Part Six, Chapter Three: On Ripening Hard Cheese in a Jar (Khābiya) and Ways For Cooking It; and Remedying Butter and Milk

2021 ◽  
pp. 400-402
Keyword(s):  
2020 ◽  
Vol 56 (4) ◽  
pp. 18-20
Author(s):  
A.D. Koval ◽  
◽  
A.N. Belov ◽  
A.V. Grishkova ◽  
A.V. Mironova ◽  
...  

2021 ◽  
Vol 28 ◽  
pp. 100190
Author(s):  
Jaqueline Auer ◽  
Michael Reiter ◽  
Sascha Senck ◽  
Andreas Reiter ◽  
Johann Kastner ◽  
...  

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.


Author(s):  
Wenfan Cao ◽  
Julie Aubert ◽  
Marie-Bernadette Maillard ◽  
Françoise Boissel ◽  
Arlette Leduc ◽  
...  

2007 ◽  
Vol 17 (7) ◽  
pp. 826-834 ◽  
Author(s):  
Jeremiah J. Sheehan ◽  
Jorge C. Oliveira ◽  
Alan L. Kelly ◽  
Paul L.H. Mc Sweeney
Keyword(s):  

2021 ◽  
Vol 149 ◽  
pp. 110654 ◽  
Author(s):  
Gabriele Rocchetti ◽  
Sara Michelini ◽  
Valentina Pizzamiglio ◽  
Francesco Masoero ◽  
Luigi Lucini

2010 ◽  
Vol 73 (1) ◽  
pp. 88-91 ◽  
Author(s):  
C. ZWEIFEL ◽  
N. GIEZENDANNER ◽  
S. CORTI ◽  
G. KRAUSE ◽  
L. BEUTIN ◽  
...  

Food is an important vehicle for transmission of Shiga toxin–producing Escherichia coli (STEC). To assess the potential public health impact of STEC in Swiss raw milk cheese produced from cow's, goat's, and ewe's milk, 1,422 samples from semihard or hard cheese and 80 samples from soft cheese were examined for STEC, and isolated strains were further characterized. By PCR, STEC was detected after enrichment in 5.7% of the 1,502 raw milk cheese samples collected at the producer level. STEC-positive samples comprised 76 semihard, 8 soft, and 1 hard cheese. By colony hybridization, 29 STEC strains were isolated from 24 semihard and 5 soft cheeses. Thirteen of the 24 strains typeable with O antisera belonged to the serogroups O2, O22, and O91. More than half (58.6%) of the 29 strains belonged to O:H serotypes previously isolated from humans, and STEC O22:H8, O91:H10, O91:H21, and O174:H21 have also been identified as agents of hemolytic uremic syndrome. Typing of Shiga toxin genes showed that stx1 was only found in 2 strains, whereas 27 strains carried genes encoding for the Stx2 group, mainly stx2 and stx2vh-a/b. Production of Stx2 and Stx2vh-a/b subtypes might be an indicator for a severe outcome in patients. Nine strains harbored hlyA (enterohemorrhagic E. coli hemolysin), whereas none tested positive for eae (intimin). Consequently, semihard and hard raw milk cheese may be a potential source of STEC, and a notable proportion of the isolated non-O157 STEC strains belonged to serotypes or harbored Shiga toxin gene variants associated with human infections.


2017 ◽  
Vol 24 (1) ◽  
pp. 67-77 ◽  
Author(s):  
Facundo Cuffia ◽  
Carina V Bergamini ◽  
Irma V Wolf ◽  
Erica R Hynes ◽  
María C Perotti

2016 ◽  
Vol 60 ◽  
pp. 165-173 ◽  
Author(s):  
Marta Ávila ◽  
Natalia Gómez-Torres ◽  
David Delgado ◽  
Pilar Gaya ◽  
Sonia Garde

Sign in / Sign up

Export Citation Format

Share Document