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Size Exclusion Chromatography of Soybean Proteins and Isoflavones
High-performance size exclusion chromatography was used to separate soybean extracts. The separation of the major storage proteins, including glycinin and beta-conglycinin, was determined by analysis of the subunits on sodium dodecyl sulfate gel electrophoresis. The extracts of defatted flour and wh...
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Published in: | Journal of agricultural and food chemistry 1994-12, Vol.42 (12), p.2713-2720 |
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container_end_page | 2720 |
container_issue | 12 |
container_start_page | 2713 |
container_title | Journal of agricultural and food chemistry |
container_volume | 42 |
creator | Cole, Kenneth D Cousin, Sydney L |
description | High-performance size exclusion chromatography was used to separate soybean extracts. The separation of the major storage proteins, including glycinin and beta-conglycinin, was determined by analysis of the subunits on sodium dodecyl sulfate gel electrophoresis. The extracts of defatted flour and whole beans showed a high degree of polymerization of the storage proteins. Addition of a disulfide reducing agent (dithiothreitol) resulted in a decrease of the polymerized forms. The separation of the major glucoside isoflavones (genistin, daidzin, and glycitein 7-beta-glucoside) was determined. The isoflavone glucosides eluted well past the elusion time of a small totally included molecule, indicating that they are separating by mechanisms other than size exclusion. Size exclusion chromatography was used to monitor the separation of the soybean extract in an aqueous two-phase extraction system. The major storage proteins partitioned to the salt phase, and the isoflavones and other hydrophobic compounds partitioned to the poly(ethylene glycol) phase |
doi_str_mv | 10.1021/jf00048a013 |
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The separation of the major storage proteins, including glycinin and beta-conglycinin, was determined by analysis of the subunits on sodium dodecyl sulfate gel electrophoresis. The extracts of defatted flour and whole beans showed a high degree of polymerization of the storage proteins. Addition of a disulfide reducing agent (dithiothreitol) resulted in a decrease of the polymerized forms. The separation of the major glucoside isoflavones (genistin, daidzin, and glycitein 7-beta-glucoside) was determined. The isoflavone glucosides eluted well past the elusion time of a small totally included molecule, indicating that they are separating by mechanisms other than size exclusion. Size exclusion chromatography was used to monitor the separation of the soybean extract in an aqueous two-phase extraction system. The major storage proteins partitioned to the salt phase, and the isoflavones and other hydrophobic compounds partitioned to the poly(ethylene glycol) phase</description><identifier>ISSN: 0021-8561</identifier><identifier>EISSN: 1520-5118</identifier><identifier>DOI: 10.1021/jf00048a013</identifier><identifier>CODEN: JAFCAU</identifier><language>eng</language><publisher>Washington, DC: American Chemical Society</publisher><subject>Animal, plant, fungal and microbial proteins, edible seaweeds and food yeasts ; Biological and medical sciences ; CHROMATOGRAPHIE ; CROMATOGRAFIA ; FLAVONOIDE ; FLAVONOIDES ; Food industries ; Fundamental and applied biological sciences. 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Agric. Food Chem</addtitle><description>High-performance size exclusion chromatography was used to separate soybean extracts. The separation of the major storage proteins, including glycinin and beta-conglycinin, was determined by analysis of the subunits on sodium dodecyl sulfate gel electrophoresis. The extracts of defatted flour and whole beans showed a high degree of polymerization of the storage proteins. Addition of a disulfide reducing agent (dithiothreitol) resulted in a decrease of the polymerized forms. The separation of the major glucoside isoflavones (genistin, daidzin, and glycitein 7-beta-glucoside) was determined. The isoflavone glucosides eluted well past the elusion time of a small totally included molecule, indicating that they are separating by mechanisms other than size exclusion. Size exclusion chromatography was used to monitor the separation of the soybean extract in an aqueous two-phase extraction system. The major storage proteins partitioned to the salt phase, and the isoflavones and other hydrophobic compounds partitioned to the poly(ethylene glycol) phase</description><subject>Animal, plant, fungal and microbial proteins, edible seaweeds and food yeasts</subject><subject>Biological and medical sciences</subject><subject>CHROMATOGRAPHIE</subject><subject>CROMATOGRAFIA</subject><subject>FLAVONOIDE</subject><subject>FLAVONOIDES</subject><subject>Food industries</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>GLUCOSIDE</subject><subject>GLUCOSIDOS</subject><subject>PROTEINAS VEGETALES</subject><subject>PROTEINE VEGETALE</subject><subject>SEPARACION</subject><subject>SEPARATION</subject><subject>SOJA</subject><issn>0021-8561</issn><issn>1520-5118</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1994</creationdate><recordtype>article</recordtype><recordid>eNptkMFPwjAUhxujiYievHnawcSDmbZru3VHJIhEoiQDrs1baWE4VtIOA_71zswQD57e4fveL-_3ELom-IHgiDyuDcaYCcCEnqAO4REOOSHiFHVwg0PBY3KOLrxfN5rgCe6gXlZ86WCwV-XOF7YK-itnN1DbpYPt6hBYE2T2kGuogomztS4qH0C1CEbemhI-baX9JTozUHp99Tu7aPY8mPZfwvH7cNTvjUOgLK1DhTUYpTFZ8DROWZ5EC8UiHKdGM2xUHotEJxBRsVB5ngvFhaKMYM4YJ8yQlHbRfZurnPXeaSO3rtiAO0iC5U97-ad9Y9-29ha8gtI4qFThjyuUChox0WhhqxW-1vsjBvch44QmXE4nmXwbZvPXOXmSSePftL4BK2HpmshZlsY4EjFv4F0LQXm5tjtXNf_497pvS7l9Ow</recordid><startdate>19941201</startdate><enddate>19941201</enddate><creator>Cole, Kenneth D</creator><creator>Cousin, Sydney L</creator><general>American Chemical Society</general><scope>FBQ</scope><scope>BSCLL</scope><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>19941201</creationdate><title>Size Exclusion Chromatography of Soybean Proteins and Isoflavones</title><author>Cole, Kenneth D ; Cousin, Sydney L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a349t-c0eafce01d59694b72dc42069fe40fcb687e7a238dcbbb8c58c3410544514f193</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1994</creationdate><topic>Animal, plant, fungal and microbial proteins, edible seaweeds and food yeasts</topic><topic>Biological and medical sciences</topic><topic>CHROMATOGRAPHIE</topic><topic>CROMATOGRAFIA</topic><topic>FLAVONOIDE</topic><topic>FLAVONOIDES</topic><topic>Food industries</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>GLUCOSIDE</topic><topic>GLUCOSIDOS</topic><topic>PROTEINAS VEGETALES</topic><topic>PROTEINE VEGETALE</topic><topic>SEPARACION</topic><topic>SEPARATION</topic><topic>SOJA</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cole, Kenneth D</creatorcontrib><creatorcontrib>Cousin, Sydney L</creatorcontrib><collection>AGRIS</collection><collection>Istex</collection><collection>Pascal-Francis</collection><collection>CrossRef</collection><jtitle>Journal of agricultural and food chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cole, Kenneth D</au><au>Cousin, Sydney L</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Size Exclusion Chromatography of Soybean Proteins and Isoflavones</atitle><jtitle>Journal of agricultural and food chemistry</jtitle><addtitle>J. Agric. Food Chem</addtitle><date>1994-12-01</date><risdate>1994</risdate><volume>42</volume><issue>12</issue><spage>2713</spage><epage>2720</epage><pages>2713-2720</pages><issn>0021-8561</issn><eissn>1520-5118</eissn><coden>JAFCAU</coden><abstract>High-performance size exclusion chromatography was used to separate soybean extracts. The separation of the major storage proteins, including glycinin and beta-conglycinin, was determined by analysis of the subunits on sodium dodecyl sulfate gel electrophoresis. The extracts of defatted flour and whole beans showed a high degree of polymerization of the storage proteins. Addition of a disulfide reducing agent (dithiothreitol) resulted in a decrease of the polymerized forms. The separation of the major glucoside isoflavones (genistin, daidzin, and glycitein 7-beta-glucoside) was determined. The isoflavone glucosides eluted well past the elusion time of a small totally included molecule, indicating that they are separating by mechanisms other than size exclusion. Size exclusion chromatography was used to monitor the separation of the soybean extract in an aqueous two-phase extraction system. The major storage proteins partitioned to the salt phase, and the isoflavones and other hydrophobic compounds partitioned to the poly(ethylene glycol) phase</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><doi>10.1021/jf00048a013</doi><tpages>8</tpages></addata></record> |
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source | ACS CRKN Legacy Archives |
subjects | Animal, plant, fungal and microbial proteins, edible seaweeds and food yeasts Biological and medical sciences CHROMATOGRAPHIE CROMATOGRAFIA FLAVONOIDE FLAVONOIDES Food industries Fundamental and applied biological sciences. Psychology GLUCOSIDE GLUCOSIDOS PROTEINAS VEGETALES PROTEINE VEGETALE SEPARACION SEPARATION SOJA |
title | Size Exclusion Chromatography of Soybean Proteins and Isoflavones |
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