Concepedia

TLDR

The study evaluated carvacrol, (+)-carvone, thymol, and trans‑cinnamaldehyde for antibacterial activity against *E. coli* O157:H7 and *S. typhimurium*, assessed their toxicity to *Photobacterium leiognathi* using a bioluminescence assay, and examined cell‑surface effects via NPN uptake, detergent/lysozyme sensitization, and release of cell material.

Abstract

Carvacrol, (+)-carvone, thymol, and trans-cinnamaldehyde were tested for their inhibitory activity against Escherichia coli O157:H7 and Salmonella typhimurium. In addition, their toxicity to Photobacterium leiognathi was determined, utilizing a bioluminescence assay. Their effects on the cell surface were investigated by measuring the uptake of 1-N-phenylnaphthylamine (NPN), by measuring their sensitization of bacterial suspensions toward detergents and lysozyme, and by analyzing material released from cells upon treatment by these agents. Carvacrol, thymol, and trans-cinnamaldehyde inhibited E. coli and S. typhimurium at 1−3 mM, whereas (+)-carvone was less inhibitory. trans-Cinnamaldehyde was the most inhibitory component toward P. leiognathi. Carvacrol and thymol disintegrated the outer membrane and released outer membrane-associated material from the cells to the external medium; such release by (+)-carvone or trans-cinnamaldehyde was negligible. Of the tested components, carvacrol and thymol decreased the intracellular ATP pool of E. coli and also inreased extracellular ATP, indicating disruptive action on the cytoplasmic membrane. Keywords: Essential oils; carvacrol; carvone; cinnamaldehyde; thymol; antimicrobial activity; outer membrane; lipopolysaccharide

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