Nitrogen metabolism in durum wheat under salinity: accumulation of proline and glycine betaine
Petronia Carillo A C , Gabriella Mastrolonardo A , Francesco Nacca A , Danila Parisi A , Angelo Verlotta A B and Amodio Fuggi AA Dipartimento di Scienze della Vita, Seconda Università degli Studi di Napoli, Via Vivaldi 43, 81100 Caserta, Italy.
B Istituto Sperimentale per la Cerealicoltura C. R. A., SS 16 Km 675, 71100 Foggia, Italy.
C Corresponding author. Email: petronia.carillo@unina2.it
Functional Plant Biology 35(5) 412-426 https://doi.org/10.1071/FP08108
Submitted: 3 March 2008 Accepted: 29 April 2008 Published: 11 July 2008
Abstract
We studied the effect of salinity on amino acid, proline and glycine betaine accumulation in leaves of different stages of development in durum wheat under high and low nitrogen supply. Our results suggest that protective compounds against salt stress are accumulated in all leaves. The major metabolites are glycine betaine, which preferentially accumulates in younger tissues, and proline, which is found predominantly in older tissues. Proline tended to accumulate early, at the onset of the stress, while glycine betaine accumulation was observed during prolonged stress. Nitrate reductase (NR) and glutamate synthase (GOGAT) are positively correlated with these compatible solutes: proline is associated with NR in the oldest leaves of high-nitrate plants and glycine betaine is associated with GOGAT in the youngest leaves of both low- and high-nitrate plants. In high-nitrate conditions proline accounts for more than 39% of the osmotic adjustment in the cytoplasmic compartments of old leaves. Its nitrogen-dependent accumulation may offer an important advantage in that it can be metabolised to allow reallocation of energy, carbon and nitrogen from the older leaves to the younger tissues. The contribution of glycine betaine is higher in young leaves and is independent of nitrogen nutrition.
Additional keywords: compatible solutes, glutamate synthase, nitrate reductase, nitrogen metabolism, salt stress.
Acknowledgements
The research was supported by ‘Ministero dell’Istruzione, dell’Università e della Ricerca’ and ‘Seconda Universitá di Napoli (Fondi di Ateneo)’. We gratefully acknowledge the kind gift of the rabbit antiserum raised against purified GOGAT from Dr Brian Forde (Department of Biological Science, Lancaster University, UK). We gratefully acknowledge Dr Ronan Sulpice and Dr John E. Lunn (Max Planck Institute of Molecular Plant Physiology, Golm, Germany) for advice during the course of this work and Dr Gareth S. Catchpole (Max Planck Institute of Molecular Plant Physiology, Golm, Germany) for his critical and constructive review of the manuscript.
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