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pubmed-article:15862867pubmed:abstractTextA homogeneous fucogalactoxyloglucan, isolated from the leaves of Hymenaea courbaril, was analysed by methylation-GC-MS. These procedures involved derived partially O-methylated alditol acetates and acetylated aldononitriles, which demonstrated the presence of both 2-O- and 4-O-substituted Xylp units in the side-chains. The presence of the unusual, latter structure was confirmed by 2D NMR spectroscopy with a correlated HMQC C-4/H-4 signal at delta 77.8/3.73. A similar 4-O-substituted xylosyl structure was present in a decasaccharide Glc4Xyl3Gal2Fuc obtained via endo-glucanase treatment of the polysaccharide, which gave rise to a molecular ion with m/z 1555 (ESI-MS, Na+ form).lld:pubmed
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pubmed-article:15862867pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:15862867pubmed:articleTitleNew 4-O-substituted xylosyl units in the xyloglucan from leaves of Hymenaea courbaril.lld:pubmed
pubmed-article:15862867pubmed:affiliationDepartamento de Bioquímica e Biologia Molecular, Universidade Federal do Paraná, CP 19046, 81531-990 Curitiba, Paraná, Brazil.lld:pubmed
pubmed-article:15862867pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:15862867pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed