A method for simultaneous fluorometry and rheology of connective tissue in bulk meat

A probe tipped with optical fibres was mounted on the load cell of a compression tester and pushed into well-aged beef rib roasts (Canada Grade AAA, n = 6, 33 ± 3.6 days post-mortem). Fluorescence (F; excitation 365 nm, emission >420 nm) and reflectance (R; 365 nm) were measured through single optical fibres. Diffuse R was measured using different fibres for illumination and detection, thus responding to tissue between the two fibres. Replication was by a matrix pattern of penetrations on single roasts. For example, in a typical roast, F was correlated with the force of penetration (mean r = 0.86 ± 0.06, n = 20, all P < 0.001). R was less (P < 0.001) strongly correlated with penetration force (mean r = 0.46 ± 0.10, n = 20, all P < 0.001). F signals from connective tissue contained less peaks than R signals from both connective and adipose tissue (respectively, 2.75 ± 0.43 versus 5.57 ± 0.67 peaks cm⁻¹, P < 0.001, n = 20 pairs) and F peaks were wider than R peaks (respectively, 3.54 ± 0.88 versus 1.38 ± 0.19 mm, P < 0.001, n = 20 pairs). For the spinales dorsi aponeurosis, the depth at which peak force was reached was strongly correlated with the depths at which both peak F and peak R were reached (r = 0.98, P < 0.001, n = 20 for both). Diffuse R was only weakly correlated with penetration force (mean r = 0.29 ± 0.12 with only 5/10 correlations significant P < 0.001). This new method showed the primary resistance to dorso-ventral penetrometry of well-aged beef rib roasts originated from connective tissue.     

Evaluation of the antioxidant potential of grape seed and bearberry extracts in raw and cooked pork

The effect of grape seed extract (GSE) and bearberry (BB), on lipid oxidation (TBARS, mg malondialdehyde (MDA)/kg muscle), colour (CIE ‘a’ redness value), pH, microbial status (log₁₀CFU colony forming units/g pork) and sensorial properties of cooked pork patties was investigated. GSE (0–1000 μg/g muscle) and BB (0–1000 μg/g muscle) were added to raw pork (M. longissimus dorsi) patties which were stored in modified atmosphere packs (MAP) (75% O₂:25% CO₂) for up to 12 days at 4 °C. Cooked pork patties were stored in MAP (70% N₂:30% CO₂) for up to 4 days at 4 °C. Mesophilic plate counts and pork pH were unaffected by GSE and BB. GSE and BB addition decreased (P < 0.05) lipid oxidation (TBARS) in raw pork patties on days 9 and 12 of storage, relative to controls. Antioxidant activity of GSE and BB was observed in cooked pork patties demonstrating the thermal stability of GSE and BB. The ‘a’ redness values of raw and cooked pork patties marginally increased with increasing GSE concentration. The sensory properties of cooked pork patties were unaffected by GSE and BB addition. Results obtained demonstrate the potential for using health promoting nutraceuticals in meat and meat products.     

Effect of Duroc content, sex and ageing period on meat and eating quality attributes of pork loin

This study was conducted to determine the effect of percentage Duroc content of entire male and female pigs and ageing period on meat and eating quality attributes of pork loin (M. longissimus thoracis et lumborum). A total of 84 pigs [entire males (n=42) and female (n=42)] of 0% Duroc (100% Large White), 50% Duroc (Duroc×Large White) or 100% Duroc (n=14 pigs per sex×genotype combination) were slaughtered at a liveweight of 100 kg. Steaks from the M. longissimus lumborum of female pigs were aged for either 2 or 7 days post-slaughter and evaluated using a consumer taste panel. Eating quality attributes of tenderness, flavour and overall liking of pork loin steaks from female pigs were not (P>0.05) influenced by Duroc content. Pork from 100% Duroc pigs was juicier (P=0.05) and had a higher (1.84%, P=0.05) intramuscular fat content than pork from 0 and 50% Duroc pigs (1.40 and 1.25%, respectively). Pork from entire male pigs had a lower (P<0.001) intramuscular fat content, was darker (P<0.01) in colour and recorded higher (P<0.01) Warner Bratzler shear force values compared with pork from female carcasses. Ageing pork loin steaks in vacuum bags for 7 days improved tenderness (P<0.01), flavour (P<0.05) and overall liking (P<0.05) compared with steaks aged for 2 days post-slaughter. Ageing of pork steaks for 7 days post-slaughter improved eating quality attributes far more effectively than increasing percentage Duroc content of pigs, which only influenced consumer scores for juiciness.     

Effect of low voltage electrical stimulation of pig carcasses and ageing on sensory attributes of fresh pork

The effect of electrically stimulating pig carcasses and ageing on sensory attributes of pork was evaluated in this study. A total of 48 female pigs [Duroc×Large White/Landrace (A; n=24) and Large White/Landrace (B; n=24)] were randomly allocated immediately prior to slaughter to one of two low voltage stimulation treatments; no stimulation or 150 mA applied for 30 s at 2 min post-exsanguination. Each side of the carcass was then randomly allocated to an ageing treatment of either 2 or 7 days post-slaughter. Muscle pH of the M. longissimus lumborum was lower (P<0.001) in electrically stimulated carcasses when measured from 40 min to 8 h post-slaughter compared with non-stimulated carcasses. Percentage drip loss, muscle lightness and PSE incidence were not influenced (P>0.05) by electrical stimulation. Electrical stimulation of pig carcasses and ageing pork for 7 days post-slaughter both improved (P<0.001) consumer scores for tenderness, juiciness, overall liking and quality category, however the interaction term of electrical stimulation and ageing was not significant for any of the sensory attributes. Pork from non-stimulated carcasses that was aged for 2 day post-slaughter was less tender (P<0.01) compared with pork in all other treatments. These results indicate that electrical stimulation (150 mA applied for 30 sec at 2 min post-exsanguination) was effective in improving eating quality attributes of pork, particularly when pork was aged for only 2 days post-slaughter, without detrimentally affecting colour or drip loss.     

Identification of halothane genotypes by calcium accumulation and their meat quality using live pigs

The three halothane genotypes (NN, Nn, and nm) were identified by measuring the capacity for Ca²⁺ accumulation by sarcoplasmic reticulum in whole muscle homogenate preparations of M. longissimus dorsi with a Ca²⁺ specific electrode at 35°C. Significant differences (P < 0·001) in deterioration (%) of Ca²⁺ accumulation, 12% for NN, 35% for Nn, and 81% for nn pigs, were observed after ageing the whole muscle homogenate preparations for 24 h in ice.

Predictions of meat quality in live pigs (n = 34) based on the values for water-holding capacity, assessed as fluid (g/0·5 g wet wt LD), and pH (fluid) by using small biopsy LD samples (Cheah et al. 1993) were performed on all the halothane genotypes. The halothane genotype NN (n = 11) showed a fluid value of 0·37 ± 0·01 and a pH (fluid) value of 6·62 ± 0·03 as compared with 0·61 ± 0·02 and 5·84 ± 0·04, respectively, for the halothane genotype nn (n = 13). The Nn pigs (n = 10) showed fluid (0·49 ± 0·03) and pH (fluid) (6·19 ± 0·11) values between those values observed for the two homozygotes (NN and nn). Predictions of meat quality in live pigs from biopsy LD muscles were confirmed from assessments on post-mortem LD muscles based on pH₁ and fibre optic probe (FOP) measurements.

The extent of deterioration (%) in Ca²⁺ accumulation showed high correlations with fluid (r = −0·861) and pH (fluid) (r = −0·831) in the biopsy LD samples, and with pH₁ (r = 0·663), FOP (r = −0·812), and drip (%) loss (r = −0·777) in the post-mortem LD samples.     

Influence of ultimate pH on bovine meat tenderness during ageing

The aim of this work was to evaluate the influence of ultimate pH and ageing at 2±2°C on the tenderness of beef. The m.longissimus thoracis et lumborum from 23 young bulls excised at 28 h post mortem were grouped into: Normal (pH 5.5 to 5.8) moderate DFD (mod DFD) (5.8p<0.05) lower in the DFD group than in the Normal one and a significant (p<0.001) linear relationship was found between ultimate pH and tenderness as evaluated by both methods. The myofibrillar protein solubility (MPS) at pH 7.0 was significantly higher in the DFD group at all post mortem times whereas for myofibrillar fragmentation index (MFI) higher values (p<0.05) were only found in the DFD group at day 1. In all three groups toughness decreased (p<0.05) from 1 to 6 days, with no further decrease to 13 days. This decrease in toughness was associated with an increase of MFI in all pH groups. Collagen solubility in all three groups was not affected by ageing. No significant (p>0.05) differences in soluble collagen and myofibrillar protein solubility (MPS) at pH 5.5 were found between the pH groups at any time. The tenderness evaluated by both methods was significantly (p<0.05) related to MFI, MPS at pH 7.0, cooking loss and juiciness. Total and soluble collagen, sarcomere length, intramuscular fat and MPS at pH 5.5 were not significantly (p>0.05) related with tenderness.     

Performance of new clean-up column for the determination of ochratoxin A in cereals and foodstuffs by HPLC-FLD

The performance of the newly developed Mycosep® 229 Ochra and Multisep® 229 Ochra clean-up columns for ochratoxin A (OTA) determination was evaluated. OTA was subsequently analysed using RP-HPLC with fluorescence detection. Recoveries for frequently contaminated commodities, like cereals, red wine, raisins and green coffee, were estimated. The recoveries obtained for the Mycosep 229 Ochra column were in the range from 87.9 ± 12.5% (n = 6) for wheat to 99.4 ± 2.7% (n = 24) for raisins. For Multisep 229 Ochra, recoveries from 76.5 ± 8.0% (n = 6) for barley to 86.4 ± 1.4% (n = 24) for raisins were achieved. Limits of detection for all matrices investigated (maize, wheat, rice, barley, raisins, green coffee beans, red wine) were in the range 0.4-2.4 μg kg^-1. The trueness of the method was tested using a certified reference material.     

Effect of genetic origin, diet and weaning weight on carcass composition, muscle physicochemical and histochemical traits in the rabbit

Fifty rabbits originating from the crossing of one dam strain with three sire strains, Hy+, INRA 9077 and INRA 3889, were studied. The adult body weights of the sire strains were 5·1, 4·1 and 3·1 kg, respectively. After weaning, the Hy+ and the INRA 9077 rabbits were fed either an H (11·99 MJ DE kg DM⁻¹) or L diet (9·67 MJ DE kg DM⁻¹). The INRA 3889 rabbits were fed only the H diet. In each of these five blocks, two weaning weights were studied and the rabbits were slaughtered when the average body weight of each block reached 2·5 kg. Slaughter yield, carcass fatness and hindleg meat to bone ratio were determined. Muscular tissue was described using (1) physicochemical criteria (ultimate pH, L^*a^*b^* colour) of the biceps femoris (BFE), tensor fasciae latae (TFL) and semimembranosus accessorius (SMA) muscles and (2) histochemical characteristics of the longissimus lumborum muscle (LL) through computerised image analysis (fibre type composition, cross-sectional area). At slaughter, the rabbits of INRA 3889 sire origin, which had the highest degree of maturity (72%), gave the best slaughter yield (p<0·01), the heaviest reference carcass weight (p<0·01), and highest LL proportion (p<0·01), hindleg meat to bone ratio (p<0·05) and fatness (p<0·01); their LL muscle showed the lowest percentage of βR fibres, while the cross-sectional area of their muscular fibres was the highest (p<0·05). When all sire × diet combinations were put together, the heavier the weaning weight, the lower the daily gain (p<0·01) and the lightness (L*) of thigh muscles (p<0·05). The lower the DE content of the diet, the lower the growth rate, the slaughter yield, the reference carcass weight (p<0·01) and the cross-sectional area of all types of muscle fibres of the rabbits of both Hy+ and INRA 9077 sire origin.     

Stability of catalase and its potential role in lipid oxidation in meat

The activity of catalase in microbial growth-controlled and uncontrolled ground beef muscle (semimembranosus, SM) did not change (P>0.05) during 6-day storage at 4°C. Likewise, catalase activity in ground, beef SM and longissimus dorsi (LD), pork LD, and chicken breast (B) and thigh (T) muscles was not affected (P>0.05) by 2-month storage at −20°C, with or without mid-month thawing/refreezing. When sodium azide (a catalase inhibitor) was added to ground beef SM, lipid oxidation (as measured by peroxide values) during 4-day refrigeration was higher (P<0.05) in treated samples — 43 and 55% higher at day 2 and day 4, respectively — than in the controls. It was concluded that catalase would be stable during meat storage/distribution and contribute significantly to the antioxidative process in raw meat products.     

Secondary sexual development (Masculinity) of bovine males: 2. Influence on certain meat quality characteristics

Differences in meat quality traits between bulls with secondary sexual development (bulls(+), n = 10), those without this development (bulls(−), n = 10) and steers (n = 10) were investigated. All animals had no permanent incisors (A-age group). Significant differences (P < 0·05) between bulls(+) and bulls(−) were found for the cooking loss percentage of the M. splenius (27·83% versus 31·11%, respectively), iron content of the M. splenius (56·02μg/g versus 49·43μg/g, respectively) and total collagen content of the M. splenius (3·74 versus 4·73 measured as Hyp N/Tot N x 1000, respectively). Drip loss of the wingrib cut (4·01% versus 5·18%, respectively) was also significantly different between bulls(+) and bulls(−). For the M. longissimus thoracis, no significant (P < 0·05) differences in any of the quality-indicating parameters investigated could be found. It is concluded that the M. splenius can be used as an indicator muscle for masculinity, based on meat quality attributes. This is supported by the correlation coefficients obtained between masculinity and the intramuscular collagen content of the M. splenius (r = −0·55) and the iron content of the M. splenius (r = 0·46). For all the other quality attributes investigated, non-significant (P > 0·05) differences between the three sex condition groups were found. It is concluded that the influence of masculinity on meat quality traits of young bulls is of little practical importance in a classification and grading system.     

Postmortem regulation of glycolysis by 6-phosphofructokinase in bovine M. Sternocephalicus pars mandibularis

This experiment addressed the hypothesis that 6-phosphofructokinase (6-PFK) regulates glycolysis in postmortem in M. sternocephalicus pars mandibularis. In two separate experiments, muscle samples were excised from randomly-selected steers that would typically be found on a commercial slaughter floor. In the first experiment, two samples were obtained from each of 6 steers immediately post-exsanguination; one sample was immersed immediately in liquid nitrogen and the other was stored at 4 °C for 4 d, to compare 6-PFK enzyme activity and glycolytic intermediate concentrations between fresh and d 4 postmortem samples. The greatest activity of 6-PFK was measured in fresh muscle extracts at pH 7.4, whereas little activity was detectable at pH 7.0. 6-PFK activity measured at pH 7.4 in d 4 samples also was barely detectable. Hill coefficient values for 6-PFK in fresh samples measured at pH 7.4 or 7.0, and d 4 samples measured at pH 7.4 were 2.9, 0.8, and 0.7, respectively, indicating loss of cooperativity with both lowered pH during assay and with time postmortem. Glycogen concentrations decreased 45% from d 0 to d 4, to 39.6 μmol glycogen/g muscle. Muscle concentrations of free glucose increased (P < 0.001) from 0.84 μmol/g at d 0 to 6.54 μmol/g at d 4. Fructose-6-phosphate and glucose-6-phosphate increased (P < 0.001) from d 0 to d 4 (2.8-fold and 4.7-fold, respectively). Lactate began accumulating immediately (3.33 μmol/g) and was elevated to 45.9 μmol/g by d 4. In the second experiment, conversion of [U-¹⁴C]glucose to lactate, glycogen, and CO₂ was measured in vitro at pH 7.4 and 7.0 in fresh M. sternocephalicus pars mandibularis strips from four steers. Total [U-¹⁴C]glucose was less in muscle strips incubated at pH 7.0 than in those incubated at pH 7.4 (55.5 vs. 123 nmol glucose utilized per 100 mg muscle per h; P = 0.04), due primarily to a reduction in glucose conversion to lactate. The conversion of glucose to glycogen or CO₂ in vitro was unaffected by media pH. These results suggest that the postmortem decline in pH in M. sternocephalicus pars mandibularis ultimately inactivates 6-PFK; this occurs prior to the depletion of glycogen reserves.     

Factors regulating lamb longissimus tenderness are affected by age at slaughter

The objective of this experiment was to determine age-related changes in collagen concentration, sarcomere length, calpain (μ- and m-) and calpastatin activities, postmortem proteolysis and Warner–Bratzler shear force (WBSF) in ovine longissimus thoracis et lumborum. Rambouillet lambs were slaughtered at 2, 4, 6, 8 and 10 months of age and samples of longissimus were collected at 0, 2 and 10 days postmortem. Collagen concentration and sarcomere lengths were determined from the cores used for WBSF measurements and reflected changes in the background toughness. Longissimus collagen concentration did not change (P>0.05) due to lamb age. Sarcomere lengths also showed age-related changes, increasing (P<0.05) from 1.35 μm at 6 months to 1.48 and 1.55 μm at 8 and 10 months, respectively. The extent of calpain mediated proteolysis determines the improvement in meat tenderness with postmortem storage. The most notable change in the calpain proteolytic system was the decline (P<0.05) in calpastatin activity from 4.18 to 1.91 U/g muscle between 2 and 10 months. The activity of μ-calpain showed a 16% increase (P<0.05) from 4 to 6 months, before it dropped again at 8 and 10 months. There was a gradual decline (P<0.05) in m-calpain activity with age, and by 10 months m-calpain activity had reduced to 80% of 2 months levels. The ratio of μ-calpain to calpastatin activities increased (P<0.05) from 2 to 6 months (from 0.31 to 0.56) with no further changes (P>0.05) at 8 or 10 months. There were no age-related changes (P>0.05) in desmin degradation at day 2, however, examination of day 10 samples showed increased (P<0.05) degradation from 2 to 6 months. Thus, the changes observed in the ratio of μ-calpain to calpastatin activities are reflected in the extent of postmortem proteolysis. Meat tenderness was measured using WBSF at 2 and 10 days postmortem. Because little proteolysis had taken place at 2 days postmortem, the decline in day 2 WBSF from 6 to 8 months could be explained by changes in sarcomere length. However, at 10 days postmortem, where WBSF was shown to decrease from 2 to 8 months, the improvement in tenderness could be explained by the amount of postmortem proteolysis. The data presented in this paper show evidence that sarcomere length is the main determinant of background toughness in ovine longissimus, and that postmortem proteolysis, resulting from μ-calpain activity regulated by calpastatin, is the main determinant of ovine longissimus tenderization during aging. Thus, lamb longissimus tenderness after refrigerated storage is determined by postmortem proteolysis and its interaction with sarcomere length.     

Prediction of fluid losses from pork using subjective and objective paleness

Meat paleness in pork Longissimus dorsi (LD) 1 day post-mortem (p-m) was measured subjectively using Japanese Pork Colour Scores (JPCS) and objectively using a Colormet fibre-optic (FO) meat probe (400–700 nm). Water-holding capacity (WHC), fluid loss during thin-slicing, and drip loss were measured in unfrozen and in frozen and thawed (FT) samples. FT caused a decrease in WHC, and an increase in slicing and drip loss (P < 0·001). FO interactance (i) was correlated (P < 0·01) with unfrozen WHC (R = 0·55), with FT WHC (r = −0·45 at 440 nm), with FT slicing loss (R = 0·81), with unfrozen drip loss (R = 0·66), and with FT drip loss (R = 0·61). Objective measurements proved that the development of pork paleness takes several days p-m and that paleness is increased by FT. Where fluid losses were predictable from paleness, the FO probe was superior to subjective evaluation by JPCS.     

The influence of season on quality characteristics of hot-boned beef m. longissimus thoracis

Samples of m. longissimus thoracis (LT) muscle were randomly collected from 70 Omani beef cattle 1 h after slaughter between August 2001 and July 2002 in the Muscat Municipality central slaughterhouse to investigate the effect of seasonal parameters on meat quality during the hot and cool seasons of Oman. The collection period (12 months) was divided into two seasons according to ambient temperatures and relative humidity and termed: Cool Season (November–March with average temperature of 21.2±1.40 °C and 57.9±1.61% relative humidity) and Hot Season (April–October with average temperature of 34.3±1.67 °C and 48.8±7.57% relative humidity). The season had a significant effect on meat quality characteristics of the LT muscle. Muscles collected during the hot season had significantly (P<0.001) higher ultimate pH values (6.24) with significantly (P<0.001) lower Warner–Bratzler (WB) shear force values (10.12) than those collected during the cool season (5.54 and 15.58). In these hot-boned samples, there was a linear relationship between ultimate pH and WB shear values. Cooking loss was significantly (P<0.001) higher for cool season samples (26.01%) than from hot season samples (19.75%). Beef from the hot season group had significantly (P<0.001) darker meat than that of the cold season group, based on L* (31.45 vs 35.58), a* (18.53 vs 23.19) and b* (4.16 vs 6.40) colour measurements. There was a linear relationship between ultimate pH and cooking loss, L*, a* and b*. These results indicated that heat stress (>30 °C) lead to physiological stress in beef cattle, which in turn increased muscle ultimate pH and influenced related meat quality characteristics.     

Microbiological effects of acid decontamination of pork carcasses at various locations in processing

The microbiological effect of hot (55° C), 1% (v/v) lactic acid sprayed on the surface of pork carcasses (n = 36) immediately after dehairing, after evisceration (immediately before chilling) or at both locations in slaughter/ processing was determined. Mean aerobic plate counts (APCs) of all acid-treated carcass surfaces were numerically lower than those of control carcasses: however, in most cases these reductions were not statistically significant (P>0·05). All samples tested for the presence of Salmonella and Listeria were negative. No significant differences in sensory characteristics or microbiological counts were evident for acid-treated and control carcass loins that were vacuum packaged and stored 0–14 days post-fabrication. Mean pH value and scores of sensory attributes such as lean color, surface discoloration, fat color, overall appearance and off-odor of chops from acid-treated carcasses were not significantly and/or consistently different from chops of comparable control carcasses. The role of bacterial attachment to pork skin and its effect on the decontaminating efficiency of lactic acid are discussed.     

Positional distribution of fatty acids in triacylglycerols from subcutaneous adipose tissue of pigs fed diets enriched with conjugated linoleic acid, corn oil, or beef tallow

This study was conducted to determine the effects of dietary beef tallow, corn oil, and conjugated linoleic acid (CLA) on the distribution of fatty acids among positions within triacylglycerols. Crossbred barrows (n=6 per treatment group) received diets containing 1.5% beef tallow, 1.5% corn oil, or 1.5% CLA for 5 weeks. Subcutaneous adipose tissue samples were obtained immediately postmortem. The fatty acid composition was determined for the sn-2 positions of the triacylglycerols by digestion with Rhizopus arrhizus lipase. Fatty acids in the sn-1/3 position were calculated from these data. Feeding CLA increased (P<0.05) the concentration of total saturated fatty acids (SFA, especially 16:0) and isomers of CLA in adipose tissue lipids, but reduced (P<0.05) the concentration of total monounsaturated fatty acids (MUFA, especially 18:1n−9). Dietary CLA caused an accumulation of total SFA in the sn-1/3 position, with a proportional decrease in total MUFA and 18:2n−6 in the outer positions. Correspondingly, lipids extracted from CLA-fed pigs had slip points that were 10 °C higher (P<0.05) than those from corn oil- or tallow-fed pigs. These data suggest that dietary CLA increases the melting point of lipids in porcine adipose tissue by increasing the proportion of SFA at the sn-1/3 position of lipids.     

Effect of selection for growth rate on biochemical, quality and texture characteristics of meat from rabbits

Biochemical characteristics, including myosin heavy chain I (MHC-I) percentage, isocitrate dehydrogenase and aldolase activities, meat quality traits and instrumental texture properties of rabbits selected for different growth rates were studied. The animals of the control (C) group (7th generation; n=60) were raised in parallel with those of selection (S) group (21st generation; n=60). Carcass weights (1230.1 ± 19.8 and 1348.3 ± 20.1 g, for C and S, respectively) and perirenal and scapular fat content differed significantly (P<0.01) between the two groups. Water holding capacity was expressed as the percentage of pressure released water and was significantly different (P<0.05) between groups C and S (33.29% and 35.57%). MHC-I percentage and aldolase activity also differed significantly (P<0.05) between groups, group C showing higher oxidative traits than group S (MHC-I: 12.5% and 9.8%; aldolase: 597.11 and 636.83 UI/g muscle). Texture properties from the Warner-Bratzler test showed higher (P<0.001) shear firmness for loin in the S group (1.69 kg/s cm²) than in the C group (1.34 kg/s cm²). In addition, the texture profile analysis indicated that chewiness, gumminess and hardness were also higher in the S group (P<0.01). In conclusion, the results confirmed a positive effect of the selection on productive traits and a negative effect on instrumental texture properties and on the water holding capacity of the meat.     

Determination of aflatoxin B1 in tiger nut-based soft drinks

An analytical method for the determination of aflatoxin B₁ in a tiger nut-based soft drinks named 'horchata' is described. The method is based on an immunoaffinity clean-up, followed by HPLC separation and fluorescence detection after electrochemical post-column derivatization. The detection limit (S/N = 3) and the quantification limit (S/N = 10) were 0.02 and 0.06 µg kg^-1, respectively. The mean recovery at a level of 2 µg l^-1 was 88% (n = 6) and the coefficient of variation was 9%. The method was applied to conduct a small market survey for a beverage named 'horchata' that is frequently consumed by parts of the population in Southern Europe. Twenty-two samples from Spanish and Belgian supermarkets were analysed. As a result, only one sample was found to contain aflatoxin B₁ at the limit of quantitation of the method.     

Muscle composition of steers treated with the β-agonist, cimaterol

The effect of the β-adrenergic agonist, cimaterol, on the nature and amount of collagen in three individual muscles (Longissimus dorsi, Vastus lateralis and Semitendinosus) from young steers was investigated.

β-Agonist-treated animals showed similar rates of liveweight gain to those of control animals but the weight and protein content of the Longissimus dorsi and Vastus lateralis muscles were significantly increased (muscle weights 1216 versus 1494 g, P < 0·05; 514 versus 642 g, P < 0·01, respectively, for control and cimaterol animals). The Semitendinosus muscle, however, showed no significant increase in weight or protein content (P > 0·05).

The total collagen content and the proportion of heat-soluble collagen varied considerably between muscles, but no significant muscle × treatment interactions were detected (P > 0·05). Cimaterol treatment reduced total muscle collagen content (controls 15·2, cimaterol 12·5mg/g fresh tissue, P < 0·05) and also reduced the percentage of heat-soluble collagen (controls 18·9%, cimaterol 13·0%, P < 0·05).