Correlation between Cheese Meltability Determined with a Computer Vision Method and with Arnott and Schreiber Tests

ABSTRACT: Meltability of different brands of Cheddar and Mozzarella cheeses was determined with a novel computer vision method as well as with 2 traditional methods, that is, the Arnott and Schreiber tests. Correlation between the results of these methods was analysed and it showed that the meltability determined with a computer vision system was significantly (P < 0.0001) interrelated with the Arnott (R²= 0.69) and Schreiber (R²= 0.88) meltabilities. The computer vision method provided an accurate quantitative account of the physical changes in cheese during melting, and thus was capable of revealing meltability differences of cheese that were difficult to distinguish by the traditional methods. The new approach was also applicable to a wide range of cheeses.     

Powder X-ray diffraction can differentiate between enantiomeric variants of calcium lactate pentahydrate crystal in cheese

Powder X-ray diffraction has been used for decades to identify crystals of calcium lactate pentahydrate in Cheddar cheese. According to this method, diffraction patterns are generated from a powdered sample of the crystals and compared with reference cards within a database that contains the diffraction patterns of known crystals. During a preliminary study of crystals harvested from various Cheddar cheese samples, we observed 2 slightly different but distinct diffraction patterns that suggested that calcium lactate pentahydrate may be present in 2 different crystalline forms. We hypothesized that the 2 diffraction patterns corresponded to 2 enantiomeric forms of calcium lactate pentahydrate (l- and dl-) that are believed to occur in Cheddar cheese, based on previous studies involving enzymatic analyses of the lactate enantiomers in crystals obtained from Cheddar cheeses. However, the powder X-ray diffraction database currently contains only one reference diffraction card under the title “calcium lactate pentahydrate.” To resolve this apparent gap in the powder X-ray diffraction database, we generated diffraction patterns from reagent-grade calcium l-lactate pentahydrate and laboratory-synthesized calcium dl-lactate pentahydrate. From the resulting diffraction patterns we determined that the existing reference diffraction card corresponds to calcium dl-lactate pentahydrate and that the other form of calcium lactate pentahydrate observed in cheese crystals corresponds to calcium l-lactate pentahydrate. Therefore, this report presents detailed data from the 2 diffraction patterns, which may be used to prepare 2 reference diffraction cards that differentiate calcium l-lactate pentahydrate from calcium dl-lactate pentahydrate. Furthermore, we collected crystals from the exteriors and interiors of Cheddar cheeses to demonstrate the ability of powder X-ray diffraction to differentiate between the 2 forms of calcium lactate pentahydrate crystals in Cheddar cheeses. Powder X-ray diffraction results were validated using enzymatic assays for lactate enantiomers. These results demonstrated that powder X-ray diffraction can be used as a diagnostic tool to quickly identify different forms of calcium lactate pentahydrate that may occur in Cheddar cheese.     

High Pressure Treatment of Milk and Effects on Microbiological and Sensory Quality of Cheddar Cheese

The effect of cycled high pressure treatment of milk on the yield, sensory, and microbiological quality of Cheddar cheese was investigated. Cheddar cheeses were made from pasteurized, raw, or pressure treated milk according to traditional methods. Flavor scores from trained dairy judges were not different for pasteurized and pressurized milk cheeses (P≤0.05). Percent moisture and wet weight yields of pressure treated milk cheeses were higher than pasteurized or raw milk cheeses (P≤0.05). Microbiological quality of pressurized milk cheeses was comparable to pasteurized milk cheeses. Texture defects were present in pressurized milk cheeses and were attributed to excess moisture. High pressure treatment of milk shows promise as an alternative to heat pasteurization prior to cheesemaking.     

Microstructure of milk gel and cheese curd observed using cryo scanning electron microscopy and confocal microscopy

Cryo scanning electron microscopy (cryo SEM) and confocal laser scanning microscopy (CLSM) were used to visualise changes in the microstructure of milk, rennet-induced gel and curd during the manufacture of Cheddar cheese. Our results show that cryo preservation did not alter the microstructure of the sample when it was fixed by rapid freezing in slush liquid nitrogen due to the formation of amorphous ice. Artefacts such as the formation of ice crystals could be observed in samples when immersed directly into liquid nitrogen (−196 °C) at atmospheric pressure. These ice crystals changed the shape of sample pores increasing their size to >20 μm. The etching time, thickness of gold coating, accelerating voltage and type of detector used for cryo SEM observation were varied in order to minimise the formation of such artefacts and optimise conditions for imaging. Chains and clusters of casein micelles and fat globules were best observed in the gel and the cooked curd when the samples were freeze fractured and etched for 30 min, coated with a mixture of gold and palladium alloy approximately 6 nm thick at −140 °C and observed using a backscattered electron detector at 15 kV. The structure of the gel, curd and cheese was also observed using CLSM. Spherical fat globules were mostly present in the serum pores of the gel prepared from unhomogenised milk but were found embedded in the aggregated chains of the casein network within the gel prepared from homogenised milk when observed using CLSM. The porosity measurements obtained using cryo SEM were similar to those obtained using CLSM. These two complementary techniques can potentially be used to assist studies for the control of cheese texture and functionality.     

Viscoelastic Property Changes in Cheddar Cheese During Ripening

The rheological properties of pasteurized and raw milk Cheddar cheese were studied using oscillatory dynamic measurements, and a specially designed rheometer fixture that prevented specimen slippage. Dynamic measurements within the linear viscoelastic range were made throughout ripening. Within-cheese changes, as related to ripening time, as well as between-cheese-type differences in G’ and G” were observed. Differences in rheological characteristics were attributed to proteolytic activities in Cheddar cheese during ripening. Specific peptide profiles associated with proteolysis during ripening may affect cheese rheological properties.     

Release and identification of angiotensin-converting enzyme-inhibitory peptides as influenced by ripening temperatures and probiotic adjuncts in Cheddar cheeses

The aim of the study was to examine the release of angiotensin-converting enzyme (ACE)-inhibitory peptides in Cheddar cheeses made with starter lactococci and Bifidobacterium longum 1941, B. animalis subsp. lactis LAFTI^® B94, Lactobacillus casei 279, Lb. casei LAFTI^® L26, Lb. acidophilus 4962 or Lb. acidophilusLAFTI^® L10 during ripening at 4 and 8 °C for 24 weeks. ACE-inhibitory activity of the cheeses was maximum at 24 weeks. Cheeses made with the addition of Lb. casei 279, Lb. casei LAFTI^® L26 or Lb. acidophilus LAFTI^® L10 had significantly higher (P < 0.05) ACE-inhibitory activity than those without any probiotic adjunct after 24 weeks at 4 and 8 °C. The IC₅₀ of cheeses ripened at 4 °C was not significantly different (P > 0.05) to that ripened at 8 °C. The lowest value of the IC₅₀ (0.13 mg mL⁻¹) and therefore the highest ACE-inhibitory activity corresponded to the cheese with the addition of Lb. acidophilus LAFTI^® L10. Several ACE-inhibitory peptides were identified as κ-CN (f 96–102), α_s1-CN (f 1–9), α_s1-CN (f 1–7), α_s1-CN (f 1–6), α_s1-CN (f 24–32) and β-CN (f 193–209). Most of the ACE-inhibitory peptides accumulated at the early stage of ripening, and as proteolysis proceeded, some of the peptides were hydrolyzed into smaller peptides.     

Long Term Use of a Cheddar Starter and Development of Phages with Homology to its Bacteria

A mixed, homofermentative, mesophilic starter was used for more than 11 years as the only starter for production of Cheddar cheese at a Danish cheese factory. The activity of the starter at the factory was carefully recorded, and whey samples were regularly tested for bacteriophages. During the years bacteriophages, homologous to an increasing number of the strains of the starter culture, gradually evolved. After 4 years bacteriophages, homologous to more than 50%—and after 6 years to more than 90%—of 62 bacterial isolates from the starter, had appeared. For most of the strains the virulence of their phages was low at first and thereafter increased over several years. It was, however, only after more than 11 years that the cheese factory first began to observe cases of reduced activity of the bulk starter; presumably because the virulence of the bacteriophages had developed to such a degree that very low levels of contamination of the milk for bulk starter could impair the subsequent activity of the bulk starter in the curd.     

添加酿酒酵母的切达干酪风味研究

随着干酪市场的日益增长,开发新型风味干酪成为新的趋势.根据前期实验结果,研究选定了3种制作添加酿酒酵母的切达干酪(KY组、KH组、KC组)加工工艺,通过顶空固相微萃取和气相色谱-质谱联用技术、聚类分析及感官评价对干酪中挥发性风味化合物进行测定及分析,以此来评价酿酒酵母在切达干酪中的应用前景.干酪成熟过程中,3组干酪中挥...