Contribution of different carbon sources to isoprene biosynthesis in poplar leaves

This study was performed to test if alternative carbon sources besides recently photosynthetically fixed CO2 are used for isoprene formation in the leaves of young poplar (Populus x canescens) trees. In a 13CO2 atmosphere under steady state conditions, only about 75% of isoprene became 13C labeled w...

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Veröffentlicht in:Plant physiology (Bethesda) 2004-05, Vol.135 (1), p.152-160
Hauptverfasser: Schnitzler, J.P, Graus, M, Kreuzwieser, J, Heizmann, U, Rennenberg, H, Wisthaler, A, Hansel, A
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container_issue 1
container_start_page 152
container_title Plant physiology (Bethesda)
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creator Schnitzler, J.P
Graus, M
Kreuzwieser, J
Heizmann, U
Rennenberg, H
Wisthaler, A
Hansel, A
description This study was performed to test if alternative carbon sources besides recently photosynthetically fixed CO2 are used for isoprene formation in the leaves of young poplar (Populus x canescens) trees. In a 13CO2 atmosphere under steady state conditions, only about 75% of isoprene became 13C labeled within minutes. A considerable part of the unlabeled carbon may be derived from xylem transported carbohydrates, as may be shown by feeding leaves with [U-13C]Glc. As a consequence of this treatment approximately 8% to 10% of the carbon emitted as isoprene was 13C labeled. In order to identify further carbon sources, poplar leaves were depleted of leaf internal carbon pools and the carbon pools were refilled with 13C labeled carbon by exposure to 13CO2. Results from this treatment showed that about 30% of isoprene carbon became 13C labeled, clearly suggesting that, in addition to xylem transported carbon and CO2, leaf internal carbon pools, e.g. starch, are used for isoprene formation. This use was even increased when net assimilation was reduced, for example by abscisic acid application. The data provide clear evidence of a dynamic exchange of carbon between different cellular precursors for isoprene biosynthesis, and an increasing importance of these alternative carbon pools under conditions of limited photosynthesis. Feeding [1,2-13C]Glc and [3-13C]Glc to leaves via the xylem suggested that alternative carbon sources are probably derived from cytosolic pyruvate/phosphoenolpyruvate equivalents and incorporated into isoprene according to the predicted cleavage of the 3-C position of pyruvate during the initial step of the plastidic deoxyxylulose-5-phosphate pathway.
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In a 13CO2 atmosphere under steady state conditions, only about 75% of isoprene became 13C labeled within minutes. A considerable part of the unlabeled carbon may be derived from xylem transported carbohydrates, as may be shown by feeding leaves with [U-13C]Glc. As a consequence of this treatment approximately 8% to 10% of the carbon emitted as isoprene was 13C labeled. In order to identify further carbon sources, poplar leaves were depleted of leaf internal carbon pools and the carbon pools were refilled with 13C labeled carbon by exposure to 13CO2. Results from this treatment showed that about 30% of isoprene carbon became 13C labeled, clearly suggesting that, in addition to xylem transported carbon and CO2, leaf internal carbon pools, e.g. starch, are used for isoprene formation. This use was even increased when net assimilation was reduced, for example by abscisic acid application. 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Psychology</subject><subject>Glucose - metabolism</subject><subject>Glucose - pharmacology</subject><subject>Hemiterpenes - biosynthesis</subject><subject>isoprene</subject><subject>isotope labeling</subject><subject>Isotopic labeling</subject><subject>Leaves</subject><subject>Metabolism</subject><subject>Net assimilation, photosynthesis, carbon metabolism. Photorespiration, respiration, fermentation (anoxia, hypoxia)</subject><subject>Nutrition. Photosynthesis. Respiration. Metabolism</subject><subject>Pentanes</subject><subject>Photosynthesis, respiration. 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Soil science and plant productions</topic><topic>alkenes</topic><topic>assimilation (physiology)</topic><topic>atmosphere</topic><topic>Biochemical Processes and Macromolecular Structures</topic><topic>Biological and medical sciences</topic><topic>Biological Transport - drug effects</topic><topic>Biosynthesis</topic><topic>Butadienes</topic><topic>carbohydrates</topic><topic>Carbon</topic><topic>Carbon - metabolism</topic><topic>Carbon - pharmacology</topic><topic>carbon dioxide</topic><topic>Carbon Dioxide - metabolism</topic><topic>Carbon Dioxide - pharmacology</topic><topic>Carbon dioxide emissions</topic><topic>Carbon Isotopes</topic><topic>Economic plant physiology</topic><topic>emissions</topic><topic>forest trees</topic><topic>Fundamental and applied biological sciences. 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Anabolism, catabolism</topic><topic>physiological transport</topic><topic>Plant Leaves - drug effects</topic><topic>Plant Leaves - metabolism</topic><topic>Plant physiology and development</topic><topic>Plants</topic><topic>Pollutant emissions</topic><topic>Populus - drug effects</topic><topic>Populus - metabolism</topic><topic>Populus canescens</topic><topic>Starch - metabolism</topic><topic>Starches</topic><topic>woody plants</topic><topic>Xylem</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Schnitzler, J.P</creatorcontrib><creatorcontrib>Graus, M</creatorcontrib><creatorcontrib>Kreuzwieser, J</creatorcontrib><creatorcontrib>Heizmann, U</creatorcontrib><creatorcontrib>Rennenberg, H</creatorcontrib><creatorcontrib>Wisthaler, A</creatorcontrib><creatorcontrib>Hansel, A</creatorcontrib><collection>AGRIS</collection><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>MEDLINE - Academic</collection><jtitle>Plant physiology (Bethesda)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Schnitzler, J.P</au><au>Graus, M</au><au>Kreuzwieser, J</au><au>Heizmann, U</au><au>Rennenberg, H</au><au>Wisthaler, A</au><au>Hansel, A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Contribution of different carbon sources to isoprene biosynthesis in poplar leaves</atitle><jtitle>Plant physiology (Bethesda)</jtitle><addtitle>Plant Physiol</addtitle><date>2004-05-01</date><risdate>2004</risdate><volume>135</volume><issue>1</issue><spage>152</spage><epage>160</epage><pages>152-160</pages><issn>0032-0889</issn><eissn>1532-2548</eissn><coden>PPHYA5</coden><abstract>This study was performed to test if alternative carbon sources besides recently photosynthetically fixed CO2 are used for isoprene formation in the leaves of young poplar (Populus x canescens) trees. In a 13CO2 atmosphere under steady state conditions, only about 75% of isoprene became 13C labeled within minutes. A considerable part of the unlabeled carbon may be derived from xylem transported carbohydrates, as may be shown by feeding leaves with [U-13C]Glc. As a consequence of this treatment approximately 8% to 10% of the carbon emitted as isoprene was 13C labeled. In order to identify further carbon sources, poplar leaves were depleted of leaf internal carbon pools and the carbon pools were refilled with 13C labeled carbon by exposure to 13CO2. Results from this treatment showed that about 30% of isoprene carbon became 13C labeled, clearly suggesting that, in addition to xylem transported carbon and CO2, leaf internal carbon pools, e.g. starch, are used for isoprene formation. This use was even increased when net assimilation was reduced, for example by abscisic acid application. The data provide clear evidence of a dynamic exchange of carbon between different cellular precursors for isoprene biosynthesis, and an increasing importance of these alternative carbon pools under conditions of limited photosynthesis. Feeding [1,2-13C]Glc and [3-13C]Glc to leaves via the xylem suggested that alternative carbon sources are probably derived from cytosolic pyruvate/phosphoenolpyruvate equivalents and incorporated into isoprene according to the predicted cleavage of the 3-C position of pyruvate during the initial step of the plastidic deoxyxylulose-5-phosphate pathway.</abstract><cop>Rockville, MD</cop><pub>American Society of Plant Biologists</pub><pmid>15122010</pmid><doi>10.1104/pp.103.037374</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
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subjects Agronomy. Soil science and plant productions
alkenes
assimilation (physiology)
atmosphere
Biochemical Processes and Macromolecular Structures
Biological and medical sciences
Biological Transport - drug effects
Biosynthesis
Butadienes
carbohydrates
Carbon
Carbon - metabolism
Carbon - pharmacology
carbon dioxide
Carbon Dioxide - metabolism
Carbon Dioxide - pharmacology
Carbon dioxide emissions
Carbon Isotopes
Economic plant physiology
emissions
forest trees
Fundamental and applied biological sciences. Psychology
Glucose - metabolism
Glucose - pharmacology
Hemiterpenes - biosynthesis
isoprene
isotope labeling
Isotopic labeling
Leaves
Metabolism
Net assimilation, photosynthesis, carbon metabolism. Photorespiration, respiration, fermentation (anoxia, hypoxia)
Nutrition. Photosynthesis. Respiration. Metabolism
Pentanes
Photosynthesis, respiration. Anabolism, catabolism
physiological transport
Plant Leaves - drug effects
Plant Leaves - metabolism
Plant physiology and development
Plants
Pollutant emissions
Populus - drug effects
Populus - metabolism
Populus canescens
Starch - metabolism
Starches
woody plants
Xylem
title Contribution of different carbon sources to isoprene biosynthesis in poplar leaves
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