Hirano M, Kiyohara H, Matsumoto T, Yamada H
Oriental Medicine Research Center of the Kitasato Institute, Tokyo, Japan.
Carbohydr Res. 1994 Jan 3;251:145-62. doi: 10.1016/0008-6215(94)84282-5.
The endo-alpha-(1-->4)-polygalacturonase-resistant fractions (PG-1, PG-2, and PG-3) from an antiulcer pectin (Bupleuran 2IIc), isolated from the roots of Bupleurum falcatum L., were further analysed by lithium degradation. The results indicated that PG-1 contained a small proportion of long, branched arabinosyl chains and a large proportion of short, neutral oligosaccharide chains. GLC-MS analysis showed that, after methylation the short, neutral oligosaccharide fraction consisted of at least 22 kinds of di- to tetra-saccharide alditols, such as Gal-(1-->4)-Rha-ol (a major component), Ara-(1-->4)-Rha-ol, Glc-(1-->4)-Rha-ol, Ara-->Ara-->Ara-ol, and Ara-->Ara-->Ara-->Ara-ol (minor components) in addition to heteroglycosyl alditols. After deesterification, PG-2 and PG-3 were digested with endo-alpha-(1-->4)-polygalacturonase again, and the enzyme-resistant intermediate size fraction (PG-2') was purified. Component sugar analysis indicated that PG-2' contained 2-Me-Fuc, 2-Me-Xyl, apiose (Api), aceric acid (AceA), 3-deoxy-D-lyxo-heptulosaric acid (Dha), and 3-deoxy-D-manno-2-octulosonic acid (Kdo) in addition to Rha, Fuc, Ara, Xyl, Man, Gal, Glc, GalA, and GlcA. Lithium degradation of PG-2' gave mainly a pentosyl-->6-deoxyhexosyl-->6-deoxyhexosyl-->pentitol fragment, with some neutral di- and tri-saccharide alditols, including a pentosyl-->deoxyhexitol. Methylation analysis of these degradation products indicated that they contained terminal Rha, Araf, Fuc, Xyl, and Gal, 4-linked Rha, 3-linked Fuc, 3-linked Ara, and 3'-linked Api. Bupleuran 2IIc was eluted as essentially a single peak on gel filtration on Sepharose CL-6B. The neutral sugar content of the successive fractions increased with increasing molecular weight, but each fraction also contained, in addition to Rha, Ara, and Gal, 2-Me-Fuc, 2-Me-Xyl, and Api.
从柴胡(Bupleurum falcatum L.)根部分离得到的抗溃疡果胶(柴胡2IIc)中的耐内切α-(1→4)-聚半乳糖醛酸酶组分(PG-1、PG-2和PG-3),通过锂降解进一步分析。结果表明,PG-1含有一小部分长的、分支的阿拉伯糖基链和一大部分短的、中性寡糖链。气相色谱-质谱联用(GLC-MS)分析表明,甲基化后,短的中性寡糖部分由至少22种二糖至四糖糖醇组成,如Gal-(1→4)-Rha-ol(主要成分)、Ara-(1→4)-Rha-ol、Glc-(1→4)-Rha-ol、Ara→Ara→Ara-ol和Ara→Ara→Ara→Ara-ol(次要成分)以及杂糖基糖醇。脱酯后,PG-2和PG-3再次用内切α-(1→4)-聚半乳糖醛酸酶消化,并纯化了耐酶的中等大小组分(PG-2')。组成糖分析表明,PG-2'除含有鼠李糖(Rha)、岩藻糖(Fuc)、阿拉伯糖(Ara)、木糖(Xyl)、甘露糖(Man)、半乳糖(Gal)、葡萄糖(Glc)、半乳糖醛酸(GalA)和葡萄糖醛酸(GlcA)外,还含有2-甲基岩藻糖(2-Me-Fuc)、2-甲基木糖(2-Me-Xyl)、芹糖(Api)、乙酰基丙酮酸(AceA)、3-脱氧-D-阿拉伯庚酮糖酸(Dha)和3-脱氧-D-甘露糖-2-辛酮糖酸(Kdo)。PG-2'的锂降解主要产生一个戊糖基→6-脱氧己糖基→6-脱氧己糖基→戊糖醇片段,以及一些中性二糖和三糖糖醇,包括一个戊糖基→脱氧己糖醇。对这些降解产物的甲基化分析表明,它们含有末端的Rha、Araf、Fuc、Xyl和Gal、4-连接的Rha、3-连接的Fuc、3-连接的Ara和3'-连接的Api。柴胡2IIc在Sepharose CL-6B凝胶过滤上基本上以单峰形式洗脱。连续馏分的中性糖含量随分子量增加而增加,但每个馏分除含有Rha、Ara和Gal外还含有2-Me-Fuc、2-Me-Xyl和Api。