Baranowska H, Polakowska R, Putrament A
Acta Microbiol Pol. 1979;28(3):181-201.
Nitrous acid, diepoxybutane and methyl methane sulfonate induce effectively non-mitochondrial chloramphenicol-resistant mutants cross-resistant to other drugs. HNO2 induces also unstable erythromycin resistant mutants. The ability of the mutants to grow on antibiotic media can be modified by detergents, guanidine hydrochloride or increased osmotic pressure of the medium. This suggests that the resistance is due to changes in cell membrane permeability similar to those described by Rank, Robertson and Philips (1975b). Multiple drug-resistant mutants selected for chloramphenicol resistance show an increased sensitivity to ethidium bromide in glucose medium. Therefore the mutations involved increase probably nuclear envelope permeability to the latter drug. Results of genetic analyses of non-mitochondrial capr and eryr mutants suggest strongly that in most, if not all, cases the resistance is determined by interaction between nuclear and extranuclear factors.
亚硝酸、1,4 - 丁二醇二缩水甘油醚和甲基磺酸甲酯能有效诱导出对氯霉素耐药且对其他药物交叉耐药的非线粒体突变体。亚硝酸还能诱导出不稳定的红霉素耐药突变体。突变体在抗生素培养基上生长的能力可被去污剂、盐酸胍或培养基渗透压升高所改变。这表明耐药性是由于细胞膜通透性的改变,类似于Rank、Robertson和Philips(1975b)所描述的情况。为氯霉素耐药性而选择的多重耐药突变体在葡萄糖培养基中对溴化乙锭表现出更高的敏感性。因此,所涉及的突变可能增加了核膜对后一种药物的通透性。对非线粒体氯霉素耐药(capr)和红霉素耐药(eryr)突变体的遗传分析结果强烈表明,在大多数(如果不是全部)情况下,耐药性是由核因子和核外因子之间的相互作用决定的。