Possible physiological mechanisms for production of hydrogen peroxide by the ichthyotoxic flagellate Heterosigma akashiwo
Blooms of the toxic red tide phytoplankton Heterosigma akashiwo (Raphidophyceae) are responsible for substantial losses within the aquaculture industry. The toxicological mechanisms of H.akashiwo blooms are complex and to date, heavily debated. One putative type of ichthyotoxin includes the producti...
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Veröffentlicht in: | Journal of plankton research 2000-10, Vol.22 (10), p.1961-1975 |
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container_title | Journal of plankton research |
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creator | Twiner, Michael J. Trick, Charles G. |
description | Blooms of the toxic red tide phytoplankton Heterosigma akashiwo (Raphidophyceae) are responsible for substantial losses within the aquaculture industry. The toxicological mechanisms of H.akashiwo blooms are complex and to date, heavily debated. One putative type of ichthyotoxin includes the production of reactive oxygen species (ROS) that could alter gill structure and function, resulting in asphyxiation. In this study, we investigated the potential of H.akashiwo to produce extracellular hydrogen peroxide, and have investigated which cellular processes are responsible for this production. Within all experiments, H.akashiwo produced substantial amounts of hydrogen peroxide (up to 7.6 pmol min–1 104 cells–1), resulting in extracellular concentrations of ~0.5 μmol l–1 H2O2. Measured rates of hydrogen peroxide production were directly proportional to cell density, but at higher cell densities, accuracy of H2O2 detection was reduced. Whereas light intensity did not alter H2O2 production, rates of production were stimulated when temperature was elevated. Hydrogen peroxide production was not only dependent on growth phase, but also was regulated by the availability of iron in the medium. Reduction of total iron to 1 nmol l–1 enhanced the production of H2O2 relative to iron replete conditions (10 μmol l–1 iron). From this, we collectively conclude that production of extracellular H2O2 by H.akashiwo occurs through a metabolic pathway that is not directly linked to photosynthesis. |
doi_str_mv | 10.1093/plankt/22.10.1961 |
format | Article |
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The toxicological mechanisms of H.akashiwo blooms are complex and to date, heavily debated. One putative type of ichthyotoxin includes the production of reactive oxygen species (ROS) that could alter gill structure and function, resulting in asphyxiation. In this study, we investigated the potential of H.akashiwo to produce extracellular hydrogen peroxide, and have investigated which cellular processes are responsible for this production. Within all experiments, H.akashiwo produced substantial amounts of hydrogen peroxide (up to 7.6 pmol min–1 104 cells–1), resulting in extracellular concentrations of ~0.5 μmol l–1 H2O2. Measured rates of hydrogen peroxide production were directly proportional to cell density, but at higher cell densities, accuracy of H2O2 detection was reduced. Whereas light intensity did not alter H2O2 production, rates of production were stimulated when temperature was elevated. Hydrogen peroxide production was not only dependent on growth phase, but also was regulated by the availability of iron in the medium. Reduction of total iron to 1 nmol l–1 enhanced the production of H2O2 relative to iron replete conditions (10 μmol l–1 iron). From this, we collectively conclude that production of extracellular H2O2 by H.akashiwo occurs through a metabolic pathway that is not directly linked to photosynthesis.</description><identifier>ISSN: 0142-7873</identifier><identifier>ISSN: 1464-3774</identifier><identifier>EISSN: 1464-3774</identifier><identifier>DOI: 10.1093/plankt/22.10.1961</identifier><identifier>CODEN: JPLRD9</identifier><language>eng</language><publisher>Oxford: Oxford University Press</publisher><subject>Animal and plant ecology ; Animal, plant and microbial ecology ; Aquaculture ; Autoecology ; Biological and medical sciences ; Blooms ; Cell density ; Extracellular ; Fundamental and applied biological sciences. Psychology ; Heterosigma akashiwo ; Hydrogen ; Hydrogen peroxide ; Iron ; Light intensity ; Marine ; Metabolic pathways ; Noxious organisms ; Photosynthesis ; Phytoplankton ; Plants and fungi ; Raphidophyceae ; Reactive oxygen species ; Red tides ; Structure-function relationships</subject><ispartof>Journal of plankton research, 2000-10, Vol.22 (10), p.1961-1975</ispartof><rights>2000 INIST-CNRS</rights><rights>Copyright Oxford University Press(England) Oct 2000</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c477t-633ccab41d72e4770d25ce39da76c96c95a121f55a21e832e6184d590e3c61733</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1496641$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Twiner, Michael J.</creatorcontrib><creatorcontrib>Trick, Charles G.</creatorcontrib><title>Possible physiological mechanisms for production of hydrogen peroxide by the ichthyotoxic flagellate Heterosigma akashiwo</title><title>Journal of plankton research</title><addtitle>J. Plankton Res</addtitle><description>Blooms of the toxic red tide phytoplankton Heterosigma akashiwo (Raphidophyceae) are responsible for substantial losses within the aquaculture industry. The toxicological mechanisms of H.akashiwo blooms are complex and to date, heavily debated. One putative type of ichthyotoxin includes the production of reactive oxygen species (ROS) that could alter gill structure and function, resulting in asphyxiation. In this study, we investigated the potential of H.akashiwo to produce extracellular hydrogen peroxide, and have investigated which cellular processes are responsible for this production. Within all experiments, H.akashiwo produced substantial amounts of hydrogen peroxide (up to 7.6 pmol min–1 104 cells–1), resulting in extracellular concentrations of ~0.5 μmol l–1 H2O2. Measured rates of hydrogen peroxide production were directly proportional to cell density, but at higher cell densities, accuracy of H2O2 detection was reduced. Whereas light intensity did not alter H2O2 production, rates of production were stimulated when temperature was elevated. Hydrogen peroxide production was not only dependent on growth phase, but also was regulated by the availability of iron in the medium. Reduction of total iron to 1 nmol l–1 enhanced the production of H2O2 relative to iron replete conditions (10 μmol l–1 iron). From this, we collectively conclude that production of extracellular H2O2 by H.akashiwo occurs through a metabolic pathway that is not directly linked to photosynthesis.</description><subject>Animal and plant ecology</subject><subject>Animal, plant and microbial ecology</subject><subject>Aquaculture</subject><subject>Autoecology</subject><subject>Biological and medical sciences</subject><subject>Blooms</subject><subject>Cell density</subject><subject>Extracellular</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Heterosigma akashiwo</subject><subject>Hydrogen</subject><subject>Hydrogen peroxide</subject><subject>Iron</subject><subject>Light intensity</subject><subject>Marine</subject><subject>Metabolic pathways</subject><subject>Noxious organisms</subject><subject>Photosynthesis</subject><subject>Phytoplankton</subject><subject>Plants and fungi</subject><subject>Raphidophyceae</subject><subject>Reactive oxygen species</subject><subject>Red tides</subject><subject>Structure-function relationships</subject><issn>0142-7873</issn><issn>1464-3774</issn><issn>1464-3774</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><recordid>eNpdkU9r3DAQxUVoodttPkBvIoTcnOifpfUxhGa3JaQ5JCHkIrTyeK2sbbmSlsbfvtpuaKAgELz5vWFmHkJfKTmnpOIXY2eGbbpg7HyvVJIeoRkVUhRcKfEBzQgVrFALxT-hzzG-EEJlrs7QdOdjdOsO8NhO0fnOb5w1He7BtmZwsY-48QGPwdc7m5wfsG9wO9XBb2DAIwT_6mrA6wmnFrCzbWonn7JocdOZDXSdSYBXkDIZ3aY32GxNbN1v_wV9bEwX4fjtn6OH62_3V6vi5ufy-9XlTWGFUqmQnFtr1oLWikFWSM1KC7yqjZK2yq80lNGmLA2jsOAMJF2IuqwIcCup4nyOzg598w6_dhCT7l20-8EG8LuoqVJclJmco5P_wBe_C0OeTTNGWEmZkBmiB8jmfWKARo_B9SZMmhK9T0IfksiWv0pOIntO3xqbmG_bBDNYF9-NopJS7LHigLmY4PVf2YStloqrUq-envXy9ml5-4Os9CP_A37knBk</recordid><startdate>20001001</startdate><enddate>20001001</enddate><creator>Twiner, Michael J.</creator><creator>Trick, Charles G.</creator><general>Oxford University Press</general><general>Oxford Publishing Limited (England)</general><scope>BSCLL</scope><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QG</scope><scope>7SN</scope><scope>C1K</scope><scope>F1W</scope><scope>H95</scope><scope>L.G</scope><scope>M7N</scope><scope>7TN</scope><scope>H97</scope><scope>H98</scope></search><sort><creationdate>20001001</creationdate><title>Possible physiological mechanisms for production of hydrogen peroxide by the ichthyotoxic flagellate Heterosigma akashiwo</title><author>Twiner, Michael J. ; Trick, Charles G.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c477t-633ccab41d72e4770d25ce39da76c96c95a121f55a21e832e6184d590e3c61733</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Animal and plant ecology</topic><topic>Animal, plant and microbial ecology</topic><topic>Aquaculture</topic><topic>Autoecology</topic><topic>Biological and medical sciences</topic><topic>Blooms</topic><topic>Cell density</topic><topic>Extracellular</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Heterosigma akashiwo</topic><topic>Hydrogen</topic><topic>Hydrogen peroxide</topic><topic>Iron</topic><topic>Light intensity</topic><topic>Marine</topic><topic>Metabolic pathways</topic><topic>Noxious organisms</topic><topic>Photosynthesis</topic><topic>Phytoplankton</topic><topic>Plants and fungi</topic><topic>Raphidophyceae</topic><topic>Reactive oxygen species</topic><topic>Red tides</topic><topic>Structure-function relationships</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Twiner, Michael J.</creatorcontrib><creatorcontrib>Trick, Charles G.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Animal Behavior Abstracts</collection><collection>Ecology Abstracts</collection><collection>Environmental Sciences and Pollution Management</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>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Oceanic Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 3: Aquatic Pollution & Environmental Quality</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Aquaculture Abstracts</collection><jtitle>Journal of plankton research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Twiner, Michael J.</au><au>Trick, Charles G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Possible physiological mechanisms for production of hydrogen peroxide by the ichthyotoxic flagellate Heterosigma akashiwo</atitle><jtitle>Journal of plankton research</jtitle><addtitle>J. Plankton Res</addtitle><date>2000-10-01</date><risdate>2000</risdate><volume>22</volume><issue>10</issue><spage>1961</spage><epage>1975</epage><pages>1961-1975</pages><issn>0142-7873</issn><issn>1464-3774</issn><eissn>1464-3774</eissn><coden>JPLRD9</coden><abstract>Blooms of the toxic red tide phytoplankton Heterosigma akashiwo (Raphidophyceae) are responsible for substantial losses within the aquaculture industry. The toxicological mechanisms of H.akashiwo blooms are complex and to date, heavily debated. One putative type of ichthyotoxin includes the production of reactive oxygen species (ROS) that could alter gill structure and function, resulting in asphyxiation. In this study, we investigated the potential of H.akashiwo to produce extracellular hydrogen peroxide, and have investigated which cellular processes are responsible for this production. Within all experiments, H.akashiwo produced substantial amounts of hydrogen peroxide (up to 7.6 pmol min–1 104 cells–1), resulting in extracellular concentrations of ~0.5 μmol l–1 H2O2. Measured rates of hydrogen peroxide production were directly proportional to cell density, but at higher cell densities, accuracy of H2O2 detection was reduced. Whereas light intensity did not alter H2O2 production, rates of production were stimulated when temperature was elevated. Hydrogen peroxide production was not only dependent on growth phase, but also was regulated by the availability of iron in the medium. Reduction of total iron to 1 nmol l–1 enhanced the production of H2O2 relative to iron replete conditions (10 μmol l–1 iron). From this, we collectively conclude that production of extracellular H2O2 by H.akashiwo occurs through a metabolic pathway that is not directly linked to photosynthesis.</abstract><cop>Oxford</cop><pub>Oxford University Press</pub><doi>10.1093/plankt/22.10.1961</doi><tpages>15</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animal and plant ecology Animal, plant and microbial ecology Aquaculture Autoecology Biological and medical sciences Blooms Cell density Extracellular Fundamental and applied biological sciences. Psychology Heterosigma akashiwo Hydrogen Hydrogen peroxide Iron Light intensity Marine Metabolic pathways Noxious organisms Photosynthesis Phytoplankton Plants and fungi Raphidophyceae Reactive oxygen species Red tides Structure-function relationships |
title | Possible physiological mechanisms for production of hydrogen peroxide by the ichthyotoxic flagellate Heterosigma akashiwo |
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