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Journal of the Science of Food and Agriculture· 2026Q1

Elucidating the source and metabolic impact of 2‐phenylethanol on Lactiplantibacillus pentosus 1 using a fish broth fermentation model

Pei Gao, Yumeng Dou, Qixing Jiang, Xiaojing Zhang et al.

Short summary

Saccharomyces cerevisiae 31 is the primary producer of 2-phenylethanol (2-PE), which at 8 mg/L significantly inhibits Lactiplantibacillus pentosus 1 growth, glucose metabolism, and lactic acid accumulation.

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Key points

  • Saccharomyces cerevisiae 31 was confirmed as the primary producer of 2-phenylethanol (2-PE).
  • Yeast metabolites, rather than direct cell contact, were found to have a stronger influence on LAB.
  • 8 mg/L of 2-PE significantly inhibited Lactiplantibacillus pentosus 1's growth, glucose consumption, and lactic acid accumulation.
  • 2-PE showed positive correlations with alcohol formation, glucose consumption, pH, total acidity, lactic acid, and valine.

AI-generated from the title and abstract; the full text is not read.

Abstract

Abstract BACKGROUND The quality of traditional fermented sour fish is shaped by metabolic interactions between core microbiota dominated by lactic acid bacteria (LAB) and yeasts. 2‐Phenylethanol (2‐PE) is a characteristic metabolite and quorum‐sensing molecule of Saccharomyces cerevisiae . This study aims to identify the primary source of 2‐PE via pure culture of dominant strains, and preliminarily investigate its effects on LAB in a fish broth fermentation model under different fermentation modes. RESULTS Single‐strain fermentation experiments confirmed that Saccharomyces cerevisiae 31 is the main producer of 2‐PE. Comparative analysis of different fermentation modes revealed that yeast metabolites exerted a stronger influence than cell‐to‐cell contact. Although not a dominant factor, 8 mg/L 2‐PE significantly inhibited the growth, glucose metabolism, and lactic acid accumulation of Lactiplantibacillus pentosus 1. Correlation analysis showed that 2‐PE had significant positive correlations with the formation of multiple alcohols, glucose consumption, pH, total acidity, lactic acid, and valine. It is speculated that 2‐PE may regulate fermentation performance by interfering with the glycolytic pathway, fatty acid metabolism, and valine metabolism in LAB. CONCLUSION This study clarifies the primary microbial source of 2‐PE in sour fish fermentation and verifies its specific regulatory effect on LAB, though it is not the core effector molecule through which Saccharomyces cerevisiae modulates LAB metabolism. The findings provide new insights into metabolite‐mediated microbial interactions in fermented food ecosystems, and the elucidated regulatory patterns offer reference for studies on other fermentation substrates including plant‐based foods and beverages. © 2026 Society of Chemical Industry.

The authors' abstract, as published at the source. Journal of the Science of Food and Agriculture, 2026 · DOI ↗

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Field: Food Science

Food ScienceAgricultural and Biological Sciences