Front-face fluorescence spectroscopy as a tool to classify seven bovine muscles according to their chemical and rheological characteristics

Potential of front-face fluorescence spectroscopy was evaluated to classify muscles according to their chemical and rheological characteristics. Seven bovine muscles (Semitendinosus, Semimembranosus, Tensor fasciae latae, Rectus abdominis, Longissimus thoracis et lumborum, Triceps branchii and Infraspinatus) were taken from 14 animals of the Charolais breed. Chemical characteristics and rheological properties of the meat were determined including dry matter, fat, collagen, protein, peak load, energy required to rupture and cooking loss. Emission spectra in the 305–400 nm, 340–540 nm and 410–700 nm ranges were recorded using front-face fluorescence spectroscopy by fixing the excitation wavelengths at 290, 322 and 382 nm, respectively. Analysis of variance (ANOVA) applied on chemical and rheological parameters showed that these muscles were significantly different (P < 0.01) from each other. Chemical and rheological data were divided into low, medium and high range groups for each variable. The results of PLSDA showed that 305–400 nm spectra were responsible for 67% (calibration), 53% (validation), 96% (calibration) and 55% (validation) of good classification for protein and cooking loss, respectively, while 340–540 nm spectra allowed 75% of good classification (validation samples) for fat content.     

Utilisation of a rapid technique based on front-face fluorescence spectroscopy for differentiating between fresh and frozen–thawed fish fillets

The potential of front-face fluorescence spectroscopy combined with chemometric tools was investigated to differentiate frozen–thawed from fresh fish. A total of 24 fish fillets, i.e., 12 fresh samples and 12 frozen–thawed samples, were investigated. Regarding the frozen–thawed samples, two speeds of freezing and thawing were tested (fast and slow) and for each condition, three whiting fillets were analysed. The fluorescence emission spectra of tryptophan (excitation: 290 nm, emission: 305–400 nm) and nicotinamide adenine dinucleotide (NADH) (excitation: 340 nm, emission: 360–570 nm) were recorded directly on samples. In a first step, the principal component analysis (PCA) was applied separately to the tryptophan or NADH fluorescence spectra. From the NADH spectra, PCA results showed a good discrimination between fresh and frozen–thawed fish samples. But it was not the case with the tryptophan fluorescence spectra. In a second step, factorial discriminant analysis (FDA) was applied to the first five principal components (PCs) of the PCA performed on the two data sets. Considering tryptophan fluorescence spectra, correct classification was observed for 62.5% and 70.8% of the calibration and validation spectra, respectively. A better classification was obtained from NADH fluorescence spectra since 100% correct classifications were obtained for the calibration and validation spectra. It was concluded that NADH fluorescence spectra may be considered as a promising probe for the reliable differentiation between frozen–thawed and fresh fish.     

Comparison of visible and near infrared reflectance spectroscopy to discriminate between pasture-fed and concentrate-fed lamb carcasses

We compared visible and near infrared spectroscopy to distinguish pasture-fed (P) from stall concentrate-fed (S) lamb carcasses. A total of 120 P and 139 S lambs were used. The reflectance spectrum of perirenal fat was measured at wavelengths between 400 and 700 nm using a portable spectrophotometer, and at wavelengths between 400 and 2500 nm using a laboratory monochromator NIRSystem. In method W_450–510, the reflectance data were used at wavelengths between 450 and 510 nm. In methods W_400–700 and W_400–2500, a multivariate analysis was performed over the full set of reflectance data, at wavelengths in the range 400–700 nm and 400–2500 nm, respectively. The proportion of correctly classified P lambs was 89.1%, 90.8% and 97.5% for W_450–510, W_400–700 and W_400–2500, W_400–2500 performing best. The proportion of correctly classified S lambs was not significantly different between methods (98.6%, 98.6% and 97.8% for W_450–510, W_400–700 and W_400–2500, respectively).     

Potential of synchronous fluorescence spectroscopy coupled with chemometrics to determine the heterocyclic aromatic amines in grilled meat

In this study, the potential of synchronous front-face fluorescence spectroscopy (SFS) coupled with chemometrics was investigated for the determination of heterocyclic aromatic amines (HAA) in cooked meat samples. Bovine meat samples (1–2 mm thick, 5 cm diameter) taken from Longissimus thoracis muscle were cooked at an average temperature of 237 °C for 5, 7 and 10 min. Four HAA (4, 8-DiMeIQx, MeIQx, IQx and PhIP) were determined on the cooked meat samples using classical LC-APCI-MS/MS method. In parallel, SFS spectra were recorded using a spectrofluorimeter on the same cooked meat samples in an excitation wavelength range of 250–550 nm using offsets of 20, 30, 40, …, 160 nm between excitation and emission monochromators. The three-dimensional synchronous fluorescence data set was analyzed using PARAFAC (parallel factor) analysis and N-PLS (n-way partial least square) regression method. PARAFAC analysis allowed capturing the fluorescence changes occurring in meat during cooking: the best model was obtained with 2 components (core consistency of 100% and explained variance of 99.2%). Whereas the loading profile of component 1 showed a maximum excitation at about 495 nm and an optimal offset of 60 nm, the loading profile of component 2 was characterized by a maximum excitation at 367 nm and an optimal offset of 90 nm. The results obtained using N-PLS regression showed good correlation between the spectral and analytical data: average recovery of 104% for 4, 8-DiMelQx, 102% for both MelQx and IQx, and 103% for PhIP were obtained. In conclusion this study indicates that SFS along with chemometrics has the potential to be used as a rapid and non-destructive technique for the determination of HAA contents in meat.     

Southern Spain lamb types discrimination by using visible spectroscopy and basic physicochemical traits

The potential for using visible spectroscopy (400–700 nm) to classify six types (breed × production system) of lamb meat was investigated. Seven wavelengths namely 400, 410, 420, 450, 510, 610 and 670 nm were retained for the discriminant analysis. The basic meat physicochemical traits of Longissimus dorsi were also studied and a model including that information together with the spectra was developed to compare both accuracies. Then, Myoglobin content, water holding capacity, pH, a^*, 670 and 610 nm wavelengths, protein percentage, L^*, ash content, 450 and 420 nm wavelengths and moisture percentage were selected as variables for the development of the discriminant function. The data analysis showed that it was possible to discriminate the lamb types with accuracy around 83% using visible spectroscopy. However these results improved to 95% when using the reflectance together with basic physicochemical traits (12% better than using only the spectra).     

Duroc and Iberian pork neural network classification by visible and near infrared reflectance spectroscopy

Visible and near infrared reflectance spectroscopy (VIS/NIRS) was used to differentiate between Duroc and Iberian pork in the M. masseter. Samples of Duroc (n = 15) and Iberian (n = 15) pig muscles were scanned in the VIS/NIR region (350–2500 nm) using a portable spectral radiometer. Both mutual information and VIS/NIRS spectra characterization were developed to generate a ranking of variables and the data were then processed by artificial neural networks, establishing 1, 3, or 10 wavelengths as input variable for classifying between the pig breeds. The models correctly classified >70% of all problem assumptions, with a correct classification of >95% for the three-variable assumption using either mutual information ranking or VIS/NIRS spectra characterization. These results demonstrate the potential value of the VIS/NIRS technique as an objective and rapid method for the authentication and identification of Duroc and Iberian pork.     

Development of a rapid method based on front-face fluorescence spectroscopy for the monitoring of egg freshness: 2—evolution of egg yolk

This preliminary study is devoted to the application of front-face fluorescence spectroscopy to the study of egg yolks during storage. A total of 79 eggs stored for 1, 2, 3, 4, 5, 9, 10, 12, 16, 18, 23, 25 and 29 days at room temperature were analysed. The fluorescence emission spectra of tryptophan residues (excitation: 290 nm; emission: 305–430 nm) of proteins and the excitation spectra of vitamin A (emission: 410 nm; excitation: 270–350 nm) were recorded directly on egg yolk samples. Factorial discriminant analysis (FDA) was used to classify the eggs according to their date after they were laid. Using tryptophan fluorescence spectra, correct classification was observed for 57.1 and 51.9% for the calibration and the validation sets, respectively. Better classification (94.9 and 91.4% of the calibration and validation samples, respectively) was obtained from the vitamin A fluorescence spectra. The first five principal components (PCs) of the principal component analysis (PCA) extracted from each data set (tryptophan and vitamin A fluorescence spectra) were pooled (concatenated) into a single-matrix and analysed by FDA. Correct classifications were obtained for 97.5% of the calibration and 96.3.1% of the validation spectra. The discrimination of the investigated egg yolks according to their storage time was excellent. It was concluded that the concatenation of different fluorescence spectra might be considered as a promising indicator of shell egg freshness when they are used in egg products.     

A comparison and joint use of mid infrared and fluorescence spectroscopic methods for differentiating between manufacturing processes and sampling zones of ripened soft cheeses

Ten traditional M1 (n = 5) and M2 (n = 5) soft cheeses produced from raw milk, and five other stabilised M3 (n = 5) cheeses manufactured from pasteurised milk, were studied using mid infrared (MIR) and front face fluorescence (FFFS) spectroscopies. MIR (3000–900 cm⁻¹), tryptophan (excitation: 290 nm, emission: 305-450 nm), 400-640 emission spectra (excitation: 380 nm) and vitamin A (excitation: 280–350 nm, emission: 410 nm) spectra were recorded at two sampling zones (external (E) and central (C)) of the investigated cheeses. When the factorial discriminant analysis (FDA) was applied to the MIR spectra, the classification was not satisfactory. With tryptophan fluorescence spectra, correct classification of 94.4 and 69.4% was observed for the calibration and validation spectra, respectively. Better classification was obtained using vitamin A fluorescence spectra, since 91.8 and 80.6% of the calibration and validation spectra, respectively, were correctly classified. When the first five principal components (PCs) of the PCA extracted from each data set were pooled into a single matrix and analysed by FDA, the classification was considerably improved, obtaining a percentage of correct classification of 100 and 91.7% for the calibration and validation samples, respectively. It was concluded that concatenation of the physico-chemical and spectroscopic data sets is an efficient technique for the identification of soft cheese varieties.     

Synchronous Front-Face Fluorescence Spectroscopy Coupled with Parallel Factors (PARAFAC) Analysis to Study the Effects of Cooking Time on Meat

ABSTRACT:  In this study, the potential of synchronous front-face fluorescence coupled with chemometrics has been investigated for the analysis of cooked meat. Bovine meat samples (thin slices of 5 cm diameter) taken from  Longissimus dorsi  muscle were cooked at 237 °C for 0, 1, 2, 5, 7, and 10 min under control conditions. Synchronous front-face fluorescence spectra were collected on meat samples in the excitation wavelength range of 250 to 550 nm using offsets (Δλ) of 20, 30, 40, 50, 60, 70, 80, 90, 100, 110, 120, 130, 140, 150, and 160 nm between excitation and emission wavelengths. The synchronous fluorescence landscape containing 360 spectra was analyzed using PARAFAC. The best PARAFAC model presented 2 components since core consistency values for the first 2 components were 100% and the explained variance was 67.98%. The loading profiles of 1st and 2nd components had an optimal Δλ of 70 and 40 nm, respectively, allowing to determine the excitation (exc.) and emission (em.) maxima wavelengths of 1st (fluorescence band at about exc.: 340 to 400/em.: 410 to 470 nm, and peak at exc.: 468/em.: 538 nm) and 2nd (exc.: 294 nm/em.: 334 nm) components. As the loading profile of the 1st component of PARAFAC was assigned to Maillard-reaction products formed during cooking, the profile of the 2nd component corresponded with the fluorescence characteristics of tryptophan residues in proteins. Loadings and scores of the PARAFAC model developed from the synchronous fluorescence spectra enabled to get information regarding the changes occurring in meat fluorophores during cooking of meat at 237 °C from 0 to 10 min.     

Dynamic testing rheology and fluorescence spectroscopy investigations of surface to centre differences in ripened soft cheeses

The viscoelastic properties and the matrix structures of three different retailed soft cheeses (M1, M2 and M3), for which the manufacturing process was varied, were studied from the surface to the centre of the cheese using dynamic rheology and front-face fluorescence spectroscopy. The storage modulus (G′) and the loss modulus (G″) values of the samples increased from the surface to the inner part of the cheeses, while strain and tan δ decreased. Protein tryptophan (excitation: 290 nm; emission: 305–400 nm) and vitamin A (emission: 410 nm; excitation: 250–350 nm) spectra were recorded at 20°C in samples cut from the surface to the centre. For each cheese, the data sets containing fluorescence spectra and rheology data were evaluated using multidimensional statistical methods. In addition, the three cheeses were well discriminated by their spectra by applying factorial discriminant analysis. From the tryptophan fluorescence data sets, 94% and 87.7% good classifications were observed for calibration and validation groups, respectively. A better classification (100% and 96% for principal and test samples) was obtained from the vitamin A spectra. Canonical correlation analysis was performed on the rheology and tryptophan fluorescence spectral data sets, and on the rheology and vitamin A fluorescence spectra data sets. The two groups of variables were found to be highly correlated since the squared canonical coefficients for canonical variates 1, 2, 3, 4 were higher than 0.98. These high correlations indicate that cheese rheology is a reflection of its structure at the molecular level.     

Effects of rapid chilling of carcasses and time of deboning on weight loss and technological quality of pork semimembranosus muscle

The effect of rapid air chilling of carcasses in the first 3 h of chilling at −31 °C (then at 2–4 °C, till 24 h post-mortem) and the possibility of earlier deboning (8 h post-mortem) after rapid air chilling, compared to conventional air chilling (at 2–4 °C, till 24 h post-mortem) on weight loss and technological quality (pH value, tenderness, drip loss, cooking loss and colour - L^*a^*b^* values) of pork M. semimembranosus was investigated. Under the rapid chilling conditions, weight loss was 0.8% at 8 h post-mortem and increased to 1.4% at 24 h post-mortem when weight loss was 2.0% under conventional chilling. Carcasses that were rapid chilled had significantly lower (P < 0.001) internal temperature in the deep leg at 4 (25.7 °C), 6 (13.0 °C), 8 (6.2 °C) and 24 h (3.8 °C) post-mortem compared to conventional chill treatment (32.7, 24.2, 19.1 and 5.1 °C, respectively). Rapid chilling reduced significantly (P < 0.05) the rate of pH value decline at 8 h (6.02) post-mortem in M. semimembranosus compared to conventional chill treatment (5.88). Compared to conventional chilling, in M. semimembranosus deboned in different time post-mortem, rapid chilling had a positive significant effect on drip loss (P < 0.05, muscles deboned 8 h post-mortem), cooking loss (P < 0.001) and incidence of pale colour (L^* value). Rapid chilling i.e. rapid chilling and earlier deboning had neither positive nor negative significant effects (P > 0.05) on other investigated technological quality parameters of M. semimembranosus (tenderness, a^* value and b^* value) compared to conventional chilling.     

Use of meat fluorescence emission as a marker of oxidation promoted by cooking

Accumulation of fluorescent pigments in cooked bovine meat (M. Longissimus thoracis) was studied in relationship with the heating parameters (time and temperature). Muscles were aged at 4 °C for 11 days under vacuum before cooking. Meat cooking was performed by applying jets of steam. Three different heating treatments were tested: two with constant surface temperatures of 65 and 96 °C for 300 s, and one with a continuously increasing surface temperature up to 207 °C. After extraction in water/dichloromethane/ethanol, fluorescence pigments were distributed between the apolar phase (emission 420–440 nm after excitation at 360 nm) and the polar phase, where two emission peaks were seen (emission 410–430 and 515 nm after excitation at 360 nm). Fluorescence in the two phases was little affected by heating at the two constant temperatures while it increased exponentially after 1 min of treatment, as the varying temperature reached 141 °C. The maximum fluorescence increases, measured in the extreme conditions of cooking (207 °C/300 s), were of 5000% in the apolar phase and 1700% in the polar phase. Thiobarbituric acid reactive substances (TBARS) and protein carbonyls were measured in parallel. The correlations between these two parameters and the fluorescence emission demonstrated that the interaction between proteins and aldehyde products of lipid peroxidation was mainly involved in the production of fluorescent pigments in cooked meat.     

Changes in the content of biologically active polyamines during beef loin storage and cooking

Dietary polyamines putrescine (PUT), spermidine (SPD) and spermine (SPM) participate in numerous human physiological processes, including tumour growth. Reliable information on their contents in foods is thus needed. Data for processed beef are very limited. Nine experiments with beef loin (longissimus lumborum) were, therefore, carried out. Loin cuts were stored at −18 °C for 178 days or beef was stored aerobically, vacuum-packaged (VP) and packaged in a modified atmosphere (MA; 70% N₂ and 30% CO₂, v/v) at +2 °C for 9, 21 and 21 days, respectively. The effects of three usual cooking treatments were also tested. Polyamines were determined after extraction with perchloric acid as dansyl derivatives using an HPLC method. Only SPM was detected at initial levels of 23.5–27.5 mg kg⁻¹, PUT and SPD contents were below the detection limits of 1.2 and 1.7 mg kg⁻¹, respectively. SPM content increased during the initial weeks of frozen storage and then gradually decreased to about 70% of the initial values at the end of the storage period (P < 0.05). No apparent SPM decrease was observed during aerobic storage for 9 days, while in VP and MA variants the losses were about 20% of the initial values on day 21 (P < 0.05). Slightly higher mean SPM losses were observed during boiling and stewing with and without added water. The differences among the cooking treatments were not significant. However, significant differences were observed among the loins used.     

Migration of ε-caprolactam from nylon cooking utensils: validation of a liquid chromatography-ultraviolet detection method

A large amount of modern cooking utensils are made of nylon. This is the generic name of polyamides that are polymers having characteristic amide linkages. Caprolactam is the monomer used in the synthesis of nylon 6. This work presents the validation of an LC-UV method for the determination of caprolactam in the aqueous food simulant 3% acetic acid (w/v) employing capryllactam as internal standard. LC–MS/MS was the confirmation technique. The obtained detection and quantification limits were satisfactory regarding caprolactam specific migration limit; these were 0.6 and 2 mg kg⁻¹, respectively. The working range was 2–30 mg kg⁻¹ and the correlation coefficients (r) were in all cases at least 0.999. The intra-day repeatability was between 2.5 and 4.8% depending on the validation level. The global mean recovery was 100.6% with a RSD (%) of 5.0%. Different nylon cooking utensils were analyzed for the migration of caprolactam in the food simulant acetic acid 3% p/v. Conditions used were repeated exposure to the simulant for 2 h at 100 °C, and the results obtained after the third exposure were in compliance regarding Directive 2002/72/EC. With the aim of identifying the polymer used in these utensils, IR spectra were also obtained for all samples.     

Physical and chemical characteristics of donkey meat from Martina Franca breed

The rheological and chemical characteristics of meat obtained from 12 Martina Franca donkey males, slaughtered at 14 months of age and a mean final body weight of 169 kg were determined. Meat samples were taken four days post mortem from muscles Longissimus thoracis et lumborum and Biceps femoris, colorimetric parameters were measured to determine L^* (lightness), a^* (redness), b^* (yellowness) and chroma. The Longissimus was significantly lighter (P < 0.05) compared to the Biceps femoris, with L^* indexes of 35.86 and 31.34, respectively. Fatty acid composition of the intramuscular fat showed a high content of polyunsaturated fatty acids (PUFAs) in both muscles, respectively 25.16 g/100 g total fatty acids in the Longissimus and 24.97 g/100 g total fatty acids in the Biceps femoris; oleic acid and palmitic acid were the two most abundant fatty acids in both muscles. The percentages of essential amino acids were higher in both muscles compared with the total amino acid content, respectively 52.88% in the Longissimus, and 51.26% in the Biceps femoris. The high level of unsaturation of the intramuscular fat resulted in a high ratio of unsaturated to saturated fat, and the total amount of essential amino acids, exceeding 50% of the total amino acids showed that donkey meat from a health point of view is a good alternative to traditional red meats.     

Rheological characterizations of texturized whey protein concentrate-based powders produced by reactive supercritical fluid extrusion

A powder blend comprising (by weight) 94% whey protein concentrate (WPC80), 6% pre-gelatinized corn starch, 0.6% CaCl₂, and 0.6% NaCl was texturized using a supercritical fluid extrusion (SCFX) process. The blend was extruded at 90 °C in a pH range of 2.89 to 8.16 with 1% (db) supercritical carbon dioxide (SC-CO₂) and 60% moisture content. The texturized WPC-based (TWPC) samples were dried, grounded into powder, reconstituted in water, and evaluated using a range of rheological studies. Most TWPC samples exhibited shear thinning behavior and their mechanical spectra were typical of weak gel characteristics. The TWPC produced under extremely acidic condition of pH 2.89 with SC-CO₂ yielded the highest η^* (10,049 Pa s) and G′ (9,885 Pa) compared to the unprocessed WPC (η^* = 0.083 Pa s and G’ = 0.036 Pa). The SCFX process rendered WPC into a product with cold-setting gel characteristics that may be suitable for use as a food texturizer over a wide range of temperatures.     

The triacylglycerol preparation of conjugated linoleic acid reduces lipid oxidation in irradiated, cooked ground beef patties

It is proposed that conjugated linoleic acid (CLA) would depress the lipid oxidation caused by irradiation of cooked, aerobically stored ground beef patties. The free fatty acid (FFA–CLA) and triacylglycerol (TAG–CLA) preparations of CLA were added at 0%, 1%, 2%, or 4% during the grinding process. Patties were irradiated at 1.5–2.0 kGy and frozen at −20 °C. Subsequently, the patties were tempered to 4 °C, cooked to 70 °C and held at 4 °C for 7 d. Enrichment of ground beef with CLA increased the cis-9,trans-11 and CLA trans-10,cis-12 CLA isomers in ground beef patties, even after cooking. Weight loss (P = 0.03) and percentage fat (P = 0.05) were higher in irradiated beef patties than in control patties. Irradiation decreased the concentration of α-linolenic acid (18:3n − 3) in the ground beef by over 60% (P = 0.07), whereas thiobarbituric acid reactive substances (TBARS) values were higher (P = 0.004) in irradiated beef patties than in control patties. The 1% concentration of added TAG–CLA reduced TBARS in irradiated ground beef patties, whereas 2% and 4% FFA–CLA depressed TBARS (CLA type × percentage interaction P = 0.04). Irradiation increased the cardboard and painty aromatic attributes (P  0.05), and FFA–CLA preparation increased the painty aromatic attribute and afterburn aftertaste, but these effects were not observed with the TAG–CLA preparation (CLA type × treatment interaction P < 0.04). Adding 1% TAG–CLA to ground beef during grinding can reduce lipid oxidation in irradiated, cooked ground beef patties without the negative aftertastes associated with the FFA–CLA preparation.     

Detection of insect-damaged wheat kernels using near-infrared hyperspectral imaging

Insect damage in wheat adversely affects its quality and is considered one of the most important degrading factors in Canada. The potential of near-infrared (NIR) hyperspectral imaging for the detection of insect-damaged wheat kernels was investigated. Healthy wheat kernels and wheat kernels visibly damaged by Sitophilus oryzae, Rhyzopertha dominica, Cryptolestes ferrugineus, and Tribolium castaneum were scanned in the 1000–1600 nm wavelength range using an NIR hyperspectral imaging system. Dimensionality of the acquired hyperspectral data was reduced using multivariate image analysis. Six statistical image features (maximum, minimum, mean, median, standard deviation, and variance) and 10 histogram features were extracted from images at 1101.69 and 1305.05 nm and given as input to statistical discriminant classifiers (linear, quadratic, and Mahalanobis) for classification. Linear discriminant analysis and quadratic discriminant analysis classifiers correctly classified 85–100% healthy and insect-damaged wheat kernels.     

Preliminary investigations on the effects of ageing and cooking on the Raman spectra of porcine longissimus dorsi

The influence of ageing and cooking on the Raman spectrum of porcine longissimus dorsi was investigated. The rich information contained in the Raman spectrum was highlighted, with numerous changes attributed to changes in the environment and conformations of the myofibrillar proteins.Predictions equations for shear force and cooking loss were developed from the Raman spectra of both raw and cooked pork. Good correlations and standard errors of prediction were obtained for both WB shear force and cooking loss, with the raw and the cooked samples showing almost identical results R² = 0.77, root mean standard error of prediction (RMSEP)% of mean = 12% for shear force; R² = 0.71, RMSEP% of mean = 10% for cooking loss. The Raman spectra were also able to predict the extent of cooking that occurred within the pork (R²_val = 0.94, RMSEP% of range = 5.5%).Raman spectroscopy has considerable potential as a method for non-destructive and rapid determination of pork quality parameters such as tenderness. Raman spectroscopy may provide a means of determining changes during cooking and the extent to which foods have been cooked.     

Effects of teeth maturity and fatness of Nellore (Bos indicus) steer carcasses on instrumental and sensory tenderness

This study sought to evaluate the effects of teeth maturity and carcass fatness on physical and sensory traits of the beef ribeye (M. longissimus thoracis). Carcass sides (n = 60) of Nellore steers were grouped into six categories, according to teeth maturity (2, 4 and 6 permanent incisors), and fatness (2 – slight and 3 – average). The boneless ribeye cuts (6th – 9th ribs) were vacuum packed and aged for 14 days. Steaks, 2.5 cm thick, were evaluated as to sarcomere length, shear force and sensory attributes. Sarcomere length was not affected (P > 0.05) by maturity or fatness. Teeth maturity did not influence (P > 0.05) tenderness measured by instrumental or sensory analysis, however rib steaks from fatter carcasses displayed better tenderness (P < 0.01) and lower cooking losses (P < 0.01). In the Nellore steer carcasses produced in Brazil, fatness may be more important than teeth maturity to improve meat tenderness.