Neyfakh A A, Bidnenko V E, Chen L B
Belozersky Laboratory of Molecular Biology and Bioorganic Chemistry, Moscow State University, USSR.
Proc Natl Acad Sci U S A. 1991 Jun 1;88(11):4781-5. doi: 10.1073/pnas.88.11.4781.
Bacillus subtilis cells selected for their resistance to rhodamine 6G demonstrated a multidrug-resistance (MDR) phenotype resembling that of mammalian MDR cells. Like MDR in mammalian cells, MDR in bacteria was mediated by the efflux of the drugs from the cells. The bacterial multidrug efflux system transported similar drugs and was sensitive to similar inhibitors as the mammalian multidrug transporter, P-glycoprotein. The gene coding for the bacterial multidrug transporter, like the P-glycoprotein gene in mammalian MDR cells, was amplified in the resistant bacteria. On the other hand, the bacterial multidrug transporter showed no sequence similarity to P-glycoprotein but exhibited an obvious homology to tetracycline efflux pumps and carbohydrate-ion symporters. These results show that the transport of structurally unrelated molecules can be mediated by members of different families of membrane transporters.
经筛选具有对罗丹明6G抗性的枯草芽孢杆菌细胞表现出一种多药耐药(MDR)表型,类似于哺乳动物的MDR细胞。与哺乳动物细胞中的MDR一样,细菌中的MDR是由药物从细胞中流出介导的。细菌多药外排系统转运相似的药物,并且对与哺乳动物多药转运蛋白P-糖蛋白相似的抑制剂敏感。与哺乳动物MDR细胞中的P-糖蛋白基因一样,编码细菌多药转运蛋白的基因在抗性细菌中被扩增。另一方面,细菌多药转运蛋白与P-糖蛋白没有序列相似性,但与四环素外排泵和碳水化合物-离子同向转运体表现出明显的同源性。这些结果表明,结构不相关分子的转运可由不同膜转运蛋白家族的成员介导。