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从突尼斯海鲜和肉类产品中可靠分离清酒乳杆菌菌株的方法。

Method for reliable isolation of Lactobacillus sakei strains originating from Tunisian seafood and meat products.

作者信息

Najjari Afef, Ouzari Hadda, Boudabous Abdellatif, Zagorec Monique

机构信息

Laboratoire de Microbiologie et Biomolécules Actives, Département de Biologie, Faculté des Sciences de Tunis, Campus Universitaire, 2092 Tunis, Tunisia.

出版信息

Int J Food Microbiol. 2008 Feb 10;121(3):342-51. doi: 10.1016/j.ijfoodmicro.2007.11.045. Epub 2007 Nov 28.

Abstract

In Tunisia, several food products derived from meat or seafood are naturally processed, without any addition of bacterial starters. Such fermented, dried-cured, salted, or marinated products, as well as the raw meat or fish may thus provide a source to isolate the natural microflora colonizing such environments. We isolated lactic acid bacteria from a representative range of flesh-foods sold or manufactured in different parts of Tunisia, and selectively searched for Lactobacillus sakei, a lactic acid bacterium potentially useful as starter or protective culture. Eighty six (86) strains were isolated from various seafood (anchovy, sardine, sole, mullet, and octopus), or meat (pork, veal, beef, sheep, chicken, and turkey) products that were either fresh, or transformed by different traditional processes. Several methods were used in order to develop a rapid and reliable protocol for the direct identification of L. sakei. Amplified ribosomal DNA restriction analysis (ARDRA) classified the various isolates into 9 distinct groups. Search for the presence of the L. sakei specific katA gene indicated that all positive isolates were grouped in the same ARDRA group. Sequencing of 16S rDNA confirmed those isolates as L. sakei. Those 22 different L. sakei strains represent 25.6% of the total isolates, while other isolates found in the different ARDRA groups were tentatively ascribed to Lactobacillus plantarum, Lactococcus lactis/garviae, Enterococcus avium, Streptococcus parauberis, Hafnia alvei, Pediococcus pentosaceus, and Lactobacillus curvatus through 16S rDNA sequencing. A fast and reliable method to isolate and discriminate L. sakei from complex food environments is proposed.

摘要

在突尼斯,几种源自肉类或海鲜的食品是自然加工的,不添加任何细菌发酵剂。因此,这类发酵、干腌、盐渍或腌制产品,以及生肉或生鱼,可能成为分离定殖于此类环境中的天然微生物群落的来源。我们从突尼斯不同地区销售或生产的一系列具有代表性的肉类食品中分离出乳酸菌,并选择性地寻找清酒乳杆菌,这是一种有可能用作发酵剂或保护性培养物的乳酸菌。从各种海鲜(凤尾鱼、沙丁鱼、鳎鱼、鲻鱼和章鱼)或肉类(猪肉、小牛肉、牛肉、羊肉、鸡肉和火鸡)产品中分离出86株菌株,这些产品要么是新鲜的,要么经过了不同的传统加工。为了开发一种快速可靠的直接鉴定清酒乳杆菌的方法,我们采用了几种方法。扩增核糖体DNA限制性分析(ARDRA)将各种分离株分为9个不同的组。对清酒乳杆菌特异性katA基因的存在进行检测表明,所有阳性分离株都归为同一个ARDRA组。16S rDNA测序证实这些分离株为清酒乳杆菌。这22种不同的清酒乳杆菌菌株占分离株总数的25.6%,而通过16S rDNA测序,在不同ARDRA组中发现的其他分离株初步被归为植物乳杆菌、乳酸乳球菌/加氏乳球菌、鸟肠球菌、副乳房链球菌、蜂房哈夫尼亚菌、戊糖片球菌和弯曲乳杆菌。本文提出了一种从复杂食品环境中分离和鉴别清酒乳杆菌的快速可靠方法。

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