Skip Navigation

Publication Detail

Title: Characterization of a novel methanol dehydrogenase in representatives of Burkholderiales: implications for environmental detection of methylotrophy and evidence for convergent evolution.

Authors: Kalyuzhnaya, Marina G; Hristova, Krassimira R; Lidstrom, Mary E; Chistoserdova, Ludmila

Published In J Bacteriol, (2008 Jun)

Abstract: 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.

PubMed ID: 18390659 Exiting the NIEHS site

MeSH Terms: Alcohol Oxidoreductases/chemistry; Alcohol Oxidoreductases/metabolism*; Amino Acid Sequence; Bacterial Proteins/genetics*; Bacterial Proteins/metabolism*; Betaproteobacteria/enzymology*; Betaproteobacteria/genetics; Biological Evolution*; Gene Expression Regulation, Bacterial; Methanol/metabolism*; Molecular Sequence Data; Mutation; Species Specificity

Back
to Top