Metabolic strategies of free-living and aggregate-associated bacterial communities inferred from biologic and chemical profiles in the Black Sea suboxic zone
Corresponding Author
Clara A. Fuchsman
School of Oceanography, University of Washington, Seattle, WA, USA
Correspondence: Clara A. Fuchsman, School of Oceanography, University of Washington, Box 355351, Seattle, WA 98195-5351, USA. Tel.: +1 206 543 9669; fax: +1 206 685 3351; e-mail: [email protected]Search for more papers by this authorJohn B. Kirkpatrick
School of Oceanography, University of Washington, Seattle, WA, USA
Search for more papers by this authorWilliam J. Brazelton
School of Oceanography, University of Washington, Seattle, WA, USA
Search for more papers by this authorJames W. Murray
School of Oceanography, University of Washington, Seattle, WA, USA
Search for more papers by this authorJames T. Staley
Department of Microbiology, University of Washington, Seattle, WA, USA
Search for more papers by this authorCorresponding Author
Clara A. Fuchsman
School of Oceanography, University of Washington, Seattle, WA, USA
Correspondence: Clara A. Fuchsman, School of Oceanography, University of Washington, Box 355351, Seattle, WA 98195-5351, USA. Tel.: +1 206 543 9669; fax: +1 206 685 3351; e-mail: [email protected]Search for more papers by this authorJohn B. Kirkpatrick
School of Oceanography, University of Washington, Seattle, WA, USA
Search for more papers by this authorWilliam J. Brazelton
School of Oceanography, University of Washington, Seattle, WA, USA
Search for more papers by this authorJames W. Murray
School of Oceanography, University of Washington, Seattle, WA, USA
Search for more papers by this authorJames T. Staley
Department of Microbiology, University of Washington, Seattle, WA, USA
Search for more papers by this authorAbstract
The Black Sea is a permanently anoxic basin with a well-defined redox gradient. We combine environmental 16S rRNA gene data from clone libraries, terminal restriction fragment length polymorphisms, and V6 hypervariable region pyrosequences to provide the most detailed bacterial survey to date. Furthermore, this data set is informed by comprehensive geochemical data; using this combination of information, we put forward testable hypotheses regarding possible metabolisms of uncultured bacteria from the Black Sea's suboxic zone (microaerophily, nitrate reduction, manganese cycling, and oxidation of methane, ammonium, and sulfide). Dominant bacteria in the upper suboxic zone included members of the SAR11, SAR324, and Microthrix groups and in the deep suboxic zone included members of BS-GSO-2, Marine Group A, and SUP05. A particulate fraction (30 μm filter) was used to distinguish between free-living and aggregate-attached communities in the suboxic zone. The particulate fraction contained greater diversity of V6 tag sequences than the bulk water samples. Lentisphaera, Epsilonproteobacteria, WS3, Planctomycetes, and Deltaproteobacteria were enriched in the particulate fraction, whereas SAR11 relatives dominated the free-living fraction. On the basis of the bacterial assemblages and simple modeling, we find that in suboxic waters, the interior of sinking aggregates potentially support manganese reduction, sulfate reduction, and sulfur oxidation.
Supporting Information
Filename | Description |
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fem1189-sup-0001-FigureS1.docxWord document, 139.7 KB | Fig. S1. Depth profiles, using a density scale, for oxygen (squares), sulfide (triangles), nitrate (circles), nitrite (diamonds), ammonium (x), methane (crosses), and particulate manganese (bold squares) from the Western Central Gyre of the Black Sea in March 2005. |
fem1189-sup-0002-FigureS2.docxWord document, 124 KB | Fig. S2. Cluster of community similarities calculated from TRFLP profiles from depths throughout the oxygenated, suboxic, and sulfidic layers. |
fem1189-sup-0003-FigureS3.docxWord document, 318.4 KB | Fig. S3. TRFLP chromatograms from the suboxic zone, obtained using the enzyme MspI. |
fem1189-sup-0004-FigureS4.docxWord document, 258.7 KB | Fig. S4. TRFLP chromatograms from the deep suboxic and sulfidic zones, obtained using the enzyme MspI. |
fem1189-sup-0005-TableS1.docxWord document, 13.1 KB | Table S1. Cell counts from the suboxic zone. |
fem1189-sup-0006-TableS2.docxWord document, 25.7 KB | Table S2. Depth Profile Metabolic Group I: The number of normalized tags at each depth for each unique OTU in this depth profile as well as their lifestyle and taxonomy. |
fem1189-sup-0007-TableS3.docxWord document, 17 KB | Table S3. Depth Profile Metabolic Group II: The number of normalized tags at each depth for each unique OTU in this depth profile as well as their lifestyle and taxonomy. |
fem1189-sup-0008-TableS4.docxWord document, 18.8 KB | Table S4. Depth Profile Metabolic Group III: The number of normalized tags at each depth for each unique OTU in this depth profile as well as their lifestyle and taxonomy. |
fem1189-sup-0009-TableS5.docxWord document, 17.4 KB | Table S5. Depth Profile Metabolic Group IV: The number of normalized tags at each depth for each unique OTU in this depth profile as well as their lifestyle and taxonomy. |
fem1189-sup-0010-TableS6.docxWord document, 22.1 KB | Table S6. Depth Profile Metabolic Group V: The number of normalized tags at each depth for each unique OTU in this depth profile as well as their lifestyle and taxonomy. |
fem1189-sup-0011-TableS7.docxWord document, 14 KB | Table S7. Unassigned Depth Profile: The number of normalized tags at each depth for each unique OTU in this depth profile as well as their lifestyle and taxonomy. |
fem1189-sup-0012-TableS8.docxWord document, 21.8 KB | Table S8. Aggregate-attached bacteria: The number of normalized tags at each depth for each unique OTU as well as their taxonomy. |
Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.
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