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Calcium/calmodulin activation of two divergent glutamate decarboxylases from tobacco

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Date

2003-08-01

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Oxford University Press

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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.

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cDNA sequences, g-aminobutyrate, glutamate decarboxylase, recombinant protein, tobacco

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

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