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 > or = 128-fold and decreased the MICs of imipenem, ciprofloxacin, and chloramphenicol > or = 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.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Amino Acid Sequence
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Anti-Infective Agents / pharmacology
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Bacterial Proteins / chemistry
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Bacterial Proteins / genetics
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Bacterial Proteins / metabolism*
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Drug Resistance, Bacterial
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Klebsiella pneumoniae / drug effects*
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Klebsiella pneumoniae / genetics
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Klebsiella pneumoniae / metabolism*
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Microbial Sensitivity Tests
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Molecular Sequence Data
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Porins / chemistry
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Porins / genetics
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Porins / metabolism*
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Protein Structure, Secondary
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Sequence Alignment
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Sequence Homology, Amino Acid
Substances
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Anti-Infective Agents
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Bacterial Proteins
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OmpK35 porin, Klebsiella pneumoniae
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Porins