Correlation of the antimicrobial activity of ME1036 with its binding affinities to the penicillin-binding proteins from Streptococcus pneumoniae strains

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Abstract

We have correlated the binding affinities of ME1036, a carbapenem, to the penicillin-binding proteins (PBPs) from Streptococcus pneumoniae strains, with its bactericidal potency against those same strains. Certain mutations in the PBPs from S. pneumonaie strains decrease the binding affinities of Β-lactams for PBPs, which gives rise to clinical resistance to those Β-lactams. ME1036 has been shown to be strongly active against genotypic penicillin-intermediate S. pneumoniae (gPISP) strains and genotypic penicillin-resistant S. pneumoniae (gPRSP) strains that contain more than one mutation in their PBPs, owing to its strong affinity for those PBPs. © 2011 Japan Antibiotics Research Association All rights reserved.

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Hirai, Y., Takahata, S., Yamada, K., Ida, T., & Maebashi, K. (2011). Correlation of the antimicrobial activity of ME1036 with its binding affinities to the penicillin-binding proteins from Streptococcus pneumoniae strains. Journal of Antibiotics, 64(11), 741–746. https://doi.org/10.1038/ja.2011.76

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