Role of milk and honey in the tolerance of lactobacilli to oxidative stress

鼠李糖乳杆菌 益生菌 食品科学 嗜酸乳杆菌 氧化应激 脂质过氧化 过氧化氢 化学 副干酪乳杆菌 脱脂牛奶 动物双歧杆菌 人口 生物 微生物学 乳酸菌 生物化学 双歧杆菌 细菌 医学 发酵 环境卫生 遗传学
作者
Vanessa Moraes Ramalho Castro,Mariane da Mota Silva,Edlene Ribeiro Prudêncio de Souza,André Fioravante Guerra,Cristiano Jorge Riger,Roberto Laureano‐Melo,Rosa Helena Luchese
出处
期刊:Brazilian Journal of Microbiology [Springer Nature]
卷期号:52 (2): 883-893 被引量:7
标识
DOI:10.1007/s42770-021-00424-3
摘要

In the development of functional probiotic food, the carrier matrices should be carefully selected and optimized to ensure the highest levels of probiotic survival in the symbiotic food along storage. Because milk and honey food matrices are rich in antioxidant substances, the aim of the research was to evaluate their effect in protecting lactobacilli from reactive oxygen species (ROS) generated by the addition of hydrogen peroxide. Viability assays were performed with and without the addition of H2O2, in three different matrices: 0.9% peptone saline, 5% honey, or 12% reconstituted skim milk. The milk matrix provided protection for the Lacticaseibacillus paracasei DTA83 and Lacticaseibacillus rhamnosus DTA76. However, this protective effect was not observed in the survival of Lactobacillus acidophilus La 5. Honey solution did not maintain the viability of probiotic microorganisms exposed to hydrogen peroxide and, on the contrary, caused a significant reduction in the population of L. rhamnosus DTA76 (p < 0.001). Lower membrane lipid peroxidation due to H2O2 exposure was observed in L. acidophilus La 5 and L. rhamnosus DTA76, but this marker showed no relation with viability. It was concluded: (i) lactobacilli from the Lacticaseibacillus genus were the ones that benefited most from the lactic environment; (ii) the absence of the protective effect of honey was possibly due to the presence of Fe2+ which reacts with H2O2 to produce hydroxyl radicals; and (iii) cell viability did not correlate with membrane lipid peroxidation, and it is not a good marker to evaluate this type of damage in cells of different microorganisms.
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