University of Münster, Institute of Pharmaceutical Biology and Phytochemistry, Corrensstrasse 48, D-48149 Münster, Germany.
University of Münster, Institute for Hygiene, Robert-Koch-Strasse 41, D-48149 Münster, Germany.
Int J Biol Macromol. 2019 Aug 1;134:921-935. doi: 10.1016/j.ijbiomac.2019.05.056. Epub 2019 May 9.
Hot-water soluble polysaccharides H-1-3 and H-2-1 were isolated from the thalli of the lichen Xanthoria parietina (L.) Th. Fr. and purified by ion exchange and gel permeation chromatography. Structure elucidation was mainly based on 2D-NMR and nano-ESI-Q-TOF MS/MS experiments. H-1-3 (13.7 kDa) was shown to be linear α-glucan with α-d-Glcp-(1 → [→[4)-α-d-Glcp-(1] → [6)-α-d-Glcp-(1] → 4)] core backbone. The (1,4)- and (1,6)-α-d-Glcp linkages were in a 2:3 M ratio. H-2-1 (525 kDa) was characterized as a complex branched β-galacto-α-mannan with →[6)-α-d-Manp-(1 → [2,6)-α-d-Manp-(1] → [2)-α-d-Manp-(1]→] core units and main side chains of (1,3)-β-d-Galf linked at O-6 to →2)-α-d-Manp-(1→, together with minor terminal units of 1,4/1,6-α-D -Glcp units attached to the core chain at O-6 position and α-L-Rhap linked to Galf side chain at O-2 position (Manp: Galf: Glcp: Rhap linkage ratio = 9:3:2:1). H-2-1 exerted strong immunoactivity in vitro and activated murine RAW macrophages 264.7 towards significantly increased phagocytosis, TNF-α and IL-1β secretion. These effects are due to an interaction of the galactomannan with the transmembrane pattern-recognition protein Dectin-2 of the macrophages.
热水溶性多糖 H-1-3 和 H-2-1 从地衣 Xanthoria parietina(L.)Th. Fr. 的藻体中分离出来,并通过离子交换和凝胶渗透色谱进行纯化。结构阐明主要基于 2D-NMR 和纳升电喷雾四极杆飞行时间质谱/质谱(nano-ESI-Q-TOF MS/MS)实验。H-1-3(13.7 kDa)被证明是线性α-葡聚糖,具有α-d-Glcp-(1→[→[4)-α-d-Glcp-(1]→[6)-α-d-Glcp-(1]→4)]核心骨架。(1,4)-和(1,6)-α-d-Glcp 键的比例为 2:3 M。H-2-1(525 kDa)被鉴定为复杂分支β-半乳糖-α-甘露聚糖,具有→[6)-α-d-Manp-(1→[2,6)-α-d-Manp-(1]→[2)-α-d-Manp-(1]→]核心单元和主要侧链(1,3)-β-d-Galf 通过 O-6 连接至→2)-α-d-Manp-(1→,与核心链 O-6 位置上的 1,4/1,6-α-D-Glcp 单元的少量末端单元以及连接至 Galf 侧链 O-2 位置的α-L-Rhap 单元一起。(Manp:Galf:Glcp:Rhap 键比=9:3:2:1)。H-2-1 在体外具有很强的免疫活性,可激活小鼠 RAW 巨噬细胞 264.7,使其吞噬作用、TNF-α 和 IL-1β 分泌显著增加。这些作用是由于半乳甘露聚糖与巨噬细胞的跨膜模式识别蛋白 Dectin-2 相互作用所致。