首页> 外文期刊>Journal of Pure & Applied Microbiology >Phenotypic and Genotypic Characterization of Probiotic Bacteria Isolated from Gir Cow Milk for their Fortification in Soya Food
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Phenotypic and Genotypic Characterization of Probiotic Bacteria Isolated from Gir Cow Milk for their Fortification in Soya Food

机译:吉尔牛乳中分离出的益生菌的表型和基因型特征对其在大豆食品中的强化作用

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Soy foods are more and more accepted as healthy food due to its numerous health benefits. However, the one of the unfavorable property of soy food is its incomplete digestion, due to the presence of soy indigestible oligosaccharides, which resulting in undesirable symptoms, such as flatulence, cramping and bloating. One of the solution of above problem is use of probiotic microorganism and use of such probiotic to soy food would help on solution of digestion and may confer additional health benefitstoo to consumers of soy food. In present study raw milk samples collected from different taluka of Amreli district, Gujarat. Total 157 bacteria were isolated. Among 157 bacteria, 67 were selected on the basis of preliminary tests which included Gram-positive, catalase negative and non-motile. The carbohydrates fermentation was determined by modified MRS agar containing bromocresol purple as a pH indicator and supplemented with 1 % of raffinose instead of dextrose. These organisms were characterized fortheir bile salt and pH tolerance too. Furthermore, base on carbohydrate fermentation, bile salt tolerance and acid tolerance result, two bacterial isolates DHA_DHR_MR _12 and DHAJRA_M_13 were selected for 16s-rRNA identification. After identification confirm that the isolate DHA_DHR_MR _12 confirmed as Lactobacillus fermentum and DHA_JRA_M_13 confirmed Enterococcus faecium.
机译:大豆食品由于其许多健康益处而被越来越多地接受为健康食品。然而,大豆食品的不利特性之一是由于大豆不易消化的低聚糖的存在而导致其消化不完全,从而导致不良症状,例如肠胃胀气,痉挛和腹胀。解决上述问题的方法之一是使用益生菌微生物,将这种益生菌用于大豆食品将有助于解决消化问题,并且可能给大豆食品的消费者带来额外的健康益处。在本研究中,从古吉拉特邦阿姆雷里区的不同taluka采集的原奶样品。总共分离出157种细菌。在初步检验的基础上,从157种细菌中选择了67种,包括革兰氏阳性,过氧化氢酶阴性和不运动。碳水化合物的发酵通过改良的MRS琼脂测定,该琼脂含有溴甲酚紫作为pH指示剂,并补充了1%的棉子糖代替葡萄糖。这些生物也对其胆盐和pH耐受性进行了表征。此外,根据碳水化合物的发酵,胆汁盐耐性和耐酸性结果,选择了两个细菌分离株DHA_DHR_MR_12和DHAJRA_M_13进行16s-rRNA鉴定。鉴定后,确认分离株DHA_DHR_MR _12确认为发酵乳杆菌,DHA_JRA_M_13确认为粪肠球菌。

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