Biochemical, Kinetic and Biological Properties of Group V Phospholipase A2 from Dromedary

Molecules. 2022 May 26;27(11):3437. doi: 10.3390/molecules27113437.

Abstract

Secretory group V phospholipase A2 (PLA2-V) is known to be involved in inflammatory processes in cellular studies, nevertheless, the biochemical and the enzymatic characteristics of this important enzyme have been unclear yet. We reported, as a first step towards understanding the biochemical properties, catalytic characteristics, antimicrobial and cytotoxic effects of this PLA2, the production of PLA2-V from dromedary. The obtained DrPLA2-V has an absolute requirement for Ca2+ and NaTDC for enzymatic activity with an optimum pH of 9 and temperature of 45 °C with phosphatidylethanolamine as a substrate. Kinetic parameters showed that Kcat/Kmapp is 2.6 ± 0.02 mM-1 s-1. The enzyme was found to display potent Gram-positive bactericidal activity (with IC50 values of about 5 µg/mL) and antifungal activity (with IC50 values of about 25 µg/mL)in vitro. However, the purified enzyme did not display a cytotoxic effect against cancer cells.

Keywords: biological activities; characterization; kinetics; phospholipase V.

MeSH terms

  • Animals
  • Anti-Bacterial Agents* / pharmacology
  • Camelus*
  • Kinetics
  • Phospholipases A2 / pharmacology
  • Temperature

Substances

  • Anti-Bacterial Agents
  • Phospholipases A2

Grants and funding

This research received no external funding.