Characterization of the recombinant glutamate decarboxylase of lactobacillus brevis G144 isolated from Galchi Jeotgal, a Korean Salted and Fermented Seafoodopen access
- Authors
- Kim, J.A.; Park, J.Y.; Kim, J.H.
- Issue Date
- 1-Mar-2021
- Publisher
- Korean Society for Microbiolog and Biotechnology
- Keywords
- GABA; Galchi jeotgal; Glutamate decarboxylase; Lactobacillus brevis
- Citation
- Microbiology and Biotechnology Letters, v.49, no.1, pp 9 - 17
- Pages
- 9
- Indexed
- SCOPUS
- Journal Title
- Microbiology and Biotechnology Letters
- Volume
- 49
- Number
- 1
- Start Page
- 9
- End Page
- 17
- URI
- https://scholarworks.gnu.ac.kr/handle/sw.gnu/5609
- DOI
- 10.48022/MBL.2002.02019
- ISSN
- 1598-642X
- Abstract
- A γ-aminobutyric acid (GABA)-producing microorganism was isolated from galchi (hairtail fish, Trichiurus lepturus) jeotgal, a Korean salted and fermented seafood. The G144 isolate produced GABA excessively when incubated in MRS broth containing monosodium glutamate (MSG, 3%, w/v). G144 was identified as Lactobacillus brevis through 16S rRNA and recA gene sequencing. gadB and gadC encoding glutamate decarboxylase (GAD) and glutamate/GABA antiporter, respectively, were cloned and gadB was located downstream of gadC. The operon structure of gadCB was confirmed by reverse transcription (RT)-polymerase chain reaction. gadB was overexpressed in Escherichia coli and recombinant GAD was purified and its size was 54.4 kDa as evidenced by SDS-PAGE results. Maximum GAD activity was observed at pH 5.0 and 40℃ and the activity was dependent on pyridoxal 5'-phophate. The Km and Vmax of GAD were 8.6 mM and 0.01 mM/min, respectively. ? 2021, The Korean Society for Microbiology and Biotechnology
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