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从灵芝未破壁孢子水提物中分离得到的具有生物活性的β-D-葡聚糖的结构与链构象。

Structure and chain conformation of bioactive β-D-glucan purified from water extracts of Ganoderma lucidum unbroken spores.

机构信息

Institute of Edible Fungi, Shanghai Academy of Agricultural Sciences, Key Laboratory of Edible Fungi Resources and Utilization (South), Ministry of Agriculture, National Engineering Research Center of Edible Fungi, National R&D Center for Edible Fungi Processing, Shanghai 201403, China.

Institute of Edible Fungi, Shanghai Academy of Agricultural Sciences, Key Laboratory of Edible Fungi Resources and Utilization (South), Ministry of Agriculture, National Engineering Research Center of Edible Fungi, National R&D Center for Edible Fungi Processing, Shanghai 201403, China.

出版信息

Int J Biol Macromol. 2021 Jun 1;180:484-493. doi: 10.1016/j.ijbiomac.2021.03.003. Epub 2021 Mar 6.

Abstract

Two polysaccharide fractions (GLSB50 and GLSB70) with total sugar content of 82.07 wt% and 53.79 wt%, respectively, were obtained from the water extracts of unbroken Ganoderma lucidum spores by sequential ethanol precipitation treatment. Compared with GLSB70, GLSB50 exhibited better activity on stimulation of humoral immune responses in immunosuppressed mice. A novel β-D-glucan (GLSB50A-III-1) with weight average molecular weight (M) of 1.93 × 10 g/mol was purified from GLSB50 through chromatography separation. The exponent α value of Mark-Houwink-Sakurada equation was calculated to be 0.13, indicating that GLSB50A-III-1 presented globular spheres conformation in aqueous solution. Structural analysis showed that GLSB50A-III-1 mainly consisted of (1 → 3), (1 → 4), (1 → 6)-linked β-d-glucose residues in the backbone, with two single β-D-Glcp attached at O-6 of β-(1 → 3) and β-(1 → 4)-linked residues separately as side chains. The repeat unit of GLSB50A-III-1 was deduced as follows.

摘要

两种多糖级分(GLSB50 和 GLSB70)的总糖含量分别为 82.07wt%和 53.79wt%,从完整的灵芝孢子水提取物中通过顺序乙醇沉淀处理获得。与 GLSB70 相比,GLSB50 对免疫抑制小鼠体液免疫反应的刺激具有更好的活性。通过色谱分离从 GLSB50 中纯化出一种新型β-D-葡聚糖(GLSB50A-III-1),其重均分子量(M)为 1.93×10g/mol。Mark-Houwink-Sakurada 方程的指数α值计算为 0.13,表明 GLSB50A-III-1 在水溶液中呈现球状构象。结构分析表明,GLSB50A-III-1 主要由(1→3)、(1→4)、(1→6)-连接的β-d-葡萄糖残基构成主链,在β-(1→3)和β-(1→4)-连接的残基的 O-6 上分别有两个单β-D-Glcp 作为侧链。GLSB50A-III-1 的重复单元推断如下。

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