On solid-like rheological behaviors of globular protein solutions

Dynamic viscoelastic and steady flow properties of β-lactoglobulin, bovine serum albumin, ovalbumin, and α-lactalbumin aqueous solutions were investigated at 20°C. When a sinusoidal strain in the linear viscoelastic region was applied, the solutions of the globular proteins except for α-lactalbumin showed typical solid-like rheological behavior: the storage modulus G′ was always larger than the loss modulus G″ in the entire frequency range examined (0.1–100 rad/s). Under a steady shear flow, strong shear thinning behavior was observed with increasing shear rate from 0.001 to 800 s⁻¹, for the globular proteins except for α-lactalbumin. The values of the steady shear viscosity η were lower than those of the dynamic shear viscosity η* at a comparable time scale of observation, violating the Cox–Merz rule, and thus suggesting that a solid-like structure in a globular protein solution was susceptible to a steady shear strain. During isothermal gelation of the protein colloids at 70°C, no crossover between G′ and G″ was observed so that the gelation point was judged by an abrupt increase in the modulus or a sudden decrease in tanδ.     

Effect of inulin on the rheological properties of silken tofu coagulated with glucono-δ-lactone

This study investigated the rheological properties of inulin-containing silken tofu coagulated with glucono-δ-lactone (GDL) upon heating. Inulin (Raftiline^® HP-gel) was added to a soy protein isolate-enriched cooked soymilk at 0%, 1%, 2%, 3% and 4% (w/v) levels along with 0.4% (w/v) GDL to prepare acid-induced silken tofu. Gelation was induced by heating the soymilk mixture from 20 to 90 °C at a constant rate (1 °C/min) or isothermally at 90 °C for 30 min. The gelling properties were measured with dynamic small-deformation mechanical analysis and static large-deformation compression tests. The rheological changes in soymilk during gelation were dependent upon both the pH decline (hydrolysis of GDL) and the specific temperature of heating. Control samples heated to 50 °C, with the pH lowered to 5.95, started to gel, showing a rapid increase in storage (G′) and loss (G″) moduli afterwards. The addition of 2% inulin lowered the on-set gelling temperature by 2.8 °C and improved (P < 0.05) both rheological parameters of the tofu gel as well as hardness and rupture force (textural profile analysis) of the formed silken tofu. The results indicated that inulin enhances the viscoelastic properties of GDL-coagulated silken tofu, and the textural effect of inulin is an added benefit to its current application mainly as a prebiotical ingredient in food.     

Associative and segregative interactions between gelatin and low-methoxy pectin: Part 2—co-gelation in the presence of Ca

The effect of segregative interactions with gelatin (type B; pI=4.9; 0–10 wt%) on the networks formed by low-methoxy pectin on cooling in the presence of stoichiometric Ca²⁺ at pH 3.9 has been investigated by rheological measurements under low-amplitude oscillatory shear. Samples were prepared and loaded at 85 °C, cooled (1 °C/min) to 5 °C, held for 100 min, and re-heated (1 °C/min) to 85 °C, with measurement of storage and loss moduli (G′ and G″) at 10 rad s⁻¹ and 2% strain. The final values of G′ at 5 °C for mixtures prepared at the same pH without Ca²⁺ were virtually identical to those observed for the same concentrations (0.5–10.0 wt%) of gelatin alone, consistent with the conclusion from the preceding paper that electrostatic (associative) interactions between the two polymers become significant only at pH values below 3.9. Increases in moduli on cooling in the presence of Ca²⁺ occurred in two discrete steps, the first coincident with gelation of calcium pectinate alone and the second with gelation of gelatin. Both processes were fully reversible on heating, but displaced to higher temperature (by 10 °C), as was also observed for the individual components. The magnitude of the changes occurring over the temperature range of the gelatin sol–gel and gel–sol transitions demonstrates that the gelatin component forms a continuous network; survival of gel structure after completion of gelatin melting shows that the calcium pectinate network is also continuous (i.e. that the co-gel is bicontinuous). On progressive incorporation of NaCl (to induce phase separation before, or during, pectin gelation) the second melting process, coincident with loss of calcium pectinate gel structure, was progressively abolished, indicating conversion to a gelatin-continuous network with dispersed particles of calcium pectinate. These qualitative conclusions are supported by quantitative analyses reported in the following paper.     

Rheological behaviour of uncross-linked and cross-linked gelatinised waxy maize starch with pectin gels

Rheological characterisation of uncross-linked (UPS) and cross-linked (CPS) waxy maize starch with pectin was conducted to determine the influence of pectin on the properties of the starch. The viscoelastic behaviour of 5% (w/v) gel systems containing UPS and CPS polysaccharides at 25 °C was evaluated by small angle deformation oscillation rheometry. Viscoelasticity measurements of the cross-linked polysaccharides indicated that the elastic component increased after cross-linking. Among all gels studied, the properties of the CPS mixtures (ratios 2:3 and 3:2) showed quite high storage (G′) and loss (G″) moduli (compared with gels of other ratios), indicating that gels of these two particular ratios had the greatest degree of elasticity and were very well structured. The results suggest that cross-linking between starch and pectin molecules can give rise to novel rheological properties.     

Influence of complexing carboxymethylcellulose on the thermostability and gelation of α-lactalbumin and β-lactoglobulin

Thermostability and gelation of the main proteins of whey, α-lactalbumin (α-lac) and β-lactoglobulin (β-lg) recovered by selective complexation with carboxymethylcellulose (CMC) was studied to evaluate its functionality in food systems. Their behavior was compared to the non-complexed proteins. Both complexes showed a maximum stability at pH 4, that is close to the pH of obtention of β-lg/CMC coacervate (pH 4) and α-lac/CMC coacervate (pH 3.2). Protein complexation increased the thermostability of β-lg by approximately 6–8 °C and that of α-lac by approximately 26 °C due to immobilization of protein molecules in a complex, mainly by electrostatic interactions and because of different amounts of bound polysaccharide. The denaturation enthalpy of complexed proteins markedly decreased as compared to free proteins. Storage modulus (G′) and loss modulus (G″) were recorded to reflect the structure development during heating β-lg/CMC and α-lac/CMC complexes at different pH values. β-lg/CMC complex at 20 wt% was a viscoelastic liquid at pH values within 2 and 8 but upon heating turned to a particulate viscoelastic gel. However, α-lac/CMC complex formed before heating opaque, large visible white particulate aggregates that sticked together to give a solid viscoelastic structure that was not further modified by thermal processing.     

Film forming solutions based on gelatin and poly(vinyl alcohol) blends: Thermal and rheological characterizations

The objective of this work was to study the rheological and thermal properties of film forming solutions (FFS) based on blends of gelatin and poly(vinyl alcohol) (PVA). The effect of the PVA concentration and plasticizer presence on the flow behavior, and viscoelastic and thermal properties of FFS was studied by steady-shear flow and oscillatory experiments, and also, by microcalorimetry. The FFS presented Newtonian behavior at 30 °C, and the viscosity was not affected neither by the PVA concentration nor by the plasticizer. All FFS presented a phase transition during tests applying temperature scanning. It was verified that the PVA affected the viscoelastic properties of FFS by dilution of gelatin. This behavior was confirmed by microcalorimetric analysis. The behaviors of the storage (G′) and loss (G″) moduli as a function of frequency of FFS obtained at 5 °C were typical of physical gels; with the G′ higher than the G″. The strength of the gels was affected by the PVA concentration.     

Gelling properties of kefiran, a food-grade polysaccharide obtained from kefir grain

The physicochemical and gelling properties of kefiran, a water-soluble glucogalactan with probed health-promoting properties, were investigated. Gel permeation chromatograms revealed a single distribution of molecular weight corresponding to 10⁷ Da. Intrinsic viscosity of kefiran determined using Huggins extrapolations was 6.0 dl/g and using Kramer approximations was 5.95 dl/g.Kefiran has a Newtonian behaviour in diluted solutions, which becomes pseudoplastic at higher concentrations. Rheological behaviour of the solution before and after freeze drying was evaluated by small deformation oscillatory rheological measurements. The mechanical spectrum of solution corresponded to an entangled network behaviour. After freeze–thaw treatment of the solution, a rheological behaviour transition from a liquid-like system to a gel was observed. The storage modulus (G′) in cryogels was 35 times higher than the value obtained for the solution. Rheological characteristics of the cryogel were influenced by kefiran concentration. As the polymer concentration increased, higher number of interactions was evident for the increment in both moduli (G′ and G″). The behaviour of kefiran cryogels about 37 °C determines its ability to melt at mouth temperature. These results suggest that kefiran cryogels could be an interesting alternative for its application in food formulations.     

Salmon by-product storage and oil extraction

Oils extracted from wild salmon by-products are excellent sources of long chain omega-3 polyunsaturated fatty acids including eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA). However, quality loss is expected if time delays are encountered before oil extraction. The free fatty acid levels (FFA), fatty acid profile and total fat soluble antioxidant activity in extracted oil from aging pink salmon heads and viscera stored at two temperatures (6 and 15 °C) for four days were determined. The FFA values in raw salmon heads and viscera increased with storage time and temperature. A significant difference (p < 0.05) from the starting material was noted at day 1 at both temperatures for FFA. Fatty acid composition data indicated no changes in the levels of long-chain omega-3 fatty acids with the respective temperature. The concentration of long-chain omega-3 fatty acids EPA ranged from 9.3 to 11.3 g/100 g of crude oil and DHA ranged from 12.3 to 13.1 g/100 g of crude oil. The antioxidant activity of the pink salmon oils at day 0 was 0.89 ± 0.15 μmole Trolox equivalent/g of crude oil. Significant decreases (p < 0.05) from the starting material were noted on day 2 for 15 °C samples and day 3 for 6 °C samples. After four days of storage antioxidant levels (Trolox equivalent/g of crude oil) were approximately 25% of initial values. Oil extracted from raw salmon heads and viscera remained a good source of long chain omega-3 fatty acids even after 4 days of raw material storage at 15 °C; however, fat soluble antioxidant activity was reduced and free fatty acid levels increased with increased raw material storage temperature and time.     

Role of cosolutes in gelation of high-methoxy pectin. Part 1. Comparison of sugars and polyols

Mixtures of high-methoxy pectin (DE 70; 1.0 wt%; pH 3.0) with ethan-1,2-diol, glycerol, xylitol, sorbitol, glucose, fructose or sucrose at concentrations of 50, 55, 60 and 65 wt% were prepared at 95 °C and changes in storage modulus (G′) and loss modulus (G″) during cooling to 5 °C, heating to 90 °C and re-cooling to 5 °C (at 1 °C/min) were measured at 1 rad s⁻¹ and 0.5% strain. In all cases, the onset temperature for gelation during cooling and the moduli recorded at 5 °C increased with increasing concentration of cosolute. Both values, however, were substantially lower for the liquid cosolutes (ethan-1,2-diol and glycerol) than for mixtures incorporating the same concentrations of the solid cosolutes. The difference is attributed to inhibition of pectin–pectin interactions by pectin–cosolute interactions, which in turn are inhibited by cosolute–cosolute interactions, these being weaker for the liquid cosolutes than for the solids (as indicated by lower melting points). On heating, there was an initial reduction in modulus, with the same temperature-course as the increase on cooling; for the solid cosolutes, this was followed by an increase attributable to hydrophobic association of methyl ester substituents. No such increase was seen with the liquid cosolutes, but differential scanning calorimetry studies showed two (reversible) thermal transitions in all cases, one over the temperature-range of the initial gelation process on cooling and the other coincident with the increase in modulus on heating in the presence of the solid cosolutes. The absence of any detectable increase in modulus on heating with the liquid cosolutes is attributed to accumulation of cosolute around the polymer chains (i.e. pectin–cosolute interactions) promoting hydrophobic association between methyl ester groups on the same chain, or within small clusters of chains, with, therefore, no contribution to network structure. At high concentrations of the solid cosolutes, the increase in modulus on heating was followed by a decrease at higher temperature; this is attributed to excessive aggregation, and was reflected in lower moduli on subsequent re-cooling to 5 °C, in contrast to the enhancement in gel strength after heating and cooling that was observed at lower concentrations of the same cosolutes.     

Characterization of gelation time and texture of gelatin and gelatin–polysaccharide mixed gels

The effects of cooling rate, holding temperature, pH and polysaccharide concentration on gelation characteristics of gelatin and gelatin–polysaccharide mixtures were investigated using a mechanical rheometer which monitored the evolution of G′ and G″. At low holding temperatures of 0 and 4 °C, elastic gelatin gels were formed whereas a higher holding temperature of 10 °C produced less elastic gels. At slow cooling rates of 1 and 2 °C/min, gelling was observed during the cooling phase in which the temperature was decreased from room temperature to the holding temperature. On the other hand, at higher cooling rates of 4 and 8 °C/min, no gelation was observed during the cooling phase. Good gelling behavior similar to that of commercial Strawberry Jell-O^® Gelatin Dessert was observed for mixtures of 1.5 and 15 g sucrose in 100 ml 0.01 M citrate buffer containing 0.0029–0.0066 g low-acyl gellan. Also, these mixed gels were stronger than Strawberry Jell-O^® Gelatin Desserts as evidenced by higher G′ and gel strength values. At a very low gellan content of 0.0029 g, increasing pH from 4.2 to 4.4 led to a decrease in the temperature at the onset of gelation, G′ at the end of cooling, holding and melting as well as an increase in gel strength. The gelation time was found to decrease to about 40 min for gelatin/sucrose dispersions in the presence of 0.0029 g gellan at pH 4.2 whereas the corresponding time at pH 4.4 was higher (79 min). In general, the gelation time of gelatin/sucrose dispersions decreased by a factor of 2 to 3 in the presence of low-acyl gellan. The addition of low-acyl gellan resulted in an increase in the gelation rate constant from 157.4 to 291 Pa. There was an optimum low-acyl gellan content for minimum gelation time, this optimum being pH dependent. Addition of guar gum also led to a decrease in gelation time to 73 min with a corresponding increase in the gelation rate constant to 211 Pa/min though these values were not sensitive to guar gum content in the range of 0.008–0.05 g. The melting temperature of gelatin/sucrose/gellan as well as gelatin/sucrose/guar mixtures did not differ significantly from that of pure gelatin or Strawberry Jell-O^® Gelatin Desserts. At pH 4.2, the melting rate constant was highest at a low-acyl gellan content of 0.0029 g whereas the rate constant was insensitive to low-acyl gellan content at pH 4.4. Addition of guar did not seem to affect the melting temperature or the melting rate constant.     

Physicochemical properties of pectins from okra (Abelmoschus esculentus (L.) Moench)

Okra pectin obtained by hot buffer extraction (HBSS) consists of an unusual pectic rhamnogalacturonan I structure in which acetyl groups and alpha galactose residues are substituted on rhamnose residues within the backbone. The okra Chelating agent Soluble Solids (CHSS) pectin consists of slightly different structures since relatively more homogalacturonan is present within the macromolecule and the rhamnogalacturonan I segments carry slightly longer side chains. The rheological properties of both okra pectins were examined under various conditions in order to understand the unusual slimy behaviour of okra pectins. The viscosity of the okra HBSS pectin was 5–8 times higher than the viscosity of the okra CHSS pectin. The okra HBSS pectin showed an elastic behaviour (G′ > G″) over a wide range of frequencies (10⁻¹–10 Hz), at a strain of 10%, while okra CHSS and saponified okra HBSS/CHSS pectin showed predominantly viscous responses (G′ < G″) over the same frequency range. The results suggest that the structural variation within the okra pectins greatly affect their rheological behaviour and it is suggested that acetylation of the pectin plays an important role through hydrophobic associations. Dynamic light scattering was used to study the association behaviour of both okra pectins at low concentration (0.001–0.1% w/w). Results showed that the saponified okra pectins did not exhibit a tendency to aggregate in the concentration range studied, whereas both non saponified samples showed a substantial degree of association. These results suggest that the unusual slimy behaviour of the non saponified samples may be related to the tendency of these pectins to associate, driven by hydrophobic interactions.     

Maturation effects in fish gelatin and HPMC composite gels

This study assessed the effectiveness of using hydroxylpropylmethylcellulose (HPMC) to enhance mechanical strength and thermal stability in fish skin gelatin (FG). The significant increase in absorbance (A₄₀₀) observed after HPMC had been added to FG and then matured indicated successful formation of a composite gel. Increased gel strength and storage modulus (G′) indicated the enhanced gelation ability of the matured composite gel, while increased melting temperature (T_m) and enthalpy (ΔH) indicated its improved thermal stability. Maturation-related rheological property improvements were more noticeable at 4 °C than 10 °C, but no apparent differences in T_m improvement were observed between 4 °C and 10 °C maturation. Nevertheless, the composite gel exhibited reversible cold and thermal gelation properties.     

Survival kinetics of Ephestia kuehniella eggs during 46–75 °C heat treatment

The effect of heat treatment on the survival of Ephestia kuehniella eggs was examined. Samples of 60 eggs were immersed in hot water at constant temperature in the 46–75 °C range for 5–1200 s. Following heat treatment and cooling, the eggs were stored at 24 ± 1 °C in a growth chamber for 7 days before survival evaluation. Statistical analysis of the data demonstrated that the thermal survival kinetics were best represented by a first-order reaction. The rate constant had an Arrhenius-type dependence over the 54–75 °C temperature range. Kinetic parameters were estimated by non-linear regression. The activation energy (E_a) and rate constant (k_ref) at the reference temperature (T_ref = 64.8 °C), were determined as 102.2 ± 6.2 kJ mol⁻¹ and 0.061 ± 0.003 s⁻¹, respectively, over the 54–75 °C temperature range. A 0.01% survival rate was obtained after 50 s at 75 °C. The data at temperatures below 50 °C were not in accordance with those at higher temperatures. Above this temperature, mortality was likely due to physiological disorders, as noted on a DSC thermogram.     

Enzymatic modification of protein preparation obtained from water-washed mechanically recovered poultry meat

Studies were conducted on a protein preparation obtained from washed mechanically recovered poultry meat (MRPM). The effect of addition of 3 g/kg microbial transglutaminase (MTG) to poultry meat protein was evaluated in terms of texture changes by dynamic mechanical analysis (DMA) and nuclear magnetic resonance (NMR) to determine water content in the preparation and its effect on protein. Samples with the addition of MTG were pre-incubated at 5–6 °C for 1.5, 3, 4.5, 6, 7.5, 9 and 24 h. The largest changes for both texture parameters and rheological properties were observed in the interval of approx. 4–7 h incubation. The protein preparation with the enzyme added had significantly higher values of the moduli of elasticity (G₁) and losses (G₂) in comparison to the control system. Samples with the addition of MTG also showed a higher water-binding capacity. From the NMR studies it was found that the greatest amount of water was bound by protein in the period of approx. 2.5–5 h incubation. After that time an increase was found in the amount of free water in the sample, which suggests that it was displaced from the system by stronger protein–protein bonds.     

Thermomechanical properties of biodegradable films based on blends of gelatin and poly(vinyl alcohol)

The aim of this work was to study the effect of the poly(vinyl alcohol) (PVA) concentration on the thermal and viscoelastic properties of films based on blends of gelatin and PVA using differential scanning calorimetry (DSC) and dynamic-mechanical analysis (DMA). One glass transition was observed between 43 and 49 °C on the DSC curves obtained in the first scanning of the blended films, followed by fusion of the crystalline portion between 116 and 134 °C. However, the DMA results showed that only the films with 10% PVA had a single peak in the tan δ spectrum. However, when the PVA concentration was increased the dynamic mechanical spectra showed two peaks on the tan δ curves, indicating two T_gs. Despite this phase separation behavior the Gordon and Taylor model was successfully applied to correlate T_g as a function of film composition, thus determining k=7.47. In the DMA frequency tests, the DMA spectra showed that the storage modulus values decreased with increasing temperature. The master curves for the PVA–gelatin films were obtained applying the TTS principle (T_r=100 °C). The WLF model was thus applied allowing for the determination of the constants C₁ and C₂. The values of these constants increased with increasing PVA concentrations in the blend: C₁=49–66 and C₂=463–480. These values were used to calculate the fractional free volume of the films at the T_g and the thermal expansion coefficient of the films above the T_g.     

Biochemical and thermal characterization of crude exo-polygalacturonase produced by Aspergillus sojae

Crude exo-polygalacturonase enzyme (produced by Aspergillus sojae), significant for industrial processes, was characterized with respect to its biochemical and thermal properties. The optimum pH and temperature for maximum crude exo-polygalacturonase activity were pH 5 and 55 °C, respectively. It retained 60–70% of its activity over a broad pH range and 80% of its initial activity at 65 °C for 1 h. The thermal stability study indicated an inactivation energy of E_d = 152 kJ mol⁻¹. The half lives at 75 and 85 °C were estimated as 3.6 and 1.02 h, respectively. Thermodynamic parameters, ΔH^*, ΔS^* and ΔG^*, were determined as a function of temperature. The kinetic constants K_m and V_max, using polygalacturonic acid as substrate, were determined as 0.424 g l⁻¹ and 80 μmol min⁻¹, respectively. SDS-PAGE profiling revealed three major bands with molecular weights of 36, 53 and 68 kDa. This enzyme can be considered as a potential candidate in various applications of waste treatment, in food, paper and textile industries.     

Combined effects of thymol, carvacrol and temperature on the quality of non conventional poultry patties

The combined effect of thymol (0–300 ppm), carvacrol (0–300 ppm), and temperature (0–18 °C) on the quality of non conventional poultry patties packaged in air and modified atmosphere (MAP: 40% CO_2; 30%O₂; 30% N₂) was investigated using a simplex centroid mixture design. The patties were monitored for microbiological (total viable count, Enterobacteriaceae, lactic acid bacteria, Pseudomonas spp.) physico-chemical (pH, colour) and sensory attributes. For the patties mixed with the antimicrobials and stored at low temperature (0–3 °C) a reduction of the cell load of about 1–1.5 log cfu/g was observed. The log reduction was lower at the end of storage time and decreased with the increase of the temperature. For the poultry patties packaged in MAP the higher log reduction for Pseudomonas spp. during all the storage time was observed. In both packaging atmospheres the combination of the essential oils and low temperature determined no modification for off-odour during the first 4 days of storage.     

Gelation mechanism and network structure of mixed solution of low- and high-acyl gellan studied by dynamic viscoelasticity, CD and NMR measurements

The gelation mechanism and the change of the network structure during cooling of the mixed solution of high-acyl (HA) and low-acyl (LA) gellan (containing 0.5% HA gellan and 0.5% LA gellan; hereafter called “mixed solution”) were elucidated on the basis of the results of dynamic viscoelasticity, circular dichroism (CD), and NMR measurements, which provide information about the network formation, the structural change due to random coil-double helix (C–H) transition, and the chain mobility of gellan, respectively. It was demonstrated that HA gellan chains in the mixed solution underwent C–H transition individually to form a network structure at the transition temperature for 1% HA gellan solution (75 °C), where storage modulus G′ and loss modulus G″ were steeply increased and the chain mobility of the HA gellan was restricted. The structural change of the HA gellan chains proceeded gradually with further cooling. At 25 °C, which is the C–H transition temperature for 1% LA gellan solution, LA gellan chains in the mixed solution formed a double helix, where G′ and G″ were slightly increased and the chain mobility of LA gellan was restricted. The results suggest that the double helix formation involves only the same kind of gellan chains even in the mixed solution, and that LA gellan chains decrease the mobility and promote the double helix formation of HA gellan chains, and vice versa.     

Crystalline stability of self-assembled fibrillar networks of 12-hydroxystearic acid in edible oils

The stability of organogels differs based on the organogelator concentration, storage temperature, and solvent type. Organogel post-crystallization annealing was monitored at 5 °C, 15 °C, 20 °C or 30 °C for up to 1 month. Gels, stored at 5 °C, had highly immobilized oil, as judged from large T₂ relaxation peaks at 50–70 ms determined by pulsed nuclear magnetic resonance (pNMR) and visual observations. When the gels were stored at 30 °C, the 50–70 ms T₂ relaxation peak shifted to longer relaxation times, indicating that the oil was more mobile than at 5 °C. Along with the increase in syneresis at 30 °C, the 12HSA network’s crystallinity was also greater, having fewer inclusions of liquid oil, as determined by pNMR. The highly branched network observed at 5 °C changed more in time with regards to crystallinity although it entrained the oil to a much greater extent than the gels stored at 30 °C.     

Evaluation and predictive modeling of shelf life of minced beef stored in high-oxygen modified atmosphere packaging at different temperatures

The aims were: (1) to follow the freshness decay of minced beef stored in high-oxygen modified atmosphere packaging at different temperatures (4.3, 8.1 and 15.5 °C) by applying traditional methods (microbiological counts, color evaluation, thiobarbituric acid assay TBA, headspace gas composition) and e-nose; (2) to model the decay kinetics to obtain information about the maximum shelf life as function of storage conditions. The minced beef, packaged in modified atmosphere was supplied by a manufacturer at the beginning of its commercial life. The study demonstrated the ability of the traditional methods to describe the kinetics of freshness decay. The modeling of the experimental data and the comparison with microbiological or chemical thresholds allowed the setting, for each index, of a stability time above which the meat was no longer acceptable. The quality decay of meat was also evaluated by the headspace fingerprint of the same set of samples by means of a commercial e-nose. A clear discrimination between “fresh” and “old” samples was obtained using PCA and CA, determining at each temperature a specific range of stability time. The mean value of the stability times calculated for each index was 9 days at 4.3 °C (recommended storage temperature), 3–4 days at 8.1 °C (usual temperature in household refrigerators) and 2 days at 15.5 °C (abuse temperature). Resolution of the stability times allowed calculation of mean Q₁₀ values, i.e. the increase in rate for a 10 °C increase in temperature.The results show that the Q₁₀ values from the traditional methods (3.6–4.0 range) overlapped with those estimated with e-nose and color indexes (3.4 and 3.9, respectively).