Peng Kaitao, Zhang Yujie, Zhang Qi, Wang Yunpu, Liu Yuhuan, Cui Xian
State Key Laboratory of Food Science and Resources, Engineering Research Center for Biomass Conversion, Ministry of Education, Nanchang University, Nanchang 330047, China.
Chongqing Research Institute, Nanchang University, Chongqing 402660, China.
Foods. 2025 Jan 14;14(2):246. doi: 10.3390/foods14020246.
In order to overcome the bioavailability limitation of polysaccharide (LPS) caused by its high molecular weight and complex structure, two low-molecular-weight degraded polysaccharides, namely G-LPS(8) and G-LPS(16), were prepared through enzymatic degradation. The molecular weight of LPS was significantly reduced by enzymolysis, leading to increased exposure of internal functional groups and altering the molar ratio of its constituent monosaccharides. The results of antioxidant experiments showed that enzymatic hydrolysis had the potential to enhance the antioxidant performance of LPS. fermentation experiments revealed that LPS and its derivatives exerted different prebiotic effects on intestinal microbial communities. Specifically, LPS mainly inhibited the growth of harmful bacteria such as Fusobacterium, while G-LPS(8) and G-LPS(16) tended to promote the growth of beneficial bacteria like , , and . Metabolomic analysis revealed that LPSs with varying molecular weights exerted comparable promoting effects on multiple amino acid and carbohydrate metabolic pathways. Importantly, with the reduction in molecular weight, G-LPS(16) also particularly stimulated sphingolipid metabolism, nucleotide metabolism, as well as ascorbic acid and uronic acid metabolism, leading to the significant increase in specific metabolites such as sphingosine. Therefore, this study suggests that properly degraded LPS components have greater potential as a prebiotic for improving gut health.
为了克服多糖(LPS)因其高分子量和复杂结构而导致的生物利用度限制,通过酶解制备了两种低分子量的降解多糖,即G-LPS(8)和G-LPS(16)。酶解显著降低了LPS的分子量,导致内部官能团暴露增加,并改变了其组成单糖的摩尔比。抗氧化实验结果表明,酶解有增强LPS抗氧化性能的潜力。发酵实验表明,LPS及其衍生物对肠道微生物群落具有不同的益生元效应。具体而言,LPS主要抑制诸如梭杆菌等有害细菌的生长,而G-LPS(8)和G-LPS(16)则倾向于促进诸如[具体有益细菌名称1]、[具体有益细菌名称2]和[具体有益细菌名称3]等有益细菌的生长。代谢组学分析表明,不同分子量的LPS对多种氨基酸和碳水化合物代谢途径具有相当的促进作用。重要的是,随着分子量的降低,G-LPS(16)还特别刺激鞘脂代谢、核苷酸代谢以及抗坏血酸和糖醛酸代谢,导致鞘氨醇等特定代谢物显著增加。因此,本研究表明,适当降解的LPS成分作为改善肠道健康的益生元具有更大的潜力。