Department of Marine Biology, Biology Institute, Fluminense Federal University, Niterói 24210-130, RJ, Brazil.
Mar Drugs. 2013 Nov 21;11(11):4628-40. doi: 10.3390/md11114628.
Total lipids from the Brazilian brown seaweed Sargassum vulgare were extracted with chloroform/methanol 2:1 and 1:2 (v/v) at room temperature. After performing Folch partition of the crude lipid extract, the lipids recovered from the Folch lower layer were fractionated on a silica gel column eluted with chloroform, acetone and methanol. The fraction eluted with methanol, presented a strong orcinol-positive band characteristic of the presence of sulfatides when examined by TLC. This fraction was then purified by two successive silica gel column chromatography giving rise to fractions F4I86 and F4II90 that exhibited strong activity against herpes simplex virus type 1 and 2. The chemical structures present in both fractions were elucidated by ESI-MS and ¹H/¹³C NMR analysis HSQC fingerprints based on their tandem-MS behavior as Sulfoquinovosyldiacylglycerols (SQDGs). The main SQDG present in both fractions and responsible for the anti-herpes activity observed was identified as 1,2-di-O-palmitoyl-3-O-(6-sulfo-α-D-quinovopyranosyl)-glycerol.
从巴西褐藻 Sargassum vulgare 中提取总脂质,使用氯仿/甲醇 2:1 和 1:2(v/v)在室温下进行。对粗脂质提取物进行 Folch 分区后,从 Folch 下层回收的脂质用硅胶柱层析,用氯仿、丙酮和甲醇洗脱。用甲醇洗脱的部分,当通过 TLC 检查时,呈现出强烈的间苯二酚阳性带,表明存在硫脂。该部分然后通过两次连续的硅胶柱层析进行纯化,得到 F4I86 和 F4II90 两个部分,它们对单纯疱疹病毒 1 和 2 表现出强烈的活性。通过 ESI-MS 和 ¹H/¹³C NMR 分析 HSQC 指纹图谱,基于它们的串联-MS 行为,阐明了两个部分中存在的化学结构,这些指纹图谱被鉴定为 1,2-二-O-棕榈酰基-3-O-(6-磺酸-α-D-奎诺吡喃糖基)-甘油。在两个部分中都存在的、负责观察到的抗疱疹活性的主要 SQDG 被鉴定为 1,2-二-O-棕榈酰基-3-O-(6-磺酸-α-D-奎诺吡喃糖基)-甘油。