YtkA (CtaK) and YozB (CtaM) function in the biogenesis of cytochrome <i>c</i> oxidase in <i>Bacillus subtilis</i>
Claes von Wachenfeldt, Joel Hällgren, Lars Hederstedt
Abstract
Abstract Cytochrome c oxidase in the respiratory chain of bacteria and mitochondria couples the reduction of molecular oxygen to form water with the generation of a transmembrane proton gradient. Bacillus subtilis has two heme A‐containing heme–copper oxidases: the menaquinol oxidase cytochrome aa 3 and the cytochrome c oxidase cytochrome caa 3 . By screening three collections of mutants for defective cytochrome c oxidase, we found the genes for two, new membrane‐bound assembly factors in B . subtilis : ytkA and yozB (renamed ctaK and ctaM , respectively). CtaK is a lipoprotein without sequence similarity to any protein of known function. We show that CtaK functions together with Sco1 (YpmQ) in a pathway, leading to the assembly of the Cu A center in cytochrome caa 3 and seems to be a functional analogue to proteins of the periplasmic Cu A chaperone family (PCu A C). CtaM is required for the activity of both cytochrome caa 3 and cytochrome aa 3 and dispensable for the insertion of heme A into these oxidases. The orthologous Bacillus anthracis protein and the distantly related Staphylococcus aureus CtaM complemented CtaM deficiency in B. subtilis, establishing a common function of CtaM in these bacteria. As the overall result of our work, 12 different proteins are known to function in the biosynthesis of cytochrome c oxidase in B. subtilis .