Free access
19 April 2011

Complete Genome Sequence of “Vulcanisaeta moutnovskia” Strain 768-28, a Novel Member of the Hyperthermophilic Crenarchaeal Genus Vulcanisaeta

ABSTRACT

Strain 768-28 was isolated from a hot spring in Kamchatka, Russia, and represents a novel member of the Vulcanisaeta genus. The complete genome sequence of this thermoacidophilic anaerobic crenarchaeon reveals genes for protein and carbohydrate-active enzymes, the Embden-Meyerhof and Entner-Doudoroff pathways for glucose metabolism, the tricarboxylic acid cycle, beta-oxidation of fatty acids, and sulfate reduction.

TEXT

Together with the genera Thermoproteus, Pyrobaculum, Thermocladium, Caldivirga, and Thermofilum, the genus Vulcanisaeta forms the crenarchaeal order Thermoproteales comprising rod-shaped thermophilic crenarchaeotes (5). Two currently known Vulcanisaeta species, V. distributa and V. souniana, are heterotrophic, anaerobic hyperthermophiles isolated from hot springs in Japan (3). The complete genome sequence of V. distributa DSM 14429 was determined recently (7). Strain 768-28 was isolated from the solfataric field close to Moutnovsky volcano in Kamchatka, Russia, and was found to be affiliated with the Vulcanisaeta genus based on 16S rRNA gene phylogeny (8). Vulcanisaeta sp. 768-28 is an obligately anaerobic acidophile with a pH range of growth from 3.5 to 6.5 and a temperature range from 60 to 98°C. It is a metabolically versatile archaeon capable of fermenting proteinaceous substrates and some sugars (8). Elemental sulfur and thiosulfate are reduced to hydrogen sulfide if added (8). To understand the physiological properties of this archaeon and possible ecological roles of Vulcanisaeta sp., a complete genome sequence was determined.
The genome of Vulcanisaeta sp. 768-28 was sequenced with the Roche 454 GS FLX pyrosequencing platform. We obtained two libraries of 174,571 single-strand reads and 72,003 paired-end reads containing 3-kb inserts. The reads were assembled into a single scaffold (14 contigs) by the Newbler Assembler 1.1 (454 Life Sciences, Branford, CT). The genome was finished by filling gaps with sequencing and primer walking of PCR products with an ABI 3730 capillary sequencer (Applied Biosystems, CA).
The complete genome of Vulcanisaeta sp. 768-28 consists of 2,298,983 bp in a single circular chromosome with an average G+C content of 42.4%. A total of 2,320 protein-coding genes were predicted by Glimmer (1), covering 88% of the chromosome. About 77% of these proteins showed similarity to those of V. distributa DSM 14429, while remaining 537 proteins are specific for strain 768-28, indicating that this strain may be classified as a novel species, “Vulcanisaeta moutnovskia.” A whole-genome annotation and analysis were performed with the AutoFACT tool (6), followed by a round of manual curation. Metabolic pathway analysis revealed that utilization of polysaccharides and proteins involve the function of numerous encoded hydrolytic enzymes. Similarly to Thermoproteus tenax (10), further oxidation of monomers proceeds in both the modified Embden-Meyerhof and Entner-Doudoroff pathways followed by an oxidative tricarboxylic acid cycle enabling the complete oxidation of organic substrates to CO2 and H2S (9). The genome encodes at least 14 putative esterases and a complete beta-oxidation pathway for fatty acids, suggesting the ability of V. moutnovskia to utilize lipids. The genome analysis suggests the presence of a sulfate reduction pathway that is quite unusual among archaea and to date had been reported only in the euryarchaeon Archaeoglobus fulgidus (4) and crenarchaeon Caldivirga maquilingensis (2). Making the genome sequence of V. moutnovskia 768-28 available will allow comprehensive comparisons with other members of the genus and enable further investigation into the mechanisms of adaptation to thermal acidic environments.

Nucleotide sequence accession number.

The complete genome sequence of V. moutnovskia 768-28 was deposited in GenBank under accession no. CP002529.

Acknowledgments

This work was supported by the Ministry of Education and Sciences of Russia (contract 02.512.11.2201).

REFERENCES

1.
Delcher A. L., Harmon D., Kasif S., White O., and Salzberg S. L. 1999. Improved microbial gene identification with GLIMMER. Nucleic Acids Res. 27:4636–4641.
2.
Itoh T., Suzuki K., Sanchez P. C., and Nakase T. 1999. Caldivirga maquilingensis gen. nov., sp. nov., a new genus of rod-shaped crenarchaeote isolated from a hot spring in the Philippines. Int. J. Syst. Bacteriol. 49:1157–1163.
3.
Itoh T., Suzuki K., and Nakase T. 2002. Vulcanisaeta distributa gen. nov., sp. nov., and Vulcanisaeta souniana sp. nov., novel hyperthermophilic, rod-shaped crenarchaeotes isolated from hot springs in Japan. Int. J. Syst. Evol. Microbiol. 52:1097–1104.
4.
Klenk H. P. et al. 1997. The complete genome sequence of the hyperthermophilic, sulphate-reducing archaeon Archaeoglobus fulgidus. Nature 390:364–370.
5.
Kletzin A. 2007. General characteristics and important model organisms, p. 14–92. In Cavicchioli R. (ed.), Archaea: molecular and cellular biology, ASM Press, Washington, DC.
6.
Koski L. B., Gray M. W., Langi B. F., and Burger G. 2005. AutoFACT: an automatic functional annotation and classification tool. BMC Bioinformatics 6:151.
7.
Mavromatis K. et al. 2010. Complete genome sequence of Vulcanisaeta distributa type strain (IC-017). Stand. Genomic Sci. 3:117–125.
8.
Prokofeva M. et al. 2005. Cultivated anaerobic acidophilic/acidotolerant thermophiles from terrestrial and deep-sea hydrothermal habitats. Extremophiles 9:437–448.
9.
Selig M. and Schönheit P. 1994. Oxidation of organic compounds to CO2 with sulfur or thiosulfate as electron acceptor in the anaerobic hyperthermophilic archaea Thermoproteus tenax and Pyrobaculum islandicum proceeds via the citric acid cycle. Arch. Microbiol. 162:286–294.
10.
Zaparty M., Tjaden B., Hensel R., and Siebers B. 2008. The central carbohydrate metabolism of the hyperthermophilic crenarchaeote Thermoproteus tenax: pathways and insights into their regulation. Arch. Microbiol. 190:231–245.

Information & Contributors

Information

Published In

cover image Journal of Bacteriology
Journal of Bacteriology
Volume 193Number 91 May 2011
Pages: 2355 - 2356
PubMed: 21398550

History

Received: 18 February 2011
Accepted: 28 February 2011
Published online: 19 April 2011

Permissions

Request permissions for this article.

Contributors

Authors

Vadim M. Gumerov
Centre “Bioengineering,” Russian Academy of Sciences, Moscow 117312, Russia
Andrey V. Mardanov
Centre “Bioengineering,” Russian Academy of Sciences, Moscow 117312, Russia
Alexey V. Beletsky
Centre “Bioengineering,” Russian Academy of Sciences, Moscow 117312, Russia
Maria I. Prokofeva
Winogradsky Institute of Microbiology, Russian Academy of Sciences, Moscow 117312, Russia
Elizaveta A. Bonch-Osmolovskaya
Winogradsky Institute of Microbiology, Russian Academy of Sciences, Moscow 117312, Russia
Nikolai V. Ravin [email protected]
Centre “Bioengineering,” Russian Academy of Sciences, Moscow 117312, Russia
Konstantin G. Skryabin [email protected]
Centre “Bioengineering,” Russian Academy of Sciences, Moscow 117312, Russia

Metrics & Citations

Metrics

Note: There is a 3- to 4-day delay in article usage, so article usage will not appear immediately after publication.

Citation counts come from the Crossref Cited by service.

Citations

If you have the appropriate software installed, you can download article citation data to the citation manager of your choice. Simply select your manager software from the list below and click Download.

View Options

Figures and Media

Figures

Media

Tables

Share

Share

Share the article link

Share with email

Email a colleague

Share on social media

American Society for Microbiology ("ASM") is committed to maintaining your confidence and trust with respect to the information we collect from you on websites owned and operated by ASM ("ASM Web Sites") and other sources. This Privacy Policy sets forth the information we collect about you, how we use this information and the choices you have about how we use such information.
FIND OUT MORE about the privacy policy