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Improved RP‐HPLC and anion‐exchange chromatography methods for the determination of amino acids and carbohydrates in soil solutions

Identifieur interne : 001765 ( Istex/Corpus ); précédent : 001764; suivant : 001766

Improved RP‐HPLC and anion‐exchange chromatography methods for the determination of amino acids and carbohydrates in soil solutions

Auteurs : Axel Meyer ; Holger Fischer ; Yakov Kuzyakov ; Klaus Fischer

Source :

RBID : ISTEX:2F95600B2AA916EC9605741F49D343E9A5875B2A

English descriptors

Abstract

In spite of their low concentrations in soil solutions, low–molecular weight organic substances (LMWOS) such as amino acids, sugars, and uronic acids play a major role in the cycles of C and N in soil. With respect to their low concentrations and to possible matrix interferences, their analysis in soil leachates is a challenging task. We established two HPLC (high‐performance liquid chromatography) methods for the parallel determination of amino acids and carbohydrates in soil leachates. The pre‐column derivatization of amino acids with an o‐phthaldialdehyde (OPA) mercaptoethanol solution yields quantitation limits between 0.03 and 0.44 µmol L–1 and SD values of <8.3% (n = 9). High‐performance anion‐exchange chromatography (HPAEC) on a Dionex CarboPac PA 20 column with a NaOH acetate gradient combined with pulsed amperometric detection (PAD) was used for the determination of carbohydrates. The calibration curves obtained for 11 carbohydrates showed excellent linearity over the concentration range from 0.02 to 50.0 mg L–1. Recovery studies revealed good results for all analytes (89%–108%). Interferences from Hg(II) salts and chloroform used for stabilization of the leachates did not occur with both chromatographic methods. The optimized method was successfully used for quantitative determinations of amino acids and carbohydrates in soil leachates.

Url:
DOI: 10.1002/jpln.200700235

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ISTEX:2F95600B2AA916EC9605741F49D343E9A5875B2A

Le document en format XML

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<div type="abstract" xml:lang="en">In spite of their low concentrations in soil solutions, low–molecular weight organic substances (LMWOS) such as amino acids, sugars, and uronic acids play a major role in the cycles of C and N in soil. With respect to their low concentrations and to possible matrix interferences, their analysis in soil leachates is a challenging task. We established two HPLC (high‐performance liquid chromatography) methods for the parallel determination of amino acids and carbohydrates in soil leachates. The pre‐column derivatization of amino acids with an o‐phthaldialdehyde (OPA) mercaptoethanol solution yields quantitation limits between 0.03 and 0.44 µmol L–1 and SD values of <8.3% (n = 9). High‐performance anion‐exchange chromatography (HPAEC) on a Dionex CarboPac PA 20 column with a NaOH acetate gradient combined with pulsed amperometric detection (PAD) was used for the determination of carbohydrates. The calibration curves obtained for 11 carbohydrates showed excellent linearity over the concentration range from 0.02 to 50.0 mg L–1. Recovery studies revealed good results for all analytes (89%–108%). Interferences from Hg(II) salts and chloroform used for stabilization of the leachates did not occur with both chromatographic methods. The optimized method was successfully used for quantitative determinations of amino acids and carbohydrates in soil leachates.</div>
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<p>In spite of their low concentrations in soil solutions, low–molecular weight organic substances (LMWOS) such as amino acids, sugars, and uronic acids play a major role in the cycles of C and N in soil. With respect to their low concentrations and to possible matrix interferences, their analysis in soil leachates is a challenging task. We established two HPLC (high‐performance liquid chromatography) methods for the parallel determination of amino acids and carbohydrates in soil leachates. The pre‐column derivatization of amino acids with an o‐phthaldialdehyde (OPA) mercaptoethanol solution yields quantitation limits between 0.03 and 0.44 µmol L–1 and SD values of <8.3% (n = 9). High‐performance anion‐exchange chromatography (HPAEC) on a Dionex CarboPac PA 20 column with a NaOH acetate gradient combined with pulsed amperometric detection (PAD) was used for the determination of carbohydrates. The calibration curves obtained for 11 carbohydrates showed excellent linearity over the concentration range from 0.02 to 50.0 mg L–1. Recovery studies revealed good results for all analytes (89%–108%). Interferences from Hg(II) salts and chloroform used for stabilization of the leachates did not occur with both chromatographic methods. The optimized method was successfully used for quantitative determinations of amino acids and carbohydrates in soil leachates.</p>
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<keyword xml:id="kwd3">soil leachates</keyword>
<keyword xml:id="kwd4">HPAEC‐PAD</keyword>
<keyword xml:id="kwd5">carbohydrates</keyword>
<keyword xml:id="kwd6">monosaccharides</keyword>
<keyword xml:id="kwd7">amino sugars</keyword>
<keyword xml:id="kwd8">uronic acids</keyword>
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<fundingAgency>Deutsche Forschungsgemeinschaft</fundingAgency>
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<title type="main">Abstract</title>
<p>In spite of their low concentrations in soil solutions, low–molecular weight organic substances (LMWOS) such as amino acids, sugars, and uronic acids play a major role in the cycles of C and N in soil. With respect to their low concentrations and to possible matrix interferences, their analysis in soil leachates is a challenging task. We established two HPLC (high‐performance liquid chromatography) methods for the parallel determination of amino acids and carbohydrates in soil leachates. The pre‐column derivatization of amino acids with an o‐phthaldialdehyde (OPA) mercaptoethanol solution yields quantitation limits between 0.03 and 0.44 µmol L
<sup>–1</sup>
and S
<sub>D </sub>
values of <8.3% (
<i>n</i>
= 9). High‐performance anion‐exchange chromatography (HPAEC) on a Dionex CarboPac PA 20 column with a NaOH acetate gradient combined with pulsed amperometric detection (PAD) was used for the determination of carbohydrates. The calibration curves obtained for 11 carbohydrates showed excellent linearity over the concentration range from 0.02 to 50.0 mg L
<sup>–1</sup>
. Recovery studies revealed good results for all analytes (89%–108%). Interferences from Hg(II) salts and chloroform used for stabilization of the leachates did not occur with both chromatographic methods. The optimized method was successfully used for quantitative determinations of amino acids and carbohydrates in soil leachates.</p>
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<title>Improved RP‐HPLC and anion‐exchange chromatography methods for the determination of amino acids and carbohydrates in soil solutions</title>
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<titleInfo type="alternative" contentType="CDATA" lang="en">
<title>Improved RP‐HPLC and anion‐exchange chromatography methods for the determination of amino acids and carbohydrates in soil solutions</title>
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<name type="personal">
<namePart type="given">Axel</namePart>
<namePart type="family">Meyer</namePart>
<affiliation>University of Trier, FB VI Geography/Geosciences, Analytical and Ecological Chemistry, Behringstraße, 54286 Trier, Germany</affiliation>
<affiliation>E-mail: meyerax@uni‐trier.de</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Holger</namePart>
<namePart type="family">Fischer</namePart>
<affiliation>Department of Agroecosystem Research, University of Bayreuth, Universitätsstr. 30, 95440 Bayreuth, Germany</affiliation>
<affiliation>Institute of Soil Science and Land Evaluation, University of Hohenheim, Emil‐Wolff‐Str. 27, 70593 Stuttgart, Germany</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Yakov</namePart>
<namePart type="family">Kuzyakov</namePart>
<affiliation>Department of Agroecosystem Research, University of Bayreuth, Universitätsstr. 30, 95440 Bayreuth, Germany</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Klaus</namePart>
<namePart type="family">Fischer</namePart>
<affiliation>University of Trier, FB VI Geography/Geosciences, Analytical and Ecological Chemistry, Behringstraße, 54286 Trier, Germany</affiliation>
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<dateIssued encoding="w3cdtf">2008-12</dateIssued>
<dateValid encoding="w3cdtf">2008-01-02</dateValid>
<copyrightDate encoding="w3cdtf">2008</copyrightDate>
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<abstract lang="en">In spite of their low concentrations in soil solutions, low–molecular weight organic substances (LMWOS) such as amino acids, sugars, and uronic acids play a major role in the cycles of C and N in soil. With respect to their low concentrations and to possible matrix interferences, their analysis in soil leachates is a challenging task. We established two HPLC (high‐performance liquid chromatography) methods for the parallel determination of amino acids and carbohydrates in soil leachates. The pre‐column derivatization of amino acids with an o‐phthaldialdehyde (OPA) mercaptoethanol solution yields quantitation limits between 0.03 and 0.44 µmol L–1 and SD values of <8.3% (n = 9). High‐performance anion‐exchange chromatography (HPAEC) on a Dionex CarboPac PA 20 column with a NaOH acetate gradient combined with pulsed amperometric detection (PAD) was used for the determination of carbohydrates. The calibration curves obtained for 11 carbohydrates showed excellent linearity over the concentration range from 0.02 to 50.0 mg L–1. Recovery studies revealed good results for all analytes (89%–108%). Interferences from Hg(II) salts and chloroform used for stabilization of the leachates did not occur with both chromatographic methods. The optimized method was successfully used for quantitative determinations of amino acids and carbohydrates in soil leachates.</abstract>
<note type="funding">Deutsche Forschungsgemeinschaft</note>
<subject lang="en">
<genre>keywords</genre>
<topic>low–molecular weight organic substances</topic>
<topic>amino acids</topic>
<topic>soil leachates</topic>
<topic>HPAEC‐PAD</topic>
<topic>carbohydrates</topic>
<topic>monosaccharides</topic>
<topic>amino sugars</topic>
<topic>uronic acids</topic>
</subject>
<relatedItem type="host">
<titleInfo>
<title>Journal of Plant Nutrition and Soil Science</title>
</titleInfo>
<titleInfo type="abbreviated">
<title>Z. Pflanzenernähr. Bodenk.</title>
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<genre type="journal">journal</genre>
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<topic>Regular Article</topic>
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<identifier type="ISSN">1436-8730</identifier>
<identifier type="eISSN">1522-2624</identifier>
<identifier type="DOI">10.1002/(ISSN)1522-2624</identifier>
<identifier type="PublisherID">JPLN</identifier>
<part>
<date>2008</date>
<detail type="volume">
<caption>vol.</caption>
<number>171</number>
</detail>
<detail type="issue">
<caption>no.</caption>
<number>6</number>
</detail>
<extent unit="pages">
<start>917</start>
<end>926</end>
<total>10</total>
</extent>
</part>
</relatedItem>
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<identifier type="DOI">10.1002/jpln.200700235</identifier>
<identifier type="ArticleID">JPLN200700235</identifier>
<accessCondition type="use and reproduction" contentType="copyright">Copyright © 2008 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim</accessCondition>
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