Wheat seedlings ( Tddcum vulgare) treated with 1 mM KNO3 or NaNO3, in the presence of 0.2 mM CaSO4, were compared during a 48-hour period with respect to nitrate uptake, translocatlon, accumulation and reduction; cation uptake and accumulation; and malate accumulation. Seedlngs treated with KNO3 absord and accumulated more nitrate, had higher nitrate reductase levels in leaves but less in roots, accumulated 17 times more malate in leaves, and accumulated more of the accompanying cation than seedlings treated with NaNO3. Within seedlns of each treatment, changes in nitrate reductase activity and malate accumulation were parallel in leaves and in roots. Despite the great difference in malate accumulation, leaves of the KNO3-treated seedlgs had only slightly greater levels of phosphoenolpyruvate carboxylase than leaves of NaNO3-treated seedlings. NADP-malic enzyme levels increased only slightiy in leaves and roots of both KNO3-and NaNO3-treated seedlns. The effects of K+ and Na+ on all of these parameters can best be explained by their effects on nitrate translocation, which in turn affects the other parameters. In a separate experiment, we confirmed that phospboenolpyruvate carboxylase activity increased about 2-fold during 36 hours of KNO3 treatment, and increased only slightly in the KCI control.(2), in which K+ is an integral part of a NO3--malate shuttle between roots and shoots.Jackson and Coleman (10) first showed the presence of PEP carboxylase in roots, and proposed the PEP carboxylase-malic dehydrogenase pathway for malate accumulation in roots. This pathway, together with malic enzyme for decarboxylation of malate, have been proposed as a mechanism for pH regulation during nitrate assimilation (18, 21), but the hypothesis has not been explicitly tested. We report here the effects of NO3 and its salts on changes in activity of carboxylating and decarboxylating enzymes.Dijkshoorn et al. (6) have shown that internal HCO3, from the decarboxylation of organic acids, was exchanged for external N03 . Also, Ben-Zioni et al. (2) have shown that tobacco roots can secrete more H"CO3-into the medium when N03 is supplied than when Cl-is supplied. The source of H14CO3 was most likely malate, previously synthesized from 14C02 supplied to the leaves.These data also implied an exchange of HCO3 for external NO3.Since there is no a priori reason why this exchange should depend on the presence of K+, we predicted that activity of the reputed decarboxylase, NADP malic enzyme (5), should not be affected by the cation accompanying N03 in the medium. This prediction was fulfilled by experiment.Both the effects of N03-on cation uptake (3, 11) and the effects of different cations on N03-uptake have been studied (4, 15). In some experiments N03 uptake from KNO3 and NaNO3 were nearly the same (16 (Plant Physiol. 56: S-227, 1975
MATERIALS AND METHODSSeeds of wheat (Triticum vulgare L. cv. Arthur) were cultured according to the methods of Blevins et al. (3). The seeds were soaked for 24 hr in continuously aerated deionized ...