,Arg-86均更改为Cys。在这项研究中,以大约10 -6 的频率选择AmpR突变的简便性强烈表明,在临床环境中可能会经常出现抑制表达力降低的菌株,例如AmpD或AmpR突变体。

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