Changes in antioxidant activity and postharvest quality of sweet pomegranates cv. Hicrannar under modified atmosphere packaging

The effects of different modified atmosphere packaging (MAP) on antioxidant compounds and storage quality of ‘Hicrannar’ sweet pomegranates were investigated during long term storage. Pomegranates were harvested at the commercial harvest stage and packed in two different types of MAP (MAP1 and MAP2). After packaging, all fruit were stored at 6 °C and 90–95% RH for 120 days, then removed from storage for different quality analyses. Some fruit were kept at 20 °C for 3 days to simulate a period of shelf-life. Fruit weight loss, decay index, skin color, total titratable acidity, total soluble solids content, total phenolics, total anthocyanins and antioxidant activity were determined. Internal atmospheres created by the MAP were periodically assessed during cold storage, and CO₂ concentrations increased and O₂ concentrations decreased inside the MAP. MAP significantly reduced weight loss after both 120 days of cold storage and shelf-life. MAP2 was the most effective packaging in reducing weight loss. Storage of pomegranates in MAP also reduced decay and the decay index, and maintained visual appearance compared to control fruit. During storage, a decrease in L* and C* values and an increase in h° values were observed in all treatments. However, fruit stored in MAP2 had higher L*, C* and lower h° values than in other treatments. Titratable acidity and total soluble solids decreased after cold storage and shelf-life, and no significant differences among treatments were found. Total phenolics, total anthocyanin contents and antioxidant activity increased during the storage period in control fruit.     

Effect of cold storage on vitamin C,phenolics and antioxidant activity of five orange genotypes [Citrus sinensis (L.) Osbeck]

The effect of cold storage on antioxidant profile and the antioxidant activity of five sweet orange genotypes [Citrus sinensis (L.) Osbeck], three blood (pigmented) varieties with different anthocyanin contents (‘Tarocco Messina’, ‘Tarocco Meli’ and ‘Moro’) and two blond varieties (‘Ovale’ and ‘Valencia late’), stored at 6 ± 1 °C for 65 d was investigated. During fruit storage, anthocyanins, hydroxycinnamic acids, vitamin C, flavanones and total phenolics were determined, and juice antioxidant capacity was measured by two different in vitro tests (DPPH scavenging activity and inhibition of induced linoleic acid peroxidation). The results showed an increase in anthocyanins, flavanones and hydroxycinnamic acids and a slight decrease in vitamin C in the blood oranges. Cold storage negatively affected flavanone concentration, while positively influenced vitamin C in blond orange varieties. Both antioxidant activity tests showed an increase in antioxidant capacity during storage caused mainly by phenolic accumulation (blood oranges) and vitamin C increase (blond oranges). Finally, correlations between antioxidant activity and total or individual phenolic components were examined.     

Controlled atmosphere treatment for control of grape mealybug,Pseudococcus maritimus (Ehrhorn) (Hemiptera: Pseudococcidae), on harvested table grapes

Controlled atmosphere (CA) treatments with ultralow oxygen (ULO) alone and in combinations with 50% carbon dioxide were studied to control grape mealybug, Pseudococcus maritimus (Ehrhorn) on harvested table grapes. Two ultralow oxygen levels, 30 and <0.01 μL L⁻¹, were tested in both ULO and ULO + 50% CO₂ treatments. The ULO treatments with the lower oxygen level were more effective than the ULO treatments at the higher oxygen level. The ULO + 50% CO₂ treatments were more effective than the ULO treatments. Grape mealybug eggs were significantly more tolerant of ULO and ULO + CO₂ treatments than nymphs and adults. A 14 day ULO treatment with 30 μL L⁻¹ O₂ at 2 °C did not achieve 100% mortalities of any life stage. In the presence of 50% CO₂, the 14 d treatment achieved complete mortality of all life stages of the grape mealybug. A 3 d ULO treatment with <0.01 μL L⁻¹ O₂ at 2 °C resulted in 93.3% mortality of nymphs and adults. The 3 d ULO treatment in combination with 50% CO₂ treatments, however, achieved complete control of grape mealybug nymphs and adults and caused 70.5% relative egg mortality. Complete egg mortality was achieved in a 10 d ULO + 50% CO₂ treatment with <0.01 μL L⁻¹ O₂ at 2 °C. Both the 14 d CA treatment with 30 μL L⁻¹ O₂ and 50% CO₂ and the 10 d CA treatment with <0.01 μL L⁻¹ O₂ and 50% CO₂ were tested on table grapes and grape quality was evaluated after two weeks of post-treatment storage. The CA treatments did not have a significant negative impact on grape quality and were safe for table grapes. The study indicated that CA treatments have potential to be developed for postharvest control of grape mealybug on harvested table grapes.     

Molecular analysis of the improvement in rachis quality by high CO2 levels in table grapes stored at low temperature

Rachis browning is one of the main factors reducing the quality of table grapes during storage at low temperature. To better understand the effect of a 3-day CO₂ pretreatment (20% CO₂ plus 20% O₂) on maintaining the rachis quality of table grapes (Vitis vinifera cv. Cardinal) at 0 °C, we analyzed the expression of genes codifying enzymes related to the synthesis and oxidation of phenolic compounds (phenylalanine ammonia-lyase, VcPAL; and polyphenol oxidase, GPO) and the detoxification of reactive oxygen species (catalase, GCAT; and ascorbate peroxidase, VcAPX) in rachis of treated and non-treated bunches. Furthermore, due to their role in senescence, the implication of ethylene and abscisic acid (ABA) was also investigated by studying the expression pattern of key regulatory genes for these hormones such as ACC synthase (ACS1) and oxidase (ACO1), VvNCED1 and 2. To determine whether these changes in gene expression were specifically related to rachis deterioration, their expression pattern in pulp and skin of treated and non-treated grapes were evaluated. The appearance of browning in non-treated rachis was associated with an increase in GPO and VcPAL mRNA levels, whereas high CO₂ levels arrested this accumulation. In pulp, even though browning was not evident, a slight increase in GPO1 mRNA accumulation in non-treated bunches was detected. Moreover, lipid peroxidation level revealed lower oxidative stress in rachis of CO₂-treated bunches than in non-treated ones, which seemed to be regulated by VcAPX and GCAT gene expression induction. This regulation was specific to rachis, showing a different pattern in pulp and skin. Regarding phytohormones, the effect of high CO₂ levels reducing rachis browning seems to be linked to the modulation of ethylene biosynthesis genes. On the other hand, neither VvNCED1 nor VvNCED2 expression levels were altered in rachis, but NCED1 was induced specifically by low temperature in pulp. Overall, our results suggest a specific response of rachis to high levels of CO₂ that could be related to the mitigation of rachis browning.     

Aloe vera gel coating maintains quality and safety of ready-to-eat pomegranate arils

Several postharvest treatments were performed on pomegranate arils prior to storage in rigid polypropylene boxes for 12 days at 3 °C: water (control), ascorbic + citric acids (at 0.5 or 1%), Aloe vera gel (at 50 or 100%), 50% A. vera gel + 0.5% ascorbic and 0.5% citric acid, and 100% A. vera gel + 1% ascorbic and 1% citric acid. A. vera (alone or in combination with acids) led to lower CO₂ and higher O₂ concentrations inside the packages compared with arils treated with water (control). With respect to quality attributes, A. vera coatings led to firmness retention and increased levels of total anthocyanins and total phenolics. In addition, A. vera treatments led to significantly lower counts for both mesophilic aerobics and yeast and moulds. Sensory analysis scores for flavour, texture, aroma, colour and purchase decision were higher in arils treated with A. vera, especially in those arils treated with 100% A. vera + 1% ascorbic and citric acids. Finally, no off-flavours in pomegranate arils were perceived by judges as a consequence of A. vera gel treatment.     

Individual anthocyanins and their contribution to total antioxidant capacity in response to low temperature and high CO2 in stored Cardinal table grapes

In this study, we have analyzed the profiles of individual anthocyanins in the skin of Cardinal table grapes and their contribution to the total antioxidant capacity (TAC) in response to low temperature (0 °C) and high CO₂ levels (20% for 3 days). An analysis of the representative colour parameters of this red-violet variety was also determined. The anthocyanin composition was determined using high-performance liquid chromatography coupled to diode array detector and mass spectrometry (HPLC–DAD–MS). The contribution of individual anthocyanins to the TAC value of table grapes was calculated on the basis of their concentration and antioxidant capacity measured as the TEAC value (slope of the anthocyanin/slope of Trolox). Chromatographic analysis identified six anthocyanins, including pelargonidin 3-glucoside (Pg-3-G), in the skin of Cardinal table grapes. Short-term storage at 0 °C in air had an increasing effect on the concentration of each of the identified anthocyanins. After 3 days at 0 °C, untreated grapes had the highest anthocyanin content (27.55 mg/100 g FW) and displayed the largest TAC value (52.45 mM TE/100 g FW). Peonidin 3-glucoside (Pn-3-G) was the predominant anthocyanin, and it was mainly responsible for the rise in the calculated TAC value in untreated grapes. Pn-3-G had a low average TEAC value (1.73 mM), but its contribution could be explained by the sharp increase in the content of this anthocyanin the first days of storage at 0 °C. In contrast, the Pn-3-G content in grapes at the end of the 3-day CO₂ treatment did not change, and both the total anthocyanin content and the calculated TAC value remained significantly constant in comparison to the levels in pre-stored grapes. In addition CO₂ treatment had a positive effect on the amount of Pg-3-G concomitant with a pronounced decline in delphinidin 3-glucoside (Dp-3-G) and smaller decreases in petunidin 3-glucoside (Pt-3-G) and malvidin 3-glucoside (Mv-3-G). These effects of high CO₂ levels on the profile of individual anthocyanins were progressively lost when grapes were transferred to air. Indeed, after prolonged low-temperature storage when the colour of the berries become dark violet, similar calculated TAC values were quantified in untreated grapes and in those exposed to 20% CO₂. These data provide new insights about the effect of low temperature and high CO₂ levels on the concentration of the individual anthocyanins identified in cardinal table grapes.     

Inheritance of anthocyanin content in the ripe berries of a tetraploid × diploid grape cross population

Variation patterns and inheritance of anthocyanin content in the ripe berries of a tetraploid × diploid table grape cross population were investigated in two successive years. The population segregated for three different ploid levels: dipolids, triploids, and tetraploids. A total of 28 different anthocyanins were detected and quantified in the progeny population. Transgressive segregation for the total anthocyanin content was observed in all the three ploid progeny populations. The total anthocyanin content increased as the ploid level increased. The broad sense heritabilities (H²) of the total anthocyanin content were all relatively high, ranging from 0.53 to 0.98, 0.57 to 0.97 and 0.43 to 0.94 in the diploid, triploid and tetraploid population, respectively. Our results suggested that the total anthocyanin content followed an additive inheritance model in this polyploid segregation population. We also observed that the relative contribution of individual anthocyanins to the total anthocyanin content varied significantly among different ploid populations, suggesting that genetic background has important impact on the accumulation of the individual anthocyanin compounds. These results will help develop better breeding strategies in a polyploid table grape breeding program for improving the content of anthocyanins, an important class of polyphenolics possessing antioxidant activities and many other health-related benefits.     

Changes in bioactive compounds and response to postharvest storage conditions in purple eggplants as affected by fruit developmental stage

Fruit maturity stage at harvest influences the response to postharvest storage conditions and bioactive compounds content. In this work fruit from two purple eggplant cultivars (Monarca and Perla Negra) were harvested at 12, 15, 18, 20 and 23 d after fruit set (designated as stages I through V) and changes in size, dry weight, calyx area, cell wall material (AIR, alcohol insoluble residue), firmness, respiration, and antioxidants (peel anthocyanins and pulp carotenoids, ascorbic acid, phenolics and chlorogenic acid) were determined. In a second set of experiments the postharvest performance of fruit harvested at stages I (“baby” eggplants), III and IV (traditional harvest stages) during storage at 0 or 10 °C was assessed. Fruit growth continued until late ripening in contrast to calyx expansion and peel anthocyanin accumulation, which were relatively earlier events. Fruit dry weight decreased between stages I and III, remaining constant afterwards. “Baby” eggplants had higher antioxidant capacity, chlorogenic acid (ChA), carotenoids and ascorbic acid contents than late-harvested fruit. ChA predominated in pulp placental tissues at stage I, spreading throughout the fruit core at as ripening progressed. No marked differences in dry mass, antioxidant capacity or responses to postharvest storage regimes were found between fruit harvested at stages III and IV. Late pickings increased yields and led to less dense fruit, which had lower respiration rates. Within this harvest window, storage at 10 °C maximized quality maintenance. In contrast “baby” eggplants stored better at 0 °C. Understanding the developmental changes in bioactive compounds and postharvest performance may help in the maximization of fruit antioxidant properties as well as in the selection of the optimal handling conditions for each ontogenic stage.     

Prestorage application of high carbon dioxide combined with controlled atmosphere storage as a dual approach to control Botrytis cinerea in organic ‘Flame Seedless’ and ‘Crimson Seedless’ table grapes

Pre-storage application of 40% CO₂ at 0 °C for 24 or 48 h and controlled atmosphere (12% O₂ + 12% CO₂) storage at 0 °C for up to eight weeks on decay control and quality of organic ‘Flame Seedless’ and ‘Crimson Seedless’ table grapes were studied as a postharvest disease control alternative. To simulate different potential field conditions, these organic treatments were applied to organic-grown grapes that were naturally infected (without inoculation), surface inoculated (berries inoculated by spraying with a conidia suspension), and nesting inoculated (clusters inoculated by placing in the middle an artificially infected berry) with the pathogen Botrytis cinerea, the cause of grape gray mold. Under these three conditions, a 40% CO₂ for 48 h pre-storage treatment followed by controlled atmosphere reduced the gray mold incidence from 22% to 0.6% and from 100% to 7.4% after four and seven weeks, respectively. High CO₂ pre-storage alone limited botrytis incidence in both naturally and artificially infected grapes, but was more effective when combined with CA. These treatments did not affect visual or sensory fruit quality. Exposure to high CO₂ for 24 or 48 h effectively inhibited mycelial growth of B. cinerea in PDA plates incubated at 22 °C for up to 72 h. Conidia germination in PDA plates was reduced ∼60% after 12 h incubation. In vitro studies demonstrated a fungistatic effect, but further studies on the mechanism of action could improve treatment performance. This novel high CO₂ initial fumigation followed by controlled atmosphere during storage or transportation could be a commercially feasible alternative for postharvest handling of organic and conventional table grapes. Our results encourage validating this combined physical treatment in other cultivars and under commercial conditions.     

Edible coatings containing chitosan and moderate modified atmospheres maintain quality and enhance phytochemicals of carrot sticks

Carrot sticks are increasingly in demand as ready-to-eat products, with a major quality problem in the development of white discoloration. Modified atmosphere packaging (MAP) and edible coating have been proposed as postharvest treatments to maintain quality and prolong shelf-life. The combined application of an edible coating containing 5 mL L^?1 of chitosan under two different MAP conditions (10 kPa O₂ + 10 kPa CO₂ in Pack A and 2 kPa O₂ + 15–25 kPa CO₂ in Pack B) over 12 d at 4 °C was studied. Respiration rate, microbial and sensory qualities as well as the contents of vitamin C, carotenoids and phenolics of coated and uncoated carrot sticks were evaluated. The use of the edible coating containing chitosan preserved the overall visual quality and reduced surface whiteness during storage. Microbial populations were very low and not influenced by coating or MAP. Edible coating increased respiration rates of carrot sticks, although this was only noticeable in the package with the less permeable film (Pack B). Vitamin C and carotenoids decreased during storage particularly in coated carrot sticks. In contrast, the content of total phenolics markedly increased in coated carrot sticks stored under moderate O₂ and CO₂ levels, while it was controlled under low O₂ and high CO₂ levels. The combined application of edible coating containing chitosan and moderate O₂ and CO₂ levels maintained quality and enhanced phenolic content in carrot sticks.     

Preharvest application of abscisic acid promotes anthocyanins accumulation in pericarp of litchi fruit without adversely affecting postharvest quality

Pericarp colour of litchi fruit is an important quality attribute that determines its market value and consumer acceptance. Plant growth regulators (PGR) such as abscisic acid (ABA) and ethephon are known to play important roles in peel colour development during maturation and ripening of non-climacteric fruits (e.g. grape and litchi). Our aim was to investigate the effects of preharvest application of ABA, ethephon and their combination on pericarp colour and fruit quality of litchi (cv. Calcuttia) and also to assess the potential effects on postharvest performance of fruit. Exogenous application of ABA (150 or 300 mg L⁻¹) at the colour-break stage significantly increased the concentration of total anthocyanins and cyanidin-3-O-rutinoside, the major anthocyanin contributing ∼71–96% of the total anthocyanins, in litchi pericarp compared to ethephon (500 μL L⁻¹). Among different anthocyanins quantified, the relative contribution of cyanidin-3,5-diglucoside to the total anthocyanins was significantly higher in all PGR-treated fruit compared to the control, but the concentration of cyanidin-3-O-glucoside was specifically enhanced by ABA. No significant effect on the concentrations of epicatechin, and quercetin-3-O-rutinoside was observed in response to PGR treatments. Ethephon (500 μL L⁻¹) treatment did not significantly increase the anthocyanin levels in pericarp, but it caused more degradation of chlorophyll pigments than control. Aril quality with regard to firmness, soluble solids and acidity was not significantly affected by PGR treatments, except that ethephon-treated fruit showed significant softening and lower acidity. Postharvest changes in fruit quality attributes including pericarp browning during cold storage at 5 °C for 14 d were mainly related to the storage duration effect, rather than PGR treatment. In conclusion, ABA treatment (150 or 300 mg L⁻¹) at the colour-break stage enhanced anthocyanins accumulation in litchi pericarp without adversely affecting postharvest quality and storage stability for 14 d.     

Changes in hydrophilic and lipophilic antioxidant activity and related bioactive compounds during postharvest storage of yellow and purple plum cultivars

Eight plum cultivars (four dark-purple and four yellow) were harvested at the commercial ripening stage, and changes of fruit quality properties were evaluated during cold storage and subsequent shelf-life, with special emphasis on bioactive compounds (phenolics, anthocyanins and carotenoids) and antioxidant activity (TAA). From the eight plum cultivars, four showed the typical climacteric ripening pattern (‘Blackamber’, ‘Larry Ann’, ‘Golden Globe’ and ‘Songold’) while four behaved as suppressed-climacteric types (‘Golden Japan’ ‘Angeleno’, Black Diamond’ and ‘TC Sun’), the latter being described for the first time. At harvest, large variations in phytochemicals and antioxidant activity were found among cultivars in peel and pulp tissues, although phytochemical concentration and antioxidant activity were higher in the peel than in the flesh (2–40-fold depending on the bioactive compound). During storage, increases in total phenolics for all cultivars (peel and pulp), in total anthocyanin content in the peel of the dark-purple plums, and total carotenoids in the peel and pulp of the yellow cultivars were observed. This behaviour of the bioactive compounds was reflected in TAA changes, since hydrophilic-TAA (H-TAA) was correlated with both phenolics and anthocyanins, while lipophilic-TAA (L-TAA) was correlated with carotenoids. L-TAA comprised about 30–50% of the TAA in plum tissues. Carotenoids and phenolics (and among them the anthocyanins) could be the main lipophilic and hydrophilic compounds contributing to L-TAA and H-TAA, respectively. No significant loss of bioactive compounds and TAA occurred during prolonged plum storage. Moreover, for a better evaluation of the antioxidant potential of plums, the contribution to carotenoids should not be overlooked.     

Influence of UV-C treatment on antioxidant capacity,antioxidant enzyme activity and texture of postharvest shiitake (Lentinus edodes) mushrooms during storage

Shiitake (Lentinus edodes) mushrooms were exposed to UV-C light (4 kJ/m²) and stored in modified atmosphere packaging (MAP) prior to 15 days at 1 ± 1 °C and 95% relative humidity plus 3 days at 20 °C. Mushroom firmness, total phenolics, total flavonoids, ascorbic acid and H₂O₂ contents, superoxide anion (O₂⁻) production rate and activities of catalase (CAT), superoxide dismutase (SOD), ascorbate peroxidase (APX) and glutathione reductase (GR) were measured. UV-C treatment resulted in maintenance of a high level of firmness during 15 days at low temperature and reduced the decrease in firmness during shelf-life storage. Furthermore, treated samples showed higher total flavonoids, ascorbic acid, and delayed the increases in both O₂⁻ production rate and H₂O₂ contents. However, no clear treatment effects were seen in total phenolics contents. The treatment also increased the antioxidant enzyme activities of CAT, SOD, APX and GR throughout the storage period. These results indicate that postharvest application of UV-C radiation can delay softening and enhance antioxidant capacity in shiitake mushrooms.     

Reduction of gray mold development in table grapes by preharvest sprays with ethanol and calcium chloride

Preharvest applications of a 16% ethanol (EtOH) solution, containing 1% CaCl₂, reduced gray mold development in ‘Chasselas’ table grapes picked at a late harvest date. The losses due to rotten clusters dropped from 15% in controls to 5% in grapes treated with EtOH + CaCl₂. Over 6 weeks cold storage, the losses due to gray mold rots were reduced by 50% in EtOH + CaCl₂ treated clusters, compared to untreated controls. Preliminary experiments had shown that a 2% EtOH solution was already inducing a significant reduction in gray mold growth. A range of concentrations up to 50% ethanol had been tested in preliminary trials without observing damage to the vines and clusters. The treatments did not induce significant changes in fruit quality assessed by sensory analysis of healthy berries.     

Application of abscisic acid (ABA) at veraison advanced red color development and maintained postharvest quality of ‘Crimson Seedless’ grapes

‘Crimson Seedless’ is a popular table grape cultivar, but in warm-climates, its fruits often fail to develop adequate red color, even after they have been treated with ethephon. Application of abscisic acid (ABA) may improve color more effectively than ethephon, but its potential effects on postharvest quality must be considered before recommending its use on table grapes. Therefore, we compared the postharvest quality attributes of grapes treated preharvest with 250 μL L⁻¹ ethephon, the current industry standard, to that of grapes treated with 150 or 300 μL L⁻¹ ABA, or nontreated. Treatment with either ethephon or 150 μL L⁻¹ ABA allowed grapes to be harvested 10 d before nontreated fruit, and fruits treated with 300 μL L⁻¹ ABA attained marketable quality 30 d before nontreated fruit. Early harvest was possible because the treatments induced more rapid coloring of the grapes, and though total yield was not affected by any plant growth regulator (PGR), all PGRs doubled packable yields by improving the color of the grapes. ABA-treated grapes were characterized by superior appearance both in berries and clusters’ rachises compared to ethephon-treated and control grapes. Other quality attributes such as firmness, berry weight, decay incidence, and shatter remained unaffected among treatments. Therefore, ABA is an effective alternative to ethephon for enhancing the color and maintaining postharvest quality of ‘Crimson Seedless’ grapes.     

Physicochemical measurements in ‘Mondial Gala’ apples stored at different atmospheres: Influence on consumer acceptability

Standard quality parameters, consumer acceptability, emission of volatile compounds and ethylene production of ‘Mondial Gala^®’ apples (Malus × domestica Borkh.) were determined in relation to storage atmosphere, storage period and shelf-life period. Fruit were harvested at the commercial date and stored in AIR (21 kPa O₂:0.03 kPa CO₂) or under three different controlled atmospheres (CAs): LO (2 kPa O₂:2 kPa CO₂), ULO1 (1 kPa O₂:1 kPa CO₂), or ULO2 (1 kPa O₂:2 kPa CO₂). Fruit samples were analysed after 12 and 26 weeks of storage plus 1 or 7 d at 20 °C.Apples stored in CA maintained better standard quality parameters than AIR-stored fruit. The volatile compounds that contributed most to the characteristic aroma of ‘Mondial Gala^®’ apples after storage were butyl, hexyl and 2-methylbutyl acetate, hexyl propanoate, ethyl butanoate, ethyl hexanoate, ethyl, butyl and hexyl 2-methylbutanoate. Data obtained from fruit analysis were subjected to principal component analysis (PCA). The apples most accepted by consumers showed the highest emission of ethyl 2-methylbutanoate, ethyl hexanoate, tert-butyl propanoate and ethyl acetate, in addition to the highest titratable acidity and firmness values.     

Influence of the combination of different atmospheres on diphenylamine,folpet and imazalil content in cold-stored ‘Pink Lady®’ apples

‘Pink Lady^®’ apples were harvested at commercial maturity, treated with three different agrochemical products, and stored at 1 °C under either air or controlled atmosphere conditions (2 kPa O₂ + 2 kPa CO₂ and 1 kPa O₂ + 1 kPa CO₂) for 13 and 27 weeks, followed by 4 weeks storage in air at 1 °C. Diphenylamine, folpet and imazalil contents in both the skin and flesh were simultaneously determined after cold storage plus simulated marketing periods of 1 and 7 d at 20 °C. After 27 weeks plus 7 d, diphenylamine and folpet levels in apple skin were lower for fruit stored in low O₂ (2 kPa) or air than for those kept under ultra-low O₂ (1 kPa). An additional storage period of 4 weeks in air reduced diphenylamine and folpet contents in whole apples stored for 13 weeks in the low O₂ controlled atmosphere. For imazalil, the same result was obtained in apple skins stored for 27 weeks under an ultra-low O₂ controlled atmosphere. Differences in diphenylamine and folpet contents were found for skin and flesh samples throughout the simulated marketing period, but there were observable differences in imazalil contents only for flesh samples.     

Preharvest application of methyl jasmonate (MeJA) in two plum cultivars. 2. Improvement of fruit quality and antioxidant systems during postharvest storage

‘Black Splendor’ (BS) and ‘Royal Rosa’ (RR) plums were treated preharvest with methyl jasmonate (MeJA) at three concentrations (0.5, 1.0 and 2.0 mM) along the on-tree fruit development: 63, 77 and 98 days after full blossom (DAFB). Both control and treated fruit were harvested at the commercial ripening stage and stored in two temperature conditions: 9 days at 20 °C or at 2 °C + 1 day at 20 °C for 50 days. Preharvest MeJA at 2.0 mM significantly accelerated whereas 0.5 mM delayed the postharvest ripening process for both cultivars, since ethylene production, respiration rate and softening were reduced significantly at the two storage conditions for 0.5 mM. In these fruit, total phenolics, total antioxidant activity (hydrophilic fraction, HTAA) and the antioxidant enzymes peroxidase (POD), catalase (CAT) and ascorbate peroxidase (APX) were found at higher levels in treated than control plums during postharvest storage, which could account for the delay of the postharvest ripening process and the extension of shelf-life.     

High carbon dioxide and low oxygen storage effects on reactive oxygen species metabolism in Pleurotus eryngii

This study addressed the influence of high carbon dioxide and low oxygen levels on Pleurotus eryngii samples, stored at 20–25 °C and 90–95% RH for 5 d. Evaluations of sensory characteristics, malondialdehyde (MDA) content, superoxide anion (O₂⁻) production rate and the activities of superoxide dismutase (SOD), peroxidase (POD), catalase (CAT), and cytochrome c oxidase (CCO) were made in the mushrooms in response to high carbon dioxide and low oxygen treatments. The results showed that 2% O₂ + 30% CO₂ significantly prolonged mushroom shelf-life when compared to the control. The 2% O₂ + 30% CO₂ mixture was better suited to maintaining mushroom sensory characteristics and delaying the MDA increase and O₂⁻ production rate during storage. The activities of SOD, POD, and CAT in 2% O₂ + 30% CO₂-treated mushrooms were significantly higher than those of the control. However, the CCO activity was not affected by the atmospheric treatment (2% O₂ + 30% CO₂). These results indicated that the 2% O₂ + 30% CO₂ treatment could alleviate lipid peroxidation and enhance antioxidant enzyme activities, but it exerted little influence on the CCO activity of Pleurotus eryngii.     

1-Methylcyclopropene (1-MCP) delays senescence,maintains quality and reduces browning of non-climacteric eggplant (Solanum melongena L.) fruit

Ethylene action can be counteracted by 1-methylcyclopropene (1-MCP), which has been used during postharvest storage to maintain quality. In this work, we evaluated the effect of 1-MCP treatments on eggplant quality and phenolic metabolism during refrigerated storage. Eggplants (cv. Lucía) were harvested at commercial maturity, treated with 1-MCP (1 μL/L, 12 h at 20 °C), stored at 10 °C for 21 d and subsequently held at 20 °C for 2 d. Corresponding controls were stored at 10 °C and then transferred to 20 °C for 2 d. During storage calyx color, damage and chlorophyll content, fruit weight loss and firmness, pulp sugar content, acidity, browning and total phenolics were measured. In addition, polyphenol oxidase (PPO), pyrogallol peroxidase (POD), and phenylalanine ammonia-lyase (PAL) activities were evaluated. Fruit calyxes showed reduced damage and remained greener in 1-MCP treated than in control fruit. 1-MCP treated eggplants showed lower weight loss. Pulp browning was clearly prevented as a consequence of 1-MCP exposure, and this was associated with delayed senescence, lower accumulation of total phenolics and reduced activity of PAL. The activity of the enzymes PPO and POD involved in the oxidation of phenolics compounds was also decreased in 1-MCP treated fruit. Results suggest that 1-MCP treatments delay senescence, prevent browning and are beneficial to complement low temperature storage and maintain quality of non-climacteric eggplant fruit.