Organic acids metabolism in roots of grapevine rootstocks under severe iron deficiency

• Published in: Plant and soil Vol. 394; no. 1-2; pp. 165 - 175
• Main Authors: Covarrubias, José Ignacio, Rombolà, Adamo Domenico
• Format: Journal Article
• Language: English
• Published: Cham Springer International Publishing 01.09.2015; Springer; Springer Nature B.V
• Subjects: Acids; basins; Biomedical and Life Sciences; chlorosis; citric acid; Ecology; exudation; Flowers & plants; genotype; Genotypes; Grapes; Health aspects; Identification and classification; Iron; Iron (Nutrient); Life Sciences; malate dehydrogenase; Metabolism; nutrient deficiencies; Nutrient deficiency; nutrient solutions; Nutrients; Organic acids; Organic chemicals; phosphoenolpyruvate carboxylase; Plant metabolism; Plant Physiology; Plant Sciences; Plant-soil relationships; Regular Article; Roots; rootstocks; screening; soil; Soil Science & Conservation; Vitaceae; viticulture; Vitis; MED; Grapevine genotypes; Enzyme activity; Phosphoenolpyruvate carboxylase; Organic acids; Iron chlorosis
• ISSN: 0032-079X; 1573-5036
• DOI: 10.1007/s11104-015-2530-5

BACKGROUND AND AIMS: In many important viticultural areas of the Mediterranean basin, plants often face prolonged periods of scarce iron (Fe) availability in the soil. The objective of the present work was to perform a comparative analysis of physiological and biochemical responses of Vitis genotypes to severe Fe deficiency. METHODS: Three grapevine rootstocks differing in susceptibility to Fe chlorosis were grown with and without Fe in the nutrient solution. RESULTS: Rootstock 101-14, susceptible to Fe chlorosis, responded to severe Fe deficiency by reducing the root activity of phosphoenolpyruvate carboxylase (PEPC) and malate dehydrogenase (MDH), however, it accumulated high levels of citric acid. By contrast, rootstock 110 Richter, tolerant to Fe chlorosis, maintained an active metabolism of organic acids, but citric acid accumulation was lower than in 101-14. Similarly to 101-14, rootstock SO4 showed a strong decrease in PEPC and MDH activities. Nevertheless it maintained moderate citric acid levels in the roots, mimicking the response by 110 Richter. CONCLUSIONS: Root PEPC and MDH activities can be used as tools for screening Fe chlorosis tolerance. Conversely, organic acids accumulation in roots may not be a reliable indicator of Fe chlorosis tolerance, particularly under conditions of severe Fe deficiency, because of their probable exudation by roots. Our results show that drawing sound conclusions from screening programs involving Fe deficiency tolerance requires short as well as long-term assessment of responses to Fe deprivation.