Analysis of protein hydrolysates. 2. Characterization of casein hydrolysates by a rapid peptide quantification method

Casein hydrolysates prepared in the laboratory or purchased from a manufacturer were characterized for the proportion of amino acids in free form, in short-chain (di- and tripeptides) or larger peptides. The hydrolysates were fractionated by size exclusion chromatography on a poly(2-hydroxyethylaspa...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of agricultural and food chemistry 1994-12, Vol.42 (12), p.2783-2789
Hauptverfasser: Silvestre, M.P.C. (UFMG, Belo Horizonte, Brazil.), Hamon, M, Yvon, M
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 2789
container_issue 12
container_start_page 2783
container_title Journal of agricultural and food chemistry
container_volume 42
creator Silvestre, M.P.C. (UFMG, Belo Horizonte, Brazil.)
Hamon, M
Yvon, M
description Casein hydrolysates prepared in the laboratory or purchased from a manufacturer were characterized for the proportion of amino acids in free form, in short-chain (di- and tripeptides) or larger peptides. The hydrolysates were fractionated by size exclusion chromatography on a poly(2-hydroxyethylaspartamide)-silica column (PHEA), and the fractions were analyzed by amino acid analysis. This led to an accurate characterization of hydrolysates which allowed a classification of the hydrolysates according to the extent of hydrolysis and their nutritional quality. A rapid method for quantifying peptides in SE-HPLC fractions was also proposed. It was based on UV absorbance measurement at 230 nm, with a correction for the absorbance of aromatic amino acid measured at three wavelengths (230, 280, and 300 nm). A good correlation was obtained between corrected areas and the amino acid analysis. Because of nonideal size exclusion behavior on the PHEA column, further analysis of free amino acids would be required to correct the data obtained from the chromatographic patterns. The quantitative technique described here proved to be a valuable tool for characterizing unknown protein hydrolysates
doi_str_mv 10.1021/jf00048a025
format Article
fullrecord <record><control><sourceid>hal_fao_a</sourceid><recordid>TN_cdi_hal_primary_oai_HAL_hal_02705528v1</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>oai_HAL_hal_02705528v1</sourcerecordid><originalsourceid>FETCH-LOGICAL-f138t-495c9e54c1968cfba172ae82d180531e1e1ca48de3300503ba43f3d9233d9793</originalsourceid><addsrcrecordid>eNpdzE1LAzEQBuAgCtbqyZunXD1snSSbbvZYilqh4MF6Xqb5cFPazZqkwvrrXaknGZiBd54ZQm4ZzBhw9rBzAFAqBC7PyIRJDoVkTJ2TCYzrQsk5uyRXKe1GpmQFE3JcdLgfkk80ONrHkK3vaDuYGMYUs00zymd02WJEnW3035h96H6xxvTf0u1AkUbsvaG97bM3ln4escveeX06PNjcBnNNLhzuk735m1OyeXrcLFfF-vX5ZblYF44JlYuylrq2stSsnivttsgqjlZxwxRIwexYGktlrBAAEsQWS-GEqbkYW1WLKbk_vW1x3_TRHzAOTUDfrBbr5jcDXoGUXH2x0d6drMPQ4Ef0qXl_q-fAlarFD_sTaAI</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Analysis of protein hydrolysates. 2. Characterization of casein hydrolysates by a rapid peptide quantification method</title><source>ACS Publications</source><creator>Silvestre, M.P.C. (UFMG, Belo Horizonte, Brazil.) ; Hamon, M ; Yvon, M</creator><creatorcontrib>Silvestre, M.P.C. (UFMG, Belo Horizonte, Brazil.) ; Hamon, M ; Yvon, M</creatorcontrib><description>Casein hydrolysates prepared in the laboratory or purchased from a manufacturer were characterized for the proportion of amino acids in free form, in short-chain (di- and tripeptides) or larger peptides. The hydrolysates were fractionated by size exclusion chromatography on a poly(2-hydroxyethylaspartamide)-silica column (PHEA), and the fractions were analyzed by amino acid analysis. This led to an accurate characterization of hydrolysates which allowed a classification of the hydrolysates according to the extent of hydrolysis and their nutritional quality. A rapid method for quantifying peptides in SE-HPLC fractions was also proposed. It was based on UV absorbance measurement at 230 nm, with a correction for the absorbance of aromatic amino acid measured at three wavelengths (230, 280, and 300 nm). A good correlation was obtained between corrected areas and the amino acid analysis. Because of nonideal size exclusion behavior on the PHEA column, further analysis of free amino acids would be required to correct the data obtained from the chromatographic patterns. The quantitative technique described here proved to be a valuable tool for characterizing unknown protein hydrolysates</description><identifier>ISSN: 0021-8561</identifier><identifier>EISSN: 1520-5118</identifier><identifier>DOI: 10.1021/jf00048a025</identifier><language>eng</language><publisher>American Chemical Society</publisher><subject>ANALISIS CUANTITATIVO ; ANALYSE QUANTITATIVE ; ESPECTROMETRIA ; Food engineering ; HYDROLYSAT DE PROTEINES ; Life Sciences ; PROTEINAS HIDROLIZADAS ; RADIACION ULTRAVIOLETA ; RAYONNEMENT ULTRAVIOLET ; SPECTROMETRIE ; TECHNIQUE ANALYTIQUE ; TECNICAS ANALITICAS</subject><ispartof>Journal of agricultural and food chemistry, 1994-12, Vol.42 (12), p.2783-2789</ispartof><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://hal.inrae.fr/hal-02705528$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Silvestre, M.P.C. (UFMG, Belo Horizonte, Brazil.)</creatorcontrib><creatorcontrib>Hamon, M</creatorcontrib><creatorcontrib>Yvon, M</creatorcontrib><title>Analysis of protein hydrolysates. 2. Characterization of casein hydrolysates by a rapid peptide quantification method</title><title>Journal of agricultural and food chemistry</title><description>Casein hydrolysates prepared in the laboratory or purchased from a manufacturer were characterized for the proportion of amino acids in free form, in short-chain (di- and tripeptides) or larger peptides. The hydrolysates were fractionated by size exclusion chromatography on a poly(2-hydroxyethylaspartamide)-silica column (PHEA), and the fractions were analyzed by amino acid analysis. This led to an accurate characterization of hydrolysates which allowed a classification of the hydrolysates according to the extent of hydrolysis and their nutritional quality. A rapid method for quantifying peptides in SE-HPLC fractions was also proposed. It was based on UV absorbance measurement at 230 nm, with a correction for the absorbance of aromatic amino acid measured at three wavelengths (230, 280, and 300 nm). A good correlation was obtained between corrected areas and the amino acid analysis. Because of nonideal size exclusion behavior on the PHEA column, further analysis of free amino acids would be required to correct the data obtained from the chromatographic patterns. The quantitative technique described here proved to be a valuable tool for characterizing unknown protein hydrolysates</description><subject>ANALISIS CUANTITATIVO</subject><subject>ANALYSE QUANTITATIVE</subject><subject>ESPECTROMETRIA</subject><subject>Food engineering</subject><subject>HYDROLYSAT DE PROTEINES</subject><subject>Life Sciences</subject><subject>PROTEINAS HIDROLIZADAS</subject><subject>RADIACION ULTRAVIOLETA</subject><subject>RAYONNEMENT ULTRAVIOLET</subject><subject>SPECTROMETRIE</subject><subject>TECHNIQUE ANALYTIQUE</subject><subject>TECNICAS ANALITICAS</subject><issn>0021-8561</issn><issn>1520-5118</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1994</creationdate><recordtype>article</recordtype><recordid>eNpdzE1LAzEQBuAgCtbqyZunXD1snSSbbvZYilqh4MF6Xqb5cFPazZqkwvrrXaknGZiBd54ZQm4ZzBhw9rBzAFAqBC7PyIRJDoVkTJ2TCYzrQsk5uyRXKe1GpmQFE3JcdLgfkk80ONrHkK3vaDuYGMYUs00zymd02WJEnW3035h96H6xxvTf0u1AkUbsvaG97bM3ln4escveeX06PNjcBnNNLhzuk735m1OyeXrcLFfF-vX5ZblYF44JlYuylrq2stSsnivttsgqjlZxwxRIwexYGktlrBAAEsQWS-GEqbkYW1WLKbk_vW1x3_TRHzAOTUDfrBbr5jcDXoGUXH2x0d6drMPQ4Ef0qXl_q-fAlarFD_sTaAI</recordid><startdate>19941201</startdate><enddate>19941201</enddate><creator>Silvestre, M.P.C. (UFMG, Belo Horizonte, Brazil.)</creator><creator>Hamon, M</creator><creator>Yvon, M</creator><general>American Chemical Society</general><scope>FBQ</scope><scope>1XC</scope></search><sort><creationdate>19941201</creationdate><title>Analysis of protein hydrolysates. 2. Characterization of casein hydrolysates by a rapid peptide quantification method</title><author>Silvestre, M.P.C. (UFMG, Belo Horizonte, Brazil.) ; Hamon, M ; Yvon, M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-f138t-495c9e54c1968cfba172ae82d180531e1e1ca48de3300503ba43f3d9233d9793</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1994</creationdate><topic>ANALISIS CUANTITATIVO</topic><topic>ANALYSE QUANTITATIVE</topic><topic>ESPECTROMETRIA</topic><topic>Food engineering</topic><topic>HYDROLYSAT DE PROTEINES</topic><topic>Life Sciences</topic><topic>PROTEINAS HIDROLIZADAS</topic><topic>RADIACION ULTRAVIOLETA</topic><topic>RAYONNEMENT ULTRAVIOLET</topic><topic>SPECTROMETRIE</topic><topic>TECHNIQUE ANALYTIQUE</topic><topic>TECNICAS ANALITICAS</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Silvestre, M.P.C. (UFMG, Belo Horizonte, Brazil.)</creatorcontrib><creatorcontrib>Hamon, M</creatorcontrib><creatorcontrib>Yvon, M</creatorcontrib><collection>AGRIS</collection><collection>Hyper Article en Ligne (HAL)</collection><jtitle>Journal of agricultural and food chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Silvestre, M.P.C. (UFMG, Belo Horizonte, Brazil.)</au><au>Hamon, M</au><au>Yvon, M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Analysis of protein hydrolysates. 2. Characterization of casein hydrolysates by a rapid peptide quantification method</atitle><jtitle>Journal of agricultural and food chemistry</jtitle><date>1994-12-01</date><risdate>1994</risdate><volume>42</volume><issue>12</issue><spage>2783</spage><epage>2789</epage><pages>2783-2789</pages><issn>0021-8561</issn><eissn>1520-5118</eissn><abstract>Casein hydrolysates prepared in the laboratory or purchased from a manufacturer were characterized for the proportion of amino acids in free form, in short-chain (di- and tripeptides) or larger peptides. The hydrolysates were fractionated by size exclusion chromatography on a poly(2-hydroxyethylaspartamide)-silica column (PHEA), and the fractions were analyzed by amino acid analysis. This led to an accurate characterization of hydrolysates which allowed a classification of the hydrolysates according to the extent of hydrolysis and their nutritional quality. A rapid method for quantifying peptides in SE-HPLC fractions was also proposed. It was based on UV absorbance measurement at 230 nm, with a correction for the absorbance of aromatic amino acid measured at three wavelengths (230, 280, and 300 nm). A good correlation was obtained between corrected areas and the amino acid analysis. Because of nonideal size exclusion behavior on the PHEA column, further analysis of free amino acids would be required to correct the data obtained from the chromatographic patterns. The quantitative technique described here proved to be a valuable tool for characterizing unknown protein hydrolysates</abstract><pub>American Chemical Society</pub><doi>10.1021/jf00048a025</doi><tpages>7</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0021-8561
ispartof Journal of agricultural and food chemistry, 1994-12, Vol.42 (12), p.2783-2789
issn 0021-8561
1520-5118
language eng
recordid cdi_hal_primary_oai_HAL_hal_02705528v1
source ACS Publications
subjects ANALISIS CUANTITATIVO
ANALYSE QUANTITATIVE
ESPECTROMETRIA
Food engineering
HYDROLYSAT DE PROTEINES
Life Sciences
PROTEINAS HIDROLIZADAS
RADIACION ULTRAVIOLETA
RAYONNEMENT ULTRAVIOLET
SPECTROMETRIE
TECHNIQUE ANALYTIQUE
TECNICAS ANALITICAS
title Analysis of protein hydrolysates. 2. Characterization of casein hydrolysates by a rapid peptide quantification method
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-05T05%3A39%3A01IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-hal_fao_a&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Analysis%20of%20protein%20hydrolysates.%202.%20Characterization%20of%20casein%20hydrolysates%20by%20a%20rapid%20peptide%20quantification%20method&rft.jtitle=Journal%20of%20agricultural%20and%20food%20chemistry&rft.au=Silvestre,%20M.P.C.%20(UFMG,%20Belo%20Horizonte,%20Brazil.)&rft.date=1994-12-01&rft.volume=42&rft.issue=12&rft.spage=2783&rft.epage=2789&rft.pages=2783-2789&rft.issn=0021-8561&rft.eissn=1520-5118&rft_id=info:doi/10.1021/jf00048a025&rft_dat=%3Chal_fao_a%3Eoai_HAL_hal_02705528v1%3C/hal_fao_a%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true