IDENTIFICATION OF THE NADH-BINDING SUBUNIT OF NADH-UBIQUINONE OXIDOREDUCTASE OF PARACOCCUS-DENITRIFICANS

The NADH dehydrogenase complex isolated from Paracoccus denitrificans is composed of approximately 10 unlike polypeptides and contains noncovalently bound FMN, non-heme iron, and acid-labile sulfide [Yagi, T. (1986) Arch. Biochem. Biophys. 250, 302-311]. When the Paracoccus NADH dehydrogenase complex was irradiated by UV light in the presence of [adenylate-32P]NAD, radioactivity was incorporated exclusively into one of three polypeptides of Mг ~ 50 000. Similar results were obtained when [adenylate-32P]NADH was used. The labeling of the Mг 50000 polypeptide was diminished when UV irradiation of the enzyme with [adenylate-32P]NAD was performed in the presence of NADH, but not in the presence of NADP(H). The labeled polypeptide was isolated by preparative sodium dodecyl sulfate gel electrophoresis and was shown to cross-react with antiserum to the NADH-binding subunit (Mг = 51000) of bovine NADH-ubiquinone oxidoreductase. Its amino acid composition was also very similar to that of the bovine NADH-binding subunit. These chemical and immunological results indicate that the Mг 50 000 polypeptide is an NADH-binding subunit of the Paracoccus NADH dehydrogenase complex. © 1990, American Chemical Society.