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- W2058212918 abstract "The location of the O-acetyl substituents on th emajor nonasaccharide repeating unit of the xyloglucan isolated from sycamore extracellular polysaccharides were determined by a combination of analytical methods, including f.a.b.-m.s. and 1H-n.m.r. spectroscopy. The O-2-linked-β-d-galactosyl residue of the nonasaccharide was found to be the dominant site of O-acetyl substitution. Both mono-O-acetylated and di-O-acetylated β-d-galactosyl residues were detected. The degree of O-acetylation of the β-d-galactosyl residue, was estimated by 1H-n.m.r. spectroscopy to be 55–60% at O-6, 15-20% at O-4, and 20–25% at O-3. 1H-n.m.r. spectroscopy also indicated that ∼50% of the β-d-galactosyl residues are mono-O-acetylated, 25–30% are di-O-acetylated, and 20% are not acetylated." @default.
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- W2058212918 date "1988-02-01" @default.
- W2058212918 modified "2023-09-27" @default.
- W2058212918 title "Location of the O-acetyl substituents on a nonasaccharide repeating unit of sycamore extracellular xyloglucan" @default.
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- W2058212918 doi "https://doi.org/10.1016/s0008-6215(00)90807-3" @default.
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