Genomic Insights into Methanotrophy: The Complete Genome Sequence of Methylococcus capsulatus (Bath)

Naomi Ward, Øivind Larsen(University of Bergen), James Sakwa, Live J. Bruseth(University of Bergen), Hoda Khouri, A. Scott Durkin, George Dimitrov, Lingxia Jiang, David J. Scanlan, Katherine H. Kang, Matt Lewis, Karen E Nelson, Barbara A. Methé, Martin Wu, John F. Heidelberg, Ian T. Paulsen(Johns Hopkins University), Derrick E. Fouts, Jacques Ravel, Hervé Tettelin, Qinghu Ren, Tim Read, Robert T. DeBoy, R. Seshadri, Steven L. Salzberg(Johns Hopkins University), Harald B. Jensen(University of Bergen), Nils Kåre Birkeland(University of Bergen), William Nelson, Robert J. Dodson, Svenn Helge Grindhaug(University of Bergen), Ingeborg Holt(National Institutes of Health), Ingvar Eidhammer(University of Bergen), Inge Jonasen(University of Bergen), Susan E. Vanaken, Terry Utterback, Tamara V. Feldblyum, Claire M. Fraser(George Washington University), Johan R. Lillehaug(University of Bergen), Jonathan A. Eisen(Johns Hopkins University)
PLoS Biology
September 17, 2004
Cited by 358Open Access
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Abstract

Methanotrophs are ubiquitous bacteria that can use the greenhouse gas methane as a sole carbon and energy source for growth, thus playing major roles in global carbon cycles, and in particular, substantially reducing emissions of biologically generated methane to the atmosphere. Despite their importance, and in contrast to organisms that play roles in other major parts of the carbon cycle such as photosynthesis, no genome-level studies have been published on the biology of methanotrophs. We report the first complete genome sequence to our knowledge from an obligate methanotroph, Methylococcus capsulatus (Bath), obtained by the shotgun sequencing approach. Analysis revealed a 3.3-Mb genome highly specialized for a methanotrophic lifestyle, including redundant pathways predicted to be involved in methanotrophy and duplicated genes for essential enzymes such as the methane monooxygenases. We used phylogenomic analysis, gene order information, and comparative analysis with the partially sequenced methylotroph Methylobacterium extorquens to detect genes of unknown function likely to be involved in methanotrophy and methylotrophy. Genome analysis suggests the ability of M. capsulatus to scavenge copper (including a previously unreported nonribosomal peptide synthetase) and to use copper in regulation of methanotrophy, but the exact regulatory mechanisms remain unclear. One of the most surprising outcomes of the project is evidence suggesting the existence of previously unsuspected metabolic flexibility in M. capsulatus, including an ability to grow on sugars, oxidize chemolithotrophic hydrogen and sulfur, and live under reduced oxygen tension, all of which have implications for methanotroph ecology. The availability of the complete genome of M. capsulatus (Bath) deepens our understanding of methanotroph biology and its relationship to global carbon cycles. We have gained evidence for greater metabolic flexibility than was previously known, and for genetic components that may have biotechnological potential.


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