Abstract
Methanogenesis and anaerobic methane oxidation through methyl-coenzyme M reductase (MCR) as a key enzyme have been suggested to be basal pathways of archaea1. How widespread MCR-based alkane metabolism is among archaea, where it occurs and how it evolved remain elusive. Here, we performed a global survey of MCR-encoding genomes based on metagenomic data from various environments. Eleven high-quality mcr-containing metagenomic-assembled genomes were obtained belonging to the Archaeoglobi in the Euryarchaeota, Hadesarchaeota and different TACK superphylum archaea, including the Nezhaarchaeota, Korarchaeota and Verstraetearchaeota. Archaeoglobi WYZ-LMO1 and WYZ-LMO3 and Korarchaeota WYZ-LMO9 encode both the (reverse) methanogenesis and the dissimilatory sulfate reduction pathway, suggesting that they have the genomic potential to couple both pathways in individual organisms. The Hadesarchaeota WYZ-LMO4–6 and Archaeoglobi JdFR-42 encode highly divergent MCRs, enzymes that may enable them to thrive on non-methane alkanes. The occurrence of mcr genes in different archaeal phyla indicates that MCR-based alkane metabolism is common in the domain of Archaea.
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Code availability
All scripts and analyses necessary to perform metagenome processing can be accessed from GitHub (https://github.com/) or the websites provided in the original research articles. The specific links to the custom software are listed below: DIAMOND version 0.8.28.90: http://ab.inf.uni-tuebingen.de/software/diamond/, Sickle version 1.33: https://github.com/najoshi/sickle, MEGAHIT version 1.0.6-hotfix1: https://hku-bal.github.io/megabox/, Bowtie version 2.2.8: http://bowtie-bio.sourceforge.net/bowtie2/index.shtml, Prodigal version 2.6.3: http://compbio.ornl.gov/prodigal/, MaxBin version 2.2.4: http://sourceforge.net/projects/maxbin/, MetaBAT version 2.12.1: https://bitbucket.org/berkeleylab/metabat, CheckM version 1.0.7: http://ecogenomics.github.io/CheckM, compareM version 0.0.23: https://github.com/dparks1134/CompareM, MAFFT version 7.313: https://mafft.cbrc.jp/alignment/software/, trimAl version 1.4.rev2: http://trimal.cgenomics.org, IQ-Tree version 1.6.6: http://www.cibiv.at/software/iqtree, and RAxML version 8.0: https://github.com/stamatak/standard-RAxML.
Data availability
The data sets generated and/or analysed during the current study are available in the NCBI repository at https://www.ncbi.nlm.nih.gov/. The MAGs from the current study have been deposited in the NCBI GenBank under the project ID PRJNA475886.
References
Ueno, Y., Yamada, K., Yoshida, N., Maruyama, S. & Isozaki, Y. Evidence from fluid inclusions for microbial methanogenesis in the early Archaean era. Nature 440, 516–519 (2006).
Conrad, R. The global methane cycle: recent advances in understanding the microbial processes involved. Environ. Microbiol. Rep. 1, 285–292 (2009).
Reeburgh, W. Oceanic methane biogeochemistry. Chem. Rev. 107, 486–513 (2007).
Knittel, K. & Boetius, A. Anaerobic oxidation of methane: progress with an unknown process. Annu. Rev. Microbiol. 63, 311–334 (2009).
Krüger, M. et al. A conspicuous nickel protein in microbial mats that oxidize methane anaerobically. Nature 426, 878–881 (2003).
Hallam, S. J. et al. Reverse methanogenesis: testing the hypothesis with environmental genomics. Science 305, 1457–1462 (2004).
Scheller, S., Goenrich, M., Boecher, R., Thauer, R. K. & Jaun, B. The key nickel enzyme of methanogenesis catalyses the anaerobic oxidation of methane. Nature 465, 606–608 (2010).
Gunsalus, R. & Wolfe, R. Methyl coenzyme M reductase from Methanobacterium thermoautotrophicum. Resolution and properties of the components. J. Biol. Chem. 255, 1891–1895 (1980).
Ermler, U., Grabarse, W., Shima, S., Goubeaud, M. & Thauer, R. K. Crystal structure of methyl-coenzyme M reductase: the key enzyme of biological methane formation. Science 278, 1457–1462 (1997).
Thauer, R. K. Anaerobic oxidation of methane with sulfate: on the reversibility of the reactions that are catalyzed by enzymes also involved in methanogenesis from CO2. Curr. Opin. Microbiol. 14, 292–299 (2011).
Lever, M. A. & Teske, A. P. Diversity of methane-cycling archaea in hydrothermal sediment investigated by general and group-specific PCR primers. Appl. Environ. Microbiol. 81, 1426–1441 (2015).
Evans, P. N. et al. Methane metabolism in the archaeal phylum Bathyarchaeota revealed by genome-centric metagenomics. Science 350, 434–438 (2015).
Vanwonterghem, I. et al. Methylotrophic methanogenesis discovered in the archaeal phylum Verstraetearchaeota. Nat. Microbiol. 1, 16170 (2016).
Laso-Pérez, R. et al. Thermophilic archaea activate butane via alkyl-coenzyme M formation. Nature 539, 396–401 (2016).
Boetius, A. et al. A marine microbial consortium apparently mediating anaerobic oxidation of methane. Nature 407, 623–626 (2000).
McGlynn, S. E., Chadwick, G. L., Kempes, C. P. & Orphan, V. J. Single cell activity reveals direct electron transfer in methanotrophic consortia. Nature 526, 531–535 (2015).
Wegener, G., Krukenberg, V., Riedel, D., Tegetmeyer, H. E. & Boetius, A. Intercellular wiring enables electron transfer between methanotrophic archaea and bacteria. Nature 526, 587–590 (2015).
Haroon, M. F. et al. Anaerobic oxidation of methane coupled to nitrate reduction in a novel archaeal lineage. Nature 500, 567–570 (2013).
Ettwig, K. F. et al. Archaea catalyze iron-dependent anaerobic oxidation of methane. Proc. Natl Acad. Sci. USA 113, 12792–12796 (2016).
Baker, B. J. et al. Genomic inference of the metabolism of cosmopolitan subsurface Archaea, Hadesarchaea. Nat. Microbiol. 1, 16002 (2016).
Elkins, J. G. et al. A korarchaeal genome reveals insights into the evolution of the Archaea. Proc. Natl Acad. Sci. USA 105, 8102–8107 (2008).
Adam, P. S., Borrel, G., Brochier-Armanet, C. & Gribaldo, S. The growing tree of Archaea: new perspectives on their diversity, evolution and ecology. ISME J. 11, 2407–2425 (2017).
Parks, D. H. et al. A standardized bacterial taxonomy based on genome phylogeny substantially revises the tree of life. Nat. Biotechnol. 36, 996–1004 (2018).
Raymann, K., Brochier-Armanet, C. & Gribaldo, S. The two-domain tree of life is linked to a new root for the Archaea. Proc. Natl Acad. Sci. USA 112, 6670–6675 (2015).
Petitjean, C., Deschamps, P., López-García, P., Moreira, D. & Brochier-Armanet, C. Extending the conserved phylogenetic core of archaea disentangles the evolution of the third domain of life. Mol. Biol. Evol. 32, 1242–1254 (2015).
Williams, T. A. et al. Integrative modeling of gene and genome evolution roots the archaeal tree of life. Proc. Natl Acad. Sci. USA 114, E4602–E4611 (2017).
Stahl, D. A., Fishbain, S., Klein, M., Baker, B. J. & Wagner, M. Origins and diversification of sulfate-respiring microorganisms. Antonie Van Leeuwenhoek 81, 189–195 (2002).
Müller, A. L., Kjeldsen, K. U., Rattei, T., Pester, M. & Loy, A. Phylogenetic and environmental diversity of DsrAB-type dissimilatory (bi) sulfite reductases. ISME J. 9, 1152–1165 (2015).
Timmers, P. H. et al. Reverse methanogenesis and respiration in methanotrophic archaea. Archaea 2017, 1654237 (2017).
Stojanowic, A., Mander, G. J., Duin, E. C. & Hedderich, R. Physiological role of the F420-non-reducing hydrogenase (Mvh) from Methanothermobacter marburgensis. Arch. Microbiol. 180, 194–203 (2003).
Buchfink, B., Xie, C. & Huson, D. H. Fast and sensitive protein alignment using DIAMOND. Nat. Methods 12, 59–60 (2014).
Li, D., Liu, C.-M., Luo, R., Sadakane, K. & Lam, T.-W. MEGAHIT: an ultra-fast single-node solution for large and complex metagenomics assembly via succinct de Bruijn graph. Bioinformatics 31, 1674–1676 (2015).
Langmead, B. & Salzberg, S. L. Fast gapped-read alignment with Bowtie 2. Nat. Methods 9, 357–359 (2012).
Hyatt, D. et al. Prodigal: prokaryotic gene recognition and translation initiation site identification. BMC Bioinformatics 11, 119 (2010).
Kanehisa, M., Furumichi, M., Tanabe, M., Sato, Y. & Morishima, K. KEGG: new perspectives on genomes, pathways, diseases and drugs. Nucleic Acids Res. 45, D353–D361 (2016).
Dick, G. J. et al. Community-wide analysis of microbial genome sequence signatures. Genome Biol. 10, R85 (2009).
Wu, Y.-W., Simmons, B. A. & Singer, S. W. MaxBin 2.0: an automated binning algorithm to recover genomes from multiple metagenomic datasets. Bioinformatics 32, 605–607 (2015).
Kang, D. D., Froula, J., Egan, R. & Wang, Z. MetaBAT, an efficient tool for accurately reconstructing single genomes from complex microbial communities. PeerJ 3, e1165 (2015).
Parks, D. H., Imelfort, M., Skennerton, C. T., Hugenholtz, P. & Tyson, G. W. CheckM: assessing the quality of microbial genomes recovered from isolates, single cells, and metagenomes. Genome Res. 25, 1043–1055 (2015).
Karst, S. M., Kirkegaard, R. H. & Albertsen, M. mmgenome: a toolbox for reproducible genome extraction from metagenomes. Preprint at https://doi.org/10.1101/059121 (2016).
Bowers, R. M. et al. Minimum information about a single amplified genome (MISAG) and a metagenome-assembled genome (MIMAG) of bacteria and archaea. Nat. Biotechnol. 35, 725–731 (2017).
Huerta-Cepas, J. et al. eggNOG 4.5: a hierarchical orthology framework with improved functional annotations for eukaryotic, prokaryotic and viral sequences. Nucleic Acids Res. 44, D286–D293 (2016).
Kanehisa, M., Sato, Y. & Morishima, K. BlastKOALA and GhostKOALA: KEGG tools for functional characterization of genome and metagenome sequences. J. Mol. Biol. 428, 726–731 (2016).
Yarza, P. et al. Uniting the classification of cultured and uncultured bacteria and archaea using 16S rRNA gene sequences. Nat. Rev. Microbiol. 12, 635–645 (2014).
Hugenholtz, P., Skarshewski, A. & Parks, D. H. Genome-based microbial taxonomy coming of age. Cold Spring Harb. Perspect. Biol. 8, a018085 (2016).
Konstantinidis, K. T., Rosselló-Móra, R. & Amann, R. Uncultivated microbes in need of their own taxonomy. ISME J. 11, 2399–2406 (2017).
Chuvochina, M. et al. The importance of designating type material for uncultured taxa. Syst. Appl. Microbiol. https://doi.org/10.1016/j.syapm.2018.07.003 (2018).
Hug, L. A. et al. A new view of the tree of life. Nat. Microbiol. 1, 16048 (2016).
Katoh, K. & Standley, D. M. MAFFT multiple sequence alignment software version 7: improvements in performance and usability. Mol. Biol. Evol. 30, 772–780 (2013).
Capella-Gutiérrez, S., Silla-Martínez, J. M. & Gabaldón, T. trimAl: a tool for automated alignment trimming in large-scale phylogenetic analyses. Bioinformatics 25, 1972–1973 (2009).
Stamatakis, A. RAxML version 8: a tool for phylogenetic analysis and post-analysis of large phylogenies. Bioinformatics 30, 1312–1313 (2014).
Nguyen, L.-T., Schmidt, H. A., von Haeseler, A. & Minh, B. Q. IQ-TREE: a fast and effective stochastic algorithm for estimating maximum-likelihood phylogenies. Mol. Biol. Evol. 32, 268–274 (2014).
Jungbluth, S. P., Amend, J. P. & Rappé, M. S. Metagenome sequencing and 98 microbial genomes from Juan de Fuca Ridge flank subsurface fluids. Sci. Data 4, 170037 (2017).
Acknowledgements
We thank R. K. Thauer for his advice on the discussed metabolic pathways, and V. Krukenberg and J. Wang for valuable discussion and suggestions for the manuscript. We are grateful to the researchers who published their sequence data on the NCBI (https://www.ncbi.nlm.nih.gov/), and to the US Department of Energy Joint Genome Institute (http://www.jgi.doe.gov/) for providing protein sequence files in collaboration with the user community. We thank the following sources for funding: the Natural Science Foundation of China (grant numbers 91751205, 41525011 and 91428308), the National Key R&D project of China (grant number 2018YFC0309800) and China Postdoctoral Science Foundation Grant (grant number 2018T110390). This study is also a contribution to the Deep Carbon Observatory.
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Y.W. and F.W. designed the research, performed the analyses, developed the metabolic models and wrote the paper. G.W. developed the metabolic models and wrote the paper. J.H. provided useful discussion and helped with the double-blind assessments of the MAGs. F.W. and X.X. provided guidance and useful suggestion.
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Wang, Y., Wegener, G., Hou, J. et al. Expanding anaerobic alkane metabolism in the domain of Archaea. Nat Microbiol 4, 595–602 (2019). https://doi.org/10.1038/s41564-019-0364-2
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DOI: https://doi.org/10.1038/s41564-019-0364-2
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