ABSTRACT
L. paracasei subsp. paracasei E6 cells were encapsulated by complex coacervation using whey protein isolate (WPI) and gum arabic and introduced in stirred yogurts after fermentation. For comparison purposes, yogurts without addition of L. paracasei and yogurts with free cells of L. paracasei were produced. The survival of free and microencapsulated L. paracasei cells was evaluated during storage of the yogurts for 45 days at 4 °C. In addition, yogurts were exposed to simulated gastric juice and the reduction in viable numbers of L. paracasei cells was assessed. The effect of complex coacervates' addition on the rheological properties of yogurts was also evaluated. Yogurts containing encapsulated L. paracasei cells showed a slightly improved cell survival (≤0.22 log CFU g-1 reduction) during storage when compared to yogurts containing free cells (≤0.64 log CFU g-1 reduction). Moreover, the microencapsulated L. paracasei cells exhibited greater survival compared to free cells upon exposure of the yogurt samples to simulated gastric juice (pH 2.0) for 3 h. Finally, the incorporation of complex coacervates did not significantly affect the rheological properties of yogurts especially when added at concentrations less than 10% w/w. Consequently, the inclusion of microencapsulated bacteria by complex coacervation in yogurts, could become an effective vehicle for successful delivery of probiotics to the gut, and hence contributing to the improvement of the gastrointestinal tract health, without altering the texture of the product.
Subject(s)
Biopolymers/chemistry , Food Additives/chemistry , Lacticaseibacillus paracasei/chemistry , Probiotics/chemistry , Yogurt/microbiology , Animals , Drug Compounding , Food Additives/metabolism , Food Storage , Gastrointestinal Tract/metabolism , Gum Arabic/chemistry , Humans , Hydrogen-Ion Concentration , Lacticaseibacillus paracasei/growth & development , Lacticaseibacillus paracasei/metabolism , Microbial Viability , Milk/chemistry , Probiotics/metabolism , Whey Proteins/chemistry , Yogurt/analysisABSTRACT
The effect of the microstructure of the medium on the growth of the food-borne pathogen Listeria monocytogenes was studied. The pathogen's growth kinetics was evaluated using liquid substrates and gels formed from different concentrations of sodium alginate (3.0% w/w) and gelatin (0-30.0% w/w). These results were further verified using a model dairy product with solid concentrations varying from 10.0 to 40.0% w/w. The pathogen's growth was faster in the liquid media than in the gels regardless of the gelling agent employed. The substrate's microstructure, apart from altering the growth pattern from planktonic to colonial, resulted in microbial growth suppression; however, each system affected the microorganism's growth in a different way. The suppressing effect of the substrate's microstructure on microbial growth was also dependent on temperature, while the presence of glucose in the solid medium accelerated microbial growth, thus reducing substantially the difference in growth kinetics between the gels and the liquid media. Any increase in the hydrocolloid concentration, which was also reflected in the rheological properties of the structured samples, resulted in a reduction of growth rate and in an increase of the lag phase of the pathogen. Overall, the gelation of the medium was found to exert a stress on the microorganism since the sol-gel transition, when the pathogen was already at the exponential growth phase, resulted in an additional lag phase or a decrease in the growth rate. The relationship between maximum specific growth rate and loss tangent of the gels (tanδ=Gâ³/G') was explored, pointing to the possible use of a single structural parameter to describe food matrix effects on microbial growth kinetics.
