首页 | 本学科首页   官方微博 | 高级检索  
   检索      


Cloning and expression of a full-length glutamate decarboxylase gene fromLactobacillus brevis BH2
Authors:Se-Hee Kim  Bo-Hye Shin  Yeon-Hee Kim  Soo-Wan Nam  Sung-Jong Jeon
Institution:(1) Department of Biotechnology and Bioengineering, Dong-Eui University, 614-714 Busan, Korea;(2) Department of Biomaterial Control (Brain Korea 21 Program), Dong-Eui University, 614-714 Busan, Korea
Abstract:A bacterium (BH2) that was found to produce a large amount of γ-aminobutyric acid (GABA) was isolated fromKimchi, a traditional fermented food in Korea. Phylogenetic analysis based on the 16S rDNA sequence and biochemical studies indicated that BH2 belonged to the genusLactobacillus brevis. Under controlled conditions in MRS broth (Difco) with 5% monosodium glutamate, this strain produced GABA at a concentration of 194 mM with a 73% GABA conversion rate after 48 h. A full-length glutamate decarboxylase (gad) gene was cloned by the rapid amplification of cDNA ends (RACE) PCR. The open reading frame (ORF) of thegad gene was composed of 1,407 nucleotides and encoded a protein (468 amino acids) with a predicted molecular weight of 53.5 kDa. The deduced amino acid sequence of GAD fromL. brevis showed 97.5 and 82.7% identities to theL. brevis OPK-3 GAD andL. plantarum WCFS1 GAD, respectively. Thegad gene was expressed inEscherichia coli cells and the expression was confirmed by SDS-PAGE analysis and enzyme activity studies.
Keywords:Lactobacillus brevis            γ  -aminobutyric acid (GABA)                      gutamate decarboxylase (GAD)                      RACE-PCR
本文献已被 SpringerLink 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号