Trias J, Nikaido H
Department of Microbiology and Immunology, University of California, Berkeley 94720.
Antimicrob Agents Chemother. 1990 Jan;34(1):52-7. doi: 10.1128/AAC.34.1.52.
The outer membrane of imipenem-resistant mutants of Pseudomonas aeruginosa with decreased permeability to imipenem was shown by Western (immuno-) blotting to contain protein D1 and to lack protein D2. Protein D2 was purified and was shown to allow the permeation of imipenem at a rate higher than expected from its molecular weight. Spontaneous imipenem-resistant mutants of P. aeruginosa PAO1 appeared at a frequency of 10(-8) in the laboratory and did not synthesize protein D2. Experiments performed with intact cells carrying plasmid pHN4 containing the gene for L-1 beta-lactamase from Pseudomonas maltophilia showed that this channel could also be used by SM-7338, Sch 33755, and Sch 33440 but apparently not by Sch 34343 or Sch 29482.
对亚胺培南通透性降低的铜绿假单胞菌亚胺培南耐药突变体的外膜经蛋白质免疫印迹法显示含有蛋白质D1且缺乏蛋白质D2。蛋白质D2经纯化后,其对亚胺培南的通透速率高于根据其分子量预期的速率。铜绿假单胞菌PAO1的自发亚胺培南耐药突变体在实验室中的出现频率为10^(-8),且不合成蛋白质D2。对携带含有嗜麦芽窄食单胞菌L-1β-内酰胺酶基因的质粒pHN4的完整细胞进行的实验表明,该通道也可被SM-7338、Sch 33755和Sch 33440利用,但显然不能被Sch 34343或Sch 29482利用。