Inhibitory effect of plantaricin peptides (Pln E/F and J/K) against Escherichia coli

World J Microbiol Biotechnol. 2014 Nov;30(11):2829-37. doi: 10.1007/s11274-014-1708-y. Epub 2014 Aug 20.

Abstract

Plantaricins are small bioactive peptides produced by Lactobacillus plantarum strains that exhibit significant antimicrobial activity against closely-related Gram-positive bacteria, including food spoilage organisms. In comparison, bacteriocins including plantaricins, are usually less effective against Gram-negative organisms. In this study, we demonstrate that heterologously expressed and purified plantaricins, Pln E, -F, -J, and -K when tested against Gram negative model organism Escherichia coli K-12 were highly effective under certain conditions. The apparent tolerance of Gram-negative members to these peptides has been explained on the basis of the presence of the outer membrane (OM) that acts as a protective barrier. We have shown that agents and/or conditions that destabilize OM of E. coli K-12, make it susceptible to plantaricin peptides. In order to further strengthen this conclusion, an OM lipoprotein-defective lpp mutant strain of E. coli K-12 was also studied and compared. A significant loss of cell viability both in terms of CFU/ml as well as with live-dead dual staining combined with flow cytometry, could be demonstrated with the lpp mutant in comparison to the wild type strain. The results indicate that plantaricins can inhibit Gram-negative bacteria if the outer-membrane is weakened and it can be used in preservation of food with the help of some food-grade chelating agents.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anti-Bacterial Agents / metabolism
  • Anti-Bacterial Agents / pharmacology*
  • Bacteriocins / metabolism
  • Bacteriocins / pharmacology*
  • Cell Membrane / metabolism
  • Colony Count, Microbial
  • Drug Tolerance
  • Escherichia coli K12 / drug effects*
  • Lactobacillus plantarum / metabolism*
  • Microbial Viability / drug effects*
  • Peptides / metabolism
  • Peptides / pharmacology*
  • Permeability

Substances

  • Anti-Bacterial Agents
  • Bacteriocins
  • Peptides