THE MOLYBDOENZYME FORMYLMETHANOFURAN DEHYDROGENASE FROM METHANOSARCINA-BARKERI CONTAINS A PTERIN COFACTOR

Recently formylmethanofuran dehydrogenase from the archaebacterium Methanosarcina barkeri has been shown to be a novel molybdo-iron-sulfur protein. We report here that the enzyme contains one mol of a bound pterin cofactor/mol molybdenum, similar but not identical to the molybdopterin of milk xanthine oxidase. The two pterins, after oxidation with I2 at pH 2.5, showed identical fluorescence spectra and, after oxidation with permanganate at pH 13, yielded pterin 6-carboxylic acid. They differed, however, in their apparent molecular mass: the pterin of formylmethanofuran dehydrogenase was 400 Da larger than that of milk xanthine oxidase, a property also exhibited by the pterin cofactor of eubacterial molybdoenzymes. A homogeneous formylmethanofuran dehydrogenase preparation was used for these investigations. The enzyme, with a molecular mass of 220 kDa, contained 0.5 - 0.8 mol molybdenum, 0.6 - 0.9 mol pterin, 28 +/- 2 mol non-heme iron and 28 +/- 2 mol acid-labile sulfur/mol based on a protein determination with bicinchoninic acid. The specific activity was 175-mu-mol . min-1 . mg-1 (K(cat) = 640 s-1) assayed with methylviologen (app. K(m) = 0.02mM) as artificial electron acceptor. The apparent K(m) for formylmethanofuran was 0.02 mM.