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...
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Veröffentlicht in: | Journal of agricultural and food chemistry 1994-12, Vol.42 (12), p.2783-2789 |
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container_title | Journal of agricultural and food chemistry |
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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 |
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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. 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(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. 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(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> |
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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 |
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