Development of Probiotic Beverages Using Fingermillet [Eleusinecoracana (L.) Gaertn.] and Banana [Musa spp.] as Prebiotic Substrates

D. M. W. Divisekera, J. R. Samarasekera, C. Hettiarachchi, J. Gooneratne, S. Gopalakrishnan, S. D. Mazumdar
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Abstract

Aims: Development of probiotic beverages using previously isolated probiotic strains; Lactobacillus plantarum MF405176.1 and Lactobacillus curieae MF405178.1 in finger millet and banana flour substrates, respectively and monitor the microbiological, physicochemical and sensory properties of formulated probiotic beverages. Place and Duration of Study: Food Technology Section, Industrial Technology Institute, Colombo, Sri Lanka. Between November 2017 to April 2018. Methodology: Moisture content reduced (9 < 10%) finger millet (ravivar.)and banana (ambulnadee var.) flour were weighted seperately (25 g each), suspended in individual containers consisting of 100 ml potable water (n=6) and homogenised to obtain slurries. The slurries were sterilized (121 ± 1oC for 15 min) and cooled (35 ± 1oC) prior to inoculation of starter cultures. Previously isolated, freeze dried probiotic strains; L. plantarum MF405176.1 and L.curieae MF405178.1 were inoculated in to finger millet and banana slurries, respectively at probiotic cell concentration of 1010 CFU/ml. Slurries were allowed to ferment (37 ± 1°C) until the pH reaches < 3.5. Throughout fermentation,pH was monitored hourly, while probiotic cell viability was measured at every 4h. Final products were evaluated for viable probiotic cell count, chemical composition (protein, fat and ash content), physical properties (pH, moisture, total soluble solids and titrable acidity), microbiological quality (aerobic plate count, Yeasts and Mould count, Coliform and Escherichia coli), shelf-life (for 5 weeks at 4 ± 1°C) and Sensory properties (color, odor, appearance, texture and overall acceptability using 9 point hedonic scale). Results: Gradual increment of probiotic cell count with fermentation time was observed in both beverages. Compared to their respective controls, significant difference (P = .05) in physical properties (total soluble solids, titrable acidity and pH) and significant increment (P = .05) in chemical properties (fat and protein content) was observed in both beverages. Finger millet based probiotic beverage containing L. plantarum MF405176.1 exhibited better physical, chemical properties and higher acceptability. Further it demonstrated better shelf life compared to banana based beverage containing L. curieae MF405178.1. Both products could sustain the viability of probiotic starter cultures up to 109 CFU/mleven at the end of 5th week of shelf life period thus demonstrated the compatibility of finger millet and banana flour as ideal prebiotic substrates for development of probiotic food. Conclusion: Study highlighted the prebiotic potentiality of finger millet and banana flour for the development of dairy free probiotic food. It confirms the behavior of new probiotic strains L. plantarum MF405176.1 and L.curieaeMF405178.1 as starters in lactic acid fermentation.
小米益生菌饮料的研制Gaertn。和香蕉[芭蕉属]作为益生元基质
目的:利用先前分离的益生菌菌株开发益生菌饮料;分别对小米和香蕉粉基质中的植物乳杆菌MF405176.1和curieae乳杆菌MF405178.1进行检测,并对配方益生菌饮料的微生物学、理化和感官特性进行监测。学习地点和时间:斯里兰卡科伦坡工业技术学院食品技术科。2017年11月至2018年4月。方法:将含水率降低(9 < 10%)的小米粉(ravivar.)和香蕉粉(ambulnadee var.)分别称重(各25 g),悬浮在装有100 ml饮用水(n=6)的单独容器中,并均质以获得浆液。浆液在接种发酵剂前(121±1℃)灭菌15 min,冷却(35±1℃)。先前分离的冷冻干燥益生菌菌株;将L. plantarum MF405176.1和L.curieae MF405178.1分别接种于手指小米和香蕉浆中,益生菌细胞浓度为1010 CFU/ml。发酵(37±1℃)至pH < 3.5。在整个发酵过程中,每小时监测pH值,每4小时测量益生菌细胞活力。评估最终产品的活菌细胞计数、化学成分(蛋白质、脂肪和灰分含量)、物理特性(pH值、水分、可溶性固体总量和可滴定酸度)、微生物质量(好氧平板计数、酵母和霉菌计数、大肠菌群和大肠杆菌)、保质期(在4±1°C下保存5周)和感官特性(颜色、气味、外观、质地和总体可接受性,使用9分hedonic量表)。结果:两种饮料中益生菌细胞计数随发酵时间的延长而逐渐增加。与各自的对照组相比,两种饮料的物理性质(可溶性固形物总量、可滴定酸度和pH值)差异显著(P = 0.05),化学性质(脂肪和蛋白质含量)显著增加(P = 0.05)。以植物乳杆菌MF405176.1为基础的手指小米益生菌饮料具有较好的物理、化学性能和较高的可接受性。此外,与含有居里乳杆菌MF405178.1的香蕉基饮料相比,它的保质期更长。两种产品在保质期5周结束时,益生菌发酵剂的活力均维持在109 CFU/ mml以上,证明了小米和香蕉粉作为开发益生菌食品的理想益生元基质的兼容性。结论:研究强调了小米和香蕉粉在开发无乳益生菌食品中的潜力。证实了新型益生菌L. plantarum MF405176.1和L. curieaemf405178.1在乳酸发酵中的发酵剂作用。
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