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Characterization of a glutamate decarboxylase (GAD) gene from Lactobacillus zymae

Authors
Park, Ji YeongJeong, Seon-JuKim, 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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