PURIFICATION AND PROPERTIES OF A NADH-DEPENDENT 5,10-METHYLENETETRAHYDROFOLATE REDUCTASE FROM PEPTOSTREPTOCOCCUS-PRODUCTUS

The methylenetetrahydrofolate reductase from the carbon‐monoxide‐utilizing homoacetogen Peptostreptococcus productus (strain Marburg) has been purified to apparent homogeneity. The purified enzyme catalyzed the oxidation of NADH with methylenetetrahydrofolate as the electron acceptor at a specific activity of 380 μmol · min−1 mg protein−1 (37°C; pH 5.5). The apparent Km for NADH was near 10 μM. The apparent molecular mass of the enzyme was determined by gel filtration to be ∼250.0 kDa. The enzyme consists of eight identical subunits with a molecular mass of 32 kDa. It contains 4 FAD/mol octamer which were reduced by the enzyme with NADH as the electron donor; iron could not be detected. Oxygen had no effect on the enzyme. Ultracentrifugation of cell extracts revealed that about 40% of the enzyme activity was recovered in the particulate fraction, suggesting that the enzyme is associated with the membrane. The enzyme also catalyzed the methylene‐tetrahydrofolate reduction with methylene blue as an artificial electron donor. The oxidation of methyl‐tetrahydrofolate was mediated with methylene blue as the electron acceptor; neither NAD+ nor viologen dyes could replace methylene blue in this reaction. NADP(H) or FAD(H2) were not used as substrates for the reaction in either direction. The activity of the purified enzyme, which was proposed to be involved in sodium translocation across the cytoplasmic membrane, was not affected by the absence or presence of added sodium. The properties of the enzyme differ from those of the ferredoxin‐dependent methylenetetrahydrofolate reductase of the homoacetogen Clostridium formicoaceticum and of the NADP+‐dependent reductase of eucaryotes investigated so far. Copyright © 1990, Wiley Blackwell. All rights reserved