A comparative study of procedures for binding of aflatoxin M1 to Lactobacillus rhamnosus GG
Jean Claude Assaf1, Ali Atoui2, André El Khoury3
1Université Saint-Joseph de Beyrouth, Campus des Sciences et Technologies, Faculté des Sciences, Matn, Lebanon; Faculty of Sciences I Lebanese University, Department of Life and Earth Sciences, Laboratory of Microbiology, Beirut, Lebanon; Lebanese University, Doctoral School of Sciences and Technologies, Platform of Research and Analysis in Environmental Sciences (PRASE), Beirut, Lebanon; Université Saint-Joseph de Beyrouth, Ecole Doctorale "Sciences et Santé", Campus des Sciences Médicales et Infirmières, Beirut, Lebanon.
Abstract:
Several strains of lactic acid bacteria (LAB), frequently used in food fermentation and preservation, have been reported to bind different types of toxins in liquid media. This study was carried out to investigate the effect of different concentrations of Lactobacillus rhamnosus GG (ATCC 53103) to bind aflatoxin M1 (AFM1) in liquid media. AFM1 binding was tested following repetitive washes or filtration procedures in combination with additional treatments such as heating, pipetting, and centrifugation. The mixture of L. rhamnosus GG and AFM1 was incubated for 18h at 37°C and the binding efficiency was determined by quantifying the unbound AFM1 using HPLC. The stability of the complexes viable bacteria-AFM1 and heat treated bacteria-AFM1 was tested. Depending on the bacterial concentration and procedure used, the percentages of bound AFM1 by L. rhamnosus GG varied from as low as undetectable to as high as 63%. The highest reduction in the level of unbound AFM1 was recorded for the five washes procedure that involved heating and pipetting. Results also showed that binding was partially reversible and AFM1 was released after repeated washes. These findings highlight the effect of different treatments on the binding of AFM1 to L. rhamnosus GG in liquid matrix.
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