Structural Transformation of Sago Starch by Heat‐Moisture and Osmotic‐Pressure Treatment

Sago starch was modified by osmotic‐pressure treatment (OPT) and heat‐moisture treatment (HMT) and physicochemical characteristics were compared. In OPT, sago starch was suspended in saturated sodium sulfate solution and heated for 1 h at 100, 110 and 120°C, corresponding to a calculated osmotic pressure of 32,728, 33,640 and 34,552 kPa (assuming sodium sulfate dissociates completely), respectively, and in HMT, sago starch with 20% moisture content was used. Change of X‐ray diffraction pattern from C‐type to A‐type was obtained for OPT and HMT starch at 110°C and 120 °C, respectively. RVA viscograms of both OPT and HMT starch exhibited a decrease of peak and breakdown viscosity but increase of final viscosity and pasting temperature. Onset (T_o), peak (T_p), and conclusion temperature (T_c) of gelatinization of both OPT and HMT starch increased significantly with increase of treatment temperature. Biphasic broadening of T_p was observed for HMT starch indicating an inhomogeneous heat transfer during HMT. The observed narrow peaks of DSC curves indicated better homogeneity of OPT. These properties suggest that OPT starch is more suitable for large‐scale production.     

Sensitive Catalase Test for End-point Temperature of Heated Chicken Meat

Our improved method enables detection of catalase-related activities as a biochemical marker for estimating cooking end-point temperature (EPT). The broad range of inactivation temperature in chicken tissues was first determined to be > 68°C and 相似文献   

Classification of Fresh and Frozen‐thawed Fish by Near‐infrared Spectroscopy

ABSTRACT: Frozen fish usually have a much lower market price than fresh fish; therefore, adulteration could occur. This article focuses on the use of near infrared (NIR) spectroscopy to detect whether fish has been frozen‐thawed because NIR spectroscopy has demonstrated the potential for addressing some authenticity issue in foods and is known to be a nondestructive rapid technique. Horse mackerel (n = 162) were evaluated as fresh and frozen‐thawed fish sample. Dry extract spectroscopy by infrared reflection (DESIR) of fresh and frozen‐thawed fish samples was performed on the meat juices then discriminated by principal component analysis (PCA) and multiple linear regressions (MLR). In DESIR spectra, the overall absorbance level was found to decrease in frozen‐thawed samples, indicating the different chemical composition of juice, amount of dry matter, particle size, and their scattering properties. The spectral changes that take place between fresh and frozen‐thawed samples are clearly seen in the 1920‐ to 2350‐nm region. The spectra are dominated by peaks attributed to proteins, in particular, peaks at 1510, 1700, 1738, 2056, 2176, 2298, and 2346 nm. It was found that fresh and frozen‐thawed fish could be separated 100% correctly by DESIR technique.     

Assessment of Enterotoxin Production and Cross‐Contamination of Staphylococcus aureus between Food Processing Materials and Ready‐To‐Eat Cooked Fish Paste

This study evaluated Staphylococcus aureus growth and subsequent staphylococcal enterotoxin A production in tryptone soy broth and on ready‐to‐eat cooked fish paste at 12 to 37 °C, as well as cross‐contamination between stainless steel, polyethylene, and latex glove at room temperature. A model was developed using Barany and Roberts's growth model, which satisfactorily described the suitable growth of S. aureus with R²‐adj from 0.94 to 0.99. Except at 12 °C, S. aureus cells in TSB presented a lag time lower (14.64 to 1.65 h), grew faster (0.08 to 0.31 log CFU/h) and produced SEA at lower cell density levels (5.65 to 6.44 log CFU/mL) compare to those inoculated on cooked fish paste with data of 16.920 to 1.985 h, 0.02 to 0.23 log CFU/h, and 6.19 to 7.11 log CFU/g, respectively. Staphylococcal enterotoxin type A (SEA) visual immunoassay test showed that primary SEA detection varied considerably among different storage temperature degrees and media. For example, it occurred only during exponential phase at 30 and 37 °C in TSB, but in cooked fish paste it took place at late exponential phase of S. aureus growth at 20 and 25 °C. The SEA detection test was negative on presence of S. aureus on cooked fish paste stored at 12 and 15°C, although cell density reached level of 6.12 log CFU/g at 15 °C. Cross‐contamination expressed as transfer rate of S. aureus from polyethylene surface to cooked fish paste surface was slower than that observed with steel surface to cooked fish paste under same conditions. These results provide helpful information for controlling S. aureus growth, SEA production and cross‐contamination during processing of cooked fish paste.     

Antioxidant Properties of Aqueous Extract of Roasted Hulled Barley in Bulk Oil or Oil‐in‐Water Emulsion Matrix

Antioxidant properties of the aqueous extracts of hulled barley (Hordeum vulgare L.) that had been roasted at 210 °C for 20 min were determined in bulk oil and oil‐in‐water (O/W) emulsions. Bulk oils were heated at 60, 100, and 180 °C, and O/W emulsions were oxidized under riboflavin photosensitization. The content of phenolic compounds was analyzed by high‐performance liquid chromatography, and in vitro antioxidant assays were also conducted. The major phenolics contained in the aqueous extract of roasted hulled barley (AERB) were p‐coumaric, ferulic, protocatechuic, chlorogenic, 4‐hydroxybenzoic, and vanillic acids. Depending on the concentration and oxidation temperature, AERB had antioxidant or prooxidant properties in bulk oil. At 60 °C, AERB at a concentration of 0.5% acted as a prooxidant, whereas at 1.0% it acted as an antioxidant. At 100 °C, AERB acted as an antioxidant irrespective of concentration. In 180 °C conditions, 0.5% AERB acted as a prooxidant, whereas other concentrations of AERB acted as antioxidants. In the case of riboflavin photosensitized O/W emulsions, AERB showed antioxidant properties irrespective of concentration. Antioxidant abilities of AERB are affected by the food matrix, including bulk oil and O/W emulsions, and concentrations of AERB, even though diverse phenolic compounds may display high antioxidant properties in in vitro assays.     

Predictive Modeling of the Effect of ε‐Polylysine Hydrochloride on Growth and Thermal Inactivation of Listeria monocytogenes in Fish Balls

This study aimed to evaluate the effect of ε‐polylysine hydrochloride (ε‐PLH) on the growth and thermal inactivation kinetics of Listeria monocytogenes in fish balls. Samples, supplemented with ε‐PLH (0, 150, or 300 ppm, w/w), were inoculated with a three‐strain cocktail of L. monocytogenes and incubated at constant temperatures of 3.4, 8, 12, or 16 °C for growth studies, or heated at 60, 62.5, 65, or 67.5 °C for thermal inactivation tests. The growth curves were fitted to the Huang primary model, and the Huang and Ratkowsky square‐root models (SRM) were used as the secondary models to evaluate the effect of temperature on bacterial growth. The survival during heating was analyzed with a log‐linear model. The results showed that, while the lag time of L. monocytogenes was affected by both ε‐PLH concentration and temperature, the specific growth rate was unaffected by ε‐PLH. Under the same temperature, a 10‐time in increase of the lag time would be expected for every 565 ppm in the increase of ε‐PLH concentration. Using the Ratkowsky SRM, the estimated nominal minimum growth temperature was –2.04 °C, while the minimum growth temperature was 0.29 °C when estimated with the Huang SRM. Validation at 10 °C showed that the Huang primary model, in combination with either the Huang or Ratkowsky SRM, could accurately predict the growth of L. monocytogenes. On the other hand, the thermal resistance of the pathogen was significantly reduced by increase in temperature or ε‐PLH. The thermal z value of L. monocytogenes was 5.78 °C, and the ε‐PLH z value was 1642 ppm. The results of this study showed that the combined application of ε‐PLH and temperature can be used to control L. monocytogenes in fish balls and to improve food safety and reduce risks to public health.     

The rheological properties of exudates from cured porcine muscle: effects of added non‐meat proteins

Meat exudates were collected from massaged cured porcine M semimembranosus using a model massaging unit. Exudates were used to observe changes in gelation properties due to the incorporation of commercially available non‐meat proteins. These included: soya isolate (90%), sodium (Na) caseinate (85%) and high gelling whey protein concentrates (WPCs, A‐35%, B‐75% and C‐β‐lactoglobulin (55%), as well as a regular 76% protein, WPC D. Compositional analysis ( n=6) showed that incorporation of non‐meat proteins significantly (P<0.05) increased the protein concentration of test exudates in all cases compared to controls. The viscoelastic properties of control and test meat exudate samples (n=6) were analysed using control stress rheology in oscillatory mode. All exudates were heated from 20 to 80°C at 1°C min⁻¹, and subsequently cooled after 30 min back down to 20°C at 1°C min ⁻¹. Addition of WPCs at a 1, 2 and 3% residual powder level and soya isolate at a 1% residual level, resulted in increased storage modulus G′ (Pa) values compared with controls. A 1% residual level of Na caseinate was detrimental to meat exudate gelation, resulting in lower final G′ (Pa) values than those observed for the control. © 1999 Society of Chemical Industry     

Non‐destructive texture analysis of farmed Atlantic salmon using visual/near‐infrared reflectance spectroscopy

Fillets of farmed Atlantic salmon were assessed by visual/near‐infrared (VIS/NIR) reflectance spectroscopy, Kramer shear force measurement and texture profile analysis (TPA). Comparison of the Kramer measurements between pairs of subsamples gave correlation coefficients of 0.85 for pre‐rigor (2 h after slaughter), 0.78 for post‐rigor (6 days after slaughter) and 0.97 for pre‐ and post‐rigor combined. TPA gave non‐significant correlations between subsamples. VIS/NIR fibre optic probe measurements gave cross‐validated correlation coefficients for prediction of Kramer shear force of 0.76 for pre‐rigor, 0.68 for post‐rigor and 0.94 for pre‐ and post‐rigor combined. Classification using linear discriminant analysis of the VIS/NIR measurements gave up to 79% correct classification into three categories: low Kramer shear force (2.13 × 10^?2–4.41 × 10^?2 J g^?1), medium Kramer shear force (4.41 × 10^?2–6.37 × 10^?2 J g^?1) and high Kramer shear force (6.37 × 10^?2–7.90 × 10^?2 J g^?1). Using these class limits, no low‐Kramer‐shear‐force sample was misclassified as a high‐Kramer‐shear‐force sample, and vice versa. It can be concluded that non‐destructive VIS/NIR fibre optic probe measurement gives fair predictions of Kramer shear force. Its most useful application in salmon production plants may be to classify fillets into broad classes according to texture before further processing or sale. © 2001 Society of Chemical Industry     

Assessment of maximum cooking temperatures in previously heat treated beef. Part 1: Near infrared spectroscopy

Near infrared diffuse reflectance (NIR) and transmittance (NIT) spectroscopy were studied as potential methods for determination of the previous heat treatment of beef. Ninety-four samples of M longissimus dorsi from 33 bulls were heat treated at nine different temperatures between 50 and 85°C, and analysed by NIR and NIT spectroscopy. The samples were analysed by NIR and NIT in both ‘wet’ and freeze dried states. The NIR and NIT methods were able to determine the maximum temperature of previously heat treated beef with a prediction error of 2.0-2.1°C in the temperature range 50–85°C. Freeze drying of the samples prior to analysis reduced the prediction error to 1.4°C for the NIR method. NIR and NIT should be useful as fast screening methods to determine whether beef has been adequately heat treated.     

Usefulness of near infrared spectroscopy to monitor the extent of heat treatment in fish meal

The objective of this study was to explore the use of near infrared (NIR) spectroscopy and chemometrics to monitor the degree of heat treatment of fish meal. Six batches of fish meal (approximately 500 g) were split in sub‐samples of 50 g and heated at constant temperature (60 ± 5 °C) for different periods of time (15 and 30 min, 1, 2, 3, 4, 5, 6, 8, 48 and 72 h) in a force air oven and scanned in the NIR region (1100–2500 nm) in a monochromator instrument in reflectance. Principal component analysis (PCA), stepwise discriminant analysis (SLDA) and partial least square regression (PLS) models were used to interpret, classify and predict the extent to heat treatment in fish meal samples. The SLDA models correctly classified 80% and 100% of fish meal samples belonging to the untreated fish meal and after 4, 5 and 6 h of heat treatment. However, samples heated for 30 min, 1, 2 and 3 h yield poor classification rates (less than 50%). This study demonstrated the potential ability of NIR spectroscopy to predict and classify the extent of heat treatment during the production of fish meal. However, further research must carry out in order to validate the NIR calibrations to predict the degree of heat treatment in fish meal expose to a shorter time.     

Gas‐producing and spoilage potential of Enterobacteriaceae and lactic acid bacteria isolated from chilled vacuum‐packaged beef

This study aimed to enumerate and identify lactic acid bacteria and Enterobacteriaceae from spoiled and nonspoiled chilled vacuum‐packaged beef and determine their potential to cause blown pack spoilage. These microbial groups were also enumerated in nonspoiled samples and detected in abattoir samples. The potential of isolates to cause ‘blown pack’ spoilage of vacuum‐packaged beef stored at chilled temperature (4 °C) and abuse temperature (15 °C) was investigated. Populations of lactic acid bacteria in exudate of spoiled and nonspoiled samples were not significantly different (P > 0.05), whereas the number of lactic acid bacteria on the surface was significantly higher (P < 0.05) in spoiled samples as compared to nonspoiled samples. The population of Enterobacteriaceae species in exudate and on the surface of samples were significantly higher (P < 0.05) in spoiled packs in comparison with nonspoiled packs. Results of the deterioration potential showed that ‘blown pack’ spoilage was noticeable after 7 days at 15 °C and after 6 weeks at 4 °C for samples inoculated with Hafnia alvei.     

Internal Temperature and Packaging System Affect Stability of Cooked Chicken Leg Patties during Refrigerated Storage

Internal end-point temperature (EPT), packaging system and storage time affected chemical stability and microbiological quality of chicken meat. Patties of broiler leg muscle were heated to EPT of 60, 65, 70, 75, 80 or 85°C, packaged in polyethylene bags or vacuum skin packs and stored at 4°C up to 14 days. Microbial total plate counts were less than 10 colony forming units/g at EPT 70°C; with negligible growth during 7 days storage. EPT and packaging method did not affect initial thiobarbituric acid reactive substances (TBARS) but higher EPT accelerated the increases in TBARS values upon storage. Several volatiles including hexanal and pentanal increased with EPT and storage time.     

Heat resistance of Escherichia coli O157:H7 in cook‐in‐bag ground beef as affected by pH and acidulant†

Summary The heat resistance of a four‐strain mixture of Escherichia coli O157:H7 was tested. The temperature range was 55–62.5 °C and the substrate was beef at pH 4.5 or 5.5, adjusted with either acetic or lactic acid. Inoculated meat, packaged in bags, was completely immersed in a circulating water bath and cooked to an internal temperature of 55, 58, 60, or 62.5 °C in 1 h, and then held for pre‐determined lengths of time. The surviving cell population was enumerated by spiral plating meat samples on tryptic soy agar overlaid with Sorbitol MacConkey agar. Regardless of the acidulant used to modify the pH, the D ‐values at all temperatures were significantly lower (P < 0.05) in ground beef at pH 4.5 as compared with the beef at pH 5.5. At the same pH levels, acetic acid rendered E. coli O157:H7 more sensitive to the lethal effect of heat. The analysis of covariance showed evidence of a significant acidulant and pH interaction on the slopes of the survivor curves at 55 °C. Based on the thermal‐death–time values, contaminated ground beef (pH 5.5/lactic acid) should be heated to an internal temperature of 55 °C for at least 116.3 min and beef (pH 4.5/acetic acid) for 64.8 min to achieve a 4‐log reduction of the pathogen. The heating time at 62.5 °C, to achieve the same level of reduction, was 4.4 and 2.6 min, respectively. Thermal‐death–time values from this study will assist the retail food processors in designing acceptance limits on critical control points that ensure safety of beef originally contaminated with E. coli O157:H7.     

Study on the self‐assembly property of type I collagen prepared from tilapia (Oreochromis niloticus) skin by different extraction methods

Type I collagen was prepared from tilapia (Oreochromis niloticus) skin by acetic acid and pepsin process at 4 °C, respectively (ASC and PSC), and hot‐water method separately at 25, 35 and 45 °C (C‐25, C‐35 and C‐45). Their structure and self‐assembly property were discussed. SDS‐PAGE patterns suggested that pepsin hydrolysis and the 35 and 45 °C extraction produced collagen with much reduced proportions of α‐ and β‐chains. Fourier transform infrared spectroscopy spectra revealed that pepsin hydrolysis did not change the conformation of collagen, but higher extraction temperature did. Self‐assembly curves and atomic force microscopy (AFM) observations showed that only ASC, PSC and C‐25 could self‐assemble into fibrils with D‐periodicity, but the reconstruction rate of C‐25 was lower. Besides, PSC had relatively higher resolution ratio compared with others. Overall, pepsin‐extracted collagen displayed higher solubility and better fibril‐forming capacity, having the potential of applying in biomaterials and food‐packaging materials.     

Fibre‐optic method for estimation of bovine fat quality

Spectroscopy using remote surface, contact, insertion and transmission fibre‐optic probes and a sensor at wavelengths of 400 to 1100 nm was used for rapid estimation of the physio‐chemical characteristics of bovine fat. Surface reflectance of the adipose tissue was negatively correlated with the bovine fat colour score at many wavelengths and positively correlated with the contents of the polyunsaturated fatty acids at 400 to 650 nm (P < 0.05). Internal reflectance using an insertion probe at 445 to 1100 nm was positively correlated with melting point and negatively correlated with refractive index (P < 0.05). Internal reflectance using a contact probe tended to be related to saturated and monounsaturated fatty acid contents. Transmittance at almost all wavelengths was positively correlated with refractive index (P < 0.05). Internal reflectance of the intermuscular fat from 34 animals measured at a meat market was correlated (P < 0.01) with saturated fatty acid content (r = 0.72 at 650 nm) and with monounsaturated fatty acid content (r = ?0.69 at 650 nm). These results indicated the possibility of using fibre‐optic measurements, requiring 1 s in bovine adipose tissue, to evaluate the quality of depot fat and that the various types of probe can be used to evaluate different physiochemical characteristics of fat. Copyright © 2003 Society of Chemical Industry     

Preliminary study on the use of near‐infrared reflectance spectroscopy to assess nitrogen content of undried wheat plants

Near‐infrared reflectance (NIR) spectroscopy combined with chemometrics was used to assess nitrogen (N) and dry matter content (DM) and chlorophyll in whole‐wheat plant (Triticum aestivum L). Whole‐wheat plant samples (n = 245) were analysed by reference method and by visible and NIR spectroscopy, in fresh (n = 182) and dry (n = 63) presentations, respectively. Calibration equations were developed using partial least squares (PLS) and validated using full cross‐validation (leave‐one‐out method). Coefficient of determination in calibration (R²_CAL) and the standard error of cross‐validation (SECV) for N content in fresh sample presentation, after second derivative, were 0.89 (SECV: 0.64%), 0.86 (SECV: 0.66%) and 0.82 (SECV: 0.74%) using the visible + NIR, NIR and visible wavelength regions, respectively. Dry sample presentation gave better R²_CAL and SECV for N compared with fresh presentation (R²_CAL > 0.90, SECV < 0.20%) using visible + NIR. The results demonstrated that NIR is a suitable method to assess N concentration in wheat plant using fresh samples (unground and undried). Copyright © 2006 Society of Chemical Industry     

Kinetic models of non‐enzymatic browning in apple puree

The effects of thermal treatments on 11 °Brix apple puree were studied at temperatures from 80 to 98 °C. Colour changes (measured by reflectance spectroscopy, colour difference, L*, a* and b* and the evolution of 5‐hydroxymethylfurfural (HMF) and sugars (hexoses and sucrose) were used to evaluate non‐enzymatic browning. A kinetic model based on a two‐stage mechanism was applied to the evolution of colour difference and a*. A first‐order kinetic model was applied to L* evolution, while the evolution of absorbance at 420 nm (A₄₂₀) of the liquid fraction was described using a zero‐order kinetic model. Thermally treated samples became more reddish and suffered a slight loss of yellow hues. The effect of temperature on the kinetic constants was described by an Arrhenius‐type equation. The presence of pulp in the samples led to activation energies for A₄₂₀ and sucrose which were lower than those found previously for clarified juices with the same soluble solids content. © 2000 Society of Chemical Industry     

Contribution of High‐Pressure‐Induced Protein Modifications to the Microenvironment and Functional Properties of Rabbit Meat Sausages

Rabbit meat batters were subjected to high pressure (HP, 100 to 300 MPa for 3, 9, or 15 min) to elucidate their effects on proteins structures, the microenvironment, and the resulting functionalities of the subsequently heated products. To determine these effects, we investigated structural and microenvironmental changes using Raman spectroscopy and also expressible moisture content, textural characteristics, and dynamic rheological properties of batters during heating (20 to 80 °C). Untreated samples served as controls. Analysis of specific Raman spectral regions demonstrated that applications of HP to rabbit meat batters tended to induce the transformation of the all‐gauche S‐S conformation to gauche‐gauche‐trans in the batter system. HP treatment higher than 100 MPa for 9 min promoted secondary structural rearrangements, and molecular polarity enhancement in the proteins prior to cooking. Also, increases of O–H stretching intensities of rabbit meat sausages were obtained by HP treatment, denoting the strengthening of water‐holding capacity. These HP‐induced alterations resulted in improved texture and, perhaps, improved juiciness of rabbit meat sausages (P < 0.05), however they had relatively poorer rheological properties than the controls. Nevertheless, HP treatment, especially 200 MPa for 9 or 15 min, was an effective technique for improving the functionalities of gel‐type products through modification of meat proteins.     

Continuous dense‐phase CO2 processing of a coconut water beverage

Effects of dense‐phase CO₂ (DPCD) on microbial, physical, chemical and sensorial quality of coconut water (CW) beverage were evaluated. Pressure during DPCD treatment was not significant in microbial reduction whereas temperature and % CO₂ levels were significant. DPCD‐treated (34.5 MPa, 25 °C, 13% CO₂, 6 min), heat‐pasteurised (74 °C, 15 s) and untreated CW beverages were evaluated during 9 weeks of refrigerated storage (4 °C). Total aerobic bacteria of DPCD and heat‐treated samples decreased whereas that of untreated samples increased to >10⁵ CFU mL^?1 after 9 weeks. DPCD increased titratable acidity but did not change pH (4.20) and °Brix (6.0). Likeability of DPCD‐treated CW was similar to untreated. Heat‐treated samples were less liked (α = 0.05) at the beginning of storage. Off flavour and taste‐difference‐from‐control scores of heated samples were higher than DPCD during the first two weeks. DPCD extended shelf life of acidified, sweetened and carbonated CW over 9 weeks at 4 °C.     

Enhanced Thermal Resistance of Salmonella in Whole Muscle Compared to Ground Beef

Irradiated beef (whole ‐muscle and ground product with identical fat, protein, and moisture composition) was exposed to a Salmonella‐ inoculated marinade and heated in brass tubes in a water bath at 55 °C, 60 °C, and 62.5 °C. The bacterial load and thermal lag time were similar (α= 0.05) for both whole and ground muscle; therefore, all samples had equivalent composition, inoculation levels, and thermal histories. Assuming 1st‐order kinetics, the inactivation rate constants (k values) in whole muscle were 50% lower than those in ground product at each temperature (P = 0.0001), and Arrhenius‐type models described the temperature dependency of k (R² > 0.95). Because thermal processing regulations are generally based on ground product studies, thermal process validations for meat and poultry products may need to consider the physical state (whole ‐muscle versus ground) of the product being manufactured.