Tricarboxylic Anion Transporters

The kinetic and equilibrium parameters of L-malate, succinate, citrate, and a-oxoglutarate uptake have been determined in mitochondria isolated from respiratory-competent cells grown under conditions of aerobic derepression, aerobic and anaerobic catabolite repression, and inhibition of mitochondrial protein synthesis, and also in mitochondria prepared from a respiratory-deficient cytoplasmic petite strain. The activity and kinetic characteristics of the systems were similar in all cases. It may be concluded that the protein components of these transport systems are coded entirely by nuclear DNA and are synthesized on the cytoplasmic ribosomes. 

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Fig. 8. Pathways involved in the conversion of glucose to fatty acid. Reaction (1) is catalyzed by cytosolic malate dehydrogenase. Reaction (2) is catalyzed by mitochondrial malate dehydrogenase. (T) designates tricarboxylate anion transporter. Reactions catalyzed by glucose-6-phosphate dehydrogenase and 6-phosphogluconate dehydrogenase in the pentose phosphate pathway produce NADPH. CS, citrate synthase ACL, ATP citrate lyase PDH, pyruvate dehydrogenase complex ACC, acetyl-CoA carboxylase FAS, fatty acid synthase.

Cytosolic generation of acetyl-CoA ( citrate shuttle ) This pathway is shown in Figure 18-13. Citrate synthesized from oxaloacetate and acetyl-CoA is transported to the cytosol via the tricarboxylate anion carrier system and cleaved to yield acetyl-CoA and oxaloacetate. 

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