Pasteurization of grapefruit juice using a centrifugal ultraviolet light irradiator

Studies are lacking on the nonthermal pasteurization of liquid foods using UV irradiators that centrifugally form very thin films to overcome the problem of limited penetration depth of UV. Grapefruit juice inoculated with Escherichia coli or Saccharomyces cerevisiae was processed at the following conditions: UV dose 4.8–24 mJ/cm²; treatment time 3.2 s, cylinder rotational speed 450–750 rpm, cylinder inclination angle 15–45°, outlet temperature 11 °C, and flow rate 300 ml/min, and was stored for 35 days. Appropriate dilutions of the samples were pour plated with TSA and TSA + 3% NaCl for E. coli and Sabouraud dextrose agar (SDA) and SDA + 5% NaCl for S. cerevisiae. Nonthermal UV processing at 19 mJ/cm², 450 rpm and 15° reduced E. coli in grapefruit juice by 5.1 log₁₀. A dose of 14 mJ/cm² reduced S. cerevisiae by 6.0 log₁₀. Inactivation increased linearly with increasing UV dose. The inactivations at 600 and 750 rpm were similar, and were better than at 450 rpm. The results at 30° and 45° were similar, and were better than at 15°. The occurrence of sublethal injury in either microorganism was not detected. Storing UV processed grapefruit juice at 4 and 10 °C reduced the surviving E. coli to below 1 log₁₀ cfu/ml in 14 days. Processing UV juice reduced the population of S. cerevisiae to less than 1 log₁₀ cfu/ml where it remained for 35 days during refrigerated storage. These results suggest that grapefruit juice may be pasteurized using a nonthermal UV irradiator that centrifugally forms a thin film.     

Biochemical characterization and process stability of polyphenoloxidase extracted from Victoria grape (Vitis vinifera ssp. Sativa)

Polyphenol oxidase (PPO) was isolated from Victoria grapes (Vitis vinifera ssp. Sativa) grown in South Africa and its biochemical characteristics were studied. Optimum pH and temperature for grape PPO activity were pH 5.0 and T = 25 °C with 10 mM catechol in McIlvaine buffer as substrate. PPO showed activity using the following substances: catechol, 4 methyl catechol, d, l-DOPA, (+) catechin and chlorogenic acid. K_m and V_max values were 52.6 ± 0.00436 mM and 653 ± 24.0 OD_400 nm/min in the case of 10 mM catechol as a substrate. Eight inhibitors were tested in this study and the most effective inhibitors were found to be ascorbic acid, l-cysteine and sodium metabisulfite. Kinetic studies showed that the thermal inactivation of Victoria grape PPO followed first-order kinetics, with an activation energy, E_a = 225 ± 13.5 of kJ/mol. Both in semipurified extract and in grape juice, PPO showed a pronounced high pressure stability.     

Short-wave ultraviolet-C light effect on pitaya (Stenocereus griseus) juice inoculated with Zygosaccharomyces bailii

Fresh pitaya (Stenocereus griseus) juice was inoculated with Zygosaccharomyces bailii to be processed using a continuous ultraviolet-C light (UV-C) (57 μW/cm²) system. Inoculated and uninoculated juices were processed at selected flow rates (16.49, 23.78, and 30.33 mL/s) and treatment times (5, 10, 15, 20, 25, and 30 min). Untreated, inoculated, and uninoculated pitaya juices were stored at 4 °C during 25 days. Microbiological (yeasts plus molds and total counts) and physicochemical (pH, total soluble solids, color, phenolic compounds, betalains, and antioxidant activity) characteristics were evaluated in fresh and processed juices. The net change in color increased as treatment time increased, reaching a maximum value of 3.9. A substantial reduction of phenolic compounds (11.6%), betalains (14.6%), and antioxidant activity (37.0%) were observed in juice treated at 30.33 mL/s during 30 min. A reduction of 1.8 log cycles of Z. bailii was observed at the highest UV-C light treatment.     

Effects of high pressure CO2 treatments on microflora, enzymes and some quality attributes of apple juice

The inactivation of microorganisms and enzymes of cloudy apple juice, and some physico-chemical properties of the juice were investigated after continuous high pressure carbon dioxide (HPCD) at 25 MPa and 43 °C, for 2 min and at 22 MPa and 60 °C for 3, 5 and 10 min, respectively. The coliform bacteria were completely inactivated in all the cases. Total aerobic bacteria was reduced by 3.72 log cycles, pectin methylesterase was reduced by 54.3% and polyphenol oxidase was completely inactivated after 10 min treatment at 22 MPa and 60 °C. The yeasts and molds were completely inactivated and the turbidity increased at 22 MPa and 60 °C regardless of time, while the L and a value reduced, but browning degree did not change. The particle size distributions of the juice changed after HPCD but were regained as treatment time was prolonged. The pH was reduced at 22 MPa and 60 °C for 3 or 5 min.     

Analysis of mathematical models of Pseudomonas spp. growth in pallet-package pork stored at different temperatures

Pseudomonas of pallet-packaged raw pork grown at 0, 5, 10, 15, 20 and 25 °C has been studied in this paper. The modified Gompertz, Baranyi and Huang models were used for data fitting. Statistical criteria such as residual sum of squares, mean square error, Akaike's information criterion, and pseudo-R² were used to evaluate model performance. Results showed that there was an apparent decline in Pseudomonas growth at initial-storage phase at low temperatures. The modified Gompertz model outperformed the others at 5, 15, and 20 °C, while Baranyi model was appropriate for 0 and 25 °C. The Huang model was optimal at 10 °C. No single model can give a consistently preferable goodness-of-fit for all growth data. The Gompertz model, with the smallest average values of RSS, AIC, MSE and the biggest pseudo-R² at all temperatures, is the most appropriate model to describe the growth of Pseudomonas of raw pork under pallet packaging.     

Inhibition of A. carbonarius growth and reduction of ochratoxin A by bacteria and yeast composites of technological importance in culture media and beverages

Five composites of yeast and six of bacterial isolates from fermented products were studied, in order to assess their ability to inhibit Aspergillus carbonarius growth and reduce OTA concentration in culture media and beverages. The antagonistic effect of the above composites against A. carbonarius growth was studied in synthetic grape medium of pH 3.5 and a_w 0.98, 0.95, 0.92 after incubation at 25 °C. Different combinations of initial inocula of bacteria or yeast composites and fungi were used (10² cfu/mL vs 10⁵ spores/mL; 10⁵ cfu/mL vs 10² spores/mL; and 10⁵ cfu/mL vs 10⁵ spores/mL). Regarding the OTA reduction experiment, 10³ and 10⁷ cfu/mL of the bacteria and yeast composites were inoculated in liquid media of different pH (3.0, 4.0, 5.0, and 6.1 or 6.5) and initial OTA concentration (50 and 100 μg/L) and incubated at 30 °C. Moreover, grape juice, red wine, and beer were supplemented with 100 μg/L of OTA and inoculated with composites of 16 yeasts (16YM) and 29 bacterial (29BM) strains (10⁷ cfu/mL) to estimate the kinetics of OTA reduction at 25 °C for 5 days. Fungal inhibition and OTA reduction were calculated in comparison to control samples. None of the bacterial composites inhibited A. carbonarius growth. The high inoculum of yeast composites (10⁵ cfu/mL) showed more efficient fungal inhibition compared to cell density of 10² cfu/mL. All yeast composites showed higher OTA reduction (up to 65%) compared to bacteria (2-25%), at all studied assays. The maximum OTA reduction was obtained at pH 3.0 by almost all yeast composites. For all studied beverages the decrease in OTA concentration was higher by yeasts (16YM) compared to bacteria (29BM). The highest OTA reduction was observed in grape juice (ca 32%) followed by wine (ca 22%), and beer (ca 12%). The present findings may assist in the control of A. carbonarius growth and OTA production in fermented foodstuffs by the use of proper strains of technological importance.     

Heat resistance of Neosartorya fischeri in various juices

Heat resistance of Neosartorya fischeri was studied in three different juices (apple, pineapple and papaya). The optimum heat activation temperature and time for the ascospores of the N. fischeri (growth for 30 days at 30 °C) was 85 °C for 10 min. Of the three juices tested, apple juice exhibited maximum 1/k values at 80, 85 and 90 °C (208.3, 30.1 and 2.0 min, respectively). The 1/k values for papaya juice (129.9, 19.0 and 1.9 min) and pineapple juice (73.5, 13.2 and 1.5 min) decreased with acidity and °Brix/acidity (ratio) level. The Z^* values for apple, papaya and pineapple juices were 5, 5.5 and 5.9 °C, respectively. The sterilization F values (4-log reduction) for apple, pineapple and papaya juices were 56.3, 38.0 and 7.2 s, respectively. Considering the thermal treatments commercially applied to pineapple (96 °C/30 s) and apple juices (95 °C/30 s), it is concluded that such treatments will not guarantee that less than 1 ascospore in each set of 10³ packs survive. Only the treatment applied to papaya juice (100 °C/30 s) will be sufficient because the F value is less than 30 s.     

Probiotic beverage from cashew apple juice fermented with Lactobacillus casei

This study optimized the conditions of Lactobacillus casei NRRL B-442 cultivation in cashew apple juice, as well as, determined the proper inoculum amount and fermentation time. Moreover, it was investigated the survivability ability of L. casei in cashew apple juice during refrigerated storage (4 °C) for 42 days. The optimum conditions for probiotic cashew apple juice production were initial pH 6.4, fermentation temperature of 30 °C, inoculation level of 7.48 Log CFU/mL (L. casei) and 16 h of fermentation process. It was observed that the L. casei grew during the refrigerated storage. Viable cell counts were higher than 8.00 Log CFU/mL throughout the storage period (42 days). The values of lightness, yellowness and total color change increased and the values of redness reduced along the fermentation and refrigerated storage periods. The fermented juice with L. casei is a good and healthy alternative functional food containing probiotics. Cashew apple juice showed to be as efficient as dairy products for L. casei growth.     

Evaluation of processing qualities of tomato juice induced by thermal and pressure processing

Effects of processing conditions including hot-break processing (92 °C for 2 min), cold-break processing (60 °C for 2 min) and hydrostatic pressure treatments (100-500 MPa) at different temperatures (4, 25 and 50 °C) for 10 min on quality aspects of tomato juice were investigated. Both hot- and cold-break processing induced significant changes in color, viscosity and radical-scavenging capacity of tomato juice compared with control (fresh tomato juice); moreover, hot-break processing induced a specific range of reduction of pectin methylesterase (PME) and polygalacturonase (PG) activities. Pressure treatments at and below 200 MPa at 4 and 25 °C maintained the color, extractable total carotenoids and lycopene, and radical-scavenging capacity; further, those at 500 MPa at 4 and 25 °C improved all the quality attributes the most except inactivation of PME in this study. The residual activity of PME showed the lowest after treating by 200 MPa at 25 °C; however, the PME activity was enhanced by treatments at 300-500 MPa and various temperatures. The residual activity of PG decreased gradually to 72% with pressure elevated from 100 to 400 MPa at 4 and 25 °C, further, that declined quickly to 10% after 500 MPa treatments. This research clearly shows that it is possible to selectively produce good tomato juice products by high pressure processing at ambient temperature.     

Characterization of juice in fruits of different Chaenomeles species

The juice in fruits of 21 genotypes of Japanese quince (Chaenomeles japonica), 1 genotype of Chinese quince (C. cathayensis), 1 genotype of flowering quince (C. speciosa) and 1 genotype of a hybrid taxon (C. ×superba), representing plant breeding material, was extracted and characterized. The content of juice in the fruits varied between 41% and 52%, on fresh weight basis. The juice was very acidic (pH 2.6 and a titratable acidity of 3.5% calculated as anhydrous citric acid, on average) and transparent (52 NTU, on average), with low density and viscosity. The content of soluble solids was also low (7.1°Brix, on average). Proteins constituted 26 mg/100 ml juice on average, but no soluble polysaccharides were present. A high content of vitamin C (59 mg/100 ml juice, on average) and phenols (284 mg/100 ml juice, on average), beside the high acidity of the juice, suggests that chaenomeles juice may be an interesting raw material as ingredient for the food industry and a source of valuable substances. A principal components analysis separated the Japanese quince genotypes from the other genotypes studied, thus indicating a clear difference in the characteristics and chemical composition of the juice.     

Aseptically packaged UHPH-treated apple juice: Safety and quality parameters during storage

Ultra-high pressure homogenization (UHPH) at 300 MPa and 4 °C inlet temperature were used to preserve apple juice, and shelf-life evaluation of aseptically packaged juice was investigated. After processing Tetra Brik containers were stored at temperatures of 4, 10, 20 and 30 °C during 60 days. In this article, the effect of processing on the spoilage inactivation was evaluated after processing and during the storage trial. Non-germinated and germinated spores were found in the UHPH-treated juice, being an inactive population during storage. Patulin content was also not modified by UHPH processing, but a significant decrease was observed during storage at 30 °C (P < 0.05). Polyphenoloxidase (PPO) and pectinmethylesterase (PME) activity was not found after UHPH-processing and during storage.A kinetic study of post-processing quality loss was conducted. Vitamin C, chlorogenic acid, total polyphenols and color change were measured during storage study and were used to model the UHPH-treated apple juice shelf-life. Loss of vitamin C was correlated with the hydroxymethylfurfural (HMF) accumulation (0.59, P < 0.05). A limiting quality parameter was polyphenolic content. UHPH-treated apple juice stored at 4 °C was found to show a shelf-life for about 21 months by preserving the color characteristics of the juice with low HMF accumulation. From 15 °C changes in quality parameters were more evident.     

Storage quality of pineapple juice non-thermally pasteurized and clarified by microfiltration

Microfiltration (MF) is classified as a non-thermal process for the fruit juice industry. It could provide a better preservation of the phytochemical property and flavor of the juice. This work aimed to study the stability of phytochemical properties including vitamin C, total phenolic content, antioxidant capacity (2-Diphenly-1-picrylhydrazyl: DPPH, free radical scavenging capacity and Oxygen Radical Absorbance Capacity: ORAC assays), microbial and chemical–physical (color, browning index, pH and total soluble solid) properties of MF-clarified pineapple juice during storage at various temperatures (i.e. 4, 27, and 37 °C). The juices were clarified by microfiltration using hollow fiber module. The results showed that most of the phytochemical properties and soluble components were retained in the juice after microfiltration. No microbial growth was detected after 6 months of storage. The storage time and temperature did not affect total soluble solids and pH (P > 0.05). The color (L^*) of clarified juice stored at 4 °C was lighter than the juices stored at higher temperature levels (P < 0.05). The phytochemical properties and total phenol content of the juice significantly decreased as storage time and temperature increased (P < 0.05). Vitamin C content was the attribute that affected storage time and temperature most as indicated by reaction rate constant and activated energy. Storage of non-thermally pasteurized and clarified pineapple juice at 4 °C was the most suitable since it allowed the best quality preservation.     

A novel acidic and low-temperature-active endo-polygalacturonase from Penicillium sp. CGMCC 1669 with potential for application in apple juice clarification

An endo-polygalacturonase gene (pg I) was cloned from Penicillium sp. CGMCC 1669 and expressed in Pichia pastoris. The full-length cDNA consists of 1140 bp and encodes a glycoside hydrolase family 28 protein with a calculated molecular mass of 37.5 kDa. The optimal pH and temperature of purified recombinant endo-PG I were 3.5 and 40 °C, respectively. At 0 °C, endo-PG I still retained 7.3% of the maximal activity. The enzyme had a high affinity and specificity towards polygalacturonic acid. The Km_app and Vmax_app values were 19.5 mg/ml and 909.1 U/min/mg, respectively. Addition of endo-PG I (3.4 U/ml) reduced the intrinsic viscosity of apple juice by 4.5%, and increased the light transmittance by 71.8%. Combination of a commercial pectin lyase and endo-PG I showed higher efficiency in juice clarification than the pectin lyase alone or the commercial pectinase widely used. These properties make endo-PG I an interesting biocatalyst for juice clarification.     

A mathematical model of inactivation kinetics for a four-strain composite of Salmonella Enteritidis and Oranienburg in commercial liquid egg yolk

The goal of this study was to develop a general model of inactivation of salmonellae in commercial liquid egg yolk for temperatures ranging from 58 °C to 66 °C by studying the inactivation kinetics of Salmonella in liquid egg yolk. Heat-resistant salmonellae (three serovars of Enteritidis [two of phage type 8 and one PT 13] and one Oranienburg) were grown to stationary phase in Tryptic Soy Broth and concentrated 10-fold by centrifugation. Each inoculum was added to liquid egg yolk and mixed thoroughly, resulting in a final population of ca. 7 log CFU/ml egg yolk. Inoculated yolk was injected into sterile glass capillary tubes, flame-sealed and heated in a water bath at 58, 60, 62, 64, and 66 °C. Capillary tubes were ethanol sanitized, rinsed, and contents were extracted. Yolk was diluted, surface plated onto Tryptic Soy Agar + 0.1% sodium pyruvate and 50 μg/ml nalidixic acid and incubated at 37 °C for 24 h before colonies were enumerated. Decimal reduction values were calculated from survivor curves with a minimum inactivation of 6 log CFU/ml at each temperature. Survival curves (except for 66 °C) featured initial lag periods before first order linear inactivation. Estimated asymptotic D-values were 1.83 min at 58 °C, 0.69 min at 60 °C, 0.26 min at 62 °C, 0.096 min at 64 °C and 0.036 min at 66 °C. The estimate of the asymptotic z-value was ca. 4.7 °C with standard error of 0.07 °C. A linear relationship between the log₁₀ of the lag times and temperature was observed. A general kinetic model of inactivation was developed. The results of the study provide information that can be used by processors to aid in producing safe pasteurized egg yolk products and for satisfying pasteurization performance standards and developing industry guidance.     

Strategy to inactivate Clostridium perfringens spores in meat products

The current study aimed to develop an inactivation strategy for Clostridium perfringens spores in meat through a combination of spore activation at low pressure (100–200 MPa, 7 min) and elevated temperature (80 °C, 10 min); spore germination at high temperatures (55, 60 or 65 °C); and inactivation of germinated spores with elevated temperatures (80 and 90 °C, 10 and 20 min) and high pressure (586 MPa, at 23 and 73 °C, 10 min). Low pressures (100–200 MPa) were insufficient to efficiently activate C. perfringens spores for germination. However, C. perfringens spores were efficiently activated with elevated temperature (80 °C, 10 min), and germinated at temperatures lethal for vegetative cells (≥55 °C) when incubated for 60 min with a mixture of l-asparagine and KCl (AK) in phosphate buffer (pH 7) and in poultry meat. Inactivation of spores (∼4 decimal reduction) in meat by elevated temperatures (80–90 °C for 20 min) required a long germination period (55 °C for 60 min). However, similar inactivation level was reached with shorter germination period (55 °C for 15 min) when spore contaminated-meat was treated with pressure-assisted thermal processing (568 MPa, 73 °C, 10 min). Therefore, the most efficient strategy to inactivate C. perfringens spores in poultry meat containing 50 mM AK consisted: (i) a primary heat treatment (80 °C, 10 min) to pasteurize and denature the meat proteins and to activate C. perfringens spores for germination; (ii) cooling of the product to 55 °C in about 20 min and further incubation at 55 °C for about 15 min for spore germination; and (iii) inactivation of germinated spores by pressure-assisted thermal processing (586 MPa at 73 °C for 10 min). Collectively, this study demonstrates the feasibility of an alternative and novel strategy to inactivate C. perfringens spores in meat products formulated with germinants specific for C. perfringens.     

Sugar metabolism and involvement of enzymes in sugarcane (Saccharum officinarum L.) stems during storage

Sugarcane (Saccharum officinarum L. cv. Badila) was harvested at the mature stage and stored at 2, 10, and 20 °C for 30, 90, and 120 days, respectively. Metabolic changes in the contents of sucrose and reducing sugar in relation to the activities of soluble acid invertase (SAI), neutral invertase (NI) and sucrose-phosphate synthase (SPS), in sugarcane juice, were studied. Extractable juice, sucrose and vitamin C declined significantly with increasing storage temperatures, while respiration rate increased. There was a rapid increase in titratable acidity during storage, with a more rapid rate at higher temperatures. A sharp increase in reducing sugar was observed within 20 days at 20 °C and 70 days at 10 °C, followed by a rapid decrease. Both SAI and NI activities showed a sharp increase within 15 days at 20 °C, followed by a rapid decrease, while a moderate increase occurred within 40–60 days at 10 °C. Slight increases were observed in SPS activity within 20 days at 20 °C and 50 days at 10 °C. Enzyme activities remained steady or underwent a small change in canes stored at 2 °C. Enzyme activities were significantly correlated with reducing sugar content.     

Bacteriocinogenic Lactobacillus plantarum ST16Pa isolated from papaya (Carica papaya) — From isolation to application: Characterization of a bacteriocin

Strain ST16PA, isolated from papaya was identified as Lactobacillus plantarum based on biochemical tests, PCR with species-specific primers and 16S rDNA sequencing. L. plantarum ST16PA produces a 6.5 kDa bacteriocin, active against different species from genera Enterobacter, Enterococcus, Lactobacillus, Pseudomonas, Streptococcus and Staphylococcus and different serotypes of Listeria spp. The peptide is inactivated by proteolytic enzymes, but not when treated with ??-amylase, catalase, lipase, Triton X-100, SDS, Tween 20, Tween 80, urea, NaCl and EDTA. However, presence of 1% Triton X-114 deactivates the bacteriocin. No change in activity was recorded after 2 h at pH values between 2.0 and 12.0, and after treatment at 100 °C for 120 min or 121 °C for 20 min. The mode of activity against Lactobacillus sakei ATCC 15521, Enterococcus faecalis ATCC 19443 and Listeria innocua 2030C was bactericidal, resulting in cell lysis and enzyme-leakage. No significant differences in cell growth and bacteriocin production were observed when strain ST16Pa was cultured in MRS broth at 26 °C and 30 °C for 24 h (25 600 AU/ml). However, even though strain ST16PA grows well in MRS broth at 15 °C and 37 °C, a reduction of bacteriocin production was observed (400 AU/ml and 1600 AU/ml, respectively). In addition, effect of MRS medium components, different initial pH and additions of glycerol or vitamins to the media on bacteriocin ST16Pa production was studied.Peptide ST16PA adsorbs (400 AU/ml) to producer cells. However, bacteriocin ST16Pa was adsorbed at 50% to cells of L. innocua 2030C and at 75% to L. sakei ATCC 15521 and E. faecalis ATCC 19433 when experiments were conducted at 30 °C and pH 6.5. Adsorption of bacteriocin ST16Pa to target cells at different temperatures, pH and in presence of potassium sorbate, sodium nitrate, sodium chloride, ascorbic acid, Tween 80 and Tween 20 were also studied. To the best of our knowledge, this is the first report on detection of L. plantarum in papaya.     

The stability of gal-polyols and oligosaccharides during pasteurization at a low pH

The aim of the work was to compare the stability of gal-xylitol and gal-sorbitol (synthesized with β-galactosidase from lactose and polyols) with the stability of lactitol, galactooligosaccharides (GOSs) and fructooligosaccharides (FOSs) in the conditions of pasteurization of juices and fruit drinks. Juice and drinks of a pH ranging from 2.7 to 4.2 were used. Pasteurization was carried out in the following variants (depending on the juice or fruit drink used): 95 °C 30 s; 95 °C 30 s+84 °C 10 or 20 min; 99 °C 30 s+88 °C 25 min. It has been shown that galactosyl derivatives of polyols demonstrate high stability in the pasteurization conditions. It is comparable to the resistance to heating that is characteristic of GOSs and lactitol. The minimum of 97% of the initial amount of gal-polyols remains in an unchanged form after thermal preservation, while FOSs are hydrolysed during pasteurization. The degree of hydrolysis of these saccharides is higher the lower the pH and the longer the pasteurization time. The pasteurization of a black currant drink (pH=3.1; 95 °C 30 s+84 °C 10 min) causes the loss of approx. 50% of tetrasaccharide and up to 30% of trisaccharides.     

Inactivation of Saccharomyces cerevisiae in conference pear with high pressure carbon dioxide and effects on pear quality

This work explores the use of high pressure carbon dioxide (HPCD) for the inactivation of Saccharomyces cerevisiae in fresh-cut conference pears. This fruit was chosen as an example of a ready to eat and minimally processed food. Assays were carried out with continuous CO₂ flow at different pressures (6–30 MPa), temperatures (25–55 °C), and exposure times (10–90 min). Heat treatments at similar temperatures and times were compared to the use of HPCD, wherein it was observed that HPCD was more effective. The total inactivation (5 log₁₀ cycles) of the yeast took place at 55 °C with HPCD while it was necessary to reach 70 °C when only heat was applied. Required pressures and exposure times were relatively low (?6 MPa and on the order of minutes) because of the direct contact between the CO₂ and the pear. The pH and °Brix were not affected by the HPCD treatment; however, the pears lost their texture and became darker due to a decrease in vitamin C and enzymatic browning. Peroxidase activity was only partially reduced. The addition of an antioxidant did not help to prevent darkening. Therefore, HPCD could be a low temperature conservation method that is superior to conventional thermal treatments for the preparation of fruit preserves where a firm texture is not essential.     

Changes in qualities of minimally processed litchis: Effect of antibrowning agents, osmo-vacuum drying and moderate vacuum packaging

Litchi fruits (litchis) are highly susceptible to pericarp browning which lowers their commercial value even though the edible portion (aril) remains in excellent condition. Therefore, minimal processing of litchis was carried out. Litchis were peeled, destoned, and arils were treated with antibrowning agents (4.9 g/kg cysteine, 20 g/kg ascorbic acid and 0.134 g/kg 4-hexyl resorcinol) along with osmo-vacuum dehydration (OVD) (502 g/kg sucrose syrup for 10 min at 570 mmHg vacuum followed by a relaxation of 10 min at atmospheric pressure) and stored at 4±2 °C. The samples were analyzed for physicochemical, sensory and microbiological qualities during storage. Changes were found to become significant (P?0.05) after 4 days of storage. During storage for 24 days, a decrease in pH, TSS (°brix), sugars (g/kg), ascorbic acid (g/kg), total phenolics (g/kg), firmness (N), color (L^* value) and sensory characteristics was observed whereas an increase in microbial counts (log cfu/g), acidity (g/kg) and drip losses (ml/kg) was observed. The combined treatment of litchis with antibrowning agents and osmo-vacuum dehydration treatment were found to be most effective in preventing the changes and the samples were acceptable (sensory score >7.0) upto 24 days, whereas the samples given only OVD treatment lost acceptability due to poor color after 16 days as compared to 8 days for the control samples (dipped in water for 10 min) during refrigerated storage.