Mathematically modeling the repair of heat-injured Listeria monocytogenes as affected by temperature, pH, and salt concentration

Heat-injured cells of Listeria monocytogenes were inoculated into Listeria repair broth (LRB) adjusted to various pH levels (4.2, 5.0, 6.6, 8.0 and 9.6) and salt concentrations (0.5%, 2.5%, 5.0%, 7.5% and 10.0% w/v) at controlled temperatures (4, 10, 22, 37 and 43 °C) in a complete factorial manner (5³). Repair of the injured microorganisms was evaluated using selective and non-selective plating media. The Gompertz parameters, which were generated by fitting the equation with the bacterial counts, were used to calculate the repair percentage as a function of time from which the repair time was estimated. All growth curves fit the Gompertz equation well (R² ≥ 0.972). A first-order model described the repair trend closely (R² = 0.989 ± 0.011). Heat-injured Listeria could fully repair in LRB only under 63 of 125 conditions tested during 21 days of incubation. Refrigeration temperature was the most effective means to prevent the repair of heat-injured Listeria. The minimum temperature required for repair increased with an increase in NaCl concentration. The pH ranges at which the repair could occur were narrower at 4 and 10 °C than those at higher temperature. The repair was observed in media containing 10% NaCl between temperatures of 22 and 43 °C at pH 6.6.     

Effect of NaCl, polydextrose, and storage conditions on the functional characteristics and microbial quality of pre- and post-rigor salted beef

The functionality and microbial storage life of pre-rigor beef mince stored at −1.5 °C under vacuum or a saturated carbon dioxide atmosphere, or at −18 °C in polyethylene bags, was investigated. Salt (2% w/w) or salt plus the cryoprotectant Polydextrose^® (2%/2.6% w/w) was added pre-rigor to some samples. Chilled storage decreased salt soluble protein (SSP) by 13–18% (P < 0.01); frozen storage decreased SSP content by 20%. Pre-rigor salted mince in saturated carbon dioxide packs had a satisfactory microbial quality after 12 weeks storage. The cook yield of finely comminuted sausage batters made from that mince and from fresh pre-rigor mince were similar, although batter stress and strain decreased with chilled storage. Adding Polydextrose^® to salted mince improved batter strain compared with the non-additive and salt-only samples and improved batter stress compared with the salt-only samples. The microbial storage life of chilled vacuumpacked unsalted mince was less than 6 weeks; pre-rigor salting increased its storage life.     

Modeling the effect of inoculum size and acid adaptation on growth/no growth interface of Escherichia coli O157:H7

The objective of this study was to model with logistic regression the growth/no growth interface of different initial inoculation levels (10¹, 10³ and 10⁵ CFU/ml; study 1), or nonadapted vs acid-adapted (study 2) Escherichia coli O157:H7 as influenced by pH, NaCl concentration and incubation temperature. Study 1 was conducted with a mixture of four E. coli O157:H7 strains grown (35 °C, 24 h) in tryptic soy broth (TSB). Study 2 was conducted with the same mixture of four E. coli O157:H7 strains grown (35 °C, 24 h) in glucose-free TSB with 1% added glucose (final pH 4.83), or in diluted lactic acid meat decontamination runoff fluids (washings; final pH 4.92), or nonadapted cultures prepared in glucose-free TSB (final pH 6.45), or in water washings (final pH 6.87). Parameters included incubation temperature (10–35 °C), pH (3.52–7.32), and NaCl concentration (0–10% w/v). Growth responses were evaluated for 60 days turbidimetrically (610 nm) every 5 days in 160 (study 1) and 360 (study 2) combinations in quadruplicate samples, with a microplate reader. The lower the initial inoculum the higher were the minimum pH and a_w values permitting growth. Differences in the pH and a_w growth limits among inoculum concentrations increased at 15 and 10 °C. Acid-adapted cultures were able to grow at lower pH than nonadapted cultures, while at temperatures below 25 °C, growth initiation of nonadapted cultures stopped at higher a_w compared to acid-adapted cultures for the whole pH range of 3.52 to 7.32. A comparison with available data indicated that our model for acid-adapted E. coli O157:H7 in different environments may provide representative growth probabilities covering both nonadapted and stress-adapted contaminants.     

Physiological properties of Lactobacillus paracasei, L. danicus and L. curvatus strains isolated from Estonian semi-hard cheese

Growth and survival of Lactobacillus paracasei (six strains), L. danicus sp. nov. (four isolates, two strains) and L. curvatus (two strains) from semi-hard Estonian cheeses were comparatively studied in different environmental conditions of relevance for their growth in cheese and survival in gastric environment. Maximum specific growth rates for L. paracasei strains varied between 0.40 and 0.57 h⁻¹, and all strains were tolerant to low water activities, heating at 60 °C for 30 min and pH 3. The newly discovered genetically distinct species L. danicus was characterized by low maximum growth rates (0.26–0.38 h⁻¹) and low temperature optimum (<30 °C). It was acid and heat sensitive and inhibited at salt concentrations from 4% and water activities below 0.93. L. curvatus was characterized by the highest growth rates (0.65–0.70 h⁻¹), tolerance to high NaCl concentrations, but sensitivity to heating, bile salts and low pH. The study showed that genetically different LAB species isolated from cheese could be distinguished by simple cultivation experiments.     

Optimisation of calcium-dependent protease and cathepsin D assays in ostrich muscle and the effect of chemical and physical dry-curing parameters

The best conditions for the assay of cathepsin D and Ca²⁺-dependent pro tease (CDP) activity in ostrich muscle was established in order to have a simple, rapid and reliable method for its determination. Measurements of A_280nm of TCA-soluble peptides and amino acid digests of casein and haemoglobin were used for measuring proteolytic activity in muscle extracts. The best conditions for the reliable determination of cathepsin D activity were found to be the incubation of an enzyme extract for 1 hr at 55 °C in a reaction mixture containing 0.9% (w/v) haemoglobin in 50 mM sodium formate buffer, pH 3.7. Characterization of the assay system for CDPs, obtained after phenyl-Sepharose chromatography, indicated that proteolytic degradation of casein by CDPs was linear with time up to 30 min at 30 °C and up to 0.1 units of activity. The effect of NaCl, KCl, nitrate, ascorbic acid, phosphate, glucose and sucrose on ostrich muscle CDP and cathepsin D activities has been studied. Salt (NaCl and KCl) acts as a strong inhibitor of proteolytic activity. Sodium and potassium nitrates (in the range 0–1000 mg l⁻¹) affected activity to varying degrees. CDP activity was enhanced by sodium nitrate concentrations below 700 mg l⁻¹ and unchanged by potassium nitrate. Cathepsin D activity was inhibited to some extent by sodium nitrate above 200 mg l⁻¹ and completely by potassium nitrate. Results showed that phosphate is an inhibitor of both activities. High concentrations of ascorbic acid (above 6 g l⁻¹) inhibited cathepsin D activity. Glucose (up to 2g l⁻¹) activated cathepsin D activity and inhibited CDP activity (up to 1 g l⁻¹). Sucrose activated enzyme activities at very low concentrations (1 × 10⁻³ M) and inhibited activities above 1 × 10⁻³ M.     

Separation and characteristics of different mucopolysaccharides from bovine trachea cartilage

Bovine trachea cartilage may be used as a source of mucopolysaccharides (MPS) for medical and cosmetic purposes. The content of MPS in bovine cartilage ranged from 10 to 11%, on a dry weight basis. Grade MPS isolation involved hydrolysis of the tissue with papain at 60 °C for 24 h at a tissue to enzyme solution ratio of 1:3 (w/v), separation of enzyme and some peptides with trichloroacetic acid and subsequent precipitation of MPS with ethanol. The MPS contained 54% of polysaccharides and about 27% of residual peptides. The crude MPS were purified and separated into four fractions by precipitation with ethanol at concentrations in reaction media of 20, 30, 40 and 66% (v/v). These fractions contributed 88, 16.5, 1.5 and 8%, respectively, to the hexosamines present in crude MPS. Total MPS recovery in all fractions was 71% of crude MPS weight. The main components of fractions I, II and IV were chondroitin sulphates, hyaluronic acid, and keratosulphates, respectively. However, fraction III contained 1.6% of total MPS of an unidentified polysaccharide.     

Prediction of Listeria spp. growth as affected by various levels of chemicals, pH, temperature and storage time in a model broth

The effects of concentration of NaCl (0.5 to 12.5%), methyl paraben (0.0 to 0.2%), sodium propionate (0.3%), sodium benzoate (0.1%), potassium sorbate (0.3%), pH (>5.9) temperature (4 to 30°C), storage time (up to 58 d) and inoculum (>10⁵ to >10⁻² per ml) on the log₁₀ probability percentage of one cell of Listeria spp. to initiate growth in a broth system were evaluated in a factorial design study. At pH 5.96 and temperature ranging from 4 to 30°C the concentrations of sodium propionate, potassium sorbate, and sodium benzoate examined allowed growth of L. monocytogenes with lag phases at 4°C of 18, 27 and 21 days, respectively. For 0.1 and 0.2% methyl paraben growth of all Listeria spp. was initiated at 8°C and 30°C, respectively. At pH 6, concentration of 12% NaCl supported the growth of L. monocytogenes at 8 to 30°C, whereas 12.5% inhibited all Listeria species. Four regression equations were derived relating probability of growth initiation to temperature, concentrations of NaCl and preservatives storage time, and Listeria species specific effects. From these equations, the number of cells needed for growth initiation can be calculated. The impact of this type of quantitative study and its possible application on the development of microbial standards for foods is discussed.     

Preparation, nutrient composition and digestibility of fermented shrimp head silage

Raw heads of the river prawn, Macrobrachium vollenhovenii, were fermented with Lactobacillus plantarum at 30 °C using molasses or cassava starch as the carbohydrate source. After incubation for 7 days, a desirable and stable pH < 4.5 was attained, and the carbohydrate source did not affect non-protein nitrogen (NPN) content or the proximate composition of the liquid silage after 30 days incubation. Hydrolysed feather meal, poultry by-product meal or soybean meal, used as alternative filler, was blended with the liquid silage (85:15, w/w) and solar-dried. The dried shrimp head silage meals were incorporated as protein supplements into pelleted semi-purified diets for catfish, Clarias gariepinus. Apparent digestibility coefficients of dry matter, crude protein, gross energy and essential amino acids in the silage by catfish fingerlings was high (> 70%). It was concluded that dried fermented fish silage is suitable and has a potential as a protein feedstuff in fish diets.     

A modified hot processing strategy for beef: functionality of electrically-stimulated and hot-boned meat preblended with different NaCl concentrations

Chucks from 20 electrically-stimulated hot-boned (HB) and cold-boned (CB) beef carcasses were preblended with different concentrations of NaCl (0, 0·5, 1·0, 1·5 and 2·0% w/w). Preblends were analysed for pH, 2-thiobarbituric acid (TBA) values, protein extraction and emulsifying capacities. Bologna (with and without added sodium tripolyphosphate) and ground meat patties prepared from these preblends were also evaluated for cooking yield, color and texture parameters. Ultimate pH values of HB preblends increased with increasing NaCl concentration. At 1% NaCl, HB had higher ultimate pH than CB preblends (P ≤ 0·05) but preblending HB meat with 2% NaCl reduced TBA values (P ≤ 0·05) because the pH was maintained above 6·0. Higher amounts of protein were extracted from HB than from CB preblends (P ≤ 0·01), but boning and salting treatments did not affect their emulsifying capacities (P > 0·05). Two percent NaCl was required to fully achieve the prerigor salting effect. At this concentration, cooking yields of bologna prepared from HB preblends and phosphate containing bologna prepared from CB preblends were not different (P > 0·05) and were higher than those of bologna without added phosphate made from CB preblends (P ≤ 0·05). No meaningful effects were observed on color and texture parameters. Cooking losses were lower in patties made from HB than CB preblends (P ≤ 0·05) independent of NaCl concentration, but boning and salting treatments had no further effects on color or textural parameters (P > 0·05). Therefore, the superior functional properties of electrically stimulated prerigor meat can be maintained by the addition of 2% NaCl up to 2 h post-mortem.     

Quality attributes of jams from low-usage tropical fruits

The chemical, sensory and storage properties of jams produced from two low-usage tropical fruits are presented. High-solids jams, either singly or blends, were produced from mature-ripe pulps of African star apple (Chrysophyllum albidum) and African plum (Spondias mombin) using the open-kettle process. Analytical data on the apple and plum jams showed that values obtained for fruit contents (43–45%), soluble solids (68·6–68·9%), reducing sugar (35·6–40·6%) and pH (2·80–3·40) are within the range typical of table jams. Whilst sensory evaluation indicated that the apple jams were preferred to the plum jams, storage trials showed that the fruit jams maintained good stability even when stored at tropical ambient conditions.