Complete genome sequence of the genetically tractable hydrogenotrophic methanogen Methanococcus maripaludis

被引:164
作者
Hendrickson, EL
Kaul, R
Zhou, Y
Bovee, D
Chapman, P
Chung, J
de Macario, EC
Dodsworth, JA
Gillett, W
Graham, DE
Hackett, M
Haydock, AK
Kang, A
Land, ML
Levy, R
Lie, TJ
Major, TA
Moore, BC
Porat, I
Palmeiri, A
Rouse, G
Saenphimmachak, C
Söll, D
Van Dien, S
Wang, T
Whitman, WB
Xia, Q
Zhang, Y
Larimer, FW
Olson, MV
Leigh, JA [1 ]
机构
[1] Univ Washington, Dept Med, Div Med Genet, Genome Ctr, Seattle, WA 98195 USA
[2] Univ Washington, Dept Microbiol, Genome Ctr, Seattle, WA 98195 USA
[3] Univ Washington, Dept Chem Engn, Genome Ctr, Seattle, WA 98195 USA
[4] Univ Washington, Dept Genome Sci, Genome Ctr, Seattle, WA 98195 USA
[5] United Metab, Seattle, WA USA
[6] SUNY Albany, Wadsworth Ctr, New York State Dept Hlth, Div Mol Med, Albany, NY 12222 USA
[7] Univ Texas, Dept Chem & Biochem, Austin, TX 78712 USA
[8] Oak Ridge Natl Lab, Oak Ridge, TN USA
[9] Univ Georgia, Dept Microbiol, Athens, GA 30602 USA
[10] Yale Univ, Dept Mol Biophys & Biochem, New Haven, CT USA
关键词
D O I
10.1128/JB.186.20.6956-6969.2004
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The genome sequence of the genetically tractable, mesophilic, hydrogenotrophic methanogen Methanococcus maripaludis contains 1,722 protein-coding genes in a single circular chromosome of 1,661,137 bp. Of the protein-coding genes (open reading frames [ORFs]), 44% were assigned a function, 48% were conserved but had unknown or uncertain functions, and 7.5% (129 ORFs) were unique to M. maripaludis. Of the unique ORFs, 27 were confirmed to encode proteins by the mass spectrometric identification of unique peptides. Genes for most known functions and pathways were identified. For example, a full complement of hydrogenases and methanogenesis enzymes was identified, including eight selenocysteine-containing proteins, with each being paralogous to a cysteine-containing counterpart. At least 59 proteins were predicted to contain iron-sulfur centers, including ferredoxins, polyferredoxins, and subunits of enzymes with various redox functions. Unusual features included the absence of a Cdc6 homolog, implying a variation in replication initiation, and the presence of a bacterial-like RNase HI as well as an RNase HII typical of the Archaea. The presence of alanine dehydrogenase and alanine racemase, which are uniquely present among the Archaea, explained the ability of the organism to use L- and D-alanine as nitrogen sources. Features that contrasted with the related organism Methanocaldococcus jannaschii included the absence of inteins, even though close homologs of most intein-containing proteins were encoded. Although two-thirds of the ORFs had their highest Blastp hits in Methanocaldococcus jannaschii, lateral gene transfer or gene loss has apparently resulted in genes, which are often clustered, with top Blastp hits in more distantly related groups.
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页码:6956 / 6969
页数:14
相关论文
共 128 条
[1]   Regulation of the synthesis of H2-forming methylenetetrahydromethanopterin dehydrogenase (Hmd) and of HmdII and HmdIII in Methanothermobacter marburgensis [J].
Afting, C ;
Kremmer, E ;
Brucker, C ;
Hochheimer, A ;
Thauer, RK .
ARCHIVES OF MICROBIOLOGY, 2000, 174 (04) :225-232
[2]   Bacterial chemotaxis:: Rhodobacter sphaeroides and Sinorhizobium meliloti -: variations on a theme? [J].
Armitage, JP ;
Schmitt, R .
MICROBIOLOGY-UK, 1997, 143 :3671-3682
[3]   Molecular biology of S-layers [J].
Bahl, H ;
Scholz, H ;
Bayan, N ;
Chami, M ;
Leblon, G ;
GulikKrzywicki, T ;
Shechter, E ;
Fouet, A ;
Mesnage, S ;
TosiCouture, E ;
Gounon, P ;
Mock, M ;
deMacario, EC ;
Macario, AJL ;
FernandezHerrero, LA ;
Olabarria, G ;
Berenguer, J ;
Blaser, MJ ;
Kuen, B ;
Lubitz, W ;
Sara, M ;
Pouwels, PH ;
Kolen, CPAM ;
Boot, HJ ;
Palva, A ;
Truppe, M ;
Howorka, S ;
Schroll, G ;
Lechleitner, S ;
Resch, S .
FEMS MICROBIOLOGY REVIEWS, 1997, 20 (1-2) :47-98
[4]   LYSINE BIOSYNTHESIS IN METHANOBACTERIUM-THERMOAUTOTROPHICUM IS BY THE DIAMINOPIMELIC ACID PATHWAY [J].
BAKHIET, N ;
FORNEY, FW ;
STAHLY, DP ;
DANIELS, L .
CURRENT MICROBIOLOGY, 1984, 10 (04) :195-198
[5]   Transcription and translation in Archaea: A mosaic of eukaryal and bacterial features [J].
Bell, SD ;
Jackson, SP .
TRENDS IN MICROBIOLOGY, 1998, 6 (06) :222-228
[6]  
BERGHOFER Y, 1994, MOL GEN GENET, V242, P369
[7]   Chromosome replication, nucleoid segregation and cell division in Archaea [J].
Bernander, R .
TRENDS IN MICROBIOLOGY, 2000, 8 (06) :278-283
[8]   The archaeal cell cycle: current issues [J].
Bernander, R .
MOLECULAR MICROBIOLOGY, 2003, 48 (03) :599-604
[9]   Archaea and the cell cycle [J].
Bernander, R .
MOLECULAR MICROBIOLOGY, 1998, 29 (04) :955-961
[10]   Development of a gene knockout system for the halophilic archaeon Haloferax volcanii by use of the pyrE gene [J].
Bitan-Banin, G ;
Ortenberg, R ;
Mevarech, M .
JOURNAL OF BACTERIOLOGY, 2003, 185 (03) :772-778