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Genomic and proteomic characterization of “ Candidatus Nitrosopelagicus brevis”: An ammonia-oxidizing archaeon from the open ocean
Open accessAbstract
Thaumarchaeota are among the most abundant microbial cells in the ocean, but difficulty in cultivating marine Thaumarchaeota has hindered investigation into the physiological and evolutionary basis of their success. We report here a closed genome assembled from a highly enriched culture of the ammonia-oxidizing pelagic thaumarchaeon CN25, originating from the open ocean. The CN25 genome exhibits strong evidence of genome streamlining, including a 1.23-Mbp genome, a high coding density, and a low number of paralogous genes. Proteomic analysis recovered nearly 70% of the predicted proteins encoded by the genome, demonstrating that a high fraction of the genome is translated. In contrast to other minimal marine microbes that acquire, rather than synthesize, cofactors, CN25 encodes and expresses near-complete biosynthetic pathways for multiple vitamins. Metagenomic fragment recruitment indicated the presence of DNA sequences >90% identical to the CN25 genome throughout the oligotrophic ocean. We propose the provisional name "Candidatus Nitrosopelagicus brevis" str. CN25 for this minimalist marine thaumarchaeon and suggest it as a potential model system for understanding archaeal adaptation to the open ocean.
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“These tradeoffs include the replacement of a Fe-containing superoxide dismutase with a Nicontaining version (Dupont et al., 2012), exchanging an Fe protein with a Cu protein in the electron transport chains in photosynthesis (Peers and Price, 2006) and ammonia oxidation (Santoro et al., 2015), and using B12 instead of Fe for ribonucleotide reductase.”
From Trace elements at the intersection of marine biological and geochemical evolution (2016) · cites this paper as Santoro et al., 2015
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Citations
Cites
Cell biology and molecular basis of denitrification
Zumft, W. G. (1997) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.61.4.533-616.1997 · Cited by 3,560
Isolation of an autotrophic ammonia-oxidizing marine archaeon
Könneke, M., Bernhard, A. E., de la Torre, J. R., Walker, C. B., Waterbury, J. B., & Stahl, D. A. (2005) · Nature · doi:10.1038/nature03911 · Cited by 2,864
Archaea in coastal marine environments.
DeLong, E. F. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.12.5685 · Cited by 2,758
Rusch, D. B., Halpern, A. L., Sutton, G. G., Heidelberg, K. B., Williamson, S. J., Yooseph, S., Wu, D., Eisen, J. A., Hoffman, J., Remington, K., et al. (2007) · PLoS Biology · doi:10.1371/journal.pbio.0050077 · Cited by 2,044
Ammonia oxidation kinetics determine niche separation of nitrifying Archaea and Bacteria
Martens‐Habbena, W., Berube, P. M., Urakawa, H., de la Torre, J. R., & Stahl, D. A. (2009) · Nature · doi:10.1038/nature08465 · Cited by 1,707
Archaeal dominance in the mesopelagic zone of the Pacific Ocean
Karner, M. B., DeLong, E. F., & Karl, D. M. (2001) · Nature · doi:10.1038/35054051 · Cited by 1,630
Mesophilic crenarchaeota: proposal for a third archaeal phylum, the Thaumarchaeota
Brochier‐Armanet, C., Boussau, B., Gribaldo, S., & Forterre, P. (2008) · Nature Reviews Microbiology · doi:10.1038/nrmicro1852 · Cited by 1,249
The Black Queen Hypothesis: Evolution of Dependencies through Adaptive Gene Loss
Morris, J., Lenski, R. E., & Zinser, E. R. (2012) · mBio · doi:10.1128/mbio.00036-12 · Cited by 1,231
Genome Streamlining in a Cosmopolitan Oceanic Bacterium
Giovannoni, S. J., Tripp, H. J., Givan, S. A., Podar, M., Vergin, K. L., Baptista, D., Bibbs, L., Eads, J. R., Richardson, T. H., Noordewier, M. O., et al. (2005) · Science · doi:10.1126/science.1114057 · Cited by 1,224
Nitrososphaera viennensis , an ammonia oxidizing archaeon from soil
Tourna, M., Stieglmeier, M., Spang, A., Könneke, M., Schintlmeister, A., Urich, T., Engel, M., Schloter, M., Wagner, M., Richter, A. A., et al. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1013488108 · Cited by 962
Walker, C. B., de la Torre, J. R., Klotz, M. G., Urakawa, H., Pinel, N., Arp, D. J., Brochier‐Armanet, C., Chain, P., Chan, P. P., Anbarani, A., et al. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0913533107 · Cited by 960
Ocean's least productive waters are expanding
Polovina, J. J., Howell, E. A., & Abecassis, M. (2008) · Geophysical Research Letters · doi:10.1029/2007gl031745 · Cited by 836
Deletional bias and the evolution of bacterial genomes
Mira, Á., Ochman, H., & Moran, N. A. (2001) · Trends in Genetics · doi:10.1016/s0168-9525(01)02447-7 · Cited by 834
A moderately thermophilic ammonia-oxidizing crenarchaeote from a hot spring
Hatzenpichler, R., Lebedeva, E. V., Spieck, E., Stoecker, K., Richter, A. A., Daims, H., & Wagner, M. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0708857105 · Cited by 688
Explaining Microbial Population Genomics through Phage Predation
Rodriguez-Valera, F., Martin-Cuadrado, A.-B., Rodriguez-Brito, B., Pašić, L., Thingstad, T. F., Rohwer, F., & Mira, A. (2009) · Nature Reviews Microbiology · doi:10.1038/nrmicro2235 · Cited by 663
The genome of a motile marine Synechococcus
Palenik, B. P., Brahamsha, B., Larimer, F. W., Land, M., Hauser, L., Chain, P., Lamerdin, J. E., Regala, W., Allen, E. E., McCarren, J., et al. (2003) · Nature · doi:10.1038/nature01943 · Cited by 657
Genomic studies of uncultivated archaea
Schleper, C., Jurgens, G., & Jonuscheit, M. (2005) · Nature Reviews Microbiology · doi:10.1038/nrmicro1159 · Cited by 635
Aerobic production of methane in the sea
Karl, D. M., Beversdorf, L. J., Björkman, K. M., Church, M. J., Martinez, A., & DeLong, E. F. (2008) · Nature Geoscience · doi:10.1038/ngeo234 · Cited by 554
Cultivation of an obligate acidophilic ammonia oxidizer from a nitrifying acid soil
Lehtovirta‐Morley, L. E., Stoecker, K., Vilcinskas, A., Prosser, J. I., & Nicol, G. W. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1107196108 · Cited by 550
Genomic insights to SAR86, an abundant and uncultivated marine bacterial lineage
Dupont, C. L., Rusch, D. B., Yooseph, S., Lombardo, M., Richter, R. A., Valas, R. E., Novotny, M. A., Yee-Greenbaum, J. L., Selengut, J., Haft, D. H., et al. (2011) · The ISME Journal · doi:10.1038/ismej.2011.189 · Cited by 538
Self-citationAmmonia-oxidizing archaea use the most energy-efficient aerobic pathway for CO 2 fixation
Könneke, M., Schubert, D. M., Brown, P. C., Hügler, M., Standfest, S., Schwander, T., von Borzyskowski, L. S., Erb, T. J., Stahl, D. A., & Berg, I. A. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1402028111 · Cited by 502
Spang, A., Hatzenpichler, R., Brochier‐Armanet, C., Rattei, T., Tischler, P., Spieck, E., Streit, W. R., Stahl, D. A., Wagner, M., & Schleper, C. (2010) · Trends in Microbiology · doi:10.1016/j.tim.2010.06.003 · Cited by 474
Comparative Genomics of the Vitamin B12 Metabolism and Regulation in Prokaryotes
Rodionov, D. A., Vitreschak, A. G., Mironov, A. A., & Gelfand, M. S. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m305837200 · Cited by 472
Dufresne, A., Salanoubat, M., Partensky, F., Artiguenave, F., Axmann, I. M. I., Barbe, V., Duprat, S., Galperin, M. Y., Koonin, E. V., Gall, F. L., et al. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1733211100 · Cited by 469
Genomic Islands and the Ecology and Evolution of Prochlorococcus
Coleman, M. L., Sullivan, M. B., Martiny, A. C., Steglich, C., Barry, K., DeLong, E. F., & Chisholm, S. W. (2006) · Science · doi:10.1126/science.1122050 · Cited by 461
Quantifying archaeal community autotrophy in the mesopelagic ocean using natural radiocarbon
Ingalls, A. E., Shah, S. R., Hansman, R. L., Aluwihare, L. I., Santos, G. M., Druffel, E. R. M., & Pearson, A. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0510157103 · Cited by 458
Isotopic Signature of N 2 O Produced by Marine Ammonia-Oxidizing Archaea
Santoro, A. E., Buchwald, C., McIlvin, M. R., & Casciotti, K. L. (2011) · Science · doi:10.1126/science.1208239 · Cited by 448
Self-citationGenomic analysis of the uncultivated marine crenarchaeote Cenarchaeum symbiosum
Hallam, S., Konstantinidis, K., Putnam, N. H., Schleper, C., Watanabe, Y., Sugahara, J., Preston, C. M., de la Torre, J. R., Richardson, P. M., & DeLong, E. F. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0608549103 · Cited by 446
Minireviews: A Sea of Change: Biogeochemical Variability in the North Pacific Subtropical Gyre
Karl, D. M. (1999) · Ecosystems · doi:10.1007/s100219900068 · Cited by 442
Prevalent genome streamlining and latitudinal divergence of planktonic bacteria in the surface ocean
Swan, B. K., Tupper, B., Sczyrba, A., Lauro, F. M., Martínez‐García, M., González, J. M., Luo, H., Wright, J. J., Landry, Z., Hanson, N. W., et al. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1304246110 · Cited by 414
Marine ammonia-oxidizing archaeal isolates display obligate mixotrophy and wide ecotypic variation
Qin, W., Amin, S. A., Martens‐Habbena, W., Walker, C. B., Urakawa, H., Devol, A. H., Ingalls, A. E., Moffett, J. W., Armbrust, E. V., & Stahl, D. A. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1324115111 · Cited by 372
Aerobic nitrous oxide production through N-nitrosating hybrid formation in ammonia-oxidizing archaea
Stieglmeier, M., Mooshammer, M., Kitzler, B., Wanek, W., Zechmeister‐Boltenstern, S., Richter, A. A., & Schleper, C. (2014) · The ISME Journal · doi:10.1038/ismej.2013.220 · Cited by 369
Microbial metatranscriptomics in a permanent marine oxygen minimum zone
Stewart, F. J., Ulloa, O., & DeLong, E. F. (2011) · Environmental Microbiology · doi:10.1111/j.1462-2920.2010.02400.x · Cited by 355
Spang, A., Poehlein, A., Offre, P., Zumbrägel, S., Haider, S., Rychlik, N., Nowka, B., Schmeisser, C., Lebedeva, E. V., Rattei, T., et al. (2012) · Environmental Microbiology · doi:10.1111/j.1462-2920.2012.02893.x · Cited by 339
Genome reduction as the dominant mode of evolution
Wolf, Y. I., & Koonin, E. V. (2013) · BioEssays · doi:10.1002/bies.201300037 · Cited by 327
Synthesis of Methylphosphonic Acid by Marine Microbes: A Source for Methane in the Aerobic Ocean
Metcalf, W. W., Griffin, B. M., Cicchillo, R. M., Gao, J., Janga, S. C., Cooke, H. A., Circello, B. T., Evans, B. S., Martens‐Habbena, W., Stahl, D. A., et al. (2012) · Science · doi:10.1126/science.1219875 · Cited by 322
Blainey, P. C., Mosier, A. C., Potanina, A., Francis, C. A., & Quake, S. R. (2011) · PLoS ONE · doi:10.1371/journal.pone.0016626 · Cited by 317
Streamlining and Core Genome Conservation among Highly Divergent Members of the SAR11 Clade
Grote, J., Thrash, J. C., Huggett, M. J., Landry, Z., Carini, P., Giovannoni, S. J., & Rappé, M. S. (2012) · mBio · doi:10.1128/mbio.00252-12 · Cited by 292
Self-citationCharacterization of the cobalamin (vitamin B12) biosynthetic genes of Salmonella typhimurium
Roth, J. R., Lawrence, J. G., Rubenfield, M., Kieffer-Higgins, S., & Church, G. M. (1993) · Journal of Bacteriology · doi:10.1128/jb.175.11.3303-3316.1993 · Cited by 281
Production of oceanic nitrous oxide by ammonia-oxidizing archaea
Löscher, C. R., Kock, A., Könneke, M., LaRoche, J., Bange, H. W., & Schmitz, R. A. (2012) · Biogeosciences · doi:10.5194/bg-9-2419-2012 · Cited by 258
Streamlining and Simplification of Microbial Genome Architecture
Lynch, M. (2006) · Annual Review of Microbiology · doi:10.1146/annurev.micro.60.080805.142300 · Cited by 256
Quantitative analysis of a deeply sequenced marine microbial metatranscriptome
Gifford, S., Sharma, S., Rinta‐Kanto, J. M., & Moran, M. A. (2010) · The ISME Journal · doi:10.1038/ismej.2010.141 · Cited by 215
Santoro, A. E., & Casciotti, K. L. (2011) · The ISME Journal · doi:10.1038/ismej.2011.58 · Cited by 208
Self-citationMultiple B-vitamin depletion in large areas of the coastal ocean
Sañudo‐Wilhelmy, S. A., Cutter, L. S., Durazo, R., Smail, E. A., Gómez‐Consarnau, L., Webb, E. A., Prokopenko, M. G., Berelson, W. M., & Karl, D. M. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1208755109 · Cited by 206
The Impact of Genome Analyses on Our Understanding of Ammonia-Oxidizing Bacteria
Arp, D. J., Chain, P., & Klotz, M. G. (2007) · Annual Review of Microbiology · doi:10.1146/annurev.micro.61.080706.093449 · Cited by 206
Beaumont, H. J. E., Lens, S. I., Reijnders, W. N. M., Westerhoff, H. V., & van Spanning, R. J. M. (2004) · Molecular Microbiology · doi:10.1111/j.1365-2958.2004.04248.x · Cited by 192
Aquatic metagenomes implicate Thaumarchaeota in global cobalamin production
Doxey, A. C., Kurtz, D. A., Lynch, M. D. J., Sauder, L. A., & Neufeld, J. D. (2014) · The ISME Journal · doi:10.1038/ismej.2014.142 · Cited by 183
Lehtovirta‐Morley, L. E., Ge, C., Ross, J. L., Yao, H., Nicol, G. W., & Prosser, J. I. (2014) · FEMS Microbiology Ecology · doi:10.1111/1574-6941.12353 · Cited by 153
Occurrence of phosphate acquisition genes in Prochlorococcus cells from different ocean regions
Martiny, A. C., Huang, Y., & Li, W. (2009) · Environmental Microbiology · doi:10.1111/j.1462-2920.2009.01860.x · Cited by 152
Carini, P., Campbell, E. O., Morré, J. T., Sañudo‐Wilhelmy, S. A., Thrash, J. C., Bennett, S. E., Temperton, B., Begley, T. P., & Giovannoni, S. J. (2014) · The ISME Journal · doi:10.1038/ismej.2014.61 · Cited by 142
Self-citationDecker, K. B., & Hinton, D. M. (2013) · Annual Review of Microbiology · doi:10.1146/annurev-micro-092412-155756 · Cited by 127
Hollibaugh, J. T., Gifford, S., Sharma, S., Bano, N., & Moran, M. A. (2010) · The ISME Journal · doi:10.1038/ismej.2010.172 · Cited by 121
General transcription factor specified global gene regulation in archaea
Facciotti, M. T., Reiss, D. J., Pan, M., Kaur, A., Vuthoori, M., Bonneau, R., Shannon, P. T., Srivastava, A., Donohoe, S., Hood, L., et al. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0611663104 · Cited by 115
Baker, B. J., Lesniewski, R. A., & Dick, G. J. (2012) · The ISME Journal · doi:10.1038/ismej.2012.64 · Cited by 110
Single-cell genomics shedding light on marine Thaumarchaeota diversification
Luo, H., Tolar, B. B., Swan, B. K., Zhang, C. L., Stepanauskas, R., Moran, M. A., & Hollibaugh, J. T. (2013) · The ISME Journal · doi:10.1038/ismej.2013.202 · Cited by 99
Amin, S. A., Moffett, J. W., Martens-Habbena, W., Jacquot, J. E., Han, Y., Devol, A., Ingalls, A. E., Stahl, D. A., & Armbrust, E. V. (2013) · Limnology and Oceanography · doi:10.4319/lo.2013.58.6.2037 · Cited by 85
Swan, B. K., Chaffin, M. D., Martínez‐García, M., Morrison, H. G., Field, E. K., Poulton, N. J., Masland, E. D. P., Harris, C. C., Sczyrba, A., Chain, P., et al. (2014) · PLoS ONE · doi:10.1371/journal.pone.0095380 · Cited by 72
Metagenomic analysis of a complex marine planktonic thaumarchaeal community from the Gulf of Maine
Tully, B., Nelson, W. C., & Heidelberg, J. F. (2011) · Environmental Microbiology · doi:10.1111/j.1462-2920.2011.02628.x · Cited by 64
Niche adaptation by expansion and reprogramming of general transcription factors
Turkarslan, S., Reiss, D. J., Gibbins, G., Su, W. L., Pan, M., Bare, J. C., Plaisier, C. L., & Baliga, N. S. (2011) · Molecular Systems Biology · doi:10.1038/msb.2011.87 · Cited by 42
Status quo in physiological proteomics of the uncultured Riftia pachyptila endosymbiont
Markert, S., Gardebrecht, A., Felbeck, H., Sievert, S. M., Klose, J., Becher, D., Albrecht, D., Thürmer, A., Daniel, R., Kleiner, M., et al. (2011) · PROTEOMICS · doi:10.1002/pmic.201100059 · Cited by 34
Methanococcus jannaschiiGenerates l- Proline by Cyclization of l- Ornithine
Graupner, M., & White, R. H. (2001) · Journal of Bacteriology · doi:10.1128/jb.183.17.5203-5205.2001 · Cited by 33
Pellitteri-Hahn, M. C., Halligan, B. D., Scalf, M., Smith, L. M., & Hickey, W. J. (2010) · Journal of Proteomics · doi:10.1016/j.jprot.2010.12.003 · Cited by 26
Seawater Activation of Escherichia coli Gene Promoter Elements: Dominance of rpoS Control
Rozen, Y., Dyk, T. K. V., LaRossa, R. A., & Belkin, S. (2001) · Microbial Ecology · doi:10.1007/s00248-001-1012-x · Cited by 26
Role of the precorrin 6‐X reductase gene in cobamide biosynthesis in Methanococcus maripaludis
Kim, W., Major, T. A., & Whitman, W. B. (2005) · Archaea · doi:10.1155/2005/903614 · Cited by 8
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Metadata
- Authors
- Santoro, A. E., Dupont, C. L., Richter, R. A., Craig, M. T., Carini, P., McIlvin, M. R., Yang, Y., Orsi, W. D., Moran, D. M., & Saito, M. A.
- Affiliations
- University of Maryland Center for Environmental Science (US)
- Microbial and Environmental Genomics and
- J. Craig Venter Institute (US)
- University of San Diego (US)
- Woods Hole Oceanographic Institution (US)
- ORCID
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 2015-01-13
- Volume
- 112
- Issue
- 4
- Pages
- 1173-1178
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC4313803
- OpenAlex
- W2032670022
- Cited by
- 268
- References
- 64
- Citations by year
- 2026: 12 · 2025: 22 · 2024: 23 · 2023: 23 · 2022: 26 · 2021: 25 · 2020: 30 · 2019: 31 · 2018: 21 · 2017: 18 · 2016: 25 · 2015: 12
- FWCI
- 22.97
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Proceedings of the National Academy of Sciences (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- eScholarship (California Digital Library) (submittedVersion)
- Funders
- Gordon and Betty Moore Foundation (GBMF3307, GBMF3782, GBMF2724)
- Topics
- Physical Sciences › Environmental Science › Ecology › Microbial Community Ecology and Physiology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Phylogenetic Studies
- Physical Sciences › Environmental Science › Pollution › Wastewater Treatment and Nitrogen Removal
- Keywords
- ammonia-oxidizing archaea, Thaumarchaeota, marine archaea, genome streamlining, minimal genome, vitamin biosynthesis, cofactor biosynthesis, proteome, genome assembly
- MeSH terms
- Amino Acid Sequence, Archaea, Molecular Sequence Data, Oceans and Seas, Water Microbiology, Archaeal Proteins, Gene Expression Regulation, Archaeal, Proteome, Proteomics, Metagenomics
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