Effect of anionic polysaccharides on conformational changes and antioxidant properties of protein-polyphenol binary covalently-linked complexes
[Display omitted] •Anionic polysaccharides were added to interact with the covalently-linked complexes.•The interaction is through steric hindrance and electrostatic repulsion.•Compared the effects of CMC or pectin on the binary complexes.•Complexes emulsion with pectin added had better stability an...
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Veröffentlicht in: | Process biochemistry (1991) 2020-02, Vol.89, p.89-97 |
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creator | Zhao, Yue Wang, Xu Li, Dan Tang, Honglin Yu, Dianyu Wang, Liqi Jiang, Lianzhou |
description | [Display omitted]
•Anionic polysaccharides were added to interact with the covalently-linked complexes.•The interaction is through steric hindrance and electrostatic repulsion.•Compared the effects of CMC or pectin on the binary complexes.•Complexes emulsion with pectin added had better stability and antioxidant activity.
This work evaluated the anionic polysaccharides to improve the functional properties and antioxidant activities, and compared the effects on covalently-linked the soy protein isolate (SPI)- (–)-epigallocatechin-3-gallat (EGCG) binary complexes. The increasing molecular weight via covalent insertion of (–)-epigallocatechin-3-gallat (EGCG) into the soy protein isolate (SPI) was verified by SDS-PAGE. The addition of polysaccharides had no obvious effects on the molecular weight, indicating noncovalent insertion by adsorption. Fourier transform infrared spectroscopy (FT-IR) analysis suggested that SPI-EGCG complexes mixed with polysaccharides changed the secondary structures of SPI with a decrease in α-helix and an increase in β-turn. The emulsions exhibited better stability index (ESI) by adding polysaccharides than the binary complexes emulsion, with decreased particle sizes and increased absolute ζ-potential values, while the value of ESI for the pectin mixed increased more. The 1,1-diphenyl-2-picrylhydrazyl radical (DPPH•) scavenging capacity of SPI-EGCG complexes with the addition of polysaccharides were both greater than 70 %. These findings indicated that anionic polysaccharides could be potentially used as a natural and safe alternative for regulating covalently-linked SPI-EGCG emulsion stability and improving emulsion oxidation resistance. |
doi_str_mv | 10.1016/j.procbio.2019.10.021 |
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•Anionic polysaccharides were added to interact with the covalently-linked complexes.•The interaction is through steric hindrance and electrostatic repulsion.•Compared the effects of CMC or pectin on the binary complexes.•Complexes emulsion with pectin added had better stability and antioxidant activity.
This work evaluated the anionic polysaccharides to improve the functional properties and antioxidant activities, and compared the effects on covalently-linked the soy protein isolate (SPI)- (–)-epigallocatechin-3-gallat (EGCG) binary complexes. The increasing molecular weight via covalent insertion of (–)-epigallocatechin-3-gallat (EGCG) into the soy protein isolate (SPI) was verified by SDS-PAGE. The addition of polysaccharides had no obvious effects on the molecular weight, indicating noncovalent insertion by adsorption. Fourier transform infrared spectroscopy (FT-IR) analysis suggested that SPI-EGCG complexes mixed with polysaccharides changed the secondary structures of SPI with a decrease in α-helix and an increase in β-turn. The emulsions exhibited better stability index (ESI) by adding polysaccharides than the binary complexes emulsion, with decreased particle sizes and increased absolute ζ-potential values, while the value of ESI for the pectin mixed increased more. The 1,1-diphenyl-2-picrylhydrazyl radical (DPPH•) scavenging capacity of SPI-EGCG complexes with the addition of polysaccharides were both greater than 70 %. These findings indicated that anionic polysaccharides could be potentially used as a natural and safe alternative for regulating covalently-linked SPI-EGCG emulsion stability and improving emulsion oxidation resistance.</description><identifier>ISSN: 1359-5113</identifier><identifier>EISSN: 1873-3298</identifier><identifier>DOI: 10.1016/j.procbio.2019.10.021</identifier><language>eng</language><publisher>Barking: Elsevier Ltd</publisher><subject>Anionic polysaccharides ; Antioxidant activity ; Antioxidants ; Conformation ; Covalence ; Emulsions ; Epigallocatechin-3-gallate ; Fourier analysis ; Fourier transforms ; Gel electrophoresis ; Infrared analysis ; Infrared spectroscopy ; Insertion ; Interactions ; Molecular weight ; Oxidation ; Oxidation resistance ; Pectin ; Polysaccharides ; Proteins ; Saccharides ; Scavenging ; Sodium lauryl sulfate ; SPI-EGCG complexes ; Stability</subject><ispartof>Process biochemistry (1991), 2020-02, Vol.89, p.89-97</ispartof><rights>2019 Elsevier Ltd</rights><rights>Copyright Elsevier BV Feb 2020</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c403t-5d009bf26bfc1866cb5fe9d81213150785691ad0d1eb2d739ecb3e3692c589fb3</citedby><cites>FETCH-LOGICAL-c403t-5d009bf26bfc1866cb5fe9d81213150785691ad0d1eb2d739ecb3e3692c589fb3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.procbio.2019.10.021$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,778,782,3539,27907,27908,45978</link.rule.ids></links><search><creatorcontrib>Zhao, Yue</creatorcontrib><creatorcontrib>Wang, Xu</creatorcontrib><creatorcontrib>Li, Dan</creatorcontrib><creatorcontrib>Tang, Honglin</creatorcontrib><creatorcontrib>Yu, Dianyu</creatorcontrib><creatorcontrib>Wang, Liqi</creatorcontrib><creatorcontrib>Jiang, Lianzhou</creatorcontrib><title>Effect of anionic polysaccharides on conformational changes and antioxidant properties of protein-polyphenol binary covalently-linked complexes</title><title>Process biochemistry (1991)</title><description>[Display omitted]
•Anionic polysaccharides were added to interact with the covalently-linked complexes.•The interaction is through steric hindrance and electrostatic repulsion.•Compared the effects of CMC or pectin on the binary complexes.•Complexes emulsion with pectin added had better stability and antioxidant activity.
This work evaluated the anionic polysaccharides to improve the functional properties and antioxidant activities, and compared the effects on covalently-linked the soy protein isolate (SPI)- (–)-epigallocatechin-3-gallat (EGCG) binary complexes. The increasing molecular weight via covalent insertion of (–)-epigallocatechin-3-gallat (EGCG) into the soy protein isolate (SPI) was verified by SDS-PAGE. The addition of polysaccharides had no obvious effects on the molecular weight, indicating noncovalent insertion by adsorption. Fourier transform infrared spectroscopy (FT-IR) analysis suggested that SPI-EGCG complexes mixed with polysaccharides changed the secondary structures of SPI with a decrease in α-helix and an increase in β-turn. The emulsions exhibited better stability index (ESI) by adding polysaccharides than the binary complexes emulsion, with decreased particle sizes and increased absolute ζ-potential values, while the value of ESI for the pectin mixed increased more. The 1,1-diphenyl-2-picrylhydrazyl radical (DPPH•) scavenging capacity of SPI-EGCG complexes with the addition of polysaccharides were both greater than 70 %. These findings indicated that anionic polysaccharides could be potentially used as a natural and safe alternative for regulating covalently-linked SPI-EGCG emulsion stability and improving emulsion oxidation resistance.</description><subject>Anionic polysaccharides</subject><subject>Antioxidant activity</subject><subject>Antioxidants</subject><subject>Conformation</subject><subject>Covalence</subject><subject>Emulsions</subject><subject>Epigallocatechin-3-gallate</subject><subject>Fourier analysis</subject><subject>Fourier transforms</subject><subject>Gel electrophoresis</subject><subject>Infrared analysis</subject><subject>Infrared spectroscopy</subject><subject>Insertion</subject><subject>Interactions</subject><subject>Molecular weight</subject><subject>Oxidation</subject><subject>Oxidation resistance</subject><subject>Pectin</subject><subject>Polysaccharides</subject><subject>Proteins</subject><subject>Saccharides</subject><subject>Scavenging</subject><subject>Sodium lauryl sulfate</subject><subject>SPI-EGCG complexes</subject><subject>Stability</subject><issn>1359-5113</issn><issn>1873-3298</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNqFUMtKBDEQHETB9fEJwoDnWdOJ88hJRHyB4EXPIZN03KyzyZiM4n6Fv2wP691D6HR1VdFdRXEGbAkMmov1ckzR9D4uOQNJ2JJx2CsW0LWiElx2-_QXtaxqAHFYHOW8ZkwAAFsUP7fOoZnK6EodfAzelGMctlkbs9LJW8xlDKWJwcW00RMx9FDSKLzRRAdLj8Bvb6mWtMaIafKzyM3dhD5Us9-4whCHsvdBpy3ZfekBwzRsq8GHd7SEbMYBvzGfFAdODxlP_-px8Xp3-3LzUD093z_eXD9V5pKJqaotY7J3vOmdga5pTF87lLYDDgJq1nZ1I0FbZgF7blsh0fQCRSO5qTvpenFcnO98acuPT8yTWsfPRMdlxUXbtPwSuo5Y9Y5lUsw5oVNj8hs6QQFTc_Zqrf6yV3P2M0zZk-5qp0M64ctjUtl4DAatT5S2stH_4_ALURmUbQ</recordid><startdate>202002</startdate><enddate>202002</enddate><creator>Zhao, Yue</creator><creator>Wang, Xu</creator><creator>Li, Dan</creator><creator>Tang, Honglin</creator><creator>Yu, Dianyu</creator><creator>Wang, Liqi</creator><creator>Jiang, Lianzhou</creator><general>Elsevier Ltd</general><general>Elsevier BV</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7QO</scope><scope>7T7</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope></search><sort><creationdate>202002</creationdate><title>Effect of anionic polysaccharides on conformational changes and antioxidant properties of protein-polyphenol binary covalently-linked complexes</title><author>Zhao, Yue ; Wang, Xu ; Li, Dan ; Tang, Honglin ; Yu, Dianyu ; Wang, Liqi ; Jiang, Lianzhou</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c403t-5d009bf26bfc1866cb5fe9d81213150785691ad0d1eb2d739ecb3e3692c589fb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Anionic polysaccharides</topic><topic>Antioxidant activity</topic><topic>Antioxidants</topic><topic>Conformation</topic><topic>Covalence</topic><topic>Emulsions</topic><topic>Epigallocatechin-3-gallate</topic><topic>Fourier analysis</topic><topic>Fourier transforms</topic><topic>Gel electrophoresis</topic><topic>Infrared analysis</topic><topic>Infrared spectroscopy</topic><topic>Insertion</topic><topic>Interactions</topic><topic>Molecular weight</topic><topic>Oxidation</topic><topic>Oxidation resistance</topic><topic>Pectin</topic><topic>Polysaccharides</topic><topic>Proteins</topic><topic>Saccharides</topic><topic>Scavenging</topic><topic>Sodium lauryl sulfate</topic><topic>SPI-EGCG complexes</topic><topic>Stability</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhao, Yue</creatorcontrib><creatorcontrib>Wang, Xu</creatorcontrib><creatorcontrib>Li, Dan</creatorcontrib><creatorcontrib>Tang, Honglin</creatorcontrib><creatorcontrib>Yu, Dianyu</creatorcontrib><creatorcontrib>Wang, Liqi</creatorcontrib><creatorcontrib>Jiang, Lianzhou</creatorcontrib><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Process biochemistry (1991)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhao, Yue</au><au>Wang, Xu</au><au>Li, Dan</au><au>Tang, Honglin</au><au>Yu, Dianyu</au><au>Wang, Liqi</au><au>Jiang, Lianzhou</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of anionic polysaccharides on conformational changes and antioxidant properties of protein-polyphenol binary covalently-linked complexes</atitle><jtitle>Process biochemistry (1991)</jtitle><date>2020-02</date><risdate>2020</risdate><volume>89</volume><spage>89</spage><epage>97</epage><pages>89-97</pages><issn>1359-5113</issn><eissn>1873-3298</eissn><abstract>[Display omitted]
•Anionic polysaccharides were added to interact with the covalently-linked complexes.•The interaction is through steric hindrance and electrostatic repulsion.•Compared the effects of CMC or pectin on the binary complexes.•Complexes emulsion with pectin added had better stability and antioxidant activity.
This work evaluated the anionic polysaccharides to improve the functional properties and antioxidant activities, and compared the effects on covalently-linked the soy protein isolate (SPI)- (–)-epigallocatechin-3-gallat (EGCG) binary complexes. The increasing molecular weight via covalent insertion of (–)-epigallocatechin-3-gallat (EGCG) into the soy protein isolate (SPI) was verified by SDS-PAGE. The addition of polysaccharides had no obvious effects on the molecular weight, indicating noncovalent insertion by adsorption. Fourier transform infrared spectroscopy (FT-IR) analysis suggested that SPI-EGCG complexes mixed with polysaccharides changed the secondary structures of SPI with a decrease in α-helix and an increase in β-turn. The emulsions exhibited better stability index (ESI) by adding polysaccharides than the binary complexes emulsion, with decreased particle sizes and increased absolute ζ-potential values, while the value of ESI for the pectin mixed increased more. The 1,1-diphenyl-2-picrylhydrazyl radical (DPPH•) scavenging capacity of SPI-EGCG complexes with the addition of polysaccharides were both greater than 70 %. These findings indicated that anionic polysaccharides could be potentially used as a natural and safe alternative for regulating covalently-linked SPI-EGCG emulsion stability and improving emulsion oxidation resistance.</abstract><cop>Barking</cop><pub>Elsevier Ltd</pub><doi>10.1016/j.procbio.2019.10.021</doi><tpages>9</tpages></addata></record> |
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subjects | Anionic polysaccharides Antioxidant activity Antioxidants Conformation Covalence Emulsions Epigallocatechin-3-gallate Fourier analysis Fourier transforms Gel electrophoresis Infrared analysis Infrared spectroscopy Insertion Interactions Molecular weight Oxidation Oxidation resistance Pectin Polysaccharides Proteins Saccharides Scavenging Sodium lauryl sulfate SPI-EGCG complexes Stability |
title | Effect of anionic polysaccharides on conformational changes and antioxidant properties of protein-polyphenol binary covalently-linked complexes |
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