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首页> 外文期刊>Journal of Microencapsulation: Microcapsules Liposomes Nanoparticles Microcells Microspheres >Microentrapment of probiotic bacteria in a Ca~(2+) -induced whey protein gel and effects on their viability in a dynamic gastro-intestinal model
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Microentrapment of probiotic bacteria in a Ca~(2+) -induced whey protein gel and effects on their viability in a dynamic gastro-intestinal model

机译:Ca〜(2+)诱导的乳清蛋白凝胶中益生菌的微包埋及其对动态胃肠道模型生存力的影响

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Entrapping probiotic bacteria in gels with ionic cross-linking is typically achieved with polysaccharides (alginate,pectin,carraghenan).In this study,whey proteins were used for this purpose by carrying out the Ca~(2+)-induced gelation of pre-heated whey protein isolate (WPI).A Lactobacillus rhamnosus cell suspension was added in a denatured WPI solution in a 30:70 volume ratio.Gelation was carried out by extrusion of the cell suspension in a CaCl_2 solution.Beads of approx 3 mm diameter were formed.The population in the beads was 8.0 x 10~8 cells g~(-1).Entrapment efficiency in gel beads was 96%,with a survival level of 23%.Scanning electron microscopy of beads before freeze-drying showed a tight protein network containing encapsulated Lb.rhamnosus cells homogeneously distributed throughout the matrix.The survival to freeze-drying of the bead-entrapped cells was 41%.Viability of micro-entrapped cells in a dynamic gastro-intestinal (GI) model was studied and the results were compared to free cells freeze-dried in a milk-based cryoprotective solution,as well as in a pre-denatured WPI solution.Results showed that protein gelation provided protection against acidic conditions in the stomach after 90 min,as well as against bile after 30,60 and 90 min in the duodenum.Moreover,the milk-based cryoprotective solution was equally effective after 90 min in the duodenum.It is concluded that the gelation of whey proteins induced by Ca~(2+) ions can protect the cells against adverse conditions of the GI system.However,certain stages in the entrapment process,particularly extrusion in the solution of CaCl_2,still need to be optimized in order to reduce the mortality of the cells during gelation.
机译:通常通过多糖(藻酸盐,果胶,角叉菜胶)将益生菌通过离子交联截留在凝胶中。在这项研究中,为什么使用蛋白质通过Ca〜(2+)诱导的预凝胶化而用于此目的。将鼠李糖乳杆菌细胞悬液以30:70的体积比添加到变性WPI溶液中,通过将细胞悬液在CaCl_2溶液中挤出进行凝胶化,形成直径约3 mm的珠凝胶珠的包埋率为96%,存活率为23%。冻干前的扫描电镜显示紧密包被的鼠李糖单胞菌细胞的蛋白质网络均匀地分布在整个基质中。包被珠子的细胞的冻干存活率为41%。研究了微包被的细胞在动态胃肠(GI)模型中的生存​​力并结果进行比较o在基于牛奶的冷冻保护溶液以及预先变性的WPI溶液中冷冻干燥的游离细胞。结果表明,蛋白质凝胶化可以在90分钟后防止胃中的酸性条件,在30分钟后防止胆汁中的酸性,在十二指肠分别为60和90分钟。此外,乳基冷冻保护溶液在十二指肠中同样有效。结论是Ca〜(2+)离子诱导的乳清蛋白凝胶化可以保护细胞免受不良影响然而,仍然需要优化包封过程的某些阶段,尤其是在CaCl_2溶液中的挤出,以降低胶凝过程中细胞的死亡率。

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