Physiological stabilization of Euglena gracilis cells by high extracellular calcium (100 mM)
Experiments were performed to test whether or not high concentrations of CaCl2 (100 mM) are able to arrest and stabilize internal structures and associated functions in Euglena gracilis Z cells stored in darkness at 4 degrees C. Storage of photoheterotrophically grown green cells in high Ca2+ media...
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Veröffentlicht in: | Applied microbiology and biotechnology 1989-12, Vol.32 (2), p.211-217 |
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creator | Tamponnet, C Barbotin, J.N Calvayrac, R |
description | Experiments were performed to test whether or not high concentrations of CaCl2 (100 mM) are able to arrest and stabilize internal structures and associated functions in Euglena gracilis Z cells stored in darkness at 4 degrees C. Storage of photoheterotrophically grown green cells in high Ca2+ media (2-100 mM) retards pheophytinization of the chlorophylls, preserves photosynthetic activities and stabilizes the structural organization of the associated light-harvesting complexes of the photosystem II units. Alterations of photosynthesis and respiration by chlorpromazine or by temperature are strongly reduced in cells stored under such conditions. More precisely, a chlorpromazine inhibition site is evidenced in the mitochondrial electron pathway and its location in the chloroplastic electron pathway is clarified. Adaptation of Euglena cells from 2 mM to 100 mM Ca2+ medium is accompanied by an increase both in the externally bound and total internal calcium concentration. A mechanism involving a Ca2+ deposit on internal membranes is proposed. Such interpretation is extended to the storage of cells immobilized in Ca2+-alginate gel. |
doi_str_mv | 10.1007/BF00165890 |
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Storage of photoheterotrophically grown green cells in high Ca2+ media (2-100 mM) retards pheophytinization of the chlorophylls, preserves photosynthetic activities and stabilizes the structural organization of the associated light-harvesting complexes of the photosystem II units. Alterations of photosynthesis and respiration by chlorpromazine or by temperature are strongly reduced in cells stored under such conditions. More precisely, a chlorpromazine inhibition site is evidenced in the mitochondrial electron pathway and its location in the chloroplastic electron pathway is clarified. Adaptation of Euglena cells from 2 mM to 100 mM Ca2+ medium is accompanied by an increase both in the externally bound and total internal calcium concentration. A mechanism involving a Ca2+ deposit on internal membranes is proposed. Such interpretation is extended to the storage of cells immobilized in Ca2+-alginate gel.</description><identifier>ISSN: 0175-7598</identifier><identifier>EISSN: 1432-0614</identifier><identifier>DOI: 10.1007/BF00165890</identifier><identifier>CODEN: AMBIDG</identifier><language>eng</language><publisher>Berlin: Springer</publisher><subject>Biological and medical sciences ; calcium ; Cell physiology ; Euglena gracilis ; extracellular spaces ; Freshwater ; Fundamental and applied biological sciences. Psychology ; immobilization ; immobilized cells ; light-harvesting proteins ; photosynthesis ; Plant physiology and development ; Plasma membrane and permeation ; respiration ; stabilization</subject><ispartof>Applied microbiology and biotechnology, 1989-12, Vol.32 (2), p.211-217</ispartof><rights>1990 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c313t-545dedfd755f6427d711194cd9cd0b5b89cabe4a97c521462d6ed55a28b24beb3</citedby><cites>FETCH-LOGICAL-c313t-545dedfd755f6427d711194cd9cd0b5b89cabe4a97c521462d6ed55a28b24beb3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=6655790$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Tamponnet, C</creatorcontrib><creatorcontrib>Barbotin, J.N</creatorcontrib><creatorcontrib>Calvayrac, R</creatorcontrib><title>Physiological stabilization of Euglena gracilis cells by high extracellular calcium (100 mM)</title><title>Applied microbiology and biotechnology</title><description>Experiments were performed to test whether or not high concentrations of CaCl2 (100 mM) are able to arrest and stabilize internal structures and associated functions in Euglena gracilis Z cells stored in darkness at 4 degrees C. Storage of photoheterotrophically grown green cells in high Ca2+ media (2-100 mM) retards pheophytinization of the chlorophylls, preserves photosynthetic activities and stabilizes the structural organization of the associated light-harvesting complexes of the photosystem II units. Alterations of photosynthesis and respiration by chlorpromazine or by temperature are strongly reduced in cells stored under such conditions. More precisely, a chlorpromazine inhibition site is evidenced in the mitochondrial electron pathway and its location in the chloroplastic electron pathway is clarified. Adaptation of Euglena cells from 2 mM to 100 mM Ca2+ medium is accompanied by an increase both in the externally bound and total internal calcium concentration. A mechanism involving a Ca2+ deposit on internal membranes is proposed. Such interpretation is extended to the storage of cells immobilized in Ca2+-alginate gel.</description><subject>Biological and medical sciences</subject><subject>calcium</subject><subject>Cell physiology</subject><subject>Euglena gracilis</subject><subject>extracellular spaces</subject><subject>Freshwater</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>immobilization</subject><subject>immobilized cells</subject><subject>light-harvesting proteins</subject><subject>photosynthesis</subject><subject>Plant physiology and development</subject><subject>Plasma membrane and permeation</subject><subject>respiration</subject><subject>stabilization</subject><issn>0175-7598</issn><issn>1432-0614</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1989</creationdate><recordtype>article</recordtype><recordid>eNpFkF9LwzAUxYMoOKcvfgHzIKJCNf_TPurYVJgo6N6EkqZpF0lbTVpwfnozN_Tpwj2_ezj3AHCM0RVGSF7fzhDCgqcZ2gEjzChJkMBsF4wQljyRPEv3wUEI75EiqRAj8Pa8XAXbua62WjkYelVYZ79Vb7sWdhWcDrUzrYK1VzoKAWrjXIDFCi5tvYTmq49CXA1OeRgdtB0aeB6zwObx4hDsVcoFc7SdY7CYTV8n98n86e5hcjNPNMW0TzjjpSmrUnJeCUZkKTHGGdNlpktU8CLNtCoMU5nUnGAmSClMybkiaUFYYQo6Bmcb3w_ffQ4m9HljwzqVak03hBxzJmlKeQQvN6D2XQjeVPmHt43yqxyjfF1g_l9ghE-3rirEzyqvWm3D34UQnMtf7GSDVarLVe0jsnghCFNERIppKugPgq94lw</recordid><startdate>19891201</startdate><enddate>19891201</enddate><creator>Tamponnet, C</creator><creator>Barbotin, J.N</creator><creator>Calvayrac, R</creator><general>Springer</general><scope>FBQ</scope><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>8FD</scope><scope>F1W</scope><scope>FR3</scope><scope>H95</scope><scope>H99</scope><scope>L.F</scope><scope>L.G</scope><scope>M7N</scope><scope>P64</scope></search><sort><creationdate>19891201</creationdate><title>Physiological stabilization of Euglena gracilis cells by high extracellular calcium (100 mM)</title><author>Tamponnet, C ; Barbotin, J.N ; Calvayrac, R</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c313t-545dedfd755f6427d711194cd9cd0b5b89cabe4a97c521462d6ed55a28b24beb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1989</creationdate><topic>Biological and medical sciences</topic><topic>calcium</topic><topic>Cell physiology</topic><topic>Euglena gracilis</topic><topic>extracellular spaces</topic><topic>Freshwater</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>immobilization</topic><topic>immobilized cells</topic><topic>light-harvesting proteins</topic><topic>photosynthesis</topic><topic>Plant physiology and development</topic><topic>Plasma membrane and permeation</topic><topic>respiration</topic><topic>stabilization</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tamponnet, C</creatorcontrib><creatorcontrib>Barbotin, J.N</creatorcontrib><creatorcontrib>Calvayrac, R</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Engineering Research Database</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources</collection><collection>ASFA: Marine Biotechnology Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Marine Biotechnology Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Applied microbiology and biotechnology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tamponnet, C</au><au>Barbotin, J.N</au><au>Calvayrac, R</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Physiological stabilization of Euglena gracilis cells by high extracellular calcium (100 mM)</atitle><jtitle>Applied microbiology and biotechnology</jtitle><date>1989-12-01</date><risdate>1989</risdate><volume>32</volume><issue>2</issue><spage>211</spage><epage>217</epage><pages>211-217</pages><issn>0175-7598</issn><eissn>1432-0614</eissn><coden>AMBIDG</coden><abstract>Experiments were performed to test whether or not high concentrations of CaCl2 (100 mM) are able to arrest and stabilize internal structures and associated functions in Euglena gracilis Z cells stored in darkness at 4 degrees C. Storage of photoheterotrophically grown green cells in high Ca2+ media (2-100 mM) retards pheophytinization of the chlorophylls, preserves photosynthetic activities and stabilizes the structural organization of the associated light-harvesting complexes of the photosystem II units. Alterations of photosynthesis and respiration by chlorpromazine or by temperature are strongly reduced in cells stored under such conditions. More precisely, a chlorpromazine inhibition site is evidenced in the mitochondrial electron pathway and its location in the chloroplastic electron pathway is clarified. Adaptation of Euglena cells from 2 mM to 100 mM Ca2+ medium is accompanied by an increase both in the externally bound and total internal calcium concentration. A mechanism involving a Ca2+ deposit on internal membranes is proposed. Such interpretation is extended to the storage of cells immobilized in Ca2+-alginate gel.</abstract><cop>Berlin</cop><pub>Springer</pub><doi>10.1007/BF00165890</doi><tpages>7</tpages></addata></record> |
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subjects | Biological and medical sciences calcium Cell physiology Euglena gracilis extracellular spaces Freshwater Fundamental and applied biological sciences. Psychology immobilization immobilized cells light-harvesting proteins photosynthesis Plant physiology and development Plasma membrane and permeation respiration stabilization |
title | Physiological stabilization of Euglena gracilis cells by high extracellular calcium (100 mM) |
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