Methanogen diversity evidenced by molecular characterization of methyl coenzyme M reductase A (mcrA) genes in hydrothermal sediments of the Guaymas Basin

被引:109
作者
Dhillon, A
Lever, M
Lloyd, KG
Albert, DB
Sogin, ML
Teske, A
机构
[1] Univ N Carolina, Dept Marine Sci, Chapel Hill, NC 27510 USA
[2] Josephine Bay Paul Ctr Comparat Mol Biol & Evolut, Marine Biol Lab, Woods Hole, MA USA
关键词
D O I
10.1128/AEM.71.8.4592-4601.2005
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The methanogenic community in hydrothermally active sediments of Guaymas Basin (Gulf of California, Mexico) was analyzed by PCR amplification, cloning, and sequencing of methyl coenzyme M reductase (mcrA) and 16S rRNA genes. Members of the Methanomicrobiales and Methanosarcinales dominated the mcrA and 16S rRNA clone libraries from the upper 15 cm of the sediments. Within the H-2/CO2- and formate-utilizing family Methanomicrobiales, two mcrA and 16S rRNA lineages were closely affiliated with cultured species of the genera Methanoculleus and Methanocorpusculum. The most frequently recovered mcrA PCR amplicons within the Methanomicrobiales did not branch with any cultured genera. Within the nutritionally versatile family Methanosarcinales, one 16S rRNA amplicon and most of the mcrA PCR amplicons were affiliated with the obligately acetate utilizing species Methanosaeta concilii. The mcrA clone libraries also included phylotypes related to the methyll-disproportionating genus Methanococcoides. However, two mcrA and two 16S rRNA lineages within the Methanosarcinales were unrelated to any cultured genus. Overall, the clone libraries indicate a diversified methanogen community that uses H-2/CO2, formate, acetate, and methylated substrates. Phylogenetic affiliations of mcrA and 16S rRNA clones with thermophilic and nonthermophilic cultured isolates indicate a mixed mesophilic and thermophillic methanogen community in the surficial Guaymas sediments.
引用
收藏
页码:4592 / 4601
页数:10
相关论文
共 59 条
[51]  
TESKE A, 2000, ABSTR ASLO AQ SCI M
[52]   Biochemistry of methanogenesis: a tribute to Marjory Stephenson [J].
Thauer, RK .
MICROBIOLOGY-UK, 1998, 144 :2377-2406
[53]   CLUSTAL-W - IMPROVING THE SENSITIVITY OF PROGRESSIVE MULTIPLE SEQUENCE ALIGNMENT THROUGH SEQUENCE WEIGHTING, POSITION-SPECIFIC GAP PENALTIES AND WEIGHT MATRIX CHOICE [J].
THOMPSON, JD ;
HIGGINS, DG ;
GIBSON, TJ .
NUCLEIC ACIDS RESEARCH, 1994, 22 (22) :4673-4680
[54]   Dimethylsulfoniopropionate in anoxic intertidal sediments: A precursor of methanogenesis via dimethyl sulfide, methanethiol, and methiolpropionate [J].
vanderMaarel, MJEC ;
Hansen, TA .
MARINE GEOLOGY, 1997, 137 (1-2) :5-12
[55]   Bacterial sulfate reduction in hydrothermal sediments of the Guaymas Basin, Gulf of California, Mexico [J].
Weber, A ;
Jorgensen, BB .
DEEP-SEA RESEARCH PART I-OCEANOGRAPHIC RESEARCH PAPERS, 2002, 49 (05) :827-841
[56]  
WELHAN JA, 1987, AAPG BULL, V71, P215
[57]   ORIGINS OF METHANE IN HYDROTHERMAL SYSTEMS [J].
WELHAN, JA .
CHEMICAL GEOLOGY, 1988, 71 (1-3) :183-198
[58]   Deep marine biosphere fuelled by increasing organic matter availability during burial and heating [J].
Wellsbury, P ;
Goodman, K ;
Barth, T ;
Cragg, BA ;
Barnes, SP ;
Parkes, RJ .
NATURE, 1997, 388 (6642) :573-576
[59]   Methane formation from long-chain alkanes by anaerobic microorganisms [J].
Zengler, K ;
Richnow, HH ;
Rosselló-Mora, R ;
Michaelis, W ;
Widdel, F .
NATURE, 1999, 401 (6750) :266-269