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Serrano, M. Melatonin Treatment of Pomegranate Trees. Encyclopedia. Available online: https://encyclopedia.pub/entry/11229 (accessed on 28 March 2024).
Serrano M. Melatonin Treatment of Pomegranate Trees. Encyclopedia. Available at: https://encyclopedia.pub/entry/11229. Accessed March 28, 2024.
Serrano, María. "Melatonin Treatment of Pomegranate Trees" Encyclopedia, https://encyclopedia.pub/entry/11229 (accessed March 28, 2024).
Serrano, M. (2021, June 24). Melatonin Treatment of Pomegranate Trees. In Encyclopedia. https://encyclopedia.pub/entry/11229
Serrano, María. "Melatonin Treatment of Pomegranate Trees." Encyclopedia. Web. 24 June, 2021.
Melatonin Treatment of Pomegranate Trees
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With the aim to study the effect of melatonin treatment of pomegranate trees on crop yield and fruit quality at harvest and during storage, two experiments were carried out in two consecutive years: 2017 and 2018. In the first year, trees were treated with melatonin (at 0.1 and 1 mM) along the developmental growth cycle and fruit quality parameters were evaluated at harvest and during storage at 10 °C for 90 days. Treatments with melatonin led to an increase of crop yield (number of fruits per tree and kg per tree), as well as higher fruit quality attributes, such as fruit size (diameter and weight), color, total soluble solids (TSS), and total acidity (TA), especially with the 0.1 mM dose. Then, in the second year, melatonin at 0.1 mM was selected for repeating the pre-harvest treatments with similar results in terms of crop yield and fruit quality parameters. During storage, pomegranate fruit treated with 0.1 mM melatonin maintained higher quality attributes than controls, such as TSS, TA, and firmness and lower weight losses were observed in fruit from treated trees, in both trials. In addition, the content of the major sugars (glucose and fructose) and organic acids (malic, succinic and ascorbic acid) were higher in melatonin-treated than in non-treated fruit. These results suggest that pre-harvest melatonin treatment could be a useful tool to increase pomegranate crop yield as well as fruit quality parameters at harvest and their maintenance during storage due to an effect of melatonin on reducing the postharvest ripening process.

Punica granatum firmness color sugars organic acids ripening

1. Introduction

Melatonin (N-acetyl-5-methoxytryptamine) is a natural-occurring compound derivative of tryptamine, and plays important roles in plant growth, such as delay of senescence process and increased tolerance to both biotic and abiotic stress [1]. These effects have been attributed to the melatonin action as a natural antioxidant molecule scavenging free radicals either in vitro as in vivo studies using different vascular plants [2]. The melatonin content in edible fruit has been associated with health-benefits, since high levels of this compound in foods are beneficial for consumers. Thus, the consumption of a Jerte Valley cherry product enhances mood and increases 5-hydroxyindoleacetic acid but reduces cortisol levels in urine, which may protect against stress and act as a mood enhancer by increasing serotonin availability in the organism, particularly with advancing age [3].
As postharvest treatments, melatonin delayed physiological deterioration of cassava roots and reduced the accumulation of H2O2 while increasing the activity of antioxidant enzymes, and thus maintaining homeostasis of cellular reactive oxygen species (ROS) through increasing the endogenous melatonin levels [4]. In tomato fruit, postharvest treatment with melatonin at 50 µM stimulated the content of anthocyanins, and might be positively related to fruit ripening but negatively related to fruit senescence, since the proteins related with senescence were downregulated while an increase of catalase and peroxidase was observed in treated fruit [5]. In peaches, postharvest application of melatonin at 0.1 mM reduced weight loss, decay incidence, and respiration rate as well as maintained firmness, total soluble solids and ascorbic acid contents during seven days of storage at 25–28 °C, with a concomitant increase in antioxidant enzymes and maintenance of membrane integrity, which might be a part of the mechanism implicated on delaying senescence in peach fruit [6].
As pre-harvest treatment, very little evidence exists about the role of melatonin on fruit growth and ripening, and different effects have been reported depending on fruit species, concentration, or time of application. Thus, melatonin was naturally found in grape tissues (skin, flesh and seed), and, during ripening, melatonin content decreased in skin, while it increased in both seed and flesh tissues [7]. Melatonin at 100 mg L−1 (0.43 mM), applied once or twice to grapevines at pre-veraison stage, significantly increased (6.6%) the grape berry size, which was correlated with increased concentration of endogenous melatonin [8]. In two cherry cultivars (‘Hondeng’ and ‘Rainier’), melatonin was evaluated during the growth cycle, and a maximum peak at stage 2 was found, which coincided with endocarp lignification in both cherry cultivars [9] and in ‘Prime Giant’ sweet cherry, melatonin 0.1 and 0.01 mM applied at pit hardening inhibited fruit ripening [10]. However, irrigation of tomato plants with 0.1 mM melatonin increased sugar and lycopene concentration in fruits, showing a positive effect on fruit ripening [11], while, in apricots, foliar spray melatonin treatment increased yield and fruit weight, although no effect on on-tree ripening was observed [12].
Pomegranate is one of the oldest known edible fruits which has gained popularity and scientific interest in the last several years due to its nutritional value and health benefits, since it is very rich in bioactive compounds with antioxidant activity [13][14]. The quality parameters for pomegranate are based on external attributes such as size, shape, and color of the skin, as well as on internal ones such as aril color, sugar and acid content, and the presence of small and soft seeds [15][16]. The color of the pomegranate increases in both skin and arils during ripening, due to the accumulation of anthocyanins, the major in the sweet varieties being cyanidin 3-glucoside, followed by delphinidin 3,5-diglucoside and pelargonidin 3-glucoside, as well as sugar content, while decreases occur on acid content and fruit firmness [16][17][18][19]. However, during postharvest storage, pomegranate exhibits important quality losses due to several physiological and enzymatic disorders, the major ones being weight loss, together with loss of firmness, aril color, and acidity, which lead to a reduction of consumers’ acceptability in terms of freshness, juiciness, and taste [15][16][19][20][21].

2. Effect of Pre-Harvest Melatonin Treatment on Crop Yield

Fruit diameter was recorded during on-tree fruit growth and ripening and results are shown in Figure 1, in which a simple-sigmoid growth curve from full blossom (FB) to harvest (155 d after full blossom, DAFB) can be observed. In addition, results showed that melatonin treatment at 0.1 mM concentration stimulated fruit growth from the second application (T2), leading to pomegranates with significantly higher size (p < 0.05) in 0.1 mM melatonin-treated trees (≈84 mm) than in 1 mM or control ones (≈79 and 77 mm, respectively) at the first harvest date. The increase of fruit size as a consequence of 0.1 mM melatonin treatment was not due to an increased peel width but to an increase in the portion of the arils, as can be observed in the photograph of cut pomegranate fruit detailed below.
Figure 1. Evolution of fruit size (diameter) during pomegranate development from full blossom (FB) to harvest, in fruit from control and 0.1 or 1 mM melatonin-treated trees. T1–T5 represent the day of treatment. Data are the mean ± SE.
With respect to yield, the results of the 2017 experiment are presented in Table 1, showing that both the number of fruit harvested by tree and kg of fruit harvested by tree were significantly higher (p < 0.05) in 0.1 mM melatonin-treated trees than in controls, although these increases were not significant in 1 mM melatonin treated trees. In addition, fruit ripening was delayed in treated trees, since yield at the first harvest date was significantly (p < 0.05) higher in control trees (28.65 ± 3.16 kg tree−1) than in those treated with 0.1 and 1 mM melatonin doses (ca. 21 kg tree−1), as well as the number of fruit per tree (78.0 ± 7.9, 61.40 ± 4.01 and 65.00 ± 3.83 for control and 0.1 and 1 mM melatonin treated trees, respectively). The average fruit weight, taking into account data from the two harvest dates, was significantly higher (p < 0.05) in fruit from 0.1 mM melatonin treated than from controls, although no significant effect was observed with 1 mM melatonin treatment. However, since total yield per tree was only significantly increased in 0.1 mM melatonin treated trees, this concentration was used in the next year, in which these effects were confirmed. Thus, higher values of kg tree−1, the number of fruits per tree and average fruit weight were obtained in 0.1 mM-melatonin treated trees compared with control ones (Table 2).
Table 1. Data for yield (kg tree−1 and number of fruit tree−1), and fruit weight in control and melatonin-treated pomegranate trees (0.1 and 1 mM) at two harvest dates (1 and 2). Year 2017.
Parameter Control Melatonin 0.1 mM Melatonin 1 mM
Yield (kg tree−1)      
Harvest 1 28.65 ± 3.16 a 21.68 ± 2.02 b 20.66 ± 2.84 b
Harvest 2 9.10 ± 0.98 a 20.36 ± 3.60 b 18.05 ± 2.29 b
Total 37.75 ± 3.28 a 42.04 ± 1.06 b 38.71 ± 2.49 a
Yield (number of fruit tree−1)      
Harvest 1 78.0 ± 7.9 a 61.40 ± 4.01 b 65.00 ± 3.83 b
Harvest 2 29.8 ± 3.21 a 58.00 ± 3.98 c 46.60 ± 5.65 b
Total 107.8 ± 5.16 a 119.40 ± 3.96 b 111.60 ± 4.15 ab
Fruit weight (g)      
Harvest 1 367.31 ± 11.29 a 353.09 ± 9.14 a 317.84 ± 10.21 b
Harvest 2 305.37 ± 7.62 a 351.03 ± 9.95 b 387.33 ± 8.45 c
Average 350.18 ± 6.19 a 352.03 ± 12.97 a 346.86 ± 9.15 b
Data are the mean ± SE. For each parameter and harvest date, different letters within a row show significant differences at p < 0.05.
Table 2. Data for yield (kg tree1 and number of fruit tree1), total number of fruits in 5 trees and fruit weight in control and 0.1 melatonin-treated pomegranate trees at two harvest dates (1 and 2). Year 2018.
Parameter Control Melatonin 0.1 mM
Yield (kg tree−1)    
Harvest 1 26.73 ± 1.72 a 22.91 ± 2.34 b
Harvest 2 10.37 ± 1.37 a 20.34 ± 3.19 b
Total 37.10 ± 1.56 a 43.25 ± 1.57 b
Yield (number of fruit tree−1)    
Harvest 1 72.40 ± 3.64 a 60.90 ± 3.85 b
Harvest 2 36.75 ± 4.02 a 60.40 ± 5.92 b
Total 109.15 ± 3.92 a 121.30 ± 4.96 b
Fruit weight (g)    
Harvest 1 369.20 ± 9.55 a 376.19 ± 7.45 a
Harvest 2 282.17 ± 6.46 a 336.75 ± 6.17 b
Average 339.90 ± 5.15 a 357.43 ± 8.07 b
Data are the mean ± SE. For each parameter and harvest date, different letters within a row show significant differences at p < 0.05.

3. Effect of Melatonin on Fruit Quality Parameters

Weight losses increased during storage in pomegranate fruit from control and treated trees, although these increases were significantly reduced by melatonin treatment, with significant differences (p < 0.05) after 60 days of storage (Table 3). With respect to TSS, levels at harvest in the 2017 experiment were 15.17 ± 0.26 g 100 g−1 in fruit from control trees and significantly higher (p < 0.05) in those from 0.1 mM treated trees, although no significant differences were observed due to 1 mM melatonin treatment (Table 3). TSS content increased during storage in fruit from control and treated trees and these increases occurred later in fruit from melatonin treated trees with respect to those from controls (Table 3). Acidity levels (TA) at harvest were also significantly increased at harvest by melatonin treatments and they decreased during storage, but the decrease was much lower in melatonin-treated fruit (both 0.1 and 1 mM) than in controls (Table 3). The ratio between TSS/TA, also known as ripening index (RI), increased during storage, but it was reduced by the pre-harvest application of melatonin (Table 3). Melatonin treatments also affected pomegranate skin and aril color, since significantly lower (p < 0.05) values of Hue angle were recorded in fruit from melatonin treated trees than in controls and those differences were maintained during the whole storage period, although Hue angle of skin and arils decreased in all pomegranate fruit (Table 3).
Table 3. Physiological and biochemical parameters in pomegranate fruits from control and melatonin-treated trees (0.1 and 1 mM) at harvest (day 0) and during 90 days of storage at 10 °C. Year 2017.
Parameter Days Control Melatonin 0.1 mM Melatonin 1 mM
Weight loss (%) 0 - - -
30 3.94 ± 0.19 aA 3.67 ± 0.15 aA 3.75 ± 0.20 aA
60 4.82 ± 0.49 bA 3.83 ± 0.48 aB 4.38 ± 0.11 bB
90 6.87 ± 1.09 cA 4.86 ± 0.26 bC 5.59 ± 0.17 cB
TSS (g 100 g−1) 0 15.17 ± 0.26 aA 16.37 ± 0.22 aB 15.38 ± 0.35 aA
30 16.68 ± 0.12 bA 16.38 ± 0.10 aA 16.40 ± 0.12 aA
60 16.93 ± 0.23 bcA 16.48 ± 0.16 aA 17.18 ± 0.26 a,bA
90 17.42 ± 0.15 cA 17.25 ± 0.19 bA 17.32 ± 0.12 bA
TA (g 100 g−1) 0 0.45 ± 0.03 aA 0.56 ± 0.01 aA 0.56 ± 0.05 aA
30 0.38 ± 0.01 bA 0.51 ± 0.02 bB 0.57 ± 0.03 aB
60 0.32 ± 0.02 bcA 0.46 ± 0.01 bB 0.45 ± 0.02 bB
90 0.21 ± 0.01 cA 0.38 ± 0.02 cB 0.30 ± 0.01 cB
RI (TSS/TA) 0 35.04 ± 0.51 aA 29.23 ± 0.52 aB 27.46 ± 0.54 aB
30 43.88 ± 0.73 bA 32.01 ± 0.54 bB 28.77 ± 0.38 aB
60 52.91 ± 0.84 cA 35.82 ± 0.74 cB 38.18 ± 0.56 bB
90 82.95 ± 1.22 dA 45.39 ± 0.41 dB 57.73 ± 0.62 cC
External Color Hue 0 68.30 ± 1.01 aA 58.84 ± 1.47 aC 62.69 ± 1.12 aB
30 64.71 ± 1.07 abA 55.89 ± 1.88 abB 57.71 ± 1.03 abB
60 61.53 ± 1.09 bcA 53.66 ± 1.88 bcB 55.80 ± 1.68 bB
90 59.93 ± 1.57 cB 52.26 ± 1.89 cB 54.48 ± 1.42 bB
Internal Color Hue 0 34.13 ± 1.71 aA 30.34 ± 1.18 aB 31.92 ± 1.29 aAB
30 31.78 ± 1.04 abA 28.34 ± 0.73 abB 28.77 ± 1.22 abB
60 28.91 ± 0.53 bA 26.00 ± 0.64 bB 26.93 ± 0.65 bcB
90 26.91 ± 0.83cA 23.84 ± 0.55 cB 24.74 ± 0.69 cAB
Data are the mean ± SE. For each parameter, different lowercase letters within a column show significant differences at p < 0.05 during storage, while capital letters show significant differences at p < 0.05 among treatments for each sampling date.
Fruit firmness at harvest, in the 2017 experiment, was significantly higher (p < 0.05) in fruit from 0.1 mM melatonin treated trees than in controls (26.52 ± 0.50 and 28.93 ± 0.710 N mm−1, respectively), while no significant effect was observed with 1 mM melatonin treatment. During storage, fruit firmness decreased in pomegranates from control and treated trees, although firmness levels were the highest in 0.1 mM melatonin treated fruit until the last sampling date (Figure 2).
Figure 2. Fruit firmness evolution (Nmm−1) during refrigerated storage in two consecutive production cycles (2017 and 2018), in control fruit and 0.1 or 1mM melatonin-treated trees. Data are the mean ± SE.
Similar results with respect to firmness (Figure 2), weight loss, TSS, TA, and RI were obtained in the experiment assayed in 2018 (Table 4), in which 0.1 mM melatonin concentration was chosen, since better results were obtained compared with 1 mM dose in the 2017 experiment. Accordingly, melatonin treatments did not affect skin color, although aril color was affected by treatment, since Hue angle values were significantly lower in melatonin treated than in control fruit, either at harvest or during storage (Table 4), which indicated a darker red color of the arils. These differences are evident in Figure 3, in which the visual aspect of pomegranates from control and melatonin-treated trees (0.1 mM) at harvest and during storage is shown. Small shrivelling symptoms were observed on pomegranate fruit after 90 days of storage in fruits from control and treated ones without differences attributed to melatonin treatment (data not shown).
Figure 3. Photography displays the visual aspect of pomegranates from control and 0.1 mM melatonin-treated trees during storage in the 2018 experiment.
Table 4. Quality parameters in control and 0.1 mM melatonin-treated pomegranate fruits at harvest (day 0) and during postharvest storage at 10 °C. Year 2018.
Parameter Treatment Day 0 Day 30 Day 60 Day 90
Weight loss (%) Control - 7.07 ± 0.49 Aa 8.49 ± 0.48 Ab 9.88 ± 0.54 Ac
Melatonin 6.03 ± 0.14 Aa 7.18 ± 0.25 Bb 7.98 ± 0.24 Bc
TSS (g 100 g−1) Control 16.05 ± 0.10 Aa 17.03 ± 0.15 Ab 17.52 ± 0.16 Ab 17.41 ± 0.22 Ab
Melatonin 17.18 ± 0.12 Ba 17.02 ± 0.13 Aa 17.13 ± 0.18 Aa 17.25 ± 0.36 Aa
TA (g 100 g−1) Control 0.35 ± 0.03 Aa 0.31 ± 0.03 Ab 0.21 ± 0.02 Ac 0.19 ± 0.04 Ac
Melatonin 0.42 ± 0.04 Ba 0.37 ± 0.03 Ba,b 0.34 ± 0.02 Bb,c 0.29 ± 0.01 Bc
Ripening index (TSS/TA) Control 45.85 ± 1.74 Aa 54.93 ± 2.15 Ab 83.42 ± 1.65 Ac 91.63 ± 1.97 Ad
Melatonin 40.90 ± 1.03 Ba 48.62 ± 0.78 Bb 50.38 ± 2.18 Bb 59.48 ± 2.18 Bc
External Color Hue Control 66.41 ± 1.22 Aa 64.20 ± 1.52 Aa 60.02 ± 1.34 Ab 58.38 ± 0.99 Ab
Melatonin 60.02 ± 0.51 Ba 56.70 ± 1.57 Bbc 54.07 ± 1.24 Bcd 52.49 ± 1.61 Bd
Internal Color Hue Control 33.13 ± 0.58 Aa 30.75 ± 1.90 Aab 29.23 ± 0.56 Ab 27.65 ± 1.07 Ac
Melatonin 30.56 ± 1.24 Ba 27.22 ± 1.40 Bab 26.02 ± 1.18 Bb 22.79 ± 1.17 Bc
Data are the mean ± SE. For each parameter, different lowercase letters within a row show significant differences at p < 0.05 during storage, while capital letters show significant differences at p < 0.05 between treatments for each sampling date.
Individual sugars are mainly responsible for TSS in pomegranate and their quantification by HPLC showed that the major one was fructose, followed by glucose, while sucrose was found at very low concentrations (Table 5). Interestingly, fruit from melatonin treated trees had significantly higher p < 0.05 content of fructose and glucose at harvest than controls. With respect to organic acids, the major one found in ‘Mollar de Elche’ pomegranate was malic acid, followed by succinic and citric acids, which were also found at higher concentration in fruit from melatonin-treated trees, while no significant differences were observed in the minor ones, citric, fumaric, and oxalic acid. However, it is worth mentioning the effect of pre-harvest melatonin treatment on increasing ascorbic acid content in the arils, with concentrations being 1.5 higher in treated than in control fruit (Table 5).
Table 5. Reducing sugars and organic acids in fruits from control and 0.1 mM melatonin-treated trees at harvest. Year 2018.
Parameter Control Melatonin 0.1 mM
Sugars (g 100 g−1)    
Sucrose 0.06 ± 0.01 a 0.06 ± 0.02 a
Glucose 4.17 ± 0.10 a 4.81 ± 0.24 b
Fructose 11.61 ± 0.33 a 12.54 ± 0.26 b
Organic acids (g 100 g−1)    
Malic acid 0.32 ± 0.03 a 0.36 ± 0.04 b
Succinic acid 0.07 ± 0.01 a 0.12 ± 0.01 b
Citric acid 0.09 ± 0.01 a 0.09 ± 0.01 a
Ascorbic acid 0.04 ± 0.01 a 0.06 ± 0.01 b
Fumaric acid 0.03 ± 0.01 a 0.03 ± 0.01 a
Oxalic acid 0.01 ± 0.01 a 0.01 ± 0.01 a
Data are the mean ± SE. For each parameter, different letters within a row show significant differences at p < 0.05.

4. Discussion

As far as we know, this is the first report showing the effects of melatonin, applied as pre-harvest treatment, in pomegranate yield and fruit quality properties, although some evidence exists in other plant species. In a recent study performed on Arabidopsis treated with melatonin and grown at 4 °C, melatonin-treated plants had significantly greater fresh weight, primary root length, and shoot height compared with untreated plants, the effect being both time and concentration dependence [22]. However, the yield increase found in the present study was higher with 0.1 mM melatonin treatment than with 1 mM dose, and due to an increase in fruit size (diameter and weight). This effect was due to an increased aril portion but to an increase in peel width as can be observed in the photograph of cut pomegranates in Figure 3. On the other hand, the amount of fruit harvested by tree was also increased by melatonin treatment. Given the fact that treatments were applied when fruit was in its active phase of growth, the higher amount of fruit harvested from treated fruit could be attributed to the effect of melatonin on decreasing the normal fruit abscission that occurs during fruit development due to environmental factors, such as wind or rain. In addition, the effect of melatonin on alleviating biotic and abiotic stress in plants has been reported [22][23]. Thus, giving the semi-arid climate conditions of Southern Spain, the melatonin treatment could increase net photosynthesis rate and productivity throughout enhancement of tree tolerance to heat and drought stresses. Accordingly, grape berries treated with melatonin at pre-veraison exhibited higher endogenous melatonin accumulation and increased berry size and weight [8]. These authors attributed this effect to an increase of the sink strength of the berry, leading the fruit to uptake more sugars and develop a larger size at harvest. On the other hand, melatonin foliar spray treatment increased fruit weight and yield for ‘Canino’ apricot [12]. In addition, we have found increased crop yield ‘Colorado’ and ‘Mikado’ apricot cultivars after melatonin treatment (unpublished data), which were attributed to increases in tree net photosynthesis, due to enhanced total chlorophyll and leaf area.
‘Mollar de Elche’ pomegranate is very much appreciated by consumers due to the high content of sugars and low acidity, which confer a sweet taste while also being very aromatic [15][16][17][18]. In this sense, the higher values of TSS, TA, sugars, and organic acids found at harvest in pomegranates of melatonin treated trees show that they had higher quality attributes than controls. However, this cultivar is characterized by having a pale aril color compared with other cultivars [15][17][24] and thus several research papers have been performed with the aim to increase aril color while enhancing anthocyanin synthesis, by applying water restrictions in summer, during the linear phase of fruit growth [25], as well as treatment with methyl jasmonate or salicylates during on-tree pomegranate fruit development [16][26]. Results of the present research show that melatonin-treated fruit had a deeper red color than controls (lower Hue angle) at harvest and during storage, showing a stimulation of the anthocyanin biosynthesis by melatonin treatment, which is the pigment contributing to the red color of pomegranates [15][16][20][26]. On the other hand, no effects of melatonin treatments on fruit taste and flavour were appreciated either at harvest or during storage, although a proper sensorial analysis would be useful to a scientific validation of this observation.
On the other hand, results show that pre-harvest melatonin treatment delayed the postharvest ripening process during storage, since weight, firmness, and acidity losses were delayed in fruit from melatonin-treated trees with respect to controls, these effects being higher for 0.1 mM dose than for 1 mM. No previous reports are available in the literature regarding the effect of preharvest melatonin treatment on the evolution of fruit quality parameters during storage, although information exists about postharvest treatments. Thus, in banana, exogenous application of melatonin (at 0.05, 0.2 and 0.5 mM) resulted in a delay of postharvest ripening, although in this report the effect was dose dependent [27]. The lower weight losses observed in fruits from melatonin treated trees with respect to those of controls might be attributed to an effect of melatonin on increasing cuticle thickness, as recently proposed for nectarines [28] and mangos [29] after postharvest melatonin treatment. Accordingly, postharvest 0.1 mM melatonin treatment delayed the postharvest ripening process during cold storage in apples [30], peaches [31], nectarines [28], pears [32], and mangos [33], which was attributed to a inhibition of ethylene production, although similar effects have been reported in non-climacteric fruits such as sweet cherries [34].

References

  1. Arnao, M.B.; Hernandez-Ruiz, J. Functions of melatonin in plants: A review. J. Pineal Res. 2015, 59, 133–150.
  2. Reiter, R.T.; Tan, D.X.; Zhou, Z.; Coelho-Cruz, M.E.; Fuentes-Broto, L.; Galano, A. Phytomelatonin: Assisting plants to survive and thrive. Molecules 2015, 20, 7396–7437.
  3. Garrido, M.; Espino, J.; González-Gómez, D.; Lozano, M.; Barriga, C.; Paredes, S.D.; Rodríguez, A.B. The consumption of a Jerte Valley cherry product in humans enhances mood and increases 5-hydroxyindoleacetic acid but reduces cortisol levels in urine. Exp. Gerontol. 2012, 47, 573–580.
  4. Ma, Q.; Zhang, T.; Zhang, P.; Wang, X.Y. Melatonin attenuates postharvest physiological deterioration of cassava storage roots. J. Pineal Res. 2016, 60, 424–434.
  5. Sun, Q.; Zhang, N.; Wang, J.; Cao, Y.; Li, X.; Zhang, H.; Zhang, L.; Tan, D.X.; Guo, Y.D. A label-free differential proteomics analysis reveals the effect of melatonin on promoting fruit ripening and anthocyanin accumulation upon postharvest in tomato. J. Pineal Res. 2016, 61, 138–153.
  6. Gao, H.; Lu, Z.; Yang, Y.; Wang, D.; Cao, M.; Cao, W. Melatonin treatment reduces chilling injury in peach fruit through its regulation of membrane fatty acid contents and phenolic metabolism. Food Chem. 2018, 45, 659–666.
  7. Vitalini, S.; Gardana, C.; Zanzotto, A.; Simonetti, P.; Faoro, F.; Fico, G.; Iriti, M. The presence of melatonin in grapevine (Vitis vinifera L.) berry tissues. J. Pineal Res. 2011, 51, 331–337.
  8. Meng, J.F.; Xu, T.F.; Song, C.Z.; Yu, Y.; Hu, F.; Zhang, L.; Zhang, Z.W.; Xi, Z.M. Melatonin treatment of pre-veraison grape berries to increase size and synchronicity of berries and modify wine aroma components. Food Chem. 2015, 185, 127–134.
  9. Zhao, Y.; Tan, D.X.; Lei, Q.; Chen, H.; Wang, L.; Li, Q.; Gao, Y.; Kong, J. Melatonin and its potential biological functions in the fruits of sweet cherry. J. Pineal Res. 2012, 55, 79–88.
  10. Tijero, V.; Muñoz, P.; Munné-Bosch, S. Melatonin as an inhibitor of sweet cherries ripening in orchard trees. Plant Physiol. Biochem. 2019, 140, 88–95.
  11. Liu, J.; Zhang, R.; Sun, Y.; Liu, Z.; Jin, W.; Sun, Y. The beneficial effects of exogenous melatonin on tomato fruit properties. Sci. Hortic. 2016, 207, 14–20.
  12. Abd El-Naby, S.K.M.A.; Mohamed, A.A.A.; El-Naggar, Y.I.M. Effect of melatonin, GA3 and NAA on vegetative growth, yield and quality of ’Canino’ apricot fruits. Acta Sci. Pol. Hortorum Cultus 2019, 18, 167–174.
  13. Asgary, S.; Keshvari, M.; Sahebkar, A.; Sarrafzadegan, N. Pomegranate consumption and blood pressure: A review. Curr. Pharm. Des. 2017, 23, 1042–1050.
  14. Panth, N.; Manandhar, B.; Paudel, K.R. Anticancer activity of Punica granatum (pomegranate): A review. Phytother. Res. 2017, 31, 568–578.
  15. Pareek, S.; Valero, D.; Serrano, M. Postharvest biology and technology of pomegranate. J. Sci. Food Agr. 2015, 95, 2360–2369.
  16. García-Pastor, M.E.; Zapata, P.J.; Castillo, S.; Martínez-Romero, D.; Guillén, F.; Valero, D.; Serrano, M. The effects of salicylic acid and its derivatives on increasing pomegranate fruit quality and bioactive compounds at harvest and during storage. Front. Plant Sci. 2020, 11, 668.
  17. Cano-Lamadrid, M.; Galindo, A.; Collado-González, J.; Rodríguez, P.; Cruz, Z.N.; Legua, P.; Burló, F.; Morales, D.; Carbonell-Barrachina, A.; Hernández, F. Influence of deficit irrigation and crop load on the yield and fruit quality in Wonderful and Mollar de Elche pomegranates. J. Sci. Food Agric. 2018, 98, 3098–3108.
  18. Nuncio-Jáuregui, N.; Calín-Sánchez, A.; Carbonell-Barrachina, A.; Hernández, F. Changes in quality parameters, proline, antioxidant activity and color of pomegranate (Punica granatum L.) as affected by fruit position within tree, cultivar and ripening stage. Sci. Hortic. 2014, 165, 181–189.
  19. Kulkarni, A.P.; Aradhya, S.M. Chemical changes and antioxidant activity in pomegranate arils during fruit development. Food Chem. 2005, 93, 319–324.
  20. García-Pastor, M.E.; Serrano, M.; Guillén, F.; Giménez, M.J.; Martínez-Romero, D.; Valero, D.; Zapata, P.J. Preharvest application of methyl jasmonate increases crop yield, fruit quality and bioactive compounds in pomegranate ‘Mollar de Elche’ at harvest and during postharvest storage. J. Sci. Food Agric. 2020, 100, 145–153.
  21. Valero, D.; Serrano, M. Postharvest Biology and Technology for Preserving Fruit Quality; CRC Press: Boca Raton, FL, USA, 2010; p. 288.
  22. Arnao, M.B.; Hernandez-Ruiz, J. Melatonin: A New Plant Hormone and/or a Plant Master Regulator? Trends Plant Sci. 2019, 24, 38–48.
  23. Kołodziejczyk, I.; Posmyk, M.M. Melatonin—A new plant biostimulator? J. Elem. 2016, 21, 1187–1198.
  24. Li, X.; Wasila, H.; Liu, L.; Yuan, T.; Gao, Z.; Zhao, B.; Ahmad, I. Physicochemical characteristics, polyphenol compositions and antioxidant potential of pomegranate juices from 10 Chinese cultivars and the environmental factors analysis. Food Chem. 2015, 175, 575–584.
  25. Bartual, J.; Pérez-Gago, M.B.; Pomares, F.; Palou, L.; Intrigliolo, D.S. Nutrient status and irrigation management affect anthocyanins in ‘Mollar de Elche’ pomegranate. Acta Hortic. 2015, 1106, 85–92.
  26. Gil, M.I.; García-Viguera, C.; Artés, F.; Tomás-Barberán, F.A. Changes in pomegranate juice pigmentation during ripening. J. Sci. Food Agric. 1995, 68, 77–81.
  27. Hu, W.; Yang, H.; Tie, W.W.; Yan, Y.; Ding, Z.; Liu, Y.; Wu, C.; Wang, J.; Reiter, R.J.; Tan, D.X.; et al. Natural variation in banana varieties highlights the role of melatonin in postharvest ripening and quality. J. Agric. Food Chem. 2017, 65, 9987–9994.
  28. Bal, E. Physicochemical changes in ‘Santa Rosa’ plum fruit treated with melatonin during cold storage. J. Food Measur. Charact. 2019, 13, 1713–1720.
  29. Rastegar, S.; Khankahdani, H.H.; Rahimzadeh, M. Effects of melatonin treatment on the biochemical changes and antioxidant enzyme activity of mango fruit during storage. Sci. Hortic. 2020, 259, 108835.
  30. Onik, J.C.; Wai, S.C.; Li, A.; Lin, Q.; Sun, Q.; Wang, Z.; Duan, Y. Melatonin treatment reduces ethylene production and maintains fruit quality in apple during postharvest storage. Food Chem. 2021, 337, 127753.
  31. Gao, H.; Zhang, Z.K.; Chai, H.K.; Cheng, N.; Yang, Y.; Wang, D.N.; Yang, T.; Cao, W. Melatonin treatment delays postharvest senescence and regulates reactive oxygen species metabolism in peach fruit. Postharvest Biol. Technol. 2016, 118, 103–110.
  32. Zhai, R.; Liu, J.; Liu, F.; Zhao, Y.; Liu, L.; Fang, C.; Wang, H.; Li, X.; Wang, Z.; Ma, F.; et al. Melatonin limited ethylene production, softening and reduced physiology disorder in pear (Pyrus communis L.) fruit during senescence. Postharvest Biol. Technol. 2018, 139, 38–46.
  33. Liu, S.; Huang, H.; Huber, D.J.; Pan, Y.; Shi, X.; Zhang, Z. Delay of ripening and softening in ‘Guifei’ mango fruit by postharvest application of melatonin. Postharvest Biol. Technol. 2020, 163, 111136.
  34. Wang, F.; Zhang, X.; Yang, Q.; Zhao, Q. Exogenous melatonin delays postharvest fruit senescence and maintains the quality of sweet cherries. Food Chem. 2019, 301, 125311.
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