Nordström K, Burman L G, Eriksson-Grennberg K G
J Bacteriol. 1970 Mar;101(3):659-68. doi: 10.1128/jb.101.3.659-668.1970.
Class II ampicillin-resistant mutants of Escherichia coli are defined as having a twofold increase in penicillinase-mediated ampicillin resistance when determined by colony formation tests on plates. In this paper, one class II mutant has been compared to its parent strain. In liquid medium, the mutant was less resistant than the parent strain both in the absence and in the presence of R1 and R-factor mediating penicillinase activity. The penicillinase activity was found to be almost completely bound to the cells in the parent strain, whereas it was excreted to a great extent in the class II mutant strain. In liquid medium, resistance was well correlated to the cell-bound penicillinase activity, whereas the excreted penicillinases were also of great importance for survival on ampicillin plates. The mutant also had a changed resistance to a great number of other antibacterial drugs. The mutant was found to be more sensitive than the parent strain to osmotic shock, especially when treated with ethylenediaminetetraacetic acid or washed with sodium ions. However, the osmotic stability was restored by the presence of 1 mm Mg(2+) ions. The class II mutant was more sensitive than the parent strain to sodium cholate, and it adsorbed the phages T4 and T3-1 at a slower rate than did the parent strain. The two strains adsorbed T6 at the same rate. The class II phenotype could be gradually reversed by increasing concentrations of divalent cations. The pleiotropic changes in the phenotype are apparently unrelated to the specific targets for the antibacterial agents tested. They are secondary consequences of a cell envelope mutation. The findings indicate that the class II mutation mediates a structural change in the lipopolysaccharide of the cell envelope.
大肠杆菌的II类氨苄青霉素抗性突变体被定义为通过平板上的菌落形成试验测定时,青霉素酶介导的氨苄青霉素抗性增加两倍。在本文中,将一个II类突变体与其亲本菌株进行了比较。在液体培养基中,无论有无R1和介导青霉素酶活性的R因子,该突变体的抗性均低于亲本菌株。发现亲本菌株中的青霉素酶活性几乎完全与细胞结合,而在II类突变体菌株中它大量分泌到细胞外。在液体培养基中,抗性与细胞结合的青霉素酶活性密切相关,而分泌的青霉素酶对在氨苄青霉素平板上存活也非常重要。该突变体对许多其他抗菌药物的抗性也发生了变化。发现该突变体比亲本菌株对渗透休克更敏感,尤其是在用乙二胺四乙酸处理或用钠离子洗涤时。然而,1 mM Mg(2+)离子的存在可恢复其渗透稳定性。II类突变体比亲本菌株对胆酸钠更敏感,并且它吸附噬菌体T4和T3-1的速度比亲本菌株慢。这两个菌株吸附T6的速度相同。通过增加二价阳离子的浓度,II类表型可逐渐逆转。表型的多效性变化显然与所测试抗菌剂的特定靶点无关。它们是细胞膜突变的次要后果。研究结果表明,II类突变介导了细胞膜脂多糖的结构变化。