Transcription profiling of interactions between Lactococcus lactis subsp. cremoris SK11 and Lactobacillus paracasei ATCC 334 during Cheddar cheese simulation

2014 ◽  
Vol 178 ◽  
pp. 76-86 ◽  
Author(s):  
Émilie Desfossés-Foucault ◽  
Gisèle LaPointe ◽  
Denis Roy
2014 ◽  
Vol 4 (1) ◽  
pp. 343-351
Author(s):  
Ouiam El Galiou ◽  
Juan Antonio Centeno ◽  
Said Zantar ◽  
Mohammed Bakkali ◽  
Javier Carballo ◽  
...  

The effect of adding four Lactococcus lactis subsp. Lactis, Lactococcus lactis subsp. lactis Bv. diacetylactis and Lactobacillus paracasei autochthonous strains as single starters (A and B) on the microbiological, physicochemical and sensory characteristics of Moroccan goat’s milk cheese was investigated. Batches with a commercial starter (C) and with raw goat’s milk without starter (D) were also made as controls. The results indicated that the different starter cultures used significantly affected the compositional characteristics of Moroccan goat’s cheese. At the first day of ripening, the pH values of cheeses manufactured with any type of starter were significantly higher than those made without starter. No significant differences (P >0.05) in values of total solids (T.S.), proteins, ash, FAT and lactose content were found between any of the batches after 7 days of ripening. The autochthonous starters in Moroccan cheesemaking were successful at reducing the levels of coliforms earlier in ripening than in cheeses made without starter and even in those made with the commercial starter. These results suggest that the combined activity of L. Lactis subsp. lactis, L. Lactis. subsp. Lactis bv. diacetylactis and L. paracasei, produces cheese with good sensory characteristics.


1995 ◽  
Vol 5 (5) ◽  
pp. 451-472 ◽  
Author(s):  
Vaughan L. Crow ◽  
Frank G. Martley ◽  
Tim Coolbear ◽  
Sally J. Roundhill

1998 ◽  
Vol 8 (10-11) ◽  
pp. 843-850 ◽  
Author(s):  
Christopher J. Pillidge ◽  
Selvarani Govindasamy-Lucey ◽  
Pramod K. Gopal ◽  
Vaughan L. Crow

Foods ◽  
2021 ◽  
Vol 10 (4) ◽  
pp. 898
Author(s):  
Hebatoallah Hassan ◽  
Daniel St-Gelais ◽  
Ahmed Gomaa ◽  
Ismail Fliss

Clostridium tyrobutyricum spores survive milk pasteurization and cause late blowing of cheeses and significant economic loss. The effectiveness of nisin-producing Lactococcus lactis ssp. lactis 32 as a protective strain for control the C. tyrobutyricum growth in Cheddar cheese slurry was compared to that of encapsulated nisin-A. The encapsulated nisin was more effective, with 1.0 log10 reductions of viable spores after one week at 30 °C and 4 °C. Spores were not detected for three weeks at 4 °C in cheese slurry made with 1.3% salt, or during week 2 with 2% salt. Gas production was observed after one week at 30 °C only in the control slurry made with 1.3% salt. In slurry made with the protective strain, the reduction in C. tyrobutyricum count was 0.6 log10 in the second week at 4 °C with both salt concentration. At 4 °C, nisin production started in week 2 and reached 97 µg/g after four weeks. Metabarcoding analysis targeting the sequencing of 16S rRNA revealed that the genus Lactococcus dominated for four weeks at 4 °C. In cheese slurry made with 2% salt, the relative abundance of the genus Clostridium decreased significantly in the presence of nisin or the protective strain. The results indicated that both strategies are able to control the growth of Clostridium development in Cheddar cheese slurries.


2017 ◽  
Vol 80 (12) ◽  
pp. 2137-2146 ◽  
Author(s):  
Dimitrios Noutsopoulos ◽  
Athanasia Kakouri ◽  
Eleftheria Kartezini ◽  
Dimitrios Pappas ◽  
Efstathios Hatziloukas ◽  
...  

ABSTRACT This study evaluated in situ expression of the nisA gene by an indigenous, nisin A–producing (NisA+) Lactococcus lactis subsp. cremoris raw milk genotype, represented by strain M78, in traditional Greek Graviera cheeses under real factory-scale manufacturing and ripening conditions. Cheeses were produced with added a mixed thermophilic and mesophilic commercial starter culture (CSC) or with the CSC plus strain M78 (CSC+M78). Cheeses were sampled after curd cooking (day 0), fermentation of the unsalted molds for 24 h (day 1), brining (day 7), and ripening of the brined molds (14 to 15 kg each) for 30 days in a fully controlled industrial room (16.5°C; 91% relative humidity; day 37). Total RNA was directly extracted from the cheese samples, and the expression of nisA gene was evaluated by real-time reverse transcription PCR (qRT-PCR). Agar overlay and well diffusion bioassays were correspondingly used for in situ detection of the M78 NisA+ colonies in the cheese agar plates and antilisterial activity in whole-cheese slurry samples, respectively. Agar overlay assays showed good growth (>8 log CFU/g of cheese) of the NisA+ strain M78 in coculture with the CSC and vice versa. The nisA expression was detected in CSC+M78 cheese samples only, with its expression levels being the highest (16-fold increase compared with those of the control gene) on day 1, followed by significant reduction on day 7 and almost negligible expression on day 37. Based on the results, certain intrinsic and mainly implicit hurdle factors appeared to reduce growth prevalence rates and decrease nisA gene expression, as well as the nisin A–mediated antilisterial activities of the NisA+ strain M78 postfermentation. To our knowledge, this is the first report on quantitative expression of the nisA gene in a Greek cooked hard cheese during commercial manufacturing and ripening conditions by using a novel, rarely isolated, indigenous NisA+ L. lactis subsp. cremoris genotype as costarter culture.


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