dc.contributorUniversidade Estadual Paulista (Unesp)
dc.contributorUniversidade Estadual de Londrina (UEL)
dc.contributorThe Biological Research Center (CIB)
dc.date.accessioned2018-12-11T17:19:33Z
dc.date.available2018-12-11T17:19:33Z
dc.date.created2018-12-11T17:19:33Z
dc.date.issued2018-08-01
dc.identifierInternational Journal of Biological Macromolecules, v. 115, p. 106-113.
dc.identifier1879-0003
dc.identifier0141-8130
dc.identifierhttp://hdl.handle.net/11449/176196
dc.identifier10.1016/j.ijbiomac.2018.04.035
dc.identifier2-s2.0-85045569361
dc.identifier2-s2.0-85045569361.pdf
dc.identifier8845835550637809
dc.identifier0000-0002-4292-3298
dc.description.abstractA fucomannogalactan from Rhizoctonia solani biomass was obtained after hot aqueous extraction and purified by freeze-thaw cycles and gel filtration chromatography on Sepharose CL-6B. The polysaccharide was homogeneous after HPSEC/RID analysis (Mw/Mn ~ 1.1), displaying an average molecular weight of 15.4 × 103 Da. Its chemical structure was determined by methylation analysis (GC/MS) and spectroscopy (FTIR, 1D and 2D NMR). The polysaccharide had a branched α-1,6-linked Galp backbone with 66% linear residues, a number of which were at O-3 methylated. Side chains (34%) were always linked at O-2 positions of the main chain and consisted of single, non-reducing ends of α-D-Manp (6%) and α-L-Fucp (28%). Analysis of its biological activity showed that the highly purified fucomannogalactan from R. solani inhibited the proliferation of colon cancer cells in vitro, but that it did not have the same activity against lung cancer cells.
dc.languageeng
dc.relationInternational Journal of Biological Macromolecules
dc.relation0,917
dc.rightsAcesso aberto
dc.sourceScopus
dc.subjectAntiproliferative activity
dc.subjectFucomannogalactan
dc.subjectGel filtration chromatography
dc.subjectNMR spectroscopy
dc.subjectRhizoctonia solani
dc.titleRhizoctonia solani fucomannogalactan: Chemical characterization and antiproliferative activity
dc.typeArtículos de revistas


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