Sun Kunlai, Chen Yin, Niu Qingfeng, Zhu Weiming, Wang Bin, Li Peipei, Ge Xuejun
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.
Int J Biol Macromol. 2016 Jan;82:387-94. doi: 10.1016/j.ijbiomac.2015.11.001. Epub 2015 Nov 4.
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.
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。