Gardiner G, Ross R P, Collins J K, Fitzgerald G, Stanton C
Dairy Products Research Center, Moorepark, Fermoy, County Cork, Ireland.
Appl Environ Microbiol. 1998 Jun;64(6):2192-9. doi: 10.1128/AEM.64.6.2192-2199.1998.
Cheddar cheese was manufactured with either Lactobacillus salivarius NFBC 310, NFBC 321, or NFBC 348 or L. paracasei NFBC 338 or NFBC 364 as the dairy starter adjunct. These five strains had previously been isolated from the human small intestine and have been characterized extensively with respect to their probiotic potential. Enumeration of these strains in mature Cheddar cheese, however, was complicated by the presence of high numbers (>10(7) CFU/g of cheese) of nonstarter lactic acid bacteria, principally composed of lactobacilli which proliferate as the cheese ripens. Attempts to differentiate the adjunct lactobacilli from the nonstarter lactobacilli based on bile tolerance and growth temperature were unsuccessful. In contrast, the randomly amplified polymorphic DNA method allowed the generation of discrete DNA fingerprints for each strain which were clearly distinguishable from those generated from the natural flora of the cheeses. Using this approach, it was found that both L. paracasei strains grew and sustained high viability in cheese during ripening, while each of the L. salivarius species declined over the ripening period. These data demonstrate that Cheddar cheese can be an effective vehicle for delivery of some probiotic organisms to the consumer.
切达干酪是以唾液乳杆菌NFBC 310、NFBC 321或NFBC 348,或副干酪乳杆菌NFBC 338或NFBC 364作为乳制品发酵剂添加剂制造而成。这五株菌株先前是从人类小肠中分离出来的,并且就其益生菌潜力已进行了广泛的特性分析。然而,由于在成熟切达干酪中存在大量(>10⁷ CFU/g奶酪)的非发酵剂乳酸菌,主要由随着奶酪成熟而增殖的乳杆菌组成,因此对这些菌株进行计数变得复杂。基于胆汁耐受性和生长温度来区分添加的乳杆菌和非发酵剂乳杆菌的尝试未成功。相比之下,随机扩增多态性DNA方法能够为每个菌株生成离散的DNA指纹图谱,这些指纹图谱与奶酪天然菌群产生的指纹图谱明显不同。采用这种方法发现,在奶酪成熟过程中,两株副干酪乳杆菌均能生长并保持高活力,而唾液乳杆菌的各个菌株在成熟期间数量下降。这些数据表明,切达干酪可以成为向消费者传递某些益生菌的有效载体。