Title of the manuscript: Water-soluble microencapsulation using gum Arabic and skim milk enhances viability and efficacy of Pediococcus acidilactici probiotic strains for application in broiler chickens
ABSTRACTObjectives: This study aimeds to develop and evaluate the effectiveness of a water-soluble microencapsulation method for probiotic strains using gum Arabic (GA) and skim milk (SKM) over a three-month storage period following processing.Methods: A total of fFourour Four strains of Pediococcus acidilactici (BYF26, BYF20, BF9, and BF14) that were typical lactic acid bacteria (LAB) strains isolated from the chicken gut were used for mixed with different ratios ofa different wall material gum Arabic (GA) and skim milk (SKM) as coating agents ratio before spray drying at anthe inlet temperature 140°C.After processing, their survivability and probiotic qualities of the strains were assessed from two weeks to three months of storage at varied temperatures, and the de-encapsulation method was performed tofor confirm the soluble properties. Finally,At last, the confirmed of antibacterial activity of the probiotic properties wasere assessed underconducted as performance in simulated gastrointestinal conditions and antibacterial activity.Results: As shown by scanning electron microscopy, spray-drying produced a spherical, whiteyellow powder. The encapsulation efficacy (EE percent) was greatest for a coating containing a combination of 30% gum Arabic : 30% skim milk (w/v) (GA:SKM30) compared to lower concentrations of the two ingredients (p<0.05). Coating with GA:SKM30 (w/v) significantly enhanced (p<0.05) BYF26 survival under simulated gastrointestinal conditions (pH 2.5-3) and maintained higher survival rates compared to non-encapsulated cells underat an artificial A c c e p t e d A r t i c l e 4 intestinal juices (AIJ) condition of pH 6. De-encapsulation tests indicated that the encapsulated powder dissolved in water while keeping viable cell counts within the effective range of 10 6 for 6 hours. In addition, following three months storage at 4°C, microencapsulation of BYF26 in GA:SKM30 maintained both the number of viable cells (p<0.05) and the preparation's antibacterial efficacy against pathogenic bacteria, specifically strains of Salmonella spp.
Conclusion:Our prototype water-soluble probiotic microencapsulation GA:SKM30 effectively maintains LAB characteristics and survival rates, demonstrating its potential for use in preserving probiotic strains that can be used in chickens and potentially in other livestock.