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1.
Appl Environ Microbiol ; 74(14): 4516-29, 2008 Jul.
Article in English | MEDLINE | ID: mdl-18515485

ABSTRACT

Marine sediments of coastal margins are important sites of carbon sequestration and nitrogen cycling. To determine the metabolic potential and structure of marine sediment microbial communities, two cores were collected each from the two stations (GMT at a depth of 200 m and GMS at 800 m) in the Gulf of Mexico, and six subsamples representing different depths were analyzed from each of these two cores using functional gene arrays containing approximately 2,000 probes targeting genes involved in carbon fixation; organic carbon degradation; contaminant degradation; metal resistance; and nitrogen, sulfur, and phosphorous cycling. The geochemistry was highly variable for the sediments based on both site and depth. A total of 930 (47.1%) probes belonging to various functional gene categories showed significant hybridization with at least 1 of the 12 samples. The overall functional gene diversity of the samples from shallow depths was in general lower than those from deep depths at both stations. Also high microbial heterogeneity existed in these marine sediments. In general, the microbial community structure was more similar when the samples were spatially closer. The number of unique genes at GMT increased with depth, from 1.7% at 0.75 cm to 18.9% at 25 cm. The same trend occurred at GMS, from 1.2% at 0.25 cm to 15.2% at 16 cm. In addition, a broad diversity of geochemically important metabolic functional genes related to carbon degradation, nitrification, denitrification, nitrogen fixation, sulfur reduction, phosphorus utilization, contaminant degradation, and metal resistance were observed, implying that marine sediments could play important roles in biogeochemical cycling of carbon, nitrogen, phosphorus, sulfate, and various metals. Finally, the Mantel test revealed significant positive correlations between various specific functional genes and functional processes, and canonical correspondence analysis suggested that sediment depth, PO(4)(3-), NH(4)(+), Mn(II), porosity, and Si(OH)(4) might play major roles in shaping the microbial community structure in the marine sediments.


Subject(s)
Bacteria/metabolism , Genetic Variation , Geologic Sediments/chemistry , Geologic Sediments/microbiology , Oligonucleotide Array Sequence Analysis , Atlantic Ocean , Bacteria/genetics , Bacteria/isolation & purification , Biodiversity , Carbon/metabolism , Cluster Analysis , Genes, Bacterial , Genome, Bacterial , Nitrogen/metabolism , Oligonucleotide Probes , Phosphorus/metabolism , Sulfur/metabolism , Water Microbiology
2.
Appl Environ Microbiol ; 69(10): 6073-81, 2003 Oct.
Article in English | MEDLINE | ID: mdl-14532064

ABSTRACT

This study examined the natural diversity and distributions of sulfate-reducing bacteria along a natural carbon gradient extending down the shelf-slope transition zone of the eastern Pacific continental margin. Dissimilatory (bi)sulfite reductase gene sequences (dsrAB) were PCR amplified and cloned from five different sampling sites, each at a discrete depth, from two different margin systems, one off the Pacific coast of Mexico and another off the coast of Washington State. A total of 1,762 clones were recovered and evaluated by restriction fragment length polymorphism (RFLP) analysis. The majority of the gene sequences recovered showed site and depth restricted distributions; however, a limited number of gene sequences were widely distributed within and between the margin systems. Cluster analysis identified 175 unique RFLP patterns, and nucleotide sequences were determined for corresponding clones. Several different continental margin DsrA sequences clustered with those from formally characterized taxa belonging to the delta subdivision of the class Proteobacteria (Desulfobulbus propionicus, Desulfosarcina variabilis) and the Bacillus-Clostridium (Desulfotomaculum putei) divisions, although the majority of the recovered sequences were phylogenetically divergent relative to all of the other DsrA sequences available for comparison. This study revealed extensive new genetic diversity among sulfate-reducing bacteria in continental margin sedimentary habitats, which appears to be tightly coupled to slope depth, specifically carbon bioavailability.


Subject(s)
Genetic Variation , Sulfur-Reducing Bacteria/classification , Deltaproteobacteria/classification , Deltaproteobacteria/enzymology , Deltaproteobacteria/genetics , Deltaproteobacteria/isolation & purification , Environment , Geologic Sediments/microbiology , Hydrogensulfite Reductase , Mexico , Molecular Sequence Data , Oxidoreductases Acting on Sulfur Group Donors/genetics , Pacific Ocean , Phylogeny , Polymorphism, Restriction Fragment Length , Seawater/microbiology , Sequence Analysis, DNA , Sulfates/metabolism , Sulfur-Reducing Bacteria/enzymology , Sulfur-Reducing Bacteria/genetics , Sulfur-Reducing Bacteria/isolation & purification , Washington
3.
Appl Environ Microbiol ; 69(6): 3549-60, 2003 Jun.
Article in English | MEDLINE | ID: mdl-12788762

ABSTRACT

To understand the composition and structure of denitrifying communities in the oxygen-deficient zone off the Pacific coast of Mexico, the molecular diversity of nir genes from sediments obtained at four stations was examined by using a PCR-based cloning approach. A total of 50 operational taxonomic units (OTUs) for nirK and 82 OTUs for nirS were obtained from all samples. Forty-four of the nirS clones and 31 of the nirK clones were sequenced; the levels of similarity of the nirS clones were 52 to 92%, and the levels of similarity of the nirS clones were 50 to 99%. The percentages of overlapping OTUs between stations were 18 to 30% for nirS and 5 to 8% for nirK. Sequence analysis revealed that 26% of the nirS clones were related to the nirS genes of Alcaligenes faecalis (80 to 94% similar) and Pseudomonas stutzeri (80 to 99%), whereas 3 to 31% of the nirK clones were closely related to the nirK genes of Pseudomonas sp. strain G-179 (98 to 99%), Bradyrhizobium japonicum (91%), Blastobacter denitrificans (83%), and Alcaligenes xylosoxidans (96%). The rest of the clones, however, were less than 80% similar to nirS and nirK sequences available in sequence databases. The results of a principal-component analysis (PCA) based on the percentage of OTUs and biogeochemical data indicated that the nitrate concentration and oxygen have an effect on the denitrifying communities. The communities at the stations in oxygen-deficient zones were more similar than the communities at the stations in the oxygenated zone. The denitrifying communities were more similar at the stations that were closer together and had similar nitrate levels. Also, the results of PCA based on biogeochemical properties suggest that geographic location and biogeochemical conditions, especially the nitrate and oxygen levels, appear to be the key factors that control the structure of denitrifying communities.


Subject(s)
Genetic Variation , Geologic Sediments/microbiology , Nitrite Reductases/genetics , Oxygen/pharmacology , Proteobacteria/enzymology , Seawater/microbiology , Cloning, Molecular , Geologic Sediments/chemistry , Molecular Sequence Data , Nitrates/metabolism , Phylogeny , Polymorphism, Restriction Fragment Length , Proteobacteria/genetics , Proteobacteria/growth & development , Sequence Analysis, DNA
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