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Stability of tryptophan during food processing and storage. 1. Comparative losses of tryptophan, lysine and methionine in different model systems
The stability of tryptophan was evaluated in several different food model systems using a chemical method (high pressure liquid chromatography after alkaline-hydrolysis) and rat assays. Losses of tryptophan were compared with the losses of lysine and methionine. Whey proteins stored in the presence...
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Published in: | British journal of nutrition 1985-03, Vol.53 (2), p.281-292 |
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description | The stability of tryptophan was evaluated in several different food model systems using a chemical method (high pressure liquid chromatography after alkaline-hydrolysis) and rat assays. Losses of tryptophan were compared with the losses of lysine and methionine. Whey proteins stored in the presence of oxidizing lipids showed large losses of lysine and extensive methionine oxidation but only minor losses of tryptophan as measured chemically. The observed decrease in bioavailable tryptophan was explained by a lower protein digestibility. Casein treated with hydrogen peroxide to oxidize all methionine to methionine sulphoxide showed a 9% loss in bioavailable tryptophan. When casein was reacted with caffeic acid at pH 7 in the presence of monophenol monooxygenase (tyrosinase; EC 1.14.18.1), no chemical loss of tryptophan occurred, although fluorodinitrobenzene-reactive lysine fell by 23%. Tryptophan bioavailability fell 15%, partly due to an 8% reduction in protein digestibility. Alkali-treated casein (0.15 M-sodium hydroxide, 80 degrees, 4 h) did not support rat growth. Chemically-determined tryptophan, available tryptophan and true nitrogen digestibility fell 10, 46 and 23% respectively. Racemization of tryptophan was found to be 10% (D/(D+L)). In whole-milk powder, which had undergone "early' or "advanced' Maillard reactions, tryptophan, determined chemically or in rat assays, was virtually unchanged. Extensive lysine losses occurred. It was concluded that losses of tryptophan during food processing and storage are small and of only minor nutritional importance, especially when compared with much larger losses of lysine and the more extensive oxidation of methionine. |
doi_str_mv | 10.1079/BJN19850035 |
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Comparative losses of tryptophan, lysine and methionine in different model systems</title><source>Free Full-Text Journals in Chemistry</source><source>Cambridge University Press:JISC Collections:Full Collection Digital Archives (STM and HSS) (218 titles)</source><creator>Nielsen, H.K ; De Weck, D ; Finot, P.A ; Liardon, R ; Hurrell, R.F</creator><creatorcontrib>Nielsen, H.K ; De Weck, D ; Finot, P.A ; Liardon, R ; Hurrell, R.F</creatorcontrib><description>The stability of tryptophan was evaluated in several different food model systems using a chemical method (high pressure liquid chromatography after alkaline-hydrolysis) and rat assays. Losses of tryptophan were compared with the losses of lysine and methionine. Whey proteins stored in the presence of oxidizing lipids showed large losses of lysine and extensive methionine oxidation but only minor losses of tryptophan as measured chemically. The observed decrease in bioavailable tryptophan was explained by a lower protein digestibility. Casein treated with hydrogen peroxide to oxidize all methionine to methionine sulphoxide showed a 9% loss in bioavailable tryptophan. When casein was reacted with caffeic acid at pH 7 in the presence of monophenol monooxygenase (tyrosinase; EC 1.14.18.1), no chemical loss of tryptophan occurred, although fluorodinitrobenzene-reactive lysine fell by 23%. Tryptophan bioavailability fell 15%, partly due to an 8% reduction in protein digestibility. Alkali-treated casein (0.15 M-sodium hydroxide, 80 degrees, 4 h) did not support rat growth. Chemically-determined tryptophan, available tryptophan and true nitrogen digestibility fell 10, 46 and 23% respectively. Racemization of tryptophan was found to be 10% (D/(D+L)). In whole-milk powder, which had undergone "early' or "advanced' Maillard reactions, tryptophan, determined chemically or in rat assays, was virtually unchanged. Extensive lysine losses occurred. It was concluded that losses of tryptophan during food processing and storage are small and of only minor nutritional importance, especially when compared with much larger losses of lysine and the more extensive oxidation of methionine.</description><identifier>ISSN: 0007-1145</identifier><identifier>EISSN: 1475-2662</identifier><identifier>DOI: 10.1079/BJN19850035</identifier><identifier>PMID: 3933549</identifier><language>eng</language><publisher>England</publisher><subject>Animals ; Caffeic Acids - pharmacology ; Drug Stability ; Drug Storage ; Food Handling ; food processing ; foods ; Hydrogen Peroxide ; Lipids - pharmacology ; lysine ; Lysine - metabolism ; Male ; methionine ; Methionine - metabolism ; Oxidation-Reduction ; processing technology ; Rats ; Rats, Inbred Strains ; Sodium Hydroxide - pharmacology ; stability ; storage ; tryptophan ; Tryptophan - metabolism</subject><ispartof>British journal of nutrition, 1985-03, Vol.53 (2), p.281-292</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c229t-61ea483f8ac58c5b9dc86a67bee6721df4c0a5a5e0b89da877c9ee8d797e851f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/3933549$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Nielsen, H.K</creatorcontrib><creatorcontrib>De Weck, D</creatorcontrib><creatorcontrib>Finot, P.A</creatorcontrib><creatorcontrib>Liardon, R</creatorcontrib><creatorcontrib>Hurrell, R.F</creatorcontrib><title>Stability of tryptophan during food processing and storage. 1. Comparative losses of tryptophan, lysine and methionine in different model systems</title><title>British journal of nutrition</title><addtitle>Br J Nutr</addtitle><description>The stability of tryptophan was evaluated in several different food model systems using a chemical method (high pressure liquid chromatography after alkaline-hydrolysis) and rat assays. Losses of tryptophan were compared with the losses of lysine and methionine. Whey proteins stored in the presence of oxidizing lipids showed large losses of lysine and extensive methionine oxidation but only minor losses of tryptophan as measured chemically. The observed decrease in bioavailable tryptophan was explained by a lower protein digestibility. Casein treated with hydrogen peroxide to oxidize all methionine to methionine sulphoxide showed a 9% loss in bioavailable tryptophan. When casein was reacted with caffeic acid at pH 7 in the presence of monophenol monooxygenase (tyrosinase; EC 1.14.18.1), no chemical loss of tryptophan occurred, although fluorodinitrobenzene-reactive lysine fell by 23%. Tryptophan bioavailability fell 15%, partly due to an 8% reduction in protein digestibility. Alkali-treated casein (0.15 M-sodium hydroxide, 80 degrees, 4 h) did not support rat growth. Chemically-determined tryptophan, available tryptophan and true nitrogen digestibility fell 10, 46 and 23% respectively. Racemization of tryptophan was found to be 10% (D/(D+L)). In whole-milk powder, which had undergone "early' or "advanced' Maillard reactions, tryptophan, determined chemically or in rat assays, was virtually unchanged. Extensive lysine losses occurred. It was concluded that losses of tryptophan during food processing and storage are small and of only minor nutritional importance, especially when compared with much larger losses of lysine and the more extensive oxidation of methionine.</description><subject>Animals</subject><subject>Caffeic Acids - pharmacology</subject><subject>Drug Stability</subject><subject>Drug Storage</subject><subject>Food Handling</subject><subject>food processing</subject><subject>foods</subject><subject>Hydrogen Peroxide</subject><subject>Lipids - pharmacology</subject><subject>lysine</subject><subject>Lysine - metabolism</subject><subject>Male</subject><subject>methionine</subject><subject>Methionine - metabolism</subject><subject>Oxidation-Reduction</subject><subject>processing technology</subject><subject>Rats</subject><subject>Rats, Inbred Strains</subject><subject>Sodium Hydroxide - pharmacology</subject><subject>stability</subject><subject>storage</subject><subject>tryptophan</subject><subject>Tryptophan - metabolism</subject><issn>0007-1145</issn><issn>1475-2662</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1985</creationdate><recordtype>article</recordtype><recordid>eNqFkT2P1DAQhi0EOpaDihrhigay2HH8VR4rPnWC4rg6cuzxnlESB9uLlJ_BP8bLrhBUVKNX88w7mnkRekrJlhKpX7_59JlqxQlh_B7a0E7yphWivY82hBDZUNrxh-hRzt-qVJToC3TBNGO80xv086aYIYyhrDh6XNK6lLjcmRm7QwrzHvsYHV5StJDzUZvZ4VxiMnvYYrrFuzgtJpkSfgAeY86Q__V5hce1DsLvwQnKXYjzUYa6IXgPCeaCp-hgxHnNBab8GD3wZszw5Fwv0e27t193H5rrL-8_7q6uG9u2ujSCgukU88pYriwftLNKGCEHACFb6nxnieGGAxmUdkZJaTWAclJLUJx6dolenHzrdd8PkEs_hWxhHM0M8ZB7KTohqOL_BWnHCO2IrODLE2hT_UQC3y8pTCatPSX9Man-r6Qq_exsexgmcH_YczS1__zU9yb2Zp9C7m9vWkIZaUWNWCr2C0Jumqc</recordid><startdate>198503</startdate><enddate>198503</enddate><creator>Nielsen, H.K</creator><creator>De Weck, D</creator><creator>Finot, P.A</creator><creator>Liardon, R</creator><creator>Hurrell, R.F</creator><scope>FBQ</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>7QL</scope><scope>C1K</scope><scope>7X8</scope></search><sort><creationdate>198503</creationdate><title>Stability of tryptophan during food processing and storage. 1. Comparative losses of tryptophan, lysine and methionine in different model systems</title><author>Nielsen, H.K ; De Weck, D ; Finot, P.A ; Liardon, R ; Hurrell, R.F</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c229t-61ea483f8ac58c5b9dc86a67bee6721df4c0a5a5e0b89da877c9ee8d797e851f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1985</creationdate><topic>Animals</topic><topic>Caffeic Acids - pharmacology</topic><topic>Drug Stability</topic><topic>Drug Storage</topic><topic>Food Handling</topic><topic>food processing</topic><topic>foods</topic><topic>Hydrogen Peroxide</topic><topic>Lipids - pharmacology</topic><topic>lysine</topic><topic>Lysine - metabolism</topic><topic>Male</topic><topic>methionine</topic><topic>Methionine - metabolism</topic><topic>Oxidation-Reduction</topic><topic>processing technology</topic><topic>Rats</topic><topic>Rats, Inbred Strains</topic><topic>Sodium Hydroxide - pharmacology</topic><topic>stability</topic><topic>storage</topic><topic>tryptophan</topic><topic>Tryptophan - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nielsen, H.K</creatorcontrib><creatorcontrib>De Weck, D</creatorcontrib><creatorcontrib>Finot, P.A</creatorcontrib><creatorcontrib>Liardon, R</creatorcontrib><creatorcontrib>Hurrell, R.F</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Environmental Sciences and Pollution Management</collection><collection>MEDLINE - Academic</collection><jtitle>British journal of nutrition</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nielsen, H.K</au><au>De Weck, D</au><au>Finot, P.A</au><au>Liardon, R</au><au>Hurrell, R.F</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Stability of tryptophan during food processing and storage. 1. Comparative losses of tryptophan, lysine and methionine in different model systems</atitle><jtitle>British journal of nutrition</jtitle><addtitle>Br J Nutr</addtitle><date>1985-03</date><risdate>1985</risdate><volume>53</volume><issue>2</issue><spage>281</spage><epage>292</epage><pages>281-292</pages><issn>0007-1145</issn><eissn>1475-2662</eissn><abstract>The stability of tryptophan was evaluated in several different food model systems using a chemical method (high pressure liquid chromatography after alkaline-hydrolysis) and rat assays. Losses of tryptophan were compared with the losses of lysine and methionine. Whey proteins stored in the presence of oxidizing lipids showed large losses of lysine and extensive methionine oxidation but only minor losses of tryptophan as measured chemically. The observed decrease in bioavailable tryptophan was explained by a lower protein digestibility. Casein treated with hydrogen peroxide to oxidize all methionine to methionine sulphoxide showed a 9% loss in bioavailable tryptophan. When casein was reacted with caffeic acid at pH 7 in the presence of monophenol monooxygenase (tyrosinase; EC 1.14.18.1), no chemical loss of tryptophan occurred, although fluorodinitrobenzene-reactive lysine fell by 23%. Tryptophan bioavailability fell 15%, partly due to an 8% reduction in protein digestibility. Alkali-treated casein (0.15 M-sodium hydroxide, 80 degrees, 4 h) did not support rat growth. Chemically-determined tryptophan, available tryptophan and true nitrogen digestibility fell 10, 46 and 23% respectively. Racemization of tryptophan was found to be 10% (D/(D+L)). In whole-milk powder, which had undergone "early' or "advanced' Maillard reactions, tryptophan, determined chemically or in rat assays, was virtually unchanged. Extensive lysine losses occurred. It was concluded that losses of tryptophan during food processing and storage are small and of only minor nutritional importance, especially when compared with much larger losses of lysine and the more extensive oxidation of methionine.</abstract><cop>England</cop><pmid>3933549</pmid><doi>10.1079/BJN19850035</doi><tpages>12</tpages></addata></record> |
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subjects | Animals Caffeic Acids - pharmacology Drug Stability Drug Storage Food Handling food processing foods Hydrogen Peroxide Lipids - pharmacology lysine Lysine - metabolism Male methionine Methionine - metabolism Oxidation-Reduction processing technology Rats Rats, Inbred Strains Sodium Hydroxide - pharmacology stability storage tryptophan Tryptophan - metabolism |
title | Stability of tryptophan during food processing and storage. 1. Comparative losses of tryptophan, lysine and methionine in different model systems |
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