| Summary: | Respiratory supercomplexes are found in mitochondria of eukaryotic cells and some bacteria. A hypothetical role of these supercomplexes is electron channeling, which in principle should increase the respiratory chain efficiency and ATP synthesis. In addition to the four classic respiratory complexes and the ATP synthase, <i>U. maydis</i> mitochondria contain three type II NADH dehydrogenases (NADH for reduced nicotinamide adenine dinucleotide) and the alternative oxidase. Changes in the composition of the respiratory supercomplexes due to energy requirements have been reported in certain organisms. In this study, we addressed the organization of the mitochondrial respiratory complexes in <i>U. maydis</i> under diverse energy conditions. Supercomplexes were obtained by solubilization of <i>U. maydis</i> mitochondria with digitonin and separated by blue native polyacrylamide gel electrophoresis (BN-PAGE). The molecular mass of supercomplexes and their probable stoichiometries were 1200 kDa (I<sub>1</sub>:IV<sub>1</sub>), 1400 kDa (I<sub>1</sub>:III<sub>2</sub>), 1600 kDa (I<sub>1</sub>:III<sub>2</sub>:IV<sub>1</sub>), and 1800 kDa (I<sub>1</sub>:III<sub>2</sub>:IV<sub>2</sub>). Concerning the ATP synthase, approximately half of the protein is present as a dimer and half as a monomer. The distribution of respiratory supercomplexes was the same in all growth conditions. We did not find evidence for the association of complex II and the alternative NADH dehydrogenases with other respiratory complexes.
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