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Purification, characterization, and antioxidant activity of polysaccharides from Grifola frondosa by hydrogen peroxide/ascorbic acid-assisted extraction
To increase the production of Grifola frondosa polysaccharides (GFPs), a hydrogen peroxide/ascorbic acid (H 2 O 2 /Vc)-assisted extraction method was established. The extraction conditions were optimized by response surface methodology. Purification of the crude GFP by DEAE-52 and Sephadex G100 colu...
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Published in: | Journal of food measurement & characterization 2024, Vol.18 (1), p.797-811 |
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description | To increase the production of
Grifola frondosa
polysaccharides (GFPs), a hydrogen peroxide/ascorbic acid (H
2
O
2
/Vc)-assisted extraction method was established. The extraction conditions were optimized by response surface methodology. Purification of the crude GFP by DEAE-52 and Sephadex G100 column chromatography yielded three fractions, GFP0, GFP1, and GFP3. Monosaccharide composition analysis revealed that these GFPs mainly consisted of mannose, glucose, galactose and
l
-fucose, together with a low proportion of xylose, glucuronic acid and ribose. Chemical antioxidant assays indicated that these GFPs possessed considerable reducing power and radical (DPPH
·
, HO
·
and ABTS
·
+
) scavenging ability. They were also observed to availably protect RAW264.7 cells from H
2
O
2
-induced oxidative stress, reduce intracellular ROS and MDA levels, and increase intracellular SOD and CAT activities. These GFPs were able to up-regulate the mRNA expression of SOD1, CAT, HO-1 and Nrf2, indicating that regulation of antioxidant enzymes and Nrf2 signaling pathway could be their important antioxidant mechanism. |
doi_str_mv | 10.1007/s11694-023-02194-y |
format | article |
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Grifola frondosa
polysaccharides (GFPs), a hydrogen peroxide/ascorbic acid (H
2
O
2
/Vc)-assisted extraction method was established. The extraction conditions were optimized by response surface methodology. Purification of the crude GFP by DEAE-52 and Sephadex G100 column chromatography yielded three fractions, GFP0, GFP1, and GFP3. Monosaccharide composition analysis revealed that these GFPs mainly consisted of mannose, glucose, galactose and
l
-fucose, together with a low proportion of xylose, glucuronic acid and ribose. Chemical antioxidant assays indicated that these GFPs possessed considerable reducing power and radical (DPPH
·
, HO
·
and ABTS
·
+
) scavenging ability. They were also observed to availably protect RAW264.7 cells from H
2
O
2
-induced oxidative stress, reduce intracellular ROS and MDA levels, and increase intracellular SOD and CAT activities. These GFPs were able to up-regulate the mRNA expression of SOD1, CAT, HO-1 and Nrf2, indicating that regulation of antioxidant enzymes and Nrf2 signaling pathway could be their important antioxidant mechanism.</description><identifier>ISSN: 2193-4126</identifier><identifier>EISSN: 2193-4134</identifier><identifier>DOI: 10.1007/s11694-023-02194-y</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Antioxidants ; Ascorbic acid ; Chemistry ; Chemistry and Materials Science ; Chemistry/Food Science ; Chromatography ; Column chromatography ; Engineering ; Food Science ; Free radicals ; Fucose ; Galactose ; Gene expression ; Grifola frondosa ; Hydrogen peroxide ; Intracellular ; Mannose ; Methods ; Molecular weight ; Monosaccharides ; Original Paper ; Oxidative stress ; Polysaccharides ; Purification ; Response surface methodology ; Rheology ; Ribose ; Saccharides ; Scavenging ; Signal transduction ; Superoxide dismutase</subject><ispartof>Journal of food measurement & characterization, 2024, Vol.18 (1), p.797-811</ispartof><rights>The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c319t-2e4481526267cd7d0ae711027dc220d66a0e56cc873ffce1ec83c64a8c43007e3</citedby><cites>FETCH-LOGICAL-c319t-2e4481526267cd7d0ae711027dc220d66a0e56cc873ffce1ec83c64a8c43007e3</cites><orcidid>0000-0003-4510-3639</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.proquest.com/docview/2918142135?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,25752,27923,27924,37011,44589</link.rule.ids></links><search><creatorcontrib>Ding, Xi-Min</creatorcontrib><creatorcontrib>Xu, Ying-Ying</creatorcontrib><creatorcontrib>Liu, Weiming</creatorcontrib><creatorcontrib>Wang, Xingli</creatorcontrib><creatorcontrib>Tang, Meng-Ting</creatorcontrib><creatorcontrib>Zhang, Xu</creatorcontrib><creatorcontrib>Gu, Qing</creatorcontrib><creatorcontrib>Zhou, Tao</creatorcontrib><title>Purification, characterization, and antioxidant activity of polysaccharides from Grifola frondosa by hydrogen peroxide/ascorbic acid-assisted extraction</title><title>Journal of food measurement & characterization</title><addtitle>Food Measure</addtitle><description>To increase the production of
Grifola frondosa
polysaccharides (GFPs), a hydrogen peroxide/ascorbic acid (H
2
O
2
/Vc)-assisted extraction method was established. The extraction conditions were optimized by response surface methodology. Purification of the crude GFP by DEAE-52 and Sephadex G100 column chromatography yielded three fractions, GFP0, GFP1, and GFP3. Monosaccharide composition analysis revealed that these GFPs mainly consisted of mannose, glucose, galactose and
l
-fucose, together with a low proportion of xylose, glucuronic acid and ribose. Chemical antioxidant assays indicated that these GFPs possessed considerable reducing power and radical (DPPH
·
, HO
·
and ABTS
·
+
) scavenging ability. They were also observed to availably protect RAW264.7 cells from H
2
O
2
-induced oxidative stress, reduce intracellular ROS and MDA levels, and increase intracellular SOD and CAT activities. These GFPs were able to up-regulate the mRNA expression of SOD1, CAT, HO-1 and Nrf2, indicating that regulation of antioxidant enzymes and Nrf2 signaling pathway could be their important antioxidant mechanism.</description><subject>Antioxidants</subject><subject>Ascorbic acid</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Chemistry/Food Science</subject><subject>Chromatography</subject><subject>Column chromatography</subject><subject>Engineering</subject><subject>Food Science</subject><subject>Free radicals</subject><subject>Fucose</subject><subject>Galactose</subject><subject>Gene expression</subject><subject>Grifola frondosa</subject><subject>Hydrogen peroxide</subject><subject>Intracellular</subject><subject>Mannose</subject><subject>Methods</subject><subject>Molecular weight</subject><subject>Monosaccharides</subject><subject>Original Paper</subject><subject>Oxidative stress</subject><subject>Polysaccharides</subject><subject>Purification</subject><subject>Response surface methodology</subject><subject>Rheology</subject><subject>Ribose</subject><subject>Saccharides</subject><subject>Scavenging</subject><subject>Signal transduction</subject><subject>Superoxide dismutase</subject><issn>2193-4126</issn><issn>2193-4134</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNp9UctKAzEUHUTBUvsDrgJuHZubpJnpUopWQdCFrkOa3GlT2klNptLxS_xcM07RnYvLPUnOA3Ky7BLoDVBajCOAnIqcMp4GEmpPskECPBfAxekvZvI8G8W4ppQCFEJIPsi-XvbBVc7oxvn6mpiVDto0GNzn8UbXNk3CB2fTJunVfbimJb4iO79pozadyFmMpAp-S-bJz290d6itj5osWrJqbfBLrMkOQ2eEYx2NDwtnkp-zuY7RxQYtwUPT5afki-ys0puIo-MeZm_3d6-zh_zpef44u33KDYdpkzMUooQJk0wWxhaWaiwAKCusYYxaKTXFiTSmLHhVGQQ0JTdS6NIInv4O-TC76n13wb_vMTZq7fehTpGKTaEEwYBPEov1LBN8jAErtQtuq0OrgKquBNWXoFIJ6qcE1SYR70Uxkeslhj_rf1Tfc6COnw</recordid><startdate>2024</startdate><enddate>2024</enddate><creator>Ding, Xi-Min</creator><creator>Xu, Ying-Ying</creator><creator>Liu, Weiming</creator><creator>Wang, Xingli</creator><creator>Tang, Meng-Ting</creator><creator>Zhang, Xu</creator><creator>Gu, Qing</creator><creator>Zhou, Tao</creator><general>Springer US</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X2</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>HCIFZ</scope><scope>L6V</scope><scope>M0K</scope><scope>M7S</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PTHSS</scope><orcidid>https://orcid.org/0000-0003-4510-3639</orcidid></search><sort><creationdate>2024</creationdate><title>Purification, characterization, and antioxidant activity of polysaccharides from Grifola frondosa by hydrogen peroxide/ascorbic acid-assisted extraction</title><author>Ding, Xi-Min ; Xu, Ying-Ying ; Liu, Weiming ; Wang, Xingli ; Tang, Meng-Ting ; Zhang, Xu ; Gu, Qing ; Zhou, Tao</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c319t-2e4481526267cd7d0ae711027dc220d66a0e56cc873ffce1ec83c64a8c43007e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Antioxidants</topic><topic>Ascorbic acid</topic><topic>Chemistry</topic><topic>Chemistry and Materials Science</topic><topic>Chemistry/Food Science</topic><topic>Chromatography</topic><topic>Column chromatography</topic><topic>Engineering</topic><topic>Food Science</topic><topic>Free radicals</topic><topic>Fucose</topic><topic>Galactose</topic><topic>Gene expression</topic><topic>Grifola frondosa</topic><topic>Hydrogen peroxide</topic><topic>Intracellular</topic><topic>Mannose</topic><topic>Methods</topic><topic>Molecular weight</topic><topic>Monosaccharides</topic><topic>Original Paper</topic><topic>Oxidative stress</topic><topic>Polysaccharides</topic><topic>Purification</topic><topic>Response surface methodology</topic><topic>Rheology</topic><topic>Ribose</topic><topic>Saccharides</topic><topic>Scavenging</topic><topic>Signal transduction</topic><topic>Superoxide dismutase</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ding, Xi-Min</creatorcontrib><creatorcontrib>Xu, Ying-Ying</creatorcontrib><creatorcontrib>Liu, Weiming</creatorcontrib><creatorcontrib>Wang, Xingli</creatorcontrib><creatorcontrib>Tang, Meng-Ting</creatorcontrib><creatorcontrib>Zhang, Xu</creatorcontrib><creatorcontrib>Gu, Qing</creatorcontrib><creatorcontrib>Zhou, Tao</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Agricultural Science Collection</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Engineering Collection</collection><collection>Agriculture Science Database</collection><collection>Engineering Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>Engineering Collection</collection><jtitle>Journal of food measurement & characterization</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ding, Xi-Min</au><au>Xu, Ying-Ying</au><au>Liu, Weiming</au><au>Wang, Xingli</au><au>Tang, Meng-Ting</au><au>Zhang, Xu</au><au>Gu, Qing</au><au>Zhou, Tao</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Purification, characterization, and antioxidant activity of polysaccharides from Grifola frondosa by hydrogen peroxide/ascorbic acid-assisted extraction</atitle><jtitle>Journal of food measurement & characterization</jtitle><stitle>Food Measure</stitle><date>2024</date><risdate>2024</risdate><volume>18</volume><issue>1</issue><spage>797</spage><epage>811</epage><pages>797-811</pages><issn>2193-4126</issn><eissn>2193-4134</eissn><abstract>To increase the production of
Grifola frondosa
polysaccharides (GFPs), a hydrogen peroxide/ascorbic acid (H
2
O
2
/Vc)-assisted extraction method was established. The extraction conditions were optimized by response surface methodology. Purification of the crude GFP by DEAE-52 and Sephadex G100 column chromatography yielded three fractions, GFP0, GFP1, and GFP3. Monosaccharide composition analysis revealed that these GFPs mainly consisted of mannose, glucose, galactose and
l
-fucose, together with a low proportion of xylose, glucuronic acid and ribose. Chemical antioxidant assays indicated that these GFPs possessed considerable reducing power and radical (DPPH
·
, HO
·
and ABTS
·
+
) scavenging ability. They were also observed to availably protect RAW264.7 cells from H
2
O
2
-induced oxidative stress, reduce intracellular ROS and MDA levels, and increase intracellular SOD and CAT activities. These GFPs were able to up-regulate the mRNA expression of SOD1, CAT, HO-1 and Nrf2, indicating that regulation of antioxidant enzymes and Nrf2 signaling pathway could be their important antioxidant mechanism.</abstract><cop>New York</cop><pub>Springer US</pub><doi>10.1007/s11694-023-02194-y</doi><tpages>15</tpages><orcidid>https://orcid.org/0000-0003-4510-3639</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Antioxidants Ascorbic acid Chemistry Chemistry and Materials Science Chemistry/Food Science Chromatography Column chromatography Engineering Food Science Free radicals Fucose Galactose Gene expression Grifola frondosa Hydrogen peroxide Intracellular Mannose Methods Molecular weight Monosaccharides Original Paper Oxidative stress Polysaccharides Purification Response surface methodology Rheology Ribose Saccharides Scavenging Signal transduction Superoxide dismutase |
title | Purification, characterization, and antioxidant activity of polysaccharides from Grifola frondosa by hydrogen peroxide/ascorbic acid-assisted extraction |
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