Whole-Genome Analysis of the Methyl <i>tert</i> -Butyl Ether-Degrading Beta-Proteobacterium <i>Methylibium petroleiphilum</i> PM1

  • Staci R. Kane
    Lawrence Livermore National Laboratory, Livermore, California
  • Anu Y. Chakicherla
    Lawrence Livermore National Laboratory, Livermore, California
  • Patrick S. G. Chain
    Lawrence Livermore National Laboratory, Livermore, California
  • Radomir Schmidt
    Department of Land Air and Water Resources, University of California, Davis, California
  • Maria W. Shin
    Lawrence Livermore National Laboratory, Livermore, California
  • Tina C. Legler
    Lawrence Livermore National Laboratory, Livermore, California
  • Kate M. Scow
    Department of Land Air and Water Resources, University of California, Davis, California
  • Frank W. Larimer
    Genome Analysis Group, Oak Ridge National Laboratory, Oak Ridge, Tennessee
  • Susan M. Lucas
    Joint Genome Institute Production Genomics Facility, Walnut Creek, California
  • Paul M. Richardson
    Joint Genome Institute Production Genomics Facility, Walnut Creek, California
  • Krassimira R. Hristova
    Department of Land Air and Water Resources, University of California, Davis, California

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<jats:title>ABSTRACT</jats:title> <jats:p> <jats:italic>Methylibium petroleiphilum</jats:italic> PM1 is a methylotroph distinguished by its ability to completely metabolize the fuel oxygenate methyl <jats:italic>tert</jats:italic> -butyl ether (MTBE). Strain PM1 also degrades aromatic (benzene, toluene, and xylene) and straight-chain (C <jats:sub>5</jats:sub> to C <jats:sub>12</jats:sub> ) hydrocarbons present in petroleum products. Whole-genome analysis of PM1 revealed an ∼4-Mb circular chromosome and an ∼600-kb megaplasmid, containing 3,831 and 646 genes, respectively. Aromatic hydrocarbon and alkane degradation, metal resistance, and methylotrophy are encoded on the chromosome. The megaplasmid contains an unusual t-RNA island, numerous insertion sequences, and large repeated elements, including a 40-kb region also present on the chromosome and a 29-kb tandem repeat encoding phosphonate transport and cobalamin biosynthesis. The megaplasmid also codes for alkane degradation and was shown to play an essential role in MTBE degradation through plasmid-curing experiments. Discrepancies between the insertion sequence element distribution patterns, the distributions of best BLASTP hits among major phylogenetic groups, and the G+C contents of the chromosome (69.2%) and plasmid (66%), together with comparative genome hybridization experiments, suggest that the plasmid was recently acquired and apparently carries the genetic information responsible for PM1's ability to degrade MTBE. Comparative genomic hybridization analysis with two PM1-like MTBE-degrading environmental isolates (∼99% identical 16S rRNA gene sequences) showed that the plasmid was highly conserved (ca. 99% identical), whereas the chromosomes were too diverse to conduct resequencing analysis. PM1's genome sequence provides a foundation for investigating MTBE biodegradation and exploring the genetic regulation of multiple biodegradation pathways in <jats:italic>M. petroleiphilum</jats:italic> and other MTBE-degrading beta-proteobacteria. </jats:p>

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