Expression of expansin genes during postharvest lignification and softening of ‘Luoyangqing’ and ‘Baisha’ loquat fruit under different storage conditions

Four expansin cDNA fragments, EjEXPA1, EjEXPA2, EjEXPA3 and EjEXPA4, were isolated and characterized from loquat (Eriobotrya japonica Lindl.) fruit. EjEXPA1 mRNA accumulated consistently with the increase in fruit firmness in 0 °C storage of ‘Luoyangqing’ (LYQ) fruit, where chilling injury with increased fruit firmness due to lignification was observed. EjEXPA1 mRNA levels were lower in fruit that underwent low temperature conditioning (LTC, 6 d at 5 °C then 4 d at 0 °C), and in 1-methylcyclopropene (1-MCP) treated fruit, in both cases where chilling injury was alleviated. Fruit of the ‘Baisha’ (BS) cultivar soften after harvest rather than increase in firmness, and high expression levels of EjEXPA1 and EjEXPA4 accompanied the softening of BS fruit stored at 20 °C; such mRNA accumulation was much lower when fruit were stored at 0 °C, where softening was significantly inhibited by the low temperature. Very low expression of EjEXPA2 and EjEXPA3 was observed during storage of both LYQ and BS fruit under the different storage conditions. Our results showed that of the four genes characterized, EjEXPA1 might be associated with chilling-induced lignification while both EjEXPA1 and EjEXPA4 were closely related to softening of loquat fruit during the postharvest period.     

Storage performance of Fortune mandarins following hot water dips

Commercially ripe ‘Fortune’ mandarins were dipped in water at 50 °C (Dip50), 52 °C (Dip52), 54 °C (Dip54), 56 °C (Dip56), or 58 °C (Dip58) for 3 min before storage at 6 °C for 30 days and 3 additional days at 20 °C (simulated shelf-life). Untreated fruits were used as control. Scanning electron microscopy of untreated fruit revealed rough and granular wax surface structures with a number of deep surface cracks. In contrast, fruits dipped at 50–54 °C did not exhibit similar fractures and the fruit surface appeared relatively homogeneous. Dip56 resulted in parts of the surface with no apparent epicuticular wax and zones with an accumulation of waxy deposits. With Dip58, the fruit surface appeared as if the treatment had melted and completely removed epicuticular waxes. Dip50–54 reduced chilling injury and levels of decay, both during cold storage and simulated shelf-life. Dip56–58 showed no advantages compared with untreated fruit. Neither Dip50 nor Dip52 caused adverse effects to rind surface, either during or after simulated shelf-life. Conversely, higher dip temperatures induced heat damage in the form of rind browning, the extent and number of fruits affected increasing as bath temperature increased. Water loss was consistently lower in untreated fruit. Peel water loss was consistently higher in Dip56 and Dip58 fruit. Differences in external appearance, physiological behaviour and internal quality attributes between untreated and Dip50–54 fruit were minimal. Dip56 and especially Dip58 had negative effects on the external appearance of fruits. The off-flavour found in Dip58 was probably due to increased levels of ethanol in the juice.     

Mortality of eggs and third instar larvae of Anastrepha ludens and A. obliqua with insecticidal controlled atmospheres at high temperatures

The in vitro mortality of eggs and third instar larvae of Anastrepha ludens and A. obliqua was determined after exposure to 21 treatments of air or controlled atmospheres (CA) at high temperatures and 50% RH. Air at 44°C for 160 min caused very low mortality, which increased significantly by CA. Higher temperatures caused a more rapid kill. One hundred percent mortality was achieved for third instar larvae of both species in air or CA at 48°C for 220 min. A 100% mortality of eggs of A. ludens was achieved in air at 51°C for 240 min or in CA at 52°C for 240 min, and 100% mortality of eggs of A. obliqua was achieved in air or in CA at 55°C for 240 min. A. obliqua was slightly more tolerant than A. ludens, and eggs were more tolerant than third instar larvae in both species. CA had a synergistic effect at <50°C, but was slightly less effective than air at higher temperatures. Low O₂ concentrations were more effective than high CO₂ levels. The mean estimated temperatures for 50, 99 and 99.9968% mortality (LT₅₀s, LT₉₉s, LT_99.9968s) of eggs of A. obliqua (the most tolerant) exposed to 0 kPa O₂+50 kPa CO₂ for 240 min were 49.4, 54.8 and 60.9°C, respectively. We conclude that dry hot air at ≥44°C and 50% RH in CA (0 kPa O₂+50 kPa CO₂), for 160 min or longer, is effective in increasing mortality of eggs and third instar larvae of A. ludens and A. obliqua.     

Phospholipase A2 and postharvest peel pitting in citrus fruit

The role of phospholipase A₂ (PLA₂) activity in development of postharvest peel pitting in mature ‘Fallglo’ tangerines [Bower citrus hybrid (Citrus reticulata Blanco × C. reticulata Blanco × C. paradisi Macf.) × Temple (C. reticulata Blanco × Citrus sinensis L.)] and ‘Navel’ oranges (Citrus sinensis L. Osbeck) was investigated. Changes in RH from 30% to 90% followed by fruit waxing increased electrolyte leakage and PLA₂ activity in flavedo, and induced pitting. Treatment with an aqueous dip of aristolochic acid (AT), a specific inhibitor of secretory phospholipase A₂ (sPLA₂) activity, immediately before transfer from 30% to 90% RH storage, markedly reduced peel pitting symptoms. Five genes encoding various phospholipase As isolated from citrus (three patatin-like and two sPLA₂-like sequences) differentially accumulated in healthy areas, areas with developing lesions and necrotic lesions of disordered fruit. Other PLA₂, phospholipase C, and phospholipase D inhibitors also reduced peel pitting; however, PLA₂ inhibitors were the most effective in preventing the disorder. In addition, phospholipase inhibitors promoted fruit decay, suggesting that innate resistance is impacted by phospholipase action. Together, the results provide evidence for involvement of phospholipase activity in development of postharvest peel pitting symptoms in citrus fruit.     

Chilling-induced oxidative stress and antioxidant responses in mume (Prunus mume) fruit during low temperature storage

Mume (Prunus mume Sieb. et Zucc.) fruit are harvested and consumed at the mature green stage and have a short storage life at ambient temperature. While cold temperature extends their storage life, improper refrigeration causes severe chilling injury (CI), with fruit suffering more severe CI at of 5–6 °C than at 1 °C. The objective of this research was to determine the involvement of reactive oxygen species (ROS) and antioxidant systems in fruit under chilling stress. ‘Nankou’ fruit were stored at 1 °C or 6 °C for 15 days. Hydrogen peroxide, a preventive ROS, decreased at a slower rate at 6 °C than 1 °C during storage. Malondialdehyde (MDA), an indicator of lipid peroxidation caused by ROS, increased during storage and the contents were higher in fruit stored at 6 °C than at 1 °C. On the other hand, fruit stored at 6 °C had a lower total antioxidant capacity (TAC) and lower activities of antioxidant-related enzymes including superoxide dismutase (SOD), catalase (CAT), and ascorbate peroxidase (APX) than at 1 °C. These results indicate that the fruit at 6 °C had more oxidative stress; thus the fruit had more severe CI symptoms than at 1 °C.     

Effect of high-pressure hot water washing treatment on fruit quality, insects, and disease in apples and pears: Part II. Effect on postharvest decay of d’Anjou pear fruit

A hot water pressure process (HWP) was evaluated for its effect on conidia of Penicillium expansum and on development of blue mold, gray mold, and mucor rot of d’Anjou pear fruit. Spores were removed from the water system through dilution and also as a result of hot water in the system that was lethal to the spores. When the system was heated, viable spores were not detected after 2–4 h of operation. Reductions in decay in the HWP system were 36, 29, and 13% for Botrytis cinerea, Mucor piriformis, and P. expansum, respectively. The response of P. expansum appeared related to the length of time fruit was in cold storage. Heat injury was observed on fruit treated with 40 and 50 °C water but not on fruit at 30 °C nozzle temperature. The HWP system described in this study should be considered as a component of an integrated decay control strategy.     

Effect of high-pressure hot-water washing treatment on fruit quality, insects, and disease in apples and pears: Part I. System description and the effect on fruit quality of ‘d’Anjou’ pears

A manually operated high-pressure hot-water washing system consisting of a boiler, hot-water mixing tank, contact loop, heat exchanger, spray mixing tank, high-pressure hot-water washing manifold, low-pressure fresh water rinse manifold, and pressure pump was constructed and installed in a packingline. The system developed 20–50 °C washing water at pressures up to 980 kPa. ‘d’Anjou’ pears (Pyrus communis L.), shortly after harvest, and after storage for 3 and 4 months in regular air (RA) or for 4, 7 and 8 months in controlled atmosphere (CA) at −1 °C were washed through the packingline with different wetting agents (0.1% Silwet, 0.01 and 0.1% Defoamer, and water), water pressures (regular and high-pressure (210–980 kPa)), water temperatures (control (tap water, 4–22 °C), 40 °C, and 50 °C), and brushes (soft and firm), respectively. The effect of the washing conditions on fruit quality was investigated after 1 month of storage at −1 °C to simulate shipping condition, and then again after 1 week at 20 °C to simulate marketing condition. Hot-water caused severe heat scald. When nozzle temperature was 50 °C, the incidence of heat scald increased to over 50% for the fruit stored in RA for 3 months. Combined with hot-water, 540 kPa high-pressure washing increased the incidence of friction discoloration. There were lower incidences of friction discoloration and heat scald for fruit stored in CA for 7 months, in comparison to that in RA for 3 months. However, those fruit did not ripen properly as indicated by a high extractable juice content. Fruit washed at harvest had minor incidences of friction discoloration regardless of different brushes, water pressures, and wetting agents. Fruit washed after storages in either 4 months RA or 4 or 8 months CA suffered a high incidence of friction discoloration including scuffing symptoms and pressure marking. The firm brushes caused a higher incidence of friction discoloration mainly because of scuffing symptoms. However, no differences were found between different water pressures and wetting agents with respect to friction discoloration. Fruit stored for 4 months RA suffered 26–28% friction discoloration in comparison to 16–18% in CA stored fruit with firm brush washing. Extended CA storage increased friction discoloration even with soft brush washing. The results suggest that a washing system with high-pressure spray, <30 °C warm water, wetting agent Defoamer and rotating soft brushes were significantly effective in removing surface pests and decay control without causing internal or external damage of fruit.     

Effect of high temperature stress on ethylene biosynthesis, respiration and ripening of ‘Hayward’ kiwifruit

Temperatures up to 35°C have been shown to increase ethylene production and ripening of propylene-treated kiwifruit (Stavroulakis, G., Sfakiotakis, E.M., 1993. We attempted to study the regulation by high stress temperature of the propylene induced ethylene biosynthesis and ripening in ‘Hayward’ kiwifruit. ‘Hayward’ kiwifruit were treated with 130 μl/l propylene at temperatures from 30 to 45°C up to 120 h. Ethylene biosynthesis pathway and fruit ripening were investigated. Propylene induced normal ripening of kiwifruit at 30–34°C. Fruit failed to ripe normally at 38°C and above 40°C ripening was inhibited. Propylene induced autocatalytic ethylene production after a lag period of 24 h at 30–34°C. Ethylene production was drastically reduced at 38°C and almost nil at 40°C. The 1-aminocyclopropane-1-carboxylic acid (ACC) content was similar at 30–38°C and was very low at 40°C. The 1-aminocyclopropane-1-carboxylate synthase (ACC synthase) and 1-aminocyclopropane-1-carboxylate oxidase (ACC oxidase) activities decreased with a temperature increase above 30°C, but ACC oxidase decreased at a faster rate than ACC synthase. Fruit not treated with propylene showed no ripening response or ethylene production. However, kiwifruit respiration rate increased with temperature up to 45°C, reaching the respiration peak in 10 h. At temperatures up to 38°C, propylene treatment enhanced the respiration rate. After 48 h at 45°C, fruit showed injury symptoms and a larger decrease in CO₂. The results suggest that high temperature stress inhibits ripening by inhibiting ethylene production and sensitivity while respiration proceeds until the breakdown of tissues.     

Cold quarantine responses of ‘Tarocco’ oranges to short hot water and thiabendazole postharvest dip treatments

This study investigated the effects of brief hot water and thiabendazole (TBZ) postharvest dip treatments on ultrastructural changes of fruit epicuticular wax (ECW), TBZ residues, decay development and quality traits of ‘Tarocco’ oranges [Citrus sinensis (L.) Osbek] subjected to cold quarantine, subsequent simulated transport and shelf-life. Commercially mature fruit were submerged in water at 20 °C (control fruit) or TBZ at 1000 mg/L and 20 °C for 60 s, or in hot water without or with TBZ at 300 mg/L and 53, 56, or 59 °C for 60, 30, and 15 s respectively. Following treatments, fruit were stored for 3 weeks at 1 °C (simulated quarantine conditions for fruit disinfestations against Mediterranean fruit fly, Medfly), followed by 4 days at 3 °C (simulated long distance transport), and finally kept at 20 °C for 3 days (shelf-life, SL). Scanning electron microscopy (SEM) analysis of ‘Tarocco’ orange surface showed that the typical wax platelets, lifting around edges of wax plates and areas free of epicuticular wax (ECW), that disappeared after hot water dips at 53–59 °C for 60–15 s, become visible again after storage for 21 days at 1 °C (quarantine conditions), and changes involving the appearance of rough ultrastructure, presence large curled plates, fissured wax crusts, and areas with ECW deficiencies, became much more pronounced after shelf-life. These occurrences were related to the transient effect of hot water treatment in decay control. Conversely, treatments with 300 mg/L TBZ 53 °C for 60 s or 56 °C for 30 s effectively reduced decay after quarantine. These treatments were as effective as standard treatment with 1000 mg/L TBZ at 20 °C and produced similar TBZ residue levels in fruit, without impairing fruit quality traits such as visual appearance, weight loss, compression test, sensory attributes, juice color parameters (a*, b*, h, L*, and Chroma), and juice chemical characteristics (soluble solids content, titratable acidity, ascorbic acid, glucose, sucrose, citric acid, total phenols, total anthocyanins, and total antioxidant activity).     

Effects of the yeast Pichia guilliermondii against Rhizopus nigricans on tomato fruit

The yeast Pichia guilliermondii was examined for its ability to control Rhizopus nigricans on tomato fruit during storage, and in order to highlight the reason for biocontrol, a possible mode of action is discussed. Results showed that autoclaved yeast culture and culture filtrate had no effect on controlling the postharvest disease caused by R. nigricans, although inoculation of P. guilliermondii prior to R. nigricans resulted in enhanced biocontrol efficacy. Moreover, rapid colonization of the yeast on wound sites was observed during the initial 3 days at 20 °C, and then the population stabilized for the remaining 4 days. This phenomenon indicated that at room temperature, P. guilliermondii could acclimatize itself to the environment of tomato fruit wounds and occupy the living space quickly. The results indicate that P. guilliermondii did not produce an antifungal substance, however, competition for nutrients and space on wounds appeared to play a role in the activity of the biocontrol and could be one of the mechanisms. In addition, the fruit inoculated with P. guilliermondii demonstrated changes in peroxidase (POD), polyphenoloxidase (PPO), superoxide dismutase (SOD), catalase (CAT), phenylalanine ammonia-lyase (PAL), chitinase (CHI) and β-1,3-glucanase activities, all of which were correlated with the onset of induced resistance. This result suggests that tomato fruit is capable of responding to the yeast P. guilliermondii, which could activate defensive enzymes and thereby induce host disease resistance.     

Plant oil emulsion modifies internal atmosphere, delays fruit ripening, and inhibits internal browning in Chinese pears

'Laiyang Chili’ and ‘Ya Li’ (Pyrus bertschneideri Reld) pears were treated with 3, 6, and 9% emulsions of commercial or refined (reduced -tocopherol levels) plant (soybean, corn, peanut, linseed, and cottonseed) oils at harvest an stored at 0°C for 6 months. Effects of oil treatments on ethylene production, respiration, fruit firmness, fruit color, soluble solid content (SSC), titratable acids (TA), internal browning (IB), and internal CO₂, O₂, and ethanol were studied. At the same concentration, oil treatments induced similar responses regardless of their sources or their -tocopherol concentrations. In both cultivars, ethylene production and respiration in fruit treated with 9% oils were lower in early storage and higher in late storage than that in the controls. Oils at 6% reduced IB, at 9% inhibited IB completely, and at 3% was not effective after 6 months at 0°C and 7 days at 20°C. Plant oil treatment maintained fruit color, firmness, SSC, and TA in a concentration-dependent manner during storage. In the first 4 months storage, 9% corn oil-treated fruit contained similar partial pressure of CO₂ and O₂ as the controls. After 5 months storage, oil-treated fruit contained higher partial pressure of CO₂ and lower levels of O₂ than the controls. When held at 20°C for 7 days, changes of internal CO₂ and O₂ were slower but partial pressure of CO₂ were higher, and O₂ were lower, in 9% corn oil-treated fruit than in the controls. Internal ethanol was not affected by oil treatment compared with control, either during storage or 7 days at 20°C. No off-flavor was detected in either oil-treated and control fruit by sensory evaluation.     

Extending the postharvest life of carnations with nitric oxide—comparison of fumigation and in vivo delivery

The ability of nitric oxide (NO) to extend the postharvest life at 20 °C of carnations (Dianthus caryophyllus L. cv. White-Sim) was investigated using delivery by gas-based fumigation and in vivo release via a solution containing the NO donor compound 2,2′-(hydroxynitrosohydrazino)-bisethanamine (DETA/NO). Treatment with NO gas in air at 1 and 5 μl l⁻¹ produced about a 30% increase in postharvest life while DETA/NO applied in solution at 10 mg l⁻¹ extended postharvest life by about 50% when dissolved in water. For flowers, use of solid delivery appears to offer a more convenient and more effective method of NO treatment than gaseous fumigation to extend postharvest life.     

The components of lucerne (Medicago sativa) leaf area index respond to temperature and photoperiod in a temperate environment

Irrigated crops of ‘Grasslands Kaituna’ lucerne were grown for 5 years in a temperate climate at Lincoln University, Canterbury, New Zealand (43°38′S, 172°28′E). From these the response of the components of leaf area index (LAI) to environmental factors was determined. A broken stick temperature threshold with a base temperature (T_b) of 1 °C at air temperatures (T_a) <15 °C and a T_b = 5 °C for T_a ≥ 15 was required to accumulate thermal time (Tt). Using this, the appearance of nodes on the main-stem (phyllochron) was constant in Tt within a re-growth cycle (30–42 days). The phyllochron was 37 ± 7 °Cd but declined from 60 to 37 °Cd as photoperiod decreased from 15.7 to 11.4 h. Branching began at the appearance of the fifth main-stem node with 2.5 secondary nodes produced per main-stem node in spring re-growth cycles but only 1.7 produced in summer. Leaf senescence increased from 0.3 to 1.08 leaves per main-stem node after the appearance of the ninth node. Spring re-growth cycles had a mean individual leaf area of 170 mm² compared with 400 mm² for summer re-growth cycles. These results demonstrate systematic variation in LAI components and suggest they need to be considered separately in response to environmental factors to provide a quantitative framework for crop simulation analyses of lucerne canopy development.     

The effect of delays in establishment of a static or dynamic controlled atmosphere on the quality of ‘Hass’ avocado fruit

The effect of delays of 1, 5, 10 or 15 d after harvest in establishing a static controlled atmosphere (SCA) or dynamic controlled atmosphere (DCA) on the quality of ‘Hass’ avocados (Persea americana Mill.) was investigated. Fruit were stored at 5 °C in SCA (5% O₂/5% CO₂) or DCA (<3% O₂/0.5% CO₂) for 6 weeks and compared with fruit stored in air. In addition, to determine whether increasing the CO₂ in the DCA would affect the fruit quality, DCA-stored fruit were compared with fruit held in a DCA with 5% CO₂ (DCA + CO₂) established 1 d after harvest. The quality of fruit was assessed at the end of storage and after ripening at 20 °C. DCA-stored fruit ripened in 4.6 d compared with 7.2 d for SCA-stored fruit, or 4.8 d for air-stored fruit. In addition, the incidences of stem end rot (SER), body rot (BR) and vascular browning (VB) were lower in DCA-stored fruit (35%, 29% and 29%, respectively) than in SCA-stored fruit (57%, 52% and 49%, respectively), or air-stored fruit (76%, 88% and 95%, respectively). Delaying the establishment of both SCA and DCA for 15 d resulted in significantly more advanced skin colour at the end of storage (average rating score 11.9) compared with other delay periods (4.6–5.1). There was no significant effect of delay on the time to ripen, skin colour when ripe or any ripe fruit disorder incidence. The incidence of diffuse flesh discolouration (DFD) was not only <1% when averaged over all delays but only occurred at >0.5% incidence in the 15 d delay treatment in DCA (4.8%) and not in SCA. The incidence of diffuse flesh discolouration was 62% in air-stored fruit. Inclusion of 5% CO₂ in DCA retarded fruit ripening from 4.7 to 6.9 d and increased the incidence of rots at the end of storage from 5% to 14%, and increased the incidence in ripe fruit of SER from 30% to 56% and of BR from 27% to 55%. It is concluded that fruit quality was better after CA storage than after air storage, and that DCA storage was better than SCA. The effect of DCA is to independently reduce the time to ripen after storage and the incidence of rots when ripe. Delaying the application of SCA or DCA did not affect the expression of rots, but may increase the incidence of DFD. Inclusion of CO₂ at 5% in CA retarded fruit ripening but stimulated rot expression and should not be used for CA storage of New Zealand grown ‘Hass’ avocados.     

Improved management of mango fruit though orchard and packinghouse treatments to reduce lenticel discoloration and prevent decay

Mango fruit are exposed to complex postharvest handling management, intended to improve postharvest quality retention during export shipment. Susceptibility to lenticel discoloration and to Alternaria side rots and Phomopsis stem-end rot under current handling conditions led us to re-evaluate and modify the chain of postharvest treatments, from the orchard to the packinghouse. The previously developed hot-water brushing (HWB) treatment was found effective in reducing incidence of Alternaria and stem-end rots, but it significantly induced development of red lenticels. Two factors were key to improving fruit quality, by simultaneously reducing lenticel discoloration and decay development: (a) postharvest water and/or NaOH washes in the orchard, and (b) hot-water spray (HWS) applied over rollers without brushes in the packinghouse. The present results indicate that optimal management involves combinations of water washes in the orchard with packinghouse HWS treatment; this significantly reduced the severity of lenticel discoloration by 50–60%, and the incidence and extent of postharvest side rots caused by Alternaria by 60% or more. These results indicate that appropriate handling of fruit can appreciably improve their quality during prolonged storage and shipment.     

A high temperature/low oxygen pulse improves cold storage disinfestation

Short periods of elevated temperature under controlled atmospheres (CA) effectively control insect pests. Cold treatment is also an effective non-chemical disinfestation process. If synergistic effects can be found by combining treatments, these may provide opportunities for cost reduction. Tests were performed to evaluate the tolerance of Packham's Triumph pears (Pyrus communis L.) to a range of temperatures (30–40 °C) combined with low oxygen (O₂ < 1 kPa). Treatment duration was 16–48 h and was followed by 1 month storage at 0 °C under air. When held at 30 °C, pears withstood up to 30 h of hypoxia. After cold storage, pears ripened slightly faster than controls but were undamaged. A temperature of 35 °C induced slight skin browning, and 40 °C resulted in substantial skin blackening. Some treatments were also tested on survival of lightbrown apple moth (LBAM), Epiphyas postvittana (Walker). All developmental stages were subjected to either 16 h at 30 °C, or 16 h under hypoxia, or 1 month at 0 °C, or a combination of the three treatments. With all treatments combined, all eggs, larvae and adults were killed. Only 4% of the pupae produced adults and combined treatments led to an increase in pupa mortality of 38%. A combined treatment (tolerated by pears) consisting of 30 h at 30 °C under low O₂ plus 1 month cold storage under air, killed 100% of LBAM pupae, and 100% of 5th instar larvae of both codling moth, Cydia pomonella (L.), and oriental fruit moth, Grapholita molesta (Busck). Implementation of such treatments would not require substantial investments for fruit industries equipped with CA storage facilities.     

Effects of exogenous putrescine on improving shelf life of four plum cultivars

Four plum cultivars (‘Golden Japan’, ‘Black Diamond’, ‘Black Star’ and ‘Santa Rosa’) were treated with 1 mM putrescine, and then stored at 20 °C. Storage duration was different for each cultivar, but the effect of putrescine in terms of increased shelf life, delayed ripening process, and higher quality attributes when compared with controls was significant for all cultivars. In addition, putrescine-treated plums showed delay and/or reduction on ethylene production, the intensity of reduction being dependent on the maximum of ethylene production at the climacteric peak. Also, higher fruit and flesh firmness, lower soluble solids concentration and titratable acidity evolution, reduced weight loss and delayed colour changes were found after putrescine treatment during storage. Moreover, higher putrescine and spermidine levels (free forms) were observed in putrescine-treated plums. The results revealed that plum storability could be extended by putrescine treatment due to its effect on delaying the ripening processes.     

Effect of heat treatments on gene expression and enzyme activities associated to cell wall degradation in strawberry fruit

Strawberries at white ripening stage were heat treated at 45 °C for 3 h in an air oven and then stored at 20 °C for 72 h. Firmness, activity of enzymes associated to cell wall degradation, and expression of related genes were determined during the storage. Fruit firmness decreased during the incubation time, and after 24 h of storage the heat-treated fruit softened less than the control fruit. However, after 3 days at 20 °C no differences in firmness were detected between control and heat-treated fruit. Immediately after heat treatment application, the activity of endo-1,4-β-d-glucanase (EGase), β-xylosidase and β-galactosidase decreased, while polygalacturonase activity remained at a level similar to the control fruit. However, lower activities of all these enzymes, including polygalacturonase, were detected in heat-treated fruit after 24 h at 20 °C. The enzyme activity of β-xylosidase, β-galactosidase and polygalacturonase increased after 72 h up to similar or higher values than those of controls. However, endo-1,4-β-d-glucanase activity remained lower in heat-treated samples even after 72 h at 20 °C. The expression of genes encoding endoglucanase (FaCel1), β-xylosidase (FaXyl1), polygalacturonase (FaPG1) and expansin (FaExp2) was reduced immediately after treatment and during the following 4 h, and then increased after 24 h to levels similar to or higher than those of control fruit.

Therefore, the selected treatment (45 °C, 3 h in air) effectively reduced strawberry softening and caused a temporary reduction of both the expression of above-mentioned genes and the activity of a set of enzymes involved in cell wall disassembly.     

Metschnikowia pulcherrima strain MACH1 outcompetes Botrytis cinerea, Alternaria alternata and Penicillium expansum in apples through iron depletion

A new strain of Metschnikowia pulcherrima (MACH1) was studied for its efficacy as a biocontrol agent against Botrytis cinerea, Penicillium expansum and Alternaria alternata on apples stored for 8 months at 1 °C. The results of two semi-commercial trials demonstrated the efficacy of the biocontrol strain MACH1. In order to understand the mechanism of action involved, the yeast strain was investigated for its competitive ability for iron against postharvest pathogens of apple. M. pulcherrima strain MACH1 was cultivated on PDA with different concentrations of iron (supplemented as FeCl₃) against A. alternata and B. cinerea. The yeast strain MACH1 produced a wider pigmented inhibition zone against both pathogens in low iron amendments while less inhibition was measured with increased iron concentrations. At the coloured inhibition zone, B. cinerea and A. alternata conidia did not germinate and mycelial degeneration was observed. In addition, a high reduction in infection by both pathogens was recorded in apples treated with M. pulcherrima strain MACH1 supplemented with low iron amendments compared to higher iron concentrations. The same experiments were carried out in vivo and in vitro against P. expansum. M. pulcherrima strain MACH1 amended with low iron concentration (5 μg mL⁻¹ FeCl₃), showing modest lesion diameter reduction and no effect on P. expansum under increased iron and without iron amendments. This study illustrated that iron depletion by the yeast strain MACH1 under low iron conditions could reduce the growth of some postharvest pathogens in vitro and in vivo. Although, iron depletion seems to be a primary mode of action against the postharvest pathogens studied, other mechanisms of action cannot be excluded in the biocontrol employed by M. pulcherrima strain MACH1.