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Peer-reviewedCC BYJournal of microbiology and biotechnology

Isolation and Characterization of Levilactobacillus brevis FBL-3 from Godeulppaegi Kimchi and Screening of Medium Components for γ-Aminobutyric Acid Production.

  1. 1Department of Food Science and Technology, Yeungnam University, Gyeongsan 38541, Republic of Korea.
  2. 2Department of Microbiology, Yogi Vemana University, Kadapa, AP 516005, India.
  3. 3Department of Food Science & Technology, Chonnam National University, Gwangju 61186, Republic of Korea.

Abstract

γ-Aminobutyric acid (GABA) is an amino acid with a variety of biological functions and is now becoming an essential food ingredient. In this work, a GABA-producing lactic acid bacterium was isolated from godeulppaegi kimchi and characterized by phenotypic, biochemical and molecular parameters. The isolate was identified as FBL-3, which produced acid colonies in MRS agar containing CaCO₃ and L-glutamic acid, was Gram positive, catalase-negative and rod-shaped, and had 99.1% similarity to Levilactobacillus brevis by API 50 CHL analysis and 100% 16S rRNA gene sequence similarity to Lvb. brevis ATCC 14869. Further, sequence analysis of 16S rRNA gene confirmed that it was Lvb. brevis FBL-3. The effects of carbon source, nitrogen source, and L-glutamic acid concentration on cell growth and TLC-densitometrically estimated GABA production were evaluated sequentially using a one-factor-at-a-time approach. Of the carbon sources tested, xylose had the highest GABA production (12.2 ± 2.34 g/L) and dry cell weight (0.75 ± 0.00 g/L) and 10 g/L xylose was selected as a good concentration for GABA production. Yeast extract was the most promising for nitrogen sources producing 4.65 ± 0.45 g/L GABA, and 20 g/L yeast extract was selected as a practical concentration since it produced 9.12 ± 1.48 g/L GABA with lower nitrogen input than 50 g/L yeast extract. L-Glutamic acid was a necessary precursor to GABA production. Although the highest GABA titer in the L-glutamic acid concentration experiment was found for 50 g/L L-glutamic acid (19.6 ± 1.03 g/L), 10 g/L L-glutamic acid supported the highest cell growth and was considered as a more balanced precursor.

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BibTeX
@article{jang2026isolation,
  title = {{Isolation and Characterization of Levilactobacillus brevis FBL-3 from Godeulppaegi Kimchi and Screening of Medium Components for γ-Aminobutyric Acid Production.}},
  author = {Eun-Ju Jang and Veeranjaneya Reddy Lebaka and Young-Min Kim and Young-Jung Wee},
  journal = {Journal of microbiology and biotechnology},
  year = {2026},
  month = sep,
  doi = {10.4014/jmb.2608.08011},
  url = {https://europepmc.org/article/MED/42870455},
  note = {CC BY},
}
RIS
TY  - JOUR
TI  - Isolation and Characterization of Levilactobacillus brevis FBL-3 from Godeulppaegi Kimchi and Screening of Medium Components for γ-Aminobutyric Acid Production.
AU  - Eun-Ju Jang
AU  - Veeranjaneya Reddy Lebaka
AU  - Young-Min Kim
AU  - Young-Jung Wee
PY  - 2026
DA  - 2026/09/22
JO  - Journal of microbiology and biotechnology
DO  - 10.4014/jmb.2608.08011
UR  - https://europepmc.org/article/MED/42870455
AB  - γ-Aminobutyric acid (GABA) is an amino acid with a variety of biological functions and is now becoming an essential food ingredient. In this work, a GABA-producing lactic acid bacterium was isolated from godeulppaegi kimchi and characterized by phenotypic, biochemical and molecular parameters. The isolate was identified as FBL-3, which produced acid colonies in MRS agar containing CaCO₃ and L-glutamic acid, was Gram positive, catalase-negative and rod-shaped, and had 99.1% similarity to Levilactobacillus brevis by API 50 CHL analysis and 100% 16S rRNA gene sequence similarity to Lvb. brevis ATCC 14869. Further, sequence analysis of 16S rRNA gene confirmed that it was Lvb. brevis FBL-3. The effects of carbon source, nitrogen source, and L-glutamic acid concentration on cell growth and TLC-densitometrically estimated GABA production were evaluated sequentially using a one-factor-at-a-time approach. Of the carbon sources tested, xylose had the highest GABA production (12.2 ± 2.34 g/L) and dry cell weight (0.75 ± 0.00 g/L) and 10 g/L xylose was selected as a good concentration for GABA production. Yeast extract was the most promising for nitrogen sources producing 4.65 ± 0.45 g/L GABA, and 20 g/L yeast extract was selected as a practical concentration since it produced 9.12 ± 1.48 g/L GABA with lower nitrogen input than 50 g/L yeast extract. L-Glutamic acid was a necessary precursor to GABA production. Although the highest GABA titer in the L-glutamic acid concentration experiment was found for 50 g/L L-glutamic acid (19.6 ± 1.03 g/L), 10 g/L L-glutamic acid supported the highest cell growth and was considered as a more balanced precursor.
SN  - 1017-7825
SN  - 1738-8872
ER  -