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从一种与珊瑚相关的真菌中分离出的一种胞外多糖及其硫酸化衍生物可激活巨噬细胞。

An exopolysaccharide isolated from a coral-associated fungus and its sulfated derivative activates macrophages.

作者信息

Sun Kunlai, Chen Yin, Niu Qingfeng, Zhu Weiming, Wang Bin, Li Peipei, Ge Xuejun

机构信息

College of Food and Pharmacy, Zhejiang Ocean University, 1 South Haida Road, Zhoushan 316000, PR China; Zhejiang Provincial Engineering Technology Research Center of Marine Biomedical Products, 1 South Haida Road, Zhoushan 316000, PR China.

College of Food and Pharmacy, Zhejiang Ocean University, 1 South Haida Road, Zhoushan 316000, PR China.

出版信息

Int J Biol Macromol. 2016 Jan;82:387-94. doi: 10.1016/j.ijbiomac.2015.11.001. Epub 2015 Nov 4.

Abstract

A coral-associated fungus Penicillium sp.gxwz446 that produced exopolysaccharde was isolated from the coral Echinogorgia flora in South China. Two neutral exopolysaccharides GX1-1 and GX2-1 were obtained from the fermented broth of the fungus and purified by anion-exchange and gel-permeation chromatography. Chemical and spectroscopic analyses showed that GX1-1 was a glucan, primarily composed of glucose, with a molecular weight of 5.0 kDa. GX1-1 mainly consists of (1→4)-linked α-d-glucopyranose units as the backbone, substituted at C-2 with a single α-d-glucopyranose on every sixth sugar residues. GX2-1 was a galactofuranose-containing mannogalactoglucan with a molecular weight of 9.5 kDa. The main linkages were composed of (1→4)-β-d-Glcp, (1→5)-β-d-Galf, (1→3,5)-β-d-Galf, (1→6)-α-d-Manp and (1→2, 6)-α-d-Manp. GX1-1 showed RAW264.7 macrophage activation activity. After subjecting GX1-1 to sulfated modification, there was about one sulfate substitution on every sugar ring, primarily at O-6. The sulfated derivative of GX1-1 exhibited a more significant ability to promote the pinocytic activity of RAW264.7 cells and induce the production of NO.

摘要

从中国南方的刺柳珊瑚(Echinogorgia flora)中分离出一种产生胞外多糖的珊瑚相关真菌青霉属(Penicillium sp.)gxwz446。从该真菌的发酵液中获得了两种中性胞外多糖GX1-1和GX2-1,并通过阴离子交换和凝胶渗透色谱法进行了纯化。化学和光谱分析表明,GX1-1是一种葡聚糖,主要由葡萄糖组成,分子量为5.0 kDa。GX1-1主要由(1→4)连接的α-d-吡喃葡萄糖单元作为主链,每六个糖残基在C-2位被一个单一的α-d-吡喃葡萄糖取代。GX2-1是一种含半乳呋喃糖的甘露半乳葡聚糖,分子量为9.5 kDa。主要连接键由(1→4)-β-d-葡萄糖、(1→5)-β-d-半乳糖、(1→3,5)-β-d-半乳糖、(1→6)-α-d-甘露糖和(1→2,6)-α-d-甘露糖组成。GX1-1具有RAW264.7巨噬细胞激活活性。对GX1-1进行硫酸化修饰后,每个糖环上约有一个硫酸取代基,主要位于O-6位。GX1-1的硫酸化衍生物表现出更显著的促进RAW264.7细胞胞饮活性和诱导NO产生的能力。

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