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从陆生蓝细菌发状念珠藻中分离出一种抗病毒多糖——念珠藻聚糖。

Isolation of an antiviral polysaccharide, nostoflan, from a terrestrial cyanobacterium, Nostoc flagelliforme.

作者信息

Kanekiyo Kenji, Lee Jung-Bum, Hayashi Kyoko, Takenaka Hiroyuki, Hayakawa Yumiko, Endo Shunro, Hayashi Toshimitsu

机构信息

Faculty of Pharmaceutical Sciences, Toyama Medical and Pharmaceutical University, 2630 Sugitani, Toyama 930-0194, Japan.

出版信息

J Nat Prod. 2005 Jul;68(7):1037-41. doi: 10.1021/np050056c.

Abstract

A novel acidic polysaccharide, nostoflan, was isolated from a terrestrial cyanobacterium, Nostoc flagelliforme. Nostoflan exhibited a potent anti-herpes simplex virus type 1 (HSV-1) activity with a selectivity index (50% cytotoxic concentration/50% inhibitory concentration against viral replication) of 13,000. Sugar composition and methylation analyses revealed that it was mainly composed of -->4)-D-Glcp-(1-->, -->6,4)-D-Glcp-(1-->, -->4)-D-Galp-(1-->, -->4)-D-Xylp-(1-->, D-GlcAp-(1-->, D-Manp-(1--> with a ratio of ca. 1:1:1:1:0.8:0.2. Two pyridylaminated oligosaccharides were prepared by partial acid hydrolysis and pyridylamination. On the basis of MALDI-TOF-MS and NMR analyses, they were found to be beta-D-Glcp-(1-->4)-D-Xyl-PA and beta-D-GlcAp-(1-->6)-beta-D-Glcp-(1-->4)-D-Gal-PA. From these results, nostoflan might be mainly composed of the following two types of sugar sequence: -->4)-beta-D-Glcp-(1-->4)-D-Xylp-(1--> and -->4)-[beta-D-GlcAp-(1-->6)-]-beta-D-Glcp-(1-->4)-D-Galp-(1-->. Besides anti-HSV-1 activity, nostoflan showed potent antiviral activities against HSV-2, human cytomegalovirus, and influenza A virus, but no activity against adenovirus and coxsackie virus was observed. Therefore, nostoflan has a broad antiviral spectrum against enveloped viruses whose cellular receptors are carbohydrates. Furthermore, nostoflan showed no antithrombin activity, unlike sulfated polysaccharides.

摘要

从陆生蓝藻发状念珠藻中分离出一种新型酸性多糖——念珠藻聚糖。念珠藻聚糖表现出强大的抗1型单纯疱疹病毒(HSV-1)活性,其选择性指数(细胞毒性浓度的50%/病毒复制抑制浓度的50%)为13000。糖组成和甲基化分析表明,它主要由→4)-D-葡萄糖-(1→、→6,4)-D-葡萄糖-(1→、→4)-D-半乳糖-(1→、→4)-D-木糖-(1→、D-葡萄糖醛酸-(1→、D-甘露糖-(1→组成,比例约为1:1:1:1:0.8:0.2。通过部分酸水解和吡啶胺化制备了两种吡啶胺化寡糖。基于基质辅助激光解吸电离飞行时间质谱(MALDI-TOF-MS)和核磁共振(NMR)分析,发现它们是β-D-葡萄糖-(1→4)-D-木糖-PA和β-D-葡萄糖醛酸-(1→6)-β-D-葡萄糖-(1→4)-D-半乳糖-PA。根据这些结果,念珠藻聚糖可能主要由以下两种糖序列组成:→4)-β-D-葡萄糖-(1→4)-D-木糖-(1→和→4)-[β-D-葡萄糖醛酸-(1→6)-]-β-D-葡萄糖-(1→4)-D-半乳糖-(1→。除了抗HSV-1活性外,念珠藻聚糖还对HSV-2、人巨细胞病毒和甲型流感病毒表现出强大的抗病毒活性,但未观察到对腺病毒和柯萨奇病毒的活性。因此,念珠藻聚糖对细胞受体为碳水化合物的包膜病毒具有广泛的抗病毒谱。此外,与硫酸化多糖不同,念珠藻聚糖没有抗凝血酶活性。

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