C-13-NUCLEAR MAGNETIC-RESONANCE SPECTRA OF COMPOUNDS CONTAINING BETA-D-FRUCTOFURANOSYL GROUPS OR RESIDUES

被引:67
作者
SEYMOUR, FR
KNAPP, RD
ZWEIG, JE
BISHOP, SH
机构
[1] BAYLOR UNIV,COLL MED,DIV ATHEROSCLEROSIS & LIPOPROT RES,HOUSTON,TX 77030
[2] METHODIST HOSP,TEXAS MED CTR,HOUSTON,TX 77030
[3] STEVENS INST TECHNOL,HOBOKEN,NJ 07030
[4] BAYLOR UNIV,COLL MED,TEXAS MED CTR,MARRS MCLEAN DEPT BIOCHEM,HOUSTON,TX 77030
基金
美国国家卫生研究院;
关键词
D O I
10.1016/S0008-6215(00)83923-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
13C-N.m.r. spectra have been recorded for sucrose, melezitose, levan, inulin, palatinose, and D-fructose. Except for the last, each compound contains a different O-substituted D-fructofuranose residue or group, or β-D-fructofuranosyl residue or group. On the basis of chemical-shift displacements, resulting from O-substitution at specific carbon atoms, resonances can be assigned to the carbon atoms of the β-D-fructofuranosyl residue. Fortuitously, the α-D-glucopyranosyl group present in some of these compounds exhibits resonances that do not obscure the β-D-fructofuranosyl resonances. O-Substitution of the β-D-fructofuranosyl residue causes a downfield displacement of the corresponding, linked-C resonance; however, the other major resonances of this residue are not affected by bulky substituents. Members of a series of levan fractions, the products of partial, acid hydrolysis of Streptoccoccus salivarius levan, were then examined for changes in relative degree of branching. © 1979.
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收藏
页码:57 / 69
页数:13
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