Please use this identifier to cite or link to this item: https://repository.cihe.edu.hk/jspui/handle/cihe/1491
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dc.contributor.authorBligh, Annie Sim Wanen_US
dc.contributor.otherWang, H.-
dc.contributor.otherWei, G.-
dc.contributor.otherLiu, F.-
dc.contributor.otherBanerjee, G.-
dc.contributor.otherJoshi, M.-
dc.contributor.otherShi, S.-
dc.contributor.otherLian, H.-
dc.contributor.otherFan, H.-
dc.contributor.otherGu, X.-
dc.contributor.otherWang, S.-
dc.date.accessioned2021-10-08T10:24:21Z-
dc.date.available2021-10-08T10:24:21Z-
dc.date.issued2014-
dc.identifier.urihttps://repository.cihe.edu.hk/jspui/handle/cihe/1491-
dc.description.abstractTwo natural homogalacturonan (HG) pectins (MW ca. 20 kDa) were isolated from green tea based on their immunomodulatory activity. The crude tea polysaccharides (TPS1 and TPS2) were obtained from green tea leaves by hot water extraction and followed by 40% and 70% ethanol precipitation, respectively. Two homogenous water soluble polysaccharides (TPS1-2a and TPS1-2b) were obtained from TPS1 after purification with gel permeation, which gave a higher phagocytic effect than TPS2. A combination of composition, methylation and configuration analyses, as well as NMR (nuclear magnetic resonance) spectroscopy revealed that TPS1-2a and TPS1-2b were homogalacturonan (HG) pectins consisting of a backbone of 1,4-linked α-d-galacturonic acid (GalA) residues with 28.4% and 26.1% of carboxyl groups as methyl ester, respectively. The immunological assay results demonstrated that TPS1-2, which consisted mainly of HG pectins, showed phagocytosis-enhancing activity in HL-60 cells.en_US
dc.language.isoenen_US
dc.publisherMDPIen_US
dc.relation.ispartofInternational Journal of Molecular Sciencesen_US
dc.titleCharacterization of two homogalacturonan pectins with immunomodulatory activity from green teaen_US
dc.typejournal articleen_US
dc.identifier.doi10.3390/ijms15069963-
dc.contributor.affiliationSchool of Health Sciencesen_US
dc.relation.issn1422-0067en_US
dc.description.volume15en_US
dc.description.issue6en_US
dc.description.startpage9963en_US
dc.description.endpage9978en_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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