The effect of Egyptian honeybee propolis on the growth of Aspergillus versicolor and sterigmatocystin biosynthesis in Ras cheese

Propolis is a natural product collected by honeybee workers. The product was tested for its antifungal effect against Aspergillus versicolor ATCC 12996 as well as biosynthesis of sterigmatocystin during ripening of Egyptian Ras cheese. The use of different concentrations of aqueous propolis extract 250, 500 and 1000 part per million (ppm) on the cheese surface was investigated. Mould growth and toxin production were completely inhibited at the highest concentration 1000 ppm, while the lower concentrations exhibited definite fungistatic activity during 90 days of ripening. Control cheese demonstrated that the amount of sterigmatocystin produced was proportional to the growth of Asp. versicolor during three months of ripening. It could be concluded that propolis concentration of 1000 ppm could prevent mould growth and sterigmatocystin production in Ras cheese. The economic as well as the public health importance of propolis as a natural preservative in cheese manufacture is discussed.     

Manufacture and quality of UF Ras cheese

Ras cheese was made by means of the traditional method from cow's milk and milk concentrated by ultrafiltration to concentration factors 2 and 5, and from diafiltered x5 retentate. The fresh cheese yield was determined and cheese was ripened for 3 months, changes in moisture, fat, nitrogen fractions, pH, acidity and ripening indices were followed periodically during the ripening period. The organoleptic properties of the cheese were also assessed. UF Milk retentate gave higher cheese yield depending on concentration factor. UF Ras cheese from high concentrated retentate was characterized by slow protein degradation, flavour development and hard texture. The composition and properties of UF Ras cheese from x2 retentate were close to that of traditional Ras cheese.     

β-Galactosidase in the acceleration of Ras cheese ripening

An attempt has been carried out to accelerate Ras cheese ripening by pre-treatment of cheese milk with β-galactosidase. Milk was treated with a β-galactosidase enzyme preparation, namely lactozym (1 ml/kg milk), at 33°C for 1 h or at 4°C for 18 h and used for Ras cheese making. Flavour intensity, formation of soluble nitrogen compounds, free amino acids and liberation of free fatty acids were enhanced in cheese made from β-galactosidase treated milk. In addition, the ripening period was reduced to 2 months compared with 4 months required for control cheese. Treatment of cheese milk with β-galactosidase at 4°C or 33°C showed a similar effect on the properties of cheese.     

Manufactore of Ras cheese from ultrafiltered milk supplemented with caseinates

Whole cow's milk was ultrafiltered (conc. Factor 5), sodium and calcium caseinate were added to the milk retentate at the rate of 0.5 and 0.75% (w/w) of the milk. Ras cheese was made from milk retentate supplemented with different levels of caseinate salts, as well as unsupplemented retentates, and compared with Ras cheese made by the traditional method. Retentate supplemented with 0.5% Na and Ca caseinate was suitable for Ras cheese-making with limited whey drainage, supplementation of retentate with 0.75% Ca caseinate gave defective cheese at the end of ripening, while Na caseinate increased soluble N and free fatty acids in the cheese. Organoleptic scoring showed that supplementation with Na caseinate enhanced cheese ripening.     

The effect of ripening and cooking temperatures on proteolysis and lipolysis in Manchego cheese

The influence of ripening temperature on proteolysis and lipolysis was studied on four lots of raw ewe's milk Manchego cheese held for 60 days at 5, 10, 15 or 20°C. Mean levels of pH 4·6, trichloroacetic acid and phosphotungstic acid soluble N in 20°C cheeses were 52%, 78% and 95% higher than the respective levels in 5°C cheeses at the end of the ripening period. Free fatty acids content after 60 days was 90% higher in 20°C cheeses than in 5°C cheeses. Significant effects of the cooking temperature of the curd (30, 36, 38 or 40°C) on pH, moisture and NaCl content were recorded, but levels of nitrogenous fractions or free fatty acids in 60-day cheeses were not affected.     

Distribution of aflatoxin M1 in cheese obtained from milk artificially contaminated

Small-scale manufacture of cheese using artificially AFM1 contaminated milk as raw material to study the distribution of such toxin both in whey and in cheese, was carried out. Whole milk with undetectable levels of AFM1 was used. The toxin was added in concentration that varied from 1.7 to 2.0 microg/l of milk. After the home-made production of cheese, the concentration of AFM1 was determined both in whey and in cheese, using the enzymatic immunoassay technique. The greatest proportion, 60%, was detected in whey while 40% AFM1 remained in cheese.     

The manufacture of Ras cheese from gamma irradiated milk

Cheese milk exposed to gamma irradiation at a dose of 0·5 Mrad was used in the manufacture of Ras cheese. Quality and ripening of cheese made from irradiated milk were compared with those of cheese made from heat-treated milk.Gamma irradiation of cheese milk reduced the total bacterial count and spore formers by 98·98% and 95·77%, respectively, and eliminated the coliform and pathogenic bacteria. This treatment slightly increased the acid and peroxide values of milk fat, as well as the time required for complete coagulation of milk.An oxidized flavour in the fresh and 1-month-old gamma-irradiated milk (GIM) cheese disappeared during ripening. At the end of ripening, GIM cheese had a better consistency and increased flavour compared with cheese made from heated milk.Ras cheese made from GIM differed little in gross chemical composition but contained higher concentrations of soluble nitrogen compounds and of Free Fatty Acids than the control. Irradiation had a stimulating effect on the total, proteolytic and lipolytic bacterial counts during cheese ripening.     

THE CONTRIBUTION OF HERBS TO THE ACCUMULATION OF HISTAMINE IN "OTLU" CHEESE

The aim of this study was to determine the effect of herbs and the use of raw milk on histamine accumulation in “Otlu” (Herby) cheese during ripening. Cow's milk was used for the cheese production. The milk was divided into two main groups: one was used raw and the other was pasteurized at 65C for 30 min. Each group was further divided into two subparts, one of which was used as control (without herbs), while 2% (w/v) of the herbs were added into the other to produce Herby cheese. All cheeses were ripened at 7C for 90 days. The cheese samples were analyzed in terms of histamine content, titratable acidity, dry matter, salt and degree of ripening on days 5, 30, 60 and 90. Total mesophilic aerobic bacteria (MAB) were also counted during ripening. The use of raw milk and the addition of herb both increased histamine formation in Otlu cheeses (P < 0.05). Moreover, higher water‐soluble nitrogen values, as degree of ripening, were obtained from both raw milk and herb‐added cheeses. The number of MAB was higher in raw cheeses (P < 0.05) and also herb‐added cheeses. The study suggests that the addition of herbs may facilitate histamine formation in Herby cheese.     

The effect of ovine and bovine milk on the textural properties of Lighvan cheese during ripening

The effect of milk origin on the physicochemical characteristics, microstructure and texture of Lighvan cheese was investigated over a 90‐day ripening period. Besides fat, other physicochemical properties of Lighvan cheese were affected by milk type. The moisture content of Lighvan cheese decreased when half or all the ovine milk was substituted with bovine milk. The Lighvan cheese's microstructural properties and porosity were affected by type of milk and ripening time. Compaction of cheeses manufactured from ovine and mixed ovine and bovine milk is similar, and more than that of bovine Lighvan cheese. Ovine Lighvan cheese is harder and less brittle than bovine and mixed bovine and ovine.     

Nutritional Evaluation of Accelerated Ripened Cheddar Processed Cheese

Accelerated ripened Cheddar cheese was prepared by blending two parts of shredded curd made from standardized cow's milk with one part of 5.2% NaCl solution and ripening at 30°C for 8 days. On a dry matter basis, protein and fat of accelerated ripened cheese were similar to that of conventionally ripened Cheddar cheese, while lactose and total ash were greater. Similar observation was made for processed cheese samples. No change in vitamin A or in riboflavin but a fourfold increase in folic acid was observed during accelerated ripening. Protein efficiency ratio, net protein utilization and digestibility coefficient by rat tests were slightly but significantly higher for conventionally ripened processed cheese. However, no difference in biological value was observed.     

Influence of lactic starter inoculation,curd heating and ripening temperature on Staphylococcus aureus behaviour in Manchego cheese

Growth and survival of Staphylococcus aureus were investigated in 52 lots of raw ewe's milk Manchego cheese manufactured and ripened under different conditions. A 5.8-fold reduction in S. aureus counts after 60 days of ripening was obtained by inoculating milk with 1% Streptococcus lactis culture, and a further 2.0-fold reduction could be achieved by adding 0.1% Lactobacillus plantarum culture. Curd heating temperature had a significant effect on S. aureus survival, with counts 4–5 times lower in cheese from 30° C curd than in cheese from curd heated at 36–40° C. Ripening temperature was the parameter with the greatest influence on S. aureus counts, which reached in cheese cured at 10° C or 20° C for 60 days levels 10 and 100 times lower, respectively, than in cheese held at 5° C.     

Effects of processing and storage of dairy products on lindane residues and metabolites

Residue levels of lindane and its metabolites were monitored in 25 samples of raw and sterilized milk, yoghurt, Domiati & Ras cheese collected from different regions in the Great Cairo Governorates. The concentrations of lindane followed the order: raw milk > Domiati cheese > sterilized milk > yoghurt=Ras cheese. Most samples were found to contain three or more metabolites at different levels. Heat treatments (pasteurization, boiling and sterilization) reduced lindane levels. The reduction percentages were 65.0–73.0, 75.0–85.4, and 84.4% for lindane content and 0.1–43.0, 37.3–55.4, and 76.6% for total of lindane and its metabolites on pasteurization, boiling, and sterilization, respectively. A gradual reduction of lindane ranging from 1.4–8.9% was observed during the manufacture and storage of yoghurt for three days in a refrigerator. The reduction of lindane was higher in Domiati cheese made by acid-enzyme coagulation than that made by enzyme coagulation. On the other hand, the manufacturing process of Ras cheese removed 36.7% lindane after storage (ripening) periods of 6 months. This may be due to the effect of microorganisms during storage.     

Biocontrol of psychrotrophic enterotoxigenic Bacillus cereus in a nonfat hard cheese by an enterococcal strain-producing enterocin AS-48

Bacillus cereus is a food poisoning bacterium of great concern, especially in milk products. In this study, we describe the efficient control of the psychrotrophic and toxigenic strain B. cereus LWL1 in milk and in a nonfat hard cow's cheese by the enterocin AS-48 producer strain Enterococcus faecalis A-48-32 (Bac+). No viable B. cereus cells were detected after 72 h incubation in milk coinoculated with the AS-48-producing strain and B. cereus. Diarrheic toxin production was also markedly inhibited by the Bac+ strain to eightfold lower levels compared with control cultures of B. cereus. In cheeses manufactured by inoculation with a commercial starter (about 6.8 log CFU/ml) and B. cereus (about 4 log CFU/ml), the latter reached 6.27 log CFU/g after 5 days of maturation, and approximately 8 log CFU/g after 15 days. However, in cheeses made from milk inoculated with the starter along with a mixture of E. faecalis-B. cereus (2/1 ratio), counts of B. cereus decreased by approximately 1.0, 2.0, 4.32, and 5.6 log units with respect to control cheeses after 5, 10, 15, and 30 days of ripening, respectively. Growth of E. faecalis A-48-32 was associated with enterocin AS-48 production and persistence in cheese. Interestingly, growth of starter cultures was not affected by the Bac+ strain, and neither was lactic acid production. These results clearly indicate that E. faecalis A-48-32 produced satisfactory amounts of bacteriocin in cheese and support the potential use of AS-48-producing strains as culture adjuncts to inhibit B. cereus during cheese manufacture and ripening.     

Influence of milk centrifugation, brining and ripening conditions in preventing gas formation by Clostridium spp. in Gouda cheese

This study examined milk centrifugation, increased salt concentration, and low ripening temperature as potential strategies to prevent late blowing caused by gas-forming Clostridium spp. in Gouda cheese. The survival of clostridia spores in cheese brine and their ability to enter Gouda cheese during brining was also evaluated. Centrifugation (3000 x g for 30 s) of contaminated milk resulted in > 60% spore reduction, with increased spore reduction at greater centrifugal forces. Low levels of C. tyrobutyricum and C. sporogenes spores survived in saturated (23%, w/v) brine with 2% (v/v) added whey at 15 degrees C for 63 days, while C. beijerinckii and C. butyricum spores were not detectable on days 4 and 35, respectively. Spores of C. tyrobutyricum in brine infiltrated Gouda cheese during 2 h of brining at 13 degrees C resulted in production of small gas holes during ripening. In Gouda cheese slurry stored at 13 degrees C, three C. tyrobutyricum strains plus one of three C. sporogenes strains germinated in the slurry with no added salt. Of three C. tyrobutyricum strains stored at 13 degrees C in slurries with higher water-phase salt concentrations of 2.4 and 3.6%, two strains and one strain germinated, respectively. No germination of spores was detected in any cheese slurry stored at 5 or 8 degrees C. Milk centrifugation, increased percent water-phase salt, absence of spores in brine, and decreased ripening temperature are all potentially important measures against gas production by Clostridium spp. in Gouda cheese.     

Proteolytical,Chemical, Textural and Sensorial Changes During the Ripening of Turkish White Cheese Made of Pasteurized Cows' Milk

Turkish White Cheese (TWC), manufactured from pasteurized cows' milk, was ripened over 90 days at 4°C, and proteolytical, chemical, textural, and sensorial changes were investigated. The main compositional characteristics of TWC are low content of total solids (TS) (39.80–41.75 g/100 g of cheese), high content of fat (49.12–49.91 g/100 g of TS) and salt (8.69–9.35 g/100 g of TS). The lactose level, pH values, and titratable acidity of samples were found between 0.74–2.05 g/100 g of TS, 4.39–4.68, and 0.73–1.12 g lactic acid/100 g of cheese, respectively. Changes in nitrogenous fractions, Urea-PAGE electrophoregram and RP-HPLC chromatograms showed that TWC undergoes a slight proteolysis. Textural attributes of TWC were significantly (p?<?0.05) affected by the ripening period. The highest overall acceptance scores were found at the 60 days of ripening. Bitterness was identified at the end of the 60 and 90 days of ageing period.     

Evaluation of cheese authenticity and proteolysis by HPLC and urea–polyacrylamide gel electrophoresis

Chromatographic and electrophoretic methods have been established as useful tools in characterising cheese ripening and in the detection of milk adulteration. The purpose of this work was to evaluate casein proteolysis of cheeses made from bovine, ovine or mixtures of bovine and ovine milks, as well as ovine cheese authenticity, for 30 days of ripening by HPLC and urea–polyacrylamide gel electrophoresis.Complementary information was obtained by both techniques when applied to the study of casein proteolysis during 30 days of ripening of ovine milk cheeses, ovine milk cheeses with 10% and 20% of bovine milk and bovine milk cheeses, manufactured according to the traditional Terrincho technology. For ovine cheeses, α-casein was the fraction that showed the higher degradation during cheese ripening. A similar behaviour was observed for ovine milk cheese with 10% of bovine milk. The profile for ovine milk cheese with 20% of bovine milk was more similar to that obtained for bovine cheese. Concerning bovine milk cheeses, electrophoresis was the most sensitive technique for the evaluation of proteolysis in these cheeses.Ten and 20% of bovine milk could be detected in ovine milk cheeses by urea–polyacrylamide gel electrophoresis and HPLC, respectively, even after 30 days of ripening.     

Fate of pyrrolizidine alkaloids during processing of milk of cows treated with ragwort

ABSTRACT

To investigate the fate of pyrrolizidine alkaloids (PAs) during milk processing, milk of cows treated via rumen fistula with a mixture of 84% (w/w) ragwort (Jacobaea vulgaris, syn. Senecio jacobaea) and 16% narrow-leaved ragwort (Senecio inaequidens) was processed using laboratory scale heating systems with industrial settings. Pasteurised and sterilised (UHT) milk were produced, as well as set-type yoghurt and cheese. Samples were analysed for 29 PAs using LC-MS/MS, of which 11 PAs were detected above LOQ in the samples (0.1 µg l^?1). Alterations in the PA concentration and composition between the standardised milk and the corresponding end-product(s) were evaluated. The heat treatments applied for pasteurisation and UHT sterilisation to prepare semi-skimmed consumption milk did not affect the PA levels in the end-products. In yoghurt, after fermentation of standardised milk (6 h, pH 4.4), 73% of total PAs were recovered. The PA concentration, specifically dehydrojacoline, was decreased, although not quantifiable, during cheese production. A further decrease of 38% during 6 weeks of ripening was observed. The results show that the PA concentration of natural contaminated cow’s milk is not affected by heat treatment applied for pasteurised and sterilised milk, but that microbial fermentation of the milk leads to a lowered PA concentration in yoghurt and cheese. This is probably due to microbiological degradation, since PAs are fairly stable under acidic conditions.     

Free amino acid content of goat's milk cheese made with animal rennet and plant coagulant

BACKGROUND: Enzymes present in the flowers of Cynara cardunculus (cyprosins) are used in the production of some traditional Spanish and Portuguese cheeses, replacing animal rennet. The aim of this work was to study the changes that take place in free amino acids during the ripening of a goat's milk cheese (Murcia al Vino) manufactured with plant coagulant (PC) or animal rennet (AR). RESULTS: The total free amino acid (TFAA) concentration increased during ripening, with Ile, Val, Ala, Phe, Gaba, Arg and Lys representing more than 50% of the TFAA content at 60 days in both types of cheese. The TFAA concentration was significantly higher in cheeses made with PC (854 mg 100 g^?1 total solids (TS)) than those made with AR (735 mg 100 g^?1 TS). The concentration of most free amino acids, especially His, Ser, Gln, Thr, Ala, Met and Ile, was higher in the PC cheese. CONCLUSION: Cheese made using PC as coagulant presented higher contents of free amino acid throughout the ripening period than cheese made using AR. Therefore we can conclude that the use of PC to produce Murcia al Vino goat's cheese would accelerate the ripening process as a result of increased cyprosin proteolytic activity. Copyright © 2011 Society of Chemical Industry     

Improving the quality of Ras-type cheese made from recombined milk containing high levels of total solids

Ras type cheese was made from recombined milk (RM) containing normal (12·5%) or high levels of Total Solids (TS) (25%, 32% or 40%) using fresh or recombined cream. Cheese curds obtained from RM containing high TS levels were moulded directly or after washing with warm water (50°C) for 10 min before moulding. The cheeses were matured at 7°C or 15°C. Cheese made from fresh milk was better in flavour and consistency than any of the cheeses made from RM. Use of RM in which fresh cream was used gave cheeses of better quality than those made from RM containing recombined cream. Washing the curd made from all RMs resulted in cheeses with better flavour and body characteristics than those made from unwashed curd. Cheese made from RM containing 25% TS with or without washing of the curds was of better quality than those made from RM containing 32% or 40% TS.The changes of nitrogenous fractions, degradation of α_sI- and β-caseins, accumulation of free amino acids and the formation of free fatty acids were reduced as the level of TS in RM was increased. All cheeses made from washed RM curd showed greater proteolysis and lipolysis compared with those made from unwashed curd. Storage of RM cheese at 15°C accelerated its ripening and improved cheese quality compared with ripening at 7°C.     

FATE OF AFLATOXIN M1 IN KASHAR CHEESE

The distribution and stability of aflatoxin M₁ (AFM₁) in Kashar cheese were investigated. Raw milk samples were spiked with AFM₁ at the levels of 50, 250 and 750 ng/L. Distribution of toxin in milk, cheese curd, whey, kneading brine and cheese, and its stability during ripening were determined by high‐performance liquid chromatography. Concentrations of AFM₁ in curds for each contamination level were 2.93, 3.19 and 3.37 times higher than those in milk. After syneresis, the percentage distribution of AFM₁ was 40–46% in curds and 53–58% in whey indicating that relatively higher concentration of toxin passed to whey. Moreover, by the kneading process approximately 2–5% of AFM₁ passed to kneading brine. Compared to the initial spiking level, the percentage of toxin in cheeses varied between 35–42%. Over a 60‐day storage period, there was no decrease in the concentration of AFM₁, suggesting that the toxin was stable during ripening.