Some members of Burkholderiales are able to grow on methanol but lack the genes (mxaFI) responsible for the well-characterized two-subunit pyrroloquinoline quinone-dependent quinoprotein methanol dehydrogenase that is widespread in methylotrophic Proteobacteria. Here, we characterized novel, mono-subunit enzymes responsible for methanol oxidation in four strains, Methyloversatilis universalis FAM5, Methylibium petroleiphilum PM1, and unclassified Burkholderiales strains RZ18-153 and FAM1. The enzyme from M. universalis FAM5 was partially purified and subjected to matrix-assisted laser desorption ionization-time of fight peptide mass fingerprinting. The resulting peptide spectrum was used to identify a gene candidate in the genome of M. petroleiphilum PM1 (mdh2) predicted to encode a type I alcohol dehydrogenase related to the characterized methanol dehydrogenase large subunits but at less than 35% amino acid identity. Homologs of mdh2 were amplified from M. universalis FAM5 and strains RZ18-153 and FAM1, and mutants lacking mdh2 were generated in three of the organisms. These mutants lost their ability to grow on methanol and ethanol, demonstrating that mdh2 is responsible for oxidation of both substrates. Our findings have implications for environmental detection of methylotrophy and indicate that this ability is widespread beyond populations possessing mxaF, the gene traditionally used as a genetic marker for environmental detection of methanol-oxidizing capability. Our findings also have implications for understanding the evolution of methanol oxidation, suggesting a convergence toward the enzymatic function for methanol oxidation in MxaF and Mdh2-type proteins.Methanol dehydrogenase (MDH) is a key enzyme in utilization of methane and methanol by methylotrophic proteobacteria (1, 2). This is a pyrroloquinoline quinone (PQQ)-dependent quinoprotein that acts in the periplasm. Like other quinoproteins, MDH is assayed in vitro in a dye-linked system using artificial electron acceptors such as phenazine methosulphate and dichlorophenolindophenol. It is typically measured at high pH (9-11) in the presence of ammonia as an essential activator (1-3). MDH oxidizes a wide range of primary alcohols but has especially high affinity for methanol (K m value of about 20 M). MDH and its prosthetic group were first described more than 40 years ago, making it one of the most thoroughly studied quinoprotein dehydrogenases (9,12,32,44,46). Gene clusters encoding the structural subunits of MDH (mxaFI), the specific electron acceptor cytochrome c L (mxaG), and a number of accessory proteins (mxaJRSACKLD) have been found well conserved in a variety of methylotroph genomes (5, 6, 25, 42), and the gene encoding the large subunit, mxaF, has been used as a marker for methylotrophy in environmental studies (27,28). However, a few methylotrophic isolates have been described that appear to lack mxa genes. In some cases this is evidenced by the analysis of complete genomes (10, 20) and in others by the inability to PCR amplify the mxaF gen...