Effect of harvest maturity and cold storage on correlations between fruit properties during ripening of apricot (Prunus armeniaca)

Apricots (Prunus armeniaca) were held in air storage at 0 °C and ripened at 20 °C, or ripened at 20 °C straight after harvest, and changes in fruit quality quantified using postharvest and sensory evaluations. Maturity at harvest significantly affected flesh firmness and other quality factors. Mealiness and gel formation only developed in fruit that had been stored at low (0 °C) temperatures. Mealiness did not develop until firmness dropped below approximately 20 N, whereas gel formation began to develop when firmness was as high as 35 N. Development of mealiness and loss of juiciness were correlated; however, slight mealiness was perceived when fruit were still considered juicy. Specific cultivar-related differences were evident in the changes in firmness and development of gel formation during and after cold storage. Fruit were less liked by the sensory panel when firmness dropped below 20 N, as juiciness decreased and mealiness and gel formation increased. Cell wall studies showed changes in yields of water-soluble and CDTA (trans-1,2-cyclohexanediamine tetraacetic acid)-soluble pectin. In fruit ripened after cold storage, mealiness and gel formation was accompanied by an increase in water-soluble pectin and an increase in CDTA-soluble pectin, whereas in apricots ripened straight after harvest, water-soluble pectin increased but CDTA-soluble pectin slightly decreased. All fruit, regardless of maturity or having chilling disorders or not, fitted the same correlation between firmness and uronic acid content of water-soluble pectin, but no pattern was evident for CDTA-soluble pectin. We concluded that the increasing solubilisation of pectin was a major feature of fruit softening in apricot, whereas the differences in CDTA-soluble pectin may reflect differences in strength of cell adhesion.     

缓慢降温对石榴果实冷害发生及生理变化的影响

对缓慢降温处理后石榴果实在冷害温度下的生理反应进行了研究,旨在为石榴果实采后保鲜提供理论依据。以新疆大籽石榴为试材,研究了0℃低温胁迫及缓慢降温对石榴果实采后生理的影响结果表明,与0℃的低温相比,缓慢降温处理减缓石榴果皮细胞膜透性的升高以及膜脂质过氧化物丙二醛的积累,抑制了多酚氧化酶活性的增加及减少了酚类物质的氧化,明显推迟和减轻石榴果实冷害症状的发生,减轻了果皮的褐变,保持果实品质。     

Mode of action of nitric oxide in inhibiting ethylene biosynthesis and fruit softening during ripening and cool storage of ‘Kensington Pride’ mango

The mode of action of nitric oxide (NO) in inhibiting ethylene biosynthesis and fruit softening during ripening and cool storage of mango fruit was investigated. Hard mature green mango (Mangifera indica L. cv. ‘Kensington Pride’) fruit were fumigated with 20 μL L⁻¹ NO for 2 h at 21 °C and allowed to ripen at 21 ± 1 °C for 10 d, or stored at 13 ± 1 °C for 21 d. During ripening and cool storage, ethylene production and respiration rate from whole fruit were determined daily. The 1-aminocyclopropane-1-carboxylic acid (ACC) content, activities of ACC synthase (ACS), ACC oxidase (ACO), and fruit softening enzymes such as pectin esterase (PE), endo-1,4-β-d-glucanase (EGase), exo- and endo-polygalacturonase (exo-PG, endo-PG) as well as firmness and rheological properties of pulp were determined at two- and seven-day intervals during ripening and cool storage, respectively. NO fumigation inhibited ethylene biosynthesis and respiration rate, and maintained higher pulp firmness, springiness, cohesiveness, chewiness, adhesiveness, and stiffness. NO-fumigated fruit during cool storage and ripening had lower ACC contents through inhibiting the activities of both ACS and ACO in the fruit pulp. NO-fumigated fruit showed decreased activities of exo-PG, endo-PG, EGase, but maintained higher PE activity in pulp tissues during ripening and cool storage. In conclusion, NO fumigation inhibited ethylene biosynthesis through inhibition of ACS and ACO activities leading to reduced ACC content in the fruit pulp which consequently, reduced the activities of fruit softening enzymes during ripening and cool storage.     

Texture profiling of blueberries (Vaccinium spp.) during fruit development,ripening and storage

Blueberries are ‘soft fruit’, a name which underlies the impact that fruit texture plays in their marketability. Worldwide blueberry production has been increasing in the last years, and they are now the second most economically important soft fruit after strawberry. During pre- and postharvest ripening, fruit softening represents the most dramatic change, leading to important losses in quality during storage. To support the FEM breeding program toward the creation of new blueberry accessions with superior texture, we used a novel texture analyzer TAXTplus to improve the phenotyping resolution, a fundamental step for a more reliable and precise selection of the most suitable ideotypes. In this work change in the mechanical profile of the blueberry cultivar ‘Brigitta Blue’ was initially assessed during berry development, maturation and postharvest ripening, revealing important textural variations. In addition, this novel equipment was exploited to compare the fruit texture behavior at two specific stages, maturity and after postharvest cold storage, on a set of 49 different blueberry and hybrids cultivars and selections. A multivariate statistical approach, including principal component analysis, was employed to analyze the dataset related to the textural parameters, according to their performance. Finally a storage index, originally defined for apple fruit texture, was adopted to depict the different storage potential of a set of blueberry cultivars.     

Assessment of chilling injury during storage: chlorophyll fluorescence characteristics of chilling-susceptible and triazole-induced chilling tolerant basil leaves

Chlorophyll (Chl) fluorescence analysis by pulse-amplitude modulation (PAM) measurements was performed to assess the extent of chilling injury (CI) in stored sweet basil (Ocimum basilicum L.) leaves. Changes in three photosynthetic characteristics, in relation to visible CI rating, were monitored in leaves following modification of their chilling susceptibility by varying storage temperature and duration in two basil cultivars, or by soil application of triazole. Basil leaves developed severe or moderate visible symptoms of CI after 4 days of storage at 4 or 8 °C, respectively, but remained undamaged when stored at 12 °C. The chilling-dependent changes obtained in the ratios of variable to maximal fluorescence (F_v/F_m), represented chilling sensitivity rather than membrane damage. The photochemical quenching coefficient (qP) was unaffected by low temperatures and did not seem to be correlated with CI. On the other hand, changes in the non-photochemical quenching coefficient (qNP) were positively correlated with the appearance of visual CI symptoms in leaves of the two cultivars at all storage temperatures and durations. Similarly, the chilling-alleviating effect of triazole was accompanied by a corresponding reduction in the chilling-induced decrease of qNP. Therefore, qNP may be associated with an irreversible transition step in the CI process, which precedes the appearance of visual symptoms. As such, changes in qNP may provide a suitable, rapid and non-destructive criterion for estimation of chilling damage in green tissues.     

Residual effects of low oxygen storage of mature green fruit on ripening processes and ester biosynthesis during ripening in bananas

Mature green banana (Musa sapientum L. cv. Cavendish) fruit were stored in 0.5%, 2%, or 21% O₂ for 7 days at 20 °C before ripening was initiated by ethylene. Residual effects of low O₂ storage in mature green fruit on ripening and ester biosynthesis in fruit were investigated during ripening for up to 6 d at 20 °C. Concentrations of ethanol in mature green fruit did not change during storage in both 21% and 2% O₂ atmospheres, but increased in fruit stored in 0.5% O₂. The activities of alcohol dehydrogenase (ADH) in 2% and 21% O₂ atmospheres remained very low throughout the storage period, but significantly increased with 0.5% O₂. After transferring fruit to regular air and trigging ripening with ethylene, yellowing of peel, fruit softening and hydrolysis of starch in fruit stored in low O₂ atmospheres were slower than in the control. Fruit stored in low O₂ also showed a delayed onset of the climacteric peak. The activities of ADH were lower in the low O₂ stored fruit than in the control fruit. Productions of ethyl acetate, isoamyl acetate, and isobutyl acetate were remarkably suppressed by low O₂ storage. Alcohol acetyltransferase activity increased gradually with storage time in all treatments, being significantly lower in fruit with low O₂ pretreatments. The results indicate that low O₂ plus room temperature storage can extend storage life of bananas with the sacrifice of a low production of ester volatiles.     

Postharvest application of gum arabic and essential oils for controlling anthracnose and quality of banana and papaya during cold storage

Management of anthracnose caused by Colletotrichum spp. is the most important issue for the tropical fruit industry because of resulting financial losses. Antifungal effects of gum arabic (GA) (10%), lemongrass oil (LG) (0.05%), cinnamon oil (CM) (0.4%), and their combinations were investigated in vitro and in vivo for controlling postharvest anthracnose of banana and papaya. LG at 0.05% and 0.4% CM showed fungicidal effects against Colletotrichum musae and Colletotrichum gloeosporioides, causal organisms of banana and papaya anthracnose, respectively. GA alone did not show any fungicidal effects while the combination of 0.05% LG and 0.4% CM with Ten percent GA alone showed more fungicidal effects. However, potato dextrose agar (PDA) medium modified with 10% GA combined with 0.4% CM showed the most promising results among all treatments against C. musae and C. gloeosporioides in suppressing the mycelial growth (73.4%) and (70.0%) and spore germination inhibition (88%) and (85%), respectively. In vivo studies also revealed that 10% GA combined with 0.4% CM was the optimal concentration in controlling decay (80%) and (71%), showing a synergistic effect in the reduction of C. musae and C. gloeosporioides, respectively, in artificially inoculated bananas and papayas. The results regarding quality evaluation also confirmed the efficacy of 10% GA combined with 0.4% CM coatings since ripening was significantly delayed, in terms of percentage weight loss, fruit firmness, soluble solids concentration and titratable acidity. The results suggest the possibility of using 10% gum arabic combined with 0.4% cinnamon oil as a biofungicide for controlling postharvest anthracnose in major tropical fruit such as banana and papaya.     

Colour development and quality of mangosteen (Garcinia mangostana L.) fruit during ripening and after harvest

The colour of mangosteen (Garcinia mangostana L.) fruit changes from green to purple black after harvest as the fruit ripens, and is used as a quality guide for growers and consumers. We determined the relationship between anthocyanin composition and content during fruit colour development in relation to fruit maturity and postharvest quality. Fruit at different stages of maturity (light greenish yellow with 5% scattered pink spots to purple black) were harvested and kept at 25 °C (85–90% RH). Fruit from each maturity stage all developed to the final purple black stage. During the postharvest period, hue angle values and pericarp firmness decreased significantly, while soluble solids contents increased. Anthocyanin contents in the outer pericarp were higher than in the inner pericarp and increased to a maximum at the final colour stage. Sensory evaluation and fruit quality (hue angle values, soluble solids and titratable acidity) of fruit harvested at the different stages did not differ once the fruit had finally developed to the purple black stage. The anthocyanins in the outer pericarp mainly consisted of five compounds, identified by HPLC/MS as cyanidin-sophoroside, cyanidin-glucoside, cyanidin-glucoside-pentoside, cyanidin-glucoside-X, cyanidin-X₂ and cyanidin-X, where X denotes an unidentified residue of m/z 190, a mass which does not correspond to any common sugar residue. Cyanidin-3-sophoroside and cyanidin-3-glucoside were the major compounds and the only ones that increased with fruit colour development.     

Influence of Md-ACS1 allelotype and harvest season within an apple germplasm collection on fruit softening during cold air storage

Previous studies have demonstrated a relationship between Md-ACS1 allelotype and apple fruit softening at ambient temperatures. The present study was undertaken to further examine the influence of this allelotype (-1/1, -1/2 or -2/2) and its interaction with harvest season (early or late) on changes in internal ethylene concentrations (IEC) and fruit softening during cold air storage. This was carried out by describing natural differences found among old apple cultivars/species and modern commercial cultivars. For late maturing cultivars, Md-ACS1-1/1 was firmer at harvest than Md-ACS1-2/2 with the heterozygote intermediate. However harvest firmness showed no differences among for the early season Md-ACS1 allelotypes. The Md-ACS1-2/2 allelotype had a slower rate of postharvest IEC increase and flesh softening compared with Md-ACS1-1/1 and -1/2 allelotypes, and late maturing cultivars had a slower rate of fruit softening than early maturing cultivars, which was independent of postharvest IEC. All three late season allelotypes and early season Md-ACS1-2/2 were firmer after storage than early season Md-ACS1-1/1 and -1/2 allelotypes, reflecting differences in both harvest firmness and softening rates. While cultivar variation in final firmness could be explained partially through Md-ACS1-mediated postharvest ethylene increases and subsequent softening, much more variation was accounted for by their differences in harvest firmness. These results are discussed in relation to strategies for breeding cultivars with superior flesh textures that are maintained during storage.     

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

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

Postharvest application of ethylene and 1-methylcyclopropene either before or after curing affects onion (Allium cepa L.) bulb quality during long term cold storage

The storability of onion bulbs is dependent on the incidence and rate of sprout growth. Exogenous ethylene applied continuously has been demonstrated to act as a sprout suppressant in onion. However, the ethylene binding inhibitor, 1-methylcyclopropene (1-MCP), can also suppress sprouting in onion. Given this seemingly contradictory result, the precise role that ethylene plays during onion storage and the effect of curing on its efficacy is not understood.‘Sherpa’ and ‘Wellington’ onion bulbs were treated before or after curing (28 °C for 6 weeks) with a single dose of 10 μL L⁻¹ ethylene or 1 μL L⁻¹ 1-MCP for 24 h at 20 °C, or no treatment (control). Replicated out-turns were sampled during 38 weeks storage at 0–1 °C. Sprout growth (31 weeks after harvest) was reduced in ‘Sherpa’ treated before curing with ethylene or before or after curing with 1-MCP. However, sprout growth of ‘Wellington’ was not affected by any treatment. Following treatment, the cured, thick-skinned ‘Wellington’ released a lower concentration of treatment gas compared with the newly harvested, thin-skinned ‘Sherpa’. Onion bulb respiration rate increased immediately after being treated with ethylene but to a lesser extent or not at all when treated with 1-MCP. Fructose concentrations of onions treated with ethylene or 1-MCP before curing were not significantly different, however, after curing concentrations were about 2-fold higher compared with the control. Mean glucose and sucrose concentrations for both cultivars were higher immediately after being treated before curing with ethylene or 1-MCP than control bulbs. It appears that inhibition of sprout growth can be achieved using just a short 24 h treatment with ethylene or 1-MCP. However, skin thickness or permeability, which is dependent on cultivar and curing, may affect ethylene or 1-MCP influx and therefore efficacy of sprout suppressant action.     

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.     

Influence of year and genetic factors on chilling injury susceptibility in peach (<Emphasis Type="Italic">Prunus persica</Emphasis> (L.) Batsch)

Chilling injury (CI) is a major physiological problem limiting consumption and export of peach and nectarine (Prunus persica (L.) Batsch). To clarify the genetic basis for chilling injury, inheritance of the major CI symptoms mealiness, flesh browning, flesh bleeding, and flesh leatheriness were examined over three years in two related peach progenies. In addition, genetic relationships among traits and the year-to-year variation in trait performance in these progenies were tracked. Both populations also segregated for Freestone-Melting flesh (F-M) and yellow flesh. There were significant differences in CI symptoms among years. The major gene endoPG, which controls the F-M locus, provides resistance to mealiness in non-melting flesh fruit. Only fruit with melting flesh can develop mealiness if the tree possesses other genetic susceptibility factors and/or experiences inducing conditions. The F-M locus also greatly influences susceptibility to flesh bleeding, although the physiological mechanism for this disorder is unclear and may be controlled by a different gene closely linked to endoPG. Unlike mealiness, flesh bleeding occurred primarily in non-melting flesh fruit, particularly when the fruit is white-fleshed. Flesh browning incidence was greater in mealy fruit and was not associated with flesh bleeding. Breeding for CI resistance is thus a viable long-term strategy to reduce losses in the fresh and processed peach and nectarine industries. This study is an important first step to understanding genetic control of CI symptoms in peach.     

Calcium chloride extends the keeping quality of fig fruit (Ficus carica L.) during storage and shelf-life

The effects of postharvest application of fruit hardening chemical agents on fig (Ficus carica L. cv. Poona) fruit were compared with untreated figs during storage. The impact of calcium chloride (4%) was notable in terms of retention of fruit color, texture and increased accumulation of ascorbic acid, compared to untreated control figs. Pretreatment with calcium chloride (4%) was found to be most effective in checking the growth of both mesophilic aerobic bacteria and yeast and molds at low temperature (1 ± 0.5 °C; 95–98% RH) storage and it further delayed ripening and senescence of figs and was beneficial in prolonging the postharvest life twofold. Treated figs without microbial spoilage could be used for short term storage, transportation, distribution and marketing for long distance domestic markets in India.     

Combining ability and patterns of inheritance for plant and fruit traits in Japanese quince (Chaenomeles japonica)

Phenotypic variation and pattern ofinheritance was investigated for plant andfruit traits in Japanese quince (Chaenomeles japonica, Maloideae). Japanesequince is a minor fruit crop in Latvia andLithuania, and is presently being developedfor production of juice, aroma and fruitfibre in Sweden and Finland. General andspecific combining ability was estimatedfor five plant vegetative traits, eightfruit yield and morphology traits, and fivefruit biochemistry traits in a studypopulation consisting of 14 hybridfamilies. Thorniness seems to be controlledprimarily by a single locus. All othertraits studied appear to be governedprimarily by additive genes, as judged fromgeneral combining ability estimates.Significant specific combining ability(SCA) was detected for yield, plant heightand some fruit traits. However, therelative contribution of SCA to the overallgenetic variance was in general low. Anefficient breeding strategy for Japanesequince could therefore be based onrecurrent selection.