-The aim of this work was to gain a comprehensive view of the microbiological characteristics of milk, natural whey starter, and cheese during the first months of ageing of Parmigiano Reggiano. A significant presence of different microbial groups in raw milk from the initial moments of production was rapidly substituted by various lactic acid bacteria. Natural whey starter contained a large number of thermophilic lactic acid bacteria (Lactobacillus helveticus, L. delbrueckii ssp. lactis, L. delbrueckii ssp. bulgaricus) and some facultatively heterofermentative lactic acid bacteria belonging to L. rhamnosus. Thermophilic lactic acid bacteria disappeared within 30 d. Rod-shaped mesophilic facultatively heterofermentative lactic acid microflora, consisting of L. casei, L. paracasei ssp. paracasei, L. paracasei ssp. tolerans, L. rhamnosus and pediococci, progressively increased up to the fifth month of ageing. Results showed that thermophilic lactobacilli were derived from natural whey starter whereas Streptococcus thermophilus originated from raw milk. Further, natural whey starter was the source of L. rhamnosus which was present throughout the entire period of the cheese ageing. The other components of non-starter lactic acid microflora derived from raw milk.

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Arribas, M.V., Selection and technological potential of Lactobacillus plantarum bacteria suitable for wine malolactic fermentation and grape aroma release,

Parmigiano Reggiano is a hard, cooked cheese produced in specific areas of Northern Italy. The raw material is obtained by mixing the partly skimmed evening milk and whole morning milk. The mixture is then heated to 22°C, and natural whey starter is added at 28–30 g/l after 1–2 min, bringing the pH of the mixture to 6·2–6·3. After coagulation, which takes ∼15 min and occurs at 32–33°C owing to the addition of calf rennet powder, the curd is broken up for 2–4 min, cut into fragments and cooked at a temperature raised gradually to 42–44°C and then more quickly to 55–56°C over 10–15 min. The curd is left undisturbed, covered by the whey, for 40–60 min, then removed and placed inside a circular wooden mould. The cheese is held at ∼20°C for 3 d during which it is turned at frequent intervals to facilitate complete whey drainage. The cheese, which now has its typical shape and size, is then salted by immersion in brine (260–280 g NaCl/l at 16–17°C) for 20–24 d. During this period the cheese absorbs 15–18 g NaCl/kg and its weight decreases by 4%. During the subsequent period of ripening (12–24 months) in store rooms at 16–18°C and 85% moisture, the cheese is frequently turned. At the end of ripening the cheese is cylindrical in shape, with a slightly convex side, 0·22–0·24 m high, 0·40–0·45 m diam. weighs 35–36 kg, has 320–330 g fat/kg dry matter and a minutely granulated internal structure with small holes formed by the activity of some heterofermentative lactic acid bacteria.

In this study, for the first time, we examined some of the physico-chemical properties of the cell surface of Akkermansia muciniphila DSM 22959, comparing it with those of Lactobacillus rhamnosus GG—one of the most extensively studied probiotic microorganisms. In particular, hydrophobicity, auto-aggregation, co-aggregation, and biofilm formation were investigated. In addition, antibiotic susceptibility, co-culture, and antimicrobial activity of the two strains were compared. Hydrophobicity was evaluated using xylene and toluene, showing that A. muciniphila DSM 22959 possessed moderate hydrophobicity. A. muciniphila showed a faster and higher auto-aggregation ability than Lb. rhamnosus GG, but a lower aptitude in biofilm formation. In the co-aggregation test, the best performance was obtained by Lb. rhamnosus GG. Regarding the susceptibility to antibiotics, the differences between the two strains were remarkable, with A. muciniphila DSM 22959 showing resistance to half of the antibiotic tested. Interesting results were also obtained with regard to the stimulating effect of Lb. rhamnosus GG on the growth of A. muciniphila when co-cultured.