Faculty of Fisheries Sciences, Hokkaido University, Hakodate 041-8611, Japan.
Department of Food Science and Technology, Tokyo University of Marine Science and Technology, Tokyo 108-8477, Japan.
Mar Drugs. 2023 Apr 28;21(5):276. doi: 10.3390/md21050276.
A separation process was established to sequentially fractionate and recover three anti-inflammatory components derived from sugars, phycobiliprotein, and chlorophyll from the hot-air-dried thalli of the red alga dulse (). The developed process consisted of three steps, without the use of organic solvents. In Step I, the sugars were separated by disrupting the cell wall of the dried thalli with a polysaccharide-degrading enzyme, and a sugar-rich extract (E1) was obtained by precipitating the other components, which were simultaneously eluted by acid precipitation. In Step II, the residue suspension from Step I was digested with thermolysin to obtain phycobiliprotein-derived peptides (PPs), and a PP-rich extract (E2) was obtained by separating the other extracts using acid precipitation. In Step III, solubilized chlorophyll was obtained by heating the residue, which was acid-precipitated, neutralized, and re-dissolved to concentrate the chlorophyll-related components (Chls)-rich extract (E3). These three extracts suppressed inflammatory-cytokine secretion by lipopolysaccharide (LPS)-stimulated macrophages, confirming that the sequential procedure had no negative effects on the activities of any of the extracts. The E1, E2, and E3 were rich in sugars, PPs, and Chls, respectively, indicating that the anti-inflammatory components were effectively fractionated and recovered through the separation protocol.
建立了一种分离工艺,可顺序分级并从红藻巨藻的热空气干燥藻体中回收三种源自糖、藻蓝蛋白和叶绿素的抗炎成分()。所开发的工艺由三个步骤组成,不使用有机溶剂。在步骤 I 中,通过用多糖降解酶破坏干燥藻体的细胞壁来分离糖,并且通过酸沉淀同时洗脱其他成分来获得富含糖的提取物 (E1)。在步骤 II 中,用胰凝乳蛋白酶消化来自步骤 I 的残渣悬浮液以获得藻蓝蛋白衍生肽 (PP),并通过酸沉淀分离其他提取物获得富含 PP 的提取物 (E2)。在步骤 III 中,通过加热酸沉淀、中和和重新溶解来获得可溶的叶绿素,以浓缩与叶绿素相关的成分 (Chls)-富含提取物 (E3)。这三种提取物抑制了脂多糖 (LPS)刺激的巨噬细胞中炎症细胞因子的分泌,证实顺序程序对任何提取物的活性都没有负面影响。E1、E2 和 E3 分别富含糖、PP 和 Chls,表明通过分离方案有效地分级和回收了抗炎成分。