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酶辅助提取对荷叶多糖的理化性质和生物活性的影响。

Effect of enzyme-assisted extraction on the physicochemical properties and bioactive potential of lotus leaf polysaccharides.

机构信息

Korea Food Research Institute, Wanju-gun, Jeollabuk-do 55365, Republic of Korea.

Korea Food Research Institute, Wanju-gun, Jeollabuk-do 55365, Republic of Korea.

出版信息

Int J Biol Macromol. 2020 Jun 15;153:169-179. doi: 10.1016/j.ijbiomac.2020.02.252. Epub 2020 Feb 24.

Abstract

Lotus leaf polysaccharides were extracted by enzyme-assisted extraction using α-amylase (LLEP-A), cellulose (LLEP-C), pectinase (LLEP-P) or protease (LLEP-PR). Their physicochemical properties and immunostimulatory activities were compared with those of hot-water extracted polysaccharides (LLWP). HPAEC-PDA and HPSEC-RI profiles indicated that variations in their molecular weight patterns and chemical compositions. Moreover, their effects on proliferation, phagocytic activity, and cytokine production in macrophages could be ordered as LLEP-P > LLEP-C > LLEP-A > LLWP > LLEP-PR, suggesting that LLEP-P by pectinase-assisted extraction was the most potent enhancer of macrophage activation. LLEP-P was further purified by gel filtration, and the main fraction (LLEP-P-І) was obtained to elucidate the structural and functional properties. LLEP-P-І (14.63 × 10 g/mol) mainly consisted of rhamnose, arabinose, galactose, and galacturonic acid at molar percentages of 15.5:15.8:20.1:32.8. FT-IR spectra indicated the predominant acidic and esterified form, suggesting the pectic-like structure. Above all, LLEP-P-І exerted greater stimulation effects on NO and cytokines production and the phagocytic activity in macrophages. Transcriptome analysis also demonstrated that LLEP-P and LLEP-P-І could upregulate macrophage immune response genes, including cytokines, chemokines, and interferon via TLR and JAK-STAT signaling. Thus, these results suggest that pectinase application is most suitable to obtain immunostimulatory polysaccharides from lotus leaves.

摘要

采用α-淀粉酶(LLEP-A)、纤维素酶(LLEP-C)、果胶酶(LLEP-P)或蛋白酶(LLEP-PR)辅助酶解提取荷叶多糖。将其理化性质和免疫刺激活性与热水提取的多糖(LLWP)进行比较。HPAEC-PDA 和 HPSEC-RI 图谱表明,它们的分子量分布和化学成分存在差异。此外,它们对巨噬细胞增殖、吞噬活性和细胞因子产生的影响可以排序为 LLEP-P > LLEP-C > LLEP-A > LLWP > LLEP-PR,表明果胶酶辅助提取的 LLEP-P 是最有效的巨噬细胞激活增强剂。进一步通过凝胶过滤对 LLEP-P 进行纯化,得到主要级分(LLEP-P-І),以阐明其结构和功能特性。LLEP-P-І(14.63×10⁴g/mol)主要由鼠李糖、阿拉伯糖、半乳糖和半乳糖醛酸组成,摩尔百分比为 15.5:15.8:20.1:32.8。FT-IR 光谱表明其主要为酸性和酯化形式,提示其具有果胶样结构。总之,LLEP-P-І 对巨噬细胞 NO 和细胞因子产生及吞噬活性的刺激作用更强。转录组分析还表明,LLEP-P 和 LLEP-P-І 可通过 TLR 和 JAK-STAT 信号通路上调巨噬细胞免疫应答基因,包括细胞因子、趋化因子和干扰素。因此,这些结果表明,果胶酶的应用最适合从荷叶中获得免疫刺激多糖。

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