Gamma irradiation increases storability and shelf life of minimally processed ready-to-cook (RTC) ash gourd (Benincasa hispida) cubes

Radiation treatment in a dose range of 0.5–2.5 kGy in combination with low temperature storage (4–15 °C) was attempted for improvement in shelf life of ready-to-cook (RTC) ash gourd (Benincasa hispida). Parameters such as microbial load, color, firmness and sensory attributes were monitored during storage. Optimum processing conditions (2 kGy; 10 °C) resulted in improved shelf life of seven days compared to the non-irradiated controls. Total bacterial count of 1.57 × 10³ CFU/g was recorded at the end of storage period (12 d). Higher total phenolic content and total antioxidant activity was observed in irradiated samples as compared to control. Irradiated samples had total phenolic content of 103.3 ± 5.2 mg kg⁻¹ and total antioxidant activity of 384.2 ± 9.7 mg kg⁻¹ while corresponding values for control samples were 67.8 ± 5.4 and 115.5 ± 7.0 mg kg⁻¹ at the end of storage period. Irradiated samples (2 kGy) showed excellent sensory and visual qualities during entire storage period.     

Effect of 60Coγ-irradiation doses on nutrients and sensory quality of fresh walnuts during storage

Fresh Liaohe walnuts (Juglans regia cv. Liaoning4) were given ⁶⁰Coγ-irradiation doses of 0, 0.1, 0.5, 1.0 and 5.0 kGy and stored at 0 ± 1 °C for 120 d. The concentrations of fat, protein, fatty acid, soluble sugar, water and vitamin E (V_E), peroxide value (PV) and the sensory quality were determined at regular intervals during storage. Irradiation at 0.1, 1.0 and 5.0 kGy accelerated lipid oxidation, increased the PV, and decreased the sensory quality and V_E content of walnuts during storage. However, an irradiation dose of 0.5 kGy resulted in less oxidative degradation, reduced PV, and maintained a higher V_E concentration and better sensory quality of walnuts during the 90 d storage. We conclude that a dose of 0.5 kGy is the optimal dose for the preservation of fresh walnuts over a 90 d storage period.     

Efficacy of gamma irradiation for protection against postharvest insect damage and microbial contamination of adlay

This study examines the protective effects of gamma irradiation against postharvest insect damage and microbial contamination and its effect on the nutritive value of adlay (Coix lacryma-jobi L.). Adlay was treated with doses of 0–20 kGy gamma irradiation and subsequently stored at ambient temperature. The number of insects, microbial quality and chemical properties of irradiated and non-irradiated adlay were evaluated immediately after treatment and after 6 months of storage. Before irradiation, total aerobic microbial counts ranged from 5.6 × 10² to 1.4 × 10⁵ CFU g⁻¹ and the mean total number of insects was 3.2 ± 2.1 per 100 g of polished kernel. Two kilograys was the lowest dose that provided 100% insect control. A radiation-resistant bacterium, Deinococcus radiodurans RC1, was found in 2 of 10 adlay samples. Four kilograys was a sufficient dose for Enterobacteriaceae inactivation, and 6 kGy was a sufficient dose for yeast and fungi inactivation. Twenty and 8 kGy sufficed for the inactivation of all mesophilic microbes in samples with and without D. radiodurans, separately. Moreover the moisture, ash, crude fiber, crude fat, crude protein and riboflavin content all remained constant. However, 8 kGy irradiation reduced vitamin B1 concentration by 24.2%, but did not measurably reduce the amount of amino acids, except methionine and cysteine. Fatty acid contents did not alter after 8 kGy irradiation, but changes were observed after the 6 months of storage. These changes caused by irradiation were no greater than those caused by the 6-month storage. Irradiation up to 8 kGy did not markedly increase the acid value, but did increase the peroxide value to 13% of the initial value right after irradiation. However, significant changes in acid value and peroxide value were noted after 6 months of storage both in non-irradiated and post-irradiated storage samples. Additionally, 8 kGy irradiation did not significantly change the adlay appearance. The improvement in the hygiene of this vital food source compensates for the small loss of some nutritional constituents. Hence 8 kGy of gamma irradiation can be used in cold decontamination of adlay to prolong shelf-life, to improve postharvest quality, and to reduce the risk of food-borne disease.     

Effect of gamma irradiation on the physico-chemical and visual properties of mango (Mangifera indica L.), cv. ‘Dushehri’ and ‘Fazli’ stored at 20 °C

The effect of γ-irradiation doses (0.3, 0.5, 0.7, 1.0, 6.0, 10.0 kGy) on different physico-chemical and visual properties of two Indian cultivars of mango, cv. ‘Dushehri’ and ‘Fazli’ was observed during storage at 20 °C for the evaluation of delayed ripening and extension of shelf-life. Visually all the irradiated fruit showed greener peel and lighter pulp throughout the storage, however, radiation injuries were present in ‘Dushehri’ treated with 6–10 kGy and in ‘Fazli’ with 1–10 kGy. Loss of fruit due to rotting was less in the irradiated samples, treated up to 1 kGy of both the cultivars. Irradiated fruit of both the cultivars at high doses (6–10 kGy) showed increased sugar content from 0 d, however, all the treated fruit registered a slower rate of increase of sugars with storage compared to the respective controls and those treated with the lower doses of 0.5 and 0.7 kGy attained peak sugar concentration later. Significant (p ≤ 0.05) textural deterioration could be detected immediately after irradiation, in ‘Dushehri’ at doses ≥1 kGy and in ‘Fazli’ at doses ≥0.7 kGy. However, low dose treated fruit (0.3–1 kGy) of both the cultivars softened at a considerably slower rate during storage and registered significantly greater fruit firmness (compression strength) throughout the storage period. Similarly, ‘Dushehri’ treated with 0.3–0.7 kGy and Fazli treated with 0.7 kGy registered significantly greater flesh firmness (shear strength). ‘Dushehri’ treated with 0.3–1 kGy and ‘Fazli’ with 0.5–1 kGy also registered significantly harder and tougher peel, as determined by puncture test, throughout the storage. Scanning electron microscopy (SEM) performed on 3rd and 2nd d of storage of ‘Dushehri’ and ‘Fazli’ respectively, revealed microstructural breakdown at and above 1 kGy in both cultivars. Cell separation could be observed in ‘Fazli’ even at 0.7 kGy. SEM also revealed that the control fruit were in a more advanced stage of ripening than the low dose treated fruit. The study showed the feasibility of low dose γ-irradiation on ‘Dushehri’ (0.3–0.7 kGy) and ‘Fazli’ (0.5 and 0.7 kGy) that induced useful delay in ripening and extension of shelf-life by a minimum of 3 and 4 d, respectively.     

Neutral and acidic electrolyzed water as emergent sanitizers for fresh-cut mizuna baby leaves

The effects of 40, 70 or 100 mg L^?1 free chlorine neutral and acidic electrolyzed water (NEW and AEW) during the washing and disinfection step, on quality attribute changes during shelf life of fresh-cut mizuna baby leaves, were studied. Physiological, nutritional, enzymatic, sensory, and microbial changes throughout 11 days at 5 °C were monitored. Results were compared to those reached with a conventional industrial treatment of 100 mg L^?1 NaClO at pH 6.5 and with a control washing with deionised water. Both NEW and AEW showed an inhibitory effect on natural microflora growth and retained the main quality attributes. Total chlorophyll content was preserved after shelf life. Initial total phenolic contents ranged between 1868 and 2518 mg CAE kg^?1 fw for AEW 40 and AEW 100 treatments respectively and slightly increased throughout shelf life. In contrast, after shelf life the total antioxidant activity recorded on the processing day decreased around 35%. Throughout shelf life EW induced an increase in catalase activity while superoxide dismutase activity decreased. Scanning electron microscopy of the leaves showed that neither NEW nor AEW affected their surface structure. To the best of our knowledge, the effects of NEW and AEW on bioactive quality parameters, as well as on antioxidant enzyme activities for fresh-cut baby leaves are first reported here. EW provides an alternative sanitizing technique to NaClO for maintaining the quality of fresh-cut mizuna baby leaves up to 11 days at 5 °C.     

Postharvest UV-B irradiation maintains sensory qualities and enhances antioxidant capacity in tomato fruit during storage

Mature-green tomato fruit (Lycopersicon esculentum cv. Zhenfen 202) were exposed to different doses of UV-B irradiation (10, 20, 40 and 80 kJ/m²) and stored in the dark at 14 °C, 95% RH for up to 37 d. Of the four doses, 20 or 40 kJ/m² was most effective in maintaining a high level of firmness and delaying the colour development. Furthermore, 20 or 40 kJ/m² promoted the accumulation of total phenolics and total flavonoids, and enhanced antioxidant capacity during storage, though UV-B irradiation could reduce the ascorbic acid content. A dose of 10 kJ/m² had similar effects but to a lesser extent. The highest dose of 80 kJ/m² resulted in higher lycopene content, but showed negative effects on texture, colour, and other antioxidants. The optimum dose of UV-B for maintaining sensory qualities and enhancing antioxidant capacity was 20 or 40 kJ/m². These results suggest that UV-B irradiation appears to be a useful non-chemical way of maintaining postharvest quality and enhancing antioxidant capacity in tomato fruit.     

UV-C inactivation of Escherichia coli and dose uniformity on apricot fruit in a commercial setting

A UV-C treatment system (two treatment chambers connected by an inclined belt to rotate apricots between chambers) was tested in a commercial setting. Escherichia coli ATCC 25922, used as a surrogate for E. coli O157:H7 to determine the system's antimicrobial efficacy, was inoculated onto fruit surfaces at a population of 6.8 log CFU/fruit. UV-C dosage was evaluated by attaching film dosimeters to six fixed locations on each apricot. Results suggested that reduction of inoculated E. coli ATCC 25922 populations on the apricot fruit by UV-C treatment was small (only 0.5–0.7 logs). There were large variations in UV-C doses among varying apricot surface locations. Approximately 1/3 of apricots had individual surfaces receiving less than 0.2 kJ m⁻² UV-C exposure, even though fruit received, on average, more than 1 kJ m⁻². Low reductions of E. coli may be attributed, in part, to non-uniform UV-C exposure. This study demonstrates the need to use a fruit rotation device more capable of delivering uniform UV-C dosage to the surface of apricots for inactivating bacteria in a commercial setting.     

Effects of ozone treatments on microbial quality and some chemical properties of lettuce,spinach, and parsley

The effects of distilled, ozonated (12 mg L⁻¹) and chlorinated (100 mg L⁻¹) water treatments on inactivation of Escherichia coli and Listeria innocua inoculated on lettuce, spinach, and parsley and on some chemical characteristics (chlorophyll a, chlorophyll b, ascorbic acid, and total phenolic contents and antioxidant activity) of these vegetables were investigated. Chlorine and ozone washes resulted in average log reductions (±standard error) of 2.9 ± 0.1 and 2.0 ± 0.3 for E. coli in the vegetables tested, respectively, while the efficiency of ozone (2.2 ± 0.1 log) was very close to that of chlorine (2.3 ± 0.1 log) on L. innocua. Aqueous ozone did not cause any detrimental effects on the chemical characteristics of the vegetables. The effect of gaseous ozone treatment (950 μL L⁻¹, 20 min) on microbial inactivation and the chemical characteristics of parsley were also determined. This treatment resulted in 1.0–1.5 log reductions in the numbers of both microorganisms but caused significant losses in important bioactive compounds of parsley. Ascorbic acid and total phenolic contents and antioxidant activity in ozone-treated samples were 40.1, 14.4, and 41.0%, respectively, less than the control samples.     

Effects of pulsed light treatments on quality and antioxidant properties of fresh-cut mushrooms (Agaricus bisporus)

This study investigated the impact of pulsed light treatments on microbial quality, enzymatic browning, texture and antioxidant properties of fresh-cut mushrooms. The reduction of the native microflora of sliced mushrooms ranged from 0.6 to 2.2 log after 15 days of refrigerated storage by flashing at 4.8, 12 and 28 J cm⁻². Pulsed light treatments allowed extension of the microbiological shelf life of fresh-cut mushrooms by 2–3 days in comparison to untreated samples, while providing a high quality product. The use of high pulsed light fluencies (12 and 28 J cm⁻²) dramatically affected the texture of sliced mushrooms due to thermal damage induced by the treatments. Enzymatic browning was also promoted by an increase in polyphenol oxidase activity when the highest dose of pulsed light was applied. At 28 J cm⁻², phenolic compounds, vitamin C and antioxidant capacity were significantly reduced. Our results suggest that the application of pulsed light at doses of 4.8 J cm⁻² could extend the shelf life of fresh-cut mushrooms without dramatically affecting texture and antioxidant properties.     

Effect of gamma irradiation on the physico-mechanical and chemical properties of potato (Solanum tuberosum L.), cv. ‘Kufri Sindhuri’, in non-refrigerated storage conditions

The effects of γ-irradiation doses, 0.04, 0.08, 0.12 and 1 kGy, applied at two different postharvest times (5 and 30 days after harvest), were studied on the textural behaviour (puncture force, shear force, work done to puncture and shear, cohesiveness and gumminess), microstructure, reducing sugar, total sugar and tuber losses of potato (Solanum tuberosum L.), cv. ‘Kufri Sindhuri’, during storage at 22 °C (RH: 85–90%). The lowest dose (0.04 kGy) was sufficient to inhibit sprouting in potatoes exposed on day 5 but not in the tubers exposed on day 30. The irradiated, non-sprouted potatoes maintained their appearance during storage. Potatoes irradiated early appeared more sensitive to radiation-induced damage, resulting in excessive loss of tubers at 1 kGy but low doses (up to 0.12 kGy) did not increase the susceptibility of the tubers to rotting. No significant differences between reducing sugar and total sugar contents of the control and low dose irradiated tubers were observed after 120 d. High dose (1 kGy) induced blackening of the bud tissue, increased rotting percentage and poor textural quality. Increasing low doses (up to 0.12 kGy) progressively reduced the textural deterioration in the tubers during storage. The scanning electron micrographs of potatoes irradiated with 0.08–0.12 kGy showed intact cells with rigid cell walls, accounting for the higher textural values registered by the samples. Among the two treatment timings, ‘K. Sindhuri’ irradiated early after harvest (i.e., on day 5) with 0.08–0.12 kGy doses retained higher textural parameters compared to those irradiated after a delay (day 30). The study showed the potential effect of γ-irradiation for enhancing the storage life of potatoes in non-refrigerated storage.     

Effects of gamma and UV-C irradiation on the postharvest control of papaya anthracnose

Anthracnose is the main postharvest disease in papaya fruit. Today, there is considerable interest on alternative methods of control to promote resistance against pathogens and supplement or replace the use of fungicides. The goal of this work was to evaluate the effects of gamma and UV-C irradiation on Colletotrichum gloeosporioides, the causal agent of anthracnose. Mycelial growth, sporulation, and conidial germination were evaluated in vitro after fungal exposition to different irradiation doses. In the in vivo assays, ‘Golden’ papaya fruit were inoculated through subcuticular injections of a conidial suspension or mycelium discs. Next, fruit were submitted to different irradiation doses (0, 0.12, 0.25, 0.5, 0.75, and 1 kGy), using Co⁶⁰ as source, or UV-C (0, 0.2, 0.4, 0.84, 1.3, and 2.4 kJ m⁻²). To check the possibility of resistance induction by irradiation, papayas were also inoculated 24, 48, or 72 h after the treatments. The fruit were stored at 25 °C/80% RH for 7 days and evaluated for incidence and rot severity. The results showed that the 0.75 and 1 kGy doses inhibited conidial germination and mycelial growth in vitro. All doses increased fungal sporulation. The 0.75 and 1 kGy doses reduced anthracnose incidence and severity, but did not reduce them when the fruit were inoculated after irradiation. All UV-C doses inhibited conidial germination and those higher than 0.84 kJ m⁻² inhibited mycelial growth. The 0.4, 0.84, and 1.3 kJ m⁻² UV-C doses reduced fungal sporulation in vitro. There was no effect of UV-C doses and time intervals between treatment and inoculation on anthracnose control and fungal sporulation in fruit lesions. Moreover, all UV-C doses caused scald on the fruit. Thus, gamma irradiation can contribute for the reduction of postharvest losses caused by anthracnose and reduce the use or doses of fungicides on disease control.     

Irradiation of ‘Boufeggous’ dates: Effects on chemical composition during storage

Moroccan dates Phoenix dactylifera L. cv. Boufeggous were treated with 0.6, 0.9 and 1.8 kGy of gamma irradiation and subsequently stored at ambient temperatures. Chemical properties were evaluated for irradiated and non-irradiated dates immediately after the treatment, 4 and 8 months of storage. No significant changes were noted in dry matter, total lipid and protein contents. Irradiation at higher doses (0.9 and 1.8 kGy) increased titratable acidity immediately after the treatment. After 8 months of storage, the treatment increased ash and decreased amino acids. Irradiation at 0.9 kGy significantly increased glucose and total sugars contents after 8 months of storage. Fructose amounts were, however, not affected by the treatment. The increase in storage time resulted in a decrease in starch contents in both irradiated and non-irradiated dates. Pectic substances (water-, oxalate- and hydrochloride-soluble fractions) were significantly reduced by the treatment with a 27% decrease in water-soluble pectins at a dose of 1.8 kGy at the end of the storage time.     

UV-C treatment delays postharvest senescence in broccoli florets

Central broccoli heads (cv. de Cicco) were harvested and treated with UV-C light (4, 7, 10, or 14 kJ m⁻²). All treatments delayed yellowing and chlorophyll degradation at 20 °C but the irradiation dose of 10 kJ m⁻² allowed retaining the highest chlorophyll content yet had lower amounts of pheophytins than every treatment other than 7 kJ m⁻². This dose was selected to analyze the effect of UV-C on postharvest broccoli senescence at 20 °C. The UV-C treatment delayed yellowing, chlorophyll a and b degradation, and also the increase in pheophytins during storage. The activity of chlorophyll peroxidase and chlorophyllase was lower in UV-C treated broccoli. Instead, Mg-dechelatase activity increased immediately after the treatment, but after 4 and 6 d this activity was lower in UV-C treated florets than in controls. Treated broccoli also displayed lower respiration rate, total phenols and flavonoids, along with higher antioxidant capacity. The results suggest that UV-C treatments could be a useful non-chemical method to delay chlorophyll degradation, reduce tissue damage and disruption, and maintain antioxidant capacity in broccoli.     

Temperature abuse timing affects the rate of quality deterioration of commercially packaged ready-to-eat baby spinach. Part I: Sensory analysis and selected quality attributes

Temperature abuse of fresh-cut products occurs routinely during transport and retail store display. However, the stage of product shelf life during temperature abuse and its impact on sensory attributes have not been studied. This study evaluated the effect of temperature abuse occurring immediately after processing and late in shelf life through measurements of sensory attributes, and membrane integrity of commercially packaged ready-to-eat baby spinach. The packaged products were received within 2 days of processing. Samples subject to early temperature abuse were immediately placed at 1, 4, 8, 12, 16 and 20 °C storage upon arrival, and those subject to late temperature abuse were stored at 1 °C for six days, and then transferred to 4, 8, 12, 16 and 20 °C storage. Package headspace gas composition, in-package visual appeal, purchase intent, product color, off-odor, decay, texture, overall quality, and tissue electrolyte leakage were evaluated every 1–2 day up to 16 day total. Results indicate that when the product temperature is maintained at 1–4 °C, the quality of commercially packaged baby spinach can be retained for up to 18 days post-processing. However, storage temperature of 8 °C or above, significantly (P < 0.001) shortened product shelf life as exhibited by accelerated tissue electrolyte leakage, product yellowing, decay and off-odor development. Most importantly, the product's shelf life stage significantly affected its response to temperature. Quality deterioration proceeded more rapidly when temperature abuse occurred in late as opposed to early shelf life stage.     

Changes in antioxidative metabolism accompanying pitting development in stored blueberry fruit

Blueberries (Vaccinium spp. ‘LanFeng’) are harvested and consumed at maturation and have a short storage life at room temperature. Changes in blueberry quality and physiological parameters differ under room or low temperature storage conditions. The storage life of blueberries can be extended at low temperature, but pitting can develop associated with refrigeration, especially during subsequent shelf-life. The objective of this research was to understand the antioxidative metabolism accompanying pitting development of stored blueberry fruit, involving reactive oxygen species and antioxidant systems. Physiological and metabolic disorders, including low firmness, increased cell membrane electrolyte leakage and malondialdehyde (MDA) content, and changes in enzyme activity, were observed in pitting blueberries. Blueberries were stored at 20 °C and 0 °C for 10 days and 60 days, respectively. Hydrogen peroxide and superoxide radical production rate increased more rapidly during shelf-life after cold storage than at room temperature. On the other hand, blueberries during shelf-life after cold storage, when pitting occurred, had lower activity of antioxidant-related enzymes, including superoxide dismutase (SOD), catalase (CAT), and ascorbate peroxidase (APX), than those stored at room temperature. The severity of pitting was paralleled by higher cell membrane electrolyte leakage and MDA content, and lower SOD, CAT, and APX activities.     

Determination of optimal sulfur dioxide time and concentration product for postharvest control of gray mold of blueberry fruit

Highbush blueberries (Vaccinum spp.) are a major export fruit crop of Chile which is stored at 0 °C and transported to markets in Asia, Europe, and the USA, using more than 15 d of maritime transportation. Under these conditions, gray mold caused by Botrytis cinerea can produce important economic losses. The effectiveness of sulfur dioxide (SO₂) concentration × time treatments on gray mold control was determined in the laboratory and validated prior to refrigerating the fruit, using pallet scale SO₂ fumigation treatment on the following blueberry cultivars: ‘Brigitta’, ‘Legacy’, ‘Liberty’ and ‘O’Neal’. In inoculated ‘Brigitta’ and ‘Liberty’ blueberries, gray mold prevalence varied from 97.2% to 97.5% in non-treated fruit, and this value was reduced from 7.9% to 6.1% in blueberries that were exposed to a SO₂ concentration × time (Ct) product of 400 (μL L⁻¹) h. The relationship between SO₂ Ct products and gray mold prevalence under laboratory conditions was best explained by exponential models, which had a determination coefficient (R²) that ranged from 0.88 to 0.96. The estimated EC₉₀ values varied between 245 and 400 (μL L⁻¹) h, and the SO₂ Ct between 250 and 350 (μL L⁻¹) h was validated using a pallet scale application treatment to obtain the best control and minimal variation. No visual phytotoxicity symptoms of SO₂ were observed with the Ct that was tested in this study. Therefore, SO₂ fumigation was demonstrated to be an effective and practical technology for reducing the risk of blueberry gray mold decay during storage, and further effort should be given to register the use of this product for blueberries in the main Chilean export markets.     

Modified atmosphere packaging preserves quality of SO2-free ‘Superior seedless’ table grapes

‘Superior seedless’ table grapes were stored for 7 days at 0 °C followed by 4 days at 8 °C + 2 days at 20 °C under modified atmosphere packaging (MAP). Two polypropylene films (PP) were used to generate the MAP, the micro-perforated PP-30 and an oriented PP (OPP). The OPP film was applied with and without fungicide (10 μL of trans-2-hexenal or 0.4 g Na₂S₂O₅ kg⁻¹). As control a macro-perforated PP was used. PP-30 packages reached the lowest O₂ and the highest CO₂ levels. Control clusters showed the highest weight losses and decay while almost no losses occurred under MAP treatments. No changes in softness, skin and/or pulp browning, or cluster shatter were found. After shelf life MAP-treated clusters showed slight to moderate stem browning, except under SO₂ where practically no browning occurred while control clusters showed an extreme stem browning. After shelf life, MAP treatments showed good visual appearance and crunchiness, while control fruits were unmarketable. No off-flavors were detected for MAP treatments except for hexenal-treated berries. No remarkable changes for color, firmness, soluble solids content, pH, titratable acidity and maturity index were detected. Total sugars content at harvest was 200 g L⁻¹ and only slight decreases were found after shelf life for most treatments. Total organic acids content at harvest was 15.4 mg 100 mL⁻¹, which remained quite constant after cold storage and shelf life. The main phenolic compounds were flavan-3-ols (over 85% from the total content), hydroxycinnamic acid derivatives and flavonols, whose total amount at harvest was 140 mg kg⁻¹ in a fresh weight basis. After shelf life only slight decreases in total phenolics occurred in all treatments. As a main conclusion, SO₂-free MAP kept the overall quality of clusters close to that at harvest, with few differences when SO₂ was added.     

Blueberry leaf extracts incorporated chitosan coatings for preserving postharvest quality of fresh blueberries

The phenolic compounds in blueberry (Vaccinium spp.) fruit and leaf extracts (BLE) were determined based on HPLC analysis. Antimicrobial assays against Staphylococcus aureus, Listeria monocytogenes, Salmonella typhimurium and Escherichia coli, as well as fungi isolated from the rotting blueberry fruit were conducted. The effects of chitosan coating incorporating different concentrations of BLE on the quality of fresh fruit during postharvest storage at 2 ± 1 °C and 95 ± 2% relative humidity (RH) for 35 d and then at room conditions for 3 d were also investigated. Five different coating treatments were applied including 2% (w/v) chitosan coating (T1), 2% (w/v) chitosan coating containing 4% (w/v, T2), 8% (w/v, T3), or 12% (w/v, T4) BLE, and 2% (w/v) chitosan coating containing 12% BLE plus modified atmosphere packaging (MAP at 3 kPa O₂ + 12 kPa CO₂) (T5). A sample of blueberries dipped into distilled water was used as control (T0). BLE had a greater variety of phenolic compounds than fruit extracts with syringic acid the highest concentration (0.259 ± 0.003 g kg⁻¹), but the total phenolic content in BLE was lower (P < 0.05) than in fruit extracts. BLE showed good antimicrobial activity against all tested microorganisms, with a minimum inhibition concentration from 25 to 50 g L⁻¹. The 2% chitosan coating that incorporated 8% or 12% BLE showed some degree of decreasing decay rate of fruit compared with the control, and the coating with BLE plus MAP had more effective control of fruit decay. All treated samples maintained higher total phenolic content and radical scavenging activity than the control. This study suggested that chitosan coating incorporating BLE can be employed to extend shelf-life and maintain high nutritional value of fresh blueberries during postharvest storage.     

The effect of modified atmospheres on the rate of firmness change of ‘Hayward’ kiwifruit

Gas exchange rates and softening of kiwifruit (Actinidia deliciosa (A Chev) Liang et Ferguson cv Hayward) were measured during two seasons under a range of modified atmosphere (MA) conditions (0–21 kPa O₂, 0–5 kPa CO₂) at 0–10 °C to characterise their functional relationship. The kinetics of gas exchange and softening were the same for the two seasons studied.CO₂ partial pressures delayed softening but did not inhibit the rate of gas exchange. Lowering the O₂ levels to near 0 kPa did not inhibit softening completely, suggesting that the rate of softening was driven by energy provided by both oxidative and fermentative processes.An integrated modelling approach was used to link the rate of softening to the rate of gas exchange explaining 88% of the effect of MA on both the rate of gas exchange and fruit softening. Shelf life simulations showed that during storage at 0 °C, lowering O₂ or raising CO₂ gave a substantial benefit towards extending shelf life. At temperatures higher than 3 °C, the additional effect of MA was already limited.