13C-isotope analyses reveal that chemolithoautotrophic Gamma- and Epsilonproteobacteria feed a microbial food web in a pelagic redoxcline of the central Baltic Sea
Summary Marine pelagic redoxclines are zones of high dark CO2 fixation rates, which can correspond up to 30% of the surface primary production. However, despite this significant contribution to the pelagic carbon cycle, the identity of most chemolithoautotrophic organisms is still unknown. Therefore...
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creator | Glaubitz, Sabine Lueders, Tillmann Abraham, Wolf-Rainer Jost, Günter Jürgens, Klaus Labrenz, Matthias |
description | Summary
Marine pelagic redoxclines are zones of high dark CO2 fixation rates, which can correspond up to 30% of the surface primary production. However, despite this significant contribution to the pelagic carbon cycle, the identity of most chemolithoautotrophic organisms is still unknown. Therefore, the aim of this study was to directly link the dark CO2 fixation capacity of a pelagic redoxcline in the central Baltic Sea (Landsort Deep) with the identity of the main chemolithoautotrophs involved. Our approach was based on the analysis of natural carbon isotope signatures in fatty acid methyl esters (FAMEs) and on measurements of CO2 incorporation in 13C‐bicarbonate pulse experiments. The incorporation of 13C into chemolithoautotrophic cells was investigated by rRNA‐based stable isotope probing (RNA‐SIP) and FAME analysis after incubation for 24 and 72 h under in situ conditions. Our results demonstrated that fatty acids indicative of Proteobacteria were significantly enriched in 13C slightly below the chemocline. RNA‐SIP analyses revealed that two different Gammaproteobacteria and three closely related Epsilonproteobacteria of the Sulfurimonas cluster were active dark CO2‐fixing microorganisms, with a time‐dependent community shift between these groups. Labelling of Archaea was not detectable, but after 72 h of incubation the 13C‐label had been transferred to a potentially bacterivorous ciliate related to Euplotes sp. Thus, RNA‐SIP provided direct evidence for the contribution of chemolithoautotrophic production to the microbial food web in this marine pelagic redoxcline, emphasizing the importance of dark CO2‐fixing Proteobacteria within this habitat. |
doi_str_mv | 10.1111/j.1462-2920.2008.01770.x |
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Marine pelagic redoxclines are zones of high dark CO2 fixation rates, which can correspond up to 30% of the surface primary production. However, despite this significant contribution to the pelagic carbon cycle, the identity of most chemolithoautotrophic organisms is still unknown. Therefore, the aim of this study was to directly link the dark CO2 fixation capacity of a pelagic redoxcline in the central Baltic Sea (Landsort Deep) with the identity of the main chemolithoautotrophs involved. Our approach was based on the analysis of natural carbon isotope signatures in fatty acid methyl esters (FAMEs) and on measurements of CO2 incorporation in 13C‐bicarbonate pulse experiments. The incorporation of 13C into chemolithoautotrophic cells was investigated by rRNA‐based stable isotope probing (RNA‐SIP) and FAME analysis after incubation for 24 and 72 h under in situ conditions. Our results demonstrated that fatty acids indicative of Proteobacteria were significantly enriched in 13C slightly below the chemocline. RNA‐SIP analyses revealed that two different Gammaproteobacteria and three closely related Epsilonproteobacteria of the Sulfurimonas cluster were active dark CO2‐fixing microorganisms, with a time‐dependent community shift between these groups. Labelling of Archaea was not detectable, but after 72 h of incubation the 13C‐label had been transferred to a potentially bacterivorous ciliate related to Euplotes sp. Thus, RNA‐SIP provided direct evidence for the contribution of chemolithoautotrophic production to the microbial food web in this marine pelagic redoxcline, emphasizing the importance of dark CO2‐fixing Proteobacteria within this habitat.</description><identifier>ISSN: 1462-2912</identifier><identifier>EISSN: 1462-2920</identifier><identifier>DOI: 10.1111/j.1462-2920.2008.01770.x</identifier><identifier>PMID: 18793316</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Animals ; Archaea ; Archaea - classification ; Archaea - genetics ; Archaea - metabolism ; Biodiversity ; Carbon Dioxide - metabolism ; Carbon Isotopes - metabolism ; DNA, Bacterial - chemistry ; DNA, Bacterial - genetics ; DNA, Ribosomal - chemistry ; DNA, Ribosomal - genetics ; Epsilonproteobacteria - classification ; Epsilonproteobacteria - genetics ; Epsilonproteobacteria - metabolism ; Euplotes ; Euplotes - classification ; Euplotes - genetics ; Euplotes - metabolism ; Fatty Acids - chemistry ; Food Chain ; Gammaproteobacteria - classification ; Gammaproteobacteria - genetics ; Gammaproteobacteria - metabolism ; Molecular Sequence Data ; Proteobacteria ; RNA - chemistry ; RNA, Ribosomal, 16S - genetics ; Seawater - microbiology ; Sequence Analysis, DNA ; Staining and Labeling</subject><ispartof>Environmental microbiology, 2009-02, Vol.11 (2), p.326-337</ispartof><rights>2008 The Authors. Journal compilation © 2008 Society for Applied Microbiology and Blackwell Publishing Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1462-2920.2008.01770.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1462-2920.2008.01770.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18793316$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Glaubitz, Sabine</creatorcontrib><creatorcontrib>Lueders, Tillmann</creatorcontrib><creatorcontrib>Abraham, Wolf-Rainer</creatorcontrib><creatorcontrib>Jost, Günter</creatorcontrib><creatorcontrib>Jürgens, Klaus</creatorcontrib><creatorcontrib>Labrenz, Matthias</creatorcontrib><title>13C-isotope analyses reveal that chemolithoautotrophic Gamma- and Epsilonproteobacteria feed a microbial food web in a pelagic redoxcline of the central Baltic Sea</title><title>Environmental microbiology</title><addtitle>Environ Microbiol</addtitle><description>Summary
Marine pelagic redoxclines are zones of high dark CO2 fixation rates, which can correspond up to 30% of the surface primary production. However, despite this significant contribution to the pelagic carbon cycle, the identity of most chemolithoautotrophic organisms is still unknown. Therefore, the aim of this study was to directly link the dark CO2 fixation capacity of a pelagic redoxcline in the central Baltic Sea (Landsort Deep) with the identity of the main chemolithoautotrophs involved. Our approach was based on the analysis of natural carbon isotope signatures in fatty acid methyl esters (FAMEs) and on measurements of CO2 incorporation in 13C‐bicarbonate pulse experiments. The incorporation of 13C into chemolithoautotrophic cells was investigated by rRNA‐based stable isotope probing (RNA‐SIP) and FAME analysis after incubation for 24 and 72 h under in situ conditions. Our results demonstrated that fatty acids indicative of Proteobacteria were significantly enriched in 13C slightly below the chemocline. RNA‐SIP analyses revealed that two different Gammaproteobacteria and three closely related Epsilonproteobacteria of the Sulfurimonas cluster were active dark CO2‐fixing microorganisms, with a time‐dependent community shift between these groups. Labelling of Archaea was not detectable, but after 72 h of incubation the 13C‐label had been transferred to a potentially bacterivorous ciliate related to Euplotes sp. Thus, RNA‐SIP provided direct evidence for the contribution of chemolithoautotrophic production to the microbial food web in this marine pelagic redoxcline, emphasizing the importance of dark CO2‐fixing Proteobacteria within this habitat.</description><subject>Animals</subject><subject>Archaea</subject><subject>Archaea - classification</subject><subject>Archaea - genetics</subject><subject>Archaea - metabolism</subject><subject>Biodiversity</subject><subject>Carbon Dioxide - metabolism</subject><subject>Carbon Isotopes - metabolism</subject><subject>DNA, Bacterial - chemistry</subject><subject>DNA, Bacterial - genetics</subject><subject>DNA, Ribosomal - chemistry</subject><subject>DNA, Ribosomal - genetics</subject><subject>Epsilonproteobacteria - classification</subject><subject>Epsilonproteobacteria - genetics</subject><subject>Epsilonproteobacteria - metabolism</subject><subject>Euplotes</subject><subject>Euplotes - classification</subject><subject>Euplotes - genetics</subject><subject>Euplotes - metabolism</subject><subject>Fatty Acids - chemistry</subject><subject>Food Chain</subject><subject>Gammaproteobacteria - classification</subject><subject>Gammaproteobacteria - genetics</subject><subject>Gammaproteobacteria - metabolism</subject><subject>Molecular Sequence Data</subject><subject>Proteobacteria</subject><subject>RNA - chemistry</subject><subject>RNA, Ribosomal, 16S - genetics</subject><subject>Seawater - microbiology</subject><subject>Sequence Analysis, DNA</subject><subject>Staining and Labeling</subject><issn>1462-2912</issn><issn>1462-2920</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc9y0zAQxj0MDC2FV2B04majP7EsHzhAJg2dSeDQAkfNxl4TBdkyktImz8OLIpMSjkgH7Wh_32q1X5YRRguW1ttdwWaS57zmtOCUqoKyqqLF4Ul2eU48PceMX2QvQtjRRImKPs8umKpqIZi8zH4xMc9NcNGNSGAAewwYiMd7BEviFiJpttg7a-LWwT666N24NQ1ZQt9DnhQtWYzBWDeM3kV0G2giegOkQ2wJkN403m1MKtY515IH3BAzpPsRLXxPdTy27tBYMyBxXXoQSYND9In_ADYm4BbhZfasAxvw1eN5lX25XtzNP-arz8ub-ftVbqbf50IylEq1nSyZUMCFUrJSpZSUVmmXNA2i4SV2bWqSVbNazPhMVVB3tKMllOIqe3Oqm77yc48h6t6EBq2FAd0-aClVPZMl_S_IqRCpozqBrx_B_abHVo_e9OCP-u_8E_DuBDwYi8d_eaonn_VOTxbqyU49-az_-KwPerG-maKkz096EyIeznrwP7RMXpf626elXt19va3WfK2vxW9-o6sx</recordid><startdate>200902</startdate><enddate>200902</enddate><creator>Glaubitz, Sabine</creator><creator>Lueders, Tillmann</creator><creator>Abraham, Wolf-Rainer</creator><creator>Jost, Günter</creator><creator>Jürgens, Klaus</creator><creator>Labrenz, Matthias</creator><general>Blackwell Publishing Ltd</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7QL</scope><scope>7SN</scope><scope>7T7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>M7N</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>200902</creationdate><title>13C-isotope analyses reveal that chemolithoautotrophic Gamma- and Epsilonproteobacteria feed a microbial food web in a pelagic redoxcline of the central Baltic Sea</title><author>Glaubitz, Sabine ; Lueders, Tillmann ; Abraham, Wolf-Rainer ; Jost, Günter ; Jürgens, Klaus ; Labrenz, Matthias</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-i1770-361e688df65138a238867856600707050912c25efdbac1749342487a9f0f05a53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Animals</topic><topic>Archaea</topic><topic>Archaea - classification</topic><topic>Archaea - genetics</topic><topic>Archaea - metabolism</topic><topic>Biodiversity</topic><topic>Carbon Dioxide - metabolism</topic><topic>Carbon Isotopes - metabolism</topic><topic>DNA, Bacterial - chemistry</topic><topic>DNA, Bacterial - genetics</topic><topic>DNA, Ribosomal - chemistry</topic><topic>DNA, Ribosomal - genetics</topic><topic>Epsilonproteobacteria - classification</topic><topic>Epsilonproteobacteria - genetics</topic><topic>Epsilonproteobacteria - metabolism</topic><topic>Euplotes</topic><topic>Euplotes - classification</topic><topic>Euplotes - genetics</topic><topic>Euplotes - metabolism</topic><topic>Fatty Acids - chemistry</topic><topic>Food Chain</topic><topic>Gammaproteobacteria - classification</topic><topic>Gammaproteobacteria - genetics</topic><topic>Gammaproteobacteria - metabolism</topic><topic>Molecular Sequence Data</topic><topic>Proteobacteria</topic><topic>RNA - chemistry</topic><topic>RNA, Ribosomal, 16S - genetics</topic><topic>Seawater - microbiology</topic><topic>Sequence Analysis, DNA</topic><topic>Staining and Labeling</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Glaubitz, Sabine</creatorcontrib><creatorcontrib>Lueders, Tillmann</creatorcontrib><creatorcontrib>Abraham, Wolf-Rainer</creatorcontrib><creatorcontrib>Jost, Günter</creatorcontrib><creatorcontrib>Jürgens, Klaus</creatorcontrib><creatorcontrib>Labrenz, Matthias</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Ecology Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Environmental microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Glaubitz, Sabine</au><au>Lueders, Tillmann</au><au>Abraham, Wolf-Rainer</au><au>Jost, Günter</au><au>Jürgens, Klaus</au><au>Labrenz, Matthias</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>13C-isotope analyses reveal that chemolithoautotrophic Gamma- and Epsilonproteobacteria feed a microbial food web in a pelagic redoxcline of the central Baltic Sea</atitle><jtitle>Environmental microbiology</jtitle><addtitle>Environ Microbiol</addtitle><date>2009-02</date><risdate>2009</risdate><volume>11</volume><issue>2</issue><spage>326</spage><epage>337</epage><pages>326-337</pages><issn>1462-2912</issn><eissn>1462-2920</eissn><abstract>Summary
Marine pelagic redoxclines are zones of high dark CO2 fixation rates, which can correspond up to 30% of the surface primary production. However, despite this significant contribution to the pelagic carbon cycle, the identity of most chemolithoautotrophic organisms is still unknown. Therefore, the aim of this study was to directly link the dark CO2 fixation capacity of a pelagic redoxcline in the central Baltic Sea (Landsort Deep) with the identity of the main chemolithoautotrophs involved. Our approach was based on the analysis of natural carbon isotope signatures in fatty acid methyl esters (FAMEs) and on measurements of CO2 incorporation in 13C‐bicarbonate pulse experiments. The incorporation of 13C into chemolithoautotrophic cells was investigated by rRNA‐based stable isotope probing (RNA‐SIP) and FAME analysis after incubation for 24 and 72 h under in situ conditions. Our results demonstrated that fatty acids indicative of Proteobacteria were significantly enriched in 13C slightly below the chemocline. RNA‐SIP analyses revealed that two different Gammaproteobacteria and three closely related Epsilonproteobacteria of the Sulfurimonas cluster were active dark CO2‐fixing microorganisms, with a time‐dependent community shift between these groups. Labelling of Archaea was not detectable, but after 72 h of incubation the 13C‐label had been transferred to a potentially bacterivorous ciliate related to Euplotes sp. Thus, RNA‐SIP provided direct evidence for the contribution of chemolithoautotrophic production to the microbial food web in this marine pelagic redoxcline, emphasizing the importance of dark CO2‐fixing Proteobacteria within this habitat.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>18793316</pmid><doi>10.1111/j.1462-2920.2008.01770.x</doi><tpages>12</tpages></addata></record> |
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subjects | Animals Archaea Archaea - classification Archaea - genetics Archaea - metabolism Biodiversity Carbon Dioxide - metabolism Carbon Isotopes - metabolism DNA, Bacterial - chemistry DNA, Bacterial - genetics DNA, Ribosomal - chemistry DNA, Ribosomal - genetics Epsilonproteobacteria - classification Epsilonproteobacteria - genetics Epsilonproteobacteria - metabolism Euplotes Euplotes - classification Euplotes - genetics Euplotes - metabolism Fatty Acids - chemistry Food Chain Gammaproteobacteria - classification Gammaproteobacteria - genetics Gammaproteobacteria - metabolism Molecular Sequence Data Proteobacteria RNA - chemistry RNA, Ribosomal, 16S - genetics Seawater - microbiology Sequence Analysis, DNA Staining and Labeling |
title | 13C-isotope analyses reveal that chemolithoautotrophic Gamma- and Epsilonproteobacteria feed a microbial food web in a pelagic redoxcline of the central Baltic Sea |
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