The effect of light on the vitamin B2 and the vitamin A content of cheese

Edam type cheese was exposed to sunlight at ambient temperature and to fluorescent light at 5 °C. The loss of vitamin B₂ (riboflavin) and vitamin A was monitored in both the surface and inner layers of the cheese and the results compared with control samples kept in the dark. The loss of riboflavin when exposed to sunlight was shown to be primarily a surface effect but losses of vitamin A were similar throughout the cheese. When exposed to fluorescent light at 5 °C and monitored at intervals for 10 days the loss of riboflavin was still greatest at the surface but a trend to lower values than the control was evident throughout the cheese. Vitamin A losses followed a different pattern in both sunlight and fluorescent light. There was a heavy initial loss throughout the cheese. Under fluorescent light this was followed by a period in which further loss was mainly in the surface layer. Vacuum packaging reduced the loss of riboflavin but had no effect on the loss of vitamin A.     

Preliminary evaluation of endogenous milk fluorophores as tracer molecules for curd syneresis

A front-face fluorescence spectroscopy probe was installed in the wall of a laboratory-scale cheese vat. Excitation and emission filters were chosen for the selective detection of vitamin A, tryptophan, and riboflavin fluorescence. The evolution of the fluorescence of each fluorophore during milk coagulation and syneresis was monitored to determine if they had the potential to act as intrinsic tracers of syneresis and also coagulation. The fluorescence profiles for 2 of the fluorophores during coagulation could be divided into 3 sections relating to enzymatic hydrolysis of κ-casein, aggregation of casein micelles, and crosslinking. A parameter relating to coagulation kinetics was derived from the tryptophan and riboflavin profiles but this was not possible for the vitamin A response. The study also indicated that tryptophan and riboflavin may act as tracer molecules for syneresis, but this was not shown for vitamin A. The evolution of tryptophan and riboflavin fluorescence during syneresis followed a first-order reaction and had strong relationships with curd moisture and whey total solids content (r = 0.86-0.96). Simple 1- and 2-parameter models were developed to predict curd moisture content, curd yield, and whey total solids using parameters derived from the sensor profiles (standard error of prediction = 0.0005-0.394%; R² = 0.963-0.999). The results of this study highlight the potential of tryptophan and riboflavin to act as intrinsic tracer molecules for noninvasive inline monitoring of milk coagulation and curd syneresis. Further work is required to validate these findings under a wider range of processing conditions.     

Detection of aflatoxin M1 in milk and dairy products consumed in Adana, Turkey

A total of 70 dairy products consisting of 20 sterilized milk, 10 butter, 20 white cheese and 20 Kashar cheese samples were analysed for aflatoxin M₁ (AFM₁) by enzyme-linked immunosorbent assay (ELISA). The detection limit was 5 ng/L for milk and 25 ng/kg for butter, white cheese and Kashar cheese. Of the 70 dairy products analysed, AFM₁ in 49 samples (70%) was found to range from 10 to 388 ng/kg. Moreover, AFM₁ levels in three samples of milk, two samples of butter, one sample of white cheese and one sample of Kashar cheese were found to be higher than the Turkish legal limits.     

Light-Induced Changes in Taste,Appearance, Odor,and Riboflavin Content of Cheese

Light-induced changes in taste, appearance, odor, and riboflavin content of common cheeses stored under controlled laboratory conditions and in the dairy cases of four local grocery stores were investigated. Sensory evaluation was performed by 25 untrained panelists, and the riboflavin content was determined by HPLC method. The data obtained from controlled storage indicated that light intensity, type of packaging paper, and piece thickness affected riboflavin retention and color in stored cheese. However, under the display conditions used in the four local stores, retail cheese retained its riboflavin after a display time of 14 d with no significant change in taste, appearance, or odor.     

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.     

Fast detection of cyclopiazonic acid in cheese using Fourier transform mid-infrared ATR spectroscopy

A simple and rapid Fourier transform mid-infrared spectroscopic method with attenuated total reflection was developed for the detection of cyclopiazonic acid in ewe's cheese samples. A partial least-squares calibration model for the prediction of cyclopiazonic acid content in ewe medium-ripened cheese, based on spectra data, revealed to be the best approach. The PLS model was tested by cross-validation in order to minimize standard error of the model and the relevant RMSECV (root of mean-squared error in cross-validation) was calculated to be 0.05 μg/g. In parallel experiments, cyclopiazonic acid content was estimated using the developed SPME-HPLC/UV method and different cheese samples were analysed using both techniques. The method appears to be useful for a qualitative and semi-quantitative screening of a large number of cheese samples, important in food contaminants monitoring. Since no sample pretreatment is required at all, the analysis times are dramatically shortened in comparison with any chromatographic procedure.     

Fate of ivermectin residues in ewes' milk and derived products

The fate of ivermectin (IVM) residues was studied throughout the processing of daily bulk milk from 30 ewes (taken up to 33 d following subcutaneous administration of 0.2 mg IVM/kg b.w.) in the following milk products: yoghurt made from raw and pasteurized milk; cheese after pressing; 30- and 60-day ripened cheese; and whey, secondary whey and whey proteins obtained after cheese-making (albumin cheese). The concentration of the H2B1a component of IVM was analysed in these dairy products using an HPLC method with fluorescence detection. The mean recovery of the method was, depending on the matrix, between 87 and 100%. Limits of detection in the order of only 0.1 microg H2B1a/kg of product were achieved. Maximum concentrations of IVM were detected mostly at 2 d after drug administration to the ewes. The highest concentration of IVM was found on day 2 in 60-day ripened cheese (96 microg H2B1a/kg cheese). Secondary whey was the matrix with the lowest concentration of IVM (<0.6 microg H2B1a/ kg). Residue levels fell below the limits of detection between day 5 (for secondary whey) and day 25 (for all cheese samples). In the matrices investigated, linear correlations between daily concentrations of IVM, milk fat and solid content were evident. During yoghurt production, fermentation and thermal stability of IVM was observed. During cheese production, approximately 35% of the IVM, present in the raw (bulk) milk samples, was lost. From the results it was concluded that the processing of ewes' milk did not eliminate the drug residues under investigation. The consequences of IVM in the human diet were discussed. Milk from treated animals should be excluded from production of fat products like cheese for longer after treatment with IVM than for lower fat products.     

Nutritional Evaluation of Typical and Reformulated Italian Cheese

The aim of this work was the nutritional evaluation of reformulated dairy products (caciotta-type cheese) and manufactured either with a low-sodium chloride content (different salting time and/or composition of the brine) or low-fat content (different partially skimmed milks). These cheeses were intended for people on low-energy or low-sodium diets. A comparison was made between these new products and three typical Italian cheeses (Provolone, Taleggio and Pecorino Romano). The nutrient content of the products was determined. Amino acids by chromatographic methods, protein digestibility by an enzymatic method and lysine availability determined spectrophotometrically were shown not to be influenced by the salt reduction. The salt reduction also did not affect vitamin contents (riboflavin, retinols, carotenes and tocopherols) measured by HPLC methods, while the reduced fat contents (310 g kg^-1, 160 g kg^-1 and 87 g kg^-1) led to significant decreases in concentrations of fat-soluble vitamins (38% for tocopherols and 7% for total retinols) and a decrease in riboflavin (13%) due to the loss of riboflavin enzymes located on the fat globules (ie xanthine oxidase). Both the typical cheeses and the new formulations represent good sources of calcium and protein. Protein digestibility was affected by the ripening time; in fact, in Pecorino Romano, ripened for 6–9 months it reached 62% in 6 h, whereas in Taleggio and in all caciotta–cheeses it reached only 32–37%. The nutritional profiles of the reformulated caciotta cheese showed that these products could represent a good choice in low-energy and low-sodium diets, but an enrichment of fat-soluble vitamins is advisable in the low-fat products. © 1997 SCI.     

Prediction of Inorganic Salt and Moisture Content of Process Cheese Using Dielectric Spectroscopy

The development of on-line sensors for compositional analysis during cheese manufacture is desirable for improved quality control. Dielectric properties of a food product are principally determined by its moisture and salt content. This indicates that dielectric spectroscopy may offer a rapid, on-line and non-destructive method for the determination of moisture and salt content of process cheese. However limited information is available in the literature on the dielectric properties of process cheese. Therefore the aims of this study are to investigate the dielectric properties of process cheese samples over a range of compositional parameters and to assess the potential of dielectric spectroscopy to improve process control during process cheese manufacture. Dielectric spectra of process cheese samples were measured using a coaxial line probe between 300 MHz and 3 GHz. A clear tend was observed between higher moisture content and increases in the dielectric constant. Inorganic salt content was found to have a major influence on the loss factor. The dielectric data obtained was used to develop chemometric models for the prediction of moisture and inorganic salt content of two experimental sets of process cheese samples (exp A and exp B). The root mean square error of prediction (RMSEP) for the models developed to predict moisture content were 0.524% (w/w) (exp A), and 0.423% (w/w) (exp B), while the RMSEP of the inorganic salt models were 0.220% (w/w) (exp A), and 0.263% (w/w) (exp B). It was concluded that dielectric spectroscopy has potential application for compositional analysis in process cheese manufacture.     

HPLC Determination of Riboflavin in Eggs and Dairy Products

An isocratic HPLC method has been developed to determine riboflavin in eggs, whole milk, 2% fat milk, skim milk, dry milk, yogurt, cottage cheese, and cheddar cheese. The developed method involves acidification, centrifugation, and quantification of riboflavin in the supernatant with HPLC. The HPLC system consisted of a μ Bondapak C₁₈ column, a solvent system of water-methanol-acetic acid (68:32:0.1 v/v), a flow rate of 1.0 ml/min, and a UV detector. The method is simple, rapid, sensitive, and specific for riboflavin. Recoveries of more than 90% were obtained in all samples analyzed.     

Short communication: Detection of human Torque teno virus in the milk of water buffaloes (Bubalus bubalis)

Forty-four raw milk and 15 serum samples from 44 healthy water buffaloes reared in Caserta, southern Italy, the most important region in Europe for buffalo breeding, were examined to evaluate the presence of Torque teno viruses (TTV) using molecular tools. Furthermore, 8 pooled pasteurized milk samples (from dairy factories having excellent sanitary conditions) and 6 Mozzarella cheese samples were also tested. Four of the cheese samples were commercial Mozzarella cheese; the remaining 2 were prepared with TTV-containing milk. Human TTV were detected and confirmed by sequencing in 7 samples of milk (approximately 16%). No TTV were found in serum, pooled pasteurized milk, or Mozzarella cheese samples. The samples of Mozzarella cheese prepared with TTV-containing milk did not show any presence of TTV, which provides evidence that standard methodological procedures to prepare Mozzarella cheese seem to affect viral structure, making this food fit for human consumption. The 7 TTV species from water buffaloes were identified as genotypes corresponding to the tth31 (3 cases), sle 1981, sle 2031, and NLC030 (2 cases each) human isolates. Although cross-species infection may occur, detection of TTV DNA in milk but not in serum led us to believe that its presence could be due to human contamination rather than a true infection. Finally, the mode of transmission of TTV has not been determined. Contaminated of the food chain with TTV may be a potential risk for human health, representing one of the multiple routes of infection.     

Detection of biogenic amine producer bacteria in a typical Italian goat cheese

The aim of this study was to research decarboxylating bacterial strains and biogenic amine content in a typical Italian goat cheese (Robiola di Roccaverano). The study was performed on fresh and ripened samples of goat cheese manufactured from industrial and artisanal producers. Sixty-seven bacterial strains isolated showed decarboxylating activity, and Enterococcus faecalis was the most widespread decarboxylating species in all artisanal and industrial products. Pediococcus acidilactici and Enterococcus malodoratus were also identified as biogenic amine producers in Robiola di Roccaverano cheese. All the E. faecalis strains isolated in this study were able to decarboxylate tyrosine. Tyramine was the most abundant biogenic amine in cheese samples, while histamine was the most widespread. High amounts of these two biogenic amines were found in ripened samples (up to 2,067 mg/kg for tyramine and 1,786 mg/kg for histamine), whereas 2-phenylethylamine and tryptamine were present in almost all ripened cheeses at low concentrations. The detection of strains producing biogenic amines and the high concentrations of tyramine and histamine found in ripened Robiola di Roccaverano could represent a potential risk to the consumer.     

Inhibitory potential of herb,fruit, and fungal-enriched cheese against key enzymes linked to type 2 diabetes and hypertension

In the current study, three different types of cheese, cheddar, feta, and Roquefort, were screened to determine the variations in phenolic-linked antioxidant activity and the potential to inhibit key enzymes relevant to type 2 diabetes and related hypertension. The cheese samples were assayed for total phenolic content, related antioxidant activity, and inhibition of α-glucosidase, pancreatic α-amylase inhibitory activity, and the angiotensin-converting enzyme (ACE)-I inhibitory activity. The three fungal-enriched Roquefort cheese samples had the highest total phenolic content. The phenolic content in the herb cheese was slightly but not significantly higher compared to plain cheese. Roquefort cheese samples had the highest antioxidant-linked DPPH (free radical) scavenging activity and as expected DPPH radical scavenging activity was higher in the herb cheese compared to plain cheese. All samples had some α-glucosidase and α-amylase inhibitory activities, with cranberry-enriched cheese having the highest activities. However, no correlation to soluble phenolic content was observed. All the cheese samples had very high anti-ACE-I inhibitory activity, indicating no correlation to phenolic content and activity was even high in 10× diluted samples. The highest ACE-I inhibitory activity was observed in plain and herb-enriched cheddar cheese as well as cranberry-enriched cheese. These studies indicate that cranberry-enriched cheese had the best potential for inhibition of α-glucosidase and α-amylase relevant for type 2 diabetes management, whereas any cheese product had potential for ACE-I inhibition linked to hypertension management, indicating likely the role of other factors such as peptides from cheese fermentation.Industrial relevanceThis research is focused on screening of different types of commercial plain, herbal, fruit, and fungal-enriched to provide a strong biochemical rationale for further design of functional cheese products for anti-type 2 diabetic and relevant hypertension management. A better understanding of these functional attributes provides a strong biochemical rationale for design in vivo and clinical studies from which right design of functional food can be established.     

Effect of fermentation on the thiamin, riboflavin and niacin contents of melon seed (Citrullus vulgaris) and African oil bean seed (Pentaclethra macrophylla)

An automated thiochrome method and high performance liquid chromatography (HPLC) with fluorescence detection were used to determine thiamin and riboflavin, respectively, in unfermented, and fermented melon seeds (Citrullus vulgaris) and African oil bean seeds (Pentaclethra macrophylla). Niacin was determined microbiologically. In all the methods used, fermentation significantly increased the content of thiamin, riboflavin and niacin in African oil bean seeds and thiamin and riboflavin in melon seeds. There was no change in the niacin content of melon seeds.     

Determination of zearalenone in corn flour and a cheese snack product using high-performance liquid chromatography with fluorescence detection

The presence of the mycotoxin zearalenone in corn flour and a cheese snack derived from this was determined. Thirty-eight samples (corn flour and cheese snacks) of different brands were analysed for zearalenone using high-performance liquid chromatography with fluorescence detection. Zearalenone was detected in corn flour and cheese snack samples with average content of 0.377 ppm (maximum, 0.889 ppm) and 0.832 ppm (maximum, 1.471 ppm) respectively. The recovery from spiked corn flour and cheese snack samples ranged from 70-87%. The method had a limit of detection of 0.01 µg ml^-1. The linearity of method was determined (y = 5.88 x + 0.25, r² = 0.9999), and optimum assay range was 0.05-30 µg ml^-1. The occurrence of zearalenone in the maize product confirms the need to assess the exposure of the Iranian population to this mycotoxin.     

Characterization of major and trace minerals,fatty acid composition,and cholesterol content of Protected Designation of Origin cheeses

Cheese provides essential nutrients for human nutrition and health, such as minerals and fatty acids (FA). Its composition varies according to milk origin (e.g., species and breed), rearing conditions (e.g., feeding and management), and cheese-making technology (e.g., coagulation process, addition of salt, ripening period). In recent years, cheese production has increased worldwide. Italy is one of the main producers and exporters of cheese. This study aimed to describe mineral, FA, and cholesterol content of 133 samples from 18 commercial cheeses from 4 dairy species (buffalo, cow, goat, and sheep) and from 3 classes of moisture content (hard, <35% moisture; semi-hard, 35–45%; and soft, >45%). Mineral concentrations of cheese samples were determined by inductively coupled plasma optical emission spectrometry, and FA and cholesterol contents were determined by gas chromatography. Moisture and species had a significant effect on almost all traits: the highest levels of Na, Ca, and Fe were found in cheeses made from sheep milk; the greatest level of Cu was found in cow milk cheese, the lowest amount of K was found in buffalo milk cheese, and the lowest amount of Zn was found in goat cheeses. In all samples, Cr and Pb were not detected (below the level of detection). In general, total fat, protein, and minerals significantly increased when the moisture decreased. Buffalo and goat cheeses had the highest saturated FA content, and sheep cheeses showed the highest content of unsaturated and polyunsaturated FA, conjugated linoleic acid, and n-3 FA. Goat and sheep cheeses achieved higher proportions of minor FA than did cow and buffalo cheeses. Buffalo cheese exhibited the lowest cholesterol level. Our results confirm that cheese mineral content is mainly affected by the cheese-making process, whereas FA profile mainly reflects the FA composition of the source milk. This study allowed the characterization of mineral and FA composition and cholesterol content and revealed large variability among different commercial cheeses.     

Detection and quantification of goat's cheese in ewe's cheese using a monoclonal antibody and two ELISA formats

A stable hybridoma cell line (B2B) has been produced secreting a monoclonal antibody (MAb) specific for the s α_s2‐casein of goats. The MAb B2B was used in two enzyme‐linked immunosorbent assays (ELISA) formats for the detection and quantification of the presence of goat's cheese in ewe's cheese samples. In the indirect ELISA format the limit of detection was 1–25% (w/w) substitution of ewe's cheese samples by goat's cheese. Afterwards, a competitive indirect ELISA was successfully developed for the detection of 0.5 to 25% (w/w) of goat's cheese in ewe's cheese samples. This competitive indirect ELISA is a very sensitive assay, can be performed in less than 5 h and is not influenced by the ripening process in cheese. © 1999 Society of Chemical Industry     

Effect of sodium citrate on structure-function relationships of Cheddar cheese

The objective of this study was to determine the effect of sodium citrate on the structure and functionality of Cheddar cheese. The hypothesis was that citrate (sodium citrate) injection would affect cheese properties mainly through its effect on bound calcium (calculated as the difference between total calcium and the water-soluble calcium content of a cheese extract). A 9-kg block of Cheddar cheese was made, vacuum-packaged, and then stored for 2 wk at 4 degrees C. After storage, the cheese was cut into 0.5- to 0.6-kg blocks that were vacuum-packaged and stored for 1 wk at 4 degrees C prior to injection. Cheese blocks were then high-pressure injected with a buffer solution (pH 5.27) containing 40% (wt/ wt) citric acid trisodium dihydrate and 6.25% (wt/wt) anhydrous citric acid, from zero (control) to five times (successive injections performed 24 h apart). Increased citric acid content of cheese from 0.22 (uninjected) to 1.39% (after five injections) caused phosphate solubilization. Thus, the calculated bound phosphate content of cheese decreased from 0.54 to 0.45 mmol/g of protein. However, unexpectedly, the soluble calcium content decreased from 0.34 (control) to 0.28 mmol/g of protein (after five injections), whereas the bound calcium content remained unchanged (0.42 mmol/g of protein). The decrease in soluble calcium probably resulted from the formation and concentration of crystals in the cheese surface, which was not included in samples for analysis, and from the expulsion of serum from within the cheese. Higher concentration of solutes in the water phase of cheese would increase the volume of serum, but the cheese had limited holding capacity and serum was expelled. Citrate injection increased the sodium content of cheese from 0.63 to 0.93%, but it had no effect on cheese pH (5.2). After five injections, the protein matrix expanded, occupying an increased area of cheese matrix (83 vs. 78%). Even though citrate injection had no effect on bound calcium, and thus the rate and extent of cheese flow were unaffected, increased phosphate solubilization, and possibly decreased ionic calcium content, resulted in expansion of the protein matrix and increased cheese hardness.     

Short communication: Viable Mycobacterium avium subspecies paratuberculosis in retail artisanal Coalho cheese from Northeastern Brazil

Mycobacterium avium ssp. paratuberculosis (MAP) is the etiologic agent of paratuberculosis and it potentially plays a role in Crohn’s disease. In humans, the main route of transmission of MAP might be the intake of contaminated milk and dairy products. Considering that MAP has already been detected in many types of cheese in different counties, and that Coalho cheese is an important dairy product in northeastern Brazil, the aim of this study was to report the first detection of MAP in retail Coalho cheese in Brazil by PCR and culture. Of 30 retail Coalho cheese samples, 3 (10%) amplified fragments of a similar size to that expected (626 bp) were obtained and viable MAP was recovered by culture from 1 (3.3%) sample. The DNA from the positive culture sample was sequenced and showed 99% identity with the insertion sequence IS900 deposited in GenBank. It was possible to identify the presence of MAP-specific DNA in the analyzed samples for the first time in Brazil, and to recover viable cells from retail Coalho cheese.     

Aflatoxin M1 in Parmesan Cheese: HPLC Determination

A method was developed to determine aflatoxin M, in Parmesan cheese produced in the Modena area during 1991. The analytical method was based on extraction of aflatoxin M, from the cheese by chloroform and clean-up by liquid-liquid extraction. The determination was made by high-pressure liquid chromatography. Of 200 fresh Parmesan cheese samples analyzed, 18 showed presence of aflatoxin M, in low concentrations (max. 0.190 μG/kg). Italian food law does not establish any maximum allowed level for this aflatoxin. The maximum limit proposed by the Swiss Federal Bureau of Health was 0.250 μg/kg.