Comparison of Gum Arabic, Modified Starch, and Whey Protein Isolate as Emulsifiers: Influence of pH, CaCl2 and Temperature

ABSTRACT: The particle size and zeta potential of model beverage emulsions (0.01 wt% soybean oil-in-water emulsions, d ≅ 1 mm) stabilized by gum arabic, modified starch, or whey protein isolate (WPI) were studied with varying pH (3 to 9), CaCl₂ concentration (0 to 25 mM), and temperature (30 °C to 90 °C). Temperature, pH, CaCl₂ strongly influenced emulsions stabilized by WPI because its stabilizing mechanism was mainly electrostatic repulsion, but not those stabilized by gum arabic or modified starch because their stabilizing modes of action were mainly steric repulsion. This study may have important implications for the application of WPI as an emulsifier in beverage emulsions.     

Effect of irradiation and modified atmosphere packaging on the microbiological safety of minced pork stored under temperature abuse conditions

The safety of irradiated pork packed in 25% CO₂:75% N₂ and stored at abuse temperature (10 or 15°C) was assessed by inoculation studies involving Salmonella typhimurium, Listeria monocytogenes, Escherichia coli, Yersinia enterocolitica and Clostridium perfringens . Irradiation to a dose of 1.75 kGy reduced pathogen numbers to below the detection limit of 10² cells g^-1. When higher inoculum levels were used (10⁶ cells g^-1) irradiation at 1.75 kGy reduced pathogen numbers by 1 –>5 log₁₀ cycles depending on strain. Clostridium perfringens was the most resistant, and Y. enterocolitica the most sensitive of the pathogens studied.
In all cases when high numbers (10⁶ to 10⁷g^-1) of spoilage and/or pathogenic bacteria were present initially on the pork the meat appeared spoiled, and although irradiation reduced the number of microorganisms, the meat was still unacceptable from a sensory viewpoint after treatment.
It was concluded that the microbiological safety of irradiated, modified atmosphere packaged (MAP) pork is better than that of unirradiated MAP pork.     

Thermal Resistance of Spores of Five Strains of Clostridium botulinum Type E in Ground Whitefish Chubs

SUMMARY– Thermal death-time determinations in the temperature range of 165°F (73.9°C) to 185°F (85°C) were made of spores of five strains of Clostridium botulinum type E in tubed fish paste prepared from whole Great Lakes whitefish chubs. Estimated F₁₇₆ (80°C) values for the destruction of approximately 1×10⁶ spores per gram of fish paste were as follows: for strain Alaska, 34.2 min; Beluga, 17.0 min; 8E, 14.0 min; Iwanai, 12.5 min; and Tenno, 13.2 min. Estimated 95% confidence limits about these F₁₇₆ values were for strain Alaska, 23.4-49.5 min; Beluga, 14.2-20.2 min; 8E, 8.2-17.7 min; Iwanai, 10.2–15.4 min; and Tenno, 9.3–18.5 min. D₁₇₆ values calculated from our F₁₇₆ values by Schmidt's (1957) equation were for strain Alaska, 4.3 min; Beluga, 2.1 min; 8E, 1.8 min; Iwanai, 1.6 min; and Tenno, 1.6 min. Z_y values obtained from thermal death-time determinations were for strain Alaska, 13.2; Beluga, 13.3; 8E, 10.3; Iwanai, 13.6; and Tenno, 13.1°F.     

Colour loss during extrusion cooking of β-carotene-wheat flour mixes as an indicator of the intensity of thermal and oxidative processing

The thermal and/or oxidative colour loss from a wheat flour/all-trans β-carotene (20–80 mg kg⁻¹) mix during extrusion cooking follows first order kinetics. The intensity of processing in extrusion is reflected in the overall rate constant ( K ) of colour loss. K -values were in the range 3–20x10⁻³ s⁻¹. They increased markedly with decreasing water content of the mix (24–14%), and with increasing barrel temperature (100–220°C). Results were independent of the type of twin-screw extruder (Werner-Pfleiderer Continua 37 or Clextral BC-45). Modelling of the overall rate constant K and of the 'equivalent plug flow' residence time was used to define 'iso-destructive' extrusion conditions giving approximately the same residence time and the same mean product temperature. Extrusion under N₂ or O₂, or in the presence of 1 mg BHT per g of β-carotene, slightly affected colour loss. Adsorption chromatography on alumina indicated that within a barrel temperature range of 125–200°C, 38–73% of the initial all-trans β-carotene was destroyed, and that 2/3 to 1/2 of this loss corresponded to the formation of 9-cis plus 13-cis β-carotene isomers. The formation of smaller amounts of unknown β-carotene derivatives may be responsible for the colour loss.     

Rheological behaviour of acorn starch dispersions: effects of concentration and temperature

Rheological properties of acorn starch dispersions at different concentrations (4%, 5%, 6% and 7%) were evaluated under steady and dynamic shear conditions. The flow behaviours of the acorn starch dispersions at different temperatures (25, 40, 55 and 70 °C) were determined from the rheological parameters provided by the power law model. The acorn starch dispersions at 25 °C exhibited high shear-thinning fluid characteristics ( n  = 0.23–0.36). Consistency index (K) and apparent viscosity (η_a,100) increased with an increase in starch concentration, and were also reduced with increasing temperature. Within the temperature range of 25–70 °C, the η_a,100 obeyed the Arrhenius temperature relationship with a high determination coefficient ( R ² = 0.97–0.99), with activation energies (E_a) ranging between 16.5 and 19.0 kJ mol⁻¹. Both the power law and exponential type models were employed in order to establish the relationship between concentration and apparent viscosity (η_a,100) in the temperature range of 25–70 °C. Magnitudes of storage ( G' ) and loss ( G ") moduli increased with an increase in the starch concentration and frequency (ω). The magnitudes of G ' were higher than those of G " over most of the frequency range (0.63–62.8 rad s⁻¹). The dynamic (η*) and steady shear (η_a) viscosities of acorn starch dispersion at 7% concentration follow the Cox–Merz superposition rule.     

COLORIMETRY OF FOODS. 3. Carrot Puree

SUMMARY– A series of 10 carrot purees was prepared with added FD&C Green No. 1 food color in increments of 0.015 ppm. The samples were evaluated visually for color differences under illumination of 7400°K and measured with a G.E. spectrophotometer with D&H tristimulus integrator and a Hun terlab D₂₅ colorimeter in cells varying from 2–8 mm in thickness against both a white and black background. The instrumental data were calculated in conventional and K/S ratios and correlated with visual and theoretical rankings. The panelists could reasonably well rank samples differing by 0.10–0.15 delta E units, calculated as [(delta L)²+ (delta a)²+ (delta b)² 1/2. Highest correlations with the theoretical order were obtained with a black background and sample thicknesses of 6 mm or more. Adequate rankings with either instrument required a multiple correlation with all 3 color parameters (X Y Z or L a b). Optimum separation of samples with the G.E. spectrophotometer was obtained with a white background and a sample thickness of 5 mm or more. The Hunterlab D₂₅ colorimeter was superior to the G.E. spectrophotometer for separation of samples. Optimum separation was with a 2-in.-diameter aperture and a cell 4 mm or more in thickness against a white background. Correlations of Hunter data with theoretical order were higher than those with visual vs. theoretical ranking. Individual K and S values may be useful in characterizing purees for colorimetry.     

Rheology and Oxidative Stability of Whey Protein Isolate-Stabilized Menhaden Oil-in-Water Emulsions as a Function of Heat Treatment

ABSTRACT:  Menhaden oil-in-water emulsions (20%, v/v) were stabilized by 2 wt% whey protein isolate (WPI) with 0.2 wt% xanthan gum (XG) in the presence of 10 mM CaCl₂ and 200 μM EDTA at pH 7. Droplet size, lipid oxidation, and rheological properties of the emulsions were investigated as a function of heating temperature and time. During heating, droplet size reached a maximum at 70 °C and then decreased at 90 °C, which can be attributed to both heating effect on increased hydrophobic attractions and the influence of CaCl₂ on decreased electrostatic repulsions. Combination of effects of EDTA and heat treatment contributed to oxidative stability of the heated emulsions. The rheological data indicate that the WPI/XG-stabilized emulsions undergo a state transition from being viscous like to an elastic like upon substantial thermal treatment. Heating below 70 °C or for less than 10 min at 70 °C favors droplet aggregation while heating at 90 °C or for 15 min or longer at 70 °C facilitates WPI adsorption and rearrangement. WPI adsorption leads to the formation of protein network around the droplet surface, which promotes oxidative stability of menhaden oil. Heating also aggravates thermodynamic incompatibility between XG and WPI, which contributes to droplet aggregation and the accumulation of more WPI around the droplet surfaces as well.     

Temperature-Sensitive Microcapsules Containing Lactoferrin and Their Action Against Carnobacterium viridans on Bologna

ABSTRACT:  Lactoferrin (LF) was encapsulated in 2 types of emulsion to protect it from contact with agents like divalent cations, which interfere with its antimicrobial activity. First, paste-like microcapsules were prepared as water-in-oil (W₁/O) emulsions from mixtures of 20% w/v LF in distilled water, 20% w/v LF in 3% w/v sodium lactate or in 20 mM sodium bicarbonate, which were emulsified with an oil mixture of 22% butter fat plus 78% corn oil and 0.1% polyglycerol polyricinoleate. Second, freeze-dried double emulsion (W₁/O/W₂), powdered microcapsules were produced following emulsification of paste-like microcapsules in an external aqueous phase (W₂) consisting of a denatured whey protein isolate (WPI) solution. The release of LF from the W₁/O microcapsules was dependent on temperature and NaCl concentration. LF was not released from the W₁/O emulsion at <5.5 °C. Its release was greater from W₁/O microcapsules when suspended in 5% aqueous NaCl than in water at ≥10 °C, whereas LF release from freeze-dried microcapsules was not controlled by temperature change. Paste-like microcapsules were incorporated in edible WPI packaging film to test the antimicrobial activity of LF against a meat spoilage organism Carnobacterium viridans . The film was applied to the surface of bologna after its inoculation with the organism and stored under vacuum at 4 or 10 °C for 28 d. The growth of C. viridans was delayed at both temperatures and microencapsulated LF had greater antimicrobial activity than when unencapsulated. The temperature-sensitive property of the W₁/O microcapsules was reduced when they were incorporated into a WPI film.     

EVALUATION OF THE HOLE PRESSURE METHOD TO MEASURE THE FIRST NORMAL STRESS DIFFERENCE OF CORN MEAL DOUGH DURING EXTRUSION COOKING

Rheological properties of food dough melt, such as steady shear viscosity (η) and first normal stress difference (N₁), were measured using an in-line slit die rheometer attached to a laboratory model single-screw extruder. The flow rate through the rheometer was varied by altering the screw speed. Alternatively, a sidestream valve, to vary the flow rate through the rheometer at fixed screw speed, was also used to obtain rheological data. The slit die rheometer was tested with corn meal at three different experimental conditions: 25% and 35% moisture contents at 180C barrel temperature and 35% moisture content at 150C barrel temperature. N₁ was measured using the hole-pressure and exit-pressure method. Exit pressure measurements were found to be erratic and unreliable. Hole pressure increased monotonically with increasing flow rate and was found to be affected by the processing history. The magnitude of the hole pressure ranged between 2% and 21% of pressure of the flush mounted transducer. For the experimental conditions used in this study, N₁ ranged from 3 × 10⁴ to 6 × 10⁵ Pa for shear rates between 30 to 400 s⁻¹. Possible sources of errors in the hole pressure measurements are discussed.     

BOUND WATER IN FRUIT PRODUCTS BY THE FREEZING METHOD

SUMMARY— An insulated heat-sink containing Freon-12® (N.B.P. −21.6°F) provides a reproducible system for measurement of thermal properties of fruit products. The difference in time required to remove the latent heat of fusion of the "eutectic" mixture in comparison with distilled water measures the "bound" water. The 34-37%"bound" water in papaya (var. solo) pulp is unaffected by varying pH in the range 3.0–6.0. Less than 10% water is bound in guava, passion fruit and pineapple juice products with up to 35% sucrose added. Thermal conductivity of the solid phase "eutectic" mixture in the 5–50% soluble solids range fits the regression Y = AB^x, Y = (3.69) (0.96)^x where x = percent total soluble solids (TSS) and Y = thermal conductivity (Cal x 10³/(cm²) (sec) (°C/cm)). The relationship of freezing point to TSS values as 1.10 + 0.64 (TSS) in the test system is significant (P < 0.01) in the range 5–50% TSS. The time for fusion (θ_w) of sucrose/water in the range 5–50% TSS fits the regression: log θ_w= (−0.8325) (−0.0165) (TSS) or θ_w= (0.984) (0.164)^TSS sec. Addition of solutes such as sucrose will inhibit gelation without affecting "bound" water values. Pectin gel structures apparently are dependent on secondary bonding and independent of "bound" water per se.     

The yeast flora of stored ready-to-use carrots and their role in spoilage

Spoilage of ready-to-use grated raw carrots packaged in polymeric films and stored at 10°C was investigated for involvement of yeasts. Cryptococcus albidus was only isolated during the first 3 days of storage, increasing to levels of 10⁵–10⁶g^-1. Candida lambica was more commonly isolated after 3–7 days of storage, and reached 10⁷–10⁸g^-1 after 12 days. Candida sake was present throughout storage, increasing from 10⁵–10⁶ after 3 days to 10⁷–10⁸ after 12 days. In some samples, Candida parapsilosis and Candida tropicalis were also isolated at levels similars to C. sake . All the yeasts isolated at the end of storage were fermentative species and their metabolism was characterized with a Warburg apparatus. Neither the number of yeasts nor the composition of the yeast flora were related to the deterioration of the product. Although Candida lambica inoculated on grated carrots caused spoilage after 12 days at 10°C, the high O₂ permeable film was most effective in reducing exudate.     

Rapid dye reduction tests for the determination of microbiological quality of meat

Rapid dye reduction tests have been developed to determine the quality of meat. Three chemical indicators, resazurin and two tetrazolium compounds, were used to correlate the microbial numbers and reduction times in meat samples. Twenty-five surface samples from sheep carcasses were subjected to each reduction test. Total viable counts given were obtained at 37°C. Resazurin reduction time was 90–120 min when the bacterial counts ranged from 1.5×10⁶ to 7.7×10⁶/cm². Samples showing bacterial counts between 1.5×10⁶ and 6.0×10⁶/cm² reduced tetrazolium (NBT) in 360–390 min whereas samples containing bacterial counts of 2.1×10⁶/cm² took 420–450 min to reduce iodophenyl nitrophenyl tetrazolium (INT) dye. Regression equations relating the number of organisms per cm² and reduction time were applied to predict the microbiological quality of meat samples from reduction time data. Among the three dyes, resazurin gave the lowest reduction time.     

The Effects of Residual Oxygen on the Storage Life of Retail-Ready Fresh Beef Steaks Masterpackaged Under a CO2 Atmosphere

ABSTRACT:  Retail-packed rump ( Gluteus medius , GM) and striploins ( Longissiumus dorsi, LD) steaks were masterpackaged under carbon dioxide (CO₂) and stored at 1 °C ± 1 °C for 14, 28, 35, and 42 d. A commercial oxygen (O₂) scavenger (ATCO HV1000®, Standa Industrie, Caen, France) was used in the masterpacks to achieve an O₂-free atmosphere. Similar packages without the O₂ scavengers were also prepared. At each storage time, 2 masterpacks of each treatment were opened and the retail trays were placed in a display case at 4 °C ± 2 °C for 1 and 48 h for microbiological and sensorial evaluations. The low growth rate of aerobic psychrotrophic flora on the stored beefsteaks demonstrated the bacteriostatic effect of CO₂ during storage. The maximum level of psychrotrophic aerobic bacteria reached during storage was approximately 10⁶ CFU/g. The steaks stored in masterpacks with scavengers bloomed to the desirable red color associated with freshly cut meat in the display case for all of the storage periods, except in the case of GM steaks, which showed a cycle of transient discoloration. GM and LD steaks were well accepted (65% and 82%, respectively) after 42 d under CO₂ at 1 °C ± 1 °C. The GM and LD steaks stored without the O₂ scavenger showed variable fractions of discoloration that significantly detracted from the appearance of the samples.     

STUDY ON INTERACTION AMONG EXTRUSION-COOKING PROCESS VARIABLES AND ENZYME ACTIVITY: EVALUATION OF EXTRUDATE STRUCTURE

A blend of wheat flour (moisture content 11.61%) and different amounts of two commercial enzymes like GRINDAMYL (GA) amylase 1000 (0–0.1 g/kg) and GA protease 41 (0–1.0 g/kg) were extruded through a co-rotating twin-screw extruder.
The effects of barrel temperature (60–120C), dough moisture (20–36%), screw speed (100–400 rpm) and different amounts of enzymes on structure of extrudates (porosity and break strength) were studied using response surface methodology.
Results showed that the highest value of porosity (62.47%  ±  4.07) was obtained at the highest value of barrel temperature (120C) and at the largest amounts of GA protease 41 (1.0 g/kg) or GA amylase 1000 (0.1 g/kg). However, the simultaneous addition of large amounts of both enzymes caused a negative effect on expansion degree (porosity  <  30%). Large amounts of moisture dough and GA amylase 1000 resulted in a high value of break strength (25.7 N/mm²) and in stiff-textured extrudates .

PRACTICAL APPLICATIONS

This research could provide some information about the effects of and the interactions between extrusion parameters and enzyme activities, which are commonly used to produce bakery products, in order to improve the texture of extrudates processed at low barrel temperatures, i.e., 60C, for example, extrudates with thermolabile components like vitamins or extrudates with high lipid fraction like breakfast cereals, pet food, etc.     

Biochemical composition and storage stability of a yogurt-like product from African yam bean (Sphenostylis stenocarpa)

The biochemical and storage properties of African yam bean ( Sphenostylis stenocarpa ) yoghurt-like product were evaluated. Milk extracted from the bean flour using hot water was supplemented with 4% milk protein concentrate (MPC), 0.15% dairy calcium (DC) and 0.5% gelatine (G) (singly or in combination). The milk was fermented with Streptococcus thermophilus and Lactobacillus delbrueckii spp bulgaricus at 43 °C for 3–5 h. Supplemented African yam bean (AYB) yoghurts had a gel-like consistency unlike the control (unsupplemented) sample. Total solids, protein, fat, ash, lactic acid bacterial count, lightness (L-value) and viscosity were improved by supplementation. Riboflavin and antioxidants were reduced; macroelements and thiamine were increased by 0.71–15.6% and 16.7%, respectively, because of fermentation. The stability of the product during storage at 4 °C was improved by supplementation and stirring. The pH of the supplemented product ranged from 4.45 to 4.54 and microbial counts from 2.6 × 10⁶ to 1.6 × 10⁸ during storage for not more than 3 weeks.     

Production of Enterotoxin-B in Cured Meats

SUMMARY— A variety of laboratory cured hams were inoculated with 10³−10⁶ cells of S. aureus strain S-6 and incubated at 10, 22 and 30°C anaerobically for up to 16 weeks. Enterotoxin-B was detected by gel-diffusion in hams with original pH over 5.30, up to 9.2% NaCl (brine) and 0.54 ppm undissociated nitrous acid. There was better toxin production at 30° than at 22° or 10°C. Toxin was detected at 10°C after at least 2 weeks incubation and in most samples after 8 weeks when pH was greater than 5.6. Toxic hams had more than 4 × 10⁶ cells/g. Contaminants were always less than 10⁵/g. Tween 80 inhibited toxin production at 30° but not at 10°C. Toxic hams looked normal even after 2 months incubation at 10°C.     

Texture of rehydrated dried bell peppers modified by low-temperature blanching and calcium addition

Diced green bell pepper was blanched twice, once at 51–79 °C for 19–61 min, and once at 95 °C for 3 min, and dried. The firmness of rehydrated samples was measured by puncture, and optimum conditions assessed by response surface methodology. The optimized model showed that, blanching at 65 °C for 49 min gave a 64% increase in puncture force over the control. The optimum temperature was used to evaluate the effect of adding CaCl₂. The dices were blanched twice, once at 65 °C for 3 min in either 0 or 4% CaCl₂, secondly in either 0 or 2% CaCl₂ solution at 95 °C for 3 min. In the second case the dices had been held at room temperature for 0–30 min before treatment. Adding CaCl₂ increased puncture force significantly ( P  ≤ 0.05). The best results, those which gave greatest firmness, were obtained by blanching at 65 °C for 3 min in 4% CaCl₂, holding for 16 min after blanching, followed by a secondary blanching at 95 °C in 2% CaCl₂.     

Water desorption isotherms of two varieties of sweet potato

Water desorption isotherms were determined for New Zealand sweet potato at 25, 40 and 55°C, and for Philippines sweet potato at 28°C. The isotherms were sigmoid in shape and of type II according to the BET classification. The data were fitted to eight two-parameter equations reported in the literature. The effect of water activity, a_w, and temperature, T °C, on the equilibrium moisture content, M _e g water/100g dry solids, was best described for New Zealand sweet potato by: Me = 20.51 T-^0.204 (a_w/(1-a_w)0.39 for a_w= 0.06–0.81     

OXALACETATE SYNTHESIS IN APPLES AND BANANAS AT LOW TEMPERATURES

¹⁴CO₂ was applied to apples and bananas that were stored at various temperatures and the incorporation of ¹⁴C into oxalacetate was determined. Apples that were susceptible to internal breakdown showed an initial decrease in incorporation as the storage temperature was reduced but incorporation then increased at temperatures below 10°C (Jonathan) or 5°C (Twenty Ounce). Apples that were not susceptible to breakdown (Delicious and Granny Smith) showed no incorporation at any temperature. Green bananas showed a minimum incorporation at 10°C but in ripe bananas, incorporation markedly increased at all temperatures less than 20°C. The respiration rate of the apple varieties at 20°C was found to be higher in fruit that were more susceptible to breakdown whereas at O°C the higher rates of respiration were from fruit less susceptible to the disorder.     

GROWTH OF STAPHYLOCOCCUS AUREUS AND ENTEROTOXIN A PRODUCTION IN FOODS CONTAINING POLYPHOSPHATES

Effects of pyro-, tripoly- and hexametaphosphates (0.5 and 1%, w/w) on growth of Staphylococcus aureus strain 196E and enterotoxin A (SEA) production were studied in cooked custard and beef at 22 and 30°C. No effect was observed in custard, where cell numbers/g increased from 10³ to 10⁸ and SEA reached 4.2 ng/g after 48 h at 22°C, irrespective of treatment. Cell numbers in cooked beef were ca. 10⁹/g after 48 h, and reduced numbers (by 1.5–2 log cycles) were found in samples containing 0.5 and 1% pyrophosphate during incubation at 22%, but not at 30°C. SEA concentrations in beef were 28 ng/g after 48 h at 22°C, and 93 and 184 ng/g after 24 and 48 h, respectively, at 30°C. SEA concentration correlated with amount of growth, and was nondetectable when cell numbers were ± 10⁶/g. Reduction of the meat pH by sodium acid pyrophosphate contributed to the observed inhibitory effect.