Ponce Nora M A, Pujol Carlos A, Damonte Elsa B, Flores María L, Stortz Carlos A
Departamento de Química Orgánica-CIHIDECAR, Facultad de Ciencias Exactas y Naturales, Univ. Buenos Aires, Pab.2 Ciudad Universitaria, 1428 Buenos Aires, Argentina.
Carbohydr Res. 2003 Jan 20;338(2):153-65. doi: 10.1016/s0008-6215(02)00403-2.
The brown seaweed Adenocystis utricularis (family Adenocystaceae, order Ectocarpales sensu lato) was extracted in parallel with three solvents usually utilized for obtaining fucoidans: distilled water, 2% calcium chloride solution and diluted hydrochloric acid (pH 2) solution. In each case, the extraction was effected at room temperature and then at 70 degrees C. The extraction yields and characteristics of the products were similar in the three cases, with only minor differences. The analytical features of the products indicate that two different types of fucoidans are present in this seaweed. One of them, mostly extracted at room temperature, is composed mainly of L-fucose, D-galactose and ester sulfate (the 'galactofucan'). The other product (the 'uronofucoidan') is the major component of the extracts obtained at 70 degrees C. It is composed mainly of fucose, accompanied by other monosaccharides (mostly Man, but also Glc, Xyl, Rha and Gal), significant amounts of uronic acids and low proportions of sulfate ester. Fractionation with the cationic detergent cetrimide has allowed achieving a better separation of the galactofucan and uronofucoidan components. The galactofucans show a high inhibitory activity against herpes simplex virus 1 and 2, with no cytotoxicity, whereas the uronofucoidans carry no antiviral activity. Structural studies on the galactofucan fractions were carried out by methylation analysis, desulfation and NMR spectroscopy. The fucan constituent is mainly composed of 3-linked alpha-L-fucopyranosyl backbone, mostly sulfated at C-4, and branched at C-2 with non-sulfated fucofuranosyl and fucopyranosyl units, and 2-sulfated fucopyranosyl units. The galactan moiety is more heterogeneous, with predominant D-galactopyranose units linked on C-3 and C-6, and sulfation mostly on C-4, even in terminal non-reducing units. It may be inferred that at least some of these galactose units carry the alpha-configuration.
棕色海藻腺囊藻(腺囊藻科,广义的网地藻目)与通常用于提取岩藻聚糖的三种溶剂同时进行提取:蒸馏水、2%氯化钙溶液和稀盐酸(pH 2)溶液。在每种情况下,提取均在室温下进行,然后在70℃下进行。三种情况下提取物的产率和特性相似,只有细微差异。产物的分析特征表明,这种海藻中存在两种不同类型的岩藻聚糖。其中一种主要在室温下提取,主要由L-岩藻糖、D-半乳糖和硫酸酯(“半乳岩藻聚糖”)组成。另一种产物(“糖醛岩藻聚糖”)是在70℃下获得的提取物的主要成分。它主要由岩藻糖组成,伴有其他单糖(主要是甘露糖,但也有葡萄糖、木糖、鼠李糖和半乳糖)、大量糖醛酸和低比例的硫酸酯。用阳离子去污剂十六烷基三甲基溴化铵进行分级分离,可以更好地分离半乳岩藻聚糖和糖醛岩藻聚糖成分。半乳岩藻聚糖对单纯疱疹病毒1和2表现出高抑制活性,且无细胞毒性,而糖醛岩藻聚糖则无抗病毒活性。通过甲基化分析、脱硫酸和核磁共振光谱对半乳岩藻聚糖级分进行了结构研究。岩藻聚糖成分主要由3-连接的α-L-岩藻吡喃糖基主链组成,大部分在C-4位硫酸化,并在C-2位带有非硫酸化的岩藻呋喃糖基和岩藻吡喃糖基单元,以及2-硫酸化的岩藻吡喃糖基单元。半乳聚糖部分更加不均一,主要的D-半乳吡喃糖单元连接在C-3和C-6位,硫酸化主要在C-4位,即使在末端非还原单元也是如此。可以推断,这些半乳糖单元中至少有一些具有α-构型。