Characterization of a glutamate decarboxylase (GAD) gene from Lactobacillus zymae
- Authors
- Park, Ji Yeong; Jeong, Seon-Ju; Kim, Jeong Hwan
- Issue Date
- Sep-2014
- Publisher
- SPRINGER
- Keywords
- gamma-Aminobutyric acid; gad gene cloning; Glutamate decarboxylase; Lactobacillus zymae
- Citation
- BIOTECHNOLOGY LETTERS, v.36, no.9, pp 1791 - 1799
- Pages
- 9
- Indexed
- SCI
SCIE
SCOPUS
- Journal Title
- BIOTECHNOLOGY LETTERS
- Volume
- 36
- Number
- 9
- Start Page
- 1791
- End Page
- 1799
- URI
- https://scholarworks.gnu.ac.kr/handle/sw.gnu/18825
- DOI
- 10.1007/s10529-014-1539-9
- ISSN
- 0141-5492
1573-6776
- Abstract
- Lactic acid bacteria (LAB) were isolated from Kimchi, a Korean traditional fermented vegetable food. LAB accumulating GABA (gamma-aminobutyric acid) in the culture media were screened by TLC analysis. One isolate, GU240, produced the highest amount of GABA among the 3,000 isolates and identified as a Lactobacillus zymae strain. Glutamate decarboxylase (GAD) gene was cloned and over-expressed in E. coli BL21(DE3) using pET26b(+). The recombinant GAD was purified by using a Ni-NTA column. Its size was 53 kDa by SDS-PAGE. Maximum GAD activity was at pH 4.5 and 41 A degrees C and the activity was dependent on pyridoxal 5'-phosphate. K-m and V-max of LzGAD were 1.7 mM and 0.01 mM/min, respectively, when glutamate was used as a substrate.
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