Effect of On-Farm Heating and Storage of Milk on Cottage Cheese Yield

Effect of on-farm heat treatment of milk on cottage cheese yields was studied. Fresh, raw milk heated to 74°C for 10 s was cooled and stored for 7 days at 3°C. Control and experimental lots of milk were separated and pasteurized at 72°C for 15 s and were used to make cottage cheese. Microbiological, shelf-life, flavor, and texture studies showed the experimental lots of cheese were as good as or better than control lots. Yield of cottage cheese was significantly higher when made from heated milk.     

Detection of aflatoxin M1 in milk,cheese and sour cream samples from Costa Rica using enzyme-assisted extraction and HPLC

Aflatoxins are toxic fungal metabolites, which can be found in feed. Aflatoxin M₁ (AFM₁) is excreted into milk when ruminants ingest aflatoxin B₁ contaminated feedstuffs. Due to its carcinogenic potential, contamination of milk and dairy products with AFM₁ may pose a risk for consumers. Hence, it is considered a public health concern. In this survey, the level of AFM₁ contamination of dairy products marketed in Costa Rica was determined by enzyme-assisted extraction, immunoaffinity clean-up and high-performance liquid chromatography coupled with a fluorescent detector (HPLC-FLD) in fluid milk (n = 70), fresh cheese (n = 70) and sour cream (n = 70) collected at local convenience stores and supermarkets. AFM₁ concentrations in milk and fresh cheese ranged from 19 to 629 ng/L and from 31 to 276 ng/L, with mean values of 136 ng/L and 74 ng/L, respectively, whereas none of the sour cream samples analysed tested positive for this aflatoxin. In 30 milk samples, and 10 cheese samples, AFM₁ concentrations surpassed threshold concentrations as established by the European Commission. Thus, sour cream and – to a lesser extent – cheese manufacturing seems to reduce the amount of AFM₁ present in milk, possibly due to fraction redistribution or microbiological degradation. The survey results reveal improper quality control procedures in the Costa Rican dairy industry. Therefore, a surveillance programme for dairy products in our country is recommended.     

Assessment of aflatoxin M1 levels in selected dairy products in north‐western Iran

The purpose of this survey was to evaluate the natural occurrence and content of aflatoxin M_1, AFM_1, in dairy products marketed in Urmia. During September 2007, 40 samples of pasteurised milk, 40 samples of ultra high temperature‐treated (UHT) milk, 40 samples of creamy cheese and 40 samples of Iranian Feta cheese were collected from different supermarkets in Urmia city. AFM₁ contents were determined by the competitive enzyme‐linked imunosorbent assay (ELISA) technique. All milk samples analysed showed a mean of AFM₁ concentrations lower than the permissible level of 50 ng/kg in Iran (23.22 and 19.53 ng/kg in pasteurised milk and UHT milk respectively). The mean levels of AFM₁ contamination were 43.31 ng/kg in Feta cheeses and 21.96 ng/kg in creamy cheeses. The potential risk of human exposure to aflatoxin M₁ via consumption of milk and milk products is well known. Dairy products must therefore be evaluated for aflatoxin and kept free from fungal contamination as much as possible.     

Cottage Cheese from Ultrafiltered Skim Milk Retentates in Industrial Cheese Making

Ultrafiltered skim milk retentates were transported to a large industrial cottage cheese plant for milk supplementation leading to cottage cheese. The resulting industrial products were observed for composition, yields, whey component losses, and quality.Ten lots of small curd cottage cheese were made in vats containing up to 6593 kg skim milk. Retentate supplemented skim milks, concentrated approximately 10% (1.1:1) and 20% (1.2:1) in total protein, were very similar in initial composition to the controls. Mean cheese yield values from milks supplemented to 1.2:1 total protein were significantly higher than mean unsupplemented control milk values. Cheese yield efficiencies, per kilogram total solids, were also significantly higher in the retentate cheese but not when calculated per kilogram total protein.Total solids, total protein, and ash were higher in cottage cheese wheys from retentate supplemented cheese and were directly related to retentate supplementation concentration. Mean whey component loss per kilogram cheese exhibited significant decreases from milks of higher retentate supplementation. Retentate supplemented skim milk produced industrial cottage cheese of comparable quality to cheese made from unsupplemented control skim milks.     

Estimation of Residual Pepsin and Chymosin Activity in Curd,

Pasteurized milk (225 g) adjusted to pH 6.2 was set with 3.5 milk clotting units of chymosin (EC 3.4.23.4). The same amount of milk at pH 5.8 was set with 3.5 milk clotting units of porcine pepsin (EC 3.4.23.1). Fifteen minutes after clotting, the curd was broken, and curd and whey were separated by centrifugation at 3500 × g for 20 min. The curd (30 g) was extracted at pH 6.8 in 450 ml water or at pH 6.2 (chymosin) or 5.8 (pepsin) in 450 ml 1 M sodium chloride.Chymosin was completely released from the curd and accounted for by both methods of extraction. Pepsin was completely released and accounted for after extraction in 1 M sodium chloride at pH 5.8 but was partly inactivated during extraction at pH 6.8.Assay of curd extracts and whey by a linear agar diffusion test accounted for 102 ± 6% of the pepsin activity added to milk when the curd was extracted in 1 M sodium chloride. Extraction at pH 6.8 allowed recovery of only 63% of the activity. Chymosin recovery was 100 ± 5% by both methods of curd extraction.     

Ultrafiltration of Milk on French Farms and in the Making of a New Specialty Cheese Industry

Ultrafiltration and thermization of milk on dairy farms in France have been under study since 1979. More recently five dairy farms in Brittany have been routinely producing 2:1 whole milk retentate for Emmental and St. Paulin cheese making. The milk processed is ultrafiltered at 35°C and thermized at 72°C for 15 s in an Ultratherm unit. Cheese quality generally appears satisfactory.In Eastern France a new specialty cheese industry has been started utilizing 4.5:1 whole milk retentate produced by ultrafiltration conducted at 40°C. The specialty cheese attains its characteristic white surface from Penicillium album mold. It has a bland, nutty flavor and very soft, smooth texture. A surface bluing phenomenon occurs after 14 d.     

Survey of aflatoxin M1 in milk and dairy products consumed in Burdur,Turkey

The aim of this study was to investigate the occurrence of aflatoxin M₁ (AFM₁) in dairy product samples in Burdur city. A total of 315 samples of dairy products were collected during 2008. Of the 315 samples analysed, AFM₁ in 246 samples (78.1%) was found to range from 5.5 to 800 ng/kg. In addition, AFM₁ levels of 16 raw milk, two pasteurised milk, only one milk powder and three white cheese samples were above the Turkish Food Codex. It is concluded that the occurrence of AFM₁ in dairy products may be considered as a possible hazard for public health.     

Genetic analysis of coagulation properties,curd firming modeling,milk yield,composition, and acidity in Sarda dairy sheep

Sheep milk is an important source of food, especially in Mediterranean countries, and is used in large part for cheese production. Milk technological traits are important for the sheep dairy industry, but research is lacking into the genetic variation of such traits. Therefore the aim of this study was to estimate the heritability of traditional milk coagulation properties and curd firmness modeled on time t (CF_t) parameters, and their genetic relationships with test-day milk yield, composition (fat, protein, and casein content), and acidity in Sarda dairy sheep. Milk samples from 1,121 Sarda ewes from 23 flocks were analyzed for 5 traditional coagulation properties by lactodynamographic tests conducted for up to 60 min: rennet coagulation time (min), curd-firming time (k₂₀, min), and 3 measures of curd firmness (a₃₀, a₄₅, and a₆₀, mm). The 240 curd firmness observations (1 every 15 s) from each milk sample were recorded, and 4 parameters for each individual sample equation were estimated: rennet coagulation time estimated from the equation (RCT_eq), the asymptotic potential curd firmness (CF_P), the curd firming instant rate constant (k_CF), and the syneresis instant rate constant (k_SR). Two other derived traits were also calculated (CF_max, the maximum curd firmness value; and t_max, the attainment time). Multivariate analyses using Bayesian methodology were performed to estimate the genetic relationships of milk coagulation properties and CF_t with the other traits; statistical inference was based on the marginal posterior distributions of the parameters of concern. The marginal posterior distribution of heritability estimates of milk yield (0.16 ± 0.07) and composition (0.21 ± 0.11 to 0.28 ± 0.10) of Sarda ewes was similar to those often obtained for bovine species. The heritability of rennet coagulation time as a single point trait was also similar to that frequently obtained for cow milk (0.19 ± 0.09), whereas the same trait calculated as an individual equation parameter exhibited larger genetic variation and a higher heritability estimate (0.32 ± 0.11). The other curd firming and syneresis traits, whether as traditional single point observations or as individual equation parameters and derived traits, were characterized by heritability estimates lower than for coagulation time and for the corresponding bovine milk traits (0.06 to 0.14). Phenotypic and additive genetic correlations among the 11 technological traits contribute to describing the interdependencies and meanings of different traits. The additive genetic relationships of these technological traits with the single test-day milk yield and composition were variable and showed milk yield to have unfavorable effects on all measures of curd firmness (a₃₀, a₄₅, a₆₀, CF_P, and CF_max) and t_max, but favorable effects on both instant rate constants (k_CF and k_SR). Milk fat content had a positive effect on curd firmness traits, especially on those obtained from CF_t equations, whereas the negative effects on both coagulation time traits were attributed to the milk protein and casein contents. Finally, in view of the estimated heritabilities and additive genetic correlations, enhancement of technological traits of sheep milk through selective breeding could be feasible in this population.     

Proteolysis in Milk Associated with Increasing Somatic Cell Counts

Individual cow samples were collected and preserved with potassium dichromate. Somatic cells counts were determined. Tyrosine value was used as an index of proteolysis. Sixty-six samples ranged in somatic cell count from < 50,000 to > 2,000,000/ml. Initial milk tyrosine values and tyrosine values for milks incubated for 24 h at 37°C showed proteolytic activity increased with increasing somatic cell count. The increase in proteolysis in preserved milk refrigerated for 72 h at 6.7°C was over 1.5 times greater in milks with > 1,000,000 cells/ml than in milks with < 60,000 cells/ml. When preserved milks were laboratory pasteurized, cooled, and stored at 6.7°C for 14 d, some proteolytic activity was detected in milks at all concentrations of somatic cells, and proteolysis increased as somatic cell counts increased. Laboratory-pasteurized samples of milk with various somatic cell counts were also incubated at 30°C for 3 and 6 h to duplicate the proteolysis that could occur during the ripening, coagulation, cutting, and cooking steps of cheese making. Again, the greatest increases in tyrosine were in milks with high somatic cell count. Protease(s) associated with elevated somatic cell counts will damage raw milk quality upon storage, pasteurized fluid milk over shelf-life, and milk during cheese making.     

Production of conjugated linoleic acid enriched milk and dairy products from cows receiving grass silage supplemented with a cereal-based concentrate containing rapeseed oil

Opportunities for the production of milk and dairy products enriched with cis-9, trans-11 conjugated linoleic acid (CLA) were investigated. Eighteen mid-lactation cows were used in a continuous-design for 7 weeks. During the first week, cows received grass silage ad libitum supplemented with 10 kg per day of a cereal-based concentrate (control) that was replaced with a concentrate containing 50 g kg⁻¹ of rapeseed oil (RO). Changes in milk fatty acid composition were monitored on a weekly basis and milk produced was used to manufacture Edam cheese and butter. Inclusion of RO in the concentrate supplement increased the mean levels of trans-octadecanoic, monounsaturated, CLA and polyunsaturated fatty acid in the milk fat from 1.6, 25.7, 0.46 and 2.8 to 4.3, 35.3, 1.02 and 3.9 g 100 g⁻¹ total fatty acids, respectively. In contrast, the mean level of saturated fatty acids decreased from 71.4 to 60.7 g  100 g⁻¹ total fatty acids. Changes in milk fatty acid composition due to RO occurred within 7 days, with responses reaching a plateau after 21 days. Furthermore, the CLA concentrations in the milk fat from individual cows ranged between 0.37 and 0.65 and 0.43 and 2.06 g 100 g⁻¹ total fatty acids for the control and RO diet, respectively. CLA enriched milk was used successfully to manufacture of Edam cheese and butter with softer textures but with acceptable organoleptic and storage properties. Processing milk into butter or cheese had no effect on the CLA concentrations indicating that enrichment of dairy products is dependent on the content in raw milk fat.     

Aflatoxin M1 in raw,UHT milk and dairy products in Sicily (Italy)

A survey on 73 milk samples from different animal breeds and 24 dairy products samples from Sicily, Italy, was carried out for the presence of aflatoxin M₁ (AFM1) by LC-fluorescence detection after immunoaffinity cleanup. AFM1 was detected in 48% and 42% of the milk and dairy samples at concentration ranges between <5.0–16.0 and <5.0–18.0 ng L^?1, respectively. Within the raw milk samples, 92% had an AFM1 content below 5.0 ng L^?1, in 7% of the cases it was in the range 5.0–10.0 ng L^?1 and 1% was contaminated between 10.0 and 20.0 ng L^?1. For the dairy products, ultra-high-temperature treated (UHT) milk, milk cream and cheese, the incidence was 42%, of which 83% contained less than 5.0 ng L^?1 and 17% contained 10.0–20.0 ng L^?1 AFM1. The levels of contamination found justify continuous monitoring for public health and to reduce consumer exposure.     

Manufacture of Cheddar cheese from high-pressure-treated whole milk

The cheese-making characteristics of high-pressure (HP)-treated milk were examined. The rennet coagulation time of pasteurised milk decreased after HP treatment at 400 MPa but increased after treatment at 600 MPa. The L-value (whiteness) of milk decreased directly after HP treatment but, over the course of coagulation, whiteness of HP-treated milk increased to the same level as in the control. Cheddar cheese was then manufactured from raw whole milk or whole milk treated by high-pressure (HP) at 400 MPa (HP400) or 600 MPa (HP600) for 10 min at 20 °C. HP treatment of raw milk at 600 MPa resulted in a 3.66 log reduction in the initial counts of non-starter lactic acid bacteria (NSLAB), decreased protein and fat content, as well as a lower pH compared to the control. Furthermore, higher treatment pressures resulted in increased incorporation of β-lactoglobulin into the cheese curd, with parallel increases in yield by 1.23% and 7.78% for HP400 and HP600 cheeses, respectively. Overall, this study showed that the effects of HP treatment on milk proteins increased rennet coagulation times and changes in cheese composition at day 1.Industrial relevanceHigh-pressure treatment is a novel technology which has been applied to a number of commercial food products. In this study, HP-induced changes in milk proteins resulted in increased cheese yields and increased cheese whiteness. In addition, HP treatment significantly reduced the microflora of raw milk cheese. Those attributes could be of interest for both industry and consumer.     

Occurrence of Aflatoxin M1 in raw and processed milk and assessment of daily intake in Lahore,Multan cities of Pakistan

In this survey aflatoxin, M₁ was quantified in raw and processed milk from various areas of two big cities of Punjab province, i.e. Lahore and Multan. The results indicated that approximately 90% of the raw milk samples collected from Lahore city was contaminated with aflatoxin M₁. Similarly, around 92% of the raw milk samples collected from Multan city was contaminated with aflatoxin M₁. All samples of processed milk and tea whiteners were contaminated and 56% of the contaminated processed milk samples and 66% of the contaminated tea whitener samples were violating the maximum limits. The dietary exposure data of AFM₁ among six different groups was calculated, which indicated that the male children population was the most vulnerable group to AFM₁, up to 6.68 ng L^?1 per day and the least affected one was the female group above 20 years of age with 1.13 ng L^?1 per day.     

Characterization of Cheese Curd Ripened with Penicillium caseicolum for Producing a Flavor Concentrate

Camembert cheese was prepared from homogenized milk containing veal oral lipase and ripened in a loose curd form to speed up the ripening process. Traditional hooped cheese was a control. Free fatty acid titer increased from 58 μmole in the fresh cheese to 359 μmole in control cheese and 2,289 μmole/g of cheese fat in loose curd cheese. After 3 wk of ripening, the cheese had 70% of its total protein as water soluble protein as compared to 39% in the hooped cheese. Polyacrylamide gel electrophoresis showed 86% of α_S1-caseins and 35% of β-casein had been degraded in the loose curd cheese. Sensory analysis demonstrated that the loose curd process rapidly produced cheese with intense flavor.     

Improved Complexometric Determination of Calcium in Cheese

Accuracy and repeatability of complexometric methods for measuring calcium in cheese are limited by titration endpoints that are difficult to recognize. Much of this difficulty results from turbidity during titration. An alternative procedure is described in which 2 to 3 g of cheese are ashed, dissolved in dilute acid, and added calcium chloride is back titrated with ethylenediaminetetraacetic acid using hydroxy naphthol blue as indicator. Samples remain free of turbidity, and the titration endpoint is recognized easily.Recovery of calcium from solutions containing magnesium and phosphate was 100.9 ± .3%, indicating that a portion of sample magnesium (about 12%) also was measured. Error caused by magnesium recovery represented less than 1% of true calcium content.Analyses of 10 Cheddar cheese samples by the proposed method and by atomic emission differed by an average of .010% calcium. Mean values of the 10 samples did not differ significantly (P>.05) between methods. Duplicate analyses of 67 Cheddar cheese samples differed by an average of .008 ± .006% calcium. Similar repeatability was achieved by several inexperienced analysts. The method is applied readily to other dairy products.     

Amino acid and soluble nitrogen evolution throughout ripening of Serra da Estrela cheese

Four batches of Serra da Estrela cheese originating from as many dairy farms were sampled throughout the ripening period, and assayed for the evolution of free amino acid (FAA) content, total nitrogen content (TN), water-soluble nitrogen content (WSN), trichloroacetic acid-soluble nitrogen content (TCASN) and phosphotungstic acid-soluble nitrogen content (PTASN). The WSN content increased from 1% (on the day of manufacture) up to 43% of TN by 180 d of ripening, thus reflecting the intense proteolytic activity of the enzymes contributed by the plant coagulant utilized. The TCASN was also found to be high in this cheese by the end of ripening (16–20%), which suggests a high extent of FAA release throughout maturation. The major FAA by 180 d of ripening were Glu, Val, Leu and Lys, representing 56–70% of the total in all four dairies sampled. Cheeses produced from refrigerated milk possessed higher amounts of γ-amino-n-butyric acid (Gaba) and lower amounts of Glu when compared with those manufactured with non-refrigerated milk.     

Alternative Test for Phosphorous in Cheese

A modified test for phosphorous in cheese based on quantitative precipitation, filtration, and indirect titration of milligram quantities of phosphorous is presented. The procedure was designed specifically for Cheddar cheese and was used to analyze a wide range of Cheddar samples including some with atypically high and low calcium and phosphorous. A modification of the procedure permitted measurement of total ash, calcium, and phosphorous in the same cheese sample. With reagent adjustments it is possible to test other cheese varieties as well as other dairy products.Average recovery of phosphorous from 10 replicate solutions containing known amounts of calcium and phosphorous was 99.1 ± .7%. Average recovery of phosphorous added to 10 replicate Cheddar cheese samples was 98.9 ± 1.5%. Ten Cheddar cheeses were analyzed in duplicate by the proposed method and by atomic emission. Results of the two methods differed by an average of .015% phosphorous, a significant difference, but the methods were strongly correlated (r =.94).Duplicate analyses by the proposed method were conducted on 54 Cheddar cheese samples ranging from .427 to .555% phosphorous. The average difference between duplicate measurements was .011 ± .009% phosphorous. The principle of the proposed test and modifications required for cheese analysis are discussed.     

The use of lactoperoxidase for the bleaching of fluid whey

Lactoperoxidase (LP) is the second most abundant enzyme in bovine milk and has been used in conjunction with hydrogen peroxide (H₂O₂) and thiocyanate (SCN^–) to work as an antimicrobial in raw milk where pasteurization is not feasible. Thiocyanate is naturally present and the lactoperoxidase system purportedly can be used to bleach dairy products, such as whey, with the addition of very little H₂O₂ to the system. This study had 3 objectives: 1) to quantify the amount of H₂O₂ necessary for bleaching of fluid whey using the LP system, 2) to monitor LP activity from raw milk through manufacture of liquid whey, and 3) to compare the flavor of whey protein concentrate 80% (WPC80) bleached by the LP system to that bleached by traditional H₂O₂ bleaching. Cheddar cheese whey with annatto (15 mL of annatto/454 kg of milk, annatto with 3% wt/vol norbixin content) was manufactured using a standard Cheddar cheesemaking procedure. Various levels of H₂O₂ (5–100 mg/kg) were added to fluid whey to determine the optimum concentration of H₂O₂ for LP activity, which was measured using an established colorimetric method. In subsequent experiments, fat-separated whey was bleached for 1 h with 250 mg of H₂O₂/kg (traditional) or 20 mg of H₂O₂/kg (LP system). The WPC80 was manufactured from whey bleached with 250 mg of H₂O₂/kg or 20 mg of H₂O₂/kg. All samples were subjected to color analysis (Hunter color values and norbixin extraction) and proximate analysis (fat, protein, and moisture). Sensory and instrumental volatile analyses were conducted on WPC80. Optimal LP bleaching in fluid whey occurred with the addition of 20 mg of H₂O₂/kg. Bleaching of fluid whey at either 35 or 50°C for 1 h with LP resulted in >99% norbixin destruction compared with 32 or 47% destruction from bleaching with 250 mg of H₂O₂/kg, at 35 or 50°C for 1 h, respectively. Higher aroma intensity and increased lipid oxidation compounds were documented in WPC80 from bleached whey compared with WPC80 from unbleached whey. Monitoring of LP activity throughout cheese and whey manufacture showed that LP activity sharply decreased after 30 min of bleaching (17.01 ± 1.4 to <1 U/mL), suggesting that sufficient bleaching takes place in a very short amount of time. Lactoperoxidase averaged 13.01 ± 0.7 U/mL in unpasteurized, fat-separated liquid whey and 138.6 ± 11.9 U/mL in concentrated retentate (11% solids). Lactoperoxidase may be a viable alternative for chemical whey bleaching.     

Effect of Milk Pricing Systems on Income over Feed and Variable Costs of Dairy Cattle Breeds

An electronic spreadsheet program using a budgeting procedure was used to compare the effect of protein pricing differentials and cheese yield pricing systems on income over feed and variable costs of the six major dairy breeds. Increasing the protein differentials from $ .03 to .22/45.4 kg milk per .1 unit increase in protein percent above 3.2% decreased the difference in income over feed and variable costs between non-Holstein and Holstein breeds. With the prices and assumptions used, the income over feed and variable costs of non-Holstein breeds never equaled or surpassed that of Holsteins. With current milk, feed, and cheese prices, using a cheese pricing system caused a substantial decrease in income over feed costs for Holsteins and decreased the differences between Holsteins and non-Holsteins. Increased cheese prices, increased feed prices, and lowered milk prices also narrowed the differences in income over feed and variable costs between Holstein and non-Holstein breeds. Although changes in the milk pricing system make the non-Holstein breeds more competitive with Holsteins, non-Holstein breeds must produce between 224 and 1539 kg more milk with the various milk and feed price scenarios used for the income over feed and variable costs to equal that of Holsteins.     

Effect of Imitation or Filled Dairy Products

United States consumers are eating more fat than ever, but they are eating less animal fat. Per capita consumption of animal fat dropped 34% since 1960, and vegetable fat consumption increased by 77%. The shift to imitation dairy products is reflected in dairy product surpluses and resulting downward pressure on dairy product prices.The imitation product that threatens the dairy industry most is imitation cheese. The 205 million pounds of imitation cheese marketed in 1984 was 44% of US Department of Agriculture price support purchases of cheese.Average retail prices for various types of imitation cheese are 16 to 32% lower than natural cheese prices; pizza with imitation cheese averages 14% less in price than natural cheese pizza of the same brand. Imitation cheese takes up 16% of the shredded cheese shelf space, 2% of the unshredded and process cheese shelf space, and pizza made with imitation cheese has gained more than half the pizza shelf space in the United States.The following strategies are recommended to counter the imitation problem: 1) reduce price advantage of imported casein through negotations with the European Economic Community to reduce export subsidies: 2) work for clearer, more prominent labeling of imitation dairy products; 3) put more emphasis on butter-margarine blend products, which compete more directly with margarine than butter; 4) use more of the $197 million annual promotion funds from farmer checkoffs for promoting cheese. Buyer response to cheese promotion is three times the response from a similar investment in fluid milk promotion.