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多相分析法定量分析奶酪中严格异型发酵乳杆菌属的方法。

Polyphasic approach for quantitative analysis of obligately heterofermentative Lactobacillus species in cheese.

机构信息

ADRIA Développement-UMT 08.3 Physi'Opt, Creac'h Gwen, 29196 Quimper, France.

出版信息

Food Microbiol. 2012 Sep;31(2):271-7. doi: 10.1016/j.fm.2012.01.009. Epub 2012 Feb 17.

Abstract

Obligately heterofermentative lactobacilli (OHL) present in cheese during ripening can influence the flavour and texture of the final product. In order to better evaluate, follow and control this population, there is a current need for easy-to-use tools. In this study, a culture-dependent quantitative method (ABEV medium) was set up for direct and selective enumeration of total OHL from cheese, and a culture-independent method based on specific real time PCR (qPCR) assays was developed to target Lactobacillus fermentum and Lactobacillus parabuchneri individual species. These tools were applied for OHL quantification in manufactured Emmental and Tomme cheeses. The ABEV medium was well adapted for specific enumeration and isolation of OHL species present in milk-derived samples, even in the presence of background microbiota. qPCR assays showed 100% specificity and could accurately quantify the targeted species in various types of cheese. Culture-dependent and -independent techniques evaluated in manufactured cheese samples generated similar bacterial counts. The behaviour of L. fermentum and L. parabuchneri was characterized from milk samples to the end of ripening. In addition, PCR-TTGE was used to confirm the presence of inoculated species and to globally analyze the composition of naturally present species. This polyphasic approach illustrates the complementarity of the different methods.

摘要

在奶酪成熟过程中存在的严格异型发酵乳杆菌(OHL)会影响最终产品的风味和质地。为了更好地评估、跟踪和控制该菌群,目前需要易于使用的工具。本研究建立了一种基于培养的定量方法(ABEV 培养基),用于直接且选择性地计数奶酪中的总 OHL,以及一种基于特定实时 PCR(qPCR)检测的非培养方法,用于针对发酵乳杆菌和副干酪乳杆菌的各个物种。这些工具被应用于制造的埃曼塔尔奶酪和汤姆奶酪中的 OHL 定量。ABEV 培养基非常适合于在存在背景微生物群的情况下对牛奶衍生样品中的 OHL 物种进行特定的计数和分离。qPCR 检测显示出 100%的特异性,并能准确地在各种类型的奶酪中定量目标物种。在制造的奶酪样品中评估的培养依赖和非培养技术产生了相似的细菌计数。从牛奶样品到成熟结束,对发酵乳杆菌和副干酪乳杆菌的行为进行了研究。此外,PCR-TTGE 用于确认接种物种的存在,并全面分析天然存在物种的组成。这种多相方法说明了不同方法的互补性。

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