Ercolini Danilo, Hill Philip J, Dodd Christine E R
Division of Food Sciences, School of Biosciences, University of Nottingham, Loughborough, Leicestershire LE12 5RD, United Kingdom.
Appl Environ Microbiol. 2003 Jun;69(6):3540-8. doi: 10.1128/AEM.69.6.3540-3548.2003.
The microbial diversity occurring in Stilton cheese was evaluated by 16S ribosomal DNA analysis with PCR-denaturing gradient gel electrophoresis. DNA templates for PCR experiments were directly extracted from the cheese as well as bulk cells harvested from a variety of viable-count media. The variable V3 and V4-V5 regions of the 16S genes were analyzed. Closest relatives of Lactococcus lactis, Enterococcus faecalis, Lactobacillus plantarum, Lactobacillus curvatus, Leuconostoc mesenteroides, Staphylococcus equorum, and Staphylococcus sp. were identified by sequencing of the DGGE fragments. Fluorescently labeled oligonucleotide probes were developed to detect Lactococcus lactis, Lactobacillus plantarum, and Leuconostoc mesenteroides in fluorescence in situ hybridization (FISH) experiments, and their specificity for the species occurring in the community of Stilton cheese was checked in FISH experiments carried out with reference cultures. The combined use of these probes and the bacterial probe Eub338 in FISH experiments on Stilton cheese sections allowed the assessment of the spatial distribution of the different microbial species in the dairy matrix. Microbial colonies of bacteria showed a differential location in the different parts of the cheese examined: the core, the veins, and the crust. Lactococci were found in the internal part of the veins as mixed colonies and as single colonies within the core. Lactobacillus plantarum was detected only underneath the surface, while Leuconostoc microcolonies were homogeneously distributed in all parts observed. The combined molecular approach is shown to be useful to simultaneously describe the structure and location of the bacterial flora in cheese. The differential distribution of species found suggests specific ecological reasons for the establishment of sites of actual microbial growth in the cheese, with implications of significance in understanding the ecology of food systems and with the aim of achieving optimization of the fermentation technologies as well as preservation of traditional products.
通过聚合酶链反应-变性梯度凝胶电泳(PCR-DGGE)对16S核糖体DNA进行分析,评估了斯蒂尔顿奶酪中存在的微生物多样性。PCR实验的DNA模板直接从奶酪以及从各种活菌计数培养基中收获的大量细胞中提取。分析了16S基因的可变V3和V4-V5区域。通过对DGGE片段进行测序,鉴定了乳酸乳球菌、粪肠球菌、植物乳杆菌、弯曲乳杆菌、肠系膜明串珠菌、马胃葡萄球菌和葡萄球菌属的近缘种。开发了荧光标记的寡核苷酸探针,用于在荧光原位杂交(FISH)实验中检测乳酸乳球菌、植物乳杆菌和肠系膜明串珠菌,并在使用参考培养物进行的FISH实验中检查它们对斯蒂尔顿奶酪群落中存在的物种的特异性。在斯蒂尔顿奶酪切片的FISH实验中,将这些探针与细菌探针Eub338结合使用,可以评估不同微生物物种在乳制品基质中的空间分布。在所检查的奶酪不同部位(核心、纹理和外皮)中,细菌的微生物菌落显示出不同的位置:乳酸球菌以混合菌落的形式存在于纹理内部,以单个菌落的形式存在于核心内。仅在表面下方检测到植物乳杆菌,而明串珠菌微菌落均匀分布在所有观察到的部位。结果表明,这种组合分子方法有助于同时描述奶酪中细菌菌群的结构和位置。发现的物种差异分布表明,奶酪中实际微生物生长位点的形成存在特定的生态原因,这对于理解食品系统的生态学具有重要意义,并且有助于实现发酵技术的优化以及传统产品的保存。