| RRC ID |
66331
|
| Author |
Hasegawa M, Fujii S, Funato K, Yoshida A, Sambongi Y.
|
| Title |
Expression of two glutamate decarboxylase genes in Lactobacillus brevis during gamma-aminobutyric acid production with date residue extract.
|
| Journal |
Biosci Biotechnol Biochem
|
| Abstract |
Gamma-aminobutyric acid (GABA) is produced by Lactobacillus brevis using date residue fermentation. In this study, the GABA production method was improved, for which L. brevis strain JCM 1059T was the most efficient among the four L. brevis strains examined. This was presumably due to a difference in the expression level of the gene encoding glutamate decarboxylase that catalyzes GABA synthesis.Abbreviation: GABA: gamma-aminobutyric acid.
|
| Volume |
84(5)
|
| Pages |
1069-1072
|
| Published |
2020-5-1
|
| DOI |
10.1080/09168451.2020.1714422
|
| PMID |
31931681
|
| MeSH |
Amino Acid Sequence
Bacterial Proteins / metabolism
Fermentation
Gene Expression Regulation, Bacterial
Genes, Bacterial / genetics
Glutamate Decarboxylase / genetics*
Glutamate Decarboxylase / metabolism
Hydrogen-Ion Concentration
Levilactobacillus brevis / enzymology*
Levilactobacillus brevis / genetics*
Phoeniceae / chemistry*
Plant Extracts / metabolism*
RNA, Ribosomal, 16S / genetics
Reverse Transcriptase Polymerase Chain Reaction
gamma-Aminobutyric Acid / metabolism*
|
| Resource |
| General Microbes |
JCM1059
JCM1061
JCM1170
JCM1559 |
