Polyphasic Characterization of a Thermotolerant Siderophilic Filamentous Cyanobacterium That Produces Intracellular Iron Deposits
Despite the high potential for oxidative stress stimulated by reduced iron, contemporary iron-depositing hot springs with circum-neutral pH are intensively populated with cyanobacteria. Therefore, studies of the physiology, diversity, and phylogeny of cyanobacteria inhabiting iron-depositing hot spr...
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creator | Brown, Igor I Bryant, Donald A Casamatta, Dale Thomas-Keprta, Kathie L Sarkisova, Svetlana A Shen, Gaozhong Graham, Joel E Boyd, Eric S Peters, John W Garrison, Daniel H McKay, David S |
description | Despite the high potential for oxidative stress stimulated by reduced iron, contemporary iron-depositing hot springs with circum-neutral pH are intensively populated with cyanobacteria. Therefore, studies of the physiology, diversity, and phylogeny of cyanobacteria inhabiting iron-depositing hot springs may provide insights into the contribution of cyanobacteria to iron redox cycling in these environments and new mechanisms of oxidative stress mitigation. In this study the morphology, ultrastructure, physiology, and phylogeny of a novel cyanobacterial taxon, JSC-1, isolated from an iron-depositing hot spring, were determined. The JSC-1 strain has been deposited in ATCC under the name Marsacia ferruginose, accession number BAA-2121. Strain JSC-1 represents a new operational taxonomical unit (OTU) within Leptolyngbya sensu lato. Strain JSC-1 exhibited an unusually high ratio between photosystem (PS) I and PS II, was capable of complementary chromatic adaptation, and is apparently capable of nitrogen fixation. Furthermore, it synthesized a unique set of carotenoids, but only chlorophyll a. Strain JSC-1 not only required high levels of Fe for growth (≥40 μM), but it also accumulated large amounts of extracellular iron in the form of ferrihydrite and intracellular iron in the form of ferric phosphates. Collectively, these observations provide insights into the physiological strategies that might have allowed cyanobacteria to develop and proliferate in Fe-rich, circum-neutral environments. |
doi_str_mv | 10.1128/AEM.00662-10 |
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Therefore, studies of the physiology, diversity, and phylogeny of cyanobacteria inhabiting iron-depositing hot springs may provide insights into the contribution of cyanobacteria to iron redox cycling in these environments and new mechanisms of oxidative stress mitigation. In this study the morphology, ultrastructure, physiology, and phylogeny of a novel cyanobacterial taxon, JSC-1, isolated from an iron-depositing hot spring, were determined. The JSC-1 strain has been deposited in ATCC under the name Marsacia ferruginose, accession number BAA-2121. Strain JSC-1 represents a new operational taxonomical unit (OTU) within Leptolyngbya sensu lato. Strain JSC-1 exhibited an unusually high ratio between photosystem (PS) I and PS II, was capable of complementary chromatic adaptation, and is apparently capable of nitrogen fixation. Furthermore, it synthesized a unique set of carotenoids, but only chlorophyll a. Strain JSC-1 not only required high levels of Fe for growth (≥40 μM), but it also accumulated large amounts of extracellular iron in the form of ferrihydrite and intracellular iron in the form of ferric phosphates. Collectively, these observations provide insights into the physiological strategies that might have allowed cyanobacteria to develop and proliferate in Fe-rich, circum-neutral environments.</description><identifier>ISSN: 0099-2240</identifier><identifier>EISSN: 1098-5336</identifier><identifier>EISSN: 1098-6596</identifier><identifier>DOI: 10.1128/AEM.00662-10</identifier><identifier>PMID: 20709851</identifier><identifier>CODEN: AEMIDF</identifier><language>eng</language><publisher>Washington, DC: American Society for Microbiology</publisher><subject>Adaptations ; Bacteria ; Biological and medical sciences ; Carotenoids - analysis ; Chlorophyll ; Chlorophyll - analysis ; Cluster Analysis ; Cyanobacteria ; Cyanobacteria - classification ; Cyanobacteria - genetics ; Cyanobacteria - isolation & purification ; Cyanobacteria - metabolism ; DNA, Bacterial - chemistry ; DNA, Bacterial - genetics ; DNA, Ribosomal - chemistry ; DNA, Ribosomal - genetics ; Environmental Microbiology ; Ferric Compounds - analysis ; Fundamental and applied biological sciences. Psychology ; Hot Springs - microbiology ; Iron ; Iron - metabolism ; Leptolyngbya ; Microbiology ; Microscopy, Electron, Transmission ; Morphology ; Nitrogen - metabolism ; Nitrogen Fixation ; Photoelectron Spectroscopy ; Photosystem I Protein Complex - analysis ; Photosystem II Protein Complex - analysis ; Phylogeny ; RNA, Ribosomal, 16S - genetics ; Sequence Analysis, DNA ; Studies</subject><ispartof>Applied and Environmental Microbiology, 2010-10, Vol.76 (19), p.6664-6672</ispartof><rights>2015 INIST-CNRS</rights><rights>Copyright American Society for Microbiology Oct 2010</rights><rights>Copyright © 2010, American Society for Microbiology 2010</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c598t-daa630f1adb7d5551cb24d8d45d1af7f4b667593a69979391a92c303dfccdc163</citedby><cites>FETCH-LOGICAL-c598t-daa630f1adb7d5551cb24d8d45d1af7f4b667593a69979391a92c303dfccdc163</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/PMC2950469/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2950469/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,3175,3176,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=23285831$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20709851$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Brown, Igor I</creatorcontrib><creatorcontrib>Bryant, Donald A</creatorcontrib><creatorcontrib>Casamatta, Dale</creatorcontrib><creatorcontrib>Thomas-Keprta, Kathie L</creatorcontrib><creatorcontrib>Sarkisova, Svetlana A</creatorcontrib><creatorcontrib>Shen, Gaozhong</creatorcontrib><creatorcontrib>Graham, Joel E</creatorcontrib><creatorcontrib>Boyd, Eric S</creatorcontrib><creatorcontrib>Peters, John W</creatorcontrib><creatorcontrib>Garrison, Daniel H</creatorcontrib><creatorcontrib>McKay, David S</creatorcontrib><title>Polyphasic Characterization of a Thermotolerant Siderophilic Filamentous Cyanobacterium That Produces Intracellular Iron Deposits</title><title>Applied and Environmental Microbiology</title><addtitle>Appl Environ Microbiol</addtitle><description>Despite the high potential for oxidative stress stimulated by reduced iron, contemporary iron-depositing hot springs with circum-neutral pH are intensively populated with cyanobacteria. Therefore, studies of the physiology, diversity, and phylogeny of cyanobacteria inhabiting iron-depositing hot springs may provide insights into the contribution of cyanobacteria to iron redox cycling in these environments and new mechanisms of oxidative stress mitigation. In this study the morphology, ultrastructure, physiology, and phylogeny of a novel cyanobacterial taxon, JSC-1, isolated from an iron-depositing hot spring, were determined. The JSC-1 strain has been deposited in ATCC under the name Marsacia ferruginose, accession number BAA-2121. Strain JSC-1 represents a new operational taxonomical unit (OTU) within Leptolyngbya sensu lato. Strain JSC-1 exhibited an unusually high ratio between photosystem (PS) I and PS II, was capable of complementary chromatic adaptation, and is apparently capable of nitrogen fixation. Furthermore, it synthesized a unique set of carotenoids, but only chlorophyll a. Strain JSC-1 not only required high levels of Fe for growth (≥40 μM), but it also accumulated large amounts of extracellular iron in the form of ferrihydrite and intracellular iron in the form of ferric phosphates. Collectively, these observations provide insights into the physiological strategies that might have allowed cyanobacteria to develop and proliferate in Fe-rich, circum-neutral environments.</description><subject>Adaptations</subject><subject>Bacteria</subject><subject>Biological and medical sciences</subject><subject>Carotenoids - analysis</subject><subject>Chlorophyll</subject><subject>Chlorophyll - analysis</subject><subject>Cluster Analysis</subject><subject>Cyanobacteria</subject><subject>Cyanobacteria - classification</subject><subject>Cyanobacteria - genetics</subject><subject>Cyanobacteria - isolation & purification</subject><subject>Cyanobacteria - metabolism</subject><subject>DNA, Bacterial - chemistry</subject><subject>DNA, Bacterial - genetics</subject><subject>DNA, Ribosomal - chemistry</subject><subject>DNA, Ribosomal - genetics</subject><subject>Environmental Microbiology</subject><subject>Ferric Compounds - analysis</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Hot Springs - microbiology</subject><subject>Iron</subject><subject>Iron - metabolism</subject><subject>Leptolyngbya</subject><subject>Microbiology</subject><subject>Microscopy, Electron, Transmission</subject><subject>Morphology</subject><subject>Nitrogen - metabolism</subject><subject>Nitrogen Fixation</subject><subject>Photoelectron Spectroscopy</subject><subject>Photosystem I Protein Complex - analysis</subject><subject>Photosystem II Protein Complex - analysis</subject><subject>Phylogeny</subject><subject>RNA, Ribosomal, 16S - genetics</subject><subject>Sequence Analysis, DNA</subject><subject>Studies</subject><issn>0099-2240</issn><issn>1098-5336</issn><issn>1098-6596</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFks1v1DAQxSMEotvCjTNESBUXUvwRO_EFqVpaWKmISm3P1sR2Nq6SOLUd0HLjP8fLLqVw4WRp_JunNzMvy15gdIIxqd-dnn0-QYhzUmD0KFtgJOqCUcofZwuEhCgIKdFBdhjCLUKoRLx-mh0QVCWM4UX249L1m6mDYFW-7MCDisbb7xCtG3PX5pBfd8YPLrreeBhjfmW18W7qbJ86zm0Pgxmjm0O-3MDoml3_PKQ2iPmld3pWJuSrMSZp0_dzDz5f-ST-wUwu2BieZU9a6IN5vn-Pspvzs-vlp-Liy8fV8vSiUEzUsdAAnKIWg24qzRjDqiGlrnXJNIa2asuG84oJClyISlCBQRBFEdWtUlphTo-y9zvdaW4Go5XZWurl5O0AfiMdWPn3z2g7uXZfJREMlVwkgTd7Ae_uZhOiHGzYzgSjSQuQNS9FKXBV_5esOCEVZhgn8vU_5K2b_Zj2ICvGuUBYbJ2_3UHKuxC8ae9NYyS3GZApA_JXBlIl4S8fDnoP_z56Ao73AAQFfZvuqmz4w1FSs5o-MNfZdffNeiMhDBLMkAaQWEjOeZmgVzuoBSdh7ZPQzRVBmCJci5Q9Qn8CBTnRJQ</recordid><startdate>20101001</startdate><enddate>20101001</enddate><creator>Brown, Igor I</creator><creator>Bryant, Donald A</creator><creator>Casamatta, Dale</creator><creator>Thomas-Keprta, Kathie L</creator><creator>Sarkisova, Svetlana A</creator><creator>Shen, Gaozhong</creator><creator>Graham, Joel E</creator><creator>Boyd, Eric S</creator><creator>Peters, John W</creator><creator>Garrison, Daniel H</creator><creator>McKay, David S</creator><general>American Society for Microbiology</general><general>American Society for Microbiology (ASM)</general><scope>FBQ</scope><scope>IQODW</scope><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>7QL</scope><scope>7QO</scope><scope>7SN</scope><scope>7SS</scope><scope>7ST</scope><scope>7T7</scope><scope>7TM</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>SOI</scope><scope>F1W</scope><scope>H95</scope><scope>L.G</scope><scope>5PM</scope></search><sort><creationdate>20101001</creationdate><title>Polyphasic Characterization of a Thermotolerant Siderophilic Filamentous Cyanobacterium That Produces Intracellular Iron Deposits</title><author>Brown, Igor I ; Bryant, Donald A ; Casamatta, Dale ; Thomas-Keprta, Kathie L ; Sarkisova, Svetlana A ; Shen, Gaozhong ; Graham, Joel E ; Boyd, Eric S ; Peters, John W ; Garrison, Daniel H ; McKay, David S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c598t-daa630f1adb7d5551cb24d8d45d1af7f4b667593a69979391a92c303dfccdc163</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Adaptations</topic><topic>Bacteria</topic><topic>Biological and medical sciences</topic><topic>Carotenoids - analysis</topic><topic>Chlorophyll</topic><topic>Chlorophyll - analysis</topic><topic>Cluster Analysis</topic><topic>Cyanobacteria</topic><topic>Cyanobacteria - classification</topic><topic>Cyanobacteria - genetics</topic><topic>Cyanobacteria - isolation & purification</topic><topic>Cyanobacteria - metabolism</topic><topic>DNA, Bacterial - chemistry</topic><topic>DNA, Bacterial - genetics</topic><topic>DNA, Ribosomal - chemistry</topic><topic>DNA, Ribosomal - genetics</topic><topic>Environmental Microbiology</topic><topic>Ferric Compounds - analysis</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Hot Springs - microbiology</topic><topic>Iron</topic><topic>Iron - metabolism</topic><topic>Leptolyngbya</topic><topic>Microbiology</topic><topic>Microscopy, Electron, Transmission</topic><topic>Morphology</topic><topic>Nitrogen - metabolism</topic><topic>Nitrogen Fixation</topic><topic>Photoelectron Spectroscopy</topic><topic>Photosystem I Protein Complex - analysis</topic><topic>Photosystem II Protein Complex - analysis</topic><topic>Phylogeny</topic><topic>RNA, Ribosomal, 16S - genetics</topic><topic>Sequence Analysis, DNA</topic><topic>Studies</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Brown, Igor I</creatorcontrib><creatorcontrib>Bryant, Donald A</creatorcontrib><creatorcontrib>Casamatta, Dale</creatorcontrib><creatorcontrib>Thomas-Keprta, Kathie L</creatorcontrib><creatorcontrib>Sarkisova, Svetlana A</creatorcontrib><creatorcontrib>Shen, Gaozhong</creatorcontrib><creatorcontrib>Graham, Joel E</creatorcontrib><creatorcontrib>Boyd, Eric S</creatorcontrib><creatorcontrib>Peters, John W</creatorcontrib><creatorcontrib>Garrison, Daniel H</creatorcontrib><creatorcontrib>McKay, David S</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Environment Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>Environment Abstracts</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Applied and Environmental Microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Brown, Igor I</au><au>Bryant, Donald A</au><au>Casamatta, Dale</au><au>Thomas-Keprta, Kathie L</au><au>Sarkisova, Svetlana A</au><au>Shen, Gaozhong</au><au>Graham, Joel E</au><au>Boyd, Eric S</au><au>Peters, John W</au><au>Garrison, Daniel H</au><au>McKay, David S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Polyphasic Characterization of a Thermotolerant Siderophilic Filamentous Cyanobacterium That Produces Intracellular Iron Deposits</atitle><jtitle>Applied and Environmental Microbiology</jtitle><addtitle>Appl Environ Microbiol</addtitle><date>2010-10-01</date><risdate>2010</risdate><volume>76</volume><issue>19</issue><spage>6664</spage><epage>6672</epage><pages>6664-6672</pages><issn>0099-2240</issn><eissn>1098-5336</eissn><eissn>1098-6596</eissn><coden>AEMIDF</coden><abstract>Despite the high potential for oxidative stress stimulated by reduced iron, contemporary iron-depositing hot springs with circum-neutral pH are intensively populated with cyanobacteria. Therefore, studies of the physiology, diversity, and phylogeny of cyanobacteria inhabiting iron-depositing hot springs may provide insights into the contribution of cyanobacteria to iron redox cycling in these environments and new mechanisms of oxidative stress mitigation. In this study the morphology, ultrastructure, physiology, and phylogeny of a novel cyanobacterial taxon, JSC-1, isolated from an iron-depositing hot spring, were determined. The JSC-1 strain has been deposited in ATCC under the name Marsacia ferruginose, accession number BAA-2121. Strain JSC-1 represents a new operational taxonomical unit (OTU) within Leptolyngbya sensu lato. Strain JSC-1 exhibited an unusually high ratio between photosystem (PS) I and PS II, was capable of complementary chromatic adaptation, and is apparently capable of nitrogen fixation. Furthermore, it synthesized a unique set of carotenoids, but only chlorophyll a. Strain JSC-1 not only required high levels of Fe for growth (≥40 μM), but it also accumulated large amounts of extracellular iron in the form of ferrihydrite and intracellular iron in the form of ferric phosphates. Collectively, these observations provide insights into the physiological strategies that might have allowed cyanobacteria to develop and proliferate in Fe-rich, circum-neutral environments.</abstract><cop>Washington, DC</cop><pub>American Society for Microbiology</pub><pmid>20709851</pmid><doi>10.1128/AEM.00662-10</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adaptations Bacteria Biological and medical sciences Carotenoids - analysis Chlorophyll Chlorophyll - analysis Cluster Analysis Cyanobacteria Cyanobacteria - classification Cyanobacteria - genetics Cyanobacteria - isolation & purification Cyanobacteria - metabolism DNA, Bacterial - chemistry DNA, Bacterial - genetics DNA, Ribosomal - chemistry DNA, Ribosomal - genetics Environmental Microbiology Ferric Compounds - analysis Fundamental and applied biological sciences. Psychology Hot Springs - microbiology Iron Iron - metabolism Leptolyngbya Microbiology Microscopy, Electron, Transmission Morphology Nitrogen - metabolism Nitrogen Fixation Photoelectron Spectroscopy Photosystem I Protein Complex - analysis Photosystem II Protein Complex - analysis Phylogeny RNA, Ribosomal, 16S - genetics Sequence Analysis, DNA Studies |
title | Polyphasic Characterization of a Thermotolerant Siderophilic Filamentous Cyanobacterium That Produces Intracellular Iron Deposits |
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