Structural and biochemical characterization of VIM-26 shows that Leu224 has implications for the substrate specificity of VIM metallo-β-lactamases

FEBS J. 2015 Mar;282(6):1031-42. doi: 10.1111/febs.13200. Epub 2015 Feb 6.

Abstract

During the last decades antimicrobial resistance has become a global health problem. Metallo-β-lactamases (MBLs) which are broad-spectrum β-lactamases that inactivate virtually all β-lactams including carbapenems, are contributing to this health problem. In this study a novel MBL variant, termed VIM-26, identified in a Klebsiella pneumoniae isolate was studied. VIM-26 belongs to the Verona integron-encoded metallo-β-lactamase (VIM) family of MBLs and is a His224Leu variant of the well-characterized VIM-1 variant. In this study, we report the kinetic parameters, minimum inhibitory concentrations and crystal structures of a recombinant VIM-26 protein, and compare them to previously published data on VIM-1, VIM-2 and VIM-7. The kinetic parameters and minimum inhibitory concentration determinations show that VIM-26, like VIM-7, has higher penicillinase activity but lower cephalosporinase activity than VIM-1 and VIM-2. The four determined VIM-26 crystal structures revealed mono- and di-zinc forms, where the Zn1 ion has distorted tetrahedral coordination geometry with an additional water molecule (W2) at a distance of 2.6-3.7 Å, which could be important during catalysis. The R2 drug binding site in VIM-26 is more open compared to VIM-2 and VIM-7 and neutrally charged due to Leu224 and Ser228. Thus, the VIM-26 drug binding properties are different from the VIM-2 (Tyr224/Arg228) and VIM-7 (His224/Arg228) structures, indicating a role of these residues in the substrate specificity.

Keywords: Klebsiella pneumoniae; antibiotic resistance; drug binding site; metallo-β-lactamase; minimum inhibitory concentrations.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anti-Bacterial Agents / chemistry
  • Bacterial Proteins / chemistry*
  • Binding Sites
  • Carbapenems / chemistry
  • Catalysis
  • Cephalosporins / chemistry
  • Crystallography, X-Ray
  • Drug Resistance, Bacterial
  • Ions
  • Klebsiella pneumoniae / enzymology
  • Leucine / chemistry*
  • Penicillins / chemistry
  • Protein Binding
  • Protein Structure, Secondary
  • Protein Structure, Tertiary
  • Recombinant Proteins / chemistry
  • Serine / chemistry
  • Substrate Specificity
  • beta-Lactamases / chemistry*

Substances

  • Anti-Bacterial Agents
  • Bacterial Proteins
  • Carbapenems
  • Cephalosporins
  • Ions
  • Penicillins
  • Recombinant Proteins
  • Serine
  • beta-Lactamases
  • beta-lactamase VIM-26, Klebsiella pneumoniae
  • Leucine