Rapid activation of phenylpropanoid metabolism in elicitor-treated hybrid poplar (Populus trichocarpa Torr. & Gray X Populus deltoides Marsh) suspension-cultured cells

Elicitor induction of phenylpropanoid metabolism was investigated in suspension-cultured cells of the fast-growing poplar hybrid (Populus trichocarpa Torr. & Gray X Populus deltoides Marsh) H11-11. Treatment of cells with polygalacturonic acid lyase or two fungal elicitors resulted in rapid and...

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Veröffentlicht in:Plant physiology (Bethesda) 1992-02, Vol.98 (2), p.728-737
Hauptverfasser: De Sa, M.M, Subramaniam, R, Williams, F.E, Douglas, C.J
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Subramaniam, R
Williams, F.E
Douglas, C.J
description Elicitor induction of phenylpropanoid metabolism was investigated in suspension-cultured cells of the fast-growing poplar hybrid (Populus trichocarpa Torr. & Gray X Populus deltoides Marsh) H11-11. Treatment of cells with polygalacturonic acid lyase or two fungal elicitors resulted in rapid and transient increases in extractable L-phenylalanine ammonia lyase and 4-coumarate:coenzyme A ligase enzyme activities. The substrate specificity of the inducible 4-coumarate:coenzyme A ligase enzyme activity appeared to differ from substrate specificity of 4-coumarate:coenzyme A ligase enzyme activity in untreated control cells. Large and transient increases in the accumulation of L-phenylalanine ammonia-lyase and 4-coumarate:coenzyme A ligase mRNAs preceded the increases in enzyme activities and were detectable by 30 minutes after the start of elicitor treatment. Chalcone synthase, cinnamyl alcohol dehydrogenase, and coniferin beta-glucosidase enzyme activities were unaffected by the elicitors, but a large and transient increase in beta-glucosidase activity capable of hydrolyzing 4-nitrophenyl-beta-glucoside was observed. Subsequent to increases in L-phenylalanine ammonia-lyase and 4-coumarate:coenzyme A ligase enzyme activities, cell wall-bound thioglycolic acid-extractable compounds accumulated in elicitor-treated cultures, and these cells exhibited strong staining with phloroglucinol, suggesting the accumulation of wall-bound phenolic compounds.
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Treatment of cells with polygalacturonic acid lyase or two fungal elicitors resulted in rapid and transient increases in extractable L-phenylalanine ammonia lyase and 4-coumarate:coenzyme A ligase enzyme activities. The substrate specificity of the inducible 4-coumarate:coenzyme A ligase enzyme activity appeared to differ from substrate specificity of 4-coumarate:coenzyme A ligase enzyme activity in untreated control cells. Large and transient increases in the accumulation of L-phenylalanine ammonia-lyase and 4-coumarate:coenzyme A ligase mRNAs preceded the increases in enzyme activities and were detectable by 30 minutes after the start of elicitor treatment. Chalcone synthase, cinnamyl alcohol dehydrogenase, and coniferin beta-glucosidase enzyme activities were unaffected by the elicitors, but a large and transient increase in beta-glucosidase activity capable of hydrolyzing 4-nitrophenyl-beta-glucoside was observed. Subsequent to increases in L-phenylalanine ammonia-lyase and 4-coumarate:coenzyme A ligase enzyme activities, cell wall-bound thioglycolic acid-extractable compounds accumulated in elicitor-treated cultures, and these cells exhibited strong staining with phloroglucinol, suggesting the accumulation of wall-bound phenolic compounds.</description><identifier>ISSN: 0032-0889</identifier><identifier>EISSN: 1532-2548</identifier><identifier>DOI: 10.1104/pp.98.2.728</identifier><identifier>PMID: 16668702</identifier><identifier>CODEN: PPHYA5</identifier><language>eng</language><publisher>Rockville, MD: American Society of Plant Physiologists</publisher><subject>ACIDE PROPIONIQUE ; ACIDO PROPIONICO ; AGENT PATHOGENE ; Agronomy. 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Treatment of cells with polygalacturonic acid lyase or two fungal elicitors resulted in rapid and transient increases in extractable L-phenylalanine ammonia lyase and 4-coumarate:coenzyme A ligase enzyme activities. The substrate specificity of the inducible 4-coumarate:coenzyme A ligase enzyme activity appeared to differ from substrate specificity of 4-coumarate:coenzyme A ligase enzyme activity in untreated control cells. Large and transient increases in the accumulation of L-phenylalanine ammonia-lyase and 4-coumarate:coenzyme A ligase mRNAs preceded the increases in enzyme activities and were detectable by 30 minutes after the start of elicitor treatment. Chalcone synthase, cinnamyl alcohol dehydrogenase, and coniferin beta-glucosidase enzyme activities were unaffected by the elicitors, but a large and transient increase in beta-glucosidase activity capable of hydrolyzing 4-nitrophenyl-beta-glucoside was observed. Subsequent to increases in L-phenylalanine ammonia-lyase and 4-coumarate:coenzyme A ligase enzyme activities, cell wall-bound thioglycolic acid-extractable compounds accumulated in elicitor-treated cultures, and these cells exhibited strong staining with phloroglucinol, suggesting the accumulation of wall-bound phenolic compounds.</description><subject>ACIDE PROPIONIQUE</subject><subject>ACIDO PROPIONICO</subject><subject>AGENT PATHOGENE</subject><subject>Agronomy. Soil science and plant productions</subject><subject>Biological and medical sciences</subject><subject>CAL</subject><subject>CALLO</subject><subject>callus</subject><subject>Cell culture techniques</subject><subject>cell suspension culture</subject><subject>Cell walls</subject><subject>Cellular metabolism</subject><subject>COMPOSE PHENOLIQUE</subject><subject>COMPUESTOS FENOLICOS</subject><subject>CULTIVO DE CELULAS</subject><subject>CULTURE DE CELLULE</subject><subject>Cultured cells</subject><subject>derivatives</subject><subject>Enzyme activity</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Genetics and breeding of economic plants</subject><subject>HIBRIDOS</subject><subject>HYBRIDE</subject><subject>hybrids</subject><subject>induced resistance</subject><subject>Lignin</subject><subject>metabolism</subject><subject>METABOLISME</subject><subject>METABOLISMO</subject><subject>ORGANISMOS PATOGENOS</subject><subject>Parsley</subject><subject>Pest resistance</subject><subject>phenolic compounds</subject><subject>Plant cells</subject><subject>Plant pathogens</subject><subject>Plants</subject><subject>Populus balsamifera subsp. trichocarpa</subject><subject>POPULUS DELTOIDES</subject><subject>POPULUS TRICHOCARPA</subject><subject>propionic acid</subject><subject>RESISTANCE INDUITE</subject><subject>RESISTENCIA INDUCIDA</subject><subject>RNA</subject><subject>Varietal selection. Specialized plant breeding, plant breeding aims</subject><issn>0032-0889</issn><issn>1532-2548</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1992</creationdate><recordtype>article</recordtype><recordid>eNplkk-L1TAUxYsoznN05U5EsxD_IK1JmrTpUgYdhRFFZ8BduU1TX4a0iUkqvE_k1_Q-3nNcuErI-XHuzT23KB4yWjFGxZsQqk5VvGq5ulVsmKx5yaVQt4sNpXinSnUnxb2UrimlrGbibnHCmqZRLeWb4vdXCHYkoLP9Bdn6hfiJhK1Zdi5EH2DxqM4mw-CdTTOxCzHOapt9LHM0kM1ItrshIhV8cBDJyy8-rG5NJEert15DDEAufYwVeU7OI-zId_IXGY3LWMAk8gli2r4iaU3BLAn7KPXq8hrRXhvn0v3izgQumQfH87S4ev_u8uxDefH5_OPZ24tSC8lyOXA1MKCt4EPTGjqK2igYm4mZlk3dIEY51ZQaKsWoOD5w3oxNI1Hmk9CsqU-LFwdf_P3P1aTczzbtO4DF-DX1bV2LrsX5Ivn6QOroU4pm6kO0M8Rdz2i_D6YPoe9Uz3sMBuknR991mM34jz0mgcCzIwBJg5siLNqmG05yKRvBEHt8wK4TRnAjC94KJvcujw7yBL6HHxEdrr51TCkEUHz6v8hxJyhrJU6C1X8AFXWzzA</recordid><startdate>19920201</startdate><enddate>19920201</enddate><creator>De Sa, M.M</creator><creator>Subramaniam, R</creator><creator>Williams, F.E</creator><creator>Douglas, C.J</creator><general>American Society of Plant Physiologists</general><scope>FBQ</scope><scope>IQODW</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>19920201</creationdate><title>Rapid activation of phenylpropanoid metabolism in elicitor-treated hybrid poplar (Populus trichocarpa Torr. &amp; Gray X Populus deltoides Marsh) suspension-cultured cells</title><author>De Sa, M.M ; Subramaniam, R ; Williams, F.E ; Douglas, C.J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c451t-b28b1a0742b67e0d43e8ad6f1e71f9b4d5f300e054d82f9b226d6651e72f4c163</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1992</creationdate><topic>ACIDE PROPIONIQUE</topic><topic>ACIDO PROPIONICO</topic><topic>AGENT PATHOGENE</topic><topic>Agronomy. Soil science and plant productions</topic><topic>Biological and medical sciences</topic><topic>CAL</topic><topic>CALLO</topic><topic>callus</topic><topic>Cell culture techniques</topic><topic>cell suspension culture</topic><topic>Cell walls</topic><topic>Cellular metabolism</topic><topic>COMPOSE PHENOLIQUE</topic><topic>COMPUESTOS FENOLICOS</topic><topic>CULTIVO DE CELULAS</topic><topic>CULTURE DE CELLULE</topic><topic>Cultured cells</topic><topic>derivatives</topic><topic>Enzyme activity</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Genetics and breeding of economic plants</topic><topic>HIBRIDOS</topic><topic>HYBRIDE</topic><topic>hybrids</topic><topic>induced resistance</topic><topic>Lignin</topic><topic>metabolism</topic><topic>METABOLISME</topic><topic>METABOLISMO</topic><topic>ORGANISMOS PATOGENOS</topic><topic>Parsley</topic><topic>Pest resistance</topic><topic>phenolic compounds</topic><topic>Plant cells</topic><topic>Plant pathogens</topic><topic>Plants</topic><topic>Populus balsamifera subsp. trichocarpa</topic><topic>POPULUS DELTOIDES</topic><topic>POPULUS TRICHOCARPA</topic><topic>propionic acid</topic><topic>RESISTANCE INDUITE</topic><topic>RESISTENCIA INDUCIDA</topic><topic>RNA</topic><topic>Varietal selection. Specialized plant breeding, plant breeding aims</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>De Sa, M.M</creatorcontrib><creatorcontrib>Subramaniam, R</creatorcontrib><creatorcontrib>Williams, F.E</creatorcontrib><creatorcontrib>Douglas, C.J</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Plant physiology (Bethesda)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>De Sa, M.M</au><au>Subramaniam, R</au><au>Williams, F.E</au><au>Douglas, C.J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Rapid activation of phenylpropanoid metabolism in elicitor-treated hybrid poplar (Populus trichocarpa Torr. &amp; Gray X Populus deltoides Marsh) suspension-cultured cells</atitle><jtitle>Plant physiology (Bethesda)</jtitle><addtitle>Plant Physiol</addtitle><date>1992-02-01</date><risdate>1992</risdate><volume>98</volume><issue>2</issue><spage>728</spage><epage>737</epage><pages>728-737</pages><issn>0032-0889</issn><eissn>1532-2548</eissn><coden>PPHYA5</coden><abstract>Elicitor induction of phenylpropanoid metabolism was investigated in suspension-cultured cells of the fast-growing poplar hybrid (Populus trichocarpa Torr. &amp; Gray X Populus deltoides Marsh) H11-11. Treatment of cells with polygalacturonic acid lyase or two fungal elicitors resulted in rapid and transient increases in extractable L-phenylalanine ammonia lyase and 4-coumarate:coenzyme A ligase enzyme activities. The substrate specificity of the inducible 4-coumarate:coenzyme A ligase enzyme activity appeared to differ from substrate specificity of 4-coumarate:coenzyme A ligase enzyme activity in untreated control cells. Large and transient increases in the accumulation of L-phenylalanine ammonia-lyase and 4-coumarate:coenzyme A ligase mRNAs preceded the increases in enzyme activities and were detectable by 30 minutes after the start of elicitor treatment. Chalcone synthase, cinnamyl alcohol dehydrogenase, and coniferin beta-glucosidase enzyme activities were unaffected by the elicitors, but a large and transient increase in beta-glucosidase activity capable of hydrolyzing 4-nitrophenyl-beta-glucoside was observed. Subsequent to increases in L-phenylalanine ammonia-lyase and 4-coumarate:coenzyme A ligase enzyme activities, cell wall-bound thioglycolic acid-extractable compounds accumulated in elicitor-treated cultures, and these cells exhibited strong staining with phloroglucinol, suggesting the accumulation of wall-bound phenolic compounds.</abstract><cop>Rockville, MD</cop><pub>American Society of Plant Physiologists</pub><pmid>16668702</pmid><doi>10.1104/pp.98.2.728</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record>
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ispartof Plant physiology (Bethesda), 1992-02, Vol.98 (2), p.728-737
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source JSTOR Archive Collection A-Z Listing; EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection
subjects ACIDE PROPIONIQUE
ACIDO PROPIONICO
AGENT PATHOGENE
Agronomy. Soil science and plant productions
Biological and medical sciences
CAL
CALLO
callus
Cell culture techniques
cell suspension culture
Cell walls
Cellular metabolism
COMPOSE PHENOLIQUE
COMPUESTOS FENOLICOS
CULTIVO DE CELULAS
CULTURE DE CELLULE
Cultured cells
derivatives
Enzyme activity
Fundamental and applied biological sciences. Psychology
Genetics and breeding of economic plants
HIBRIDOS
HYBRIDE
hybrids
induced resistance
Lignin
metabolism
METABOLISME
METABOLISMO
ORGANISMOS PATOGENOS
Parsley
Pest resistance
phenolic compounds
Plant cells
Plant pathogens
Plants
Populus balsamifera subsp. trichocarpa
POPULUS DELTOIDES
POPULUS TRICHOCARPA
propionic acid
RESISTANCE INDUITE
RESISTENCIA INDUCIDA
RNA
Varietal selection. Specialized plant breeding, plant breeding aims
title Rapid activation of phenylpropanoid metabolism in elicitor-treated hybrid poplar (Populus trichocarpa Torr. & Gray X Populus deltoides Marsh) suspension-cultured cells
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