Reis Sofia F, Martins Vitor J, Bastos Rita, Lima Tânia, Correia Viviana G, Pinheiro Benedita A, Silva Lisete M, Palma Angelina S, Ferreira Paula, Vilanova Manuel, Coimbra Manuel A, Coelho Elisabete
REQUIMTE-LAQV, Department of Chemistry, University of Aveiro, 3810-193 Aveiro, Portugal.
I3S, Institute for Research in Innovation in Health, University of Porto, 4200-135 Porto, Portugal.
Foods. 2023 Jan 5;12(2):246. doi: 10.3390/foods12020246.
Brewer's spent yeast (BSY) microcapsules have a complex network of cell-wall polysaccharides that are induced by brewing when compared to the baker's yeast () microcapsules. These are rich in (β1→3)-glucans and covalently linked to (α1→4)- and (β1→4)-glucans in addition to residual mannoproteins. is often used as a drug delivery system due to its immunostimulatory potential conferred by the presence of (β1→3)-glucans. Similarly, BSY microcapsules could also be used in the encapsulation of compounds or drug delivery systems with the advantage of resisting digestion conferred by (β1→4)-glucans and promoting a broader immunomodulatory response. This work aims to study the feasibility of BSY microcapsules that are the result of alkali and subcritical water extraction processes, as oral carriers for food and biomedical applications by (1) evaluating the resistance of BSY microcapsules to in vitro digestion (IVD), (2) their recognition by the human Dectin-1 immune receptor after IVD, and (3) the recognition of IVD-solubilized material by different mammalian immune receptors. IVD digested 44-63% of the material, depending on the extraction process. The non-digested material, despite some visible agglutination and deformation of the microcapsules, preserved their spherical shape and was enriched in (β1→3)-glucans. These microcapsules were all recognized by the human Dectin-1 immune receptor. The digested material was differentially recognized by a variety of lectins of the immune system related to (β1→3)-glucans, glycogen, and mannans. These results show the potential of BSY microcapsules to be used as oral carriers for food and biomedical applications.
与面包酵母微胶囊相比,啤酒废酵母(BSY)微胶囊具有由酿造过程诱导产生的复杂细胞壁多糖网络。这些微胶囊富含(β1→3)-葡聚糖,除了残留的甘露糖蛋白外,还与(α1→4)-和(β1→4)-葡聚糖共价连接。由于其(β1→3)-葡聚糖赋予的免疫刺激潜力,面包酵母微胶囊常被用作药物递送系统。同样,BSY微胶囊也可用于化合物的包封或药物递送系统,其优势在于(β1→4)-葡聚糖赋予的抗消化性以及促进更广泛的免疫调节反应。本研究旨在探讨碱法和亚临界水提取工艺制备的BSY微胶囊作为食品和生物医学应用口服载体的可行性,具体包括:(1)评估BSY微胶囊对体外消化(IVD)的抗性;(2)IVD后其被人类Dectin-1免疫受体识别的情况;(3)不同哺乳动物免疫受体对IVD溶解物质的识别。根据提取工艺的不同,IVD消化了44%-63%的物质。未消化的物质,尽管微胶囊有一些明显的凝集和变形,但仍保持其球形,且富含(β1→3)-葡聚糖。这些微胶囊均被人类Dectin-1免疫受体识别。消化后的物质被与(β1→3)-葡聚糖、糖原和甘露聚糖相关的多种免疫系统凝集素不同程度地识别。这些结果表明BSY微胶囊有潜力用作食品和生物医学应用的口服载体。