Abstract
A full-length cDNA encoding glutamate decarboxylase (designated as OsGAD3),
which catalyzes the conversion of glutamate to gamma-aminobutyric acid
(GABA), was isolated from the GABA-rich giant-embryo Oryza sativa (Shangshi
Jing 315). The full-length cDNA of OsGAD3 (SSJ315) has a 1479 bp open reading
frame (ORF) encoding a protein of 492 amino acid residues. The deduced
protein had an isoelectric point (pI) of 5.72 and a calculated molecular
weight of 56.1 kD. Sequence comparison showed that OsGAD3 (SSJ315) matches
the glutamate decarboxylases of other plant species reported previously.
Analysis of the structural features of the C-terminal portions of plant GADs
revealed that OsGAD3 (SSJ315) has the typical CaM-binding domain (CaMBD) in
the C-terminal region as most other plant GADs. Evolution analysis showed
that plant GADs are conserved in the process of evolution. The cloning and
characterization of the OsGAD3 (SSJ315) gene will enable us to use OsGAD3 to
enhance GABA production in O. sativa (SSJ315) by metabolic engineering in the
near future.
Original language | English |
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Pages (from-to) | 873-879 |
Number of pages | 7 |
Journal | Archives of Biological Sciences |
Volume | 62 |
Issue number | 4 |
DOIs | |
Publication status | Published - 2010 |
User-Defined Keywords
- Cloning
- Oryza sativa
- OsGAD3
- RT-PCR