Timing of molecular events following elicitor treatment of plant cells
Extracellular products with elicitor activity from the bean pathogen Colletotrichum lindemuthianum induced a multiplicity of changes in bean suspension cells. An immediate increase in luminol-mediated chemiluminescence which peaked within 30 min indicated production of activated oxygen species. Shut...
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Veröffentlicht in: | Physiological and molecular plant pathology 1991, Vol.38 (1), p.1-13 |
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creator | Anderson, Anne J. Rogers, Kim Tepper, Craig S. Blee, Kris Cardon, Jeff |
description | Extracellular products with elicitor activity from the bean pathogen
Colletotrichum lindemuthianum induced a multiplicity of changes in bean suspension cells. An immediate increase in luminol-mediated chemiluminescence which peaked within 30 min indicated production of activated oxygen species. Shut down of synthesis of discrete proteins and enhanced synthesis of other proteins was apparent by 3 h. These differences in protein profiles between elicitor-treated and control cells were more pronounced by 6 h. Other changes at 4–6 h involved perturbations in membrane functions including lipid peroxidation, altered proton efflux and uptake of a vital stain, fluorescein diacetate as well as reduced activity of the extracellular enzymes peroxidase and β glucosidase. These changes coincide with an increase in electron paramagnetic resonance signal consistent with free radical accumulation. The accumulation of phytoalexins at 6–8 h after treatment suggests that phytoalexins do not account for either free radicals detected earlier by the electron paramagnetic resonance signals or altered plant membrane function. Our data suggest that altered protein expression may be triggered by free radicals connected to activated oxygen metabolism. |
doi_str_mv | 10.1016/S0885-5765(05)80139-0 |
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Colletotrichum lindemuthianum induced a multiplicity of changes in bean suspension cells. An immediate increase in luminol-mediated chemiluminescence which peaked within 30 min indicated production of activated oxygen species. Shut down of synthesis of discrete proteins and enhanced synthesis of other proteins was apparent by 3 h. These differences in protein profiles between elicitor-treated and control cells were more pronounced by 6 h. Other changes at 4–6 h involved perturbations in membrane functions including lipid peroxidation, altered proton efflux and uptake of a vital stain, fluorescein diacetate as well as reduced activity of the extracellular enzymes peroxidase and β glucosidase. These changes coincide with an increase in electron paramagnetic resonance signal consistent with free radical accumulation. The accumulation of phytoalexins at 6–8 h after treatment suggests that phytoalexins do not account for either free radicals detected earlier by the electron paramagnetic resonance signals or altered plant membrane function. Our data suggest that altered protein expression may be triggered by free radicals connected to activated oxygen metabolism.</description><identifier>ISSN: 0885-5765</identifier><identifier>EISSN: 1096-1178</identifier><identifier>DOI: 10.1016/S0885-5765(05)80139-0</identifier><identifier>CODEN: PMPPEZ</identifier><language>eng</language><publisher>London: Elsevier India Pvt Ltd</publisher><subject>Agronomy. Soil science and plant productions ; Biological and medical sciences ; Fundamental and applied biological sciences. Psychology ; Fungal plant pathogens ; Pathology, epidemiology, host-fungus relationships. Damages, economic importance ; Phaseolus vulgaris ; Phytopathology. Animal pests. Plant and forest protection</subject><ispartof>Physiological and molecular plant pathology, 1991, Vol.38 (1), p.1-13</ispartof><rights>1991 Academic Press Limited</rights><rights>1992 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c367t-db02b60d311d54990d73313d5c37272412feb1ac839ea7550d07694fd77536a03</citedby><cites>FETCH-LOGICAL-c367t-db02b60d311d54990d73313d5c37272412feb1ac839ea7550d07694fd77536a03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/S0885-5765(05)80139-0$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,4024,27923,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=5268894$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Anderson, Anne J.</creatorcontrib><creatorcontrib>Rogers, Kim</creatorcontrib><creatorcontrib>Tepper, Craig S.</creatorcontrib><creatorcontrib>Blee, Kris</creatorcontrib><creatorcontrib>Cardon, Jeff</creatorcontrib><title>Timing of molecular events following elicitor treatment of plant cells</title><title>Physiological and molecular plant pathology</title><description>Extracellular products with elicitor activity from the bean pathogen
Colletotrichum lindemuthianum induced a multiplicity of changes in bean suspension cells. An immediate increase in luminol-mediated chemiluminescence which peaked within 30 min indicated production of activated oxygen species. Shut down of synthesis of discrete proteins and enhanced synthesis of other proteins was apparent by 3 h. These differences in protein profiles between elicitor-treated and control cells were more pronounced by 6 h. Other changes at 4–6 h involved perturbations in membrane functions including lipid peroxidation, altered proton efflux and uptake of a vital stain, fluorescein diacetate as well as reduced activity of the extracellular enzymes peroxidase and β glucosidase. These changes coincide with an increase in electron paramagnetic resonance signal consistent with free radical accumulation. The accumulation of phytoalexins at 6–8 h after treatment suggests that phytoalexins do not account for either free radicals detected earlier by the electron paramagnetic resonance signals or altered plant membrane function. Our data suggest that altered protein expression may be triggered by free radicals connected to activated oxygen metabolism.</description><subject>Agronomy. Soil science and plant productions</subject><subject>Biological and medical sciences</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Fungal plant pathogens</subject><subject>Pathology, epidemiology, host-fungus relationships. Damages, economic importance</subject><subject>Phaseolus vulgaris</subject><subject>Phytopathology. Animal pests. 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Soil science and plant productions</topic><topic>Biological and medical sciences</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Fungal plant pathogens</topic><topic>Pathology, epidemiology, host-fungus relationships. Damages, economic importance</topic><topic>Phaseolus vulgaris</topic><topic>Phytopathology. Animal pests. Plant and forest protection</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Anderson, Anne J.</creatorcontrib><creatorcontrib>Rogers, Kim</creatorcontrib><creatorcontrib>Tepper, Craig S.</creatorcontrib><creatorcontrib>Blee, Kris</creatorcontrib><creatorcontrib>Cardon, Jeff</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</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><jtitle>Physiological and molecular plant pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Anderson, Anne J.</au><au>Rogers, Kim</au><au>Tepper, Craig S.</au><au>Blee, Kris</au><au>Cardon, Jeff</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Timing of molecular events following elicitor treatment of plant cells</atitle><jtitle>Physiological and molecular plant pathology</jtitle><date>1991</date><risdate>1991</risdate><volume>38</volume><issue>1</issue><spage>1</spage><epage>13</epage><pages>1-13</pages><issn>0885-5765</issn><eissn>1096-1178</eissn><coden>PMPPEZ</coden><abstract>Extracellular products with elicitor activity from the bean pathogen
Colletotrichum lindemuthianum induced a multiplicity of changes in bean suspension cells. An immediate increase in luminol-mediated chemiluminescence which peaked within 30 min indicated production of activated oxygen species. Shut down of synthesis of discrete proteins and enhanced synthesis of other proteins was apparent by 3 h. These differences in protein profiles between elicitor-treated and control cells were more pronounced by 6 h. Other changes at 4–6 h involved perturbations in membrane functions including lipid peroxidation, altered proton efflux and uptake of a vital stain, fluorescein diacetate as well as reduced activity of the extracellular enzymes peroxidase and β glucosidase. These changes coincide with an increase in electron paramagnetic resonance signal consistent with free radical accumulation. The accumulation of phytoalexins at 6–8 h after treatment suggests that phytoalexins do not account for either free radicals detected earlier by the electron paramagnetic resonance signals or altered plant membrane function. Our data suggest that altered protein expression may be triggered by free radicals connected to activated oxygen metabolism.</abstract><cop>London</cop><pub>Elsevier India Pvt Ltd</pub><doi>10.1016/S0885-5765(05)80139-0</doi><tpages>13</tpages></addata></record> |
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subjects | Agronomy. Soil science and plant productions Biological and medical sciences Fundamental and applied biological sciences. Psychology Fungal plant pathogens Pathology, epidemiology, host-fungus relationships. Damages, economic importance Phaseolus vulgaris Phytopathology. Animal pests. Plant and forest protection |
title | Timing of molecular events following elicitor treatment of plant cells |
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