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从北川当归根部分离得到的果胶多糖的结构与抗补体活性

Structure and anti-complementary activity of pectic polysaccharides isolated from the root of Angelica acutiloba Kitagawa.

作者信息

Kiyohara H, Cyong J C, Yamada H

机构信息

Oriental Medicine Research Center, Kitasato Institute, Tokyo, Japan.

出版信息

Carbohydr Res. 1988 Nov 1;182(2):259-75. doi: 10.1016/0008-6215(88)84007-2.

DOI:10.1016/0008-6215(88)84007-2
PMID:3242805
Abstract

Four pectic polysaccharides (AR-2IIa-IId) with anti-complementary activity have been isolated from a hot-water extract of the root of Angelica acutiloba Kitagawa. Each of these polysaccharides contained a large proportion of GalA together with neutral sugars consisting mainly of Rha, Ara, and Gal. Digestion with endo-alpha-(1----4)-polygalacturonase indicated that AR-2IIa-IIc each contained a large proportion of enzyme-sensitive polygalacturonan regions, and that AR-2IId contained a large proportion of enzyme-resistant regions. When AR-2IId was de-esterified, it became sensitive to the enzyme. These polysaccharides also contained small proportions of enzyme-resistant regions (PG-1) which were rich in neutral sugars. Methylation analysis and base-catalysed beta-elimination studies suggested that each PG-1 contained a rhamnogalacturonan moiety in which 2,4-disubstituted Rha was attached to 4-substituted GalA through position 2 of Rha. Carboxyl-reduction and methyl- and de-esterification of these polysaccharides modulated their anti-complementary activities. Digestion with endo-alpha-(1----4)-polygalacturonase decreased the activities of AR-2IIa and -2IIb, but not those of AR-2IIc and -2IId. Although PG-1 fractions from AR-2IIa-IIc were more active than the original polysaccharides, oligogalacturonide fragments obtained by enzymic digestion had weak or negligible activity. AR-2IIa-IIc expressed their anti-complementary activities mainly via the classical pathway, but AR-2IId and each PG-1 expressed their activities via both the classical and alternative pathways.

摘要

从北川当归根的热水提取物中分离出了四种具有抗补体活性的果胶多糖(AR-2IIa-IId)。这些多糖中的每一种都含有大量的半乳糖醛酸(GalA)以及主要由鼠李糖(Rha)、阿拉伯糖(Ara)和半乳糖(Gal)组成的中性糖。用内切α-(1→4)-聚半乳糖醛酸酶消化表明,AR-2IIa-IIc各自含有很大比例的对该酶敏感的聚半乳糖醛酸区域,而AR-2IId含有很大比例的对该酶抗性的区域。当AR-2IId去酯化后,它变得对该酶敏感。这些多糖还含有少量富含中性糖的对该酶抗性的区域(PG-1)。甲基化分析和碱催化的β-消除研究表明,每个PG-1都含有一个鼠李半乳糖醛酸部分,其中2,4-二取代的Rha通过Rha的2位连接到4-取代的GalA上。这些多糖的羧基还原以及甲基化和去酯化作用调节了它们的抗补体活性。用内切α-(1→4)-聚半乳糖醛酸酶消化降低了AR-2IIa和-2IIb的活性,但没有降低AR-2IIc和-2IId的活性。尽管来自AR-2IIa-IIc的PG-1级分比原始多糖更具活性,但通过酶消化获得的低聚半乳糖醛酸片段活性较弱或可忽略不计。AR-2IIa-IIc主要通过经典途径表达其抗补体活性,但AR-2IId和每个PG-1通过经典途径和替代途径表达其活性。

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