Evidence map›Paper›PMID 22003381›Full record

ArticlePloS one2011

The complete genome sequence of Thermoproteus tenax: a physiologically versatile member of the Crenarchaeota.

Bettina Siebers, Melanie Zaparty, Guenter Raddatz, Britta Tjaden, Sonja-Verena Albers, Steve D Bell, Fabian Blombach, Arnulf Kletzin, Nikos Kyrpides, Christa Lanz and 8 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
2.1field-weighted citation impact, top 13% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

30 citing papers in PubMed, 53 citations in OpenAlex.

  1. Review
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  7. Genomic attributes of thermophilic and hyperthermophilic bacteria and archaea.World journal of microbiology & biotechnology · 2022
    Review
  8. Article
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  14. Article
  15. Biotechnology of extremely thermophilic archaea.FEMS microbiology reviews · 2018
    Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

18 authors at 13 institutions in 4 countries.

Bettina SiebersFaculty of Chemistry, Biofilm Centre, Molecular Enzyme Technology and Biochemistry, University of Duisburg-Essen, Essen, Germany. bettina.siebers@uni-due.de
Melanie Zaparty
Guenter Raddatz
Britta Tjaden
Sonja-Verena Albers
Steve D Bell
Fabian Blombach
Arnulf Kletzin
Nikos Kyrpides
Christa Lanz
André Plagens
Markus Rampp
Andrea Rosinus
Mathias von Jan
Kira S Makarova
Hans-Peter Klenk
Stephan C Schuster
Reinhard Hensel
Max Planck Institute for Terrestrial Microbiology · DELeibniz Institute DSMZ – German Collection of Microorganisms and Cell Cultures · DEMax Planck Institute for Developmental Biology · DEJoint Genome Institute · USMax Planck Institute for Biological Cybernetics · DEMax Planck Institute for Plasma Physics · DEMax Planck Society · DENational Institutes of Health · USPennsylvania State University · USUniversity of Duisburg-Essen · DEUniversity of Oxford · GBUniversity of Regensburg · DEWageningen University & Research · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Here, we report on the complete genome sequence of the hyperthermophilic Crenarchaeum Thermoproteus tenax (strain Kra1, DSM 2078(T)) a type strain of the crenarchaeotal order Thermoproteales. Its circular 1.84-megabase genome harbors no extrachromosomal elements and 2,051 open reading frames are identified, covering 90.6% of the complete sequence, which represents a high coding density. Derived from the gene content, T. tenax is a representative member of the Crenarchaeota. The organism is strictly anaerobic and sulfur-dependent with optimal growth at 86°C and pH 5.6. One particular feature is the great metabolic versatility, which is not accompanied by a distinct increase of genome size or information density as compared to other Crenarchaeota. T. tenax is able to grow chemolithoautotrophically (CO₂/H₂) as well as chemoorganoheterotrophically in presence of various organic substrates. All pathways for synthesizing the 20 proteinogenic amino acids are present. In addition, two presumably complete gene sets for NADH:quinone oxidoreductase (complex I) were identified in the genome and there is evidence that either NADH or reduced ferredoxin might serve as electron donor. Beside the typical archaeal A₀A₁-ATP synthase, a membrane-bound pyrophosphatase is found, which might contribute to energy conservation. Surprisingly, all genes required for dissimilatory sulfate reduction are present, which is confirmed by growth experiments. Mentionable is furthermore, the presence of two proteins (ParA family ATPase, actin-like protein) that might be involved in cell division in Thermoproteales, where the ESCRT system is absent, and of genes involved in genetic competence (DprA, ComF) that is so far unique within Archaea.

Indexed as

Amino AcidsChemoautotrophic GrowthDNA ReplicationEnergy MetabolismEvolution, MolecularGenome, ArchaealGenomicsPhylogenyProtein BiosynthesisProtein TransportProton-Motive ForceThermoproteusTranscription, GeneticAmino Acids

Identifiers

PMID22003381
PMCPMC3189178
OpenAlexW2114640216

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.