Modelling the effect of a temperature shift on the lag phase duration of Listeria monocytogenes

The aim of this work is to study and model the effect of a temperature shift on h₀, the product of the growth rate by the lag phase duration (μλ). Our work is based on the data of Whiting and Bagi [Int. J. Food Microbiol. 73 (2002) 291], who studied the influence of both the pre-incubation temperature (T_prior) and the growth temperature (T_growth) on λ values of Listeria monocytogenes. We introduce a new model to describe the evolution of the parameter h₀ as a function of T_prior and T_growth, and compare it to Whiting and Bagi's published polynomial model that describes the influence of T_prior and T_growth on λ independently of μ. For exponential as well as stationary phase cells, h₀ increases almost linearly with the magnitude of the temperature shift. A simple linear model of h₀ turns out to be more suitable to predict λ values than a polynomial model of λ.     

A model of the specific growth rate inhibition by weak acids in yeasts based on energy requirements

Zygosaccharomyces bailii, a spoilage yeast, capable of metabolic activity in food environments with low pH, low a_w and in the presence of weak acid preservatives was chosen for a study on the effect of benzoic acid on growth parameters. In batch cultures, under controlled pH, this food preservative inhibited growth, decreasing the specific growth rate (μ) and the yield coefficient (Y_S) on glucose. Data obtained at pH 3.5, 4.0 and 4.5 showed that this inhibition was exclusively promoted by the undissociated form of the acid since the effect was independent of pH when the concentration of the acid was expressed in this form. Moreover, the relationship between the values for μ and Y_S, provided evidence that the specific consumption rate of glucose (q_S) was not affected by benzoic acid, indicating that the inhibition of growth should be completely explained by a decrease of Y_S. The outcome of parallel experiments performed in continuous culture was that the decrease of Y_S was due to an increase of the maintenance coefficient (m), defined as the fraction of q_S diverted from growth to cope with stress, represented in this case by the presence of the preservative. Based on these results a model was built, assuming that m increased hyperbolically with the concentration of benzoic acid, from zero in the absence of the acid up to q_S when growth was completely inhibited. The concentration of the acid, for which m=q_S/2, is a constant (K_W), and represents a measure of the tolerance for a preservative, in this case benzoic acid. The simple equation μ/μ₀=1+W/K_W predicts the value of μ for a concentration (W) of the preservative, requiring the knowledge of two parameters: the specific growth rate in the absence of the preservative (μ₀) and K_W. The equation fitted very well the data of the effect of benzoic acid on the specific growth rate of Z. bailii, having K_W=0.96 mM benzoic acid. The model was also validated with other spoilage yeasts grown in the presence of benzoic acid in microtiter plates in an automated spectrophotometer. The values obtained for K_W under these conditions confirm Z. bailii as the most tolerant (K_W=2.1 mM) followed by Pichia sp. (K_W=0.78 mM), Saccharomyces cerevisiae (K_W=0.53 mM) and Debaryomyces hansenii (K_W=0.11 mM).     

Effect of temperature and relative humidity on yellowing rate of paddy

The effects of temperature and relative humidity (or water activity) in storage chambers on yellowing rate of paddy were investigated and then an empirical equation for predicting the yellowing rate was developed. Paddy was conditioned using saturated salt solutions at relative humidities ranging from 0.80 to 0.95 and temperatures of 35, 45, 55, 60 and 65°C. The yellowing rate was found to follow the zero order kinetics. The yellowing constant value (k) increased exponentially with temperature and increased linearly with water activity. The magnitude of apparent activation energy varied from 130–145 kJ/mol. A predictive equation for determining yellowing rate was ln k=−δa_w−/T+(γa_w)/T where a_w was water activity (valid from 0.80 to 0.95), T was absolute temperature (valid from 308 to 338 K) and , δ, and γ were constants. The results of variance analysis showed that temperature, water activity and their interaction significantly influenced the yellowing rate of paddy.     

Comparing predicting models for heat inactivation of Listeria monocytogenes and Pseudomonas aeruginosa at different pH

Under the same experimental conditions it has been demonstrated that whereas survival curves of Listeria monocytogenes in the range of temperatures from 54 to 62 °C followed a first-order kinetic, those of Pseudomonas aeruginosa in the range of temperatures from 50 to 56 °C were not linear showing a shoulder followed by a linear region. The first order kinetic model did not describe survival curves of P. aeruginosa. A model based on the Weibull distribution (Log₁₀(N_t/N₀)=(1/−2.303)*(t/b)ⁿ)) accurately described the inactivation kinetics of both microorganisms at the three pHs of 4, 5.5, 7.4 investigated. For both microorganisms, the b value depended on the treatment temperature and the pH of the treatment medium. Whereas for L. monocytogenes the n value was independent of the treatment conditions, for P. aeruginosa the n value depended on the pH of the treatment medium.

The model based on the Weibull distribution was capable of accurately predicting the treatment time to inactivate five Log₁₀ cycles of both microorganisms at the three pHs investigated.     

Effect of environmental stresses on the mean and distribution of individual cell lag times of Escherichia coli O157:H7

The effect of starvation, heat or acid stress on duration of individual cell lag time (τ) and standard deviation (SD) of τ was investigated using Escherichia coli O157:H7. Cells were stressed by exposure to acid (pH 3.5), heat (50 °C), or starvation in either glucose-free mineral medium (MOPS), tryptic soy broth (TSB) or Luria broth (LB). Stressed cells were then diluted into wells of a Bioscreen plate to obtain single cells per well. Replicate time to detection (t_d) values were obtained using the Bioscreen and used to calculate the τ and SD. Significant (P ≤ 0.05) increases in τ over untreated controls were found for the following treatments: 14 days in acid; 2 h of heating; 3 days starvation in MOPS; and 2 days starvation in either TSB or LB. The largest increase in τ was > 2-fold from 2.5 to 5.6 h observed with the heat treatment. MOPS starvation was more detrimental to the cells than was acid treatment over the same time period. A significant increase in SD was found with 21 days acid treatment, and 2 days starvation in either TSB or LB. No significant increase in SD was found for MOPS starvation or heat treatment. Lognormal, Gamma, ExtremeValue and Weibull distributions were fitted to the τ data using BestFit. The results suggest that the Lognormal distribution is suitable for fitting τ data from either stressed or unstressed cells.     

Identification of PSE in the Longissimus muscle of pigs stunned by captive-bolt

Meat quality characteristics in the longissimus muscle of 57 pigs slaughtered at approximately 100 kg liveweight were studied. They were slaughtered by captive-bolt stunning and exsanguination. The incidence of pale, soft and exudative (PSE) meat was identified by muscle colour and water holding capacity 24 h post mortem (C₂₄ and WHC₂₄). The muscle pH value 45 min post mortem (pH₁), absorption ratio (R-value) of muscle acid extract, and colour and water holding capacity 1 h post mortem (C₁ and WHC₁) were also determined. The interrelationships among pH₁, R-value, C₁, WHC₁, C₂₄ and WHC₂₄ were studied and the multiple regressions of C₁, C₂₄, WHC₁ and WHC₂₄ with pH₁ and R-value were computed. The results of simple and multiple regression analysis showed that neither muscle pH₁ nor R-value could effectively predict colour or WHC at 24 h post mortem. Combining pH₁ and R-value provided little improvement in the prediction of the ultimate meat colour and WHC.     

Thermal inactivation of the frozen thawed traditional meat starter culture, Pediococcus pentosaceus, in a meat model system

The equation, y_(t) = y₍₀₎e^kt, was fitted (R = 0.9281, 0.9220 and 0.9117, respectively) to thermal inactivation data (55, 60 and 65 °C) of the traditional meat starter culture Pediococcus pentosaceus (10⁷ cfu/ml) in a meat model system. The population reduction constant (‘k’) increased (about 2.5- and 3-fold) with an increase in the treatment temperature (from 55 to 60 °C and from 60 to 65 °C, respectively). The Q₁₀ (55–65 °C) for ‘k’ was 7.63. Thermal treatments of 19.1, 9.0 and 3.1 min (55, 60 and 65 °C, respectively) reduced the population of P. pentosaceus by 2.0 logs. The value of ‘k’ and the duration of the thermal treatment played an important role in the extent of the inactivation of the culture. The “zero inactivation” temperature (T₀) for P. pentosaceus was 49.9 °C. About 5 logs of the culture would be destroyed at 63 and 68 °C within about 15.5 and 6.5 min, respectively.     

Physical changes of significance for early post mortem water distribution in porcine M. longissimus

The post mortem changes in water mobility and distribution were followed in porcine muscle (M. longissimus dorsi) samples using continuous low-field NMR relaxation measurements and simultaneous measurement of changes in muscle impedance as an indirect measure of membrane integrity as well as muscle contraction measurements using a rigormeter instrument. Distributed exponential fitting analysis of NMR T₂ relaxation data revealed the presence of three distinct water populations (T₂₀, T₂₁, T₂₂) within the muscle during its conversion to meat. Comparison of T₂ relaxation patterns and contraction data indicates that rigor development affects the attributes of the T₂₁ water population and thereby contributes to myofibrillar water characteristics post mortem, as the T₂₁ water population is believed to reflect inter/intra-myofibrillar water. The volume of the water population believed to reflect extra-cellular water (T₂₂) in the living muscle. Early post mortem T₂₂ decreased slightly within the first 2–3 h post mortem followed by an increase and a change in its characteristic time constant. This was ascribed to an initial muscle cell swelling followed by water being expelled from the cellular space into the extra-myofibrillar space. Comparison of changes in the T₂₂ water population and impedance characteristics within the muscle during its conversion to meat revealed close relationship between progresses in the two attributes. Obtained data strongly support that the post mortem reorganization of water is closely associated with membrane properties, which moreover was found to affect the final water-holding capacity of the meat. Finally, a model for early post mortem events leading to changes in the distribution of water within muscles is proposed.     

烟草NtbZIP038的克隆、鉴定及表达模式分析

碱性亮氨酸拉链（bZIP）转录因子是植物中数量最多、最具有多样性的基因家族之一,对植物生长发育及胁迫响应具有重要作用。为探究烟草中bZIP转录因子的生物学功能,本研究在烟草K326中克隆得到一个bZIP转录因子基因NtbZIP038,并对其保守结构域进行分析,利用qRT-PCR技术检测了该基因的表达模式,进一步结合亚细胞定位及转录激活试验对其功能进行了初步鉴定。结果表明,NtbZIP038含有典型的bZIP结构域,亚细胞定位于细胞核中并具有转录激活活性。表达模式分析表明,NtbZIP038在根中表达量最高（p<0.001）,并在盐、干旱、冷、热、脱落酸（ABA）等非生物胁迫下都有明显的表达量变化,在ABA处理下尤其明显（p<0.001）。因此,作为bZIP家族中的一员,NtbZIP038转录因子可能在烟草根系发育、ABA响应与非生物胁迫中扮演着重要的角色。     

Colour of normal and high pH beef heated to different temperatures as related to oxygenation

The effects of oxygenation and thermal treatment (internal temperature, T_i: 45, 60, 75°C) on the colour and some colour related physical and biochemical properties of beef longissimus dorsi (LD) muscle, both normal (pH_u5.6) and DFD (pH_u>6.6), were studied. The colour components (L^*, a^*, b^* values) for the raw and heated LD, both before and after oxygenation, were instrumentally and sensorily evaluated. The colour of raw and heated (60°C) DFD beef before and after oxygenation differed significantly from the normal meat and contained more native muscle pigment (TMP). pH also influenced the depth of the oxygenated layer, specific activity of cytochrome c oxidase (SACCO) and the amount of oxygen consumed. An increase in internal temperature was usually accompanied by a lower SACCO and a significant decrease of TMP, as well as a change of all colour parameters. Oxygenation of the raw and heated slices (except at 75°C) of both types of meat led to higher L^*, a^* and b^* values.     

Relationships between sensory perception and water distribution determined by low-field NMR T(2) relaxation in processed pork - impact of tumbling and RN(-) allele

The relationships between water distribution, measured with low-field NMR (LF-NMR) transverse (T₂) relaxometry and sensory properties in tumbled and non-tumbled cured-smoked loins from 30 female Hampshire crossbred pigs were investigated. Upon distributed analysis of the T₂ relaxation, three populations centred at about 2, 40 and 600–800 ms, respectively, were detected. Clear differences in the characteristics of the intermediate population (T₂₁) were observed between loins from carriers and non-carriers of the RN⁻ allele, which implies differences in water–protein interactions between the two genotypes. PLS regressions between NMR T₂ variables and sensory attributes revealed significant correlations between NMR T₂ variables and the sensory attributes juiciness, acidulous taste and meat taste, which mainly could be ascribed to the T₂₁ time constant. In addition, the number of unappealing pores assessed by the sensory panel was highly related to the relative T₂ populations, implying that the microstructure is directly reflected in the NMR T₂ populations. However, prediction of the processing yield from NMR T₂ variables was poor. The correlation improved when RN genotypes and tumbling conditions were included as predictors. Thus, other effects of tumbling treatments and RN genotypes unrelated to NMR T₂ relaxation were observed.     

The significance of cooling rate on water dynamics in porcine muscle from heterozygote carriers and non-carriers of the halothane gene-a low-field NMR relaxation study

The post mortem changes in the chemical/physical state distribution of water were followed in pig muscle (M. longissimus dorsi) from heterozygote (n=12) and non-carriers (n=12) of the halothane gene exposed to two different cooling profiles using continuous low-field NMR relaxation measurements. T₂ relaxation data were analyzed using distributed exponential fitting analysis. Independent of genotype post mortem changes were observed in the two water populations characterizing water within the myofibrillar space (T₂₁) and the extra-myofibrillar space (T₂₂), respectively, as a function of chilling regime. The effect was most pronounced in samples from heterozygote carriers of the halothane gene. The obtained results strongly suggest that improved water-holding capacity of muscles upon fast chilling can be ascribed to a reduced accumulation of extra-myofibrillar water in the meat post mortem, and it is hypothesized that differences in the accumulation of extra-myofibrillar water post mortem can be ascribed largely to the time at which disruption of cell membrane integrity takes place.     

Enthalpy-Entropy compensation in food vapor adsorption

Enthalpy-entropy compensation was analysed for sorption isotherms of potatoes, macadamia nuts, apricots, figs, currants, prunes and raisins. Plots of (ΔH_dif)_T vs (ΔS_dif)_T for potatoes and macadamia nuts presented two isokinetic temperatures: T_B1 = 272.0 ± 57.7 K (− 1 °C) for potatoes, T_B1 = 265.0 ± 18.8 K (− 8 °C) for macadamia nuts and T_B2 = 382.5 ± 7.3 K (109.5 °C) for both products. The first isokinetic temperature (T_B1) appeared only at the upper portion of the temperature range tested (50, 60 and 70 °C for potatoes and 50 and 60 °C for macadamia nuts). The two isokinetic temperatures observed for potatoes and macadamia nuts suggested that during the initial stages at low a_w T_B1 is controlled by changes in the entropy of water, whereas the second isokinetic temperature (T_B2) is considered to be enthalpy-controlled. Dried fruits presented only one isokinetic curve T_B = 315.7 ± 3.5 K (42.7 °C), for raisins, currants and figs (75.2–82.3% d.b. sugars) and T_B = 317.7 ± 4.6 K (44.7 °C) for prunes and apricots (51.5–54.5% d.b. sugars), indicating an enthalpy-controlled adsorption process for the whole range of moisture contents covered.     

Variation in post-mortem rate of glycolyis does not necessarily affect drip loss of non-stimulated veal

In this study the effect of the rate of post mortem pH fall on the water-holding capacity of meat from moderately chilled veal carcasses was investigated. Also the relationship between muscle protein denaturation and drip loss of veal was examined. Three groups of 10 Friesian Holstein male veal calves each were selected on the basis of their pH in M. longissimus thoracis et lumborum (LTL) at 3 hr post mortem (pH₃): (1) fast pH-fall, pH₃ < 6.2; (2) intermediate pH-fall, 6.5 < pH₃ < 6.6; (3) slow pH-fall, pH₃ > 6.7. After 48 hr of chilling the LTL was excised from the carcass and sampled for determination of drip loss, filter paper wetness, sarcomere length, protein solubility and transmission value. Differences in pH₃ were not associated with differences in drip loss, filter paper wetness or differences in protein denaturation. It is suggested that at the relatively high veal carcass chilling rate the effect of rate of pH-fall on protein denaturation and thus on drip loss is negligible. Drip loss of veal was highly correlated with both solubility of sarcoplasmic (r = −0.67; p < 0.001) and total muscle protein (r = −0.54; p < 0.01) and with transmission values (r = 0.66; p < 0.001). These results indicate that protein denaturation measurements may be a good predictor for drip loss of veal.     

Growth energetics of Lactococcus lactis subsp. lactis biovar diacetylactis in cometabolism of citrate and glucose

Certain strains of lactic acid bacteria present in commercial cheese starters, characterized by faint transparent colonies on an agar plate containing 1 mg kg ⁻¹ crystal violet (CVT), were identified as Lactococcus lactis subsp. (ssp) lactis biovar diacetylactis. The effect of citrate on the growth of these strains (CVT strains) in the presence of glucose was studied, in comparison with L. lactis strains. Molar growth yield from glucose (Y_G, g dry weight/mole of glucose consumed) for CVT strains grown on glucose plus citrate was significantly higher than the control (i.e. without citrate), but not for other L. lactis strains tested. Enhanced Y_G was also observed at a pH-controlled experiment, indicating that enhanced Y_G did not result from a buffering effect of citrate. CVT strains, in contrast to other strains of the same species, were shown to obtain enough energy to enhance Y_G on glucose–citrate mixtures.     

Dietary vitamin E supplementation and discoloration of pork bone and muscle following modified atmosphere packaging

The effects of modified atmosphere (80% O₂: 20% CO₂) and illumination on the discoloration rate of pork bone (lumbar vertebrae) and muscle (longissimus lumborum), and on muscle lipid stability were studied in vitamin E-supplemented and unsupplemented pigs. Bone-in pork chops were placed in 80% O₂: 20% CO₂ at 0 °C and stored for 5 days in the dark. The chops were then displayed under (a) fluorescent light in air or modified atmosphere or (b) in air with or without illumination. Lipid oxidation was increased by the modified atmosphere packaging but this detrimental effect was offset by vitamin E supplementation. Higher supplementation levels (198 and 207mg/kg) improved bone color stability regardless of the packaging atmosphere or the lighting conditions. Although vitamin E supplementation improved muscle color stability during display in air or modified atmosphere, the benefit of supplementation on muscle color was detectable only for illuminated storage.     

Effect of pH at time of salting on the functional properties of pre-rigor beef

The functional properties of thawed pre-rigor beef that had been minced and salted or not salted when its pH value reached 6.8, 6.6, 6.4, 6.2 and 6.0, then immediately frozen, were determined. The mince samples were used to manufacture a finely comminuted sausage batter. Presalting before frozen storage resulted in higher (p < 0.05) thawed mince pH, and batter cook yield and shear strain, and lower (p < 0.05) mince salt soluble proteins, thaw drip and Hunter L^* and b^* values and batter shear stress than unsalted controls. The pre-rigor pH at time of salting/mincing affected (p < 0.05) thaw drip (unsalted mince only), Hunter L^* and b^* values and shear stress. Shear stress tended to increase (p < 0.01) and Hunter L^* (p < 0.05) and b^* (p < 0.01) values tended to decrease with fall in pre-rigor salting pH. No interaction (p > 0.05) between salting and pre-rigor pH at time of salting was observed.     

Evaluation of methoprene alone and in combination with diatomaceous earth to control Rhyzopertha dominica (Coleoptera: Bostrichidae) on stored wheat

A series of experiments were conducted in which different formulations of the insect growth regulator methoprene were evaluated for control of Rhyzopertha dominica (F.), the lesser grain borer, a major internal insect pest of stored wheat. In the first test, application rates of 10-ppm R,S-methoprene (a racemic mixture of the R and S isomers of methoprene) and 1 and 5-ppm S-methoprene (S-isomer only) gave 100% suppression of F₁ adult progeny of R. dominica for 24 weeks. In the second test, adult R. dominica were exposed at 27°C and 32°C, 57% and 75% relative humidity (r.h.) on untreated wheat and wheat treated with 1- to 10-ppm S-methoprene dust. Survival after a 3-week exposure decreased with increasing concentration of dust, and ranged from 69% to 99%, but no F₁ adult progeny were produced in treated wheat. In the final test, concentrations of 0, 0.25, 0.50, 0.75, and 1.0 ppm S-methoprene EC were combined with concentrations of 0, 75, 150, 225, and 300 ppm of the commercial diatomaceous earth (DE) Protect-It^®. Within each methoprene concentration, survival generally decreased with increasing concentration of DE, and was generally greater at 75% than at 57% r.h. Only the wheat treated with 0-ppm methoprene contained an appreciable number of F₁ adults. In summary, both the dust and EC formulations of S-methoprene gave 100% suppression of F₁ adult progeny R. dominica at application rates of 1 ppm, and combination treatments involving reduced rates of methoprene and DE gave effective control of R. dominica.     

Effect of electrical stimulation on post mortem biochemical characteristics and quality of Longissimus dorsi thoracis muscle from buffalo (Bubalus bubalis)

High voltage electrical stimulation (700 V, 1400 V peak, pulses 1 s on/1 s off, 60 Hz, 2 A) on buffalo carcasses resulted in a significantly more rapid pH fall in Longissimus dorsi thoracis muscle when compared to non stimulated controls (p < 0.01), during the first 24 h after slaughter. The IMP/ATP ratio on the same period showed a much more rapid increase for the stimulated muscles (1.07 and 1.16 at times 1 and 2.5 h post mortem vs control values of 0.77 and 0.83, respectively). Sensory and instrumental evaluation of texture of meat cooled by two distinct processes showed that tenderness at 24 h post mortem was higher in the stimulated muscles compared to non-stimulated controls, irrespective of the cooling process adopted. High voltage stimulation significantly decreases cohesiveness, increases myofibril fragmentation; and SDS polyacrylamide gel electrophoresis of the myofibrillar proteins showed a weakening of Troponin T band during 6 days of ageing in non-stimulated control muscles, whereas electrical stimulation accelerated the process of ageing over 3 days. This is the first report on acceleration of conditioning in buffalo muscle and the conditions described here have a high potential for application in meat industry for buffalo slaughter.     

Water status of cooked white salted noodles evaluated by MRI

Transverse relaxation time (T₂)-weighted images and T₂ maps of white salted noodles (WSN) were investigated by magnetic resonance imaging technique. T₂-weighted images and T₂ maps clearly showed the differences in water status between noodles. The migration of moisture from surface regions to central regions of boiled WSN at different migration rates were investigated during storage. The distribution of T₂ values changed differently depending on the cooking and storage times. The small differences in T₂ values between surface region and central region of noodles cooked for 5 and 15 min were attributed to the limited water absorption during short cooking time, which resulted in high firmness. The changes in starch granules morphology observed under scanning electron microscope and the increase of noodle firmness measured by texture analyzer were significantly affected by the water status in noodles. The water status can be controlled by the cooking time.