Binding of Aflatoxin B1 to Lactobacillus paracasei SNP-2 and Stability of Bacteria-AFB1 Complex

R. Utami, T. Utami, Suparmo Suparmo, E. Rahayu
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引用次数: 2

Abstract

The aim of this research was to study the binding ability of viable and non-viable of Lactobacillus paracasei SNP-2 to aflatoxin B 1 (AFB 1 ) in phosphate buffer saline (PBS) at pH 7.3. Bacterial cells were grown in MRS broth at 37 °C for 24 h, and then centrifuged at 1,800 g[a1]  for 20 min at 10 °C to get the pellet. Pellet was suspended in PBS pH 7.3 until the cell concentration was about 10 10 CFU/ml. Viable cells, the heated, and acid-killed cells were evaluated their ability to bind AFB 1 in PBS pH 7.3. Stability of the L. paracasei SNP-2/AFB 1 complexes was evaluated by determining the amount of the released AFB 1 to the PBS following five times washing. The results showed that AFB 1 binding ability to heat-and acid-kill bacteria were higher than that of by viable cells. More than 70% of bound AFB 1 was released from viable bacteria after five times washing. However, the heated and acid-killed cell treatments significantly increased the complex stability of bacteria-AFB 1
黄曲霉毒素B1与副干酪乳杆菌SNP-2的结合及细菌-AFB1复合物的稳定性
本研究的目的是研究在pH 7.3的磷酸盐缓冲盐水(PBS)中,副干酪乳杆菌SNP-2的活菌和不活菌与黄曲霉毒素B1(AFB1)的结合能力。细菌细胞在37°C的MRS肉汤中生长24小时,然后在10°C下以1800 g[a1]离心20分钟以获得颗粒。将颗粒悬浮在pH 7.3的PBS中,直到细胞浓度为约10 10 CFU/ml。评估活细胞、加热的和酸杀死的细胞在PBS pH 7.3中结合AFB1的能力。通过测定洗涤五次后释放到PBS中的AFB1的量来评估副干酪乳杆菌SNP-2/AFB 1复合物的稳定性。结果表明,AFB1对高温和酸性细菌的结合能力高于活细胞。经5次洗涤后,70%以上的结合AFB1从活菌中释放。然而,加热和酸杀死的细胞处理显著增加了细菌AFB1的复杂稳定性
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