Article

Exploring the modulation of extracellular metabolites in different Listeria monocytogenes strains under cold-stress

Hyun-Jun Kim1,, Hye-Jin Kim1,, Cheorun Jo1,2,*
Author Information & Copyright
1Department of Agricultural Biotechnology, Center for Food and Bioconvergence, and Research Institute of Agriculture and Life Science, Seoul National University, Seoul 08826, Korea.
2Institute of Green BioScience and Technology, Seoul National University, Pyeongchang 25354, Korea.

† These authors contributed equally to this work.

*Corresponding Author: Cheorun Jo. E-mail: cheorun@snu.ac.kr.

© Copyright 2024 Korean Society for Food Science of Animal Resources. This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

Received: Jul 22, 2024 ; Revised: Aug 28, 2024 ; Accepted: Sep 10, 2024

Published Online: Sep 20, 2024

Abstract

This study investigated the modulation of extracellular metabolites in Listeria monocytogenes NCCP 15743 (L5), NCCP 16594 (L6), and ATCC 19111 (L9) strains in cold-stressed culture. The strains were cultured in Mueller Hinton broth at 8°C for 22 days. Extracellular metabolites were extracted at five growth phases (initial, lag, log, early saturate, and saturate) of each strain. Under cold-stress, growth phases of L5 and L6 exhibited similarities, while L9 displayed a distinct pattern. The change in extracellular metabolites under cold-stress was dependent on growth phase and strain. The presence of L. monocytogenes was distinguished based on the concentrations of trehalose, isoleucine, arginine, and phenylalanine. During extended cold-stressed culture, all strains enhanced two metabolic pathways at the lag and log phases: energy metabolism (trehalose, lactate, propanoate, acetate, ethanol, and formic acid) and glutathione-related metabolism (acetate, histidine, arginine, proline, glutamate, glycine, serine, and methionine). The expression of these extracellular metabolites provides crucial insights into the complex metabolic adaptations of L. monocytogenes during cold-stress culture. This study introduces a distinctive approach to identifying L. monocytogenes under cold-stress, offering potential application for safety enhancement in the food industry.

Keywords: Extracellular metabolites; Multivariate analysis; Culture media; Foodborne pathogens detection method; Nuclear magnetic resonance spectroscopy