Antioxidant Properties of Kilned and Roasted Malts
Compounds possessing antioxidant activity play a crucial role in delaying or preventing lipid oxidation in foods and beverages during processing and storage. Such reactions lead to loss of product quality, especially as a consequence of off-flavor formation. The aim of this study was to determine th...
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Veröffentlicht in: | Journal of agricultural and food chemistry 2005-10, Vol.53 (20), p.8068-8074 |
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creator | Samaras, Thomas S Camburn, Philip A Chandra, Sachin X Gordon, Michael H Ames, Jennifer M |
description | Compounds possessing antioxidant activity play a crucial role in delaying or preventing lipid oxidation in foods and beverages during processing and storage. Such reactions lead to loss of product quality, especially as a consequence of off-flavor formation. The aim of this study was to determine the antioxidant activity of kilned (standard) and roasted (speciality) malts in relation to phenolic compounds, sugars, amino acids, and color [assessed as European Brewing Convention units (°EBC) and absorbance at 420 nm]. The concentrations of sugars and amino acids decreased with the intensity of the applied heat treatment, and this was attributed to the extent of the Maillard reaction, as well as sugar caramelization, in the highly roasted malts. Proline, followed by glutamine, was the most abundant free amino/imino acid in the malt samples, except those that were highly roasted, and maltose was the most abundant sugar in all malts. Levels of total phenolic compounds decreased with heat treatment. Catechin and ferulic acid were the most abundant phenolic compounds in the majority of the malts, and amounts were highest in the kilned samples. In highly roasted malts, degradation products of ferulic acid were identified. Antioxidant activity increased with the intensity of heating, in parallel with color formation, and was significantly higher for roasted malts compared to kilned malts. In kilned malts, phenolic compounds were the main identified contributors to antioxidant activity, with Maillard reaction products also playing a role. In roasted malts, Maillard reaction products were responsible for the majority of the antioxidant activity. Keywords: Kilned malt; roasted malt; antioxidant activity; 2,2‘-azinobis(3-ethylbenzothiazoline-6-sulfonic acid) radical cation scavenging activity; oxygen radical absorbance capacity; Maillard reaction; capillary electrophoresis |
doi_str_mv | 10.1021/jf051410f |
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Such reactions lead to loss of product quality, especially as a consequence of off-flavor formation. The aim of this study was to determine the antioxidant activity of kilned (standard) and roasted (speciality) malts in relation to phenolic compounds, sugars, amino acids, and color [assessed as European Brewing Convention units (°EBC) and absorbance at 420 nm]. The concentrations of sugars and amino acids decreased with the intensity of the applied heat treatment, and this was attributed to the extent of the Maillard reaction, as well as sugar caramelization, in the highly roasted malts. Proline, followed by glutamine, was the most abundant free amino/imino acid in the malt samples, except those that were highly roasted, and maltose was the most abundant sugar in all malts. Levels of total phenolic compounds decreased with heat treatment. Catechin and ferulic acid were the most abundant phenolic compounds in the majority of the malts, and amounts were highest in the kilned samples. In highly roasted malts, degradation products of ferulic acid were identified. Antioxidant activity increased with the intensity of heating, in parallel with color formation, and was significantly higher for roasted malts compared to kilned malts. In kilned malts, phenolic compounds were the main identified contributors to antioxidant activity, with Maillard reaction products also playing a role. In roasted malts, Maillard reaction products were responsible for the majority of the antioxidant activity. Keywords: Kilned malt; roasted malt; antioxidant activity; 2,2‘-azinobis(3-ethylbenzothiazoline-6-sulfonic acid) radical cation scavenging activity; oxygen radical absorbance capacity; Maillard reaction; capillary electrophoresis</description><identifier>ISSN: 0021-8561</identifier><identifier>EISSN: 1520-5118</identifier><identifier>DOI: 10.1021/jf051410f</identifier><identifier>PMID: 16190672</identifier><identifier>CODEN: JAFCAU</identifier><language>eng</language><publisher>Washington, DC: American Chemical Society</publisher><subject>Amino Acids - analysis ; antioxidant activity ; antioxidants ; Antioxidants - analysis ; Antioxidants - pharmacology ; Biological and medical sciences ; Carbohydrates - analysis ; Catechin - analysis ; Color ; Coumaric Acids - analysis ; Edible Grain - chemistry ; Food Handling - methods ; Food industries ; Fundamental and applied biological sciences. Psychology ; heat treatment ; Hot Temperature ; kilns ; Maillard Reaction ; Maillard reaction products ; malt ; malting barley ; phenolic compounds ; Phenols - analysis ; roasting ; Spectrophotometry</subject><ispartof>Journal of agricultural and food chemistry, 2005-10, Vol.53 (20), p.8068-8074</ispartof><rights>Copyright © 2005 American Chemical Society</rights><rights>2007 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a471t-9117637cd69620980c6b26e7196722fe80eb575607b545c4f580f15e31debe633</citedby><cites>FETCH-LOGICAL-a471t-9117637cd69620980c6b26e7196722fe80eb575607b545c4f580f15e31debe633</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/jf051410f$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/jf051410f$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,776,780,2752,27053,27901,27902,56713,56763</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=17170481$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16190672$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Samaras, Thomas S</creatorcontrib><creatorcontrib>Camburn, Philip A</creatorcontrib><creatorcontrib>Chandra, Sachin X</creatorcontrib><creatorcontrib>Gordon, Michael H</creatorcontrib><creatorcontrib>Ames, Jennifer M</creatorcontrib><title>Antioxidant Properties of Kilned and Roasted Malts</title><title>Journal of agricultural and food chemistry</title><addtitle>J. Agric. Food Chem</addtitle><description>Compounds possessing antioxidant activity play a crucial role in delaying or preventing lipid oxidation in foods and beverages during processing and storage. Such reactions lead to loss of product quality, especially as a consequence of off-flavor formation. The aim of this study was to determine the antioxidant activity of kilned (standard) and roasted (speciality) malts in relation to phenolic compounds, sugars, amino acids, and color [assessed as European Brewing Convention units (°EBC) and absorbance at 420 nm]. The concentrations of sugars and amino acids decreased with the intensity of the applied heat treatment, and this was attributed to the extent of the Maillard reaction, as well as sugar caramelization, in the highly roasted malts. Proline, followed by glutamine, was the most abundant free amino/imino acid in the malt samples, except those that were highly roasted, and maltose was the most abundant sugar in all malts. Levels of total phenolic compounds decreased with heat treatment. Catechin and ferulic acid were the most abundant phenolic compounds in the majority of the malts, and amounts were highest in the kilned samples. In highly roasted malts, degradation products of ferulic acid were identified. Antioxidant activity increased with the intensity of heating, in parallel with color formation, and was significantly higher for roasted malts compared to kilned malts. In kilned malts, phenolic compounds were the main identified contributors to antioxidant activity, with Maillard reaction products also playing a role. In roasted malts, Maillard reaction products were responsible for the majority of the antioxidant activity. Keywords: Kilned malt; roasted malt; antioxidant activity; 2,2‘-azinobis(3-ethylbenzothiazoline-6-sulfonic acid) radical cation scavenging activity; oxygen radical absorbance capacity; Maillard reaction; capillary electrophoresis</description><subject>Amino Acids - analysis</subject><subject>antioxidant activity</subject><subject>antioxidants</subject><subject>Antioxidants - analysis</subject><subject>Antioxidants - pharmacology</subject><subject>Biological and medical sciences</subject><subject>Carbohydrates - analysis</subject><subject>Catechin - analysis</subject><subject>Color</subject><subject>Coumaric Acids - analysis</subject><subject>Edible Grain - chemistry</subject><subject>Food Handling - methods</subject><subject>Food industries</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>heat treatment</subject><subject>Hot Temperature</subject><subject>kilns</subject><subject>Maillard Reaction</subject><subject>Maillard reaction products</subject><subject>malt</subject><subject>malting barley</subject><subject>phenolic compounds</subject><subject>Phenols - analysis</subject><subject>roasting</subject><subject>Spectrophotometry</subject><issn>0021-8561</issn><issn>1520-5118</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpt0E1P4zAQBmALsYLyceAPQC4g7SEwY8cfOaIK2BVdURW4cLGcxEYpaVzsVGL__bpqRS978kjz6B35JeQM4RqB4s3cAccCwe2REXIKOUdU-2QEaZkrLvCQHMU4BwDFJRyQQxRYgpB0ROhtP7T-q21MP2TT4Jc2DK2NmXfZY9v1tslM32Qzb-KQ5j-mG-IJ-eFMF-3p9j0mr_d3L-Nf-eTp4ff4dpKbQuKQl4hSMFk3ohQUSgW1qKiwEst0mDqrwFZccgGy4gWvC8cVOOSWYWMrKxg7Jleb3GXwnysbB71oY227zvTWr6IWSjCOVCX4cwPr4GMM1ullaBcm_NUIel2Q_i4o2fNt6Kpa2GYnt40kcLkFJtamc8H0dRt3TqKEQmFy-ca1qZmv770JH1pIJrl-mT7r8eyxmL7BRK9zLzbeGa_Ne0iZr88UkAECKxgVu8umjnruV6FP7f7nC_8AjUWOjA</recordid><startdate>20051005</startdate><enddate>20051005</enddate><creator>Samaras, Thomas S</creator><creator>Camburn, Philip A</creator><creator>Chandra, Sachin X</creator><creator>Gordon, Michael H</creator><creator>Ames, Jennifer M</creator><general>American Chemical Society</general><scope>FBQ</scope><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20051005</creationdate><title>Antioxidant Properties of Kilned and Roasted Malts</title><author>Samaras, Thomas S ; Camburn, Philip A ; Chandra, Sachin X ; Gordon, Michael H ; Ames, Jennifer M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a471t-9117637cd69620980c6b26e7196722fe80eb575607b545c4f580f15e31debe633</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Amino Acids - analysis</topic><topic>antioxidant activity</topic><topic>antioxidants</topic><topic>Antioxidants - analysis</topic><topic>Antioxidants - pharmacology</topic><topic>Biological and medical sciences</topic><topic>Carbohydrates - analysis</topic><topic>Catechin - analysis</topic><topic>Color</topic><topic>Coumaric Acids - analysis</topic><topic>Edible Grain - chemistry</topic><topic>Food Handling - methods</topic><topic>Food industries</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>heat treatment</topic><topic>Hot Temperature</topic><topic>kilns</topic><topic>Maillard Reaction</topic><topic>Maillard reaction products</topic><topic>malt</topic><topic>malting barley</topic><topic>phenolic compounds</topic><topic>Phenols - analysis</topic><topic>roasting</topic><topic>Spectrophotometry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Samaras, Thomas S</creatorcontrib><creatorcontrib>Camburn, Philip A</creatorcontrib><creatorcontrib>Chandra, Sachin X</creatorcontrib><creatorcontrib>Gordon, Michael H</creatorcontrib><creatorcontrib>Ames, Jennifer M</creatorcontrib><collection>AGRIS</collection><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of agricultural and food chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Samaras, Thomas S</au><au>Camburn, Philip A</au><au>Chandra, Sachin X</au><au>Gordon, Michael H</au><au>Ames, Jennifer M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Antioxidant Properties of Kilned and Roasted Malts</atitle><jtitle>Journal of agricultural and food chemistry</jtitle><addtitle>J. Agric. Food Chem</addtitle><date>2005-10-05</date><risdate>2005</risdate><volume>53</volume><issue>20</issue><spage>8068</spage><epage>8074</epage><pages>8068-8074</pages><issn>0021-8561</issn><eissn>1520-5118</eissn><coden>JAFCAU</coden><abstract>Compounds possessing antioxidant activity play a crucial role in delaying or preventing lipid oxidation in foods and beverages during processing and storage. Such reactions lead to loss of product quality, especially as a consequence of off-flavor formation. The aim of this study was to determine the antioxidant activity of kilned (standard) and roasted (speciality) malts in relation to phenolic compounds, sugars, amino acids, and color [assessed as European Brewing Convention units (°EBC) and absorbance at 420 nm]. The concentrations of sugars and amino acids decreased with the intensity of the applied heat treatment, and this was attributed to the extent of the Maillard reaction, as well as sugar caramelization, in the highly roasted malts. Proline, followed by glutamine, was the most abundant free amino/imino acid in the malt samples, except those that were highly roasted, and maltose was the most abundant sugar in all malts. Levels of total phenolic compounds decreased with heat treatment. Catechin and ferulic acid were the most abundant phenolic compounds in the majority of the malts, and amounts were highest in the kilned samples. In highly roasted malts, degradation products of ferulic acid were identified. Antioxidant activity increased with the intensity of heating, in parallel with color formation, and was significantly higher for roasted malts compared to kilned malts. In kilned malts, phenolic compounds were the main identified contributors to antioxidant activity, with Maillard reaction products also playing a role. In roasted malts, Maillard reaction products were responsible for the majority of the antioxidant activity. Keywords: Kilned malt; roasted malt; antioxidant activity; 2,2‘-azinobis(3-ethylbenzothiazoline-6-sulfonic acid) radical cation scavenging activity; oxygen radical absorbance capacity; Maillard reaction; capillary electrophoresis</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><pmid>16190672</pmid><doi>10.1021/jf051410f</doi><tpages>7</tpages></addata></record> |
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subjects | Amino Acids - analysis antioxidant activity antioxidants Antioxidants - analysis Antioxidants - pharmacology Biological and medical sciences Carbohydrates - analysis Catechin - analysis Color Coumaric Acids - analysis Edible Grain - chemistry Food Handling - methods Food industries Fundamental and applied biological sciences. Psychology heat treatment Hot Temperature kilns Maillard Reaction Maillard reaction products malt malting barley phenolic compounds Phenols - analysis roasting Spectrophotometry |
title | Antioxidant Properties of Kilned and Roasted Malts |
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