Abstract
Dissimilatory sulfate-reducing archaea of the genus Archaeoglobus display divergent preferences in the use of energy sources and electron acceptors. Here we present the complete genome sequence of the thermophilic Archaeoglobus sulfaticallidus strain PM70-1T, which distinctly couples chemolithoautotrophic growth on H2/CO2 to sulfate reduction in addition to heterotrophic growth.
GENOME ANNOUNCEMENT
The thermophilic euryarchaeon Archaeoglobus sulfaticallidus type strain PM70-1 belongs to the family Archaeoglobaceae and was isolated from black rust present on the steel surface of a borehole observatory on the eastern flank of Juan de Fuca Ridge, eastern Pacific Ocean (1, 2). The genus Archaeoglobus consists of five species with validly published names, A. fulgidus (3), A. profundus (4), A. veneficus (5), A. infectus (6), and A. sulfaticallidus (1), all of which were isolated from marine hydrothermal systems. A formal species description has not been published for “A. lithotrophicus,” isolated from deep oil reservoirs (7).
All members of the genus Archaeoglobus, with the exception of A. profundus and A. infectus (1, 3–6, 8), are capable of chemolithoautrotrophic growth on H2/CO2 and thiosulfate. However, A. sulfaticallidus differs from the other members of the genus Archaeoglobus by being able to couple chemolithoautotrophic growth on H2/CO2 to sulfate reduction (1). This trait has so far been reported only for “A. lithotrophicus,” which, in contrast to A. sulfaticallidus, is not capable of heterotrophic growth (7).
Whole-genome sequencing was performed using a mixed library of shotgun and 8-kb paired-end reads from a Roche 454-sequencing platform at the Norwegian Sequencing Centre in Oslo, Norway (http://www.sequencing.uio.no). Pyrosequencing reads were assembled using the Newbler assembler version 2.8 (Roche). The Newbler assembly contained 20 contigs in a single scaffold. The genome was finished by filling gaps between contigs with Sanger sequencing of targeted PCR products using an ABI 3730 sequencer (Applied Biosystems). The final assembly comprises 386,142 reads that provide 50× coverage of the genome. Gene predictions and functional assignments were performed within the Integrated Microbial Genomes—Expert Review (IMG-ER) platform (9) in combination with manual curation. Pfam families were categorized according to Pfam27.0, using the command line version of HMMER3 (10, 11).
The complete genome of A. sulfaticallidus PM70-1 comprises one circular chromosome with a total size of 2,076,931 bp and a GC content of 43.24%. The genome contains 2,216 protein-coding genes, 1 rRNA operon (one copy each of 5S, 16S, and 23S rRNA genes), and 51 tRNA genes, in addition to 6 other structural RNA genes. Similar to those in the genomes of A. fulgidus (12), A. profundus (13), A. veneficus (Genomes Online Database [GOLD] identification no. Gc01707), and Ferroglobus placidus (14), the 5S rRNA gene is not found adjacent to the 16S and 23S rRNA genes. Of the 2,216 predicted coding genes, 1,494 (67.4%) were assigned to known protein functions.
A complete set of genes for the acetyl coenzyme A (acetyl-CoA) pathway of methanogens, which may function as both the core reductive and oxidative carbon metabolic systems, was identified in the genome of A. sulfaticallidus (8, 15). Like other members of the Archaeoglobaceae, A. sulfaticallidus lacks genes for terminal methanogenesis from acetyl-CoA. Instead, the genome carries a full set of genes for dissimilatory sulfate reduction, common to a wide range of sulfate-reducing organisms (16).
Nucleotide sequence accession number.
The complete genome sequence of A. sulfaticallidus PM70-1T has been deposited in GenBank under accession number CP005290.
ACKNOWLEDGMENTS
The sequencing project was supported by the Norwegian Research Council (project no. 179560/V30 and 208491/O10).
Footnotes
Citation Stokke R, Hocking WP, Steinsbu BO, Steen IH. 2013. Complete genome sequence of the thermophilic and facultatively chemolithoautotrophic sulfate reducer Archaeoglobus sulfaticallidus strain PM70-1T. Genome Announc. 1(4):e00406-13. doi:10.1128/genomeA.00406-13.
REFERENCES
- 1. Steinsbu BO, Thorseth IH, Nakagawa S, Inagaki F, Lever MA, Engelen B, Øvreås L, Pedersen RB. 2010. Archaeoglobus sulfaticallidus sp. nov., a thermophilic and facultatively lithoautotrophic sulfate-reducer isolated from black rust exposed to hot ridge flank crustal fluids. Int. J. Syst. Evol. Microbiol. 60:2745–2752 [DOI] [PubMed] [Google Scholar]
- 2. Nakagawa S, Inagaki F, Suzuki Y, Steinsbu BO, Lever MA, Takai K, Engelen B, Sako Y, Wheat CG, Horikoshi K. Integrated Ocean Drilling Program Expedition S 2006. Microbial community in black rust exposed to hot ridge flank crustal fluids. Appl. Environ. Microbiol. 72:6789–6799 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3. Stetter KO. 1988. Archaeoglobus fulgidus gen. nov., sp. nov: a new taxon of extremely thermophilic archaebacteria. Syst.. Appl. Microbiol. 10:172–173 [Google Scholar]
- 4. Burggraf S, Jannasch HW, Nicolaus B, Stetter K. 1990. Archaeoglobus profundus sp.nov., represents a new species within the sulfate-reducing archaebacteria. Syst. Appl. Microbiol. 13:24–28 [Google Scholar]
- 5. Huber H, Jannasch HW, Rachel R, Fuchs T, Stetter K. 1997. Archaeoglobus veneficus sp.nov., a novel facultative chemolithoautotrophic hyperthermophilic sulfite reducer isolated from abyssal black smokers. Syst. Appl. Microbiol. 20:374–380 [Google Scholar]
- 6. Mori K, Maruyama A, Urabe T, Suzuki K-i, Hanada S. 2008. Archaeoglobus infectus sp. nov., a novel thermophilic, chemolithoheterotrophic archaeon isolated from a deep-sea rock collected at Suiyo seamount, Izu-Bonin arc, western Pacific Ocean. Int. J. Syst. Evol. Microbiol. 58:810–816 [DOI] [PubMed] [Google Scholar]
- 7. Stetter KO, Huber R, Blochl E, Kurr M, Eden RD, Fielder M, Cash H, Vance I. 1993. Hyperthermophilic archaea are thriving in deep North Sea and Alaskan oil reservoirs. Nature 365:743–745 [Google Scholar]
- 8. Vorholt J, Kunow J, Stetter KO, Thauer RK. 1995. Enzymes and coenzymes of the carbon monoxide dehydrogenase pathway for autotrophic CO2 fixation in Archaeoglobus lithotrophicus and the lack of carbon monoxide dehydrogenase in the heterotrophic A. profundus. Arch. Microbiol. 163:112–118 [Google Scholar]
- 9. Markowitz VM, Mavromatis K, Ivanova NN, Chen IM, Chu K, Kyrpides NC. 2009. IMG er: a system for microbial genome annotation expert review and curation. Bioinformatics 25:2271–2278 [DOI] [PubMed] [Google Scholar]
- 10. Finn RD, Clements J, Eddy SR. 2011. HMMER web server: interactive sequence similarity searching. Nucleic Acids Res. 39:W29–W37 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 11. Punta M, Coggill PC, Eberhardt RY, Mistry J, Tate J, Boursnell C, Pang N, Forslund K, Ceric G, Clements J, Heger A, Holm L, Sonnhammer EL, Eddy SR, Bateman A, Finn RD. 2012. The Pfam protein families database. Nucleic Acids Res. 40:D290–D301 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 12. Klenk HP, Clayton RA, Tomb JF, White O, Nelson KE, Ketchum KA, Dodson RJ, Gwinn M, Hickey EK, Peterson JD, Richardson DL, Kerlavage AR, Graham DE, Kyrpides NC, Fleischmann RD, Quackenbush J, Lee NH, Sutton GG, Gill S, Kirkness EF, Dougherty BA, McKenney K, Adams MD, Loftus B, Peterson S, Reich CI, McNeil LK, Badger JH, Glodek A, Zhou L, Overbeek R, Gocayne JD, Weidman JF, McDonald L, Utterback T, Cotton MD, Spriggs T, Artiach P, Kaine BP, Sykes SM, Sadow PW, D’Andrea KP, Bowman C, Fujii C, Garland SA, Mason TM, Olsen GJ, Fraser CM, Smith HO, Woese CR, Venter JC. 1997. The complete genome sequence of the hyperthermophilic, sulphate-reducing archaeon Archaeoglobus fulgidus. Nature 390:364–370 [DOI] [PubMed] [Google Scholar]
- 13. von Jan M, Lapidus A, Glavina Del Rio T, Copeland A, Tice H, Cheng J-F, Lucas S, Chen F, Nolan M, Goodwin L, Han C, Pitluck S, Liolios K, Ivanova N, Mavromatis K, Ovchinnikova G, Chertkov O, Pati A, Chen A, Palaniappan K, Land M, Hauser L, Chang Y-J, Jeffries CD, Saunders E, Brettin T, Detter JC, Chain P, Eichinger K, Huber H, Spring S, Rohde M, Göker M, Wirth R, Woyke T, Bristow J, Eisen JA, Markowitz V, Hugenholtz P, Kyrpides NC, Klenk H-P. 2010. Complete genome sequence of Archaeoglobus profundus type strain (AV18 T). Stand. Genomics Sci. 2:327–346 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14. Anderson IJ, Risso C, Holmes D, Lucas S, Copeland A, Lapidus A, Cheng J-F, Bruce D, Goodwin L, Pitluck S, Saunders E, Brettin T, Detter JC, Han C, Tapia R, Larimer F, Land M, Hauser L, Woyke T, Lovley D, Kyrpides NC, Ivanova N. 2011. Complete genome sequence of Ferroglobus placidus AEDII12DO. Stand. Genomics Sci. 5:50–60 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 15. Möller-Zinkhan D, Thauer RK. 1990. Anaerobic lactate oxidation to 3 CO2 by Archaeoglobus fulgidus via the carbon monoxide dehydrogenase pathway: demonstration of the acetyl-CoA carbon-carbon cleavage reaction in cell extracts. Arch. Microbiol. 153:215–218 [Google Scholar]
- 16. Pereira IAC, Ramos AR, Grein F, Marques MC, Da Silva SM, Venceslau SS. 2011. A comparative genomic analysis of energy metabolism in sulfate reducing bacteria and archaea. Front. Microbiol. 2:69. [DOI] [PMC free article] [PubMed] [Google Scholar]
