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Characterization and regulation of ammonium transport systems in Citrus plants

Identifieur interne : 000851 ( PascalFrancis/Corpus ); précédent : 000850; suivant : 000852

Characterization and regulation of ammonium transport systems in Citrus plants

Auteurs : M. Cerezo ; P. Tillard ; A. Gojon ; E. Primo-Millo ; P. Garcia-Agustin

Source :

RBID : Pascal:02-0149830

Descripteurs français

English descriptors

Abstract

We have investigated both the kinetics and regulation of 15NH4+ influx in roots of 3-month-old hydroponically grown Citrus (Citrus sinensis L. Osbeck x Poncirus trifoliata Blanco) seedlings. The 15NH4+ influx is saturable below an external ammonium concentration of 1 mM, indicating the action of a high-affinity transport system (HATS). The HATS is under feedback repression by the N status of the plant, being downregulated in plants adequately supplied with N during growth, and up-regulated by N-starvation. When assayed between 1 and 50 mM [15NH4+]0, the 15NH4+ influx showed a linear response typical of a low-affinity transport system (LATS). The activity of the LATS increased in plants supplied with NH4+ as compared with plants grown on an N-free medium. Transfer of the plants to N-free solution resulted in a marked decrease in the LATS-mediated 15NH4+ influx. Accordingly, resupply of NH4+ after N-starvation triggered a dramatic stimulation of the activity of the LATS. These data provide evidence that in Citrus plants, the LATS or at least one of its components is inducible by NH4+. Even when up-regulated, both the HATS and the LATS displayed a limited capacity, as compared with that usually found in herbaceous species. The use of various metabolic uncouplers or inhibitors indicated that 15NH4+ influx mediated by the HATS is strongly dependent on energy metabolism and H transmembrane electrochemical gradient. By contrast, the LATS is not affected by protonophores or inhibitors of the H+-ATPase, suggesting that its activity is mostly driven by the NH4+/NH3 transmembrane gradient. In agreement with these hypotheses, the HATS-mediated 15NH4+ influx was strongly inhibited when the solution pH was raised from 4 to 7, whereas influx mediated by the LATS was slightly stimulated.

Notice en format standard (ISO 2709)

Pour connaître la documentation sur le format Inist Standard.

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A03   1    @0 Planta
A05       @2 214
A06       @2 1
A08 01  1  ENG  @1 Characterization and regulation of ammonium transport systems in Citrus plants
A11 01  1    @1 CEREZO (M.)
A11 02  1    @1 TILLARD (P.)
A11 03  1    @1 GOJON (A.)
A11 04  1    @1 PRIMO-MILLO (E.)
A11 05  1    @1 GARCIA-AGUSTIN (P.)
A14 01      @1 Unidad de Fisiología Vegetal, Departamento de Ciencias Expérimentales, Escuela Superior de Tecnología y Ciencias Experimentales, Universitat Jaume I @2 12071 Castellón @3 ESP @Z 1 aut. @Z 5 aut.
A14 02      @1 Biochimie et Physiologie Moléculaire des plantes, UMR 5004, Agro-M, CNRS, INRA, UM2, Place Viala @2 34060 Montpellier @3 FRA @Z 2 aut. @Z 3 aut.
A14 03      @1 Departamento de Citricultura, Instituto Valenciano de Investigaciones Agrarias, Apartado Oficial @2 46113 Moncada Valencia @3 ESP @Z 4 aut.
A20       @1 97-105
A21       @1 2001
A23 01      @0 ENG
A43 01      @1 INIST @2 916 @5 354000102199970120
A44       @0 0000 @1 © 2002 INIST-CNRS. All rights reserved.
A45       @0 33 ref.
A47 01  1    @0 02-0149830
A60       @1 P
A61       @0 A
A64 01  1    @0 Planta
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C01 01    ENG  @0 We have investigated both the kinetics and regulation of 15NH4+ influx in roots of 3-month-old hydroponically grown Citrus (Citrus sinensis L. Osbeck x Poncirus trifoliata Blanco) seedlings. The 15NH4+ influx is saturable below an external ammonium concentration of 1 mM, indicating the action of a high-affinity transport system (HATS). The HATS is under feedback repression by the N status of the plant, being downregulated in plants adequately supplied with N during growth, and up-regulated by N-starvation. When assayed between 1 and 50 mM [15NH4+]0, the 15NH4+ influx showed a linear response typical of a low-affinity transport system (LATS). The activity of the LATS increased in plants supplied with NH4+ as compared with plants grown on an N-free medium. Transfer of the plants to N-free solution resulted in a marked decrease in the LATS-mediated 15NH4+ influx. Accordingly, resupply of NH4+ after N-starvation triggered a dramatic stimulation of the activity of the LATS. These data provide evidence that in Citrus plants, the LATS or at least one of its components is inducible by NH4+. Even when up-regulated, both the HATS and the LATS displayed a limited capacity, as compared with that usually found in herbaceous species. The use of various metabolic uncouplers or inhibitors indicated that 15NH4+ influx mediated by the HATS is strongly dependent on energy metabolism and H transmembrane electrochemical gradient. By contrast, the LATS is not affected by protonophores or inhibitors of the H+-ATPase, suggesting that its activity is mostly driven by the NH4+/NH3 transmembrane gradient. In agreement with these hypotheses, the HATS-mediated 15NH4+ influx was strongly inhibited when the solution pH was raised from 4 to 7, whereas influx mediated by the LATS was slightly stimulated.
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C03 05  X  ENG  @0 Carrier protein @5 05
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C03 07  X  ENG  @0 Absorption @5 07
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C03 09  X  FRE  @0 Nutrition @5 09
C03 09  X  ENG  @0 Nutrition @5 09
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C03 11  X  SPA  @0 Nitrato @2 NA @2 FX @5 16
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C03 17  X  ENG  @0 Root @5 37
C03 17  X  SPA  @0 Raíz @5 37
C03 18  X  FRE  @0 Citrus sinensis Poncirus trifoliata @2 NS @4 INC @5 77
C03 19  X  FRE  @0 Azote 15 @2 FF @4 INC @5 81
C07 01  X  FRE  @0 Agrume @5 39
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C07 01  X  SPA  @0 Agrios @5 39
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C07 02  X  ENG  @0 Rutaceae @2 NS @5 40
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C07 03  X  FRE  @0 Dicotyledones @2 NS
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Format Inist (serveur)

NO : PASCAL 02-0149830 INIST
ET : Characterization and regulation of ammonium transport systems in Citrus plants
AU : CEREZO (M.); TILLARD (P.); GOJON (A.); PRIMO-MILLO (E.); GARCIA-AGUSTIN (P.)
AF : Unidad de Fisiología Vegetal, Departamento de Ciencias Expérimentales, Escuela Superior de Tecnología y Ciencias Experimentales, Universitat Jaume I/12071 Castellón/Espagne (1 aut., 5 aut.); Biochimie et Physiologie Moléculaire des plantes, UMR 5004, Agro-M, CNRS, INRA, UM2, Place Viala/34060 Montpellier/France (2 aut., 3 aut.); Departamento de Citricultura, Instituto Valenciano de Investigaciones Agrarias, Apartado Oficial/46113 Moncada Valencia/Espagne (4 aut.)
DT : Publication en série; Niveau analytique
SO : Planta; ISSN 0032-0935; Coden PLANAB; Allemagne; Da. 2001; Vol. 214; No. 1; Pp. 97-105; Bibl. 33 ref.
LA : Anglais
EA : We have investigated both the kinetics and regulation of 15NH4+ influx in roots of 3-month-old hydroponically grown Citrus (Citrus sinensis L. Osbeck x Poncirus trifoliata Blanco) seedlings. The 15NH4+ influx is saturable below an external ammonium concentration of 1 mM, indicating the action of a high-affinity transport system (HATS). The HATS is under feedback repression by the N status of the plant, being downregulated in plants adequately supplied with N during growth, and up-regulated by N-starvation. When assayed between 1 and 50 mM [15NH4+]0, the 15NH4+ influx showed a linear response typical of a low-affinity transport system (LATS). The activity of the LATS increased in plants supplied with NH4+ as compared with plants grown on an N-free medium. Transfer of the plants to N-free solution resulted in a marked decrease in the LATS-mediated 15NH4+ influx. Accordingly, resupply of NH4+ after N-starvation triggered a dramatic stimulation of the activity of the LATS. These data provide evidence that in Citrus plants, the LATS or at least one of its components is inducible by NH4+. Even when up-regulated, both the HATS and the LATS displayed a limited capacity, as compared with that usually found in herbaceous species. The use of various metabolic uncouplers or inhibitors indicated that 15NH4+ influx mediated by the HATS is strongly dependent on energy metabolism and H transmembrane electrochemical gradient. By contrast, the LATS is not affected by protonophores or inhibitors of the H+-ATPase, suggesting that its activity is mostly driven by the NH4+/NH3 transmembrane gradient. In agreement with these hypotheses, the HATS-mediated 15NH4+ influx was strongly inhibited when the solution pH was raised from 4 to 7, whereas influx mediated by the LATS was slightly stimulated.
CC : 002A10C; 002A32E05C
FD : Caractérisation; Régulation; Transport biologique; Marquage isotopique; Protéine transport; Site haute affinité; Absorption; Site faible affinité; Nutrition; Ammonium; Nitrate; Proton; Déficit; Métabolisme énergétique; Gradient proton; Gradient concentration; Racine; Citrus sinensis Poncirus trifoliata; Azote 15
FG : Agrume; Rutaceae; Dicotyledones; Angiospermae; Spermatophyta; Elément minéral; Nutriment; Traceur; Azote Isotope
ED : Characterization; Regulation(control); Biological transport; Isotope labelling; Carrier protein; High affinity site; Absorption; Low affinity site; Nutrition; Ammonium; Nitrates; Proton; Deficiency; Energy metabolism; Proton gradient; Concentration gradient; Root
EG : Citrus fruit; Rutaceae; Dicotyledones; Angiospermae; Spermatophyta; Inorganic element; Nutrient; Tracers; Nitrogen Isotopes
SD : Caracterización; Regulación; Transporte biológico; Marcación isotópica; Proteína transportador; Sitio alta afinidad; Absorción; Sitio debil afinidad; Nutrición; Amonio; Nitrato; Protón; Déficiencia; Metabolismo energético; Gradiente protón; Gradiente concentración; Raíz
LO : INIST-916.354000102199970120
ID : 02-0149830

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Pascal:02-0149830

Le document en format XML

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<div type="abstract" xml:lang="en">We have investigated both the kinetics and regulation of
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<sup>15</sup>
NH
<sub>4</sub>
<sup>+</sup>
]
<sub>0</sub>
, the 15NH4+ influx showed a linear response typical of a low-affinity transport system (LATS). The activity of the LATS increased in plants supplied with NH
<sub>4</sub>
<sup>+</sup>
as compared with plants grown on an N-free medium. Transfer of the plants to N-free solution resulted in a marked decrease in the LATS-mediated 15NH4+ influx. Accordingly, resupply of NH
<sub>4</sub>
<sup>+</sup>
after N-starvation triggered a dramatic stimulation of the activity of the LATS. These data provide evidence that in Citrus plants, the LATS or at least one of its components is inducible by NH
<sub>4</sub>
<sup>+</sup>
. Even when up-regulated, both the HATS and the LATS displayed a limited capacity, as compared with that usually found in herbaceous species. The use of various metabolic uncouplers or inhibitors indicated that 15NH4+ influx mediated by the HATS is strongly dependent on energy metabolism and H transmembrane electrochemical gradient. By contrast, the LATS is not affected by protonophores or inhibitors of the H
<sup>+</sup>
-ATPase, suggesting that its activity is mostly driven by the NH
<sub>4</sub>
<sup>+</sup>
/NH
<sub>3</sub>
transmembrane gradient. In agreement with these hypotheses, the HATS-mediated 15NH4+ influx was strongly inhibited when the solution pH was raised from 4 to 7, whereas influx mediated by the LATS was slightly stimulated.</div>
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<s0>0032-0935</s0>
</fA01>
<fA02 i1="01">
<s0>PLANAB</s0>
</fA02>
<fA03 i2="1">
<s0>Planta</s0>
</fA03>
<fA05>
<s2>214</s2>
</fA05>
<fA06>
<s2>1</s2>
</fA06>
<fA08 i1="01" i2="1" l="ENG">
<s1>Characterization and regulation of ammonium transport systems in Citrus plants</s1>
</fA08>
<fA11 i1="01" i2="1">
<s1>CEREZO (M.)</s1>
</fA11>
<fA11 i1="02" i2="1">
<s1>TILLARD (P.)</s1>
</fA11>
<fA11 i1="03" i2="1">
<s1>GOJON (A.)</s1>
</fA11>
<fA11 i1="04" i2="1">
<s1>PRIMO-MILLO (E.)</s1>
</fA11>
<fA11 i1="05" i2="1">
<s1>GARCIA-AGUSTIN (P.)</s1>
</fA11>
<fA14 i1="01">
<s1>Unidad de Fisiología Vegetal, Departamento de Ciencias Expérimentales, Escuela Superior de Tecnología y Ciencias Experimentales, Universitat Jaume I</s1>
<s2>12071 Castellón</s2>
<s3>ESP</s3>
<sZ>1 aut.</sZ>
<sZ>5 aut.</sZ>
</fA14>
<fA14 i1="02">
<s1>Biochimie et Physiologie Moléculaire des plantes, UMR 5004, Agro-M, CNRS, INRA, UM2, Place Viala</s1>
<s2>34060 Montpellier</s2>
<s3>FRA</s3>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
</fA14>
<fA14 i1="03">
<s1>Departamento de Citricultura, Instituto Valenciano de Investigaciones Agrarias, Apartado Oficial</s1>
<s2>46113 Moncada Valencia</s2>
<s3>ESP</s3>
<sZ>4 aut.</sZ>
</fA14>
<fA20>
<s1>97-105</s1>
</fA20>
<fA21>
<s1>2001</s1>
</fA21>
<fA23 i1="01">
<s0>ENG</s0>
</fA23>
<fA43 i1="01">
<s1>INIST</s1>
<s2>916</s2>
<s5>354000102199970120</s5>
</fA43>
<fA44>
<s0>0000</s0>
<s1>© 2002 INIST-CNRS. All rights reserved.</s1>
</fA44>
<fA45>
<s0>33 ref.</s0>
</fA45>
<fA47 i1="01" i2="1">
<s0>02-0149830</s0>
</fA47>
<fA60>
<s1>P</s1>
</fA60>
<fA61>
<s0>A</s0>
</fA61>
<fA64 i1="01" i2="1">
<s0>Planta</s0>
</fA64>
<fA66 i1="01">
<s0>DEU</s0>
</fA66>
<fC01 i1="01" l="ENG">
<s0>We have investigated both the kinetics and regulation of
<sup>15</sup>
NH
<sup>4+</sup>
influx in roots of 3-month-old hydroponically grown Citrus (Citrus sinensis L. Osbeck x Poncirus trifoliata Blanco) seedlings. The
<sup>15</sup>
NH
<sub>4</sub>
<sup>+</sup>
influx is saturable below an external ammonium concentration of 1 mM, indicating the action of a high-affinity transport system (HATS). The HATS is under feedback repression by the N status of the plant, being downregulated in plants adequately supplied with N during growth, and up-regulated by N-starvation. When assayed between 1 and 50 mM [
<sup>15</sup>
NH
<sub>4</sub>
<sup>+</sup>
]
<sub>0</sub>
, the 15NH4+ influx showed a linear response typical of a low-affinity transport system (LATS). The activity of the LATS increased in plants supplied with NH
<sub>4</sub>
<sup>+</sup>
as compared with plants grown on an N-free medium. Transfer of the plants to N-free solution resulted in a marked decrease in the LATS-mediated 15NH4+ influx. Accordingly, resupply of NH
<sub>4</sub>
<sup>+</sup>
after N-starvation triggered a dramatic stimulation of the activity of the LATS. These data provide evidence that in Citrus plants, the LATS or at least one of its components is inducible by NH
<sub>4</sub>
<sup>+</sup>
. Even when up-regulated, both the HATS and the LATS displayed a limited capacity, as compared with that usually found in herbaceous species. The use of various metabolic uncouplers or inhibitors indicated that 15NH4+ influx mediated by the HATS is strongly dependent on energy metabolism and H transmembrane electrochemical gradient. By contrast, the LATS is not affected by protonophores or inhibitors of the H
<sup>+</sup>
-ATPase, suggesting that its activity is mostly driven by the NH
<sub>4</sub>
<sup>+</sup>
/NH
<sub>3</sub>
transmembrane gradient. In agreement with these hypotheses, the HATS-mediated 15NH4+ influx was strongly inhibited when the solution pH was raised from 4 to 7, whereas influx mediated by the LATS was slightly stimulated.</s0>
</fC01>
<fC02 i1="01" i2="X">
<s0>002A10C</s0>
</fC02>
<fC02 i1="02" i2="X">
<s0>002A32E05C</s0>
</fC02>
<fC03 i1="01" i2="X" l="FRE">
<s0>Caractérisation</s0>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="ENG">
<s0>Characterization</s0>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="X" l="SPA">
<s0>Caracterización</s0>
<s5>01</s5>
</fC03>
<fC03 i1="02" i2="X" l="FRE">
<s0>Régulation</s0>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="X" l="ENG">
<s0>Regulation(control)</s0>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="X" l="SPA">
<s0>Regulación</s0>
<s5>02</s5>
</fC03>
<fC03 i1="03" i2="X" l="FRE">
<s0>Transport biologique</s0>
<s5>03</s5>
</fC03>
<fC03 i1="03" i2="X" l="ENG">
<s0>Biological transport</s0>
<s5>03</s5>
</fC03>
<fC03 i1="03" i2="X" l="SPA">
<s0>Transporte biológico</s0>
<s5>03</s5>
</fC03>
<fC03 i1="04" i2="X" l="FRE">
<s0>Marquage isotopique</s0>
<s5>04</s5>
</fC03>
<fC03 i1="04" i2="X" l="ENG">
<s0>Isotope labelling</s0>
<s5>04</s5>
</fC03>
<fC03 i1="04" i2="X" l="SPA">
<s0>Marcación isotópica</s0>
<s5>04</s5>
</fC03>
<fC03 i1="05" i2="X" l="FRE">
<s0>Protéine transport</s0>
<s5>05</s5>
</fC03>
<fC03 i1="05" i2="X" l="ENG">
<s0>Carrier protein</s0>
<s5>05</s5>
</fC03>
<fC03 i1="05" i2="X" l="SPA">
<s0>Proteína transportador</s0>
<s5>05</s5>
</fC03>
<fC03 i1="06" i2="X" l="FRE">
<s0>Site haute affinité</s0>
<s5>06</s5>
</fC03>
<fC03 i1="06" i2="X" l="ENG">
<s0>High affinity site</s0>
<s5>06</s5>
</fC03>
<fC03 i1="06" i2="X" l="SPA">
<s0>Sitio alta afinidad</s0>
<s5>06</s5>
</fC03>
<fC03 i1="07" i2="X" l="FRE">
<s0>Absorption</s0>
<s5>07</s5>
</fC03>
<fC03 i1="07" i2="X" l="ENG">
<s0>Absorption</s0>
<s5>07</s5>
</fC03>
<fC03 i1="07" i2="X" l="SPA">
<s0>Absorción</s0>
<s5>07</s5>
</fC03>
<fC03 i1="08" i2="X" l="FRE">
<s0>Site faible affinité</s0>
<s5>08</s5>
</fC03>
<fC03 i1="08" i2="X" l="ENG">
<s0>Low affinity site</s0>
<s5>08</s5>
</fC03>
<fC03 i1="08" i2="X" l="SPA">
<s0>Sitio debil afinidad</s0>
<s5>08</s5>
</fC03>
<fC03 i1="09" i2="X" l="FRE">
<s0>Nutrition</s0>
<s5>09</s5>
</fC03>
<fC03 i1="09" i2="X" l="ENG">
<s0>Nutrition</s0>
<s5>09</s5>
</fC03>
<fC03 i1="09" i2="X" l="SPA">
<s0>Nutrición</s0>
<s5>09</s5>
</fC03>
<fC03 i1="10" i2="X" l="FRE">
<s0>Ammonium</s0>
<s2>NC</s2>
<s5>15</s5>
</fC03>
<fC03 i1="10" i2="X" l="ENG">
<s0>Ammonium</s0>
<s2>NC</s2>
<s5>15</s5>
</fC03>
<fC03 i1="10" i2="X" l="SPA">
<s0>Amonio</s0>
<s2>NC</s2>
<s5>15</s5>
</fC03>
<fC03 i1="11" i2="X" l="FRE">
<s0>Nitrate</s0>
<s2>NA</s2>
<s2>FX</s2>
<s5>16</s5>
</fC03>
<fC03 i1="11" i2="X" l="ENG">
<s0>Nitrates</s0>
<s2>NA</s2>
<s2>FX</s2>
<s5>16</s5>
</fC03>
<fC03 i1="11" i2="X" l="SPA">
<s0>Nitrato</s0>
<s2>NA</s2>
<s2>FX</s2>
<s5>16</s5>
</fC03>
<fC03 i1="12" i2="X" l="FRE">
<s0>Proton</s0>
<s5>18</s5>
</fC03>
<fC03 i1="12" i2="X" l="ENG">
<s0>Proton</s0>
<s5>18</s5>
</fC03>
<fC03 i1="12" i2="X" l="SPA">
<s0>Protón</s0>
<s5>18</s5>
</fC03>
<fC03 i1="13" i2="X" l="FRE">
<s0>Déficit</s0>
<s5>33</s5>
</fC03>
<fC03 i1="13" i2="X" l="ENG">
<s0>Deficiency</s0>
<s5>33</s5>
</fC03>
<fC03 i1="13" i2="X" l="SPA">
<s0>Déficiencia</s0>
<s5>33</s5>
</fC03>
<fC03 i1="14" i2="X" l="FRE">
<s0>Métabolisme énergétique</s0>
<s5>34</s5>
</fC03>
<fC03 i1="14" i2="X" l="ENG">
<s0>Energy metabolism</s0>
<s5>34</s5>
</fC03>
<fC03 i1="14" i2="X" l="SPA">
<s0>Metabolismo energético</s0>
<s5>34</s5>
</fC03>
<fC03 i1="15" i2="X" l="FRE">
<s0>Gradient proton</s0>
<s5>35</s5>
</fC03>
<fC03 i1="15" i2="X" l="ENG">
<s0>Proton gradient</s0>
<s5>35</s5>
</fC03>
<fC03 i1="15" i2="X" l="SPA">
<s0>Gradiente protón</s0>
<s5>35</s5>
</fC03>
<fC03 i1="16" i2="X" l="FRE">
<s0>Gradient concentration</s0>
<s5>36</s5>
</fC03>
<fC03 i1="16" i2="X" l="ENG">
<s0>Concentration gradient</s0>
<s5>36</s5>
</fC03>
<fC03 i1="16" i2="X" l="SPA">
<s0>Gradiente concentración</s0>
<s5>36</s5>
</fC03>
<fC03 i1="17" i2="X" l="FRE">
<s0>Racine</s0>
<s5>37</s5>
</fC03>
<fC03 i1="17" i2="X" l="ENG">
<s0>Root</s0>
<s5>37</s5>
</fC03>
<fC03 i1="17" i2="X" l="SPA">
<s0>Raíz</s0>
<s5>37</s5>
</fC03>
<fC03 i1="18" i2="X" l="FRE">
<s0>Citrus sinensis Poncirus trifoliata</s0>
<s2>NS</s2>
<s4>INC</s4>
<s5>77</s5>
</fC03>
<fC03 i1="19" i2="X" l="FRE">
<s0>Azote 15</s0>
<s2>FF</s2>
<s4>INC</s4>
<s5>81</s5>
</fC03>
<fC07 i1="01" i2="X" l="FRE">
<s0>Agrume</s0>
<s5>39</s5>
</fC07>
<fC07 i1="01" i2="X" l="ENG">
<s0>Citrus fruit</s0>
<s5>39</s5>
</fC07>
<fC07 i1="01" i2="X" l="SPA">
<s0>Agrios</s0>
<s5>39</s5>
</fC07>
<fC07 i1="02" i2="X" l="FRE">
<s0>Rutaceae</s0>
<s2>NS</s2>
<s5>40</s5>
</fC07>
<fC07 i1="02" i2="X" l="ENG">
<s0>Rutaceae</s0>
<s2>NS</s2>
<s5>40</s5>
</fC07>
<fC07 i1="02" i2="X" l="SPA">
<s0>Rutaceae</s0>
<s2>NS</s2>
<s5>40</s5>
</fC07>
<fC07 i1="03" i2="X" l="FRE">
<s0>Dicotyledones</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="03" i2="X" l="ENG">
<s0>Dicotyledones</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="03" i2="X" l="SPA">
<s0>Dicotyledones</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="04" i2="X" l="FRE">
<s0>Angiospermae</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="04" i2="X" l="ENG">
<s0>Angiospermae</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="04" i2="X" l="SPA">
<s0>Angiospermae</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="05" i2="X" l="FRE">
<s0>Spermatophyta</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="05" i2="X" l="ENG">
<s0>Spermatophyta</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="05" i2="X" l="SPA">
<s0>Spermatophyta</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="06" i2="X" l="FRE">
<s0>Elément minéral</s0>
<s5>50</s5>
</fC07>
<fC07 i1="06" i2="X" l="ENG">
<s0>Inorganic element</s0>
<s5>50</s5>
</fC07>
<fC07 i1="06" i2="X" l="SPA">
<s0>Elemento inorgánico</s0>
<s5>50</s5>
</fC07>
<fC07 i1="07" i2="X" l="FRE">
<s0>Nutriment</s0>
<s5>51</s5>
</fC07>
<fC07 i1="07" i2="X" l="ENG">
<s0>Nutrient</s0>
<s5>51</s5>
</fC07>
<fC07 i1="07" i2="X" l="SPA">
<s0>Nutriente</s0>
<s5>51</s5>
</fC07>
<fC07 i1="08" i2="X" l="FRE">
<s0>Traceur</s0>
<s5>53</s5>
</fC07>
<fC07 i1="08" i2="X" l="ENG">
<s0>Tracers</s0>
<s5>53</s5>
</fC07>
<fC07 i1="08" i2="X" l="SPA">
<s0>Trazador</s0>
<s5>53</s5>
</fC07>
<fC07 i1="09" i2="X" l="FRE">
<s0>Azote Isotope</s0>
<s2>NC</s2>
<s2>NA</s2>
<s5>54</s5>
</fC07>
<fC07 i1="09" i2="X" l="ENG">
<s0>Nitrogen Isotopes</s0>
<s2>NC</s2>
<s2>NA</s2>
<s5>54</s5>
</fC07>
<fC07 i1="09" i2="X" l="SPA">
<s0>Nitrógeno Isótopo</s0>
<s2>NC</s2>
<s2>NA</s2>
<s5>54</s5>
</fC07>
<fN21>
<s1>084</s1>
</fN21>
<fN82>
<s1>PSI</s1>
</fN82>
</pA>
</standard>
<server>
<NO>PASCAL 02-0149830 INIST</NO>
<ET>Characterization and regulation of ammonium transport systems in Citrus plants</ET>
<AU>CEREZO (M.); TILLARD (P.); GOJON (A.); PRIMO-MILLO (E.); GARCIA-AGUSTIN (P.)</AU>
<AF>Unidad de Fisiología Vegetal, Departamento de Ciencias Expérimentales, Escuela Superior de Tecnología y Ciencias Experimentales, Universitat Jaume I/12071 Castellón/Espagne (1 aut., 5 aut.); Biochimie et Physiologie Moléculaire des plantes, UMR 5004, Agro-M, CNRS, INRA, UM2, Place Viala/34060 Montpellier/France (2 aut., 3 aut.); Departamento de Citricultura, Instituto Valenciano de Investigaciones Agrarias, Apartado Oficial/46113 Moncada Valencia/Espagne (4 aut.)</AF>
<DT>Publication en série; Niveau analytique</DT>
<SO>Planta; ISSN 0032-0935; Coden PLANAB; Allemagne; Da. 2001; Vol. 214; No. 1; Pp. 97-105; Bibl. 33 ref.</SO>
<LA>Anglais</LA>
<EA>We have investigated both the kinetics and regulation of
<sup>15</sup>
NH
<sup>4+</sup>
influx in roots of 3-month-old hydroponically grown Citrus (Citrus sinensis L. Osbeck x Poncirus trifoliata Blanco) seedlings. The
<sup>15</sup>
NH
<sub>4</sub>
<sup>+</sup>
influx is saturable below an external ammonium concentration of 1 mM, indicating the action of a high-affinity transport system (HATS). The HATS is under feedback repression by the N status of the plant, being downregulated in plants adequately supplied with N during growth, and up-regulated by N-starvation. When assayed between 1 and 50 mM [
<sup>15</sup>
NH
<sub>4</sub>
<sup>+</sup>
]
<sub>0</sub>
, the 15NH4+ influx showed a linear response typical of a low-affinity transport system (LATS). The activity of the LATS increased in plants supplied with NH
<sub>4</sub>
<sup>+</sup>
as compared with plants grown on an N-free medium. Transfer of the plants to N-free solution resulted in a marked decrease in the LATS-mediated 15NH4+ influx. Accordingly, resupply of NH
<sub>4</sub>
<sup>+</sup>
after N-starvation triggered a dramatic stimulation of the activity of the LATS. These data provide evidence that in Citrus plants, the LATS or at least one of its components is inducible by NH
<sub>4</sub>
<sup>+</sup>
. Even when up-regulated, both the HATS and the LATS displayed a limited capacity, as compared with that usually found in herbaceous species. The use of various metabolic uncouplers or inhibitors indicated that 15NH4+ influx mediated by the HATS is strongly dependent on energy metabolism and H transmembrane electrochemical gradient. By contrast, the LATS is not affected by protonophores or inhibitors of the H
<sup>+</sup>
-ATPase, suggesting that its activity is mostly driven by the NH
<sub>4</sub>
<sup>+</sup>
/NH
<sub>3</sub>
transmembrane gradient. In agreement with these hypotheses, the HATS-mediated 15NH4+ influx was strongly inhibited when the solution pH was raised from 4 to 7, whereas influx mediated by the LATS was slightly stimulated.</EA>
<CC>002A10C; 002A32E05C</CC>
<FD>Caractérisation; Régulation; Transport biologique; Marquage isotopique; Protéine transport; Site haute affinité; Absorption; Site faible affinité; Nutrition; Ammonium; Nitrate; Proton; Déficit; Métabolisme énergétique; Gradient proton; Gradient concentration; Racine; Citrus sinensis Poncirus trifoliata; Azote 15</FD>
<FG>Agrume; Rutaceae; Dicotyledones; Angiospermae; Spermatophyta; Elément minéral; Nutriment; Traceur; Azote Isotope</FG>
<ED>Characterization; Regulation(control); Biological transport; Isotope labelling; Carrier protein; High affinity site; Absorption; Low affinity site; Nutrition; Ammonium; Nitrates; Proton; Deficiency; Energy metabolism; Proton gradient; Concentration gradient; Root</ED>
<EG>Citrus fruit; Rutaceae; Dicotyledones; Angiospermae; Spermatophyta; Inorganic element; Nutrient; Tracers; Nitrogen Isotopes</EG>
<SD>Caracterización; Regulación; Transporte biológico; Marcación isotópica; Proteína transportador; Sitio alta afinidad; Absorción; Sitio debil afinidad; Nutrición; Amonio; Nitrato; Protón; Déficiencia; Metabolismo energético; Gradiente protón; Gradiente concentración; Raíz</SD>
<LO>INIST-916.354000102199970120</LO>
<ID>02-0149830</ID>
</server>
</inist>
</record>

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