Regulation of stony hard peach softening with ACC treatment

Controlling the rate of fruit softening in melting-flesh peaches is a primary goal of the fruit industry. Stony hard (SH) peach varieties lack the ability to synthesize 1-aminocyclopropane-1-carboxylic acid (ACC), the precursor of ethylene, which is required for fruit maturation. SH peaches thus have crisp flesh that remains firm during ripening. In this study, we developed a simple technique to stimulate fruit softening by a single spray application of ACC at a concentration of 10–20 mM, which was sufficient to allow ethylene synthesis and fruit softening. Higher concentrations of ACC increased ethylene production, and made the fruit softer. Ethylene synthesis was limited to the first 2–3 d after ACC treatment, after which fruit ceased softening and retained its remaining firmness. These results indicate that a single application of ACC solution can be used to regulate the process of fruit softening in SH peaches.     

1-MCP regulates ethylene biosynthesis and fruit softening during ripening of ‘Tegan Blue’ plum

To investigate the effects of postharvest application of 1-MCP on ethylene production and fruit softening, activities of ethylene biosynthesis and fruit softening enzymes were measured during postharvest ripening of plum (Prunus salicina Lindl. cv. Tegan Blue) fruit after being exposed to 1-MCP (0, 0.5, 1.0 or 2.0 μL L⁻¹) at 20 ± 1 °C for 24 h. Following the treatments, fruit were allowed to ripen at ambient temperature (20 ± 1 °C), and ethylene production in fruit, activities of ACS and ACO, ACC content and fruit softening enzymes (PE, EGase, exo-PG and endo-PG) in fruit skin and pulp were recorded at different intervals. Postharvest application of 1-MCP significantly delayed and suppressed the climacteric ethylene production with reduction in the activities of ethylene biosynthesis enzymes (ACS, ACO) and ACC content, and fruit softening enzymes (PE, EGase, exo-PG and endo-PG) in the skin as well as in pulp tissues. The reduction was more pronounced with increased concentrations of 1-MCP. 1-MCP treated fruit showed different rates of fruit softening and activities of ethylene biosynthesis enzymes in the skin and pulp tissues which warrant further investigation on regulation of gene expression related to these enzymes with the inhibitory effect of 1-MCP.     

Combined treatment of aminoethoxyvinylglycine (AVG) and 1-methylcyclopropene (1-MCP) reduces melting-flesh peach fruit softening

The effects of postharvest application of aminoethoxyvinylglycine (AVG) and 1-methylcyclopropene (1-MCP) on ethylene production and fruit quality, and thus on transportation and shelf-life, were evaluated in melting-flesh peaches. AVG (150 mg L⁻¹) significantly reduced ethylene production, and the effect was enhanced in combination with 1-MCP (1 μL L⁻¹). However, fruit treated with AVG alone softened to untreated control levels 2 d after harvest (DAH). Treatment with 1-MCP significantly reduced the rate of softening until 2 DAH, but the fruit rapidly softened thereafter, and reached untreated control levels by 4 DAH. A combination of AVG and 1-MCP significantly reduced fruit tissue softening throughout ripening. The effect of each chemical on flesh firmness indicated that 1-MCP affected fruit response in the early stages of ripening up to 4 DAH, and AVG significantly reduced softening in the latter stages from 4 to 9 DAH. Peaches treated with AVG and 1-MCP retained their ground color during ripening, but the effect of each chemical on color is unclear. The present study indicates that combined treatment with AVG and 1-MCP significantly delays the ripening of melting-flesh peaches.     

The addition of rosehip oil improves the beneficial effect of Aloe vera gel on delaying ripening and maintaining postharvest quality of several stonefruit

In this work Aloe vera gel (AV) alone or with the addition of 10 or 2% rosehip oil was used as fruit edible coatings in a wide range of Prunus species and cultivars: peaches (‘Roma’ and ‘B-424-16’ flat type), plums (‘Red Beauty’ and ‘Songria’), nectarine (‘Garofa’) and sweet cherry (‘Brooks’). Following treatments, fruit were stored at 20 °C for 6 days and analysed for the effect of treatments on fruit ripening and quality parameters compared with uncoated fruit (control). The addition of the rosehip oil to AV gel reduced respiration rate in all fruit, and ethylene production in the climacteric ones (peaches, plums and nectarine). In addition, all the parameters related with fruit ripening and quality, such as weight loss, softening, colour change and ripening index, were also delayed in treated compared with control fruit, the effect being generally higher when rosehip oil was added to AV, and especially in those fruit that exhibited the highest ethylene production rates (‘Roma’ and flat type peaches). Although the highest effect was obtained with AV + rosehip oil at 10%, the sensory panel detected an excess of gloss and oiliness on the fruit surface, which was considered as a negative attribute. Thus, 2% rosehip oil added to AV could be used as an innovative postharvest tool to increase the beneficial effect of AV as an edible coating, especially in climacteric fruit showing high ethylene production rates.     

Continuous microwave treatment to control postharvest brown rot in stone fruit

Monilinia spp. are the most important causes of brown rot in stone fruit and no chemical fungicides are allowed in the European Union to be applied to stone fruit after harvest. From preliminary studies, microwave (MW) treatments at 17.5 kW for 50 s and 10 kW for 95 s were selected as effective conditions to control brown rot. Both treatments were investigated to control Monilinia fructicola in fruit with different weights and maturity levels and in naturally infected fruit. Fruit weight only had a significant effect on microwave efficacy in ‘Placido’ peaches treated by MW at 10 kW for 95 s in which better brown rot control was observed in small than large fruit. Maturity level did not have a significant effect on efficacy of MW treatments in any of the varieties evaluated. When both MW treatments were studied in naturally infected peaches and nectarines, brown rot incidence was significantly reduced to less than 14% compared with untreated fruit where brown rot incidence was higher than 45%. The effect of both treatments on fruit quality was also evaluated. Fruit firmness was not negatively affected in the varieties tested and even a delay of fruit softening was observed. However, internal damage around the stone was observed, especially in the smallest fruit in which high temperature is achieved at the end of both MW treatments.     

Physiological response of ‘Larry Ann’ plums to cold storage and 1-MCP treatment

The aim of this work was to study the specific effects of low temperature and 1-MCP treatment on ethylene metabolism and oxidative behaviour in plums (Prunus × salicina cv. Larry Ann). Control fruit were stored at 20 °C or 0 °C and the 1-MCP (625 nL L^?1) treated fruit at 0 °C. Changes in the kinetics of ethylene production upon removal were related to changes in ACC metabolism (ACC and MACC levels), oxidative behaviour (H₂O₂ content) and enzymatic antioxidant potential (SOD, CAT and POX enzymes) during cold storage. Low temperature stress inhibited the synthesis of MACC, which appeared to be the basic process that regulated ACC and ethylene production at ambient temperature. Although 1-MCP treatment inhibited ethylene production and ACC accumulation in the cold, it did not inhibit the accumulation of MACC. Neither cold nor 1-MCP treatment induced oxidative stress. Nevertheless, the 1-MCP treatment significantly impaired the increase in POX activity observed during cold storage. Collectively these results showed the underlying role that ACC metabolism plays in the ripening behaviour of cold-stored plums, confirming previous results. The results also indicate that MACC and malonyl transferase activity are the key regulatory factors that control ripening and possibly some ethylene-related disorders such as chilling injury in cold-stored plums.     

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.     

Effect of ethylene concentration on quality parameters of fresh tomatoes stored using a carbon-heat hybrid ethylene scrubber

Tomato fruit were stored in cold rooms at 8 °C containing an adsorbent–catalyst device including activated carbon–1% Pd either alone or with a heater (175 °C) programmed to heat at 3 h pulse intervals. Cold rooms without the adsorbent–catalyst system were used as controls. The use of the device led to very low concentrations of both ethylene and CO₂ inside the cold rooms when compared with activated carbon–1% Pd alone or control rooms. In addition, the parameters related to ripening such as respiration rate, ethylene production, 1-aminocylcopropane-1-carboxylic acid (ACC, free and conjugated), colour changes, softening, decrease in total acidity (mainly citric and ascorbic acids) and lycopene were significantly higher in stored tomato fruit in control rooms than in those stored in cold rooms with both adsorbent–catalyst systems. The magnitude of the delay in these parameters was always significantly greater with the use of the device with respect to activated carbon–1% Pd alone. Thus, this device could be considered as a new tool to eliminate the ethylene surrounding fruit and vegetables in storage areas, avoiding the detrimental effects of ethylene action and leading to maintenance of their postharvest quality. Other additional advantages are the auto-regeneration process, when heat pulses were applied to the adsorbent–catalyst system, and the fact that it is an environmentally friendly technology.     

Effect of host and Monilinia spp. variables on the efficacy of radio frequency treatment on peaches

Brown rot caused by Monilinia spp. is the most important postharvest disease of stone fruit. Currently, no chemical fungicides are allowed in the European Union to be applied to stone fruit after harvest. In previous work, radio frequency (RF) treatment for 4.5 min applied with fruit immersed in water at 40 °C was very promising for the control brown rot on peaches and nectarines. In the present study, the efficacy of this radio frequency treatment was studied employing different infection times, inoculum concentrations, fruit maturity levels and in naturally infected fruit. Generally, infection time and maturity level of fruit did not have a significant effect on the RF treatment efficacy and brown rot incidence was significantly reduced in fruit inoculated 0, 24 or 48 h before treatment and at all maturity levels evaluated in both peaches and nectarines. RF treatment significantly reduced brown rot incidence at all inoculum concentrations evaluated (10³, 10⁴, 10⁵ and 10⁶ conidia mL⁻¹). However, in peaches, the treatment efficacy was slightly less when the inoculum concentration was increased to 10⁵ or 10⁶ conidia mL⁻¹. In naturally infected fruit, brown rot incidence was significantly reduced from 92% among control fruit to less than 26% in peaches and complete brown rot control was achieved in nectarines. RF treatment did not have an effect on fruit firmness in the varieties tested, and even a delay of fruit softening was observed. Moreover, both external and internal fruit appearance was not affected by the treatment.     

Ethanol vapor treatment maintains postharvest storage quality and inhibits internal ethylene biosynthesis during storage of oriental sweet melons

In order to evaluate the effect of ethanol vapor treatments (0.5 mL/kg and 3 mL/kg) on postharvest storage at 23 °C, quality of oriental sweet melons, and to clarify the mechanism of the inhibition of senescence, we investigated physiological and quality changes induced by ethanol vapor, decay incidence, internal ethylene concentration (IEC) and ethylene-related enzymes activities as well as gene expression. Both ethanol vapor treatments, irrespective of concentration, significantly (P < 0.5) delayed skin color changes, retarded softening and suppressed fruit decay in ethanol vapor-treated fruit. Between the two treatments, 0.5 mL/kg of ethanol vapor maintained better quality in storage than that of 3 mL/kg. Compared with the control, both ethanol vapor treatments resulted in different profiles and composition of aromatic volatile compounds of fruit during storage, and a significant increase of ethyl esters, including ethyl acetate, ethyl butanoate, ethyl hexanoate, ethyl 2-methylbutanoate, 3-(methylthio) propionate and 2-phenethyl acetate, and five new ethyl esters were also detected. Both treatments increased alcohol acyl-transferase (AAT) activity levels, which peaked earlier than in the control, but there were no significant differences in activities of alcohol dehydrogenase (ADH). Both treatments significantly (P < 0.5) suppressed internal ethylene concentrations (IEC) during storage at 23 °C, which was evident from reducing 1-aminocyclopropane-1-carboxylic acid (ACC) synthase (ACS) and ACC oxidase (ACO) activities, and inhibiting ACC biosynthesis, and the effect of the 0.5 mL/kg treatment was better than that of 3 mL/kg. Real-time quantitative PCR (Q-PCR) analysis showed that the expression patterns of CM-ACO1, CM-ACO2, CM-ACS1 and CM-ACS2 were consistent with ethylene production during storage. These results suggest that postharvest ethanol vapor treatments markedly delayed the senescence of harvested oriental sweet melons, maintained better quality in storage and improved levels of volatile aroma compounds, especially the ethyl esters, through suppressing the expression of particular members of ethylene-forming enzyme gene families as well as ethylene biosynthesis, and the effect is dose dependent.     

1-MCP controls ripening induced by impact injury on apricots by affecting SOD and POX activities

The influence of 1-MCP on the response of apricots to mechanical injury (impact) and the potential involvement of oxidative stress was investigated. Apricots (Prunus armeniaca L. cv. Marietta) picked at an early ripening (commercial harvest) stage (11–11.5 °Brix) were dropped from 30 cm onto a flat, hard surface to simulate an impact injury; fruit were treated with 500 nl 1⁻¹ 1-MCP for 20 h at 20 °C before or after the impact injury. Injured fruit showed a substantial rise in ethylene production after 4 days, while in fruit treated with 1-MCP, this increase started after 6 days, with a production rate lower than that of injured fruit. Increase in the respiration rate was delayed for 1-MCP-treated injured fruit in comparison with untreated injured ones. Tissue softening was reduced by 1-MCP treatment, showing less tissue deformability. Scanning EM analysis of injured tissue revealed healthier cells in 1-MCP treated apricots. 1-MCP-treated the increase of superoxide dismutase activity (SOD) due to mechanical injury in the first 4 days and this behaviour was related to ethylene production. Peroxidase activity (POX) increased in injured tissue immediately but then remained stable; 1-MCP, particularly when applied before the impact, increased POX activity. These results indicate that using 1-MCP can control ripening acceleration of apricots induced by mechanical injury. SOD, POX, and ethylene relationships are discussed.     

Physiology and quality response of harvested banana fruit to cold shock

Experiments were conducted to examine softening and quality responses of harvested banana fruit to cold shock treatment intended to extend shelf-life. Fruit were immersed in ice-water for 1 h, then treated with or without 100 μL L^?1 ethylene for 24 h at 24 °C, and finally stored at 20 °C. Fruit firmness, chlorophyll content, ethylene production, respiration rates, contents of pectin, starch and sugar, and the activities of the cell wall modifying enzymes polygalacturonase (PG), pectin methylesterase (PME) and CMCase (cellulase, endo-1,4-β-glucanase) were analyzed. Total amylase activity was also measured. Immersion in ice-water for 1 h effectively inhibited ripening-associated processes, including peel de-greening and pulp softening during storage or ripening. The delay in ripening was also manifest in reduced ethylene production and respiration rates. The inhibition of softening by cold shock treatment was related to decreased PG and PME activities, that is, retardation of pectin solubilization/degradation. Reduced activities of CMCase and total amylase and conversion of starch to sugar by ice-water immersion also contributed to the delay in softening of harvested banana fruit.     

Physiology of fresh-cut ‘Galia’ (Cucumis melo var. reticulatus) from ripe fruit treated with 1-methylcyclopropene

‘Galia’ (Cucumis melo var. reticulatus L. Naud. cv. Galia) fruit were harvested at the three-quarter slip stage and treated with 1 μL L⁻¹ 1-methylcyclopropene (1-MCP) at 20 °C for 24 h. The fruit were processed and stored as fresh-cut cubes and intact fruit for 10 d at 5 °C. Ethylene production of fresh-cut cubes was approximately 4–5-fold higher than intact fruit at day 1. Afterward, the ethylene production of fresh-cut cubes declined significantly whereas that of intact fruit remained relatively constant at about 0.69–1.04 ng kg⁻¹ s⁻¹. 1-MCP delayed mesocarp softening in both fresh-cut and intact fruit and the symptoms of watersoaking in fresh-cut fruit. Continuously stored fresh-cut cubes and cubes derived from intact fruit not treated with the ethylene antagonist softened 27% and 25.6%, respectively, during 10 d storage at 5 °C while cubes derived from 1-MCP-treated fruit softened 9% and 17%, respectively. Fresh-cut tissue from 1-MCP-treated fruit exhibited slightly reduced populations of both total aerobic organisms and Enterobacterium, although the differences did not appear to be sufficient to explain the differences in keeping quality between 1-MCP-treated and control fruit. Based primarily on firmness retention and reduced watersoaking, 1-MCP treatment deferred loss of physical deterioration of fresh-cut ‘Galia’ cubes at 5 °C by 2–3 d compared with controls.     

Effects of auxin and jasmonates on 1-aminocyclopropane-1-carboxylate (ACC) synthase and ACC oxidase gene expression during ripening of apple fruit

1-Aminocyclopropane-1-carboxylate (ACC) synthase and oxidase activities, their gene expression, and ethylene production in apple fruit [Malus sylvestris (L.) Mill. Var. domestica (Borkh.) Mansf.] treated with a synthetic auxin 2,4-dichlorophenoxy-propionic acid (2,4-DP) and n-propyl dihydrojasmonate (PDJ), a jasmonic acid derivative, has been investigated to clarify the action of auxin and jasmonates on ethylene production. The fruit was harvested at 103 d after full bloom (preclimacteric). The expression of MdACS4 messenger RNA (mRNA) at 48 and 96 h after treatment was higher in fruit treated with 2,4-DP than in the untreated control, but those of MdACS1 and MdACO1 were not affected by treatment. The ethylene production in 2,4-DP-treated fruit increased at 96 h after treatment. In contrast, expression of mRNAs hybridized with MdACS1 and MdACO1 probes in the skin of PDJ-treated fruit were higher than those in the untreated control. In addition, ACC synthase activity and ethylene production also increased after treatment. These results show that the ethylene production rate may differ with the kind of genes which were stimulated by auxin or jasmonates.     

Immersion of fruit in water to improve radio frequency treatment to control brown rot in stone fruit

Brown rot caused by Monilinia spp. is the most important postharvest disease of stone fruit. Currently, no chemical fungicides are allowed in the European Union to be applied to stone fruit after harvest, which has increased the need to develop alternative methods. Radio frequency (RF) treatment at 27.12 MHz with fruit immersed in water was studied to control brown rot in peaches and nectarines artificially inoculated with M. fructicola. Additionally, RF treatment in air was also investigated to evaluate the benefit of water immersion to reduce the effect of fruit size on treatment efficacy. RF treatment with fruit immersed in water at 20 °C applied for 9 min significantly reduced brown rot incidence in both peaches and nectarines and no significant differences in RF efficacy were observed depending on fruit size. However, when RF treatment was applied in air for 18 min, brown rot reduction was significantly higher in large fruit than in small fruit. Finally, the decrease in exposure time of radio frequency treatment with fruit immersed in water with increasing water temperature was also studied. Reduction of treatment time to 6 and 4.5 min was achieved by increasing water temperature at 35 and 40 °C, respectively, to control brown rot without adverse external and internal damage in both ‘Baby Gold 9’ peaches and ‘Autumn Free’ nectarines.     

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.