Dramatic difference in the responses of phosphoenolpyruvate carboxylase to temperature in leaves of C3 and C4 plants

Temperature caused phenomenal modulation of phosphoenolpyruvate carboxylase (PEPC, EC 4.1.1.31) in leaf discs of Amaranthus hypochondriacus (NAD-ME type C-4 species), compared to the pattern in Pisum sativum (a C-3 plant). The optimal incubation temperature for PEPC in A. hypochondriacus (C-4) was 45 degreesC compared to 30 degreesC in P. sativum (C-3). A. hypochondriacus (C-4) lost nearly 70% of PEPC activity on exposure to a low temperature of 15 degreesC, compared to only about a 35% loss in the case of P. sativum (C-3)Thus, the C-4 enzyme was less sensitive to supraoptimal temperature and more sensitive to suboptimal temperature than that of the C-3 species. As the temperature was raised from 15 degreesC to 50 degreesC, there was a sharp decrease in malate sensitivity of PEPC. The extent of such a decrease in C-4 plants (45%) was more than that in C-3 species (30%). The maintenance of high enzyme activity at warm temperatures, together with a sharp decrease in the malate sensitivity of PEPC was also noticed in other C-4 plants. The temperature-induced changes in PEPC of both A. hypochondriacus (C-4) and P. sativum (C-3) were reversible to a large extent. There was no difference in the extent of phosphorylation of PEPC in leaves of A. hypochondriacus on exposure to varying temperatures, unlike the marked increase in the phosphorylation of enzyme on illumination of the leaves. These results demonstrate that (i) there are marked differences in the temperature sensitivity of PEPC in C-3 and C-4 plants, (ii) the temperature induced changes are reversible, and (iii) these changes are not related to the phosphorylation state of the enzyme. The inclusion of PEG-6000, during the assay, dampened the modulation by temperature of malate sensitivity of PEPC in A. hypochondriacus. It is suggested that the variation in temperature may cause significant conformational changes in C-4-PEPC.