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Capillary electrophoresis analysis of orange juice pectinesterases

Identifieur interne : 000917 ( PascalFrancis/Corpus ); précédent : 000916; suivant : 000918

Capillary electrophoresis analysis of orange juice pectinesterases

Auteurs : Robert J. Braddock ; Charles R. Bryan ; Jacqueline K. Burns

Source :

RBID : Pascal:01-0177851

Descripteurs français

English descriptors

Abstract

Pectinesterase (PE) was extracted from orange juice and pulp with 1 M NaCl, desalted, and separated using capillary electrophoresis (CE) gel procedures (CE-SDS-CGE) and isoelectric focusing (CE-IEF). PE resolved as a single peak using noncoated fused silica columns with CE-SDS-CGE. CE-IEF separation of PE required acryloylaminoethoxyethanol-coated columns, which had limited stability. Thermal stability of PE extracts before and after heating at 75 °C for 30 min and at 95 °C for 5 min established heat labile and heat stabile fractions with identical PE migration times by CE-SDS-CGE or CE-IEF. Peak magnitude decreased to a constant value as heating time increased at 75 °C. Regression analysis of CE-SDS-CGE peak migration times of molecular weight (MW) standards estimated both heat labile and heat stable PE at MW 36 900. Traditional SDS-PAGE gel separation of MW standards and active PE isolated by IEF allowed estimation of MW 36 000. CE-SDS-CGE allowed presumptive, but not quantitative, detection of active PE in fresh juice.

Notice en format standard (ISO 2709)

Pour connaître la documentation sur le format Inist Standard.

pA  
A01 01  1    @0 0021-8561
A02 01      @0 JAFCAU
A03   1    @0 J. agric. food chem. : (Print)
A05       @2 49
A06       @2 2
A08 01  1  ENG  @1 Capillary electrophoresis analysis of orange juice pectinesterases
A11 01  1    @1 BRADDOCK (Robert J.)
A11 02  1    @1 BRYAN (Charles R.)
A11 03  1    @1 BURNS (Jacqueline K.)
A14 01      @1 University of Florida, Citrus Research and Education Center, 700 Experiment Station Road @2 Lake Alfred, Florida 33850 @3 USA @Z 1 aut. @Z 2 aut. @Z 3 aut.
A20       @1 846-850
A21       @1 2001
A23 01      @0 ENG
A43 01      @1 INIST @2 7332 @5 354000097957750520
A44       @0 0000 @1 © 2001 INIST-CNRS. All rights reserved.
A45       @0 13 ref.
A47 01  1    @0 01-0177851
A60       @1 P
A61       @0 A
A64 01  1    @0 Journal of agricultural and food chemistry : (Print)
A66 01      @0 USA
C01 01    ENG  @0 Pectinesterase (PE) was extracted from orange juice and pulp with 1 M NaCl, desalted, and separated using capillary electrophoresis (CE) gel procedures (CE-SDS-CGE) and isoelectric focusing (CE-IEF). PE resolved as a single peak using noncoated fused silica columns with CE-SDS-CGE. CE-IEF separation of PE required acryloylaminoethoxyethanol-coated columns, which had limited stability. Thermal stability of PE extracts before and after heating at 75 °C for 30 min and at 95 °C for 5 min established heat labile and heat stabile fractions with identical PE migration times by CE-SDS-CGE or CE-IEF. Peak magnitude decreased to a constant value as heating time increased at 75 °C. Regression analysis of CE-SDS-CGE peak migration times of molecular weight (MW) standards estimated both heat labile and heat stable PE at MW 36 900. Traditional SDS-PAGE gel separation of MW standards and active PE isolated by IEF allowed estimation of MW 36 000. CE-SDS-CGE allowed presumptive, but not quantitative, detection of active PE in fresh juice.
C02 01  X    @0 002A35B09
C02 02  X    @0 002A10E05
C03 01  X  FRE  @0 Méthode analyse @5 01
C03 01  X  ENG  @0 Analysis method @5 01
C03 01  X  SPA  @0 Método análisis @5 01
C03 02  X  FRE  @0 Pectinesterase @2 FE @5 02
C03 02  X  ENG  @0 Pectinesterase @2 FE @5 02
C03 02  X  SPA  @0 Pectinesterase @2 FE @5 02
C03 03  X  FRE  @0 Jus d'orange @5 03
C03 03  X  ENG  @0 Orange juice @5 03
C03 03  X  SPA  @0 Zugo naranja @5 03
C03 04  X  FRE  @0 Electrophorèse capillaire @5 04
C03 04  X  ENG  @0 Capillary electrophoresis @5 04
C03 04  X  SPA  @0 Electroforesis capilar @5 04
C03 05  X  FRE  @0 Stabilité thermique @5 05
C03 05  X  ENG  @0 Thermal stability @5 05
C03 05  X  SPA  @0 Estabilidad térmica @5 05
C03 06  X  FRE  @0 Qualité production @5 06
C03 06  X  ENG  @0 Production quality @5 06
C03 06  X  SPA  @0 Calidad producción @5 06
C03 07  X  FRE  @0 Flaveur @5 07
C03 07  X  ENG  @0 Flavor @5 07
C03 07  X  SPA  @0 Flavor @5 07
C03 08  X  FRE  @0 Traitement thermique @5 08
C03 08  X  ENG  @0 Heat treatment @5 08
C03 08  X  SPA  @0 Tratamiento térmico @5 08
C03 09  X  FRE  @0 Propriété chimique @5 09
C03 09  X  ENG  @0 Chemical properties @5 09
C03 09  X  SPA  @0 Propiedad química @5 09
C03 10  X  FRE  @0 Citrus sinensis @2 NS @5 10
C03 10  X  ENG  @0 Citrus sinensis @2 NS @5 10
C03 10  X  SPA  @0 Citrus sinensis @2 NS @5 10
C03 11  X  FRE  @0 Inactivation @5 33
C03 11  X  ENG  @0 Inactivation @5 33
C03 11  X  SPA  @0 Inactivación @5 33
C03 12  X  FRE  @0 Caractérisation @5 34
C03 12  X  ENG  @0 Characterization @5 34
C03 12  X  SPA  @0 Caracterización @5 34
C03 13  X  FRE  @0 Masse moléculaire @5 35
C03 13  X  ENG  @0 Molecular weight @5 35
C03 13  X  SPA  @0 Masa molecular @5 35
C07 01  X  FRE  @0 Carboxylic ester hydrolases @2 FE
C07 01  X  ENG  @0 Carboxylic ester hydrolases @2 FE
C07 01  X  SPA  @0 Carboxylic ester hydrolases @2 FE
C07 02  X  FRE  @0 Esterases @2 FE
C07 02  X  ENG  @0 Esterases @2 FE
C07 02  X  SPA  @0 Esterases @2 FE
C07 03  X  FRE  @0 Hydrolases @2 FE
C07 03  X  ENG  @0 Hydrolases @2 FE
C07 03  X  SPA  @0 Hydrolases @2 FE
C07 04  X  FRE  @0 Enzyme
C07 04  X  ENG  @0 Enzyme
C07 04  X  SPA  @0 Enzima
C07 05  X  FRE  @0 Rutaceae @2 NS
C07 05  X  ENG  @0 Rutaceae @2 NS
C07 05  X  SPA  @0 Rutaceae @2 NS
C07 06  X  FRE  @0 Dicotyledones @2 NS
C07 06  X  ENG  @0 Dicotyledones @2 NS
C07 06  X  SPA  @0 Dicotyledones @2 NS
C07 07  X  FRE  @0 Angiospermae @2 NS
C07 07  X  ENG  @0 Angiospermae @2 NS
C07 07  X  SPA  @0 Angiospermae @2 NS
C07 08  X  FRE  @0 Spermatophyta @2 NS
C07 08  X  ENG  @0 Spermatophyta @2 NS
C07 08  X  SPA  @0 Spermatophyta @2 NS
C07 09  X  FRE  @0 Agrume @5 40
C07 09  X  ENG  @0 Citrus fruit @5 40
C07 09  X  SPA  @0 Agrios @5 40
N21       @1 119

Format Inist (serveur)

NO : PASCAL 01-0177851 INIST
ET : Capillary electrophoresis analysis of orange juice pectinesterases
AU : BRADDOCK (Robert J.); BRYAN (Charles R.); BURNS (Jacqueline K.)
AF : University of Florida, Citrus Research and Education Center, 700 Experiment Station Road/Lake Alfred, Florida 33850/Etats-Unis (1 aut., 2 aut., 3 aut.)
DT : Publication en série; Niveau analytique
SO : Journal of agricultural and food chemistry : (Print); ISSN 0021-8561; Coden JAFCAU; Etats-Unis; Da. 2001; Vol. 49; No. 2; Pp. 846-850; Bibl. 13 ref.
LA : Anglais
EA : Pectinesterase (PE) was extracted from orange juice and pulp with 1 M NaCl, desalted, and separated using capillary electrophoresis (CE) gel procedures (CE-SDS-CGE) and isoelectric focusing (CE-IEF). PE resolved as a single peak using noncoated fused silica columns with CE-SDS-CGE. CE-IEF separation of PE required acryloylaminoethoxyethanol-coated columns, which had limited stability. Thermal stability of PE extracts before and after heating at 75 °C for 30 min and at 95 °C for 5 min established heat labile and heat stabile fractions with identical PE migration times by CE-SDS-CGE or CE-IEF. Peak magnitude decreased to a constant value as heating time increased at 75 °C. Regression analysis of CE-SDS-CGE peak migration times of molecular weight (MW) standards estimated both heat labile and heat stable PE at MW 36 900. Traditional SDS-PAGE gel separation of MW standards and active PE isolated by IEF allowed estimation of MW 36 000. CE-SDS-CGE allowed presumptive, but not quantitative, detection of active PE in fresh juice.
CC : 002A35B09; 002A10E05
FD : Méthode analyse; Pectinesterase; Jus d'orange; Electrophorèse capillaire; Stabilité thermique; Qualité production; Flaveur; Traitement thermique; Propriété chimique; Citrus sinensis; Inactivation; Caractérisation; Masse moléculaire
FG : Carboxylic ester hydrolases; Esterases; Hydrolases; Enzyme; Rutaceae; Dicotyledones; Angiospermae; Spermatophyta; Agrume
ED : Analysis method; Pectinesterase; Orange juice; Capillary electrophoresis; Thermal stability; Production quality; Flavor; Heat treatment; Chemical properties; Citrus sinensis; Inactivation; Characterization; Molecular weight
EG : Carboxylic ester hydrolases; Esterases; Hydrolases; Enzyme; Rutaceae; Dicotyledones; Angiospermae; Spermatophyta; Citrus fruit
SD : Método análisis; Pectinesterase; Zugo naranja; Electroforesis capilar; Estabilidad térmica; Calidad producción; Flavor; Tratamiento térmico; Propiedad química; Citrus sinensis; Inactivación; Caracterización; Masa molecular
LO : INIST-7332.354000097957750520
ID : 01-0177851

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Pascal:01-0177851

Le document en format XML

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<div type="abstract" xml:lang="en">Pectinesterase (PE) was extracted from orange juice and pulp with 1 M NaCl, desalted, and separated using capillary electrophoresis (CE) gel procedures (CE-SDS-CGE) and isoelectric focusing (CE-IEF). PE resolved as a single peak using noncoated fused silica columns with CE-SDS-CGE. CE-IEF separation of PE required acryloylaminoethoxyethanol-coated columns, which had limited stability. Thermal stability of PE extracts before and after heating at 75 °C for 30 min and at 95 °C for 5 min established heat labile and heat stabile fractions with identical PE migration times by CE-SDS-CGE or CE-IEF. Peak magnitude decreased to a constant value as heating time increased at 75 °C. Regression analysis of CE-SDS-CGE peak migration times of molecular weight (MW) standards estimated both heat labile and heat stable PE at MW 36 900. Traditional SDS-PAGE gel separation of MW standards and active PE isolated by IEF allowed estimation of MW 36 000. CE-SDS-CGE allowed presumptive, but not quantitative, detection of active PE in fresh juice.</div>
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<fC03 i1="08" i2="X" l="SPA">
<s0>Tratamiento térmico</s0>
<s5>08</s5>
</fC03>
<fC03 i1="09" i2="X" l="FRE">
<s0>Propriété chimique</s0>
<s5>09</s5>
</fC03>
<fC03 i1="09" i2="X" l="ENG">
<s0>Chemical properties</s0>
<s5>09</s5>
</fC03>
<fC03 i1="09" i2="X" l="SPA">
<s0>Propiedad química</s0>
<s5>09</s5>
</fC03>
<fC03 i1="10" i2="X" l="FRE">
<s0>Citrus sinensis</s0>
<s2>NS</s2>
<s5>10</s5>
</fC03>
<fC03 i1="10" i2="X" l="ENG">
<s0>Citrus sinensis</s0>
<s2>NS</s2>
<s5>10</s5>
</fC03>
<fC03 i1="10" i2="X" l="SPA">
<s0>Citrus sinensis</s0>
<s2>NS</s2>
<s5>10</s5>
</fC03>
<fC03 i1="11" i2="X" l="FRE">
<s0>Inactivation</s0>
<s5>33</s5>
</fC03>
<fC03 i1="11" i2="X" l="ENG">
<s0>Inactivation</s0>
<s5>33</s5>
</fC03>
<fC03 i1="11" i2="X" l="SPA">
<s0>Inactivación</s0>
<s5>33</s5>
</fC03>
<fC03 i1="12" i2="X" l="FRE">
<s0>Caractérisation</s0>
<s5>34</s5>
</fC03>
<fC03 i1="12" i2="X" l="ENG">
<s0>Characterization</s0>
<s5>34</s5>
</fC03>
<fC03 i1="12" i2="X" l="SPA">
<s0>Caracterización</s0>
<s5>34</s5>
</fC03>
<fC03 i1="13" i2="X" l="FRE">
<s0>Masse moléculaire</s0>
<s5>35</s5>
</fC03>
<fC03 i1="13" i2="X" l="ENG">
<s0>Molecular weight</s0>
<s5>35</s5>
</fC03>
<fC03 i1="13" i2="X" l="SPA">
<s0>Masa molecular</s0>
<s5>35</s5>
</fC03>
<fC07 i1="01" i2="X" l="FRE">
<s0>Carboxylic ester hydrolases</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="01" i2="X" l="ENG">
<s0>Carboxylic ester hydrolases</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="01" i2="X" l="SPA">
<s0>Carboxylic ester hydrolases</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="02" i2="X" l="FRE">
<s0>Esterases</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="02" i2="X" l="ENG">
<s0>Esterases</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="02" i2="X" l="SPA">
<s0>Esterases</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="03" i2="X" l="FRE">
<s0>Hydrolases</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="03" i2="X" l="ENG">
<s0>Hydrolases</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="03" i2="X" l="SPA">
<s0>Hydrolases</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="04" i2="X" l="FRE">
<s0>Enzyme</s0>
</fC07>
<fC07 i1="04" i2="X" l="ENG">
<s0>Enzyme</s0>
</fC07>
<fC07 i1="04" i2="X" l="SPA">
<s0>Enzima</s0>
</fC07>
<fC07 i1="05" i2="X" l="FRE">
<s0>Rutaceae</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="05" i2="X" l="ENG">
<s0>Rutaceae</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="05" i2="X" l="SPA">
<s0>Rutaceae</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="06" i2="X" l="FRE">
<s0>Dicotyledones</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="06" i2="X" l="ENG">
<s0>Dicotyledones</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="06" i2="X" l="SPA">
<s0>Dicotyledones</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="07" i2="X" l="FRE">
<s0>Angiospermae</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="07" i2="X" l="ENG">
<s0>Angiospermae</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="07" i2="X" l="SPA">
<s0>Angiospermae</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="08" i2="X" l="FRE">
<s0>Spermatophyta</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="08" i2="X" l="ENG">
<s0>Spermatophyta</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="08" i2="X" l="SPA">
<s0>Spermatophyta</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="09" i2="X" l="FRE">
<s0>Agrume</s0>
<s5>40</s5>
</fC07>
<fC07 i1="09" i2="X" l="ENG">
<s0>Citrus fruit</s0>
<s5>40</s5>
</fC07>
<fC07 i1="09" i2="X" l="SPA">
<s0>Agrios</s0>
<s5>40</s5>
</fC07>
<fN21>
<s1>119</s1>
</fN21>
</pA>
</standard>
<server>
<NO>PASCAL 01-0177851 INIST</NO>
<ET>Capillary electrophoresis analysis of orange juice pectinesterases</ET>
<AU>BRADDOCK (Robert J.); BRYAN (Charles R.); BURNS (Jacqueline K.)</AU>
<AF>University of Florida, Citrus Research and Education Center, 700 Experiment Station Road/Lake Alfred, Florida 33850/Etats-Unis (1 aut., 2 aut., 3 aut.)</AF>
<DT>Publication en série; Niveau analytique</DT>
<SO>Journal of agricultural and food chemistry : (Print); ISSN 0021-8561; Coden JAFCAU; Etats-Unis; Da. 2001; Vol. 49; No. 2; Pp. 846-850; Bibl. 13 ref.</SO>
<LA>Anglais</LA>
<EA>Pectinesterase (PE) was extracted from orange juice and pulp with 1 M NaCl, desalted, and separated using capillary electrophoresis (CE) gel procedures (CE-SDS-CGE) and isoelectric focusing (CE-IEF). PE resolved as a single peak using noncoated fused silica columns with CE-SDS-CGE. CE-IEF separation of PE required acryloylaminoethoxyethanol-coated columns, which had limited stability. Thermal stability of PE extracts before and after heating at 75 °C for 30 min and at 95 °C for 5 min established heat labile and heat stabile fractions with identical PE migration times by CE-SDS-CGE or CE-IEF. Peak magnitude decreased to a constant value as heating time increased at 75 °C. Regression analysis of CE-SDS-CGE peak migration times of molecular weight (MW) standards estimated both heat labile and heat stable PE at MW 36 900. Traditional SDS-PAGE gel separation of MW standards and active PE isolated by IEF allowed estimation of MW 36 000. CE-SDS-CGE allowed presumptive, but not quantitative, detection of active PE in fresh juice.</EA>
<CC>002A35B09; 002A10E05</CC>
<FD>Méthode analyse; Pectinesterase; Jus d'orange; Electrophorèse capillaire; Stabilité thermique; Qualité production; Flaveur; Traitement thermique; Propriété chimique; Citrus sinensis; Inactivation; Caractérisation; Masse moléculaire</FD>
<FG>Carboxylic ester hydrolases; Esterases; Hydrolases; Enzyme; Rutaceae; Dicotyledones; Angiospermae; Spermatophyta; Agrume</FG>
<ED>Analysis method; Pectinesterase; Orange juice; Capillary electrophoresis; Thermal stability; Production quality; Flavor; Heat treatment; Chemical properties; Citrus sinensis; Inactivation; Characterization; Molecular weight</ED>
<EG>Carboxylic ester hydrolases; Esterases; Hydrolases; Enzyme; Rutaceae; Dicotyledones; Angiospermae; Spermatophyta; Citrus fruit</EG>
<SD>Método análisis; Pectinesterase; Zugo naranja; Electroforesis capilar; Estabilidad térmica; Calidad producción; Flavor; Tratamiento térmico; Propiedad química; Citrus sinensis; Inactivación; Caracterización; Masa molecular</SD>
<LO>INIST-7332.354000097957750520</LO>
<ID>01-0177851</ID>
</server>
</inist>
</record>

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