Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/10573
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dc.contributorDepartment of Applied Biology and Chemical Technology-
dc.creatorYan, JK-
dc.creatorWang, WQ-
dc.creatorMa, HL-
dc.creatorWu, JY-
dc.date.accessioned2015-06-23T09:10:30Z-
dc.date.available2015-06-23T09:10:30Z-
dc.identifier.issn1420-3049-
dc.identifier.urihttp://hdl.handle.net/10397/10573-
dc.language.isoenen_US
dc.publisherMdpi Agen_US
dc.rights© 2013 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).en_US
dc.rightsThe following publication Yan, J. K., Wang, W. Q., Ma, H. L., & Wu, J. Y. (2013). Sulfation and enhanced antioxidant capacity of an exopolysaccharide produced by the medicinal fungus Cordyceps sinensis. Molecules, 18(1), (Suppl. ), 167-177 is available athttps://dx.doi.org/10.3390/molecules18010167en_US
dc.subjectAntioxidant activityen_US
dc.subjectCordyceps sinensisen_US
dc.subjectExopolysaccharideen_US
dc.subjectMolecular weighten_US
dc.subjectSulfationen_US
dc.titleSulfation and enhanced antioxidant capacity of an exopolysaccharide produced by the medicinal fungus Cordyceps sinensisen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage167-
dc.identifier.epage177-
dc.identifier.volume18-
dc.identifier.issue1-
dc.identifier.doi10.3390/molecules18010167-
dcterms.abstractEPS-1 was an exopolysaccharide produced by the medicinal fungus Cordyceps sinensis (Cs-HK1). In the present study, EPS-1 was sulfated with chlorosulfonic acid (CSA)-pyridine (Pyr) at different volume ratios, yielding four sulfated derivatives, SEPS-1A, B, C and D, with different degrees of substitution (DS: 0.25-1.38) and molecular weights (17.1-4.1 kDa). The sulfation of EPS-1 occurred most frequently at the C-6 hydroxyl groups due to their higher reactivity. In aqueous solution, the native EPS-1 formed random coils or aggregated networks, but the sulfated derivatives formed single helices. The antioxidant activities of the sulfated EPS-1 derivatives for scavenging hydroxyl radicals (·OH) and 2,2-Azinobis-3-ehtylbenzothiazolin-6-sulfonic acid radicals (ABTS·+) were significantly increased with increasing DS and decreasing molecular weight (MW). Sulfation has thus been shown to be an effective and favorable strategy for improving the physico-chemical properties and bioactivities of fungal polysaccharides.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationMolecules, Jan. 2013, v. 18, no. 1, p. 167-177-
dcterms.isPartOfMolecules-
dcterms.issued2013-
dc.identifier.isiWOS:000314032900012-
dc.identifier.scopus2-s2.0-84872875547-
dc.identifier.rosgroupidr67278-
dc.description.ros2012-2013 > Academic research: refereed > Publication in refereed journal-
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberOA_IR/PIRAen_US
dc.description.pubStatusPublisheden_US
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