Huang Yan-Yan, Wu Jia-Min, Wu Wei-Tong, Lin Jia-Wei, Liang Yan-Tong, Hong Zhen-Zhen, Jia Xiang-Ze, Liu Dong-Mei
College of Food Science and Engineering, Foshan University, Foshan, Guangdong, China.
Guangdong Provincial Key Laboratory of Intelligent Food Manufacturing, Foshan University, Foshan, Guangdong, China.
Front Nutr. 2022 Dec 8;9:1073071. doi: 10.3389/fnut.2022.1073071. eCollection 2022.
This study investigated the structural, antioxidant, and immunomodulatory activities of acidic exopolysaccharide (EPS-LP2) isolated from DMDL 9010. EPS-LP2 is composed of fucose (Fuc), arabinose (Ara), galactose (Gal), glucose (Glc), mannose (Man), and D-fructose (Fru) with a molar ratio of 0.13: 0.69: 8.32: 27.57: 62.07: 0.58: 0.46, respectively. Structural analysis of EPS-LP2 exhibited a smooth irregular lamellar surface, rod-like structure with swollen ends and slippery surfaces, and good thermal stability. Based on the methylation and NMR analysis, sugar residues including t-Man, t-Glc, 2-Man, 6-Gal, 6-Glc, and 4-Glc were found to exist in EPS-LP2. In the 50∼400 μg/ml range, EPS-LP2 showed negligible neurotoxicity to RAW264.7 cells. Moreover, EPS-LP2 could protect RAW264.7 cells from oxidative injury by lowering the generation of reactive oxygen species (ROS), malondialdehyde (MDA), and the secretion of lactate dehydrogenase (LDH). In contrast, an increase in superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GSH-Px), and the concentrations of glutathione (GSH) were observed. Immunoreactivity assays showed that EPS-LP2 could suppress the expression of NO, tumor necrosis factor-α (TNF-α), and interleukin 6 (IL-6) and inhibit the activation of the mitogen-activated protein kinase (MAPK)/nuclear factor-κB-gene binding (NF-κB) cell pathway. Conclusively, EPS-LP2 could be a potential natural antioxidant and immunomodulatory agent in functional foods and medicines.
本研究调查了从DMDL 9010中分离出的酸性胞外多糖(EPS-LP2)的结构、抗氧化和免疫调节活性。EPS-LP2由岩藻糖(Fuc)、阿拉伯糖(Ara)、半乳糖(Gal)、葡萄糖(Glc)、甘露糖(Man)和D-果糖(Fru)组成,其摩尔比分别为0.13:0.69:8.32:27.57:62.07:0.58:0.46。EPS-LP2的结构分析显示其表面光滑不规则呈层状,为两端肿胀且表面光滑的棒状结构,具有良好的热稳定性。基于甲基化和核磁共振分析,发现EPS-LP2中存在包括t-Man、t-Glc、2-Man、6-Gal、6-Glc和4-Glc在内的糖残基。在50∼400μg/ml范围内,EPS-LP2对RAW264.7细胞显示出可忽略不计的神经毒性。此外,EPS-LP2可通过降低活性氧(ROS)、丙二醛(MDA)的生成以及乳酸脱氢酶(LDH)的分泌来保护RAW264.7细胞免受氧化损伤。相反,观察到超氧化物歧化酶(SOD)、过氧化氢酶(CAT)、谷胱甘肽过氧化物酶(GSH-Px)以及谷胱甘肽(GSH)浓度增加。免疫反应性测定表明,EPS-LP2可抑制一氧化氮(NO)、肿瘤坏死因子-α(TNF-α)和白细胞介素6(IL-6)的表达,并抑制丝裂原活化蛋白激酶(MAPK)/核因子-κB基因结合(NF-κB)细胞途径的激活。总之,EPS-LP2可能是功能性食品和药品中一种潜在的天然抗氧化剂和免疫调节剂。