Glutamine chelation governs the selective inhibition of Staphylococcus aureus and Salmonella typhi growth by cis-dichloro-bis(8-quinolinolato)zirconium(IV): Theory and experiment

Eur J Pharm Sci. 2020 Aug 1:151:105427. doi: 10.1016/j.ejps.2020.105427. Epub 2020 Jun 13.

Abstract

Quinolone-based Schiff base zirconium(IV) complex was studied as potential bacterial inhibitor against Gram-positive Staphylococcus aureus and Gram-negative Salmonella typhi growth, showing that the interaction of the complex with L-glutamine which presents in the membrane of wall leads cell death, and the mode of bacterial interaction was analyzed theoretically by DFT. Furthermore, the interaction of different amino acid residues L-alanine, D-alanine, L-lysine and D-glutamine with the metal complex through UV-vis docking studies was conducted observing that D-glutamine interacts efficiently among other amino acid residues. This observation is consistent with the interaction of the metal complex that was effective when participating in an insight of the peptidoglycan cell wall since the binding nature of glutamine potentially inhibits these microorganisms.

Keywords: Amino acid bindings; Salmonella typhi; Schiff base zirconium(IV) complex; Staphylococcus aureus; TD-DFT.

MeSH terms

  • Glutamine
  • Humans
  • Salmonella typhi
  • Staphylococcal Infections*
  • Staphylococcus aureus*
  • Zirconium

Substances

  • Glutamine
  • Zirconium