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Genomics and Proteomics

Complete Genome Sequence of the Genetically Tractable Hydrogenotrophic Methanogen Methanococcus maripaludis

E. L. Hendrickson, R. Kaul, Y. Zhou, D. Bovee, P. Chapman, J. Chung, E. Conway de Macario, J. A. Dodsworth, W. Gillett, D. E. Graham, M. Hackett, A. K. Haydock, A. Kang, M. L. Land, R. Levy, T. J. Lie, T. A. Major, B. C. Moore, I. Porat, A. Palmeiri, G. Rouse, C. Saenphimmachak, D. Söll, S. Van Dien, T. Wang, W. B. Whitman, Q. Xia, Y. Zhang, F. W. Larimer, M. V. Olson, J. A. Leigh
E. L. Hendrickson
1Departments of Microbiology
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R. Kaul
2Department of Medicine, Division of Medical Genetics
3University of Washington Genome Center
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Y. Zhou
3University of Washington Genome Center
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D. Bovee
3University of Washington Genome Center
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P. Chapman
3University of Washington Genome Center
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J. Chung
3University of Washington Genome Center
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E. Conway de Macario
4Wadsworth Center, New York State Department of Health, Division of Molecular Medicine, The University at Albany (SUNY), Albany, New York
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J. A. Dodsworth
1Departments of Microbiology
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W. Gillett
3University of Washington Genome Center
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D. E. Graham
5Department of Chemistry and Biochemistry, The University of Texas at Austin, Austin, Texas
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M. Hackett
6Chemical Engineering
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A. K. Haydock
1Departments of Microbiology
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A. Kang
3University of Washington Genome Center
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M. L. Land
7Genome Analysis and Systems Modeling, Oak Ridge National Laboratory, Oak Ridge, Tennessee
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R. Levy
3University of Washington Genome Center
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T. J. Lie
1Departments of Microbiology
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T. A. Major
8Department of Microbiology, University of Georgia, Athens, Georgia
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B. C. Moore
1Departments of Microbiology
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I. Porat
8Department of Microbiology, University of Georgia, Athens, Georgia
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A. Palmeiri
3University of Washington Genome Center
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G. Rouse
3University of Washington Genome Center
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C. Saenphimmachak
3University of Washington Genome Center
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D. Söll
9Department of Molecular Biophysics and Biochemistry, Yale University, New Haven, Connecticut
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S. Van Dien
10United Metabolics, Seattle, Washington
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T. Wang
1Departments of Microbiology
6Chemical Engineering
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W. B. Whitman
8Department of Microbiology, University of Georgia, Athens, Georgia
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Q. Xia
1Departments of Microbiology
6Chemical Engineering
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Y. Zhang
1Departments of Microbiology
6Chemical Engineering
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F. W. Larimer
7Genome Analysis and Systems Modeling, Oak Ridge National Laboratory, Oak Ridge, Tennessee
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M. V. Olson
2Department of Medicine, Division of Medical Genetics
3University of Washington Genome Center
11Genome Sciences, University of Washington
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J. A. Leigh
1Departments of Microbiology
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  • For correspondence: leighj@u.washington.edu
DOI: 10.1128/JB.186.20.6956-6969.2004
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  • FIG. 1.
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    FIG. 1.

    Circular map of M. maripaludis genome. First (outer) double ring, top Blastp hits; second double ring, ORFs unique to M. maripaludis; third double ring, functional categories; black single ring, deviation from average mol% G+C; inner ring, GC skew. Top Blast hits are coded as follows: blue, Methanocaldococcus jannaschii; magenta, other methanogens; green, other Archaea; brown, Bacteria and Eukarya. Sectors containing top Blast hits predominately to groups other than Methanocaldococcus jannaschii are shown, with ORF number intervals. Functional categories are coded as follows: red, replication and repair; green, energy metabolism; blue, carbohydrate metabolism; cyan, lipid metabolism; magenta, transcription; yellow, translation; sky blue, cellular processes; orange, amino acid metabolism; pink, metabolism of cofactors; light red, nucleotide metabolism; gray, conserved hypothetical proteins; white, hypothetical proteins; brown, unassigned proteins; black, other; pale green, RNAs.

  • FIG. 2.
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    FIG. 2.

    Map of major metabolic pathways in M. maripaludis. Shown are energy and redox-related pathways (shaded areas), CO2 fixation, the reductive branch of the TCA cycle, nitrogen assimilation, glycolysis and gluconeogenesis, the nonoxidative pentose phosphate pathway, and amino acid biosynthesis. Some reactions and minor substrates and products were omitted. Abbreviations: ASA, aspartate semialdehyde; CHR, chorismate; (CO), enzyme-bound carbon monoxide; CoA, coenzyme A; CoB, coenzyme B; CoM, coenzyme M; E4P, erythrose-4-phosphate; F6P, fructose-6-phosphate; FBP, fructose-bis-phosphate; Fdx, ferredoxin; FUM, fumarate; F420, coenzyme F420; GA3P, glyceraldehyde-3-phosphate; G1P, glucose-1-phosphate; G6P, glucose-6-phosphate; (2H), low-potential hydride on unknown carrier; H+ (ext), proton-motive force; H4MPT, tetrahydromethanopterin; HSE, homoserine; IND, indole-3-glycerol-phosphate; KIV, 2-ketoisovalerate; MAL, malate; mDAP, meso-diaminopimelate; MFR, methanofuran; OAA, oxaloacetate; 2OG, 2-oxoglutarate; PEP, phosphoenolpyruvate; 3PG, 3-phosphoglycerate; PP, pyrophosphate; PPA, prephenate; PRPP, phosphoribosylpyrophosphate; PYR, pyruvate; R5P, ribose-5-phosphate; SDAP, succinyldiaminopimelate; SKA, shikimate; SUCC, succinate; S7P, sedoheptulose-7-phosphate; THDP, tetrahydrodipicolinate; X5P, xylulose-5-phosphate; ?, incomplete knowledge of pathway.

Tables

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  • TABLE 1.

    General features of the M. maripaludis genome

    ParameterValue
    Total no. of bases1,661,137
    No. of protein-coding genes1,722
    No. of predicted transmembrane proteins350
    Gene density (genes/kb)1.036
    Average gene length (bp)857
    Protein-coding percentage88.9
    No. of tRNAs38
    No. of rRNA operons3
    %GC33.1
  • TABLE 2.

    Functional categories of proteins encoded by M. maripaludis genome

    FunctionaNo. of ORFs% of ORFs
    Amino acid biosynthesis824.8
    Biosynthesis of cofactors, prosthetic groups, and carriers683.9
    Cell envelope80.56
    Cellular processes (cell division, chemotaxis, and motility)301.7
    Central intermediary metabolism1126.5
    DNA metabolism402.3
    Energy metabolism (methanogenesis, hydrogen metabolism, and ATPase)814.7
    Fatty acid and phospholipid metabolism60.35
    Hypothetical proteins1025.9
    Unique proteins of unknown function271.6
    Conserved hypothetical proteins65638
    Protein fate221.3
    Protein synthesis1196.9
    Purines, pyrimidines, nucleosides, and nucleotides442.6
    Regulatory functions382.2
    Transcription221.3
    Transport and binding proteins865.0
    Unclassified and unknown function17910.4
    Total1,722100
    • ↵ a Adapted from The Institute for Genome Research's functional categories.

  • TABLE 3.

    Phylogenetic distributions and functions of clustered non-Methanocaldococcus jannaschii top Blastp hit categories

    ORF intervala (Mmp no.)Predominant group(s)bRepresented functions
    0345-0371Other ArchaeaConserved hypothetical proteins, carbohydrate metabolism
    0483-0536Other methanogens and BacteriaConserved hypothetical proteins, Fmd, Mo transport, molybdopterin biosynthesis, metal chelatase, probable cation transport
    0709-0734 Bacteria and other methanogensDivalent cation transport, UvrABC
    0753-0762 Bacteria Conserved hypothetical proteins
    0772-0862Other methanogens and BacteriaConserved hypothetical proteins, Vhc
    0973-0988Other methanogensCdh
    • ↵ a Intervals containing 70% or more top Blastp hits for other methanogens, other Archaea, and Bacteria combined.

    • ↵ b Groups containing the top Blastp hits for at least 20% of the ORFs in the interval.

Additional Files

  • Figures
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  • Supplemental material

    Files in this Data Supplement:

    • Lists S1 - Supplementary lists of unique proteins, transcriptional regulators, and transporters.
      Excel document, 23K
    • Lists S2 - Top Blast hits.
      Excel document, 958K
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Complete Genome Sequence of the Genetically Tractable Hydrogenotrophic Methanogen Methanococcus maripaludis
E. L. Hendrickson, R. Kaul, Y. Zhou, D. Bovee, P. Chapman, J. Chung, E. Conway de Macario, J. A. Dodsworth, W. Gillett, D. E. Graham, M. Hackett, A. K. Haydock, A. Kang, M. L. Land, R. Levy, T. J. Lie, T. A. Major, B. C. Moore, I. Porat, A. Palmeiri, G. Rouse, C. Saenphimmachak, D. Söll, S. Van Dien, T. Wang, W. B. Whitman, Q. Xia, Y. Zhang, F. W. Larimer, M. V. Olson, J. A. Leigh
Journal of Bacteriology Oct 2004, 186 (20) 6956-6969; DOI: 10.1128/JB.186.20.6956-6969.2004

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Complete Genome Sequence of the Genetically Tractable Hydrogenotrophic Methanogen Methanococcus maripaludis
E. L. Hendrickson, R. Kaul, Y. Zhou, D. Bovee, P. Chapman, J. Chung, E. Conway de Macario, J. A. Dodsworth, W. Gillett, D. E. Graham, M. Hackett, A. K. Haydock, A. Kang, M. L. Land, R. Levy, T. J. Lie, T. A. Major, B. C. Moore, I. Porat, A. Palmeiri, G. Rouse, C. Saenphimmachak, D. Söll, S. Van Dien, T. Wang, W. B. Whitman, Q. Xia, Y. Zhang, F. W. Larimer, M. V. Olson, J. A. Leigh
Journal of Bacteriology Oct 2004, 186 (20) 6956-6969; DOI: 10.1128/JB.186.20.6956-6969.2004
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KEYWORDS

Archaeal Proteins
Genome, Archaeal
hydrogen
methane
Methanococcus
Sequence Analysis, DNA

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