# Regulation of Arginine Metabolism and Ethanol Tolerance in Saccharomyces cerevisiae by BTN2

**Authors:** Ting Xia, Keiwei Chen, Huqi Zhou, Tangchao Chen, Wenjing Lin, Gongnian Xiao, Ruosi Fang

PMC · DOI: 10.1002/fsn3.70244 · 2025-05-01

## TL;DR

This study shows how the BTN2 gene in yeast affects arginine metabolism and ethanol tolerance, offering a way to reduce harmful urea in wine.

## Contribution

The study reveals BTN2's role in regulating arginine transport, catabolism, and urea degradation in yeast under ethanol stress.

## Key findings

- BTN2 knockout inhibits arginine intake and promotes urea reduction in Saccharomyces cerevisiae.
- BTN2 modulates gene expression of GAP1, CAN1, CAR1, and DUR1,2 in arginine metabolism.
- BTN2 enhances ethanol tolerance and reduces oxidative damage in yeast cells.

## Abstract

Ethyl carbamate (EC), primarily formed by the reaction between urea and ethanol, is a natural carcinogen prevalent in fermented alcoholic beverages. Urea is an arginine metabolite produced by 
Saccharomyces cerevisiae
. Previous studies have shown that BTN2 influences arginine metabolism. In this study, we compared the effects of BTN2‐modified strains on key metabolites, enzymes, and transcriptional gene expressions in the arginine metabolic pathway, and assessed cell growth and oxidative damage under different ethanol stresses. It revealed that the knockout of BTN2 inhibited arginine intake and promoted urea reduction. RT‐qPCR results demonstrated that BTN2 regulate arginine transportation, catabolism, and urea degradation by modulating the expression of GAP1, CAN1, CAR1, and DUR1,2. Moreover, the results showed that BTN2 enhanced ethanol tolerance and alleviated cellular damage. These findings provide a promising method for reducing arginine uptake by 
Saccharomyces cerevisiae
 and consequently urea accumulation in wine.

The impact of BTN2 modified strains on key metabolites, enzymes, and gene expression in the arginine metabolic pathway was investigated. BTN2 knock out strain was found to reduce arginine uptake and promote arginine and urea degradation. BTN2 was found to enhance ethanol tolerance and reduce ethanol‐induced oxidative damage.

## Linked entities

- **Genes:** BTN2 (Btn2p) [NCBI Gene 853043], gap-1 (C2 domain-containing protein;GTPase Activating Protein family;Ras GTPase-activating protein gap-1) [NCBI Gene 180530], CAN1 (arginine permease CAN1) [NCBI Gene 856646], CA1 (carbonic anhydrase 1) [NCBI Gene 759], DUR12 (bifunctional urea carboxylase/allophanate hydrolase) [NCBI Gene 852507]
- **Chemicals:** ethyl carbamate (PubChem CID 5641), urea (PubChem CID 1176), ethanol (PubChem CID 702), arginine (PubChem CID 232)
- **Species:** Saccharomyces cerevisiae (taxon 4932)

## Full-text entities

- **Genes:** DUR12 (bifunctional urea carboxylase/allophanate hydrolase) [NCBI Gene 852507] {aka DUR80}, BTN2 (Btn2p) [NCBI Gene 853043], GAP1 (amino acid permease GAP1) [NCBI Gene 853912], CAN1 (arginine permease CAN1) [NCBI Gene 856646], CAR1 (arginase) [NCBI Gene 855993] {aka LPH15}
- **Chemicals:** EC (MESH:D014520), Ethanol (MESH:D000431), Arginine (MESH:D001120), Urea (MESH:D014508)
- **Species:** Saccharomyces cerevisiae (baker's yeast, species) [taxon 4932]

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12045926/full.md

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Source: https://tomesphere.com/paper/PMC12045926