Inactivation of Enterobacter sakazakii by pulsed electric field in buffered peptone water and infant formula milk

The effect of high-intensity pulsed electric field (PEF) treatment on the survival of Enterobacter sakazakii suspended in buffered peptone water (BPW) and powdered infant formula milk (IFM) was evaluated. Reference medium and IFM samples were treated with PEF. Electric field intensity and treatment time were varied from 10 to 40 kV cm⁻¹ and from 60 to 3895 μs, respectively. Samples of buffered peptone water (3 g L⁻¹) and IFM were inoculated with E. sakazakii (CECT 858) (10⁹ cfu mL⁻¹) and then treated with PEF. The inactivation data were adjusted to the Weibull frequency distribution function and Bigelow model, and constants were calculated for both substrates. A maximum 2.7 log (cfu mL⁻¹) reduction was achieved in BPW after exposure of E. sakazakii to PEF for 360 μs (2.5 μs pulse width) at 40 kV cm⁻¹. In IFM, exposure of E. sakazakii to PEF, with the same conditions, led to a 1.2 log (cfu mL⁻¹) reduction. The greater the field strength and treatment time, the greater the inactivation achieved in both substrates. Even though further research will be necessary, according to the results, there are good prospects for the use of PEF in hospitals to achieve safe reconstituted infant formula before storage at refrigerated temperatures.     

Thermal death kinetics and heating rate effects for fifth-instar Cydia pomonella (L.) (Lepidoptera: Tortricidae)

Thermal death kinetic parameters of fifth-instar codling moths (Cydia pomonella (L.)) and the effect of three heating rates (1°C min⁻¹, 10°C min⁻¹, and 18°C min⁻¹) on larval mortality were determined by a heating block system. The insects were heated to four temperatures (46°C, 48°C, 50°C, and 52°C) held for predetermined periods followed by 24 h storage at 4°C before mortality evaluation. Thermal death kinetics for fifth-instar codling moths followed a 0.5th order of kinetic reaction. Minimum time required to achieve 100% mortality of a given population decreased with temperature in a semi-logarithmic manner. No larval survival was observed in samples of 600 insects after exposure to 46°C, 48°C, 50°C, and 52°C for 50, 15, 5, and 2 min, respectively. Activation energy for thermal kill of fifth-instar codling moths at the heating rate of 18°C min⁻¹ was estimated to be about 472 kJ mol⁻¹. The lethal time accumulated during the ramp period was about 1.8, 0.2, and 0.1 min for the heating rates of 1°C min⁻¹, 10°C min⁻¹, and 18°C min⁻¹, respectively.     

Thermophysical properties of processed meat and poultry products

Thermophysical properties of various meat and poultry emulsions were evaluated at four temperatures (20, 40, 60 and 80 °C). Thermal conductivities (0.26–0.48 W m⁻¹ K⁻¹) increased linearly with temperature between 20 and 60 °C. Between 60 and 80 °C, it remained constant for most products except bologna. Curves for thermal conductivity as a function of temperature could be roughly grouped into two different categories: products containing meat particles and those containing meat emulsions. The application of various models was investigated for thermal conductivity prediction. It was found that a three phase structural based Kirscher model had the potential for predicting thermal conductivities with acceptable accuracy. Densities decreased slightly as a function of temperature from 20 to 40 °C. A transition phase was observed from 40 to 60 °C, which was followed by a decrease from 60 to 80 °C. There was a decrease of about 50 kg m⁻³ between the density of a raw product at room temperature (at maximum 1070 kg m⁻³) and the product heated to 80 °C (at minimum 970 kg m⁻³), due to the gelation or setting of the structure. After a transition period from 10 to 30 °C, the heat capacity increased linearly from 30 to 80 °C, and ranged from 2850 to 3380 J kg⁻¹ °C⁻¹, respectively. Densities and heat capacities were strongly influenced by the carbohydrate content (i.e. as the carbohydrate content increased the density decreased). The salt content adversely affected thermal conductivity and thermal diffusivity values. However, these parameters increased with moisture content.     

Studies to determine the critical control points in pork slaughter hazard analysis and critical control point systems

Aerobic mesophilic counts (AMC), coliform (CC) and coliform resuscitation counts (CRCs) were obtained by swabbing 50 cm² areas at three sites (ham, belly and neck) on pig carcasses, after each of seven stages of the slaughter/dressing process (bleeding, scalding, dehairing, singeing, polishing, evisceration and chilling). In most cases, there were no statistical differences (P>0.05) among the counts derived by these three methods. Reductions in counts at individual sites were observed after scalding (3.5 log₁₀ cfu cm⁻²), and singeing (2.5 log₁₀ cfu cm⁻²). Increases in counts at individual sites were observed after dehairing (2.0 log₁₀ cfu cm⁻²) and polishing (1.5 log₁₀ cfu cm⁻²). The incidence of Salmonella on pig carcasses was also obtained by swabbing the outside surfaces of 100 half carcasses. Information on the incidence of Salmonella in scald tank water (108 samples) was also investigated. Carcass swabs and scald tank water were examined for the presence of Salmonella using standard enrichment methods. Salmonella were detected on 31% of carcasses immediately after bleeding, 7% of carcasses immediately after dehairing and evisceration, and 1% of carcasses immediately after scalding. Serovars included Salmonella Typhimurium, Salmonella Hadar, Salmonella Infantis and Salmonella Derby. No Salmonella were recovered from samples of scald tank water. The impact of pig slaughter/dressing processes on carcass microbiology and their potential use as critical control points (CCPs) during pork production are discussed.     

Drip loss of case-ready meat and of premium cuts and their associations with earlier measured sample drip loss, meat quality and carcass traits in pigs

Drip loss of 374 samples taken from porcine M. longissimus dorsi and M. semimembranosus was measured by using the “bag method” (BM), EZ-DripLoss (EZ-DL) from premium cuts (PC) and in retail tray (case-ready meat; CRM). This provided a comparison between these methods and their relationships to other meat quality and carcass traits. Samples were prepared at 24 h post-mortem (pm) and were measured 24 and 48 h after preparation (at 48 and 72 h pm) using the BM and after 48 h (at 72 h pm) with the EZ-DL and PC. Drip loss of meat kept in retail trays was measured after 7 days (CRM₇) and daily within a week (CRM_1–7). Average drip loss was 1.80% and 3.10% using the BM after 24 and 48 h, respectively. EZ-DL and CRM₇ showed higher drip losses of 4.71% and 4.00%. Daily loss of CRM_1–7 showed a concavely shaped curve and increased from 1.57% to 5.64% after 7 days. High correlations were obtained between drip loss of CRM₇ and BM (r = 0.88) or the EZ-DL (r = 0.91). The development of drip loss in case-ready meat fitted by linear-quadratic regression (y = 0.439 + 1.245x − 0.072x²) showed that high drip loss measured earlier by bag and EZ-DripLoss methods was highly associated with a high intercept (r = 0.63–0.72), a high linear increase (r = 0.77–0.81), but larger decrease in increments (r = −0.82 to −0.86) during weekly stored meat in retail trays as supplied at consumer level. Because the positive linear regression coefficient was substantially higher than the negative quadratic regression coefficient, the development of drip loss is mainly dependent on the initial drip loss. Therefore, animals with high drip loss within 72 h post-mortem also showed undesirable high drip loss curves over the entire retail period. Relationships between drip loss and other meat quality traits were similar for BM, EZ-DL and CRM₇. Of these the correlation between pH₂₄ and drip loss was highest with r = −0.54, −0.49 and −0.47 for BM, EZ-DL and CRMH₇, respectively. Interestingly, a correlation of r = −0.35 between blood pH value and CRML₇ was obtained. Carcass traits such as loin, ham, shoulder, belly weight or loin eye area showed only marginal correlations to drip loss. In conclusion, EZ-DL was the most appropriate method to predict drip loss of case-ready meat in retail trays and its development during a 7 day storage period.     

Diffusion of thiocyanate and hypothiocyanite in whey protein films incorporating the lactoperoxidase system

The diffusion of the thiocyanate (SCN⁻) and hypothiocyanite (OSCN⁻) components of a lactoperoxidase system (LPOS) in whey protein isolate (WPI) films was investigated. Diffusion coefficients for these molecules were measured for the LPOS-incorporated WPI films prepared with different WPI:glycerol ratios (1:1, 3:1, and 5:1). WPI film disks were coated on the surfaces of smoked salmon samples, and the samples were stored at 4, 10 and 22 °C. The diffusion coefficients were determined by fitting a mathematical model to the amounts of SCN⁻ and OSCN⁻ released from the disks during a period of time. The diffusion coefficients for SCN⁻ (D₁) and OSCN⁻ (D₂) in the films were 0.19–5.2 × 10⁻¹² m² s⁻¹ and 0.13–6.5 × 10⁻¹³ m² s⁻¹, respectively. The D₁ and D₂ decreased as the WPI:glycerol ratio increased and the storage temperature decreased. The E_a values for diffusion in 1:1, 3:1, and 5:1 WPI:glycerol films were 13.3, 29.5, and 35.6 kJmol⁻¹, respectively, for SCN⁻ and 15.8, 30.1, and 39.9 kJmol⁻¹, respectively, for OSCN⁻.     

Respiration of Tribolium castaneum (Herbst) at reduced oxygen concentrations

Adults, eggs, young and old larvae and pupae of Tribolium castaneum (Herbst) were exposed to atmospheres containing 1%, 2%, 3%, 5%, 10%, and 15% oxygen in nitrogen at 30°C and 70% r.h. Respiration rates were determined with a gas chromatograph. The oxygen intake and carbon dioxide output by insects were expressed in μl/insect/h or μl/mg/h.

Adults exposed to 21% oxygen required an initial acclimatization period of at least 5 h, after which the respiration rate remained stable. Based on this finding, all the respiration measurements were carried out after an initial adaptation of insects to the respirometer conditions for 24 h.

Respiration of eggs, young and old larvae, pupae, and adults at 30°C in normal atmospheric air was at rates of 0.0121, 9.25, 8.45, 1.45, and 4.67 μl CO₂/insect/h, respectively. Respiration rates of the same stages in terms of insect weight were 0.32, 29.08, 3.33, 0.59 and 2.37 μl CO₂/mg insect/h, respectively. At reduced oxygen levels respiration rates of eggs, larvae and pupae were proportional to the oxygen levels. Adult respiration was higher for 3% and 5% oxygen than for normal atmospheric air with rates of 4.77 and 4.98 μl CO₂/insect/h, respectively. In adults, RQ values for the same oxygen levels were also higher than for normal atmospheric oxygen and were 1.07 and 1.18, respectively.     

A new measure of uptake: desorption of unreacted phosphine from susceptible and resistant strains of Tribolium castaneum (Herbst) (Coleoptera: Tenebrionidae)

Previous studies of phosphine (PH₃) uptake by insects have concentrated on the process as a whole (“gross uptake”), without distinguishing between absorption of the gas and oxidation to non-volatile products. The lower gross uptake by phosphine-resistant (R) strains of stored product pests has given some insights into resistance mechanism(s). In this study, a recently described method of fumigant residue analysis in grains (microwave irradiation followed by headspace gas chromatography) was adapted to measure absorbed unreacted PH₃ (“reversible uptake”) in a susceptible (S) and an R strain of the rust red flour beetle Tribolium castaneum. At a concentration of 0.9 mg l⁻¹, S insects contained 20 ng g⁻¹ after 15 min exposure, rising slowly to 50 ng g⁻¹ after 5 h. The R strain yielded 190 ng g⁻¹ after 15 min, falling to 50 ng g⁻¹ over 5 h. Falling PH₃ content corresponded with increasing mortality in the R strain, while all except the shortest exposure killed 97% or more of the S strain. Insects of either strain, killed prior to PH₃ exposure by freezing in liquid nitrogen, contained 130–140 ng g⁻¹ after 30 min, rising to 190–200 ng g⁻¹ after 5 h. Gross uptake under the same conditions was 50 μg g⁻¹ (S) and 8 μg g⁻¹ (R) after 5 h, which accords with the literature. Reversible uptake by living insects of either strain under anoxia was 40–50 ng g⁻¹ over 30 min to 2 h. By examining the time-course of reversible PH₃ uptake, a new hypothesis of phosphine action and uptake, in which PH₃ oxidation in vivo is a consequence of reactive oxygen species generation, rather than a direct cause of toxicity, is discussed.     

Analysis of potential lard adulteration in chocolate and chocolate products using Fourier transform infrared spectroscopy

Fourier transform infrared (FTIR) spectroscopy, in combination with attenuated total reflectance (ATR) and partial least square (PLS) regression, was used to detect the presence of lard in chocolate formulation. The spectral bands associated with lard, cocoa butter and their blends (ranging from 0% to 15% of lard in cocoa butter) were recorded, interpreted and identified. A semi-quantitative approach is proposed to measure the percent of lard in blends on the basis of spectral data at the frequency region 4000–650 cm⁻¹, using the equation y = 0.9225x + 0.5539. The coefficient of determination (R²) was 0.9872 with a standard error (SE) of 1.305. In this paper, the potential of FTIR spectroscopy as a rapid analytical tool for the quantitative determination of adulterants especially lard, in chocolate, is demonstrated.     

Effect of modified atmospheres on microbiological, color and sensory properties of refrigerated pork

Pork loin samples were stored (4 °C) in nylon polyethylene plastic bags using different modified atmospheres packaging (MAP): vacuum, 100% CO₂ 99% CO₂ + 1% CO, 100% O₂ or 100% CO followed by vacuum. Throughout the storage period Pseudomonas growth was limited in loins packaged in all MAPs evaluated, except for 100% O₂. Psychrotrophs reached 10⁷ CFU g⁻¹ after 20 days of storage except for the loin samples in 100% O₂ MAP that present count above 10⁸ CFU g⁻¹. The 1% CO/99% CO₂ atmosphere was best for preserving the desirable pork loin color and the L* and a* values remained similar to the fresh meat values using this MAP. Pork loins in 99% CO₂/1% CO MAP obtained the highest consumer acceptance scores after 24 h of storage. These samples and those treated with CO and then vacuum packaged received the greatest acceptance scores even after 20 days of storage.     

Ultraviolet Light (254 nm) Inactivation of Listeria monocytogenes on Frankfurters That Contain Potassium Lactate and Sodium Diacetate

ABSTRACT:  Listeria monocytogenes , a psychrotrophic foodborne pathogen, is an occasional postprocess contaminant on ready-to-eat meat (RTE) products including frankfurters. Ultraviolet C light (UVC) is an FDA-approved technology for the decontamination of food surfaces. In this study, the ability of UVC to inactivate L. monocytogenes on frankfurters that contained potassium lactate (PL) and sodium diacetate (SDA), either before or after packaging, was investigated. UVC irradiation of frankfurters that were surface-inoculated with L. monocytogenes resulted in a 1.31, 1.49, and 1.93 log reduction at doses of 1, 2, and 4 J/cm², respectively. UVC treatment had no effect on frankfurter color or texture at UVC doses up to 4 J/cm². Frankfurter meat treated with UVC doses up to 16 J/cm² did not increase mutagenesis in bacterial or human cells, either with or without exogenous metabolic activation. UVC treatment of single-layer frankfurter packs at a dose of 2 J/cm² resulted in a 0.97 (± 0.14) log reduction of L. monocytogenes . Following 8 wk of refrigerated storage L. monocytogenes levels decreased by only 0.65 log in non-UVC-treated frankfurter packs compared with 2.5 log in the UVC-treated packs. Because the numbers of L. monocytogenes associated with contaminations of ready-to-eat meats are typically very low, the use of UVC in combination with potassium lactate and sodium diacetate has the potential to reduce the number of frankfurter recalls and foodborne illness outbreaks.     

Prediction of processed cheese instrumental texture and meltability by mid-infrared spectroscopy coupled with chemometric tools

The objective of this study was to determine the potential of mid-infrared spectroscopy coupled with multidimensional statistical analysis for the prediction of processed cheese instrumental texture and meltability attributes. Processed cheeses (n = 32) of varying composition were manufactured in a pilot plant. Following two and four weeks storage at 4 °C samples were analysed using texture profile analysis, two meltability tests (computer vision, Olson and Price) and mid-infrared spectroscopy (4000–640 cm⁻¹). Partial least squares regression was used to develop predictive models for all measured attributes. Five attributes were successfully modelled with varying degrees of accuracy. The computer vision meltability model allowed for discrimination between high and low melt values (R² = 0.64). The hardness and springiness models gave approximate quantitative results (R² = 0.77) and the cohesiveness (R² = 0.81) and Olson and Price meltability (R² = 0.88) models gave good prediction results.     

Residual susceptibility of Plodia interpunctella to deltamethrin dust: Effects of concentration and time of exposure

Wandering phase fifth instarPlodia interpunctella (Hübner) were exposed at ten weekly intervals for 6, 12 and 24 h or 1 week to 0.05% deltamethrin dust at application rates of 38, 47 and 56 mg per 0.016 m². The percentages of pupating larvae and adult emergence at all three rates were greatest at the 6-h exposure and least at the 1-week exposure, but there was no consistent decrease in pupation or emergence as the exposure was increased from 6 to 24 h. Pupation and emergence decreased with increasing application rate of deltamethrin dust at each weekly bioassay, and the percentage of emerged adults was usually less than the percentage of larvae that pupated. At the conclusion of the test (9 weeks), curve-fit adult emergence data for larvae exposed for 1 week to deltamethrin dust at application rates of 38, 47 and 56 mg per 0.016 m² were calculated by linear regression to be 26.6%, 20.5% and 17.3% respectively. For all other exposure times at each rate, adult emergence usually exceeded 20% after 2–4 weeks.     

The effect of air temperature, velocity and visual lean (VL) composition on the tempering times of frozen boneless beef blocks

Beef blocks of two compositions, 100% and 50% visual lean (VL), in standard commercial packaging with nominal dimensions of 510 × 390 × 150 mm were tempered from −18 °C to −3 °C using air at temperatures from 3 °C to −3 °C and velocities of 0.5 and 5 ms⁻¹. These conditions were then modelled using a finite difference mathematical model and the accuracy of the model assessed by comparison with the experimental results. An extended range of conditions (including an intermediate air velocity of 2 ms⁻¹ and an intermediate composition of 75% VL) was then modelled to produce data that can be used to design tempering processes.

The results show that single stage air tempering of even single blocks within their cartons needs to be a long process. In air at 3 °C and 5 ms⁻¹, blocks of 50% VL rose to deep temperatures of −10 °C and −3 °C after 4.0 and 22.5 h, respectively, while with 100% VL 4.6 and 27.3 h were required. Under these conditions, the surface layers of the meat would have spent many hours in a thawed condition that would be detrimental to both drip and optimal processing. Using lower temperatures avoids thawing and at the same time produces an optimum temperature difference for subsequent processing. However, tempering times are substantially extended. For example, times to the above temperatures using air at −1 °C and 5 ms⁻¹ were 4.8 and 37.5 h for 50% VL and 5.1 and 44.5 h for 100% VL.     

Susceptibility of Rhyzopertha dominica to ionizing radiation

The effects of ionizing radiation doses between 1 and 20 krad on all stages of Rhyzopertha dominica were studied. Adult emergence from treated eggs and larvae was prevented by 4 and 8 krad respectively. Doses up to 20 krad to pupae only slightly reduced the emergence of adults. However there was considerable (up to 30 per cent) mortality of the adults within 8 hours of eclosion. The 20 krad dose caused very high mortality of adults from irradiated pupae and of irradiated adults within 3–5 weeks. Complete sterility, as evidenced by the lack of an F₁ generation, was induced in pupae by a dose of 14 krad and in adults by 11·5 krad.     

Levels of heavy metals in candy packages and candies likely to be consumed by small children

Ninety two samples of child-consumed candies and candy packages were analyzed for seven heavy metals. Lead (Pb) was detected at concentrations of 110.3–6394.1 mg kg⁻¹ in ten of 92 candy packages. The directive factor of Pb contamination had originated in the lead-based ink of the outer cover. Particularly, Pb was detected at high concentrations in case of green- or yellow-colored packages. Chromium (Cr) was detected at high concentrations in cases where Pb was also detected at high concentrations, and the Cr levels ranged from 136.9 mg kg⁻¹ to 1429.3 mg kg⁻¹ in seven of the 92 candy packages. Hexavalent chromium [Cr(VI)] was detected at 87–105.0% of the total Cr in polypropylene-coated wrappers with printed outer covers. The migration of Cr(VI) increased with elution time up to 0.20 μg (cm²)⁻¹ for 30 days in basic (pH 10.0) solution; however, there were no migrations in acidic (pH 4.0) and neutral (pH 7.0) solutions. The migration of Pb increased with elution time up to 0.65 μg (cm²)⁻¹ and 0.28 μg (cm²)⁻¹ in basic (pH 10.0) and acidic (pH 4.0) solutions, respectively. However, any migration was hardly observed in neutral (pH 7.0) solution.     

The influence of RN genotype, including the new V199I allele, on the eating quality of pork loin

The eating quality of M. longissimus dorsi (LD) from RN⁻ homozygotes, RN⁻ heterozygotes and RN⁻ non-carriers was investigated in a Swedish Hampshire×Finnish Landrace pig population. The recently identified new allele (V199I, here denoted rn*) at the RN locus was also detected among the pigs selected and included in the sensory evaluation. The number of animals varied from 10 to 15 in the five genotype groups; RN⁻/RN⁻, RN⁻/rn+, RN⁻/rn*, rn+/rn+ and rn+/rn* (in total 59 pigs). In addition, one pig was determined to be rn*/rn* but was excluded from the analysis. The three genotypes in which the RN⁻ allele was represented (RN⁻/RN⁻, RN⁻/rn+ and RN⁻/rn*) had higher glycogen and lower protein contents as well as lower ultimate pH (measured 48 h post-mortem) in LD than the non-carriers (rn+/rn+ and rn+rn*). Of the sensory parameters evaluated (tenderness, chewing time, chewing residual, juiciness, meat flavour and acidity), the five RN genotypes only affected acidity significantly; the RN⁻ allele contributing to a more acid taste in LD. The influence of the rn* allele resembled that of rn+ on the sensory parameters. When the material was divided into three groups (homozygous, heterozygous and non-carriers of the RN⁻ allele) the juiciness was found to be significantly influenced by RN genotype, and LD from animals that were homozygous and heterozygous with respect to the RN⁻ allele exhibited a higher juiciness than LD from non-carriers. The RN⁻ allele also tended to contribute to greater tenderness, which was significantly higher in LD from heterozygous carriers than from non-carriers of the RN⁻ allele. A more rapid decline in pH (measured as pH at 45 min and 3 h post-mortem) contributed to a greater tenderness in LD (according to a trained panel and Warner-Bratzler shear force). In addition to the RN genotype, the decline in pH was influenced by carcass weight, which varied between 71 and 97 kg, and by stunning procedure, which changed during the course of the study from individual to group stunning with CO₂. The individual stunning procedure contributed to a lower pH in the initial post-mortem phase (pH₄₅), whereas a higher carcass weight and the RN⁻ allele lowered the pH in the mid-post-mortem region (pH_3h and pH_24h), significantly (P0.05). The pH continued to decline after 24 h post-mortem and the ultimate pH was not reached until 48 h post-mortem. The cooking loss, juiciness and acidity were related to the specific characteristics of the RN⁻ carriers, such as higher glycogen content, lower protein content and lower ultimate pH (pH_48h).     

Influence of various preservatives on the quality of minced beef under modified atmosphere at chilled storage

The effect of preservatives on microbial quality, pH, drip-loss, roasting-loss, colour, and sensorial properties of modified atmosphere packaged (70% O₂ and 30% CO₂) minced beef (M. semimembranosus) stored at (2 ± 0.5 °C) for 12 days was investigated. Beef cubes (approx. 20 × 20 × 20 mm size) were immersed in solutions of 2% and 5% lactic acid, 2% lactic acid combined with 0.5% sodium ascorbate, 20% potassium lactate and 20% potassium sorbate before mincing. Addition of lactic acid was associated with pH drop, which increased drip-loss and roasting-loss. Application of all additives inhibited aerobic micro-organisms (10³–10⁴ CFU g⁻¹ on day 12) compared to reference sample (9 × 10⁵ CFU g⁻¹ on day 12). Lactic acid discoloured samples, while sodium ascorbate seemed to improve colour stability. Despite good visual colour characteristics, potassium sorbate treated samples were organoleptically unacceptable with massive off-flavour.     

Effects of ultrafiltration of whole milk on some properties of spray-dried milk powders

The objective was to produce spray-dried milk powders for assessment subsequently in chocolate. Milks were ultrafiltered to increase their protein content (3.08–5.33 g 100 g⁻¹), concentrated to different solids levels (42.8–52.3 g 100 g⁻¹) and spray-dried to produce powders (26–59 g 100 g⁻¹ fat). The relationships between the milk protein content, concentrate viscosity and some powder properties were quantified. The free-fat content of the powders increased linearly to 74 g 100 g⁻¹ fat with milk protein content for 26 and 40 g 100 g⁻¹ fat powders. The particle size and moisture content of the powders increased linearly with concentrate viscosity for 26 g 100 g⁻¹ fat powders. Differences between the control and ultrafiltration-treated milk powders were explained. The free-fat content and the particle size increased with the fat content of the control powders. The vacuole volume of the powders was inversely more related to the free-fat content than to the fat content of the control powders.     

Biologically active polyamines in pig kidneys and spleen: Content after slaughter and changes during cold storage and cooking

Polyamines putrescine, spermidine (SPD) and spermine (SPM) were determined as dansyl derivatives using an HPLC method. Distribution of SPD and SPM in pair kidneys was homogenous. The mean SPD and SPM contents in pig kidneys 24 h after slaughter were 9.39 ± 3.35 and 53.1 ± 14.0 mg kg⁻¹, respectively with no significant differences between barrows and gilts. Putrescine content was below the detection limit of 1.2 mg kg⁻¹. In kidneys stored aerobically or vacuum-packaged at 2–3 °C for 7 and 21 days, respectively, SPD and SPM decreased significantly. Stewing decreased both polyamines more extensively in kidneys processed on day-1 after slaughter than on day-7 after storage at 2–3 °C. The mean SPD and SPM in 10 spleens 24 h after slaughter were 36.7 ± 5.70 and 34.0 ± 7.64 mg kg⁻¹, respectively. Thus, both pork kidney and spleen are foods with a high level of SPM and SPD.