Thermal-death kinetics of fifth-instar Amyelois transitella (Walker) (Lepidoptera: Pyralidae)

Information on kinetics for thermal mortality of navel orangeworm, Amyelois transitella (Walker) (Lepidoptera: Pyralidae), is needed for developing post-harvest phytosanitation thermal treatments of walnuts. Thermal-death kinetics for fifth-instar navel orangeworms were determined at temperatures between 46°C and 54°C at a heating rate of 18°C min⁻¹ using a heating block system. Thermal-death curves for fifth-instar navel orangeworms followed a 0.5th-order of kinetic reaction. The time required to achieve 100% mortality (N₀=600) decreased with increasing temperature in a logarithmic manner. Complete kill of 600 insects required a minimum exposure time of 140, 50, 15, 6, and 1 min at 46°C, 48°C, 50°C, 52°C, and 54°C, respectively. The reaction rate (k) was affected by treatment temperatures following an Arrhenius relationship. The activation energy for thermal kill of fifth-instar navel orangeworms was estimated to be between 510 and 520 kJ mol⁻¹.     

Thermal resistance of different life stages of codling moth (Lepidoptera: Tortricidae)

Phytosanitation regulations in several international markets require postharvest treatments to control codling moth, Cydia pomonella (L.) (Lepidoptera: Tortricidae), in various commodities. Thermal treatments are gaining acceptance to replace chemical fumigation. Determining the most thermal-tolerant life stage is essential in the development of effective postharvest insect control protocols based on thermal energy. A heating block system was used to evaluate relative heat resistance of five different life stages of codling moth: white-ring eggs, black-head eggs, third-instar, fifth-instar, and diapausing larvae, at a heating rate of 15°C/min. The fifth-instar was the most heat-resistant life stage in the tested temperature range of 50–52°C except for diapausing larvae. Thermal death kinetic data of diapausing fifth-instar larvae were determined and also compared with the published TDT curve of non-diapausing larvae using the same heating block system. Both diapausing and non-diapausing larvae were dead after treatments at 50°C for 5 min and 52°C for 2 min. However, at the lower temperatures or shorter times, diapausing larvae had lower mortality than non-diapausing larvae.     

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.     

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.     

Effects of different storage conditions on steroidal saponinsin yam (Dioscorea pseudojaponica Yamamoto) tubers

Effect of storage on steroidal saponins, furostanol and spirostanol glycosides, in yam (D. pseudojaponica Yamamoto) tubers was determined. Unpeeled and vacuum-sealed peeled tubers were stored at −18, 4, 17 and 25 °C from 5 to 80 days separately. Furostanol glycosides in unpeeled tubers could be converted by furostanol glycoside 26-O-β-glucosidase (F26G) to spirostanol glycosides after 4 °C storage for 35 days (chilling injury could be found), or 17 and 25 °C storage for 50 days. The conversion increased with storage times. Peeled tubers stored at 17 and 25 °C for 5 days could experience organoleptic injury, which would enlarge with increasing storage period. After 35 days of storage, large part of vacuum-sealed tubers transformed to juice with stench. In the early 20 days storage, saponins in these tubers were lost rapidly. F26G activity in decreasing order was 25 °C > 17 °C > 4 °C and could be inhibited under vacuum.     

Effect of vapors from fractionated samples of propolis on microbial and oxidation damage of rice during storage

The efficacy of vapors from polar and non-polar sub-fractions of propolis on microbial and oxidation control during rice (Oryza sativa, hinohikari var.) storage was evaluated. The sub-fractions (absolute ethanol, methylene chloride, hexane extracts: AEPEV, MCPEV and HEPEV, respectively) were infused in synthetic adsorbents and their volatiles released during storage (6 months). HEPEV, MCPEV and AEPEV treatments inhibited molding and post-inoculation bacterial colonization (1.1, 1.1, 0.9 and 1.3, 1.2, 1.1 log₁₀ cfu/g reductions, respectively) on brown rice. AEPEV treatment suppressed fat acidity damage of milled rice at 30 °C to conventional cold storage level (5 °C) and differential Gram staining of bacteria isolated after the treatment indicated a dominant Gram-positive bacterial distribution. The concentrations providing 50% inhibition of 2′,2′-diphenylpicrylhydrazyl free radical scavenging were 9.8, 3.2 and 2.8 μg/μl for hexane (HEPE), absolute ethanol (AEPE) and methylene chloride (MCPE) extracts, respectively. The oxidative degradation rate was lowest for AEPE (4.3 × 10⁻⁴ min⁻¹) and highest for HEPE (1.9 × 10⁻³ min⁻¹) in the β-carotene bleaching assay. Gas chromatograph mass spectrometry revealed that AEPE had the highest amount of caffeic acid and caffeic acid phenethyl ester. Ultimately, the volatiles from the propolis sub-fractions had varied potential in rice quality preservation.     

Effect of non-ionizing radiation (UVC) on the development of Trogoderma granarium Everts

Various instars of khapra beetle Trogoderma granarium were exposed to ultra-violet rays (UVC) to assess their effect on each instar and their potential in breaking the developmental cycle of the khapra beetle.

Eggs aged zero (recently laid), 24 and 48 h were exposed to UVC at a radiation intensity of 31.4±0.02 W m⁻². Doses equivalent to 3 min (56.52 J cm⁻²), 8 min (150.72 J cm⁻²), and 12 min (226.08 J cm⁻²) resulted in death of all eggs, with a hatch of 96.6% in the control.

Mortality of UVC-irradiated larvae increased proportionally with increase in UVC dose, while, for each dose, mortality was inversely related to age of larvae at irradiation. Thus, at a UVC dose of 56.52 J cm⁻², larval mortality was 98.3%, 93.3% and 83.3% and adult emergence was 1.7%, 6.7% and 11.7% for 1–9, 10–18 and 19–27 day-old larvae, respectively. Similar effects were observed for UVC doses 150.72 and 226.08 J cm⁻² with an increase in the overall mortality of larvae and a decrease in adult emergence. Effect of irradiation of 0, 24 and 48 h-old pupae with doses of UVC, was inversely related to age of pupae at irradiation. Thus, at 56.52 J cm⁻², mortality as pupae was 91.7%, 71.7% and 73.3% and adult emergence was 0%, 3.3% and 1.7% for 0, 24 and 48 h-old pupae, respectively. Premature emergence of deformed adultoids was 25% when 24 and 48 h-old pupae were irradiated with the above dose. At a dose of 225.08 52 J cm⁻² there was no adult emergence. Death as pupae was 98.3%, 96.7% and 78.3% and premature emergence was 1.7%, 3.3%, and 21.7% for pupae irradiated at 0, 24 and 48 h-old, respectively.     

Relationship between nitrate/nitrite reductase activities in meat associated staphylococci and nitrosylmyoglobin formation in a cured meat model system

Quantitative determination of catalase, nitrate reductase, nitrite reductase and nitric oxide synthase activities (NOS) was performed on 11 different bacterial strains, mainly staphylococci, isolated from fermented sausages, bacon brine or cured meat products. All except one strain possessed catalase activity in the range from 1.0 to 6.1 μmol min^− 1 ml^− 1. Ten out of 11 bacteria strains showed nitrate reductase activity in the range between 50 and 796 nmol min^− 1 ml^− 1 and nine showed nitrite reductase activity in the range between 6 and 42 nmol min^− 1 ml^− 1. No evidence of NOS activity of the selected strains was detected. In a colour formation assay containing myoglobin all strains affected nitrosylmyoglobin (MbFe^IINO) formation in assays containing nitrite, whereas only strains having nitrate reductase activity generated MbFe^IINO in assays containing nitrate as the sole nitrosylating agent. The quantitative nitrate and nitrite reductase activity did not fully explain or correlate well with the observed rate of formation of MbFe^IINO, which seemed to be more affected by the growth rate of the different strains. The mechanism of the reduction of nitrite into NO of strains not having nitrite reductase activity remains to be fully elucidated, but could be due to a dual-mode action of nitrate reductase capable of acting on nitrate.     

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.     

Impact of sorbitol on the thermostability and heat-induced gelation of bovine serum albumin

The influence of sorbitol (0–40 wt.%) on the thermal denaturation and gelation of bovine serum albumin (BSA, pH 7.0) in aqueous solution has been studied. The effect of sorbitol on heat denaturation of 0.5 wt.% BSA solutions was measured using ultrasensitive differential scanning calorimetry. The unfolding process was irreversible and was characterized by the thermal denaturation temperature (T_m). As the sorbitol concentration increased from 0 to 40 wt.%, T_m increased from 73.0 to 80.9 °C. The rise in T_m was attributed to the increased thermal stability of the globular state of BSA relative to its native state. The dynamic shear rheology of 4 wt.% BSA solutions containing 200 mM NaCl was monitored as they were heated from 30 to 90 °C at 1.5 °C min⁻¹, held at 90 °C for 120 min, and then cooled back to 30 °C at −1.5 °C min⁻¹. Sorbitol increased the protein gelation temperature (ΔT_gel +10 °C for 40 wt.% sorbitol), decreased the isothermal gelation rate at 90 °C, but increased the final shear modulus of the gels cooled to 30 °C. The impact of sorbitol on gel characteristics was attributed to its ability to increase protein thermal stability, increase the attractive force between proteins and decrease the protein–protein collision frequency.     

Some properties of the polygalacturonase from four Zimbabwean wild fruits (Uapaca kirkiana, Zizphus mauritiana, Tamarindus indica and Berchemia discolor fruits)

Polygalacturonase was extracted from ripe Uapaca kirkiana, Zizphus mauritiana, Tamarindus indica and Berchemia discolor fruits of Zimbabwe. Protein concentrations and activities of the enzymes in the extracts were determined in the four fruit extracts. The protein concentrations in the enzyme extracts ranged from 0.82 ± 0.17 to 1.97 ± 0.13 mg/ml and enzyme activities from 1.99 ± 0.13 to 6.64 ± 0.38 mmol min⁻¹ mg⁻¹ in the four fruit extracts. Optimum pH of the enzyme ranged from 4.5 to 5 and optimum temperature from 25 to 37 °C. The enzyme extracts reduced the viscosity of 1% pectin solutions in an experiment which was done together with assay for reducing sugars to prove the activities of the enzyme extracts in the four wild fruits. The K_m and V_max ranged from 0.115 to 0.252 mg/ml and 0.0057 to 0.0119 mmol reducing groups/min/mg protein, respectively, in the four polygalacturonase extracts. Calcium chloride and sodium chloride activated the PG from all sources to a greater extend than magnesium chloride and barium chloride. PG from the other three fruits had very little effect on the polysaccharide from U. kirkiana.     

Fumigation with carbonyl sulfide: a model for the interaction of concentration, time and temperature

The new fumigant carbonyl sulfide offers an alternative to both methyl bromide and phosphine as a grain fumigant. Separate mathematical models for levels of kill, based on quantitative toxicological studies were developed for adults and eggs of the rice weevil Sitophilus oryzae (L.). These models suggest that fumigation exposure times for carbonyl sulfide will be a compromise between those of methyl bromide (typically 24 h) and phosphine (7–10 d) to achieve a very high kill of all developmental stages. S. oryzae eggs were more difficult to kill with carbonyl sulfide fumigation than the adults. At 30°C, a 25 g m⁻³ fumigation killed 99.9% of adults in less than 1 d, but took 4 d to kill the same percentage of eggs. Models were generated to describe the mortality of adults at 10, 15, 20, 25 and 30°C. From these models it is predicted that fumigation with carbonyl sulfide for 1–2 d at 30 g m⁻³ will kill 99.9% of adults. Furthermore the models illustrate that fumigations with concentrations below 10 g m⁻³ are unlikely to kill all adult S. oryzae. Significant variation was observed in the response of eggs to the fumigant over the temperature range of 10 to 30°C. Models were generated to describe the mortality of eggs at 10, 15, 20, 25 and 30°C. As the temperature was reduced below 25°C, the time taken to achieve an effective fumigation increased. Extrapolating from the models, a 25 g m⁻³ fumigation to control 99.9% of S. oryzae eggs will take 95 h (4 d) at 30°C, 77 h (3.2 d) at 25°C, 120 h (5 d) at 20°C, 174 h (7.5 d) at 15°C and about 290 h (11 d) at 10°C. The role of temperature in the time taken to kill eggs with carbonyl sulfide cannot be ignored. In order to achieve the desired level of kill of all developmental stages, the fumigation rates need to be set according to the most difficult life stage to kill, in this instance, the egg stage.     

Influence of temperature and surfactant on Escherichia coli inactivation in aqueous suspensions treated by moderate pulsed electric fields

This research employed a conductometric technique to estimate the inactivation kinetics of Escherichia coli cells in aqueous suspensions (1 wt.%) during simultaneous pulsed electric fields (PEF) and thermal treatments. The electric field strength was E = 5 kV/cm, the effective PEF treatment time t_PEF was within 0–0.2 s, the pulse duration t_i was 10^− 3 s, the medium temperature was 30–50 °C, and the time of thermal treatment t_T was within 0–7000 s. The damage of E. coli was accompanied by cell size decrease and release of intracellular components. The synergy between PEF and thermal treatments on E. coli inactivation was clearly present. The non-ionic surfactant Triton X-100 additionally improved its inactivation. The characteristic damage time followed the Arrhenius law within the temperature range 30–50 °C with activation energies W = 94 ± 2 kJ mol^− 1 and W = 103 ± 5 kJ mol^− 1 with and without the presence of surfactant, respectively. Relations between cell aggregation, cell ζ-potentials and presence of surfactant were analysed.     

A new method for the measurement of the tensile strength of rice grains by using the diametral compression test

Breakage of rice grains during milling can be attributed to the presence of fissures, caused by stresses related to shrinkage during drying. These fissures are usually caused by a tensile failure in the center of the grain. Very few data of the tensile strength of rice grains have been published, which is related to experimental difficulties. An attractive method for the measurement of the tensile strength is the diametral compression test, in which a cylinder is pressed between two flat plates. In this paper, results are shown of the application of the diametral compression test on rice grains. At a temperature of 20°C, a moisture content of 5.7% (w.b.) and a deformation rate of 7·10⁻³ min⁻¹ the tensile strength of rice grains is 10 ± 2 MPa, the compressive strength is 73 ± 15 MPa and the Young's modulus is 1.1 ± 0.1 GPa. The Young’s moduli from the diametral compression tests are not significantly different from those from uniaxial compression tests, which agrees with the theory. The obtained tensile strength values are in accordance with those from the literature. The repeatability of the diametral compression tests is of the same order as the repeatability of uniaxial compression tests.     

Heating condition effects on thermal resistance of fifth-instar Amyelois transitella (Walker) (Lepidoptera: Pyralidae)

Successful development of a thermal treatment protocol depends on reliable information on fundamental thermal death kinetics of targeted insects under different heating conditions. The effects of heating rates (1, 10, and 15 °C min⁻¹), pre-treatment conditioning (30 °C+6 h), and the difference between long-term laboratory cultures and recently isolated cultures on thermal mortality of fifth-instar navel orangeworm, Amyelois transitella (Walker), were studied using a heating block system. There was no significant difference in insect mortality resulting from heating rates of 10 and 15 °C min⁻¹. Temperature control at 1 °C min⁻¹ was more uniform than for the other heating rates, resulting in reduced variability for insect mortality. The mean mortality at the heating rate of 1 °C min⁻¹ was significantly lower than for the two faster heating rates only at 48 °C+30 min. The pre-treatment conditioning of fifth-instar Amyelois transitella enhanced their thermotolerance only at certain temperature-time combinations. Fifth-instars from long-term laboratory and recently isolated cultures were equally susceptible to elevated temperatures. Therefore, thermal death kinetic information obtained from the long-term laboratory cultures can be used to develop thermal protocols against field pests.     

Pre-selection of protective colloids for enhanced viability of Bifidobacterium bifidum following spray-drying and storage, and evaluation of aguamiel as thermoprotective prebiotic

The objective of this work was to demonstrate that Bifidobacterium bifidum viability to spray-drying and with storage time could be substantially enhanced by pre-selecting protective colloids offering resistance to oxygen diffusion (high activation energy) and adding aguamiel as a thermoprotector prebiotic. Three different protective colloids blends exhibiting relatively high, medium and low activation energies were mixed with B. bifidum harvested in the late log phase, with or without aguamiel, spray-dried at 130, 140 and 155 °C, and stored at 4 °C at a water activity of 0.32. Viability was determined by cell total count in MRS agar. Best viability was achieved when microencapsulating the microorganism in the protective colloids blend exhibiting highest activation energy (40.7 kJ mol⁻¹), with aguamiel, and dried at 140 °C. Viability ranged from 1.26 × 10⁸ cfu g⁻¹ immediately after drying to 6.0 × 10⁶ cfu g⁻¹ after 5 weeks storage time at 4 °C.     

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.     

Effects of supercritical carbon dioxide extraction conditions on yields and antioxidant activity of Chlorella pyrenoidosa extracts

Yields and antioxidant activity of Chlorella pyrenoidosa extracts obtained by supercritical carbon dioxide extraction through an orthogonal experiment (L₁₆(4⁵)) were investigated to get the best extraction conditions. The results showed that extraction pressure, temperature and modifier were the main three variables that influenced the yields of extracts. The highest yield was obtained at 32 °C, 40 MPa, 20 L h⁻¹ with dosage of modifier 1 mL ethanol g⁻¹ sample for 3 h. Moreover, increasing pressure and concentrations of modifier led to the increase of extraction yields and antioxidant activity. DPPH radical scavenging method showed that almost all the extracts had significantly higher antiradical activities varying from 29.67 ± 0.29% to 54.16 ± 4.49% comparing to -tocopherol, Trolox, and BHT as references except extracts at 32 °C, 35 MPa and 15 L h⁻¹ without modifier for 1.5 h. These results indicate that supercritical extraction is a promising alternative process for recovering compounds of high antioxidant activity from C. pyrenoidosa.     

Sorption of chloroanisole vapors by raisin packaging material

The behavior and concentration of 2,4,6-trichloroanisole (TCA) vapors migrating into low-density polyethylene film (PE) of 0.39 μm at various temperatures and desorption of TCA from PE were determined. After 12 h exposure, 1642 μg g⁻¹ TCA was sorbed at 30 °C compared with 675 μg g⁻¹ at 20 °C. For PE to reach equilibrium of 4200 μg g⁻¹ at 30 °C took 48 h, but 120 h at 20 °C. The transmission of TCA through PE occurred after 12 h at 30 °C (8.9 μg kg⁻¹ m⁻² h⁻¹) and after 36 h at 20 °C (5.0 μg kg⁻¹ m⁻² h⁻¹). Desorption of TCA from PE increased with temperature. At 80 °C, 99% TCA was desorbed in 1 h compared to 51% at 40 °C, 31% at 30 °C and 17% at 20 °C. The rate of sorption, desorption and transmission of TCA vapors by PE is highly temperature-dependent.     

NMR relaxometry and differential scanning calorimetry during meat cooking

By combining simultaneous nuclear magnetic resonance (NMR) T₂ relaxometry and differential scanning calorimetry (DSC) on pork samples heated to nine temperature levels between 25 and 75 °C, the present study investigates the relationship between thermal denaturation of meat proteins and heat-induced changes in water characteristics. Principal component analysis (PCA) on the distributed ¹H NMR T₂ relaxation data revealed that the major changes in water characteristics during heating occur between 40 and 50 °C. This is probably initiated by denaturation of myosin heads, which however, could not be detected in the DSC thermograms obtained directly on the meat. In contrast, the DSC thermograms revealed endothermic transitions at 54, 65 and 77 °C, probably reflecting the denaturation of myosin (rods and light chain), sarcoplasmic proteins together with collagen and actin, respectively. Simultaneous modelling of DSC and NMR data by partial least squares regression (PLSR) revealed a correlation between denaturation of myosin rods and light chains at 53–58 °C and heat-induced changes in myofibrillar water (T₂ relaxation time 10–60 ms) as well as between actin denaturation at 80–82 °C and expulsion of water from the meat. Accordingly, the present study demonstrates a direct relationship between thermal denaturation of specific proteins/protein structures and heat-induced changes in water mobility during heating of pork.