FoodPRINT International Associated Laboratory INRAE, School of Chemical and Environmental Engineering, College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou, Jiangsu 215123, China.
Food Funct. 2021 Apr 7;12(7):2995-3008. doi: 10.1039/d0fo02906h. Epub 2021 Mar 11.
Protective agents used in spray drying protect the activity of lactic acid bacteria (LAB) by stabilizing the subcellular structures, constituting a protective layer at the cellular surface, or having mild drying kinetics. The effects of a reputed protectant, whey protein isolate (WPI), on Lactobacillus rhamnosus GG (LGG) were examined by exposing the cells to WPI solution to induce protein adsorption at the cellular surface prior to spray drying. WPI-treated LGG demonstrated enhanced thermotolerance with cell survival increased by 1.64 log after heat treatment. The survival after spray drying was significantly decreased from 45.75% to 8.6% and from 32.96% to 10.44%, when the WPI-treated cells were resuspended in trehalose solution or reconstituted skimmed milk as protectant, respectively, associated with decreased growth capability and metabolic activity. The contact with WPI appeared to stimulate the cellular response of LGG. With well-maintained cell viability and intact cellular membrane, the metabolic activity of WPI-treated LGG was decreased, and subsequent resuspension of the cells in trehalose solution led to a reduction in the stability of the cellular surface charge. The WPI-treated cells showed marginally increased surface roughness, indicating possible WPI attachment, but there was no thick protein coverage at the cellular surface and the size distribution of cells was unaffected. It was proposed that the enhanced thermotolerance and the decreased survival of spray-dried LGG could be linked to the cellular response toward WPI and protectant media, which may vary among individual LAB strains. Modulating the strain-specific interactions between the LAB cells and the protectant constituents could be crucial to maximizing cell viability retention after spray drying.
喷雾干燥中使用的保护剂通过稳定亚细胞结构、在细胞表面形成保护层或具有温和的干燥动力学来保护乳酸菌 (LAB) 的活性。通过在喷雾干燥前将细胞暴露于乳清蛋白分离物 (WPI) 溶液中以诱导细胞表面的蛋白质吸附,研究了一种受好评的保护剂乳清蛋白分离物 (WPI) 对鼠李糖乳杆菌 GG (LGG) 的影响。WPI 处理的 LGG 表现出增强的耐热性,经过热处理后细胞存活率增加了 1.64 log。当 WPI 处理的细胞分别悬浮在海藻糖溶液或还原脱脂乳中作为保护剂时,喷雾干燥后的存活率从 45.75%显著降低到 8.6%和 32.96%至 10.44%,与生长能力和代谢活性下降相关。与 WPI 的接触似乎刺激了 LGG 的细胞反应。WPI 处理的 LGG 保持良好的细胞活力和完整的细胞膜,其代谢活性降低,随后将细胞悬浮在海藻糖溶液中会降低细胞表面电荷的稳定性。WPI 处理的细胞表面粗糙度略有增加,表明可能存在 WPI 附着,但细胞表面没有厚的蛋白质覆盖,细胞的大小分布不受影响。据推测,喷雾干燥的 LGG 增强的耐热性和存活率降低可能与细胞对 WPI 和保护剂介质的反应有关,而这种反应可能因单个 LAB 菌株而异。调节 LAB 细胞与保护剂成分之间的特定于菌株的相互作用对于最大限度地保留喷雾干燥后的细胞活力至关重要。