Effect of salts on soy storage proteins defatted with supercritical CO2 and alcohols
The primary objective was to determine whether salts will stabilize soy storage proteins against the denaturing effects of alcohols or the heat and pressure used in supercritical CO2 during the defatting process. Nitrogen solubility index (NSI) and differential scanning calorimetry (DSC) were used t...
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Veröffentlicht in: | Journal of the American Oil Chemists' Society 1998-08, Vol.75 (8), p.911-916 |
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creator | Sessa, D.J. (NCAUR, USDA, ARS, Peoria, IL.) Nelson, T.C Snyder, J.M |
description | The primary objective was to determine whether salts will stabilize soy storage proteins against the denaturing effects of alcohols or the heat and pressure used in supercritical CO2 during the defatting process. Nitrogen solubility index (NSI) and differential scanning calorimetry (DSC) were used to monitor the denaturation of proteins. A variety of salt solutions used to hydrate full‐fat soy grits increased the thermal stability of both 7S and 11S storage proteins. DSC was used to monitor their denaturation temperature. Neutral salt hydrations followed the lyotropic series for protein stabilization. Of the salts evaluated, the test results indicate that the reducing salt, sodium sulfite, and the neutral salt, sodium sulfate, when used to steep beans, yielded significantly higher NSI than did the water‐steeped controls or other salt treatments after partial defatting with absolute isopropanol or ethanol and supercritical CO2. However, these same salt treatments did not as effectively stabilize the proteins against the denaturing effects of ethanol more aqueous than 84% when these alcohols were used as the defatting medium. |
doi_str_mv | 10.1007/s11746-998-0266-6 |
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(NCAUR, USDA, ARS, Peoria, IL.) ; Nelson, T.C ; Snyder, J.M</creator><creatorcontrib>Sessa, D.J. (NCAUR, USDA, ARS, Peoria, IL.) ; Nelson, T.C ; Snyder, J.M</creatorcontrib><description>The primary objective was to determine whether salts will stabilize soy storage proteins against the denaturing effects of alcohols or the heat and pressure used in supercritical CO2 during the defatting process. Nitrogen solubility index (NSI) and differential scanning calorimetry (DSC) were used to monitor the denaturation of proteins. A variety of salt solutions used to hydrate full‐fat soy grits increased the thermal stability of both 7S and 11S storage proteins. DSC was used to monitor their denaturation temperature. Neutral salt hydrations followed the lyotropic series for protein stabilization. Of the salts evaluated, the test results indicate that the reducing salt, sodium sulfite, and the neutral salt, sodium sulfate, when used to steep beans, yielded significantly higher NSI than did the water‐steeped controls or other salt treatments after partial defatting with absolute isopropanol or ethanol and supercritical CO2. However, these same salt treatments did not as effectively stabilize the proteins against the denaturing effects of ethanol more aqueous than 84% when these alcohols were used as the defatting medium.</description><identifier>ISSN: 0003-021X</identifier><identifier>EISSN: 1558-9331</identifier><identifier>DOI: 10.1007/s11746-998-0266-6</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer‐Verlag</publisher><subject>Animal, plant, fungal and microbial proteins, edible seaweeds and food yeasts ; Biological and medical sciences ; CARBON DIOXIDE ; Defatting ; differential scanning calorimetry ; DIOXIDO DE CARBONO ; DIOXYDE DE CARBONE ; ethanol extraction of oil ; Food industries ; Fundamental and applied biological sciences. Psychology ; heat denaturation ; isopropanol extraction of oil ; nitrogen solubility index ; PROTEINAS DE RESERVA ; PROTEINE DE RESERVE ; salt stabilization ; SOJA ; SOYBEANS ; STORAGE PROTEINS ; supercritical CO2 extraction of oil</subject><ispartof>Journal of the American Oil Chemists' Society, 1998-08, Vol.75 (8), p.911-916</ispartof><rights>1998 American Oil Chemists' Society (AOCS)</rights><rights>1998 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1007%2Fs11746-998-0266-6$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1007%2Fs11746-998-0266-6$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27923,27924,45573,45574</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2356167$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Sessa, D.J. (NCAUR, USDA, ARS, Peoria, IL.)</creatorcontrib><creatorcontrib>Nelson, T.C</creatorcontrib><creatorcontrib>Snyder, J.M</creatorcontrib><title>Effect of salts on soy storage proteins defatted with supercritical CO2 and alcohols</title><title>Journal of the American Oil Chemists' Society</title><description>The primary objective was to determine whether salts will stabilize soy storage proteins against the denaturing effects of alcohols or the heat and pressure used in supercritical CO2 during the defatting process. Nitrogen solubility index (NSI) and differential scanning calorimetry (DSC) were used to monitor the denaturation of proteins. A variety of salt solutions used to hydrate full‐fat soy grits increased the thermal stability of both 7S and 11S storage proteins. DSC was used to monitor their denaturation temperature. Neutral salt hydrations followed the lyotropic series for protein stabilization. Of the salts evaluated, the test results indicate that the reducing salt, sodium sulfite, and the neutral salt, sodium sulfate, when used to steep beans, yielded significantly higher NSI than did the water‐steeped controls or other salt treatments after partial defatting with absolute isopropanol or ethanol and supercritical CO2. However, these same salt treatments did not as effectively stabilize the proteins against the denaturing effects of ethanol more aqueous than 84% when these alcohols were used as the defatting medium.</description><subject>Animal, plant, fungal and microbial proteins, edible seaweeds and food yeasts</subject><subject>Biological and medical sciences</subject><subject>CARBON DIOXIDE</subject><subject>Defatting</subject><subject>differential scanning calorimetry</subject><subject>DIOXIDO DE CARBONO</subject><subject>DIOXYDE DE CARBONE</subject><subject>ethanol extraction of oil</subject><subject>Food industries</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>heat denaturation</subject><subject>isopropanol extraction of oil</subject><subject>nitrogen solubility index</subject><subject>PROTEINAS DE RESERVA</subject><subject>PROTEINE DE RESERVE</subject><subject>salt stabilization</subject><subject>SOJA</subject><subject>SOYBEANS</subject><subject>STORAGE PROTEINS</subject><subject>supercritical CO2 extraction of oil</subject><issn>0003-021X</issn><issn>1558-9331</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><recordid>eNo9kMlqwzAQhkVpoenyAD0UdOjVrUayFh-DSRcI5JAEehMTW0pcXMtYKiFvXweXnobhX_j5CHkA9gyM6ZcIoHOVFYXJGFcqUxdkBlKarBACLsmMMSZGBT6vyU2MX-NrBJczsll476pEg6cR2xRp6GgMJxpTGHDvaD-E5Jou0tp5TMnV9NikA40_vRuqoUlNhS0tV5xiV1Nsq3AIbbwjVx7b6O7_7i3Zvi425Xu2XL19lPNl5rnkcJ6Gde5Q88qgkILx3JhcqrzGaqc0cCY0GKNAy9o46SQY9AKkLqSuxQ7FLXmaenuM4w4_YFc10fZD843DyXIhFSg92vRkOzatO_3LwOwZnZ3Q2RGdPaOzys5X5ZoVAGPycUp6DBb3w1i-XUNRaKa1kVz8AtTVa2A</recordid><startdate>199808</startdate><enddate>199808</enddate><creator>Sessa, D.J. (NCAUR, USDA, ARS, Peoria, IL.)</creator><creator>Nelson, T.C</creator><creator>Snyder, J.M</creator><general>Springer‐Verlag</general><general>Springer</general><scope>FBQ</scope><scope>IQODW</scope></search><sort><creationdate>199808</creationdate><title>Effect of salts on soy storage proteins defatted with supercritical CO2 and alcohols</title><author>Sessa, D.J. (NCAUR, USDA, ARS, Peoria, IL.) ; Nelson, T.C ; Snyder, J.M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-f2521-933ad4ea72c8a353024884564dacb67120371886175d8e5e518af3157957d3ba3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Animal, plant, fungal and microbial proteins, edible seaweeds and food yeasts</topic><topic>Biological and medical sciences</topic><topic>CARBON DIOXIDE</topic><topic>Defatting</topic><topic>differential scanning calorimetry</topic><topic>DIOXIDO DE CARBONO</topic><topic>DIOXYDE DE CARBONE</topic><topic>ethanol extraction of oil</topic><topic>Food industries</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>heat denaturation</topic><topic>isopropanol extraction of oil</topic><topic>nitrogen solubility index</topic><topic>PROTEINAS DE RESERVA</topic><topic>PROTEINE DE RESERVE</topic><topic>salt stabilization</topic><topic>SOJA</topic><topic>SOYBEANS</topic><topic>STORAGE PROTEINS</topic><topic>supercritical CO2 extraction of oil</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sessa, D.J. (NCAUR, USDA, ARS, Peoria, IL.)</creatorcontrib><creatorcontrib>Nelson, T.C</creatorcontrib><creatorcontrib>Snyder, J.M</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><jtitle>Journal of the American Oil Chemists' Society</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sessa, D.J. 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DSC was used to monitor their denaturation temperature. Neutral salt hydrations followed the lyotropic series for protein stabilization. Of the salts evaluated, the test results indicate that the reducing salt, sodium sulfite, and the neutral salt, sodium sulfate, when used to steep beans, yielded significantly higher NSI than did the water‐steeped controls or other salt treatments after partial defatting with absolute isopropanol or ethanol and supercritical CO2. However, these same salt treatments did not as effectively stabilize the proteins against the denaturing effects of ethanol more aqueous than 84% when these alcohols were used as the defatting medium.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer‐Verlag</pub><doi>10.1007/s11746-998-0266-6</doi><tpages>6</tpages></addata></record> |
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source | Wiley Online Library Journals Frontfile Complete; SpringerLink Journals - AutoHoldings |
subjects | Animal, plant, fungal and microbial proteins, edible seaweeds and food yeasts Biological and medical sciences CARBON DIOXIDE Defatting differential scanning calorimetry DIOXIDO DE CARBONO DIOXYDE DE CARBONE ethanol extraction of oil Food industries Fundamental and applied biological sciences. Psychology heat denaturation isopropanol extraction of oil nitrogen solubility index PROTEINAS DE RESERVA PROTEINE DE RESERVE salt stabilization SOJA SOYBEANS STORAGE PROTEINS supercritical CO2 extraction of oil |
title | Effect of salts on soy storage proteins defatted with supercritical CO2 and alcohols |
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