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Light versus Dark Carbon Metabolism in Cherry Tomato Fruits: II. Relationship between Malate Metabolism and Photosynthetic Activity
The possible relationship between malate metabolism and photosynthetic activity in green tomato fruit tissues (Lycopersicum esculentum var. cerasiforme Dun A. Gray) was investigated. Initial experiments consisted of vacuum-infiltrating 14C-3 or 14C-4-malate into isolated tissues in darkness and then...
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Published in: | Plant physiology (Bethesda) 1977-12, Vol.60 (6), p.877-880 |
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description | The possible relationship between malate metabolism and photosynthetic activity in green tomato fruit tissues (Lycopersicum esculentum var. cerasiforme Dun A. Gray) was investigated. Initial experiments consisted of vacuum-infiltrating 14C-3 or 14C-4-malate into isolated tissues in darkness and then incubating the tissues under photosynthetic conditions. Other experiments involved a short pulse with 14C-bicarbonate in darkness to label the malate pool(s), followed by a chase in the light in the presence of nonradioactive bicarbonate. Both series of experiments were followed by the separation and identification of labeled metabolic intermediates. Label initially in carbon atoms 3 and 4 of malate, corresponding also to C-3 of pyruvate and CO2 after malate decarboxylation, was recovered as citrate + isocitrate, sugars and starch following incubations of tissues in the light. These data demonstrate that the reductive pentose phosphate cycle utilizes CO2 furnished by malate metabolism due to the operation of the citric acid cycle and perhaps also to malic enzyme activity. Some synthesis of sugars and starch from C-3 of malate was observed in darkness or in the light 3-(3,4-dichlorophenyl)-1,1-dimethyl which could be due to gluconeogenesis. Pulse-chase experiments indicated a rapidly turning over malate pool. |
doi_str_mv | 10.1104/pp.60.6.877 |
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Relationship between Malate Metabolism and Photosynthetic Activity</title><source>JSTOR Archival Journals and Primary Sources Collection</source><source>Alma/SFX Local Collection</source><creator>Farineau, J</creator><creatorcontrib>Farineau, J</creatorcontrib><description>The possible relationship between malate metabolism and photosynthetic activity in green tomato fruit tissues (Lycopersicum esculentum var. cerasiforme Dun A. Gray) was investigated. Initial experiments consisted of vacuum-infiltrating 14C-3 or 14C-4-malate into isolated tissues in darkness and then incubating the tissues under photosynthetic conditions. Other experiments involved a short pulse with 14C-bicarbonate in darkness to label the malate pool(s), followed by a chase in the light in the presence of nonradioactive bicarbonate. Both series of experiments were followed by the separation and identification of labeled metabolic intermediates. Label initially in carbon atoms 3 and 4 of malate, corresponding also to C-3 of pyruvate and CO2 after malate decarboxylation, was recovered as citrate + isocitrate, sugars and starch following incubations of tissues in the light. These data demonstrate that the reductive pentose phosphate cycle utilizes CO2 furnished by malate metabolism due to the operation of the citric acid cycle and perhaps also to malic enzyme activity. Some synthesis of sugars and starch from C-3 of malate was observed in darkness or in the light 3-(3,4-dichlorophenyl)-1,1-dimethyl which could be due to gluconeogenesis. Pulse-chase experiments indicated a rapidly turning over malate pool.</description><identifier>ISSN: 0032-0889</identifier><identifier>EISSN: 1532-2548</identifier><identifier>DOI: 10.1104/pp.60.6.877</identifier><identifier>PMID: 16660205</identifier><language>eng</language><publisher>United States: American Society of Plant Physiologists</publisher><subject>Bicarbonates ; Carbon dioxide ; Crassulacean acid metabolism ; Decarboxylation ; Enzymes ; Metabolism ; Plants ; Radioactive decay ; Starches ; Sugars</subject><ispartof>Plant physiology (Bethesda), 1977-12, Vol.60 (6), p.877-880</ispartof><rights>Copyright 1977 The American Society of Plant Physiologists</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/4265107$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/4265107$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,780,784,885,27924,27925,58238,58471</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16660205$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Farineau, J</creatorcontrib><title>Light versus Dark Carbon Metabolism in Cherry Tomato Fruits: II. Relationship between Malate Metabolism and Photosynthetic Activity</title><title>Plant physiology (Bethesda)</title><addtitle>Plant Physiol</addtitle><description>The possible relationship between malate metabolism and photosynthetic activity in green tomato fruit tissues (Lycopersicum esculentum var. cerasiforme Dun A. Gray) was investigated. Initial experiments consisted of vacuum-infiltrating 14C-3 or 14C-4-malate into isolated tissues in darkness and then incubating the tissues under photosynthetic conditions. Other experiments involved a short pulse with 14C-bicarbonate in darkness to label the malate pool(s), followed by a chase in the light in the presence of nonradioactive bicarbonate. Both series of experiments were followed by the separation and identification of labeled metabolic intermediates. Label initially in carbon atoms 3 and 4 of malate, corresponding also to C-3 of pyruvate and CO2 after malate decarboxylation, was recovered as citrate + isocitrate, sugars and starch following incubations of tissues in the light. These data demonstrate that the reductive pentose phosphate cycle utilizes CO2 furnished by malate metabolism due to the operation of the citric acid cycle and perhaps also to malic enzyme activity. Some synthesis of sugars and starch from C-3 of malate was observed in darkness or in the light 3-(3,4-dichlorophenyl)-1,1-dimethyl which could be due to gluconeogenesis. Pulse-chase experiments indicated a rapidly turning over malate pool.</description><subject>Bicarbonates</subject><subject>Carbon dioxide</subject><subject>Crassulacean acid metabolism</subject><subject>Decarboxylation</subject><subject>Enzymes</subject><subject>Metabolism</subject><subject>Plants</subject><subject>Radioactive decay</subject><subject>Starches</subject><subject>Sugars</subject><issn>0032-0889</issn><issn>1532-2548</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1977</creationdate><recordtype>article</recordtype><recordid>eNpVkUFv1DAQhS0EokvhxBUh3zigDWM7sR0kDtXSwkqLQKicLSc7aVySONjeRXvmj9doV6WcxuP53htbj5CXDArGoHw3z4WEQhZaqUdkwSrBl7wq9WOyAMhn0Lo-I89ivAUAJlj5lJwxKSVwqBbkz8bd9InuMcRdpB9t-ElXNjR-ol8w2cYPLo7UTXTVYwgHeu1Hmzy9CjuX4nu6Xhf0Ow42OT_F3s20wfQbMYttvsSHHnba0m-9Tz4eptRjci29aJPbu3R4Tp50doj44lTPyY-ry-vV5-Xm66f16mKzbDkwvexYA1pALRUXwgK3Guvcd1uVf8hk1dQK604IsLJkrWqR87rORLutsGpKK87Jh6PvvGtG3LY4pWAHMwc32nAw3jrz_2Ryvbnxe1OVXAmd9W9O-uB_7TAmM7rY4jDYCf0uGiVEqTWoKpNvj2QbfIwBu_slDMzf0Mw8GwlGmhxapl8_fNc_9pRSBl4dgduYfLifl1xWDJS4A-K4nd0</recordid><startdate>19771201</startdate><enddate>19771201</enddate><creator>Farineau, J</creator><general>American Society of Plant Physiologists</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>19771201</creationdate><title>Light versus Dark Carbon Metabolism in Cherry Tomato Fruits: II. Relationship between Malate Metabolism and Photosynthetic Activity</title><author>Farineau, J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2018-f1b0830967233a02a8e9830fd7889165b97e9f330a641c7ce2299983cd5e5b4a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1977</creationdate><topic>Bicarbonates</topic><topic>Carbon dioxide</topic><topic>Crassulacean acid metabolism</topic><topic>Decarboxylation</topic><topic>Enzymes</topic><topic>Metabolism</topic><topic>Plants</topic><topic>Radioactive decay</topic><topic>Starches</topic><topic>Sugars</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Farineau, J</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Plant physiology (Bethesda)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Farineau, J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Light versus Dark Carbon Metabolism in Cherry Tomato Fruits: II. Relationship between Malate Metabolism and Photosynthetic Activity</atitle><jtitle>Plant physiology (Bethesda)</jtitle><addtitle>Plant Physiol</addtitle><date>1977-12-01</date><risdate>1977</risdate><volume>60</volume><issue>6</issue><spage>877</spage><epage>880</epage><pages>877-880</pages><issn>0032-0889</issn><eissn>1532-2548</eissn><abstract>The possible relationship between malate metabolism and photosynthetic activity in green tomato fruit tissues (Lycopersicum esculentum var. cerasiforme Dun A. Gray) was investigated. Initial experiments consisted of vacuum-infiltrating 14C-3 or 14C-4-malate into isolated tissues in darkness and then incubating the tissues under photosynthetic conditions. Other experiments involved a short pulse with 14C-bicarbonate in darkness to label the malate pool(s), followed by a chase in the light in the presence of nonradioactive bicarbonate. Both series of experiments were followed by the separation and identification of labeled metabolic intermediates. Label initially in carbon atoms 3 and 4 of malate, corresponding also to C-3 of pyruvate and CO2 after malate decarboxylation, was recovered as citrate + isocitrate, sugars and starch following incubations of tissues in the light. These data demonstrate that the reductive pentose phosphate cycle utilizes CO2 furnished by malate metabolism due to the operation of the citric acid cycle and perhaps also to malic enzyme activity. Some synthesis of sugars and starch from C-3 of malate was observed in darkness or in the light 3-(3,4-dichlorophenyl)-1,1-dimethyl which could be due to gluconeogenesis. Pulse-chase experiments indicated a rapidly turning over malate pool.</abstract><cop>United States</cop><pub>American Society of Plant Physiologists</pub><pmid>16660205</pmid><doi>10.1104/pp.60.6.877</doi><tpages>4</tpages></addata></record> |
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source | JSTOR Archival Journals and Primary Sources Collection; Alma/SFX Local Collection |
subjects | Bicarbonates Carbon dioxide Crassulacean acid metabolism Decarboxylation Enzymes Metabolism Plants Radioactive decay Starches Sugars |
title | Light versus Dark Carbon Metabolism in Cherry Tomato Fruits: II. Relationship between Malate Metabolism and Photosynthetic Activity |
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