RESISTANCE OF HIGHLY BRANCHED (1-]3)-BETA-D-GLUCANS TO FORMOLYSIS

被引:0
作者
OHNO, N
TERUI, T
CHIBA, N
KURACHI, K
ADACHI, Y
YADOMAE, T
机构
[1] TOKYO UNIV PHARM & LIFE SCI, SCH PHARM, IMMUNOPHARMACOL MICROBIAL PROD LAB, HACHIOJI, TOKYO 19203, JAPAN
[2] KOWA CO LTD, FUJI FACTORY, FUJI, SHIZUOKA 417, JAPAN
关键词
BETA-GLUCAN; FORMOLYSIS; OLIGOSACCHARIDE; ANTITUMOR GLUCAN;
D O I
暂无
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Small molecular weight (MW) glucan derivatives could be a useful tool for studying the mechanisms of beta-glucan mediated biological activity, especially as antagonists for a beta-glucan receptor. This paper described the stability of various (1-->6) branched (1-->3)-beta-D-glucans to formolysis in the preparation of small MW derivatives. The glucans used were curdlan (linear), pachyman (few branches), GRN (one branch in every third main chain unit; 2/6), SPG (2/6), SSG (3/6), and OL-2 (4/6). Curdlan and pachyman were easily degraded to oligosaccharides by degradation for 20 min at 100 degrees C by 90% formic acid. However, branched glucans, especially the highly branched glucans, SSG and OL-2, were significantly resistant to degradation, and the majority remained high MW. SSG required a longer period and/or a higher temperature (121 degrees C treatment) to produce small MW derivatives. Branched glucans were also resistant to zymolyase (an endo-(1-->3)-beta-D-glucan hydrolase) digestion. These facts suggest that the (1-->6)-beta-D-branched residues contribute to the glucans' resistance to formic acid degradation and zymolyase digestion.
引用
收藏
页码:1057 / 1060
页数:4
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