Coordinate Changes in Carbon Partitioning and Plastidial Metabolism during the Development of Oilseed Rape Embryos
Measurements of metabolic fluxes in whole embryos and isolated plastids have revealed major changes in the pathways of carbon utilization during cotyledon filling by oilseed rape (Brassica napus L.) embryos. In the early cotyledon stage (stage A), embryos used sucrose (Suc) predominantly for starch...
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description | Measurements of metabolic fluxes in whole embryos and isolated plastids have revealed major changes in the pathways of carbon utilization during cotyledon filling by oilseed rape (Brassica napus L.) embryos. In the early cotyledon stage (stage A), embryos used sucrose (Suc) predominantly for starch synthesis. Plastids isolated from these embryos imported glucose-6-phosphate (Glc-6-P) and partitioned it to starch and fatty acids synthesis and to the oxidative pentose phosphate pathway in the ratio of 2:1:1 on a hexose basis. Of the substrates tested, Glc-6-P gave the highest rates of fatty acid synthesis by the plastids and pyruvate was used weakly. By the mid-to late-cotyledon stage (stage C), oil accumulation by the embryos was rapid, as was their utilization of Suc for oil synthesis in vitro. Plastids from C-stage embryos differed markedly from those of stage-A embryos: (a) pyruvate uptake and utilization for fatty acid synthesis increased by respectively 18- and 25-fold; (b) Glc-6-P partitioning was predominantly to the oxidative pentose phosphate pathway (respective ratios of 1:1:3); and (c) the rate of plastidial fatty acid synthesis more than doubled. This increased rate of fatty synthesis was dependent upon the increase in pyruvate uptake and was mediated through the induction of a saturable transporter activity. |
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In the early cotyledon stage (stage A), embryos used sucrose (Suc) predominantly for starch synthesis. Plastids isolated from these embryos imported glucose-6-phosphate (Glc-6-P) and partitioned it to starch and fatty acids synthesis and to the oxidative pentose phosphate pathway in the ratio of 2:1:1 on a hexose basis. Of the substrates tested, Glc-6-P gave the highest rates of fatty acid synthesis by the plastids and pyruvate was used weakly. By the mid-to late-cotyledon stage (stage C), oil accumulation by the embryos was rapid, as was their utilization of Suc for oil synthesis in vitro. Plastids from C-stage embryos differed markedly from those of stage-A embryos: (a) pyruvate uptake and utilization for fatty acid synthesis increased by respectively 18- and 25-fold; (b) Glc-6-P partitioning was predominantly to the oxidative pentose phosphate pathway (respective ratios of 1:1:3); and (c) the rate of plastidial fatty acid synthesis more than doubled. This increased rate of fatty synthesis was dependent upon the increase in pyruvate uptake and was mediated through the induction of a saturable transporter activity.</description><identifier>ISSN: 0032-0889</identifier><identifier>EISSN: 1532-2548</identifier><identifier>DOI: 10.1104/pp.122.3.767</identifier><identifier>PMID: 10712540</identifier><identifier>CODEN: PPHYA5</identifier><language>eng</language><publisher>Rockville, MD: American Society of Plant Physiologists</publisher><subject>Acetates ; Agronomy. Soil science and plant productions ; Biochemistry and Macromolecular Structure ; Biological and medical sciences ; Brassica - embryology ; Brassica - metabolism ; Carbon ; Carbon - metabolism ; Carrier Proteins - metabolism ; Economic plant physiology ; Embryos ; Enzymes ; Fatty acids ; Fatty Acids - biosynthesis ; Fundamental and applied biological sciences. Psychology ; Glucose-6-Phosphate - metabolism ; Lipid metabolism ; Lipids ; Lipids - biosynthesis ; Membrane Transport Proteins ; Net assimilation, photosynthesis, carbon metabolism. Photorespiration, respiration, fermentation (anoxia, hypoxia) ; Nutrition. Photosynthesis. Respiration. 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In the early cotyledon stage (stage A), embryos used sucrose (Suc) predominantly for starch synthesis. Plastids isolated from these embryos imported glucose-6-phosphate (Glc-6-P) and partitioned it to starch and fatty acids synthesis and to the oxidative pentose phosphate pathway in the ratio of 2:1:1 on a hexose basis. Of the substrates tested, Glc-6-P gave the highest rates of fatty acid synthesis by the plastids and pyruvate was used weakly. By the mid-to late-cotyledon stage (stage C), oil accumulation by the embryos was rapid, as was their utilization of Suc for oil synthesis in vitro. Plastids from C-stage embryos differed markedly from those of stage-A embryos: (a) pyruvate uptake and utilization for fatty acid synthesis increased by respectively 18- and 25-fold; (b) Glc-6-P partitioning was predominantly to the oxidative pentose phosphate pathway (respective ratios of 1:1:3); and (c) the rate of plastidial fatty acid synthesis more than doubled. This increased rate of fatty synthesis was dependent upon the increase in pyruvate uptake and was mediated through the induction of a saturable transporter activity.</description><subject>Acetates</subject><subject>Agronomy. Soil science and plant productions</subject><subject>Biochemistry and Macromolecular Structure</subject><subject>Biological and medical sciences</subject><subject>Brassica - embryology</subject><subject>Brassica - metabolism</subject><subject>Carbon</subject><subject>Carbon - metabolism</subject><subject>Carrier Proteins - metabolism</subject><subject>Economic plant physiology</subject><subject>Embryos</subject><subject>Enzymes</subject><subject>Fatty acids</subject><subject>Fatty Acids - biosynthesis</subject><subject>Fundamental and applied biological sciences. 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Metabolism</subject><subject>Oilseeds</subject><subject>Plant Oils - metabolism</subject><subject>Plant Proteins - biosynthesis</subject><subject>Plastids</subject><subject>Plastids - metabolism</subject><subject>Starch</subject><subject>Starch - biosynthesis</subject><subject>Starches</subject><subject>Sucrose - metabolism</subject><issn>0032-0889</issn><issn>1532-2548</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNpdktuL1DAUh4Mo7jj65qNIEPHJGXNrk4IvUtcLrOwi-hxO03QmQ5vUJF3Y_96sM6yrT7mc7xy-8AtCzynZUkrEu3neUsa2fCtr-QCtaMXZhlVCPUQrQsqeKNWcoScpHQghlFPxGJ1RImlhyArFNoTYOw_Z4nYPfmcTdh63ELvg8RXE7LIL3vkdBt_jqxFSdr2DEX-zGbowujThfom3QN5b_NFe2zHMk_UZhwFfujFZ2-PvMFt8PnXxJqSn6NEA5frZaV2jn5_Of7RfNheXn7-2Hy42RpBabkxRBSFpOcmqq4dO1YaCYpQTRSgVxhBmLdTEMKqUssKKbqjrBmTfm44yvkbvj3PnpZtsb4pShFHP0U0Qb3QAp_-teLfXu3CtK9X8aX9zao_h12JT1pNLxo4jeBuWpCVpKslZU8BX_4GHsERfnqaLWU0FY7xAb4-QiSGlaIc7D0r0bY56nnXJUXNdciz4y_vu9-BjcAV4fQIgGRiHCN649JfjjFflK6zRiyN2SDnEu7JgsqEV478BwyuwFQ</recordid><startdate>20000301</startdate><enddate>20000301</enddate><creator>Eastmond, Peter J.</creator><creator>Stephen Rawsthorne</creator><general>American Society of Plant Physiologists</general><general>American Society of Plant Biologists</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>4T-</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8AO</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>M2P</scope><scope>M7P</scope><scope>MBDVC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>S0X</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20000301</creationdate><title>Coordinate Changes in Carbon Partitioning and Plastidial Metabolism during the Development of Oilseed Rape Embryos</title><author>Eastmond, Peter J. ; Stephen Rawsthorne</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4067-c314a471c4075b6fb86c1a8213080114cc02eea60c21888e4e4bf669a7ddcb123</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Acetates</topic><topic>Agronomy. Soil science and plant productions</topic><topic>Biochemistry and Macromolecular Structure</topic><topic>Biological and medical sciences</topic><topic>Brassica - embryology</topic><topic>Brassica - metabolism</topic><topic>Carbon</topic><topic>Carbon - metabolism</topic><topic>Carrier Proteins - metabolism</topic><topic>Economic plant physiology</topic><topic>Embryos</topic><topic>Enzymes</topic><topic>Fatty acids</topic><topic>Fatty Acids - biosynthesis</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Glucose-6-Phosphate - metabolism</topic><topic>Lipid metabolism</topic><topic>Lipids</topic><topic>Lipids - biosynthesis</topic><topic>Membrane Transport Proteins</topic><topic>Net assimilation, photosynthesis, carbon metabolism. Photorespiration, respiration, fermentation (anoxia, hypoxia)</topic><topic>Nutrition. Photosynthesis. Respiration. Metabolism</topic><topic>Oilseeds</topic><topic>Plant Oils - metabolism</topic><topic>Plant Proteins - biosynthesis</topic><topic>Plastids</topic><topic>Plastids - metabolism</topic><topic>Starch</topic><topic>Starch - biosynthesis</topic><topic>Starches</topic><topic>Sucrose - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Eastmond, Peter J.</creatorcontrib><creatorcontrib>Stephen Rawsthorne</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Docstoc</collection><collection>Agricultural Science Collection</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest Pharma Collection</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Agricultural Science Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>SIRS Editorial</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>Eastmond, Peter J.</au><au>Stephen Rawsthorne</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Coordinate Changes in Carbon Partitioning and Plastidial Metabolism during the Development of Oilseed Rape Embryos</atitle><jtitle>Plant physiology (Bethesda)</jtitle><addtitle>Plant Physiol</addtitle><date>2000-03-01</date><risdate>2000</risdate><volume>122</volume><issue>3</issue><spage>767</spage><epage>774</epage><pages>767-774</pages><issn>0032-0889</issn><eissn>1532-2548</eissn><coden>PPHYA5</coden><abstract>Measurements of metabolic fluxes in whole embryos and isolated plastids have revealed major changes in the pathways of carbon utilization during cotyledon filling by oilseed rape (Brassica napus L.) embryos. In the early cotyledon stage (stage A), embryos used sucrose (Suc) predominantly for starch synthesis. Plastids isolated from these embryos imported glucose-6-phosphate (Glc-6-P) and partitioned it to starch and fatty acids synthesis and to the oxidative pentose phosphate pathway in the ratio of 2:1:1 on a hexose basis. Of the substrates tested, Glc-6-P gave the highest rates of fatty acid synthesis by the plastids and pyruvate was used weakly. By the mid-to late-cotyledon stage (stage C), oil accumulation by the embryos was rapid, as was their utilization of Suc for oil synthesis in vitro. Plastids from C-stage embryos differed markedly from those of stage-A embryos: (a) pyruvate uptake and utilization for fatty acid synthesis increased by respectively 18- and 25-fold; (b) Glc-6-P partitioning was predominantly to the oxidative pentose phosphate pathway (respective ratios of 1:1:3); and (c) the rate of plastidial fatty acid synthesis more than doubled. This increased rate of fatty synthesis was dependent upon the increase in pyruvate uptake and was mediated through the induction of a saturable transporter activity.</abstract><cop>Rockville, MD</cop><pub>American Society of Plant Physiologists</pub><pmid>10712540</pmid><doi>10.1104/pp.122.3.767</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Acetates Agronomy. Soil science and plant productions Biochemistry and Macromolecular Structure Biological and medical sciences Brassica - embryology Brassica - metabolism Carbon Carbon - metabolism Carrier Proteins - metabolism Economic plant physiology Embryos Enzymes Fatty acids Fatty Acids - biosynthesis Fundamental and applied biological sciences. Psychology Glucose-6-Phosphate - metabolism Lipid metabolism Lipids Lipids - biosynthesis Membrane Transport Proteins Net assimilation, photosynthesis, carbon metabolism. Photorespiration, respiration, fermentation (anoxia, hypoxia) Nutrition. Photosynthesis. Respiration. Metabolism Oilseeds Plant Oils - metabolism Plant Proteins - biosynthesis Plastids Plastids - metabolism Starch Starch - biosynthesis Starches Sucrose - metabolism |
title | Coordinate Changes in Carbon Partitioning and Plastidial Metabolism during the Development of Oilseed Rape Embryos |
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