INFLUENCE OF SALTS AND pH ON THE FIRMNESS OF COOKED SNAP BEANS IN RELATION TO THE PROPERTIES OF PECTIN

Solute conditions inside cooked bean pods were adjusted by soaking the pods in different solutions. Interactions of Ca⁺⁺ and Na⁺ showed increasing firmness as Ca⁺⁺ concentration was raised and decreasing firmness as Na⁺ was raised. Chelating agents removed Ca⁺⁺ and decreased firmness. Higher pH gave lower firmness except in the presence of excess Ca⁺⁺. The presence of Na⁺ decreased the effect of pH on firmness. Urea decreased firmness when pods had been previously treated with a chelator. The effects of treatments on firmness were related to the behavior of pectin solutions and gels.     

Shelf life of several marine fish species of Bangladesh during ice storage

Organoleptic, biochemical and bacteriological aspects of five tropical marine fish such as silver jewfish, Bombay duck, big-eye tuna, Chinese pomfret and ribbon fish stored in ice were studied. Organoleptically all fish were found acceptable for 10–13 days before becoming inedible. Proximate analysis showed that moisture content increased slightly; protein and lipid content decreased gradually and ash had little or no significant change. pH, TVB-N, peroxide and aerobic plate count values increased with increasing storage period but the values were within acceptable range up to 10 days of storage. Changes in myofibrillar ATPase activity and solubility of these fishes showed that Ca²⁺ ATPase in the presence of both 0.1  m and 0.5  m KCl decreased gradually whereas no marked changes were observed in the Mg⁺² ATPase activities in the presence/absence of Ca⁺². Myofibrillar protein solubility of all fish samples also decreased considerably during ice storage. The decrement in Ca²⁺ ATPase activity and solubility indicates denaturation of myofibrillar protein of fish samples during ice storage.     

Effects of Anions and Cations on Sugar Utilization in Cucumber Juice Fermentation

ABSTRACT: :
The extent of glucose and fructose utilization during cucumber juice fermentation was affected differentially by the addition of 10 to 360 mM of selected anions (chloride, nitrate, sulfate, phosphate, acetate, lactate, and citrate) and cations (Na⁺, K⁺, NH₄⁺, Ca²⁺, Mg²⁺, and Mn²⁺). Inorganic anions generally suppressed utilization of both sugars, particularly at higher concentrations. Acetate and lactate increased utilization of fructose, but not glucose, while citrate increased utilization of both sugars. Of the cations tested, 10-60 mM Mn⁺² significantly (P < 0.05) increased utilization of both sugars, but higher concentrations reduced utilization, as compared with the control. Evidence indicates that brine composition can significantly influence sugar utilization during cucumber fermentation, and may be important in developing controlled fermentation strategies for brined cucumbers.     

Technical Approach to Simplify the Purification Method and Characterization of Microbial Transglutaminase Produced from Streptoverticillium ladakanum

In order to fast and economically purify MTGase from Streptoverticillium ladakanum , a stepwise elution method was developed and compared with linear gradient elution method. MTGase was purified to electrophoretical homogeneity by using CM Sepharose CL-6B and Blue Sepharose Fast Flow chromatographies by linear gradient or stepwise methods. The recovery of MTGase by linear gradient and stepwise methods were 68.4% and 81.0%, respectively. The optimal temperature and pH were 40 °C and 5.5, respectively. It was stable at pH 5.0 to 7.0 and had a rate constant (KD) of 6.21 °o 10^-5 min^-1 for thermal inactivation at 45 °C. The purified MTGase was activated by K⁺ Na⁺, Ca²⁺, Mn²⁺, and Mg²⁺, not affected by Fe³⁺, EDTA, but inhibited by Cu²⁺, Zn²⁺, Hg²⁺, Ni²⁺, Co²⁺, Cd²⁺, PCMB, NEM, IAA, and PMSF. A simple stepwise method was developed for the purification of MTGase from S. ladakanum.     

Textural properties of a model aqueous phase in low fat products. Part 1: Alginate, caseinate and starch in isolation, and in starch containing binary mixtures

Summary The effect of increasing additions of calcium on the textural properties of alginate, caseinate and starch dispersions was investigated to provide a baseline for further work on mixtures of these biopolymers. Increasing concentrations of calcium transformed the alginate solutions into gels having a maximum rigidity at 1000 and 300 p.p.m. Ca²⁺ for 2.0 and 0.5% of the polysaccharide, respectively. Gelation was achieved by cooling which unveiled a two stage process of network formation. Caseinate solutions (12%) showed an increased viscosity with a rising Ca²⁺ concentration up to 2250 p.p.m., above which viscosity decreased. Starch (2.5%) exhibited a slight loss in storage modulus (G') with increasing levels of calcium. The texture of the alginate starch mixture was determined by the alginate component (two stage gelation process), but inverted to that of starch at high levels of added Ca²⁺. In the absence of the counterion, casein had an adverse effect on the strength and cohesion of starch networks. At 400 p.p.m. Ca²⁺, the protein forms a continuous liquid like phase which suspends the starch inclusions thus dictating the textural properties of the mixture. Caseinate continues to dominate up to 1200 p.p.m. Ca²⁺, at which point the starchy matrix influences the system once more. Finally at higher levels of the counterion the sample phase inverts back to a starch continuous gel. Part 2 of this work examines the effect of calcium on the remaining preparations in order to facilitate the formulation of improved low fat products.     

Time-temperature studies of gellan polysaccharide-high sugar mixtures: effect of sodium ions on structure formation

ABSTRACT:  Changes to the viscoelastic storage and loss moduli were measured as a function of temperature and oscillatory frequency for 0.5% (w/w) gellan:80% (w/w) cosolute dispersions with added Na⁺ (40 to 160 mM). Isothermal frequency (0.15 to 15 Hz) and thermal scans (at 0.15 Hz) were performed over a decreasing then increasing temperature range of 85 to 5 °C and 5 to 85 °C, respectively. Moduli were found to increase in magnitude with decreasing temperature and increasing levels of Na⁺ during cooling, then remained relatively thermally irreversible upon heating. Isothermal frequency (ITF) data were described using the time–temperature superposition (TTS) principle and the modified Cole–Cole (MCC) analysis. Both TTS and the MCC analyses successfully described the behavior of samples containing 40 mM added Na⁺ during cooling and heating, and at the 100-mM Na⁺ level during cooling. TTS superposed ITF data over the entire temperature range, whereas successful superposition was restricted to lower temperatures in the MCC analysis, where the viscoelastic response was dominated by the long-range relaxation of gellan chains between junction zones. Failure of both analyses was attributed to the formation of junction zones composed of polymer–polymer associations. It is proposed that the addition of Na⁺ promotes the formation of a weakly cross-linked gellan network.     

Purification and Characterization of an α-L-Rhamnosidase from Aspergillus terreus of Interest in Winemaking

ABSTRACT: An enzyme with α-L-rhamnosidase activity was purified to homogeneity from a culture filtrate of Aspergillus terreus after growth in a medium containing L-rhamnose as the sole carbon source. The biosynthesis of this enzyme was repressed by glucose. The enzyme had a molecular mass of 96 kDa on sodium dodecyl sulfate-polyacrylamide gel electrophoresis and an isoelectric point of 4.6 as determined by analytical isoelectric focusing. The pH and temperature optima for the enzyme were found to be 4.0 and 44 °C, respectively. Using p-nitrophenyl-α-L-rhamnopyranoside as a substrate, the enzyme exhibited Michaelis-Menten kinetics with K_M and V_max values of 0.17 mM and 84 U/mg, respectively. The enzyme was inhibited competitively by L-rhamnose (K₁ 2.5 mM). Divalent cations such as Ca²⁺ Mg²⁺ Zn²⁺ and Co²⁺ stimulated the a-L-rhamnosidase activity, whereas this was inhibited by Hg2+ and Cd2+. Ethanol (12% v/v) and glucose (21% w/v) decreased enzyme activity by approximately 20%, while this was not affected by SO₂.     

Alginate- and gellan-based edible films for probiotic coatings on fresh-cut fruits

ABSTRACT:  Alginate- (2% w/v) or gellan-based (0.5%) edible films, containing glycerol (0.6% to 2.0%), N-acetylcysteine (1%), and/or ascorbic acid (1%) and citric acid (1%), were formulated and used to coat fresh-cut apple and papaya cylinders. Water vapor permeability (WVP) was significantly higher ( P < 0.05) in alginate films (0.30 to 0.31 × 10⁻⁹g m/Pa s m²) than in the gellan ones (0.26 to 0.27 × 10⁻⁹g m/Pa s m²). Addition of 0.025% (w/v) sunflower oil decreased WVP of gellan films (0.20 to 0.22 × 10⁻⁹ g m/Pa s m²). Water solubility of gellan and alginate films at 25 °C (0.47 to 0.59 and 0.74 to 0.79, respectively) and their swelling ratios (2.3 to 2.6 and 1.6 to 2.0, respectively) indicate their potential for coating high moisture fresh-cut fruits. Fresh-cut apple and papaya cylinders were successfully coated with 2% (w/v) alginate or gellan film-forming solutions containing viable bifidobacteria. WVP in alginate (6.31 and 5.52 × 10⁻⁹g m/Pa s m²) or gellan (3.65 and 4.89 × 10⁻⁹ g m/Pa s m²) probiotic coatings of papaya and apple, respectively, were higher than in the corresponding cast films. The gellan coatings and films exhibited better water vapor properties in comparison with the alginate coatings. Values > 10⁶ CFU/g B. lactis Bb -12 were maintained for 10 d during refrigerated storage of fresh-cut fruits, demonstrating the feasibility of alginate- and gellan-based edible coatings to carry and support viable probiotics on fresh-cut fruit.     

Isolation of Tomato Seed Meal Proteins with Salt Solutions

Salt solutions were used in isolating tomato seed meal proteins. Na₂SO₃ and NaCl solutions at different concentrations, and pH were included in a central composite design to find optimum conditions of protein isolation. The highest total protein yield was achieved with water extraction (no salt present). Salt extraction at pH 7.5 produced isolates with protein content of 93.4% (NaCl 5% w/v) and 77.1% (Na₂SO₃ 0.5% w/v). Observed values were in good agreement with predicted values. Isolates extracted with different salt solutions ranged from less soluble but very resistant to heat and Ca²⁺, to very surface active with functional properties comparable to commercial soy isolates.     

ATLANTIC QUEEN CRAB (Chionoecetes opilio), JONAH CRAB (Cancer borealis), AND RED CRAB (Geryon quinquedens). Proximate Composition of Crabmeat from Edible Tissues and Concentrations of Some Major Mineral Constituents in the Ash

The gross composition of the edible tissues of Atlantic Queen crab, Jonah crab and Red crab was determined by standard analytical methods and results compared to those obtained for analysis of edible tissues in other species of crab. In addition, the concentrations of various cationic constituents of the ash (Na⁺, K⁺, Ca⁺⁺ and Mg⁺⁺) and phosphate were estimated in hydrogen peroxide-sulfuric acid digests of meat samples of each of the three Crab species. The nutritive value of crabmeat from these species is discussed in terms of protein content, mineral composition and overall calorific value.     

EFFECT OF ALKALI METAL IONS ON THE RHEOLOGICAL PROPERTIES OF κ-CARRAGEENAN AND AGAROSE GELS

Stress relaxation and dynamic measurements were carried out on κ-carrageenan and agarose gels to examine the effect of alkali metal ions. The elastic modulus of κ-carrageenan gels increase remarkably by adding alkali metal ions Li⁺, Na⁺, K⁺, Cs⁺. This was explained as follows: the electrostatic repulsion of sulfate groups in κ-carrageenan gels are prevented by the shielding action of the alkali metal ions stabilizing the double helical structure of κ-carrageenan gels. The increase of the modulus was in the order: Cs⁺ > K⁺≫ Na⁺ > Li⁺. The difference between these two groups (Cs⁺, K⁺) and (Na⁺, Li⁺) is that the former group belongs to the structure disordering ions while the latter group belongs to the structure ordering ions. Thus, the former group prevents the repulsion of sulfate groups more directly than the latter. Agarose gel, which lacks sulfate groups, is not influenced so much by adding the alkali metal ions.     

Determination of chloride, nitrate and calcium ions in sugar with ion selective-electrodes

Chloride, nitrate, and calcium ion-selective electrodes were tested and found satisfactory for the determination of the corresponding ions in highly refined white sugar, molasses and other impure sugar samples at different stages of sugar manufacturing or refining. The interferences by Br⁻ and I⁻ ions in Cl⁻ determination were eliminated by oxidation with 3 M HNO₃ and passing air to remove the free Br₂ and I₂ formed. The Cl⁻ concentration was then determined with a chloride-selective electrode against a calibration curve. Chloride should not be determined by ashing sugar, since this causes high losses of Cl⁻. It was found that NO₃⁻ and free Ca²⁺ ions could be determined directly in the sugar solution against corresponding calibration curves. Total calcium was determined after ashing of sugar samples. The ash was dissolved in 0.1 M HCl and passed through an anion exchange resin to remove PO³⁻₄ and SiO₂₋₃ ions, and Ca²⁺ was determined as before. Bound calcium was obtained by subtracting values of free from total calcium. Determination of bound calcium was useful to monitor the process of liming. For comparison, the three ions were also determined with acceptable precision without removing interfering ions using the method of standard addition and Gran's plot. The errors of determination for both direct and standard addition techniques were 3% for Cl⁻ and NO⁻₃ and 1–5% for Ca²⁺.     

EFFECT OF ALKALI AND ALKALI-EARTH HALIDES ON TEXTURE AND COOKING YIELD OF COOKED COMMINUTED LEAN PORK

The effects of alkali-and alkali-earth halides and sulfates on the texture and cooking yield of cooked lean comminuted pork were examined. Divalent cations (Ca²⁺ and Mg²⁺) associated with Br⁻, I⁻ and SO^2-₄ imparted a firm texture to meat (peak force values of 17.1–21.1 kg as compared to 8.4 kg for the control sample devoid of any added salt). Peak force values of samples containing monovalent cations were generally low, but for most cases, were higher (P < 0.05) than that of the control. The cooking yields of samples containing divalent cations (regardless of their anion counterparts) were not different (P>0.05) from that of the control. At 200 meq/kg sample, iodides of monovalent cations as well as sodium chloride increased the cooking yield by approximately 5–20% compared to the control.     

Characterization of a thermostable and acidic-tolerable beta-glucanase from aerobic fungi Trichoderma koningii ZJU-T

ABSTRACT:  An extreme thermostable and acidic tolerable β-glucanase was isolated and characterized from aerobic fungi Trichoderma koningii ZJU-T. The optimal reaction temperature and pH for the β-glucanase were 100 °C and pH 2.0, respectively. The β-glucanase showed increased stability at higher temperatures and lower pH values when compared to other β-glucanases. The optimum conditions for the β-glucanase stability were found to be pH 4.0 and 80 °C. Even subjected to 100 °C for 3 h, β-glucanase activity did not show significant reduction. Moreover, K⁺ significantly enhanced β-glucanase activity at the concentration of 1 mM, while EDTA and other metal ions such as Mg²⁺, Mn²⁺, Zn²⁺, Ca²⁺, Fe²⁺, Pb²⁺, and Fe³⁺ inhibited β-glucanase activity. Denaturants, including sodium dodecyl sulfate (SDS) and mercaptoethanol, also inhibited β-glucanase activity at a concentration of 5%. However, in the presence of 7 M urea, residual activity of the β-glucanase still remained 14.5%.     

Influence of some polyvalent organic acids and salts on the colloidal stability of milk

Fifteen polyvalent organic salts and acids increased, some very markedly, the heat stability of milk progressively with increasing concentration; acetate and mesaconic acid had no effect, and maleate caused destabilization. Citrate, oxalate and EDTA markedly reduced the [Ca⁺] in the milk and increased its ethanol stability by shifting the ethanol/pH profile to lower pH values. These additives ≥ 20 mmol/l prevented the coagulation of milk by rennet, but the other additives caused only slight increases in RCT .
Citrate, EDTA and oxalate disrupted casein micelles and would therefore not be suitable additives: however, the other acids and salts did not alter the appearance of the milk and might be recommended as suitable additives to improve the heat stability. In terms of the response to the level of Ca²⁺ and colloidal calcium phosphate in milk, there appeared to be a correlation between ethanol stability and rennet coagulation time.     

EFFECT OF pH AND CATIONS ON THE THERMALLY INDUCED GELATION OF OVALBUMIN

The gelation of ovalbumin in the presence of salts containing Ca⁺² and Mg⁺² at various pH values was investigated. Characteristics of the gels produced were evaluated using penetration measurements on an Ottawa Texture Measuring System as well as dynamic rheology on a Bohlin VOR rheometer. Gel properties were related to cation binding (equilibrium dialysis) and to changes in protein structure (differential scanning calorimetry). Cation binding generally increased with increasing salt concentration, and Mg⁺² bound to a greater extent than Ca⁺² at the higher levels studied. The impact of this binding on gel structure was dependent on pH and the technique used to evaluate structure. At pH 5 proteins tended to coagulate regardless of the type or amount of salt. At pH 7, the highest rigidity values from penetration measurements were obtained at salt levels of 0.005 M. At pH 9, the salt concentration for maximum rigidity varied with the salt, while the storage moduli (G') from dynamic rheology were highest at the highest salt concentration used. Based on rigidity data, the inclusion of 0.005 M MgSo₄ would give a product with the greatest rigidity over a wide pH range.     

Osmotic dehydration kinetics of carrot cubes in sodium chloride solution

Osmotic dehydration kinetics of carrot cubes in sodium chloride solution having concentrations 5%, 10% and 15% (w/v), solution temperature 35, 45 and 55 °C, sample to solution ratio (STSR) 1:4, 1:5 and 1:6 were studied up to 240 min duration. During the experimentation, effect of solution temperature and process duration was significant and that of solution concentration and STSR were non-significant on water loss. Among the different models applied (Penetration model, Magee Model, and Azuara model), Azuara model best fitted to the experimental data for water loss and solute gain during osmotic dehydration. Effective diffusivities of water and solute were calculated by using the analytical solution of Fick's unsteady state law of diffusion by iterative technique with a computer program. For the above conditions, the effective diffusivity of water was found to be in the range between 2.6323 × 10⁻⁹ and 6.2397 × 10⁻⁹ m²/s and that of solute between 3.1522 × 10⁻⁹ and 4.6400 × 10⁻⁹ m²/s.     

The Green Oat Story: Possible Mechanisms of Green Color Formation in Oat Products during Cooking

ABSTRACT:  Consumers occasionally report greenish colors generated in their oat products when cooking in tap water. Here we have investigated pH and ferrous (Fe²⁺) ion as possible mechanisms for this color change. Steel-cut oat groats can turn brown-green color when cooked in alkaline conditions (pHs 9 to 12). Extraction of this color with methanol, and high-pressure liquid chromatography indicated a direct association of this color with the phenolic acid or avenanthramide content of the oat. The presence of 50 mM NaHCO₃ in water will cause oat/water mixtures to turn alkaline when cooked as CO₂ is driven off, generating OH⁻ ion. Although tap water rarely, if ever, contains so much bicarbonate, bicarbonate is used as a leavening agent in baking applications. Industrial interests using baking soda or alkaline conditions during oat processing should be aware of possible off color generation. We have also found that as little as 10 ppm Fe²⁺ will turn oat products gray-green when cooked. The aleurone stained darker than the starchy endosperm. Other divalent cations, such as Ca²⁺ or Mg²⁺ had no effect on cooked oat color. As much as 50 ppm Fe²⁺ may be found in freshly pumped well water, but Fe²⁺ reacts quickly with oxygen and precipitates as Fe(OH)₃. Thus, some freshly pumped well water may turn oats green when cooked, but if the water is left under atmospheric conditions for several hours, no discoloration will appear in the cooked oats.     

AN ESTEROLYTIC ACTIVITY FROM A WILD EDIBLE MUSHROOM, LYCOPERDON PERLATUM

Lycoperdon perlatum Pers. (Lycoperdaceae, Agaricales, Agaricomycetidae, Agaricomycetes, Basidiomycota, Fungi) was evaluated for its esterolytic potential. Native electrophoresis of the crude extracts showed four bands having Rf values of 0.34, 0.39, 0.52 and 0.59. The esterase showed the highest activity toward a short-chain substrate, p -nitrophenyl acetate. Optimum reaction conditions for L. perlatum crude extract were attained at pH 8.0 and 40C. Esterolytic activity of enzyme extract was stimulated in the presence of Mn^{2 +} , Fe^{2 +} , Ca^{2 +} and Zn^{2 +} in the reaction mixture. The enzyme activity was stimulated by incubation at pH 6.0 but retained 77% of its original activity at its optimum pH after 24 h. Thermal inactivation was displayed after incubation for 20 min at various temperatures above 30C. At 1 mM final concentration, 2-mercaptoethanol, dithiothreitol, ethylenediamine tetraacetic acid and p -methylphenyl sulfonylfluoride inhibited the esterolytic reaction. These results support that the crude L. perlatum extract possesses an esterolytic activity having properties similar to other esterases.

PRACTICAL APPLICATIONS

Esterases catalyzing the cleavage and formation of ester bonds are known α/β-hydrolases (EC 3.1.1.X). Esterases are used for the synthesis of flavor esters for the food industry, modification of triglycerides for fat and oil industry and resolution of racemic mixtures used for the synthesis of fine chemicals for the pharmaceutical industry. Therefore, the search for new enzyme sources is important for the development of new enzymes and applications.     

Osmotic Dehydration of Tomato in Sucrose Solutions: Fick's Law Classical Modeling

ABSTRACT:  Osmotic dehydration of tomato was modeled by the classical Fick's law including shrinkage, convective resistance at the interface and the presence of water bulk flow. Tomato slices having 8 mm thickness were osmotically dehydrated in sucrose solutions at 50, 60, and 70 °Brix and at 35, 45, and 55 °C. Other experiments were done in a 70 °Brix sucrose solution at 35 °C with tomato slices of 4, 6, and 8 mm thickness and at different motion levels (velocities 0, 0.053, and 0.107 m/s). Tomato weight, water content, and °Brix of the products were measured as a function of processing time (20, 40, 80, 160, and 320 min). Results showed that temperature, concentration, thickness, and solution movement significantly influenced water loss and sucrose gain during the osmotic dehydration of tomato. The model predicted the modifications of soluble solid content and water content as a function of time in close agreement with the experimental data. Experimental Sherwood number correlations for sucrose and water were determined as Sh _s = 1.3 Re ^0.5 Sc _s^0.15 and Sh _w = 0.11 Re ^0.5 Sc _w^0.5, respectively. The effective diffusion coefficients of water (4.97 10⁻¹¹– 2.10 10⁻¹⁰ m²/s) and sucrose (3.18 10⁻¹¹– 1.69 10⁻¹⁰ m²/s) depended only on temperature through an Arrhenius-type relationship.