The application of digestive tract lactic acid bacteria with high esterase activity for zearalenone detoxification

玉米赤霉烯酮 酯酶 细菌 生物 真菌毒素 乳酸 微生物学 拉伤 戒毒(替代医学) 植物乳杆菌 食品科学 生物化学 酶 替代医学 病理 解剖 医学 遗传学
作者
Shiau‐Wei Chen,Jih‐Tay Hsu,Yan‐An Chou,H. Wang
出处
期刊:Journal of the Science of Food and Agriculture [Wiley]
卷期号:98 (10): 3870-3879 被引量:37
标识
DOI:10.1002/jsfa.8904
摘要

Abstract BACKGROUND Zearalenone (ZEA) is an estrogenic mycotoxin produced by several Fusarium species and frequently contaminates cereals used for food or animal feed. This study attempted to select lactic acid bacteria (LAB) with high esterase activity from the digestive tract, with the goal of using these bacteria for ZEA detoxification. RESULTS No ZEA activity‐related biotransformation products were observed in three isolates (B1, B2 and D10) during incubation in the presence of ZEA. All three LAB strains were Lactobacillus plantarum , but the API 50 CHL results suggested that the three isolates were different strains. Increased esterase activity was associated with an increase in cell growth, and the ZEA‐detoxifying capabilities of isolates rely on the concentration of bacteria in the culture medium. The lipolytic activity and ZEA removal assay indicated that ZEA degradation by the supernatant fraction was dependent on esterase activity; the supernatant of B2 strain showed the highest ZEA degradation ability and did not release the binding ZEA back into the medium. The D10 strain showed fast ZEA binding ability during the late log phase but began to release the bound ZEA back into the medium after the early stationary phase. All isolates showed good acid and bile salt tolerance ability but all strains showed low adhesion ability to epithelial cells. CONCLUSION Based on the ZEA removal characterization and ability of the isolates, it is suggested that the isolates could be applied to ZEA detoxification of contaminated feed, but the with the requirement of high cell number for ZEA binding and limited degradation time before absorption of ZEA in the digestive tract. © 2018 Society of Chemical Industry
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