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从 sp. 中分离、纯化、结构表征新型胞外多糖及其抗癌活性

Separation, Purification, Structural Characterization, and Anticancer Activity of a Novel Exopolysaccharide from sp.

机构信息

Drug Research & Development Center, School of Pharmacy, Wannan Medical College, Wuhu 241002, China.

Anhui Provincial Engineering Research Center for Polysaccharide Drugs, Provincial Engineering Laboratory for Screening and Re-Evaluation of Active Compounds of Herbal Medicines in Southern Anhui, Wuhu 241002, China.

出版信息

Molecules. 2022 Mar 23;27(7):2071. doi: 10.3390/molecules27072071.

Abstract

sp. has a wide range of applications in the food fermentation industry. In this study, a novel exopolysaccharide, labeled MSEPS, was separated from sp. fermentation broth through ethanol precipitation and was purified by ion-exchange chromatography, as well as gel filtration column chromatography. MSEPS was composed mostly of mannose, galactose, fucose, arabinose, and glucose with a molar ratio of 0.466:0.169:0.139:0.126:0.015 and had a molecular weight of 7.78 × 10 Da. The analysis of methylation and nuclear magnetic resonance results indicated that MSEPS mainly consisted of a backbone of →3,6)-α-d-Man-(1→3,6)-β-d-Gal-(1→, with substitution at O-3 of →6)-α-d-Man-(1→ and →6)-β-d-Gal-(1→ by terminal α-l-Ara residues. MTT assays showed that MSEPS was nontoxic in normal cells (HK-2 cells) and inhibited the proliferation of carcinoma cells (SGC-7901 cells). Additionally, morphological analysis and flow cytometry experiments indicated that MSEPS promoted SGC-7901 cell death via apoptosis. Therefore, MSEPS from sp. can be developed as a potential antitumor agent.

摘要

sp. 在食品发酵工业中有广泛的应用。在本研究中,通过乙醇沉淀从 sp. 发酵液中分离出一种新型胞外多糖,命名为 MSEPS,并通过离子交换色谱和凝胶过滤柱色谱进行纯化。MSEPS 主要由甘露糖、半乳糖、岩藻糖、阿拉伯糖和葡萄糖组成,摩尔比为 0.466:0.169:0.139:0.126:0.015,分子量为 7.78 × 10 Da。甲基化和核磁共振分析结果表明,MSEPS 主要由→3,6)-α-d-Man-(1→3,6)-β-d-Gal-(1→构成的主链组成,在→6)-α-d-Man-(1→和→6)-β-d-Gal-(1→的 O-3 位被末端α-l-Ara 残基取代。MTT 法测定结果表明,MSEPS 在正常细胞(HK-2 细胞)中无毒性,并抑制癌细胞(SGC-7901 细胞)的增殖。此外,形态分析和流式细胞术实验表明,MSEPS 通过细胞凋亡促进 SGC-7901 细胞死亡。因此, sp. 产生的 MSEPS 可以开发为一种潜在的抗肿瘤药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/43f7/9000282/57ea2c756cf4/molecules-27-02071-g001.jpg

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