Please use this identifier to cite or link to this item: https://repository.cihe.edu.hk/jspui/handle/cihe/2008
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dc.contributor.authorBligh, Annie Sim Wanen_US
dc.contributor.otherWang, S. C.-
dc.contributor.otherZhu, C. L.-
dc.contributor.otherShi, S. S.-
dc.contributor.otherWang, Z. T.-
dc.contributor.otherHu, Z. B.-
dc.contributor.otherCrowder, J.-
dc.contributor.otherBranford-White, C.-
dc.contributor.otherVella, C.-
dc.date.accessioned2021-12-09T02:41:51Z-
dc.date.available2021-12-09T02:41:51Z-
dc.date.issued2008-
dc.identifier.urihttps://repository.cihe.edu.hk/jspui/handle/cihe/2008-
dc.description.abstractChina is a major producer of oats; the annual harvested area of 350,000 ha yields approximately 465,000 tons, giving an average yield of 1.33 tons/ha. The bran is not used for animal feed as it is of poor digestibility and low nutritive content and is considered a waste byproduct. Therefore, it is advantageous to produce a value-added product from the bran. We extracted the native polysaccharide, a linear (1–3)-, (1–4)-linked β-glucan (OBG) from the oat bran and synthesized a sulfated derivative OBGS containing 36.5% sulfate. OBGS had potent activity against a primary isolate of human immunodeficiency virus (HIV-1) in peripheral blood mononuclear cells at a concentration (EC50 = 5.98 ×10<sup>−4</sup> µM) approximately 15,000 times below its cytotoxic concentration. OBGS was also active postinfection (EC<sub>50</sub> = 5.3 ×10<sup>−4</sup> µM) and protected pretreated peripheral mononuclear cells (EC<sub>50</sub> = 5.2 ×10<sup>−2</sup> µM) washed free of the compounds prior to infection. Thus, OBGS has potential as a vaginal microbicide and is the first such report for oat bran derived sulfated̃ β-glucan.en_US
dc.language.isoenen_US
dc.publisherACS Publicationsen_US
dc.relation.ispartofJournal of Agricultural and Food Chemistryen_US
dc.titleSulfated β-glucan derived from oat bran with potent anti-HIV activityen_US
dc.typejournal articleen_US
dc.identifier.doi10.1021/jf072888h-
dc.contributor.affiliationSchool of Health Sciencesen_US
dc.relation.issn1520-5118en_US
dc.description.volume56en_US
dc.description.issue8en_US
dc.description.startpage2624en_US
dc.description.endpage2629en_US
dc.cihe.affiliatedNo-
item.fulltextWith Fulltext-
item.grantfulltextopen-
item.openairecristypehttp://purl.org/coar/resource_type/c_6501-
item.cerifentitytypePublications-
item.openairetypejournal article-
item.languageiso639-1en-
crisitem.author.deptS.K. Yee School of Health Sciences-
crisitem.author.orcid0000-0002-4757-2159-
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