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利用重复元件聚合酶链反应对源自韩国食品的短乳杆菌分离株进行分子分型。

Molecular typing of Lactobacillus brevis isolates from Korean food using repetitive element-polymerase chain reaction.

作者信息

Kaur Jasmine, Sharma Anshul, Lee Sulhee, Park Young-Seo

机构信息

Department of Food Science and Biotechnology, Gachon University, Seongnam, South Korea.

出版信息

Food Sci Technol Int. 2018 Jun;24(4):341-350. doi: 10.1177/1082013217753993. Epub 2018 Jan 19.

Abstract

Lactobacillus brevis is a part of a large family of lactic acid bacteria that are present in cheese, sauerkraut, sourdough, silage, cow manure, feces, and the intestinal tract of humans and rats. It finds its use in food fermentation, and so is considered a "generally regarded as safe" organism. L. brevis strains are extensively used as probiotics and hence, there is a need for identifying and characterizing these strains. For identification and discrimination of the bacterial species at the subspecific level, repetitive element-polymerase chain reaction method is a reliable genomic fingerprinting tool. The objective of the present study was to characterize 13 strains of L. brevis isolated from various fermented foods using repetitive element-polymerase chain reaction. Repetitive element-polymerase chain reaction was performed using three primer sets, REP, Enterobacterial Repetitive Intergenic Consensus (ERIC), and (GTG), which produced different fingerprinting patterns that enable us to distinguish between the closely related strains. Fingerprinting patterns generated band range in between 150 and 5000 bp with REP, 200-7500 bp with ERIC, and 250-2000 bp with (GTG) primers, respectively. The Jaccard's dissimilarity matrices were used to obtain dendrograms by the unweighted neighbor-joining method using genetic dissimilarities based on repetitive element-polymerase chain reaction fingerprinting data. Repetitive element-polymerase chain reaction proved to be a rapid and easy method that can produce reliable results in L. brevis species.

摘要

短乳杆菌是乳酸菌大家族的一部分,存在于奶酪、酸菜、酸面团、青贮饲料、牛粪、粪便以及人类和大鼠的肠道中。它用于食品发酵,因此被认为是一种“一般认为安全”的生物体。短乳杆菌菌株被广泛用作益生菌,因此,有必要对这些菌株进行鉴定和表征。为了在亚种水平上鉴定和区分细菌物种,重复元件聚合酶链反应方法是一种可靠的基因组指纹识别工具。本研究的目的是使用重复元件聚合酶链反应对从各种发酵食品中分离出的13株短乳杆菌进行表征。使用三种引物对进行重复元件聚合酶链反应,即REP、肠杆菌重复基因间共有序列(ERIC)和(GTG),它们产生了不同的指纹图谱,使我们能够区分密切相关的菌株。REP引物产生的指纹图谱条带范围在150至5000 bp之间,ERIC引物产生的条带范围在200至7500 bp之间,(GTG)引物产生的条带范围在250至2000 bp之间。使用Jaccard差异矩阵,通过基于重复元件聚合酶链反应指纹数据的遗传差异,采用非加权邻接法获得树状图。重复元件聚合酶链反应被证明是一种快速简便的方法,能够在短乳杆菌物种中产生可靠的结果。

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