Matthew M, Harris A M
J Gen Microbiol. 1976 May;94(1):55-67. doi: 10.1099/00221287-94-1-55.
beta-Lactamases (EC. 3.5.2.6) can be directly compared by analytical isoelectric focusing. Using this technique, 242 strains from five Gram-positive and 16 Gram-negative genera were examined. A preparation of each strain focused as a single group of bands which did not match the pattern of any R factor-associated beta-lactamase. None of the strains was known to carry an R factor and resistance transfer experiments were unsuccessful. The enzymes studied were therefore thought to be chromosomally mediated. The isoelectric points ranged from 3.9 to 8.7 and were not related to the substrate profiles or other biochemical properties. The chromosomal beta-lactamases appeared to be specific for genus, species and sub-species, and strains that produced identical beta-lactamases had identical bacterial characteristics. Correlation of bacteriological differences with differences in beta-lactamase patterns is discussed with particular reference to strains of Escherichia coli and Klebsiella spp. Since beta-lactamases may be universally produced by bacteria, separation of the enzymes by analytical isoelectric focusing could be used in bacterial taxonomy.
β-内酰胺酶(EC. 3.5.2.6)可通过分析等电聚焦法直接进行比较。运用该技术,对来自5个革兰氏阳性菌属和16个革兰氏阴性菌属的242株菌株进行了检测。每株菌株的制剂聚焦为一组单一的条带,与任何R因子相关的β-内酰胺酶模式均不匹配。已知这些菌株均未携带R因子,且耐药性转移实验未成功。因此,所研究的酶被认为是由染色体介导的。其等电点范围为3.9至8.7,与底物谱或其他生化特性无关。染色体β-内酰胺酶似乎对菌属、菌种和亚种具有特异性,产生相同β-内酰胺酶的菌株具有相同的细菌特征。本文特别参照大肠杆菌和克雷伯菌属菌株,讨论了细菌学差异与β-内酰胺酶模式差异之间的相关性。由于细菌可能普遍产生β-内酰胺酶,通过分析等电聚焦法分离这些酶可用于细菌分类学。