The DOI matches its Crossref record; 4 of the 4 references it cites were found in a registry or an index.
Genomic Insights into Methanotrophy: The Complete Genome Sequence of Methylococcus capsulatus (Bath)
Open accessAbstract
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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Versatile and open software for comparing large genomes
Kurtz, S., Phillippy, A., Delcher, A. L., Smoot, M., Shumway, M., Antonescu, C., & Salzberg, S. L. (2004) · Genome Biology · doi:10.1186/gb-2004-5-2-r12 · Cited by 5,254
Self-citationWu, M., Sun, L. V., Vamathevan, J., Riegler, M., Deboy, R., Brownlie, J. C., McGraw, E. A., Martin, W., Esser, C., Ahmadinejad, N., et al. (2004) · PLoS Biology · doi:10.1371/journal.pbio.0020069 · Cited by 851 · cited 1×
“Sequence alignments and phylogenetic trees were refined using the methods described previously (Salzberg et al. 2001; Wu et al. 2004).”
MethodSelf-citationMicrobial Genes in the Human Genome: Lateral Transfer or Gene Loss?
Salzberg, S. L., White, O., Peterson, J., & Eisen, J. A. (2001) · Science · doi:10.1126/science.1061036 · Cited by 326
Self-citationWood, A. P., Aurikko, J. P., & Kelly, D. P. (2004) · FEMS Microbiology Reviews · doi:10.1016/j.femsre.2003.12.001 · Cited by 177 · cited 1×
“Lack of experimental evidence precludes speculation as to the nature of these conditions; however, catabolite repression (Wood et al. 2004) may play a role here.”
Background
Cited by
Semrau, J. D., DiSpirito, A. A., & Yoon, S. (2010) · FEMS Microbiology Reviews · doi:10.1111/j.1574-6976.2010.00212.x · Cited by 760
Methane as a Resource: Can the Methanotrophs Add Value?
Strong, P. J., Xie, S., & Clarke, W. P. (2015) · Environmental Science & Technology · doi:10.1021/es504242n · Cited by 501
Methanotrophy below pH 1 by a new Verrucomicrobia species
Pol, A., Heijmans, K., Harhangi, H. R., Tedesco, D., Jetten, M. S. M., & Op den Camp, H. J. M. (2007) · Nature · doi:10.1038/nature06222 · Cited by 432
Glass, J. B., & Orphan, V. J. (2012) · Frontiers in Microbiology · doi:10.3389/fmicb.2012.00061 · Cited by 431
The Expanding World of Methylotrophic Metabolism
Chistoserdova, L., Kalyuzhnaya, M. G., & Lidstrom, M. E. (2009) · Annual Review of Microbiology · doi:10.1146/annurev.micro.091208.073600 · Cited by 420
Metadata
- Authors
- Ward, N., Larsen, Ø., Sakwa, J., Bruseth, L., Khouri, H., Durkin, A. S., Dimitrov, G., Jiang, L., Scanlan, D., Kang, K. H., Lewis, M., Nelson, K. E., Methé, B., Wu, M., Heidelberg, J. F., Paulsen, I. T., Fouts, D., Ravel, J., Tettelin, H., Ren, Q., Read, T., DeBoy, R. T., Seshadri, R., Salzberg, S. L., Jensen, H. B., Birkeland, N. K., Nelson, W. C., Dodson, R. J., Grindhaug, S. H., Holt, I., Eidhammer, I., Jonasen, I., Vanaken, S., Utterback, T., Feldblyum, T. V., Fraser, C. M., Lillehaug, J. R., & Eisen, J. A.
- Venue
- PLoS Biology
- Publisher
- Public Library of Science (PLoS)
- Published
- 2004-09-21
- Volume
- 2
- Issue
- 10
- Pages
- e303
- ISSN
- 1544-9173 (ISSN-L)
- 1545-7885
- OpenAlex
- W1980575078
- Cited by
- 361
- References
- 4
- FWCI
- 6.34
- Type
- journal article
- Language
- en
- Open access
- gold
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