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首页> 外文期刊>Advances in Microbiology >Isolation and Characterization of Lactic Acid Bacteria Producing Bacteriocin like Inhibitory Substance (BLIS) from “Gappal”, a Dairy Product from Burkina Faso
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Isolation and Characterization of Lactic Acid Bacteria Producing Bacteriocin like Inhibitory Substance (BLIS) from “Gappal”, a Dairy Product from Burkina Faso

机译:产自布基纳法索乳制品“ Gappal”的乳酸菌如抑制性物质(BLIS)的分离和鉴定

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摘要

Indigenous fermented foods are known for their nutritional and functional properties but they are often spoiled by pathogenic bacteria that can constitute a food safety problem. “Gappal” is a no-thermal treat food based on millet dough and milk and its production conditions can constitute a food safety problem. The aim of this study was to screen and identify LAB producing Bacteriocin-like inhibitory substances using a matrix similar to “Gappal”. The detection of potential BLIS was first performed using overlaid method after enrichment of samples in whey and millet dough. The isolates demonstrating inhibiting area were preselected, purified and tested for the presence of antibacterial properties using their neutralized cell-free culture supernatant and subsequently treated with catalase in combination with protease, pepsin or trypsin. The antimicrobial effect of two isolates (Gbf48 and Gbf50) after growth on MRS broth over 12 h at 30?C were active against E. faecalis ATCC 19433, M. luteus ATCC 49732, S. aureus ATCC 2523, L. monocytogenes , B. megaterium , B. sphaericus and B. cereus with an activity of 2560 AU/mL. The 16S RNA gene sequencing identification indicated that these isolates are Pediococcus acidilactici. Gbf 48 and Gbf 50 could be used to improve preservative factors for a controlled fermentation of non thermal treatment fermented food for their potential of acidification adds to BLIS production.
机译:土著发酵食品以其营养和功能特性而闻名,但它们经常被可能构成食品安全问题的致病细菌破坏。 “ Gappal”是基于小米面团和牛奶的非热处理食品,其生产条件可能构成食品安全问题。这项研究的目的是使用类似于“ Gappal”的基质来筛选和鉴定产生LAB的类细菌抑制素的物质。在乳清和谷子面团中富集样品后,首先使用覆盖法进行潜在的BLIS检测。使用中和的无细胞培养上清液,对具有抑制区域的分离物进行预选,纯化和测试其抗菌性能,然后用过氧化氢酶与蛋白酶,胃蛋白酶或胰蛋白酶联合处理。两个分离株(Gbf48和Gbf50)在30°C下生长超过12小时后对MRS肉汤的抗微生物作用对E具有活性。粪便ATCC 19433,M.黄体ATCC 49732, S。金黄色葡萄球菌ATCC 2523, L。单核细胞增生病ter球菌和 B。蜡状细胞的活性为2560 AU / mL。 16S RNA基因测序鉴定表明,这些分离物是乳酸双球菌。 Gbf 48和Gbf 50可用于改善非热处理发酵食品受控发酵的防腐因子,因为它们的酸化潜力增加了BLIS的生产。

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