Laboratory of Food Microbiology and Hygiene, Faculty of Agriculture, Aristotle University of Thessaloniki, 54124, Thessaloniki, Greece.
Department of Genetics, Development and Molecular Biology, School of Biology, Aristotle University of Thessaloniki, 54124 Thessaloniki Greece.
Int J Food Microbiol. 2015 May 4;200:87-96. doi: 10.1016/j.ijfoodmicro.2015.02.008. Epub 2015 Feb 11.
Isolates of NSLAB were obtained from fresh (58 isolates) and mature (38) Feta cheese made at household level in three different mountainous areas, in order to study the effect of the area of production on NSLAB composition and their technological characteristics. Results obtained by SDS-PAGE of whole-cell proteins indicated that the microflora of the fresh cheese was composed of either lactococci (areas 1, 2), or lactococci and enterococci (area 3). The NSLAB microflora of mature cheese was composed almost entirely of lactobacilli species, differing according to the area of production. Species allocation by the SDS-PAGE method was confirmed by sequencing representative strains. Lactococci of cheese made in area 1 exhibited a narrow spectrum of antibacterial activity compared to isolates from areas 2 and 3, while for lactobacilli from all three areas a similar spectrum was noticed. Lactococci from area 2 exhibited higher (P<0.05) mean acidifying activity than lactococci from area 1. The isolates from the three areas also differed in respect of their caseinolytic activity, with preferences towards β-CN (areas 1 and 2) or αs-CN (area 3). Mean proteolytic activity of lactococci from area 1 was stronger (P<0.05) than that of lactococci from area 2 and the same was observed for their mean aminopeptidase activity, as well as their extent of autolysis at pH5.1. Mean acidifying activity of lactobacilli after 6h was for strains of area 3>2=1. The strains from areas 1 and 3 degraded preferentially αs-CN, while a clear preference towards β-CN was noticed for strains of area 2; their mean proteolytic activity was for strains of area 1 higher (P<0.05) than strains from area 3. The above results suggest that cheeses from the three areas differ in species composition of NSLAB and their technological properties. Principal component analysis of results on acidifying and proteolytic activities as well as autolysis allowed the distinction of lactococci according to their derivation area enabling the selection of appropriate strains as starters for cheese production in each area.
从三个不同山区家庭制作的新鲜(58 株)和成熟(38 株)菲达奶酪中分离出 NSLAB,以研究生产区域对 NSLAB 组成及其工艺特性的影响。全细胞蛋白 SDS-PAGE 结果表明,新鲜奶酪的微生物区系由乳球菌(区域 1、2)或乳球菌和肠球菌(区域 3)组成。成熟奶酪的 NSLAB 微生物区系几乎完全由乳杆菌组成,根据生产区域而有所不同。通过 SDS-PAGE 方法分配的物种通过测序代表性菌株得到确认。与来自 2 区和 3 区的分离株相比,来自 1 区的奶酪乳球菌显示出较窄的抗菌活性谱,而来自所有三个区域的乳杆菌则显示出相似的谱。来自 2 区的乳球菌的酸化活性(P<0.05)高于来自 1 区的乳球菌。来自三个区域的分离株在其对酪蛋白的水解活性方面也存在差异,对β-CN(区域 1 和 2)或αs-CN(区域 3)有偏好。来自 1 区的乳球菌的平均蛋白水解活性(P<0.05)强于来自 2 区的乳球菌,其平均氨肽酶活性以及在 pH5.1 下的自溶程度也是如此。6h 后,乳杆菌的平均酸化活性为区域 3>2=1。来自区域 1 和 3 的菌株优先降解αs-CN,而来自区域 2 的菌株则明显优先降解β-CN;来自区域 1 的菌株的平均蛋白水解活性(P<0.05)高于来自区域 3 的菌株。上述结果表明,来自三个地区的奶酪在 NSLAB 的物种组成及其工艺特性上存在差异。酸和蛋白水解活性以及自溶的主成分分析允许根据其来源区域对乳球菌进行区分,从而能够选择适当的菌株作为每个地区奶酪生产的起始菌株。