Lithotrophic iron-oxidizing bacteria produce organic stalks to control mineral growth: implications for biosignature formation
Neutrophilic Fe-oxidizing bacteria (FeOB) are often identified by their distinctive morphologies, such as the extracellular twisted ribbon-like stalks formed by Gallionella ferruginea or Mariprofundus ferrooxydans . Similar filaments preserved in silica are often identified as FeOB fossils in rocks....
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description | Neutrophilic Fe-oxidizing bacteria (FeOB) are often identified by their distinctive morphologies, such as the extracellular twisted ribbon-like stalks formed by
Gallionella ferruginea
or
Mariprofundus ferrooxydans
. Similar filaments preserved in silica are often identified as FeOB fossils in rocks. Although it is assumed that twisted iron stalks are indicative of FeOB, the stalk's metabolic role has not been established. To this end, we studied the marine FeOB
M. ferrooxydans
by light, X-ray and electron microscopy. Using time-lapse light microscopy, we observed cells excreting stalks during growth (averaging 2.2 μm h
−1
). Scanning transmission X-ray microscopy and near-edge X-ray absorption fine structure (NEXAFS) spectroscopy show that stalks are Fe(III)-rich, whereas cells are low in Fe. Transmission electron microscopy reveals that stalks are composed of several fibrils, which contain few-nanometer-sized iron oxyhydroxide crystals. Lepidocrocite crystals that nucleated on the fibril surface are much larger (∼100 nm), suggesting that mineral growth within fibrils is retarded, relative to sites surrounding fibrils. C and N 1s NEXAFS spectroscopy and fluorescence probing show that stalks primarily contain carboxyl-rich polysaccharides. On the basis of these results, we suggest a physiological model for Fe oxidation in which cells excrete oxidized Fe bound to organic polymers. These organic molecules retard mineral growth, preventing cell encrustation. This model describes an essential role for stalk formation in FeOB growth. We suggest that stalk-like morphologies observed in modern and ancient samples may be correlated confidently with the Fe-oxidizing metabolism as a robust biosignature. |
doi_str_mv | 10.1038/ismej.2010.173 |
format | Article |
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Gallionella ferruginea
or
Mariprofundus ferrooxydans
. Similar filaments preserved in silica are often identified as FeOB fossils in rocks. Although it is assumed that twisted iron stalks are indicative of FeOB, the stalk's metabolic role has not been established. To this end, we studied the marine FeOB
M. ferrooxydans
by light, X-ray and electron microscopy. Using time-lapse light microscopy, we observed cells excreting stalks during growth (averaging 2.2 μm h
−1
). Scanning transmission X-ray microscopy and near-edge X-ray absorption fine structure (NEXAFS) spectroscopy show that stalks are Fe(III)-rich, whereas cells are low in Fe. Transmission electron microscopy reveals that stalks are composed of several fibrils, which contain few-nanometer-sized iron oxyhydroxide crystals. Lepidocrocite crystals that nucleated on the fibril surface are much larger (∼100 nm), suggesting that mineral growth within fibrils is retarded, relative to sites surrounding fibrils. C and N 1s NEXAFS spectroscopy and fluorescence probing show that stalks primarily contain carboxyl-rich polysaccharides. On the basis of these results, we suggest a physiological model for Fe oxidation in which cells excrete oxidized Fe bound to organic polymers. These organic molecules retard mineral growth, preventing cell encrustation. This model describes an essential role for stalk formation in FeOB growth. We suggest that stalk-like morphologies observed in modern and ancient samples may be correlated confidently with the Fe-oxidizing metabolism as a robust biosignature.</description><identifier>ISSN: 1751-7362</identifier><identifier>EISSN: 1751-7370</identifier><identifier>DOI: 10.1038/ismej.2010.173</identifier><identifier>PMID: 21107443</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>631/326/41/1969 ; 631/326/41/2528 ; ABSORPTION ; BACTERIA ; Biomedical and Life Sciences ; Crystals ; Ecology ; ELECTRON MICROSCOPY ; encrustation ; ENVIRONMENTAL SCIENCES ; Evolutionary Biology ; Ferric Compounds - analysis ; Fibrils ; Filaments ; FINE STRUCTURE ; FLUORESCENCE ; Fossils ; Gallionella ferruginea ; Ionizing radiation ; IRON ; Iron - metabolism ; Iron-oxidizing bacteria ; Leukocytes (neutrophilic) ; Life Sciences ; Light microscopy ; METABOLISM ; Microbial Ecology ; Microbial Genetics and Genomics ; Microbiology ; MICROSCOPY ; Minerals ; Minerals - chemistry ; ORGANIC POLYMERS ; Original ; original-article ; OXIDATION ; Oxidation-Reduction ; Physiology ; Polymers ; POLYSACCHARIDES ; Proteobacteria - cytology ; Proteobacteria - growth & development ; Proteobacteria - metabolism ; Rocks ; Saccharides ; Scanning ; SILICA ; SPECTROSCOPY ; TRANSMISSION ELECTRON MICROSCOPY ; Ultrastructure</subject><ispartof>ISME Journal, 2011-04, Vol.5 (4), p.717-727</ispartof><rights>International Society for Microbial Ecology 2011</rights><rights>Copyright Nature Publishing Group Apr 2011</rights><rights>Copyright © 2011 International Society for Microbial Ecology 2011 International Society for Microbial Ecology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a606t-45fb23917e8292ffb89f2fc65ea5110ab71e3a1bd4d44304a8fe9ec67bd70d03</citedby><cites>FETCH-LOGICAL-a606t-45fb23917e8292ffb89f2fc65ea5110ab71e3a1bd4d44304a8fe9ec67bd70d03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3105749/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3105749/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21107443$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://www.osti.gov/servlets/purl/1048283$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><creatorcontrib>Chan, Clara S</creatorcontrib><creatorcontrib>Fakra, Sirine C</creatorcontrib><creatorcontrib>Emerson, David</creatorcontrib><creatorcontrib>Fleming, Emily J</creatorcontrib><creatorcontrib>Edwards, Katrina J</creatorcontrib><creatorcontrib>Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States)</creatorcontrib><title>Lithotrophic iron-oxidizing bacteria produce organic stalks to control mineral growth: implications for biosignature formation</title><title>ISME Journal</title><addtitle>ISME J</addtitle><addtitle>ISME J</addtitle><description>Neutrophilic Fe-oxidizing bacteria (FeOB) are often identified by their distinctive morphologies, such as the extracellular twisted ribbon-like stalks formed by
Gallionella ferruginea
or
Mariprofundus ferrooxydans
. Similar filaments preserved in silica are often identified as FeOB fossils in rocks. Although it is assumed that twisted iron stalks are indicative of FeOB, the stalk's metabolic role has not been established. To this end, we studied the marine FeOB
M. ferrooxydans
by light, X-ray and electron microscopy. Using time-lapse light microscopy, we observed cells excreting stalks during growth (averaging 2.2 μm h
−1
). Scanning transmission X-ray microscopy and near-edge X-ray absorption fine structure (NEXAFS) spectroscopy show that stalks are Fe(III)-rich, whereas cells are low in Fe. Transmission electron microscopy reveals that stalks are composed of several fibrils, which contain few-nanometer-sized iron oxyhydroxide crystals. Lepidocrocite crystals that nucleated on the fibril surface are much larger (∼100 nm), suggesting that mineral growth within fibrils is retarded, relative to sites surrounding fibrils. C and N 1s NEXAFS spectroscopy and fluorescence probing show that stalks primarily contain carboxyl-rich polysaccharides. On the basis of these results, we suggest a physiological model for Fe oxidation in which cells excrete oxidized Fe bound to organic polymers. These organic molecules retard mineral growth, preventing cell encrustation. This model describes an essential role for stalk formation in FeOB growth. We suggest that stalk-like morphologies observed in modern and ancient samples may be correlated confidently with the Fe-oxidizing metabolism as a robust biosignature.</description><subject>631/326/41/1969</subject><subject>631/326/41/2528</subject><subject>ABSORPTION</subject><subject>BACTERIA</subject><subject>Biomedical and Life Sciences</subject><subject>Crystals</subject><subject>Ecology</subject><subject>ELECTRON MICROSCOPY</subject><subject>encrustation</subject><subject>ENVIRONMENTAL SCIENCES</subject><subject>Evolutionary Biology</subject><subject>Ferric Compounds - analysis</subject><subject>Fibrils</subject><subject>Filaments</subject><subject>FINE STRUCTURE</subject><subject>FLUORESCENCE</subject><subject>Fossils</subject><subject>Gallionella ferruginea</subject><subject>Ionizing radiation</subject><subject>IRON</subject><subject>Iron - metabolism</subject><subject>Iron-oxidizing bacteria</subject><subject>Leukocytes (neutrophilic)</subject><subject>Life Sciences</subject><subject>Light microscopy</subject><subject>METABOLISM</subject><subject>Microbial Ecology</subject><subject>Microbial Genetics and Genomics</subject><subject>Microbiology</subject><subject>MICROSCOPY</subject><subject>Minerals</subject><subject>Minerals - chemistry</subject><subject>ORGANIC POLYMERS</subject><subject>Original</subject><subject>original-article</subject><subject>OXIDATION</subject><subject>Oxidation-Reduction</subject><subject>Physiology</subject><subject>Polymers</subject><subject>POLYSACCHARIDES</subject><subject>Proteobacteria - cytology</subject><subject>Proteobacteria - growth & development</subject><subject>Proteobacteria - metabolism</subject><subject>Rocks</subject><subject>Saccharides</subject><subject>Scanning</subject><subject>SILICA</subject><subject>SPECTROSCOPY</subject><subject>TRANSMISSION ELECTRON MICROSCOPY</subject><subject>Ultrastructure</subject><issn>1751-7362</issn><issn>1751-7370</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNp9kruP1DAQxiME4o6DlhJZUECTPT-SOKFAQide0ko011uOM0lmSezFdngV_O04u8fqQIjKj_n5m_nGk2WPGd0wKupLDDPsNpyuZynuZOdMliyXQtK7p33Fz7IHIewoLWVVyfvZGWeMyqIQ59nPLcbRRe_2IxqC3tncfcMOf6AdSKtNBI-a7L3rFgPE-UHbxIWop0-BREeMs-nxRGa04PVEBu--xvElwXk_odERnQ2kd5606AIOVsfFw3oxH2IPs3u9ngI8ulkvsuu3b66v3ufbj-8-XL3e5rqiVcyLsm-5aJiEmje879u66XlvqhJ0mazoVjIQmrVd0SVXtNB1Dw2YSradpB0VF9mro-x-aWfoDKSi9aT2HmftvyunUf0ZsTiqwX1RgqWeFU0SeHoUcCGiCgYjmDF5t2CiYrSoeS0S9Pwmi3efFwhRzRgMTJO24Jag6nLFGlEk8sV_yfVrK1ZxuZb-7C905xZvU7MSxZs6cVImanOkjHcheOhP3hg9qKnDoKh1UFQalPTgye2OnPDfk5GAyyMQUsgO4G_n_afkL-SRzX8</recordid><startdate>20110401</startdate><enddate>20110401</enddate><creator>Chan, Clara S</creator><creator>Fakra, Sirine C</creator><creator>Emerson, David</creator><creator>Fleming, Emily J</creator><creator>Edwards, Katrina J</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QL</scope><scope>7SN</scope><scope>7ST</scope><scope>7T7</scope><scope>7TM</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>P64</scope><scope>PATMY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PYCSY</scope><scope>SOI</scope><scope>7X8</scope><scope>OIOZB</scope><scope>OTOTI</scope><scope>5PM</scope></search><sort><creationdate>20110401</creationdate><title>Lithotrophic iron-oxidizing bacteria produce organic stalks to control mineral growth: implications for biosignature formation</title><author>Chan, Clara S ; Fakra, Sirine C ; Emerson, David ; Fleming, Emily J ; Edwards, Katrina J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a606t-45fb23917e8292ffb89f2fc65ea5110ab71e3a1bd4d44304a8fe9ec67bd70d03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>631/326/41/1969</topic><topic>631/326/41/2528</topic><topic>ABSORPTION</topic><topic>BACTERIA</topic><topic>Biomedical and Life Sciences</topic><topic>Crystals</topic><topic>Ecology</topic><topic>ELECTRON MICROSCOPY</topic><topic>encrustation</topic><topic>ENVIRONMENTAL SCIENCES</topic><topic>Evolutionary Biology</topic><topic>Ferric Compounds - analysis</topic><topic>Fibrils</topic><topic>Filaments</topic><topic>FINE STRUCTURE</topic><topic>FLUORESCENCE</topic><topic>Fossils</topic><topic>Gallionella ferruginea</topic><topic>Ionizing radiation</topic><topic>IRON</topic><topic>Iron - metabolism</topic><topic>Iron-oxidizing bacteria</topic><topic>Leukocytes (neutrophilic)</topic><topic>Life Sciences</topic><topic>Light microscopy</topic><topic>METABOLISM</topic><topic>Microbial Ecology</topic><topic>Microbial Genetics and Genomics</topic><topic>Microbiology</topic><topic>MICROSCOPY</topic><topic>Minerals</topic><topic>Minerals - chemistry</topic><topic>ORGANIC POLYMERS</topic><topic>Original</topic><topic>original-article</topic><topic>OXIDATION</topic><topic>Oxidation-Reduction</topic><topic>Physiology</topic><topic>Polymers</topic><topic>POLYSACCHARIDES</topic><topic>Proteobacteria - cytology</topic><topic>Proteobacteria - growth & development</topic><topic>Proteobacteria - metabolism</topic><topic>Rocks</topic><topic>Saccharides</topic><topic>Scanning</topic><topic>SILICA</topic><topic>SPECTROSCOPY</topic><topic>TRANSMISSION ELECTRON MICROSCOPY</topic><topic>Ultrastructure</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chan, Clara S</creatorcontrib><creatorcontrib>Fakra, Sirine C</creatorcontrib><creatorcontrib>Emerson, David</creatorcontrib><creatorcontrib>Fleming, Emily J</creatorcontrib><creatorcontrib>Edwards, Katrina J</creatorcontrib><creatorcontrib>Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States)</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Ecology Abstracts</collection><collection>Environment Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Nucleic Acids Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environmental Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>Environmental Science Collection</collection><collection>Environment Abstracts</collection><collection>MEDLINE - Academic</collection><collection>OSTI.GOV - Hybrid</collection><collection>OSTI.GOV</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>ISME Journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chan, Clara S</au><au>Fakra, Sirine C</au><au>Emerson, David</au><au>Fleming, Emily J</au><au>Edwards, Katrina J</au><aucorp>Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States)</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Lithotrophic iron-oxidizing bacteria produce organic stalks to control mineral growth: implications for biosignature formation</atitle><jtitle>ISME Journal</jtitle><stitle>ISME J</stitle><addtitle>ISME J</addtitle><date>2011-04-01</date><risdate>2011</risdate><volume>5</volume><issue>4</issue><spage>717</spage><epage>727</epage><pages>717-727</pages><issn>1751-7362</issn><eissn>1751-7370</eissn><abstract>Neutrophilic Fe-oxidizing bacteria (FeOB) are often identified by their distinctive morphologies, such as the extracellular twisted ribbon-like stalks formed by
Gallionella ferruginea
or
Mariprofundus ferrooxydans
. Similar filaments preserved in silica are often identified as FeOB fossils in rocks. Although it is assumed that twisted iron stalks are indicative of FeOB, the stalk's metabolic role has not been established. To this end, we studied the marine FeOB
M. ferrooxydans
by light, X-ray and electron microscopy. Using time-lapse light microscopy, we observed cells excreting stalks during growth (averaging 2.2 μm h
−1
). Scanning transmission X-ray microscopy and near-edge X-ray absorption fine structure (NEXAFS) spectroscopy show that stalks are Fe(III)-rich, whereas cells are low in Fe. Transmission electron microscopy reveals that stalks are composed of several fibrils, which contain few-nanometer-sized iron oxyhydroxide crystals. Lepidocrocite crystals that nucleated on the fibril surface are much larger (∼100 nm), suggesting that mineral growth within fibrils is retarded, relative to sites surrounding fibrils. C and N 1s NEXAFS spectroscopy and fluorescence probing show that stalks primarily contain carboxyl-rich polysaccharides. On the basis of these results, we suggest a physiological model for Fe oxidation in which cells excrete oxidized Fe bound to organic polymers. These organic molecules retard mineral growth, preventing cell encrustation. This model describes an essential role for stalk formation in FeOB growth. We suggest that stalk-like morphologies observed in modern and ancient samples may be correlated confidently with the Fe-oxidizing metabolism as a robust biosignature.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>21107443</pmid><doi>10.1038/ismej.2010.173</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 631/326/41/1969 631/326/41/2528 ABSORPTION BACTERIA Biomedical and Life Sciences Crystals Ecology ELECTRON MICROSCOPY encrustation ENVIRONMENTAL SCIENCES Evolutionary Biology Ferric Compounds - analysis Fibrils Filaments FINE STRUCTURE FLUORESCENCE Fossils Gallionella ferruginea Ionizing radiation IRON Iron - metabolism Iron-oxidizing bacteria Leukocytes (neutrophilic) Life Sciences Light microscopy METABOLISM Microbial Ecology Microbial Genetics and Genomics Microbiology MICROSCOPY Minerals Minerals - chemistry ORGANIC POLYMERS Original original-article OXIDATION Oxidation-Reduction Physiology Polymers POLYSACCHARIDES Proteobacteria - cytology Proteobacteria - growth & development Proteobacteria - metabolism Rocks Saccharides Scanning SILICA SPECTROSCOPY TRANSMISSION ELECTRON MICROSCOPY Ultrastructure |
title | Lithotrophic iron-oxidizing bacteria produce organic stalks to control mineral growth: implications for biosignature formation |
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