NAD(P)(+)-dependent isocitrate dehydrogenases in mitochondria purified from Picea abies seedlings

Isocitrate dehydrogenase (IDH) activities were measured in mitochondria isolated from aerial parts of 21-day-old spruce (Picea abies L. Karst.) seedlings. Mitochondria were purified by two methods, involving continuous and discontinuous Percoll gradients. Whatever the method of purification, the mitochondrial outer membrane was about 69% intact, and the mitochondria contained very low cytosolic, chloroplastic and peroxisomal contaminations. Nevertheless, as judged by the recovery of fumarase activity, purification on a continuous 28% Percoll gradient gave the best yield in mitochondria, which exhibited a high degree of inner membrane intactness (91%). The purified mitochondria oxidized succinate and malate with good respiratory control and ADP/O ratios. The highest oxidation rate was obtained with succinate as substrate, and malate oxidation was improved (+ 60%) by addition of exogenous NAD(+). Experiments using standard respiratory chain inhibitors indicated that, in spruce mitochondria, the alternative pathway was present. Both NAD(+)-isocitrate dehydrogenase (EC 1.1.1.41) and NADP(+)-isocitrate dehydrogenase (EC 1.1.1.42) were present in the mitochondrial matrix fraction, and NAD(+)-IDH activity was about 2-fold higher than NADP(+)-IDH activity. The NAD(+)-IDH showed sigmoidal kinetics in response to isocitrate and standard Michaelis-Menten kinetics for NAD(+) and Mg2+. The NADP(+)-IDH, in contrast, displayed lower K-m values. For NAD(+)-IDH the pH optimum was at 7.4, whereas NADP(+)-IDH exhibited a broad pH optimum between 8.3 and 9. In addition, NAD(+)-IDH was more thermolabile. Adenine nucleotides and 2-oxoglutarate were found to inhibit NAD(P)(+)-IDH activities only at high concentrations.