Effects of low temperature storage and sucrose pulsing on the vase life of Lilium cv. Brindisi inflorescences

Lilium cv. Brindisi inflorescences were stored at 2.5 °C for 5, 10, 15 or 20 d, comparing dry storage with storage of the stem ends in water. Prior to storage, inflorescences were treated with 20 or 100 g L⁻¹ sucrose in water, for 20 h at 20 °C. After storage the inflorescences were individually placed in water at 20 °C. The floral buds were still closed at the end of cold storage. In experiments carried out in summer, the time to bud opening was hastened by storage at 2.5 °C in water, more so after a longer period of cold storage. The time to tepal senescence after cold storage in water decreased with the time of storage. The time to tepal abscission was about 1 day longer than the time to tepal senescence. Repeat experiments in late fall and winter additionally showed early leaf yellowing after cold storage. Compared to the experiments in summer, more desiccated floral buds were found in the fall. Pulse treatment with 100 g L⁻¹ sucrose prior to cold storage reduced the number of desiccated buds. However, leaf yellowing was aggravated by the 100 g L⁻¹ sucrose pulse treatment. Compared to cold storage in water, dry storage at 2.5 °C further hastened the time to bud opening and also further hastened tepal senescence and abscission. Dry storage also produced more buds that desiccated or opened poorly. Sucrose treatment (100 g L⁻¹) alleviated the effects of dry storage on tepal senescence and bud desiccation. The data showed that lily cv. Brindisi inflorescences are prone to chilling injury, but can be stored, depending on the treatment, for 5–10 d, during most of the year.     

Effects of heat treatment on chlorophyll degrading enzymes in stored broccoli (Brassica oleracea L.)

Effects of heat treatment on chlorophyll (Chl) degrading enzyme activities in stored broccoli (Brassica oleracea L.) were determined. Chl contents of broccoli treated at 50 °C for 1 h or without heat treatment (control) decreased after 4 days of storage at 15 °C, whereas the contents of broccoli treated at 50 °C for 2 h showed almost no change after 4 days of storage at 15 °C. Chlorophyllase activity of broccoli heat-treated for 1 or 2 h decreased during storage before the occurrence of yellowing, while the activity of the control showed a slight decrease on day 4. Chl oxidase activity of broccoli heat-treated for 2 h remained unchanged. Chl degrading peroxidase activity in the control markedly increased after 6 days of storage at 15 °C, but an increase in the activities in broccoli treated at 50 °C, especially for 2 h, was suppressed. Six anionic and two cationic isoperoxidases were detected in broccoli on day 0. One of the isoperoxidases, C₂ (Rf 0.3) cationic isoperoxidase, was involved in Chl degradation and the increase in C₂ level was greatly reduced by treatment at 50 °C for 2 h. These results indicate that heat treatment could reduce Chl degradation due to the suppression of Chl degrading enzyme activities.     

Interactive effects of ozone and 1-methylcyclopropene on decay resistance and quality of stored carrots

Fresh carrots were treated with or without 1.0 μL L⁻¹ 1-methylcyclopropene (1-MCP) at 10 °C for 16 h, and then exposed to 300 or 1000 nL L⁻¹ ozone at 10 °C for 0, 1, 2, or 4 days. The carrots were stored at 0 °C for up to 24 weeks and evaluated every 4 weeks for resistance to challenge inoculations of Botrytis cinerea and Sclerotinia sclerotiorum. Quality attributes and stress and flavor volatiles were also quantified. Decay resistance to B. cinerea was induced by treatments with 1000 nL L⁻¹ ozone for 2 or 4 days, however no lasting resistance to S. sclerotiorum was induced. Firmness was reduced in carrots treated with either 300 or 1000 nL L⁻¹ ozone for 4 days. Treatment with ozone for 1, 2, or 4 days resulted in 60–90% greater respiration rates than controls, but this effect diminished within 4 weeks of storage. Ozone treatments stimulated the production of the stress volatiles ethanol and hexanal, which were, respectively, 43- and 11-times greater than the controls immediately after a 4-day exposure to 1000 nL L⁻¹, but this effect diminished with storage time. Sucrose concentrations were reduced, but terpene concentrations were increased. Treatment with 1-MCP reduced B. cinerea resistance induced by the ozone treatments. Respiration rates, loss of sucrose, and increase in glucose and fructose during storage were also reduced by 1-MCP treatment. Treatment with 1-MCP had no effect on weight loss or firmness. In general, the concentrations of pre-storage ozone that induced resistance to B. cinerea also reduced carrot quality and therefore are not likely of commercial value.     

Response of climacteric-type guava (Psidium guajava L.) to postharvest treatment with 1-MCP

Guava (Psidium guajava L. cv. ‘Allahabad Safeda’) fruit harvested at the mature light-green stage were exposed to 300 and 600 nL L⁻¹ 1-methylcyclopropene (1-MCP) for 6, 12 and 24 h at 20 ± 1 °C, and held in either cold storage (10 °C) for 25 days or ambient conditions (25–29 °C) for 9 days. Most of the physiological and biochemical changes during storage and ripening were affected by 1-MCP in a dose dependent manner. Ethylene production and respiratory rates were significantly suppressed during storage as well as ripening under both the storage conditions depending upon 1-MCP concentration and exposure duration. 1-MCP treatment had a pronounced effect on fruit firmness changes during storage under both the conditions. The reduced changes in the soluble solids contents (SSC), titratable acidity (TA) and vitamin C content showed the effectiveness of 1-MCP in retarding fruit ripening. Vitamin C content in 1-MCP-treated fruit was significantly higher than in non-treated fruit, and those treated with 300 nL L⁻¹ 1-MCP for 6 h. The development of chilling injury symptoms was ameliorated to a greater extent in 1-MCP-treated fruit during cold storage and ripening. A significant reduction in the decay incidence of 1-MCP-treated fruit was observed under both the storage conditions. 1-MCP at 600 nL L⁻¹ for 12 h, in combination with cold storage (10 °C) seems a promising way to extend the storage life of guava cv. ‘Allahabad Safeda’ while 1-MCP at 300 nL L⁻¹ for 12 and 24 h or 600 nL L⁻¹ for 6 h, may be used to provide 4–5 days extended marketability of fruit under ambient conditions.     

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.     

Effect of 1-methylcyclopropene (1-MCP) on storage life of durian fruit

Fruit of cv. Monthong durian (Durio zibethinus) were treated with 0 (control) or 500 nL L⁻¹ 1-MCP for 12 h at 25 °C. Fruit were then stored at 15 °C. To determine storage life, every 3 days a batch of fruit was transferred to 25 °C. The time to ripeness (adequate eating quality) at 25 °C in controls (no 1-MCP) decreased from 5 days in freshly harvested fruit to 3 days after 18 days of storage at 15 °C. Storage life was considered adequate if the time to ripeness was ≥3 days. The storage life at 15 °C of control fruit (no 1-MCP) was therefore 18 days. After the 1-MCP treatment the time to ripeness at 25 °C was 7 days in fresh fruit, while in fruit stored at 15 °C for 30 days it was about 3 days. The storage life at 15 °C of 1-MCP-treated fruit was therefore 30 days. Pulp firmness and pulp total soluble solids (TSS) were determined after 3 day storage intervals at 15 °C and when the fruit was ripe at 25 °C. These parameters were only slightly affected by the 1-MCP treatment. Furthermore, 1-MCP had no effect on pulp color, but delayed yellowing of the fruit exterior. It is concluded that treatment with 1-MCP before storage at 15 °C extended storage life from 18 to 30 days.     

Effects of phosphine fumigation on postharvest quality of four Chinese cut flower species

Chrysanthemum (White, Yellow, and Daisy), carnation (Master and Barbara), rose (Carola, Black magic, Diana, Champagne, and Avalanche), and Chinese rose (Golden Medallion, Diplomat, Marina, and Athena) are the main Chinese cut flower species produced for exportation. Cut flowers infested with quarantine pests need methyl bromide (MB) fumigation to satisfy phytosanitary requirements of importing countries. Phosphine (PH₃) is a potential alternative to methyl bromide. Development of phosphine as a phytosanitary treatment requires information regarding its phytotoxicity to cut flowers. Therefore phosphine fumigation at 24 °C and 2 °C was investigated to evaluate its effects on the postharvest quality of cut flowers. Phosphine fumigation for 6 h with dosages as high as 12.2 mg L⁻¹ at 24 °C produced no adverse effects on flower color, diameter, vase life, and other damage indices (DI) for all cultivars. However, different adverse effects on some cultivars were observed after 12 d fumigation at 2 °C. There were significant changes for color values of Carola, Black magic, Diana, Champagne, Avalanche, and Diplomat; significant decrease in flower diameter and vase life of Diana, Champagne, and Avalanche at 3.04 mg L⁻¹, white Chrysanthemum and Diploma at 1.52 and 3.04 mg L⁻¹; significant increase in DI of Champagne and Avalanche at 3.04 mg L⁻¹, and White chrysanthemum, Diana, and Diploma at 1.52 and 3.04 mg L⁻¹. In combination with information on phosphine toxicity to insect pests at ambient and low temperatures in the literature, it is suggested that phosphine fumigation could be a viable replacement of MB fumigation for quarantine treatment of these four cut flower species.     

Inhibition of browning on the surface of apple slices by short term exposure to nitric oxide (NO) gas

Freshly cut slices of apple (Malus x domestica Borkh cv. Granny Smith) were fumigated with nitric oxide (NO) gas at concentrations between 1 and 500 μl l⁻¹ in air at 20 °C for up to 6 h followed by storage at 0, 5, 10 and 20 °C in air. Exposure to nitric oxide delayed the onset of browning on the apple surface with the most effective treatment being fumigation with 10 μl l⁻¹ NO for 1 h. While nitric oxide inhibited browning in slices held at all temperatures, it was relatively more effective as the storage temperature was reduced with the extension in postharvest life over the respective untreated slices increasing from about 40% at 20 °C to about 70% at 0 °C. In a smaller study on ‘Royal Gala’, ‘Golden Delicious’, ‘Sundowner’, ‘Fuji’ and ‘Red Delicious’ slices stored at 10 °C, 10 μl l⁻¹ NO for 1 h was found to be effective in inhibiting surface browning in all cultivars.     

Responses of 1-MCP application in plums stored under air and controlled atmospheres

The potential of 1-MCP for controlling ripening in ‘Angeleno’ plum fruit under air and controlled atmosphere (CA) storage was explored, and the possibility that 1-MCP can inhibit development of brown rot caused by Monilinia laxa and internal breakdown in ‘Fortune’ and ‘Angeleno’ plums tested. After harvest, fruit were exposed to 300 and 500 nl l⁻¹ (in 2003) and 500 nl l⁻¹ 1-MCP (in 2004) at low temperatures (0–3 °C) for 24 h. After treatment the plums were stored in air at 0 °C and ‘Angeleno’ fruit were also stored in CA storage (1.8% O₂ + 2.5% CO₂). Following storage, fruit were kept at 20 °C. In ‘Angeleno’ fruit, 1-MCP was effective in delaying the loss of firmness and colour changes during holding at 20 °C. 1-MCP reduced brown rot in fruit stored in CA but no significant reduction was found in air storage. Internal breakdown, a major physiological storage disorder in plums, was inhibited by 1-MCP treatment. Furthermore, since 1-MCP applied in air storage showed better results than the control in CA conditions, an application of 1-MCP before air storage could be the best way to reduce the ripening process for short or medium storage periods (40 and 60 days). CA storage plus 1-MCP treatment could be used for long periods (80 days).     

Effects of 1-methylcyclopropene on ripening of greenhouse tomatoes at three storage temperatures

Tomatoes (Lycopersicon esculentum Mill., cv. Rapsodie) were harvested at the mature green stage and treated with 250 nl l⁻¹ 1-methylcyclopropene (1-MCP) for 24 h at 20 °C. The fruit were then stored for 24 days at 15, 20 or 25 °C at 90–95% relative humidity. Sampling was carried out at 0, 6, 12, 18 and 24 days after treatment. Treatment with 1-MCP delayed ripening as measured by changes in lycopene, chlorophyll, hue angle, polygalacturonase (PG) activity and tissue firmness. Ripening was delayed by 6 days at 25 °C, by 12 days at 20 °C, and by 18 days at 15 °C in 1-MCP-treated fruit. In general, 1-MCP only delayed the onset of ripening-related changes and did not significantly alter final values for measures of firmness, color (hue angle), PG activity, and lycopene and chlorophyll contents at a particular storage temperature. The results suggest that 1-MCP is most effective at delaying ripening of mature-green tomatoes when they are stored near the currently recommended temperature range of 12.5–15 °C.     

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 cutting on ascorbic acid oxidation and recycling in fresh-cut baby spinach (Spinacia oleracea L.) leaves

Fresh-cut spinach during processing undergoes several mechanical procedures such as cutting, which may induce stress responses. These stresses may trigger the accumulation of harmful reactive oxygen species (ROS). Plants respond through a wide range of mechanisms and ascorbic acid (AsA) has an important role. The combined effect of cutting, temperature and storage time on AsA recycling route in spinach fresh-cut leaves was studied. AsA, gene expression and activities of the enzymes involved in the AsA oxidation and recycling were considered. Spinach leaves were cut in six pieces and stored at 4 °C or 20 °C. AsA content and enzymes activities were measured over six days of storage, while gene expression analyses were performed in a time-point experiment within 24 h after cutting. Results showed that AsA decreased after cutting (from 19.41 mg/100 g FW to 15 mg/100 g FW) and generally was higher in samples stored at 4 °C. After six days, AsA was 10 mg/100 g in control and 5 mg/100 g FW in cut leaves. The expression of genes and activities of the enzymes involved in the AsA oxidation and recycling route were, for some enzymes, in accordance with AsA levels. The APX (EC 1.11.1.11) activity after cutting increased up to 290 nmol AsA mg⁻¹ prot min⁻¹ compared to the control with 190 nmol AsA mg⁻¹ prot min⁻¹. AsA reduction is firstly affected by temperature and aggravated by cutting procedures. AsA represents a valuable postharvest quality indicator of freshness in spinach leaves.     

Combination of electrolysed water,UV-C and superatmospheric O2 packaging for improving fresh-cut broccoli quality

The effects of neutral electrolysed water (NEW), ultraviolet light C (UV-C) and superatmospheric O₂ packaging (HO), single or combined, on the quality of fresh-cut kailan-hybrid broccoli for 19 days at 5 °C were studied. As controls, washing with water and sanitation with NaClO were both used. Electrolyte leakage, sensory, microbial and nutritional quality changes throughout shelf-life were studied. At day 15, the combined treatments achieved lower mesophilic and psychrophilic growth compared to the single ones. Single treatments produced higher ascorbate peroxidase (APX) reductions just after its application, while superoxide dismutase (SOD) showed the opposite behaviour. After 5 days at 5 °C, a great increase of APX and guaiacol peroxidase (GPX) activity was observed, NEW + UV-C + HO and HO-including treatments achieving the highest and the lowest APX increases, respectively. UV-C-including treatments produced the highest α-linolenic acid (ALA) decreases ranging 35–38% over control contents on the processing day. NEW-including treatments greatly reduced, throughout shelf-life, ALA and stearic acid (SA) content by 27–44% and 31–61%, respectively. Total phenolic content and antioxidant capacity (1415 mg ChAE kg⁻¹ fw and 287 mg AAE kg⁻¹ fw, respectively) remained quite constant during shelf-life. In general, the treatments and their possible combinations seem to be promising techniques to preserve, or even enhance, the quality of fresh-cut kailan-hybrid broccoli and, probably, other vegetables.     

Ethylene synthesis,ripening capacity,and superficial scald inhibition in 1-MCP treated ‘d’Anjou’ pears are affected by storage temperature

A continuing challenge for commercializing 1-methylcyclopropene (1-MCP) to extend the storage life and control superficial scald of ‘d’Anjou’ pear (Pyrus communis L.) is how to initiate ripening in 1-MCP treated fruit. ‘D’Anjou’ pears harvested at commercial and late maturity were treated with 1-MCP at 0.15 μL L⁻¹ and stored either at the commercial storage temperature −1.1 °C (1-MCP@−1.1 °C), or at 1.1 °C (1-MCP@1.1 °C) or 2.2 °C (1-MCP@2.2 °C) for 8 months. Control fruit stored at −1.1 °C ripened and developed significant scald within 7 d at 20 °C following 3–5 months of storage. While 1-MCP@−1.1 °C fruit did not develop ripening capacity due to extremely low internal ethylene concentration (IEC) and ethylene production rate for 8 months, 1-MCP@1.1 °C fruit produced significant amounts of IEC during storage and developed ripening capacity with relatively low levels of scald within 7 d at 20 °C following 6–8 months of storage. 1-MCP@2.2 °C fruit lost quality quickly during storage. Compared to the control, the expression of ethylene synthesis (PcACS1, PcACO1) and signal (PcETR1, PcETR2) genes was stable at extremely low levels in 1-MCP@−1.1 °C fruit. In contrast, they increased expression after 4 or 5 months of storage in 1-MCP@1.1 °C fruit. Other genes (PcCTR1, PcACS2, PcACS4 and PcACS5) remained at very low expression regardless of fruit capacity to ripen. A storage temperature of 1.1 °C can facilitate initiation of ripening capacity in 1-MCP treated ‘d’Anjou’ pears with relatively low scald incidence following 6–8 months storage through recovering the expression of certain ethylene synthesis and signal genes.     

Postharvest ethylene conditioning as a tool to reduce quality loss of stored mature sweet oranges

Ethylene is related to senescence but also induces protective mechanisms against stress in plants. The citrus industry only applies the hormone to induce fruit degreening. The aim of this work was to determine the effect of ethylene on the quality of colored citrus fruit stored under commercial conditions to extend postharvest life, since it protects them from stress causing postharvest disorders such as chilling injury (CI) and non-chilling peel pitting (NCPP). The effect of conditioning mature Navelate and Lane Late sweet oranges (Citrus sinensis L. Osbeck) for 4 days with 2 μL L⁻¹ ethylene at 12 °C, rather than at higher temperatures used for degreening, on the quality of fruit stored at 2 or 12 °C, was examined. The ethylene conditioning (EC) treatment did not increase color but reduced calyx abscission and NCPP in fruit of both cultivars stored at 12 °C, and also CI in Navelate fruit at 2 °C. Lane Late fruit did not develop CI but showed a new disorder in EC fruit held at 2 °C. This disorder began as scalded areas around the fruit stem end and extended over the fruit surface during storage. EC had no deleterious effect on the quality of Navelate oranges stored at either 2 or 12 °C. Similar results were found in Lane Late fruit although EC slightly increased off-flavor perception at 2 °C and the maturity index at 2 and 12 °C. Moreover, EC slightly increased the content of bioactive flavonoids in the pulp of Navelate fruit but significant differences between control and EC fruit were only found after prolonged storage at 2 °C. In Lane Late fruit, EC avoided the initial decrease in flavonoid content found in control samples. Results show, therefore, that EC at 12 °C may be a tool to extend postharvest life of NCPP and CI-sensitive oranges, and that the tolerance of citrus cultivars to the combined effect of EC and non-freezing low temperature (2 °C) should be tested to select the proper storage temperature.     

Apparent synergism between the positive effects of 1-MCP and modified atmosphere on storage life of banana fruit

Fruit of cv. Gros Michel banana were treated with 1-MCP (1000 nL L⁻¹ for 4 h at 25 °C) and then packed in non-perforated polyethylene (PE) bags for modified atmosphere storage (MAP). The bags were placed in corrugated cardboard boxes and stored at 14 °C. Fruit were removed from cool storage and ripened at room temperature using ethephon. The length of storage life was determined by the change in peel color to yellow, after this ethephon treatment. Fruit treated with 1-MCP + MAP had a storage life of 100 days. The storage life of control fruit (no 1-MCP and no MAP) was 20 days. Fruit held in PE bags without 1-MCP treatment had a 40 day storage life, and the same was found in fruit treated with 1-MCP but without PE bags. 1-MCP is an inhibitor of ethylene action, but also inhibited ethylene production, mainly through inhibition of ACC oxidase activity in the peel. MAP inhibited ethylene production mainly through inhibition of ACC oxidase, both in the peel and pulp. The combination of 1-MCP treatment and MAP storage resulted in much lower ethylene production due to inhibition of both ACC synthase and ACC oxidase activity.     

Chlorophyll fluorescence for non-destructive measurement of flavonoids in broccoli

Chlorophyll fluorescence (ChlF) by excitation with two radiation beams of different wavelengths can be used for non-destructive quantitation of epidermal flavonoids in leaves. The method was tested on marketable broccoli heads, but including red light (685 nm) and green light (530 nm) in addition to ultraviolet (UV) radiation (382 nm) and blue light (450 nm) for excitation of ChlF. As a reference, the content of flavonoids was measured with high performance liquid chromatography. To induce flavonoids, postharvest treatment during 12 days with various combinations of visible and UV radiation was tried, but the achieved changes in the flavonoid levels were not statistically significant. Instead a large natural variation of flavonoid content among the broccoli heads was used to correlate it with the fluorescence data. It was possible to estimate the content of flavonoids in flower buds by means of ChlF: relative epidermal absorbance of blue light was well correlated with flavonoid content (r = 0.69, p < 0.001). For quercetin alone the correlation was higher (r = 0.77, p < 0.001). On the other hand, relative epidermal absorbance of UV radiation or green light had a much weaker correlation with flavonoid content (r ≤ 0.40, p < 0.05). Within the broccoli heads, flower buds had 15 times higher levels of flavonoids than the floret stalks, which in turn had five times higher contents than the main stem. Repeated ChlF measurements on individual broccoli heads during cold storage could monitor small but significant changes in flower buds, possibly indicating a breakdown of constituents absorbing UV and green light.     

Biopreservation of fresh-cut melon using the strain Pseudomonas graminis CPA-7

The use of biopreservation is a promising technique to ensure microbial safety of fresh-cut produce. The objective of this work was to test the effectiveness of the strain CPA-7 of Pseudomonas graminis against a cocktail of Salmonella spp. and Listeria monocytogenes on fresh-cut melon, and evaluate its effect on its quality during shelf-life when tested in conditions simulating commercial application.Fresh-cut melon was artificially inoculated with Salmonella spp. and L. monocytogenes and with or without the biopreservative strain at different concentrations and stored at 20, 10 and 5 °C. Moreover, the effect of the strain was tested in conditions simulating commercial application. Fresh-cut melon was packaged using passive modified atmosphere (MAP) and AIR conditions and stored at 5 and 10 °C. Quality of fresh-cut melon was evaluated in CPA-7 treated and untreated samples. At laboratory scale trials, P. graminis reduced Salmonella and L. monocytogenes growth on fresh-cut melon stored at 5, 10 and 20 °C. Effectiveness depended on their concentration and on storage temperature. At low pathogen concentration and 20 °C, L. monocytogenes growth was reduced between 2.1 and 5.3 log cfu g⁻¹ units after 2 days of storage and Salmonella growth between 2.0 and 7.3 log cfu g⁻¹ depending on CPA-7 dose. At 10 °C, similar reductions of pathogens were observed after 5 days of storage. In studies simulating commercial conditions, packaging atmosphere and temperature influenced P. graminis effectiveness, with better results in samples packaged under AIR conditions and 10 °C. Reduction of pathogen growth was <1-log unit in fresh-cut melon stored in MAP whilst it was >4-log units in AIR. Soluble solids content, titratable acidity, pH and firmness of fresh-cut melon were not significantly different in CPA-7 treated and untreated (control) melon. In general, lightness, chroma and hue values of fresh-cut melon stored in AIR decreased faster in CPA-7 samples than on control ones. At 5 °C, CPA-7 treated melon was visually scored lower than untreated melon. P. graminis has demonstrated promising results at 10 °C, which is a temperature more compromised for safety. Nevertheless more detailed studies on the modified atmosphere are required because AIR packaging is not recommended due to the rapid loss of quality.     

Postharvest nitric oxide fumigation delays fruit ripening and alleviates chilling injury during cold storage of Japanese plums (Prunus salicina Lindell)

We investigated the effects of nitric oxide (NO) fumigation on fruit ripening, chilling injury, and quality of Japanese plums cv. ‘Amber Jewel’. Commercially mature fruit were fumigated with 0, 5, 10, and 20 μL L⁻¹ NO gas at 20 °C for 2 h. Post-fumigation, fruit were either allowed to ripen at 21 ± 1 °C or were stored at 0 °C for 5, 6, and 7 weeks followed by ripening for 5 d at 21 ± 1 °C. NO-fumigation, irrespective of concentration applied, significantly (P ≤ 0.5) suppressed respiration and ethylene production rates during ripening at 21 ± 1 °C. At 21 ± 1 °C, the delay in ripening caused by NO-fumigation was evident from the restricted skin colour changes and retarded softening in fumigated fruit. NO treatments (10 and 20 μL L⁻¹) delayed the decrease in titratable acidity (TA) without a significant (P ≤ 0.5) effect on soluble solids concentration (SSC) during ripening. During 5, 6, and 7 weeks of storage at 0 °C, NO-fumigation was effective towards restricting changes in the ripening related parameters, skin colour, firmness, and TA. The individual sugar (fructose, glucose, sucrose, and sorbitol) profiles of NO-fumigated fruit were significantly different from those of non-fumigated fruit after cold storage and ripening at 21 ± 1 °C. CI symptoms, manifest in the form of flesh browning and translucency, were significantly lower in NO-fumigated fruit than in non-fumigated fruit after 5, 6, and 7 weeks storage followed by ripening for 5 d at 21 ± 1 °C. NO-fumigation was effective in reducing decay incidence in plums during ripening without storage and after cold storage at 0 °C for 5, 6, and 7 weeks. In conclusion, the postharvest exposure of ‘Amber Jewel’ plums to NO gas (10 μL L⁻¹) delayed ripening by 3–4 d at 21 ± 1 °C, and also alleviated chilling injury symptoms during cold storage at 0 °C for 6 weeks.