Outer membrane protein D2 catalyzes facilitated diffusion of carbapenems and penems through the outer membrane of Pseudomonas aeruginosa

Antimicrob Agents Chemother. 1990 Jan;34(1):52-7. doi: 10.1128/AAC.34.1.52.

Abstract

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.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Anti-Bacterial Agents / metabolism*
  • Bacterial Outer Membrane Proteins / metabolism*
  • Cell Membrane Permeability
  • Diffusion
  • Imipenem / pharmacology
  • Kinetics
  • Lactams*
  • Meropenem
  • Molecular Weight
  • Plasmids
  • Pseudomonas aeruginosa / genetics
  • Pseudomonas aeruginosa / metabolism*
  • Pseudomonas aeruginosa / ultrastructure
  • Thienamycins / metabolism*

Substances

  • Anti-Bacterial Agents
  • Bacterial Outer Membrane Proteins
  • Lactams
  • Thienamycins
  • Imipenem
  • Sch 33755
  • Sch 29482
  • Sch 33440
  • Sch 34343
  • Meropenem