EsturgeonV1, PascalFrancis, Checkpoint, bibRecord, 000244

Characterization of glutathione S-transferases in juvenile white sturgeon

Identifieur interne : 000244 ( PascalFrancis/Checkpoint ); précédent : 000243; suivant : 000245

Characterization of glutathione S-transferases in juvenile white sturgeon

Auteurs : Rachel T. Donham [États-Unis] ; Dexter Morin [États-Unis] ; William T. Jewell [États-Unis] ; Stephanie A. Burns [États-Unis] ; Alyson E. Mitchell [États-Unis] ; M. W. Lame [États-Unis] ; H. J. Segall [États-Unis] ; Ronald S. Tjeerdema [États-Unis]

Source :

Aquatic toxicology [ 0166-445X ] ; 2005.

RBID : Pascal:05-0148244

Descripteurs français

Pascal (Inist)
- Caractérisation, Glutathione transferase, Milieu aquatique, Ecotoxicologie, Acipenser transmontanus.
Wicri :
- topic : Milieu aquatique.

English descriptors

KwdEn :
- Acipenser transmontanus, Aquatic environment, Characterization, Ecotoxicology, Glutathione transferase.

Abstract

Glutathione S-transferases (GSTs) are a family of detoxification enzymes that catalyze the conjugation of glutathione (GSH) to electrophiles, thus preventing toxicity. This study characterized the cytosolic GST classes of juvenile white sturgeon (Acipenser transmontanus) liver, using two methods of isolation. The first, which employed affinity chromatography, electrophoresis and immunoblotting against a polyclonal striped bass GST antibody, yielded two cytosolic GSTs. The GSTs were identified by nanospray liquid chromatography-tandem mass spectrometry (LC-MS/MS), peptide mass mapping and MS/MS sequencing, as well as de novo MS/MS sequencing as GST classes π and μ using the Mascot search engine and the NCBI non-redundant database (nrDB) for both methods. The molecular masses were determined to be 23,548 ± 23 and 26,027 ± 23 Da, respectively, using linear matrix assisted laser desorption ionization time of flight (MALDI-TOF) mass spectrometry. The second method of isolation, which used affinity chromatography and high-pressure liquid chromatography (HPLC), yielded π, μ, and possibly two a isoforms by MALDI-TOF-TOF, again searching against the NCBI nrDB. The a isoforms were determined to have molecular masses of 25,528 ± 23 and 25,348 ± 23 Da by electrospray ionization source (ESI)-MS. Overall, it appears that the HPLC method is more sensitive than immunoblotting with the current antibody. Activity of the cytosolic GSTs was evaluated using the substrate 1-chloro-2,4-dinitrobenzene (CDNB) and found to be 2.4 ± 0.6 U/mg cytosolic protein, and 0.41 ± 0.05 U/mg cytosolic protein using ethacrynic acid (ETHA).

Affiliations:

Links toward previous steps (curation, corpus...)

to stream PascalFrancis, to step Corpus: 000250
to stream PascalFrancis, to step Curation: 000126

Links to Exploration step

Pascal:05-0148244

Le document en format XML

<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Characterization of glutathione S-transferases in juvenile white sturgeon</title>
<author><name sortKey="Donham, Rachel T" sort="Donham, Rachel T" uniqKey="Donham R" first="Rachel T." last="Donham">Rachel T. Donham</name>
<affiliation wicri:level="2"><inist:fA14 i1="01"><s1>Department of Environmental Toxicology, College of Agricultural and Environmental Sciences, University of California, I Shields Avenue</s1>
<s2>Davis, CA 95616-8588</s2>
<s3>USA</s3>
<sZ>1 aut.</sZ>
<sZ>8 aut.</sZ>
</inist:fA14>
<country>États-Unis</country>
<placeName><region type="state">Californie</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Morin, Dexter" sort="Morin, Dexter" uniqKey="Morin D" first="Dexter" last="Morin">Dexter Morin</name>
<affiliation wicri:level="2"><inist:fA14 i1="02"><s1>Department of Molecular Biosciences: School of Veterinary Medicine, University of California, I Shields Avenue</s1>
<s2>Davis, CA 95616</s2>
<s3>USA</s3>
<sZ>2 aut.</sZ>
<sZ>6 aut.</sZ>
<sZ>7 aut.</sZ>
</inist:fA14>
<country>États-Unis</country>
<placeName><region type="state">Californie</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Jewell, William T" sort="Jewell, William T" uniqKey="Jewell W" first="William T." last="Jewell">William T. Jewell</name>
<affiliation wicri:level="2"><inist:fA14 i1="03"><s1>Molecular Structure Facility, University of California, 1 Shields Avenue</s1>
<s2>Davis, CA 95616</s2>
<s3>USA</s3>
<sZ>3 aut.</sZ>
</inist:fA14>
<country>États-Unis</country>
<placeName><region type="state">Californie</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Burns, Stephanie A" sort="Burns, Stephanie A" uniqKey="Burns S" first="Stephanie A." last="Burns">Stephanie A. Burns</name>
<affiliation wicri:level="2"><inist:fA14 i1="04"><s1>Department of Food Science and Nutrition, College of Agriculture and Environmental Sciences, University of California, 1 Shields Avenue</s1>
<s2>Davis, CA 95616-8588</s2>
<s3>USA</s3>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
</inist:fA14>
<country>États-Unis</country>
<placeName><region type="state">Californie</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Mitchell, Alyson E" sort="Mitchell, Alyson E" uniqKey="Mitchell A" first="Alyson E." last="Mitchell">Alyson E. Mitchell</name>
<affiliation wicri:level="2"><inist:fA14 i1="04"><s1>Department of Food Science and Nutrition, College of Agriculture and Environmental Sciences, University of California, 1 Shields Avenue</s1>
<s2>Davis, CA 95616-8588</s2>
<s3>USA</s3>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
</inist:fA14>
<country>États-Unis</country>
<placeName><region type="state">Californie</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Lame, M W" sort="Lame, M W" uniqKey="Lame M" first="M. W." last="Lame">M. W. Lame</name>
<affiliation wicri:level="2"><inist:fA14 i1="02"><s1>Department of Molecular Biosciences: School of Veterinary Medicine, University of California, I Shields Avenue</s1>
<s2>Davis, CA 95616</s2>
<s3>USA</s3>
<sZ>2 aut.</sZ>
<sZ>6 aut.</sZ>
<sZ>7 aut.</sZ>
</inist:fA14>
<country>États-Unis</country>
<placeName><region type="state">Californie</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Segall, H J" sort="Segall, H J" uniqKey="Segall H" first="H. J." last="Segall">H. J. Segall</name>
<affiliation wicri:level="2"><inist:fA14 i1="02"><s1>Department of Molecular Biosciences: School of Veterinary Medicine, University of California, I Shields Avenue</s1>
<s2>Davis, CA 95616</s2>
<s3>USA</s3>
<sZ>2 aut.</sZ>
<sZ>6 aut.</sZ>
<sZ>7 aut.</sZ>
</inist:fA14>
<country>États-Unis</country>
<placeName><region type="state">Californie</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Tjeerdema, Ronald S" sort="Tjeerdema, Ronald S" uniqKey="Tjeerdema R" first="Ronald S." last="Tjeerdema">Ronald S. Tjeerdema</name>
<affiliation wicri:level="2"><inist:fA14 i1="01"><s1>Department of Environmental Toxicology, College of Agricultural and Environmental Sciences, University of California, I Shields Avenue</s1>
<s2>Davis, CA 95616-8588</s2>
<s3>USA</s3>
<sZ>1 aut.</sZ>
<sZ>8 aut.</sZ>
</inist:fA14>
<country>États-Unis</country>
<placeName><region type="state">Californie</region>
</placeName>
</affiliation>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">INIST</idno>
<idno type="inist">05-0148244</idno>
<date when="2005">2005</date>
<idno type="stanalyst">PASCAL 05-0148244 INIST</idno>
<idno type="RBID">Pascal:05-0148244</idno>
<idno type="wicri:Area/PascalFrancis/Corpus">000250</idno>
<idno type="wicri:Area/PascalFrancis/Curation">000126</idno>
<idno type="wicri:Area/PascalFrancis/Checkpoint">000244</idno>
<idno type="wicri:explorRef" wicri:stream="PascalFrancis" wicri:step="Checkpoint">000244</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a">Characterization of glutathione S-transferases in juvenile white sturgeon</title>
<author><name sortKey="Donham, Rachel T" sort="Donham, Rachel T" uniqKey="Donham R" first="Rachel T." last="Donham">Rachel T. Donham</name>
<affiliation wicri:level="2"><inist:fA14 i1="01"><s1>Department of Environmental Toxicology, College of Agricultural and Environmental Sciences, University of California, I Shields Avenue</s1>
<s2>Davis, CA 95616-8588</s2>
<s3>USA</s3>
<sZ>1 aut.</sZ>
<sZ>8 aut.</sZ>
</inist:fA14>
<country>États-Unis</country>
<placeName><region type="state">Californie</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Morin, Dexter" sort="Morin, Dexter" uniqKey="Morin D" first="Dexter" last="Morin">Dexter Morin</name>
<affiliation wicri:level="2"><inist:fA14 i1="02"><s1>Department of Molecular Biosciences: School of Veterinary Medicine, University of California, I Shields Avenue</s1>
<s2>Davis, CA 95616</s2>
<s3>USA</s3>
<sZ>2 aut.</sZ>
<sZ>6 aut.</sZ>
<sZ>7 aut.</sZ>
</inist:fA14>
<country>États-Unis</country>
<placeName><region type="state">Californie</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Jewell, William T" sort="Jewell, William T" uniqKey="Jewell W" first="William T." last="Jewell">William T. Jewell</name>
<affiliation wicri:level="2"><inist:fA14 i1="03"><s1>Molecular Structure Facility, University of California, 1 Shields Avenue</s1>
<s2>Davis, CA 95616</s2>
<s3>USA</s3>
<sZ>3 aut.</sZ>
</inist:fA14>
<country>États-Unis</country>
<placeName><region type="state">Californie</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Burns, Stephanie A" sort="Burns, Stephanie A" uniqKey="Burns S" first="Stephanie A." last="Burns">Stephanie A. Burns</name>
<affiliation wicri:level="2"><inist:fA14 i1="04"><s1>Department of Food Science and Nutrition, College of Agriculture and Environmental Sciences, University of California, 1 Shields Avenue</s1>
<s2>Davis, CA 95616-8588</s2>
<s3>USA</s3>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
</inist:fA14>
<country>États-Unis</country>
<placeName><region type="state">Californie</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Mitchell, Alyson E" sort="Mitchell, Alyson E" uniqKey="Mitchell A" first="Alyson E." last="Mitchell">Alyson E. Mitchell</name>
<affiliation wicri:level="2"><inist:fA14 i1="04"><s1>Department of Food Science and Nutrition, College of Agriculture and Environmental Sciences, University of California, 1 Shields Avenue</s1>
<s2>Davis, CA 95616-8588</s2>
<s3>USA</s3>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
</inist:fA14>
<country>États-Unis</country>
<placeName><region type="state">Californie</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Lame, M W" sort="Lame, M W" uniqKey="Lame M" first="M. W." last="Lame">M. W. Lame</name>
<affiliation wicri:level="2"><inist:fA14 i1="02"><s1>Department of Molecular Biosciences: School of Veterinary Medicine, University of California, I Shields Avenue</s1>
<s2>Davis, CA 95616</s2>
<s3>USA</s3>
<sZ>2 aut.</sZ>
<sZ>6 aut.</sZ>
<sZ>7 aut.</sZ>
</inist:fA14>
<country>États-Unis</country>
<placeName><region type="state">Californie</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Segall, H J" sort="Segall, H J" uniqKey="Segall H" first="H. J." last="Segall">H. J. Segall</name>
<affiliation wicri:level="2"><inist:fA14 i1="02"><s1>Department of Molecular Biosciences: School of Veterinary Medicine, University of California, I Shields Avenue</s1>
<s2>Davis, CA 95616</s2>
<s3>USA</s3>
<sZ>2 aut.</sZ>
<sZ>6 aut.</sZ>
<sZ>7 aut.</sZ>
</inist:fA14>
<country>États-Unis</country>
<placeName><region type="state">Californie</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Tjeerdema, Ronald S" sort="Tjeerdema, Ronald S" uniqKey="Tjeerdema R" first="Ronald S." last="Tjeerdema">Ronald S. Tjeerdema</name>
<affiliation wicri:level="2"><inist:fA14 i1="01"><s1>Department of Environmental Toxicology, College of Agricultural and Environmental Sciences, University of California, I Shields Avenue</s1>
<s2>Davis, CA 95616-8588</s2>
<s3>USA</s3>
<sZ>1 aut.</sZ>
<sZ>8 aut.</sZ>
</inist:fA14>
<country>États-Unis</country>
<placeName><region type="state">Californie</region>
</placeName>
</affiliation>
</author>
</analytic>
<series><title level="j" type="main">Aquatic toxicology</title>
<title level="j" type="abbreviated">Aquat. toxicol.</title>
<idno type="ISSN">0166-445X</idno>
<imprint><date when="2005">2005</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
<seriesStmt><title level="j" type="main">Aquatic toxicology</title>
<title level="j" type="abbreviated">Aquat. toxicol.</title>
<idno type="ISSN">0166-445X</idno>
</seriesStmt>
</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Acipenser transmontanus</term>
<term>Aquatic environment</term>
<term>Characterization</term>
<term>Ecotoxicology</term>
<term>Glutathione transferase</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr"><term>Caractérisation</term>
<term>Glutathione transferase</term>
<term>Milieu aquatique</term>
<term>Ecotoxicologie</term>
<term>Acipenser transmontanus</term>
</keywords>
<keywords scheme="Wicri" type="topic" xml:lang="fr"><term>Milieu aquatique</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en">Glutathione S-transferases (GSTs) are a family of detoxification enzymes that catalyze the conjugation of glutathione (GSH) to electrophiles, thus preventing toxicity. This study characterized the cytosolic GST classes of juvenile white sturgeon (Acipenser transmontanus) liver, using two methods of isolation. The first, which employed affinity chromatography, electrophoresis and immunoblotting against a polyclonal striped bass GST antibody, yielded two cytosolic GSTs. The GSTs were identified by nanospray liquid chromatography-tandem mass spectrometry (LC-MS/MS), peptide mass mapping and MS/MS sequencing, as well as de novo MS/MS sequencing as GST classes π and μ using the Mascot search engine and the NCBI non-redundant database (nrDB) for both methods. The molecular masses were determined to be 23,548 ± 23 and 26,027 ± 23 Da, respectively, using linear matrix assisted laser desorption ionization time of flight (MALDI-TOF) mass spectrometry. The second method of isolation, which used affinity chromatography and high-pressure liquid chromatography (HPLC), yielded π, μ, and possibly two a isoforms by MALDI-TOF-TOF, again searching against the NCBI nrDB. The a isoforms were determined to have molecular masses of 25,528 ± 23 and 25,348 ± 23 Da by electrospray ionization source (ESI)-MS. Overall, it appears that the HPLC method is more sensitive than immunoblotting with the current antibody. Activity of the cytosolic GSTs was evaluated using the substrate 1-chloro-2,4-dinitrobenzene (CDNB) and found to be 2.4 ± 0.6 U/mg cytosolic protein, and 0.41 ± 0.05 U/mg cytosolic protein using ethacrynic acid (ETHA).</div>
</front>
</TEI>
<inist><standard h6="B"><pA><fA01 i1="01" i2="1"><s0>0166-445X</s0>
</fA01>
<fA02 i1="01"><s0>AQTODG</s0>
</fA02>
<fA03 i2="1"><s0>Aquat. toxicol.</s0>
</fA03>
<fA05><s2>71</s2>
</fA05>
<fA06><s2>3</s2>
</fA06>
<fA08 i1="01" i2="1" l="ENG"><s1>Characterization of glutathione S-transferases in juvenile white sturgeon</s1>
</fA08>
<fA11 i1="01" i2="1"><s1>DONHAM (Rachel T.)</s1>
</fA11>
<fA11 i1="02" i2="1"><s1>MORIN (Dexter)</s1>
</fA11>
<fA11 i1="03" i2="1"><s1>JEWELL (William T.)</s1>
</fA11>
<fA11 i1="04" i2="1"><s1>BURNS (Stephanie A.)</s1>
</fA11>
<fA11 i1="05" i2="1"><s1>MITCHELL (Alyson E.)</s1>
</fA11>
<fA11 i1="06" i2="1"><s1>LAME (M. W.)</s1>
</fA11>
<fA11 i1="07" i2="1"><s1>SEGALL (H. J.)</s1>
</fA11>
<fA11 i1="08" i2="1"><s1>TJEERDEMA (Ronald S.)</s1>
</fA11>
<fA14 i1="01"><s1>Department of Environmental Toxicology, College of Agricultural and Environmental Sciences, University of California, I Shields Avenue</s1>
<s2>Davis, CA 95616-8588</s2>
<s3>USA</s3>
<sZ>1 aut.</sZ>
<sZ>8 aut.</sZ>
</fA14>
<fA14 i1="02"><s1>Department of Molecular Biosciences: School of Veterinary Medicine, University of California, I Shields Avenue</s1>
<s2>Davis, CA 95616</s2>
<s3>USA</s3>
<sZ>2 aut.</sZ>
<sZ>6 aut.</sZ>
<sZ>7 aut.</sZ>
</fA14>
<fA14 i1="03"><s1>Molecular Structure Facility, University of California, 1 Shields Avenue</s1>
<s2>Davis, CA 95616</s2>
<s3>USA</s3>
<sZ>3 aut.</sZ>
</fA14>
<fA14 i1="04"><s1>Department of Food Science and Nutrition, College of Agriculture and Environmental Sciences, University of California, 1 Shields Avenue</s1>
<s2>Davis, CA 95616-8588</s2>
<s3>USA</s3>
<sZ>4 aut.</sZ>
<sZ>5 aut.</sZ>
</fA14>
<fA20><s1>203-214</s1>
</fA20>
<fA21><s1>2005</s1>
</fA21>
<fA23 i1="01"><s0>ENG</s0>
</fA23>
<fA43 i1="01"><s1>INIST</s1>
<s2>18841</s2>
<s5>354000125946860010</s5>
</fA43>
<fA44><s0>0000</s0>
<s1>© 2005 INIST-CNRS. All rights reserved.</s1>
</fA44>
<fA45><s0>27 ref.</s0>
</fA45>
<fA47 i1="01" i2="1"><s0>05-0148244</s0>
</fA47>
<fA60><s1>P</s1>
</fA60>
<fA61><s0>A</s0>
</fA61>
<fA64 i1="01" i2="1"><s0>Aquatic toxicology</s0>
</fA64>
<fA66 i1="01"><s0>NLD</s0>
</fA66>
<fC01 i1="01" l="ENG"><s0>Glutathione S-transferases (GSTs) are a family of detoxification enzymes that catalyze the conjugation of glutathione (GSH) to electrophiles, thus preventing toxicity. This study characterized the cytosolic GST classes of juvenile white sturgeon (Acipenser transmontanus) liver, using two methods of isolation. The first, which employed affinity chromatography, electrophoresis and immunoblotting against a polyclonal striped bass GST antibody, yielded two cytosolic GSTs. The GSTs were identified by nanospray liquid chromatography-tandem mass spectrometry (LC-MS/MS), peptide mass mapping and MS/MS sequencing, as well as de novo MS/MS sequencing as GST classes π and μ using the Mascot search engine and the NCBI non-redundant database (nrDB) for both methods. The molecular masses were determined to be 23,548 ± 23 and 26,027 ± 23 Da, respectively, using linear matrix assisted laser desorption ionization time of flight (MALDI-TOF) mass spectrometry. The second method of isolation, which used affinity chromatography and high-pressure liquid chromatography (HPLC), yielded π, μ, and possibly two a isoforms by MALDI-TOF-TOF, again searching against the NCBI nrDB. The a isoforms were determined to have molecular masses of 25,528 ± 23 and 25,348 ± 23 Da by electrospray ionization source (ESI)-MS. Overall, it appears that the HPLC method is more sensitive than immunoblotting with the current antibody. Activity of the cytosolic GSTs was evaluated using the substrate 1-chloro-2,4-dinitrobenzene (CDNB) and found to be 2.4 ± 0.6 U/mg cytosolic protein, and 0.41 ± 0.05 U/mg cytosolic protein using ethacrynic acid (ETHA).</s0>
</fC01>
<fC02 i1="01" i2="X"><s0>002A14D05A</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>Glutathione transferase</s0>
<s2>FE</s2>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="X" l="ENG"><s0>Glutathione transferase</s0>
<s2>FE</s2>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="X" l="SPA"><s0>Glutathione transferase</s0>
<s2>FE</s2>
<s5>02</s5>
</fC03>
<fC03 i1="03" i2="X" l="FRE"><s0>Milieu aquatique</s0>
<s5>03</s5>
</fC03>
<fC03 i1="03" i2="X" l="ENG"><s0>Aquatic environment</s0>
<s5>03</s5>
</fC03>
<fC03 i1="03" i2="X" l="SPA"><s0>Medio acuático</s0>
<s5>03</s5>
</fC03>
<fC03 i1="04" i2="X" l="FRE"><s0>Ecotoxicologie</s0>
<s5>04</s5>
</fC03>
<fC03 i1="04" i2="X" l="ENG"><s0>Ecotoxicology</s0>
<s5>04</s5>
</fC03>
<fC03 i1="04" i2="X" l="SPA"><s0>Ecotoxicología</s0>
<s5>04</s5>
</fC03>
<fC03 i1="05" i2="X" l="FRE"><s0>Acipenser transmontanus</s0>
<s2>NS</s2>
<s5>55</s5>
</fC03>
<fC03 i1="05" i2="X" l="ENG"><s0>Acipenser transmontanus</s0>
<s2>NS</s2>
<s5>55</s5>
</fC03>
<fC03 i1="05" i2="X" l="SPA"><s0>Acipenser transmontanus</s0>
<s2>NS</s2>
<s5>55</s5>
</fC03>
<fC07 i1="01" i2="X" l="FRE"><s0>Transferases</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="01" i2="X" l="ENG"><s0>Transferases</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="01" i2="X" l="SPA"><s0>Transferases</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="02" i2="X" l="FRE"><s0>Enzyme</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="02" i2="X" l="ENG"><s0>Enzyme</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="02" i2="X" l="SPA"><s0>Enzima</s0>
<s2>FE</s2>
</fC07>
<fC07 i1="03" i2="X" l="FRE"><s0>Pisces</s0>
<s2>NS</s2>
<s5>29</s5>
</fC07>
<fC07 i1="03" i2="X" l="ENG"><s0>Pisces</s0>
<s2>NS</s2>
<s5>29</s5>
</fC07>
<fC07 i1="03" i2="X" l="SPA"><s0>Pisces</s0>
<s2>NS</s2>
<s5>29</s5>
</fC07>
<fC07 i1="04" i2="X" l="FRE"><s0>Vertebrata</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="04" i2="X" l="ENG"><s0>Vertebrata</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="04" i2="X" l="SPA"><s0>Vertebrata</s0>
<s2>NS</s2>
</fC07>
<fC07 i1="05" i2="X" l="FRE"><s0>Acipenseridae</s0>
<s4>INC</s4>
<s5>70</s5>
</fC07>
<fN21><s1>101</s1>
</fN21>
<fN44 i1="01"><s1>OTO</s1>
</fN44>
<fN82><s1>OTO</s1>
</fN82>
</pA>
</standard>
</inist>
<affiliations><list><country><li>États-Unis</li>
</country>
<region><li>Californie</li>
</region>
</list>
<tree><country name="États-Unis"><region name="Californie"><name sortKey="Donham, Rachel T" sort="Donham, Rachel T" uniqKey="Donham R" first="Rachel T." last="Donham">Rachel T. Donham</name>
</region>
<name sortKey="Burns, Stephanie A" sort="Burns, Stephanie A" uniqKey="Burns S" first="Stephanie A." last="Burns">Stephanie A. Burns</name>
<name sortKey="Jewell, William T" sort="Jewell, William T" uniqKey="Jewell W" first="William T." last="Jewell">William T. Jewell</name>
<name sortKey="Lame, M W" sort="Lame, M W" uniqKey="Lame M" first="M. W." last="Lame">M. W. Lame</name>
<name sortKey="Mitchell, Alyson E" sort="Mitchell, Alyson E" uniqKey="Mitchell A" first="Alyson E." last="Mitchell">Alyson E. Mitchell</name>
<name sortKey="Morin, Dexter" sort="Morin, Dexter" uniqKey="Morin D" first="Dexter" last="Morin">Dexter Morin</name>
<name sortKey="Segall, H J" sort="Segall, H J" uniqKey="Segall H" first="H. J." last="Segall">H. J. Segall</name>
<name sortKey="Tjeerdema, Ronald S" sort="Tjeerdema, Ronald S" uniqKey="Tjeerdema R" first="Ronald S." last="Tjeerdema">Ronald S. Tjeerdema</name>
</country>
</tree>
</affiliations>
</record>

Pour manipuler ce document sous Unix (Dilib)

EXPLOR_STEP=$WICRI_ROOT/Wicri/Eau/explor/EsturgeonV1/Data/PascalFrancis/Checkpoint

HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 000244 | SxmlIndent | more

HfdSelect -h $EXPLOR_AREA/Data/PascalFrancis/Checkpoint/biblio.hfd -nk 000244 | SxmlIndent | more

Pour mettre un lien sur cette page dans le réseau Wicri

{{Explor lien
   |wiki=    Wicri/Eau
   |area=    EsturgeonV1
   |flux=    PascalFrancis
   |étape=   Checkpoint
   |type=    RBID
   |clé=     Pascal:05-0148244
   |texte=   Characterization of glutathione S-transferases in juvenile white sturgeon
}}

This area was generated with Dilib version V0.6.27.
Data generation: Sat Mar 25 15:37:54 2017. Site generation: Tue Feb 13 14:18:49 2024

	Serveur d'exploration sur l'esturgeon
	Attention, ce site est en cours de développement ! Attention, site généré par des moyens informatiques à partir de corpus bruts. Les informations ne sont donc pas validées.

Serveur d'exploration sur l'esturgeon

Characterization of glutathione S-transferases in juvenile white sturgeon

Characterization of glutathione S-transferases in juvenile white sturgeon

Source :

Descripteurs français

English descriptors

Abstract

Links toward previous steps (curation, corpus...)

Links to Exploration step

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

Pour mettre un lien sur cette page dans le réseau Wicri