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ABSTRACT OmpK35 from Klebsiella pneumoniae is the homologue of Escherichia coli OmpF porin. Expression of OmpK35 in K. pneumoniae strain CSUB10R (lacking both OmpK35 and OmpK36) decreased the MICs of cephalosporins and meropenem ≥128-fold and decreased the MICs of imipenem, ciprofloxacin, and chloramphenicol ≥8-fold. MIC reductions by OmpK35 were 4 times (cefepime), 8 times (cefotetan, cefotaxime, and cefpirome), or 128 times (ceftazidime) higher than those caused by OmpK36, but the MICs were similar or 1 dilution lower for other evaluated agents.
Sequence Homology, Amino Acid, Molecular Sequence Data, Porins, Microbial Sensitivity Tests, Protein Structure, Secondary, Klebsiella pneumoniae, Anti-Infective Agents, Bacterial Proteins, Drug Resistance, Bacterial, Amino Acid Sequence, Sequence Alignment
Sequence Homology, Amino Acid, Molecular Sequence Data, Porins, Microbial Sensitivity Tests, Protein Structure, Secondary, Klebsiella pneumoniae, Anti-Infective Agents, Bacterial Proteins, Drug Resistance, Bacterial, Amino Acid Sequence, Sequence Alignment
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