Low-affinity penicillin-binding protein associated with beta-lactam resistance in Staphylococcus aureus

BJ Hartman, A Tomasz - Journal of bacteriology, 1984 - Am Soc Microbiol
BJ Hartman, A Tomasz
Journal of bacteriology, 1984Am Soc Microbiol
Methicillin resistance in Staphylococcus aureus has been associated with alterations in the
penicillin-binding proteins (PBPs). An intriguing property of all methicillin-resistant
staphylococci is the dependence of resistance on the pH value of the growth medium.
Growth of such bacteria at pH 5.2 completely suppressed the expression of methicillin
resistance. We have examined the PBP patterns of methicillin-resistant staphylococci grown
at pH 7.0. We detected a high-molecular-weight PBP (PBP-2a; approximate size, 78,000 …
Methicillin resistance in Staphylococcus aureus has been associated with alterations in the penicillin-binding proteins (PBPs). An intriguing property of all methicillin-resistant staphylococci is the dependence of resistance on the pH value of the growth medium. Growth of such bacteria at pH 5.2 completely suppressed the expression of methicillin resistance. We have examined the PBP patterns of methicillin-resistant staphylococci grown at pH 7.0. We detected a high-molecular-weight PBP (PBP-2a; approximate size, 78,000 daltons) that was only present in the resistant bacteria but not in the isogenic sensitive strain. In cultures grown at pH 5.2, the extra PBP was not detectable.
American Society for Microbiology