Please use this identifier to cite or link to this item: https://rda.sliit.lk/handle/123456789/1203
Title: Calcium/calmodulin activation of two divergent glutamate decarboxylases from tobacco
Authors: Yevtushenko, D. P
McLean, M. D
Peiris, S
Cauwenberghe, O. R. V
Shelp, B. J
Keywords: cDNA sequences
g-aminobutyrate
glutamate decarboxylase
recombinant protein
tobacco
Issue Date: 1-Aug-2003
Publisher: Oxford University Press
Citation: Dmytro P. Yevtushenko, Michael D. McLean, Sriyani Peiris, Owen R. Van Cauwenberghe, Barry J. Shelp, Calcium/calmodulin activation of two divergent glutamate decarboxylases from tobacco*, Journal of Experimental Botany, Volume 54, Issue 389, 1 August 2003, Pages 2001–2002, https://doi.org/10.1093/jxb/erg210
Series/Report no.: Journal of experimental botany;Vol 54 Issue 389 Pages 2001-2002
Abstract: Glutamate decarboxylase (GAD, EC 4.1.1.15) catalyses the α‐decarboxylation of glutamate to produce γ‐aminobutyrate (GABA). The nucleotide sequences of two divergent GADs (designated GAD1 and GAD3) were isolated from a Nicotianatabacum L. cv. Samsun NN leaf cDNA library. Open reading frames indicated that GAD1 encodes a polypeptide of 496 amino acids and has greater than 99% identity with known tobacco GADs, whereas GAD3 encodes a polypeptide of 491 amino acids and has about 14% divergence from known tobacco GADs. Genomic DNA analysis suggested that there are at least four tobacco GAD genes, existing in pairs of highly identical genes. An in vitro assay at pH 7.3 revealed that activities of the recombinant proteins, after isolation from Escherichia coli and partial purification by nickel‐affinity chromatography, are 57–133 times the control levels in the presence of 0.5 mM calcium and 0.2 µM bovine calmodulin.
URI: http://rda.sliit.lk/handle/123456789/1203
ISSN: 1460-2431
Appears in Collections:Research Papers
Research Papers - School of Natural Sciences
Research Papers - SLIIT Staff Publications

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