Amyes S G, Towner K J, Carter G I, Thomson C J, Young H K
Department of Bacteriology, Medical School, University of Edinburgh, UK.
J Antimicrob Chemother. 1989 Aug;24(2):111-9. doi: 10.1093/jac/24.2.111.
Plasmid pUN835 was identified in an Escherichia coli strain isolated from an outbreak of porcine diarrhoea on a farm near Nottingham, UK. The trimethoprim resistance gene did not hybridize with any of the gene probes derived from known plasmid-encoded trimethoprim resistance genes. The trimethoprim resistance gene of pUN835 was shown to encode the production of a dihydrofolate reductase which confers high-level resistance on its host. This enzyme was smaller than most plasmid-encoded dihydrofolate reductases (molecular mass = 11,500) and was labile to heat. It had relatively low affinity for the substrate dihydrofolate (Km = 20 microM) and it was resistant to competitive inhibition by trimethoprim (Ki = 7.0 microM). We classify this novel enzyme as type VII.
质粒pUN835是在从英国诺丁汉附近一个农场的猪腹泻疫情中分离出的一株大肠杆菌中鉴定出来的。甲氧苄啶抗性基因与任何已知质粒编码的甲氧苄啶抗性基因衍生的基因探针均未杂交。pUN835的甲氧苄啶抗性基因被证明可编码二氢叶酸还原酶的产生,该酶赋予其宿主高水平抗性。这种酶比大多数质粒编码的二氢叶酸还原酶小(分子量 = 11,500),并且对热不稳定。它对底物二氢叶酸的亲和力相对较低(Km = 20 microM),并且对甲氧苄啶的竞争性抑制具有抗性(Ki = 7.0 microM)。我们将这种新型酶归类为VII型。