4.7 Article

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

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JOURNAL OF NATURAL PRODUCTS
卷 68, 期 7, 页码 1037-1041

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AMER CHEMICAL SOC
DOI: 10.1021/np050056c

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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)-]- -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.

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