Osmotic dehydration of guava: influence of replacing sodium metabisulphite with honey on quality

Guava slices were subjected to pre-treatment by soaking in a solution containing 0.25% (w/v) sodium metabisulphite, 0.5% (w/v) ascorbic acid, 1% (w/v) citric acid, 1% (w/v) calcium chloride and either 0%, 1% or 3% (v/v) honey. A higher concentration of metabisulphite [0.5% (w/v)], but no honey, was also prepared as a reference. After osmotic dehydration, the guava slices were dried at 60 °C. During 24 weeks of storage, the measured texture values of products indicated that an addition of honey significantly delayed the increase in hardness and cutting work in guava slices compared to other treatments ( P  ≤   0.05). Pre-treatment with 0.5% (w/v) metabisulphite without honey or 0.25% (w/v) metabisulphite with 1% (v/v) honey maintained colour during storage better than with 0 or 3% (v/v) honey. The result showed good agreement with colour score evaluation. Overall results suggested that 1% (v/v) honey was the best pre-treatment condition.     

STUDIES ON PRESERVATION OF SUGARCANE JUICE

ABSTRACT

The variety CoP 92226 was selected for preparing sugarcane juice beverage on the basis of yield and sensory attributes from eight promising varieties of sugarcane. Sugarcane juice beverage samples were prepared by pasteurizing the sugarcane juice at 70°C for 10 minutes and adding citric acid (40 mg/100 ml), ascorbic acid (40 mg/100 ml) and potassium metabisulphite (150 ppm). Samples of sugarcane juice beverage were stored at room (30±5°C) and refrigeration (4±2°C) temperature in pre-sterilized glass bottles and analyzed for physico-chemical, microbiological and sensory attributes at every 15 days interval for 90 days. The pH, total soluble solids and total sugars decreased, whereas, titratable acidity and reducing sugars increased significantly (P<0.01) during storage. An appreciable increase in total plate counts and yeast and mold counts were observed, however, no coliforms, were detected in sugarcane juice beverage during storage. The changes in different attributes were significantly (P<0.01) higher at room temperature as compared to refrigeration temperature. The sugarcane juice beverage having citric acid and potassium metabisulphite showed minimum changes in sensory qualities during storage, both at room and refrigeration temperature. An acceptable quality beverage of sugarcane juice with satisfactory storage stability for 90 days at room as well as refrigeration temperature could be prepared.     

Biomass and Patulin Production by Byssochlamys nivea in Apple Juice as Affected by Sorbate, Benzoate, SO2 and Temperature

The effects of potassium sorbate, sodium benzoate, SO₂ and incubation temperature on biomass and patulin production by Byssochlamys nivea in apple juice were determined. Growth at 21, 30 and 37°C over a 25-day incubation period was significantly retarded by 75 ppm SO₂, 150 ppm potassium sorbate and 500 ppm sodium benzoate. Biomass accumulated to approximately 500 mg/100 ml in control samples of apple juice. Patulin was produced in the highest concentrations at 21°C after 20 days incubation. After reaching a maximum concentration at 30 and 37°C, a rapid decline in patulin content was observed. Patulin production was also observed at 12°C. On the basis of concentration, SO₂ had the most significant effect on the rate of biomass and patulin production by B. nivea followed by potassium sorbate and sodium benzoate, respectively.     

Pectin lyase and polygalacturonase of Aspergillus niger pathogenic for yam tubers (Diascorea rotundata)

Polygalacturonase and pectin lyase of Aspergillus niger partially purified by ethanol, ammonium sulphate precipitation, DEAE-cellulose and Sephadex G-150 column chromatography were characterized. Polygalacturonase gave optimum activity at pH 4–5, and at 35°C. It was stable at pH 3–7 and at 20–50°C. The molecular weight was 38020. For pectin lyase optimum activity occurred at pH 5 and 45°C. The enzyme was stable at pH 3–4 and at 40–50°C. The molecular weight was 30 900. Yam tissue was optimally macerated at pH 4–5 by the enzymes. At pH 4.5, potassium sorbate (0.6 mg/ml), benzoic acid (0.8 mg/ml) and sodium benzoate (1.0 mg/ml) caused complete inhibition of polygalacturonase activity. With pectin lyase, this effect was achieved with potassium sorbate and benzoic acid each at 0.9 mg/ml, but not with sodium benzoate.     

Prediction of toxin production by Clostridium botulinum in pasteurized pork slurry

A model pork slurry system was used to study factors controlling the growth of Clostridium botulinum types A & B (Roberts, Gibson & Robinson, 1981a,b). The following factors were studied in combination: sodium chloride (2.5, 3.5, 4.5% w/v on water); sodium nitrite (100, 200, 300 μg/g); sodium nitrate (0, 500 μg/g); sodium isoascorbate (0, 1000 μg/g); polyphosphate (Curaphos 700, 0, 0.3% w/v); heat treatment (none, 8°C/7 min, 80°C/7 min + 70°C/1 hr); at two pH levels and stored at: 15, 17.5, 20 or 35°C.
Analyses of results yielded a statistical model providing two formulae (for 'low' and 'high' pH slurries) which estimate the probability of toxin production in the pork slurry system within the limits defined above.     

Antimicrobial Activity and Synergistic Effect of Cinnamon with Sodium Benzoate or Potassium Sorbate in Controlling Escherichia coli O157:H7 in Apple Juice

ABSTRACT: Antimicrobial effects of cinnamon, sodium benzoate, potassium sorbate, and combinations were examined against Escherichia coli O157:H7 in apple juice at 8°C and 25°C. E. coli O157:H7 was reduced by 1.6 log colony-forming units (CFU)/mL at 8°C and 2.0 log CFU/mL at 25°C by 0.3% cinnamon. At 8°C, 5.2 log CFU/mL of E. coli O157:H7 was eliminated in 11 d by 0.3% cinnamon with 0.1% sodium benzoate, and in 14 d by 0.3% cinnamon with 0.1% potassium sorbate. At 25°C, 5.3 log CFU/mL E. coli O157:H7 was eliminated in 3 d by the same combinations. A synergistic effect was observed between cinnamon and preservatives against E. coli O157:H7 at 8°C and 25°C.     

Factors controlling the growth of Clostridium botulinum types A and B in pasteurized, cured meats III. The effect of potassium sorbate

The growth of Clostridium botulinum types A and B spores, at 10¹ or 10³ per container, was studied in a pork slurry system containing nitrite (40 μg/g), sodium chloride (2.5, 3.5, 4.5% w/v) sodium isoascorbate (550 μg/g) at varying pH levels, with or without potassium sorbate (0.26% w/v), without heating and after two heat treatments (80°C for 7 min, and 80°C for 7 min + 70°C for 1 hr) followed by storage at 15, 17.5, 20 or 35°C for up to 6 months. At a given spore inoculum, potassium sorbate significantly decreased toxin production, as did increasing NaCl, decreasing pH or decreasing storage temperature. Heat treatment did not significantly affect spoilage or toxin production overall, but interacted significantly with some factors. The effect of sorbate was greater at 3.5% NaCl than at 2.5%, at pH values below 6.0, and at low storage temperature.     

Control of a range of food related microorganisms by a multi-parameter preservation system

Seventy-two process variables, based on a matrix of a _w nature of controlling solute, pH, and the addition of sodium citrate and sodium benzoate were examined with a view t o devising a food preservation system for ambient temperatures. Growth of a challenge'cocktail' of Staphylococcus aureus, Bacillus subtilis, Pseudomonas aeruginosa, Streptococcus faecalis, Lactobacillus casei and Clostridiurn perfringens, was assessed in a Brain Heart Infusion broth based model system. Each of the controlling factors had an effect on growth. The addition of sodium citrate (2% w /v) and sodium benzoate (2000 mg/I) enhanced the inhibitory effect. Reduction in a _w (1.00–0.94) and pH (7.0–5.5) in combination or as separate controlling factors increased any inhibition. Combinations of sodium chloride and glycerol were used as the controlling solute, and increasing the proportion of sodium chloride resulted in suppressed growth, irrespective of any change in a _w or pH. Combinations of sodium citrate and sodium benzoate with a pH less than 6.0 and an a, less than 0.95 inhibited any growth during a 42 day incubation period at 37°C, irrespective of the controlling solutes studied.     

野刺梨营养酒饮料的研制

用酒糟酒、野刺梨果汁、蜂花粉、香精为原料,通过正交试验,探索含酒营养果汁饮料的生产工艺,并对蜂花粉的破壁工艺进行了探讨。实验结果显示,花粉用曲霉培养,在pH5.4、温度55℃、10%NaCl条件下降解56h,破壁率达98.5%以上。由酒糟酒降度实验可知:用1.35mg/100ml海藻酸钠和180mg/100ml可溶淀粉联合处理20°加浆酒,18h可沉淀完全,除去大部分高级脂肪酸酯。     

Pasteurization of Fresh Orange Juice Using Low-Energy Pulsed Electrical Field

ABSTRACT: Using the hurdle approach, temperature, acidity, and number of pulses were varied to maximize microbial inactivation in orange juice. The effect of PEF combined with the addition of nisin, lysozyme, or a combination of both to orange juice was also investigated. Optimal conditions consisting of 20 pulses of an electric field of 80 kV/ cm, at pH 3.5, and a temperature of 44 °C with 100 U nisin/ml resulted in over a 6-log cycle reduction in the microbial population. The process was most influenced by a change in temperature (p < 0.0001). Following treatment, there was a 97.5% retention of vitamin C, along with a 92.7% reduction in pectinmethylesterase activity. The microbial shelf-life of the orange juice was also improved and determined to be at least 28 d when stored at 4 °C without aseptic packaging. Gas chromatography revealed no significant differences in aroma compounds before and after pulsing.     

高效液相色谱内标法测定酱油中糖精钠和苯甲酸钠

以山梨酸钾为内标物,采用高效液相色谱法测定酱油中的糖精钠和苯甲酸钠的含量。样品经体积分数为50%的乙醇溶液提取后,采用Nova-Pak C18色谱柱(3.9 mm×15 mm×5 μm)分离,以甲醇-0.02 mol/L乙酸铵（5∶95,V/V）为流动相进行洗脱,流速1 mL/min,紫外检测波长230 nm。结果表明,在0.1～1.4 mg/kg的添加范围,糖精钠、苯甲酸钠的加标回收率分别为99.5%～102.3%,95.1%～102.1%,相对标准偏差(RSD)分别为0.69%和0.82%。所测酱油中糖精钠和苯甲酸钠的含量分别为3.27 mg/kg和0.133 mg/kg。采用该方法回收率高、准确性好,可用于酱油中糖精钠和苯甲酸钠含量分析。     

Using Dimethyldicarbonate to Minimize Sulfur Dioxide for Prevention of Fermentation from Excessive Yeast Contamination in Juice and Semi-Sweet Wine

ABSTRACT: Sulfur dioxide (SO₂) at 0, 10, 25, and 50 mg/L and/or dimethyldicarbonate (DMDC) at 0, 50, 100, and 200 mg/L at different pH levels (3.0, 3.2, 3.4, and 3.6) in juice and semi-sweet wine were evaluated by monitoring yeast growth and visible fermentation at 20 °C after excessive yeast contamination (500 to 700 colony forming units/mL), using Saccharomyces bayanus. The treatments with the least preservatives that prevented yeast growth and visible fermentation at all pH levels in juice were 50 mg/L SO₂+ 100 mg/L DMDC and in wine were 10 mg/L SO₂+ 50 mg/L DMDC. DMDC and minimal SO₂ levels prevented fermentation in juice and semi-sweet wine with excessive yeast contamination.     

Thermal resistance of Alicyclobacillus acidoterrestris spores in different heating media

The aim of this work was to study the influence of temperature (85, 90, 95 and 100 °C), total soluble solids (SS: 10 and 20°Brix or % by weight of sucrose) and pH (3.5 and 4.0) on decimal reduction time ( D- value) of the Alicyclobacillus acidoterrestris strain DSM2498 spores in apple juice, orange juice and malt extract broth (MEB). The effects of SS and pH on D -values and z- values in each media were insignificant ( P  > 0.05). In apple juice, orange juice and MEB, z- values of A. acidoterrestris for pH 3.5 and pH 4.0 were 12.2 ± 1.3–14.2 ± 3.2 °C, 11.2 ± 0.3–9.4 ± 0.0 °C and 11.9 ± 0.8–10.3 ± 0.4 °C, respectively. z- values of apple juice, orange juice and MEB samples with SS = 10°Brix and SS = 20°Brix were 14.1 ± 3.2–12.2 ± 1.3 °C, 10.2 ± 0.7–10.5 ± 1.1 °C and 11.3 ± 1.5–10.9 ± 0.2 °C, respectively. However, D -values of all samples were affected by temperature significantly ( P  < 0.01). Average D -values of apple juice, orange juice and MEB were 101.2 ± 14.7, 34.4 ± 7.9, 20.3 ± 4.9 and 4.3 ± 1.3 min for 85, 90, 95 and 100 °C. This study demonstrated that A. acidoterrestris spores exhibited high resistance to thermal processing applications. pH and SS of the media did not affect thermal resistance.     

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.     

Degradation Kinetics of Capsanthin in Paprika (Capsicum annuum L.) as Affected by Heating

ABSTRACT: Diluted juice of paprika was heated at 80, 90 and 100°C with holding times of 0, 2, 4, 8 and 16 min. Capsanthin in each sample was determined by HPLC. The degradation kinetics of capsanthin was studied by two groups of reaction models including elementary reaction rate models and those of modified square root-based pseudo (MRBP-). The MRBP-1st order reaction rate model was proven as an appropriate model in this study. The pseudo Q₁₀ (PQ₁₀) value was 1.045 and the predicted half-life (capsanthin 2,850 mg/L) was 27.47, 21.23 and 15.23 min, respectively, at 80, 90 and 100°C.     

Solubilization of wheat gluten with sodium hydroxide

The solubility of wheat gluten may be increased greatly by treatment with 0.25 M sodium hydroxide. At temperatures of 40°C and above, the solubility of the protein exceeds 100 mg/ml in a reaction time of 6 hr or less. The products from the reaction of 60°C and 80°C were darker than the original gluten and had an unpleasant odour of H₂S on dissolution in water. They also contained traces of lysinoalanine. The 40°C reaction product was about the same colour as gluten, and its solutions in water did not smell of H₂S. Reaction of gluten at 20°C also caused a large increase in solubility, but after 24 hr the solubility was only 77 mg/ml. This product was also of the same colour as gluten, and did not smell of H₂S in solution. Neither the 20°C nor the 40°C products contained detectable traces of lysinoalanine. For reasons of flavour, colour, lysinoalanine content and economy of time, the optimum reaction conditions are 6 hr at 40°C.     

Thermal Inactivation of Yeasts in Fruit Juices Supplemented with Food Preservatives and Sucrose

Thermal inactivation of five yeasts (Candida krusei, Hansenula anomala, Saccharomyces bailii, S. cerevisiae and Torulopsis magnoliae) suspended in five fruit juices (apple, apricot, grape, orange and pineapple) as affected by potassium sorbate, sodium benzoate and sucrose was investigated. Yeasts were most sensitive to heat when suspended in orange juice. Both preservatives, at a concentration as low as 100 ppm, enhanced the rate of inactivation in juices containing no added sucrose. Supplementation of juices with sucrose (30 and 50%) resulted in protection against death of yeasts. The detrimental effects of potassium sorbate and sodium benzoate were reduced in the presence of high concentrations of sucrose. While neither preservative exhibited a consistent superior lethal effect compared with the other, overall, sodium benzoate was generally more effective than was potassium sorbate.     

Citric Acid and Antimicrobials Affect Microbiological Stability and Quality of Tomato Juice

Acidification, addition of dimethyl dicarbonate and a mixture of potassium sorbate and sodium benzoate and storage temperature were related to microbiological stability and quality of tomato juice. Whether iuices were acidified CDH 4.0 to 3.7) or nonacidified. dimethyl dicarbonate and sorbate/benzoate were highly effective in diminishcng mold and yeast count at 5°C and 20°C. Dimethyl dicarbonate in juices acidified to pH 3.7 and stored at 5°C was most effective in controlling plate counts, followed by sorbate/benzoate in juices acidified to pH 3.7 and stored at 5°C and 20°C. Tomato juice treated with dimethyl dicarbonate had lower amounts of ascorbic acid, total amino acids, fructose, glucose, lycopene and β-carotene.     

Prickly pear sheets: a new fruit product

Dried sheets (Teen-Edin) from prickly pear (Taifi cultivar) fruits were made and the composition of the pulp and the optimum formulation sheet was analysed. The optimum formulation was obtained by adding to fruit pulp (100%), 10% sucrose, 1.1% citric acid, 0.15% sodium metabisulphite, and 0.5% olive oil (w/w). Sodium metabisulphite improved the colour and citric acid produced a similar acid taste to the traditional apricot sheets. The sheets were highly acceptable to a small panel and have potential for manufacture as a possible alternative to apricot sheets (Kamar-Eddin). The technique could also be used for preservation in many other arid parts of the world where prickly pears grow.     

Partial purification and characterisation of banana [Musa (AAA Group) 'Gros Michel'] polyphenol oxidase

Polyphenol oxidase (PPO) from pulp of banana [Musa (AAA Group) 'Gros Michel'] was extracted and precipitated with 80% saturated ammonium sulphate followed by conventional column chromatography on Sephacryl S-200 HR and fast protein liquid chromatography on Mono Q column. The lyophilised PPO obtained from Sephacryl S-200 HR column was used for characterisation and inhibition studies. The partially purified PPO obtained from the Mono Q column exhibited at least three isoenzymes. The banana PPO had optimum pH for activity at 7 and it was stable around the same pH. Only 48% of initial enzyme activity was lost after heating at 70 °C for 30 min. The enzyme was completely inhibited by 2 m m sodium metabisulphite, 2 m m l -cysteine, 4 m m ascorbic acid, and 100 m m 4-hexylresorcinol. The K _m and V _max of banana PPO for dopamine were 2.08 m m and 0.124 m m  min⁻¹ respectively.