Lipoic acid metabolism

Lipoic acid is an essential cofactor of dehydrogenase enzymes, mainly the E₂ subunit of pyruvate dehydrogenase, branched-chain keto-acid dehydrogenase and 2-oxoglutarate dehydrogenase complexes. Lipoic acid is an organic sulphur compound derived from the 8-carbon fatty acid, octanoic acid. In most eukaryotes, lipoic acid is synthesised in mitochondrion and it is consistent with the localisation of above mentioned three complexes in mitochondria. In apicomplexan parasites, pyruvate dehydrogenase complex is localised in the plastid organelle, apicoplast. As the de novo fatty acid biosynthesis via FAS II pathway (fatty acid biosynthesis in the apicoplast) occurs in apicoplast, it is possible to suggest that these apicomplexans can de novo synthesise lipoic acid in the apicoplast. Although other dehydrogenases are located in mitochondria, de novo fatty acid biosynthesis does not take place in apicomplexan mitochondrion. The work by Crawford et al in T. gondii demonstrated that lipoylation of mitochondrial proteins is reduced when the parasites are grown in lipoic acid-deficient medium and no effect was seen with lipoylation of apicoplast proteins. This effect in mitochondrion has also shown to be reversed with exogenous lipoic acid supply [1]. This clearly shows that apicoplast synthesises lipoic acid de novo, whereas mitochondrion salvages it from host. The orthologs of all proteins annotated to this pathway in T. gondii are present in Neospora caninum genome. The plasma membrane and mitochondrial transporter which are involved in lipoic acid salvage and mitochondrial localisation are not yet identified in either T. gondii or N. caninum genomes. The lipoic acid metabolism pathway for Plasmodium falciparum in MPMP is identical to T. gondii pathway and pathway for N. caninum here.

Open in a new window

Sources and fates of metabolites