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首页> 外文期刊>Journal of dairy science >Microbial community dynamics of a blue-veined raw milk cheese from the United Kingdom
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Microbial community dynamics of a blue-veined raw milk cheese from the United Kingdom

机译:来自英国的蓝纹生乳奶酪的微生物群落动态

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摘要

A commercial blue-veined cheese made from unpasteurized milk was examined by conventional culturing and PCR denaturing gradient gel electrophoresis analysis of the bacterial community 16S rRNA genes using 3 primer sets, V3, V4V5, and V6V8. Genomic DNA for amplification was extracted directly from raw milk, starter culture, cheese at different stages of production, fully ripened cheese, and from the cultured cells grown on various media. The outer rind was sampled separately from the inner white core and blue veins. A diverse microbiota containingLactococcus lactisssp.lactis,Lactobacillus plantarum,Lactobacillus curvatus,Staphylococcus gallinarum,Staphylococcus devriesei,Microbacteriumsp.,Sphingobacteriumsp.,Mycetocolasp.,Brevundimonassp.,Enterococcus faecalis, Proteussp., andKocuriasp. was detected in the raw milk using culturing methods, but onlyLactococcus lactisssp.lactis,Lactobacillus plantarum, andEnterococcus faecalissurvived to the final cheese and were detected both in the core and the rind. Using PCR denaturing gradient gel electrophoresis analysis of the cheese process samples,Staphylococcus equorumandEnterococcus duranswere found in the rind of prepiercing samples but not in the core and veins; after piercing, these species were found in all parts of the cheese but survived only in the rind when the cheese was fully ripened.Brevibacteriumsp.,Halomonassp.,Acinetobactersp.,Alkalibacteriumsp., andCorynebacterium caseiwere identified only by PCR denaturing gradient gel electrophoresis and not cultured from the samples.Brevibacteriumsp. was initially identified in the cheese postpiercing (core and veins),Halomonassp. was found in the matured cheese (rind), andAcinetobactersp.,Alkalibacteriumsp., andCorynebacterium caseiwere also found in the prepiercing samples (rind) and then found through the subsequent process stages. The work suggests that in this raw milk cheese, a limited community from the milk survive to the final cheese, with salt addition and handling contributing to the final cheese consortium.
机译:通过常规培养和使用3个引物对(V3,V4V5和V6V8)对细菌群落16S rRNA基因进行PCR变性梯度凝胶电泳分析,检查了由未经巴氏消毒的牛奶制得的市售蓝纹奶酪。直接从原料奶,发酵剂培养,生产中不同阶段的干酪,完全成熟的干酪以及在各种培养基上生长的培养细胞中直接提取用于扩增的基因组DNA。外皮与内白芯和蓝纹分开取样。包含乳酸乳球菌,乳杆菌,植物乳杆菌,弯形杆菌,鸡葡萄球菌,德氏葡萄球菌,微细菌菌,鞘氨醇杆菌,分枝杆菌,短杆菌,短肠肠球菌,粪肠球菌和变形杆菌的多种菌群。可通过培养方法在生乳中检出,但只有乳酸乳球菌,乳杆菌,植物乳杆菌和粪肠球菌在最终的奶酪中存活,并且在核心和果皮中均检出。采用PCR变性梯度凝胶电泳对干酪样样品进行分析,发现在刺穿前的果皮中未发现核心葡萄球菌和杜伦肠球菌,但在核心和静脉中未发现。刺穿后,在干酪的所有部位都发现了这些菌种,但仅在干酪完全成熟后才能在果皮中存活。从样品中培养。最初是在奶酪后刺穿(核心和静脉)Halomonassp中发现的。在成熟的奶酪(果皮)中发现了Aβ,在预先刺穿的样品(果皮)中还发现了不动杆菌属,碱杆菌属和干酪杆菌。这项工作表明,在这种生乳奶酪中,从牛奶到最终奶酪的生存空间非常有限,而盐分的添加和处理对最终奶酪联盟起到了促进作用。

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