Korfmann G, Sanders C C, Moland E S
Department of Medical Microbiology, Creighton University School of Medicine, Omaha, Nebraska 68178.
Antimicrob Agents Chemother. 1991 Feb;35(2):358-64. doi: 10.1128/AAC.35.2.358.
A study was done to determine the genetic locus responsible for altered expression of AmpC beta-lactamase in Enterobacter cloacae 1194E and several mutants derived from E. cloacae 029. These phenotypes were defined by units of enzyme activity found in sonic extracts of cells before and after induction with cefoxitin and included (units uninduced/units induced) the wild-type (7/219), high-level constitutive (10,911/10,862), temperature-sensitive (at 30 degrees C 82/706 and at 42 degrees C 5,031/6,020), and hyperinducible (19/1,688) phenotypes. When the ampD region of each E. cloacae strain was cloned and introduced into an ampD mutant Escherichia coli strain, the altered phenotypes were found to reside within this locus. Furthermore, transformants containing wild-type ampD were poorly inducible at 42 degrees C while those with high-level constitutive or hyperinducible ampD were unaffected by temperature. Since the source of ampD was the only variable in these E. coli transformants, these results suggested that ampD encodes a protein that is involved in sensing the inducer. To test this possibility, the responses to different inducers of E. coli transformants containing various ampD regions were assessed. In the presence of wild-type ampD, transformants responded equally to cefoxitin and cefotetan, regardless of temperature. In the presence of temperature-sensitive ampD, induction by cefotetan was similar to that by cefoxitin at 30 degrees C but greater than that by cefoxitin at 42 degrees C. These results suggest that ampD encodes a protein involved in induction of AmpC beta-lactamase in E. cloacae.
开展了一项研究,以确定阴沟肠杆菌1194E及源自阴沟肠杆菌029的多个突变体中负责AmpCβ-内酰胺酶表达改变的基因位点。这些表型通过在头孢西丁诱导前后细胞超声提取物中发现的酶活性单位来定义,包括(未诱导单位/诱导单位)野生型(7/219)、高水平组成型(10911/10862)、温度敏感型(30℃时为82/706,42℃时为5031/6020)和超诱导型(19/1688)表型。当克隆每个阴沟肠杆菌菌株的ampD区域并将其导入ampD突变的大肠杆菌菌株时,发现改变的表型位于该基因位点内。此外,含有野生型ampD的转化体在42℃时诱导性较差,而具有高水平组成型或超诱导型ampD的转化体不受温度影响。由于ampD的来源是这些大肠杆菌转化体中唯一的变量,这些结果表明ampD编码一种参与感应诱导剂的蛋白质。为了验证这种可能性,评估了含有各种ampD区域的大肠杆菌转化体对不同诱导剂的反应。在存在野生型ampD的情况下,无论温度如何,转化体对头孢西丁和头孢替坦的反应相同。在存在温度敏感型ampD的情况下,头孢替坦在30℃时的诱导作用与头孢西丁相似,但在42℃时大于头孢西丁。这些结果表明ampD编码一种参与阴沟肠杆菌中AmpCβ-内酰胺酶诱导的蛋白质。