# Effect of Glutamate Concentration and Atmosphere of Incubation on the Production of ɣ-Aminobutyric Acid in Levilactobacillus brevis LB12

**Authors:** Emanuela Lavanga, Marilisa Giavalisco, Annamaria Ricciardi, Teresa Zotta

PMC · DOI: 10.3390/microorganisms14010108 · 2026-01-04

## TL;DR

This study explores how oxygen and glutamate affect GABA production and gene regulation in Levilactobacillus brevis LB12.

## Contribution

The study reveals how oxygen negatively impacts GABA production and gene expression in Levilactobacillus brevis.

## Key findings

- Aerobic conditions increased biomass but reduced GABA production from glutamate.
- Oxygen strongly reduced the transcription of gadC and gadB genes.
- Switching incubation atmosphere did not restore gene functionality under oxygen exposure.

## Abstract

Levilactobacillus brevis is able to produce ɣ-aminobutyric acid (GABA), a non-proteogenic amino acid that provides several benefits to human health. In this study, we investigated the effect of glutamate (Glu) and oxygen (O2) on biomass yield, GABA production and regulation of the gad operon in Lvb. brevis LB12. A change in incubation atmosphere from anaerobiosis (AN) to aerobiosis (AE) was applied to elucidate if AE pre-adaptation and cultivation could be exploited to improve cell density, as well as to determine the role of O2 on the expression of the gad operon. AE increased biomass yield, but impaired Glu to GABA conversion, in both the cultivation and the adaptation phases. The gad operon (gadR, gadC, gadB, gltX) was up-regulated in the presence of Glu, while O2 strongly reduced the transcription of gadC and gadB. Switching the incubation atmosphere (AE vs. AN) and Glu supplementation did not restore the gene functionality, suggesting that the negative effect of O2 was persistent and more prolonged adaptation to AN would be required. This study provides additional data on the regulation of the gad operon, but further insight on the effect of O2 upon GABA production by Lvb. brevis must be expanded to understand the possible mechanisms involved.

## Linked entities

- **Genes:** gadR (acid resistance transcriptional regulator GadR) [NCBI Gene 32488837], gadC (amino acid antiporter) [NCBI Gene 917297], gadB (glutamate decarboxylase GadB) [NCBI Gene 887580], gltX (glutamate--tRNA ligase) [NCBI Gene 882647]
- **Chemicals:** glutamate (PubChem CID 611), oxygen (PubChem CID 977)
- **Species:** Levilactobacillus brevis (taxon 1580)

## Full-text entities

- **Genes:** GAD1 (glutamate decarboxylase 1) [NCBI Gene 2571] {aka CPSQ1, DEE89, GAD, GAD-67, SCP}
- **Chemicals:** O2 (MESH:D010100), GABA (MESH:D005680), Glu (MESH:D018698)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12843658/full.md

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Source: https://tomesphere.com/paper/PMC12843658