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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
Main Author: Farineau, J
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Language:English
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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.
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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. 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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. 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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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ispartof Plant physiology (Bethesda), 1977-12, Vol.60 (6), p.877-880
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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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