Open Access

Complete genome sequence of Meiothermus ruber type strain (21T)

  • Brian J Tindall
  • , Johannes Sikorski
  • , Susan Lucas
  • , Eugene Goltsman
  • , Alex Copeland
  • , Tijana Glavina Del Rio
  • , Matt Nolan
  • , Hope Tice
  • , Jan-Fang Cheng
  • , Cliff Han,
  • , Sam Pitluck
  • , Konstantinos Liolios
  • , Natalia Ivanova
  • , Konstantinos Mavromatis
  • , Galina Ovchinnikova
  • , Amrita Pati
  • , Regine Fähnrich
  • , Lynne Goodwin,
  • , Amy Chen
  • , Krishna Palaniappan
  • , Miriam Land,
  • , Loren Hauser,
  • , Yun-Juan Chang,
  • , Cynthia D. Jeffries,
  • , Manfred Rohde
  • , Markus Göker
  • , Tanja Woyke
  • , James Bristow
  • , Jonathan A. Eisen,
  • , Victor Markowitz
  • , Philip Hugenholtz
  • , Nikos C. Kyrpides
  • , Hans-Peter Klenk
  • and Alla Lapidus
Corresponding author

DOI: 10.4056/sigs.1032748

Received: 29 July 2010

Published: 30 August 2010


Meiothermus ruber (Loginova et al. 1984) Nobre et al. 1996 is the type species of the genus Meiothermus. This thermophilic genus is of special interest, as its members share relatively low degrees of 16S rRNA gene sequence similarity and constitute a separate evolutionary lineage from members of the genus Thermus, from which they can generally be distinguished by their slightly lower temperature optima. The temperature related split is in accordance with the chemotaxonomic feature of the polar lipids. M. ruber is a representative of the low-temperature group. This is the first completed genome sequence of the genus Meiothermus and only the third genome sequence to be published from a member of the family Thermaceae. The 3,097,457 bp long genome with its 3,052 protein-coding and 53 RNA genes is a part of the Genomic Encyclopedia of Bacteria and Archaea project.




Strain 21T (= DSM 1279 = ATCC 35948 = VKM B-1258) is the type strain of the species Meiothermus ruber, which is the type species of the genus Meiothermus [1]. Strain 21T was first described as a member of the genus Thermus by Loginova and Egorova in 1975 [2], but the species name to which it was assigned was not included on the Approved Lists of Bacterial Names [3]. Consequently Thermus ruber was revived, according to Rule 28a of the International Code of Nomenclature of Bacteria [4] in 1984 [5]. It received its current name in 1996 when transferred from the genus Thermus into the then novel genus Meiothermus by Nobre et al. [1]. Currently, there are eight species placed in the genus Meiothermus [6]. The genus name derives from the Greek words ‘meion’ and ‘thermos’ meaning ‘lesser’ and ‘hot’ to indicate an organism in a less hot place [1,6]. The species epithet derives from the Latin word ‘ruber’ meaning red, to indicate the red cell pigmentation [5,6]. Members of the genus Meiothermus were isolated from natural hot springs and artificial thermal environments [1] in Russia [5], Central France [7], both Northern and Central Portugal [8,9], North-Eastern China [10], Northern Taiwan [11] and Iceland [12]. Interestingly, the genus Meiothermus is heterogeneous with respect to pigmentation. The yellow pigmented species also form a distinct group on the basis of the 16S rRNA gene sequence similarity, with the red/orange pigmented strains forming two groups, one comprising M. silvanus and the other the remaining species [9,10]. Like all members of the Deinococci the lipid composition of the cell membrane of members of the genus Meiothermus is based on unusual and characteristic structures. Here we present a summary classification and a set of features for M. ruber 21T, together with the description of the complete genomic sequencing and annotation.

Classification and features

The 16S rRNA genes of the seven other type strains in the genus Meiothermus share between 88.7% (M. silvanus) [13] and 98.8% (M. taiwanensis) [14] sequence identity with strain 21T, whereas the other type strains from the family Thermaceae share 84.5 to 87.6% sequence identity [15]. Thermus sp. R55-10 from the Great Artesian Basin of Australia (AF407749), as well as other reference strains, e.g. 16105 and 17106 [12], and the uncultured bacterial clone 53-ORF05 from an aerobic sequencing batch reactor (DQ376569) show full length 16S rRNA sequences identical to that of strain 21T. A rather large number of isolates with almost identical 16S rRNA gene sequences originates from the Great Artesian Basin of Australia, clone R03 (AF407684), and various hot springs in Hyogo, Japan (strain H328; AB442017), Liaoning Province, China (strain L462; EU418906, and others), Thailand (strain O1DQU (EU376397), a Finnish paper production facility (strain L-s-R2A-3B.2; AM229096) and others), but also the not validly published ‘M. rosaceus’ (99.9%) [16] from Tengchong hot spring in Yunnan (China). Environmental samples and metagenomic surveys do not surpass 81-82% sequence similarity to the 16S rRNA gene sequence of strain 21T, indicating a rather mixed impression about the environmental importance of strains belonging to the species M. ruber, as occurring only in very restricted extreme habitats (status August 2009).

A detailed physiological description based on five strains has been given by Loginova et al. [5]. The cells are described as Gram-negative nonmotile rods that are 3 to 6 by 0.5 to 0.8 µm (Table 1), have rounded ends, and are nonsporeforming [5]. In potato-peptone-yeast extract broth incubated at 60°C, filamentous forms (20 to 40 µm in length) are observed along with shorter rods (Figure 1) [5]. No filamentous forms are observed after 16 h of incubation. M. ruber is obligately thermophilic [5]. On potato-peptone-yeast extract medium, the temperature range for growth is approx. 35-70°C, with an optimum temperature at 60°C (the generation time is then 60 min) [5]. A bright red intracellular carotenoid pigment is produced, which resembles retro-dehydro-γ-carotene (neo A, neo B) in its spectral properties [2]. The absorption spectra of acetone, methanol-acetone (l:l), and hexane extracts show three maxima at 455, 483, and 513 nm. The major carotenoid has since been identified as a 1‘-β-glucopyranosyl-3,4,3‘,4‘-tetradehydro-1‘,2‘-dihydro-β,ψ-caroten-2-one, with the glucose acetylated at position 6 [30]. One strain (strain INMI-a) contains a bright yellow pigment resembling neurosporaxanthine in its spectral properties [5], although it may well have been misidentified, since other species within the genus Meiothermus are yellow pigmented [8,9]. M. ruber is obligately aerobic [5]. It grows in minimal medium supplemented with 0.15% (wt/vol) peptone as an N source, 0.05% (wt/vol) yeast extract, and one of the following carbon sources at a concentration of 0.25% (wt/vol): D-glucose, sucrose, maltose, D-galactose, D-mannose, rhamnose, D-cellobiose, glycerol, D-mannitol, acetate, pyruvate, succinate, fumarate, or DL-malate (sodium salts). No growth occurs if the concentration of D-glucose in the medium is raised to 0.5% (wt/vol) [5]. Only moderate growth occurs when ammonium phosphate (0.1%, wt/vol) is substituted for peptone as the N source. No growth occurs in the control medium without a carbon source. No growth occurs on minimal medium supplemented with 0.25% (wt/vol) D-glucose, 0.05% (wt/vol) yeast extract and one of the following nitrogen sources at a concentration of 0.1% (wt/vol): L-alanine, glycine, L-asparagine, L-tyrosine, L-glutamate, ammonium sulfate, nitrate, or urea. Further lists of carbon source utilization, which differ in part from the above list, are published elsewhere [7,10-12]. Nitrates are not reduced and milk is not peptonized [5], but M. ruber strain 21T is positive for catalase and oxidase [10]. The most comprehensive and updated list of physiological properties is probably given by Albuquerque et al [7].

Table 1

Classification and general features of M. ruber 21T according to the MIGS recommendations [17]




     Evidence code

     Current classification

     Domain Bacteria

     TAS [18]

     Phylum Deinococcus -Thermus

     TAS [1,3,19-23]

     Class Deinococci

     TAS [24,25]

     Order Thermales

     TAS [25,26]

     Family Thermaceae

     TAS [25,27]

     Genus Meiothermus

     TAS [1,7]

     Species Meiothermus ruber

     TAS [5]

     Type strain 21

     TAS [5]

     Gram stain


     TAS [5]

     Cell shape


     TAS [5]


     non motile

     TAS [5]


     not reported

     TAS [5]

     Temperature range


     TAS [5]

     Optimum temperature


     TAS [5]


     growth with 1% NaCl

     TAS [7]


     Oxygen requirement

     obligately aerobic

     TAS [5]

     Carbon source

     a diverse set of sugars

     TAS [5]

     Energy source


     TAS [5]



     hot springs

     TAS [5]


     Biotic relationship


     TAS [5]



     not reported

     Biosafety level


     TAS [28]


     hot spring

     TAS [5]


     Geographic location

     Kamchatka Peninsula, Russia

     TAS [5]


     Sample collection time

     1973 or before

     TAS [2]


     Latitude      Longitude

     unknown     unknown







Evidence codes - IDA: Inferred from Direct Assay (first time in publication); TAS: Traceable Author Statement (i.e., a direct report exists in the literature); NAS: Non-traceable Author Statement (i.e., not directly observed for the living, isolated sample, but based on a generally accepted property for the species, or anecdotal evidence). These evidence codes are from of the Gene Ontology project [29]. If the evidence code is IDA, then the property was directly observed by one of the authors or an expert mentioned in the acknowledgements

Figure 1

Scanning electron micrograph of M. ruber 21T

Figure 2 shows the phylogenetic neighborhood of M. ruber 21T in a 16S rRNA based tree. The sequences of the two 16S rRNA gene copies in the genome are identical and differ by only one nucleotide from the previously published sequence generated from ATCC 35948 (Z15059).

Figure 2

Phylogenetic tree highlighting the position of M. ruber 21T relative to the type strains of the other species within the genus and to the type strains of the other species within the family Thermaceae. The trees were inferred from 1,403 aligned characters [31,32] of the 16S rRNA gene sequence under the maximum likelihood criterion [33] and rooted in accordance with the current taxonomy [34]. The branches are scaled in terms of the expected number of substitutions per site. Numbers above branches are support values from 1,000 bootstrap replicates [35] if larger than 60%. Lineages with type strain genome sequencing projects registered in GOLD [36] are shown in blue, published genomes in bold (Thermus thermophilus; AP008226).


Initial reports on the polar lipids of M. ruber indicated that they consist of two major glycolipids GL1a (~ 42%) and GL1b (~ 57%) and one major phospholipid PL2 (~ 93%), with small amounts of two other phospholipids PL1 and PL3 [37]. Detailed work indicates that in strains of Thermus oshimai, T. thermophilus, M. ruber, and M. taiwanensis the major phospholipid is a 2’-O-(1, 2-diacyl-sn-glycero-3-phospho) –3’-O-(α-N-acetyl-glucosaminyl)-N-glyceroyl alkylamine [38]. This compound is related to the major phosphoglycolipid reported from Deinococcus radiodurans [39] and can be considered to be unambiguous chemical markers for this major evolutionary lineage. The glycolipids are derivatives of a Glcp -> Glcp-> GalNAcyl -> Glcp -> diacyl glycerol [40]. Based on mass spectral data it appears that there may be three distinct derivatives, differing in the fatty acid amide linked to the gatactosamine [40]. These may be divided into one compound containing exclusively 2-hydroxylated fatty acids (mainly 2-OH iso-17:0) and a mixture of two compounds that cannot be fully resolved by thin layer chromatography carrying either 3-hydroxylated fatty acids or unsubstituted fatty acids. The basic glycolipid structure dihexosyl – N-acyl-hexosaminyl – hexosyl – diacylglycerol is a feature common to all members of the genera Thermus and Meiothermus examined to date. There is currently no evidence that members of the family Thermaceae (as currently defined) produce significant amounts of polar lipids containing only two aliphatic side chains. The consequences of having polar lipids containing three aliphatic side chains on membrane structure has yet to be examined. Such peculiarities also indicate the value of membrane composition in helping to unravel evolution at a cellular level. The major fatty acids of the polar lipids are iso-C15:0 (30-40%) and iso-C17:0 (13-17%), followed by anteiso-C15:0, C16:0, iso-C16:0, anteiso-C17:0, iso-C17:0-2OH, and, at least in some studies, iso-C17:1 ω9c (the values range from 3-10%). Other fatty acid values are below 2%, including 3-OH branched chain fatty acids. The values vary slightly between the different studies [7,9,11,12,37]. Detailed structural studies suggest that long chain diols may be present in small amounts, substituting for the 1-acyl-sn-glycerol [38]. Although not routinely reported the presence of alkylamines (amide linked to the glyceric acid of the major phospholipid) can be deduced from detailed structural studies of the major phospholipid [38]. Menaquinone 8 is the major respiratory quinone, although it is not clear which pathway is used for the synthesis of the naphthoquinone ring nucleus [41]. Ornithine is the major diamino acid of the peptidoglycan in the genus Meiothermus [1].

Genome sequencing and annotation

Genome project history

This organism was selected for sequencing on the basis of its phylogenetic position [42], and is part of the Genomic Encyclopedia of Bacteria and Archaea project [43]. The genome project is deposited in the Genome OnLine Database [36] and the complete genome sequence is deposited in GenBank. Sequencing, finishing and annotation were performed by the DOE Joint Genome Institute (JGI). A summary of the project information is shown in Table 2.

Table 2

Genome sequencing project information





     Finishing quality



     Libraries used

     Three genomic libraries:     one Sanger 8 kb pMCL200 library, one fosmide library     and one 454 pyrosequence standard library


     Sequencing platforms

     ABI3730, 454 Titanium


     Sequencing coverage

     9.84× Sanger; 27.4× pyrosequence



     Newbler version, PGA


     Gene calling method

     Prodigal 1.4, GenePRIMP



     Genbank Date of Release

     March 3, 2010

     GOLD ID


     NCBI project ID


     Database: IMG-GEBA



     Source material identifier

     DSM 1279

     Project relevance

     Tree of Life, GEBA

Growth conditions and DNA isolation

M. ruber 21T, DSM 1279, was grown in DSMZ medium 256 (Nutrient Agar) [44] at 50°C. DNA was isolated from 0.5-1 g of cell paste using Qiagen Genomic 500 DNA Kit (Qiagen, Hilden, Germany) following the standard protocol as recommended by the manufacturer, with modification L for cell lysis as described in Wu et al. [43].

Genome sequencing and assembly

The genome was sequenced using a combination of Sanger and 454 sequencing platforms. All general aspects of library construction and sequencing can be found at the JGI website (Web Site). Pyrosequencing reads were assembled using the Newbler assembler version (Roche). Large Newbler contigs were broken into 3,428 overlap ping fragments of 1,000 bp and entered into assembly as pseudo-reads. The sequences were assigned quality scores based on Newbler consensus q-scores with modifications to account for overlap redundancy and adjust inflated q-scores. A hybrid 454/Sanger assembly was made using PGA assembler. Possible misassemblies were corrected and gaps between contgis were closed by primer walks off Sanger clones and bridging PCR fragments and by editing in Consed. A total of 431 Sanger finishing reads were produced to close gaps, to resolve repetitive regions, and to raise the quality of the finished sequence. Illumina reads were used to improve the final consensus quality using an in-house developed tool (the Polisher [45]). The error rate of the completed genome sequence is less than 1 in 100,000. Together, the combination of the Sanger and 454 sequencing platforms provided 37.24× coverage of the genome. The final assembly contains 30,479 Sanger reads and 371,362 pyrosequencing reads.

Genome annotation

Genes were identified using Prodigal [46] as part of the Oak Ridge National Laboratory genome annotation pipeline, followed by a round of manual curation using the JGI GenePRIMP pipeline [47]. The predicted CDSs were translated and used to search the National Center for Biotechnology Information (NCBI) nonredundant database, UniProt, TIGRFam, Pfam, PRIAM, KEGG, COG, and InterPro databases. Additional gene prediction analysis and functional annotation was performed within the Integrated Microbial Genomes - Expert Review (IMG-ER) platform [48].

Genome properties

The genome consists of a 3,097,457 bp long chromosome with a 63.4% GC content (Table 3 and Figure 3). Of the 3,105 genes predicted, 3,052 were protein-coding genes, and 53 RNAs; thirty eight pseudogenes were also identified. The majority of the protein-coding genes (71.8%) were assigned with a putative function while the remaining ones were annotated as hypothetical proteins. The distribution of genes into COGs functional categories is presented in Table 4.

Table 3

Genome Statistics



     % of Total

Genome size (bp)



DNA Coding region (bp)



DNA G+C content (bp)



Number of replicons


Extrachromosomal elements


Total genes



RNA genes



rRNA operons


Protein-coding genes



Pseudo genes



Genes with function prediction



Genes in paralog clusters



Genes assigned to COGs



Genes assigned Pfam domains



Genes with signal peptides



Genes with transmembrane helices



CRISPR repeats


Figure 3

Graphical circular map of the genome. From outside to the center: Genes on forward strand (color by COG categories), Genes on reverse strand (color by COG categories), RNA genes (tRNAs green, rRNAs red, other RNAs black), GC content, GC skew.

Table 4

Number of genes associated with the general COG functional categories








     Translation, ribosomal structure and biogenesis




     RNA processing and modification








     Replication, recombination and repair




     Chromatin structure and dynamics




     Cell cycle control, cell division, chromosome partitioning




     Nuclear structure




     Defense mechanisms




     Signal transduction mechanisms




     Cell wall/membrane/envelope biogenesis




     Cell motility








     Extracellular structures




     Intracellular trafficking and secretion, and vesicular transport




     Posttranslational modification, protein turnover, chaperones




     Energy production and conversion




     Carbohydrate transport and metabolism




     Amino acid transport and metabolism




     Nucleotide transport and metabolism




     Coenzyme transport and metabolism




     Lipid transport and metabolism




     Inorganic ion transport and metabolism




     Secondary metabolites biosynthesis, transport and catabolism




     General function prediction only




     Function unknown




     Not in COGs



We would like to gratefully acknowledge the help of Susanne Schneider (DSMZ) for DNA extraction and quality analysis. This work was performed under the auspices of the US Department of Energy Office of Science, Biological and Environmental Research Program, and by the University of California, Lawrence Berkeley National Laboratory under contract No. DE-AC02-05CH11231, Lawrence Livermore National Laboratory under Contract No. DE-AC52-07NA27344, and Los Alamos National Laboratory under contract No. DE-AC02-06NA25396, UT-Battelle, and Oak Ridge National Laboratory under contract DE-AC05-00OR22725, as well as German Research Foundation (DFG) INST 599/1-2 and SI 1352/1-2.

This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.


  1. Nobre MF, Trüper HG and Da Costa MS. Transfer of Thermus ruber (Loginova et al. 1984), Thermus silvanus (Tenreiro et al. 1995), and Thermus chliarophilus (Tenreiro et al. 1995) to Meiothermus gen. nov. as Meiothermus ruber comb. nov., Meiothermus silvanus comb. nov., and Meiothermus chliarophilus comb. nov., respectively, and emendation of the genus Thermus. Int J Syst Bacteriol. 1996; 46:604-606 View Article
  2. Loginova LG and Egorova LA. Obligate thermophilic-bacterium Thermus ruber in hot springs of Kamchatka. Mikrobiologiya. 1975; 44:661-665PubMed
  3. Skerman VBD, McGowan V and Sneath PHA. Approved Lists of Bacterial Names. Int J Syst Bacteriol. 1980; 30:225-420 View Article
  4. Lapage SP, Sneath PHA, Lessel EF, Skerman VBD, Seeliger HPR, Clark WA. 1992. International Code of Nomenclature of Bacteria (1990 Revision). Bacteriological Code. American Society for Microbiology, Washington, DC.
  5. Loginova LG, Egorova LA, Golovacheva RS and Seregina LM. Thermus ruber sp. nov., nom. rev. Int J Syst Bacteriol. 1984; 34:498-499 View Article
  6. Euzéby JP. List of bacterial names with standing in nomenclature: A folder available on the Internet. Int J Syst Bacteriol. 1997; 47:590-592 View ArticlePubMed
  7. Albuquerque L, Ferreira C, Tomaz D, Tiago I, Veríssimo A, da Costa MS and Nobre MF. Meiothermus rufus sp. nov., a new slightly thermophilic red-pigmented species and emended description of the genus Meiothermus. Syst Appl Microbiol. 2009; 32:306-313 View ArticlePubMed
  8. Tenreiro S, Nobre MF and da Costa MS. Thermus silvanus sp. nov. and Thermus chliarophilus sp. nov., two new species related to Thermus ruber but with lower growth temperatures. Int J Syst Bacteriol. 1995; 45:633-639 View ArticlePubMed
  9. Pires AL, Albuquerque L, Tiago I, Nobre MF, Empadinhas N, Veríssimo A and da Costa MS. Meiothermus timidus sp. nov., a new slightly thermophilic yellow-pigmented species. FEMS Microbiol Lett. 2005; 245:39-45 View ArticlePubMed
  10. Zhang XQ, Zhang WJ, Wei BP, Xu XW, Zhu XF and Wu M. Meiothermus cateniformans sp. nov., a slightly thermophilic species from north-eastern China. Int J Syst Evol Microbiol. 2010; 60:840-844 View ArticlePubMed
  11. Chen MY, Lin GH, Lin YT and Tsay SS. Meiothermus taiwanensis sp. nov., a novel filamentous, thermophilic species isolated in Taiwan. Int J Syst Evol Microbiol. 2002; 52:1647-1654 View ArticlePubMed
  12. Chung AP, Rainey F, Nobre MF, Burghardt J and Costa MSD. Meiothermus cerbereus sp. nov., a new slightly thermophilic species with high levels of 3-hydroxy fatty acids. Int J Syst Bacteriol. 1997; 47:1225-1230 View ArticlePubMed
  13. Nobre MF and Trüper HG. Da Costa. Transfer of Thermus ruber (Loginova et al. 1984), Thermus silvanus (Tenreiro et al. 1995), and Thermus chliarophilus (Tenreiro et al. 1995) to Meiothermus gen. nov. as Meiothermus ruber comb. nov., Meiothermus silvanus comb. nov., and Meiothermus chliarophilus comb. nov., respectively, and emendation of the genus Thermus. Int J Syst Bacteriol. 1996; 46:604-606 View Article
  14. Chen MY, Lin GH, Lin YT and Tsay SS. Meiothermus taiwanensis sp. nov., a novel filamentous, thermophilic species isolated in Taiwan. Int J Syst Evol Microbiol. 2002; 52:1647-1654 View ArticlePubMed
  15. Chun J, Lee JH, Jung Y, Kim M, Kim S, Kim BK and Lim YW. EzTaxon: a web-based tool for the identification of prokaryotes based on 16S ribosomal RNA gene sequences. Int J Syst Evol Microbiol. 2007; 57:2259-2261 View ArticlePubMed
  16. Chen C, Lin L, Peng Q, Ben K and Zhou Z. Meiothermus rosaceus sp. nov. isolated from Tengchong hot spring in Yunnan, China. FEMS Microbiol Lett. 2002; 216:263-268 View ArticlePubMed
  17. Field D, Garrity G, Gray T, Morrison N, Selengut J, Sterk P, Tatusova T, Thomson N, Allen MJ and Angiuoli SV. The minimum information about a genome sequence (MIGS) specification. Nat Biotechnol. 2008; 26:541-547 View ArticlePubMed
  18. Woese CR, Kandler O and Wheelis ML. Towards a natural system of organisms: proposal for the domains Archaea, Bacteria, and Eucarya. Proc Natl Acad Sci USA. 1990; 87:4576-4579 View ArticlePubMed
  19. Garrity GM, Lilburn TG, Cole JR, Harrison SH, Euzéby J, Tindall BJ. Taxonomic outline of the Bacteria and Archaea, Release 7.7 March 6, 2007. Part 2 - The Bacteria: Phyla "Aquificae", "Thermotogae", "Thermodesulfobacteria", "Deinococcus-Thermus", "Chrysiogenetes", "Chloroflexi", "Thermomicrobia", "Nitrospira", "Deferribacteres", "Cyanobacteria", and "Chlorobi". Web Site
  20. Weisburg WG, Giovannoni SJ and Woese CR. The Deinococcus-Thermus phylum and the effect of rRNA composition on phylogenetic tree construction. Syst Appl Microbiol. 1989; 11:128-134PubMed
  21. Brooks BW and Murray RGE. Nomenclature for Micrococcus radiodurans and other radiation resistant cocci: Deinococcaceae fam. nov. and Deinococcus gen. nov., including five species. Int J Syst Bacteriol. 1981; 31:353-360 View Article
  22. Rainey FA, Nobre MF, Schumman P, Stackebrandt E and da Costa MS. Phylogenetic diversity of the deinococci as determined by 16S ribosomal DNA sequence comparison. Int J Syst Bacteriol. 1997; 47:510-514 View ArticlePubMed
  23. Brock TD and Freeze H. Thermus aquaticus gen. n. and sp. n., a nonsporulating extreme thermophile. J Bacteriol. 1969; 98:289-297PubMed
  24. Garrity GM, Holt JG. Class I. Deinococci class. nov. In: Garrity GM, Boone DR, Castenholz RW (eds), Bergey's Manual of Systematic Bacteriology, Second Edition, Volume 1, Springer, New York, 2001, p. 395.
  25. . Validation List no. 85. Validation of publication of new names and new combinations previously effectively published outside the IJSEM. Int J Syst Evol Microbiol. 2002; 52:685-690 View ArticlePubMed
  26. Rainey FA, da Costa MS. Order II. Thermales ord. nov. In: Garrity GM, Boone DR, Castenholz RW (eds), Bergey's Manual of Systematic Bacteriology, Second Edition, Volume 1, Springer, New York, 2001, p. 403.
  27. da Costa MS, Rainey FA. Family I. Thermaceae fam. nov. In: Garrity GM, Boone DR, Castenholz RW (eds), Bergey's Manual of Systematic Bacteriology, Second Edition, Volume 1, Springer, New York, 2001, p. 403-404.
  28. Classification of bacteria and archaea in risk groups. TRBA 466.Web Site
  29. Ashburner M, Ball CA, Blake JA, Botstein D, Butler H, Cherry JM, Davis AP, Dolinski K, Dwight SS and Eppig JT. Gene Ontology: tool for the unification of biology. Nat Genet. 2000; 25:25-29 View ArticlePubMed
  30. Burgess ML, Barrow KD, Gao C, Heard GM and Glenn D. Carotenoid glycoside esters from the thermophilic bacterium Meiothermus ruber. J Nat Prod. 1999; 62:859-863 View ArticlePubMed
  31. Castresana J. Selection of conserved blocks from multiple alignments for their use in phylogenetic analysis. Mol Biol Evol. 2000; 17:540-552PubMed
  32. Lee C, Grasso C and Sharlow MF. Multiple sequence alignment using partial order graphs. Bioinformatics. 2002; 18:452-464 View ArticlePubMed
  33. Stamatakis A, Hoover P and Rougemont J. A Rapid Bootstrap Algorithm for the RAxML Web Servers. Syst Biol. 2008; 57:758-771 View ArticlePubMed
  34. Yarza P, Richter M, Peplies J, Euzeby JP, Amann R, Schleifer KH, Ludwig W, Glöckner FO and Rossello-Mora R. The All-Species Living Tree project: A 16S rRNA-based phylogenetic tree of all sequenced type strains. Syst Appl Microbiol. 2008; 31:241-250 View ArticlePubMed
  35. Pattengale ND, Alipour M, Bininda-Emonds ORP, Moret BME and Stamatakis A. How many bootstrap replicates are necessary? Lect Notes Comput Sci. 2009; 5541:184-200 View Article
  36. Liolios K, Chen IM, Mavromatis K, Tavernarakis N, Hugenholtz P, Markowitz VM and Kyrpides NC. The Genomes On Line Database (GOLD) in 2009: status of genomic and metagenomic projects and their associated metadata. Nucleic Acids Res. 2010; 38:D346-D354 View ArticlePubMed
  37. Donato ME, Seleiro EA and da Costa MS. Polar lipid and fatty acid composition of strains of Thermus ruber. Syst Appl Microbiol. 1991; 14:234-239
  38. Yang YL, Yang FL, Jao SC, Chen MY, Tsay SS, Zou W and Wu SH. Structural elucidation of phosphoglycolipids from strains of the bacterial thermophiles Thermus and Meiothermus. J Lipid Res. 2006; 47:1823-1832 View ArticlePubMed
  39. Anderson R and Hansen K. Structure of a novel phosphoglycolipid from Deinococcus radiodurans. J Biol Chem. 1985; 260:12219-12223PubMed
  40. Ferreira AM, Wait R, Nobre MF and da Costa MS. Characterization of glycolipids from Meiothermus spp. Microbiology. 1999; 145:1191-1199 View ArticlePubMed
  41. Hiratsuka T, Furihata K, Ishikawa J, Yamashita H, Itoh N, Seto H and Dairi T. An alternative menaquinone biosynthetic pathway operating in microorganisms. Science. 2008; 321:1670-1673 View ArticlePubMed
  42. Klenk HP and Göker M. En route to a genome-based classification of Archaea and Bacteria? Syst Appl Microbiol. 2010; 33:175-182 View ArticlePubMed
  43. Wu D, Hugenholtz P, Mavromatis K, Pukall R, Dalin E, Ivanova NN, Kunin V, Goodwin L, Wu M and Tindall BJ. A phylogeny-driven genomic encyclopaedia of Bacteria and Archaea. Nature. 2009; 462:1056-1060 View ArticlePubMed
  44. List of growth media used at DSMZ: Web Site
  45. Lapidus A, LaButti K, Foster B, Lowry S, Trong S, Goltsman E. POLISHER: An effective tool for using ultra short reads in microbial genome assembly and finishing. AGBT, Marco Island, FL, 2008.
  46. Hyatt D, Chen GL, Locascio PF, Land ML, Larimer FW and Hauser LJ. Prodigal Prokaryotic Dynamic Programming Genefinding Algorithm. BMC Bioinformatics. 2010; 11:119 View ArticlePubMed
  47. Pati A, Ivanova N, Mikhailova N, Ovchinikova G, Hooper SD, Lykidis A and Kyrpides NC. GenePRIMP: A gene prediction improvement ipeline for microbial genomes. Nat Methods. 2010; 7:455-457 View ArticlePubMed
  48. Markowitz VM, Ivanova NN, Chen IMA, Chu K and Kyrpides NC. IMG ER: a system for microbial genome annotation expert review and curation. Bioinformatics. 2009; 25:2271-2278 View ArticlePubMed