Randazzo Cinzia L, Vaughan Elaine E, Caggia Cinzia
DOFATA-Sezione Tecnologie Agroalimentari, University of Catania, via Santa Sofia 98, 95123 Catania, Italy.
Int J Food Microbiol. 2006 May 25;109(1-2):1-8. doi: 10.1016/j.ijfoodmicro.2005.11.002. Epub 2006 Apr 17.
Traditional artisanal Pecorino Siciliano (PS) cheeses, and two experimental PS cheeses were manufactured using either raw or pasteurised ewes' milk with the addition of starter cultures. The bacterial diversity and dynamics of the different cheese types were evaluated both by culturing and characterisation of isolates, and a culture-independent approach based on the 16S ribosomal RNA (rRNA) gene. Following cultivation, artisanal and experimental cheese types showed similar microbial counts, and isolates belonging to Lactococcus lactis, Streptococcus thermophilus, Enterococcus faecalis and Leuconostoc mesenteroides were identified by phenotypic characterisation and comparison of the restriction fragment length polymorphism (RFLP) of the 16S rRNA gene to that of reference species. The culture-independent fingerprinting technique PCR and denaturing gradient gel electrophoresis (DGGE) of V6 to V8 regions of the 16S rRNA gene of samples taken during artisanal PS cheese manufacture, from raw milk to the ripened cheese, indicated relevant shifts in the microbial community structure. The dominance of Streptococcus bovis and Lactococcus lactis species in the traditional artisanal PS was revealed by 16S rRNA gene sequencing. Comparison of DGGE profiles of samples from milk to ripened cheese, derived from artisanal procedure and the two experimental PS cheeses during production showed similar trends with the presence of intense bands in common. Nevertheless, the profiles of several artisanal cheeses from different farms appeared more diverse, and these additional species are probably responsible for the generally superior flavour and aroma development of traditional PS cheese.
传统手工制作的西西里佩科里诺奶酪(PS)以及两种实验性PS奶酪,是使用生羊乳或巴氏杀菌羊乳并添加发酵剂制作而成的。通过对分离菌株的培养和鉴定以及基于16S核糖体RNA(rRNA)基因的非培养方法,评估了不同类型奶酪的细菌多样性和动态变化。培养后,手工制作的奶酪和实验性奶酪显示出相似的微生物数量,通过表型鉴定以及将16S rRNA基因的限制性片段长度多态性(RFLP)与参考物种进行比较,鉴定出了属于乳酸乳球菌、嗜热链球菌、粪肠球菌和肠系膜明串珠菌的分离菌株。在传统手工制作PS奶酪的过程中,从原料乳到成熟奶酪,对所采集样品的16S rRNA基因V6至V8区域进行非培养指纹技术PCR和变性梯度凝胶电泳(DGGE)分析,结果表明微生物群落结构发生了显著变化。16S rRNA基因测序揭示了传统手工制作PS奶酪中牛链球菌和乳酸乳球菌的优势地位。对来自手工制作过程以及两种实验性PS奶酪生产过程中从牛奶到成熟奶酪的样品进行DGGE图谱比较,结果显示出相似的趋势,存在共同的强条带。然而,来自不同农场的几种手工制作奶酪的图谱显得更加多样,这些额外的菌种可能是传统PS奶酪通常具有更优质风味和香气的原因。