Deastringency treatment with CO2 induces oxidative stress in persimmon fruit

Because of astringency at harvest, ‘Rojo Brillante’ persimmons are regularly submitted to deastringency treatment based on exposing fruit to a high CO₂ concentration. The treatment conditions that ensure total astringency removal throughout the various maturity stages have been determined to be 95% CO₂, 20 °C, 24 h. The aim of this study was to investigate changes in the redox state of persimmon fruit associated with this deastringency treatment. The levels of reactive oxygen species (ROS) (O₂⁻ and H₂O₂), and the activities of the main ROS scavenging enzymes (CAT, POD, APX, and SOD), were determined at harvest and after deastringency in fruit at three different maturity stages.Our results showed that during ‘Rojo Brillante’ persimmon maturation, the level of O₂⁻ gradually increased, while APX activity was lowered. The deastringency treatment with CO₂ induced oxidative stress in the fruit, observed as an over-accumulation of O₂⁻ and H₂O₂. As a response to ROS accumulation, the activities of the CAT, APX and SOD scavenging enzymes were up-regulated after deastringency treatment. The response of POD enzyme was dependent on maturity stage, showing enhanced activity after CO₂ treatment only for the fruit at the most mature stage.     

Analysis of the main secondary metabolites produced in tomato (Lycopersicon esculentum,Mill.) epicarp tissue during fruit ripening using fluorescence techniques

Tomato (Lycopersicon esculentum L.) fruit are an important source of antioxidant (mainly pigment) compounds, as well as lycopene, β-carotene, ascorbic acid and polyphenols. Differentiation of the final product in the market requires an accurate evaluation of these value-adding compounds. Because of this, we have undertaken a comparison of the spectral characterisation of the tomato fruit surface pigments from the immature to over-ripe stage, using spectroscopy techniques based on visible fluorescence emission upon excitation in the same or ultraviolet spectral regions. The aim was to verify the spectral band for optimal conditions for fruit harvesting using non-destructive techniques. The pattern of pigment composition changed markedly during ripening and showed progressive disappearance of chlorophyll with a concomitant increase in carotenoids until the fully ripe stage. The main fluorescence spectral features belonging to anthocyanins, flavonoids, carotenoids and chlorophyll a after excitation of skin tomato pigments at different laser wavelengths was identified. In comparing, the fluorescence spectral ratios at the excitation wavelength λ_exc = 266 nm, significant differences were obtained for the spectral ratios of chlorophyll/flavonoids and carotenoids/chlorophyll. Positive correlation coefficients were found for the carotenoids/flavonoids (0.780) ratios and negative ones for the carotenoids/chlorophyll ratios (−0.513).Analysis of fluorescence resulted in determination of the most useful laser radiation for remote non-invasive measurements with laser-induced fluoresence (LIF): for the ripening stage, λ_exc = 266 nm was the optimal laser wavelength, since the induced fluorescence spectra obtained appeared to differ with the physiological stage of the fruit.     

Effect of antioxidants in controlling enzymatic browning of minimally processed persimmon ‘Rojo Brillante’

‘Rojo Brillante’ is an important variety of persimmon that after removal of the astringency with high levels of CO₂, maintains firmness and sweetness, making possible its commercialization as a fresh-cut commodity. However, the commercial success of the product is limited mainly by enzymatic browning. This work presents the effect of a wide range of antioxidants on enzymatic browning of ‘Rojo Brillante’ persimmon combining in vitro (extracts and precipitates) and in vivo (cut tissue) studies. Preliminary screening of the antioxidants, determined by absorbance and color measurements of persimmon extracts and pellets, showed that 4-hexylresorcinol (Hexyl), citric acid (CA) and calcium chloride (CaCl₂) were effective at controlling browning at 10 mM; whereas, ascorbic acid (AA) required a higher concentration (25 mM). Peracetic acid, cyclodextrin, cysteine, and hexametaphosphate were not effective at controlling browning, even at a concentration of 50 mM. In in vivo studies, AA (1.12%) and CA (0.21%) were the most effective treatments to control enzymatic browning of fresh-cut material, reaching the limit of marketability in 5–7 days, whereas, Hexyl and CaCl₂ did not reach 1 day of storage. The results showed that optimum concentrations in cut tissue did not always correlate with the in vitro studies, indicating that antioxidants have an effect not only in browning reactions, but also in metabolic activity and cell wall changes during wound-induced reactions. The results provide relevant information for further development of minimally processed ‘Rojo Brillante’ persimmon during storage at 5 °C.     

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.     

The use of electrical impedance spectroscopy to assess the physiological condition of kiwifruit

The electrical impedance of kiwifruit [Actinidia deliciosa (A. Chev) C.F. Liang et A.R. Ferguson, cv. Hayward] was studied during fruit ripening. Measurements were made on whole fruit, and tissues excised from the outer pericarp, inner pericarp and core. Alternating current at frequencies between 50 Hz and 1 MHz was passed through fruit and tissue samples, and complex impedance spectra were separated into the resistances of the apoplast, cytoplasm and vacuole, and capacitances of the plasma membrane and tonoplast. The differences in R_50 Hz and R_1 MHz between tissues (representative of apoplast resistance and total tissue resistance, respectively) were explained in terms of the anatomy and composition of the respective tissues. Some variations were seen from one year to the other. During ripening, there was little change in the impedance characteristics of the fruit, despite a 10-fold decrease in firmness. This was unexpected since previous studies with nectarine, persimmon and tomato fruit have shown a considerable reduction in impedance during ripening. The failure to observe any impedance change was checked using a number of different methods for measuring impedance, by two different laboratories, and confirmed by measuring electrolyte leakage from tissue discs. All the results suggested that the mobility of electrolytes within the cell wall did not change during kiwifruit ripening. We speculate that physicochemical interactions that take place within the cell wall may have a major impact on the impedance of kiwifruit tissue.     

Increasing the rate of ripening of date palm fruit (Phoenix dactylifera L.) cv. Helali by preharvest and postharvest treatments

‘Helali’ is a late season date palm cultivar. At the mature (Bisir) stage, the fruit are astringent as a result of high contents of soluble tannins, and removal of tannins is necessary for the fruit to be edible. During the harvesting season, only 30–40% of the total fruit might normally ripen (Rutab stage) on the tree and the remaining fruit fail to ripen. This study showed that bunch bagging with different materials such as black or blue polyethylene bags, white ‘agrlsafe’ (polypropylene fleece) and paper bags during the growing season significantly increased the rate of fruit ripening and increased Rutab yield per bunch. In this respect, black and blue polyethylene bags were the most effective followed by ‘agrlsafe’ and paper bags. Preharvest ethrel application significantly increased Rutab fruit yield per bunch compared to the controls. There were no significant differences in Rutab yield per bunch between sprays or injection of ethrel into the bunch peduncle. Postharvest dipping of fruit at the Bisir stage in ethrel at 4.2 ml/l and abscisic acid at 1.0 mM significantly enhanced ripening, compared to the controls. However, ABG-3168 (an ethylene blocker) application at 3.33 g/l significantly inhibited ripening, suggesting a role for ethylene in the ripening process. Ethanol vapor significantly hastened ripening of Bisir fruit over 10 days at ambient conditions in desiccators. The response of immature fruit (according to fruit density and TSS) to ethanol vapor was much greater than mature ones. Also, immersion of fruit in water for 10 h significantly increased fruit ripening compared to the controls, but to a lesser extent. It is concluded that ‘Helali’ date ripening could be hastened by bunch bagging during growth, or by exposing the Bisir fruit to ethanol vapor following harvest. Neither treatment showed any negative impact on the overall quality characteristics of ripe fruit, suggesting that they may be practical tools for increasing the ripening rate of Bisir ‘Helali’ dates.     

Relationships between internal ethylene and optical reflectance in ripening ‘Antonovka’ apples grown under sunlit and shaded conditions

The feasibility of non-destructive estimation of internal ethylene concentration (IEC) in apple fruit via fruit reflectance using recently developed approaches and a fiber-optics reflectometer was investigated. The relationships between IEC and fruit reflectance in the 400–800 nm range were studied in stored apple (Malus × domestica Borkh., cv. Antonovka) fruit. A strong correlation between IEC and optical reflectance spectra taken from sunlit surfaces of the fruit was detected whereas reflectance of the shaded fruit surface showed a weak correlation with IEC. The increase of the reflectance in the red occurred along with IEC build-up during ripening resulting a strong (r² > 0.80) correlation. By contrast, reflectance in the blue-green part of the spectrum remained low and was negatively (r² ≈ 0.65) correlated with IEC. These observations are consistent with the phenomenon of degradation of chlorophylls which often occurs in parallel with the retention of carotenoids in ripening apple skin. As a result, IEC showed a significant correlation (r² > 0.69; P < 0.001) with the index based on reflectances in the red and blue-green regions of the spectrum (R₆₇₈ ? R₄₈₀)/R₈₀₀. The effects of strong solar light on the relationships between IEC and fruit reflectance are considered. The possibilities and limitations of a non-destructive reflectance-based assay of IEC in apple fruit are discussed.     

Control of alternaria black spot in persimmon fruit by a mixture of gibberellin and benzyl adenine,and its mode of action

In Israel, alternaria black spot (ABS) disease, caused by Alternaria alternata, is the main postharvest factor that reduces quality and impairs storability of persimmon fruit Diospyros kaki cv. Triumph. The fungus infects the fruit in the orchard and remains quiescent until harvest, or renews its development just before harvest, following rain or high humidity; it then preferentially colonizes the stem-end of the fruit. Recent findings suggest the importance of ethylene and respiration during early fruit growth as factors influencing maturity, crack development, and occurrence of ABS in the stem end of the fruit. We tested the effects of the growth regulator Superlon, a mixture of gibberellin (GA₄₊₇) and benzyl adenine (BA), applied at 40 μg mL⁻¹ once a month during three consecutive months, on fruit physiological responses during growth and on ABS occurrence during storage at 0 °C. Superlon treatments during the early stages of fruit growth, i.e., starting 40 days after fruit set (daf), applied once monthly during three consecutive months, inhibited ethylene and CO₂ production in the stem end. Treatments applied starting 100 daf enhanced cell proliferation under the fruit cuticle. Regardless of application timing, Superlon delayed chlorophyll degradation, and reduced fruit cuticle cracking and ABS susceptibility during the late stages of fruit growth and during storage. Present results suggest that the phytohormone, acting as a modulator of host physiological responses that result in delayed fruit maturation, is a main factor in enhanced resistance to ABS at harvest and during storage.     

The mechanism of differential susceptibility to alternaria black spot,caused by Alternaria alternata,of stem- and bottom-end tissues of persimmon fruit

In Israel, alternaria black spot (ABS), caused by Alternaria alternata, is the main postharvest factor that reduces quality and impairs storability of persimmon fruit Diospyros kaki cv. Triumph. The fungus infects the fruit in the orchard and remains quiescent until harvest, or starts development just before harvest, following rain or high humidity. During 2–3 months of storage at 0 °C, the pathogen colonizes the fruit, eliciting ABS symptoms. Susceptibility of the fruit to A. alternata attack is characterized by colonization in the upper, stem-end tissue, in contrast to lack of development at the bottom end. Comparison between the physiology of the stem-end and the bottom-end tissues showed greater production of ethylene and CO₂ in the former during early stages of fruit growth, and greater cracked areas and reduced chlorophyll levels in the later stages of growth, before harvest. Increasing fruit weight by increasing irrigation in the orchard enhanced the cracked area and susceptibility to ABS during growth and at harvest. Wound inoculation enhanced ABS colonization in both ends of the fruit, but more significantly in the upper stem end. The present results suggest that the differential susceptibility to ABS during storage is caused by a differential ripening process, and possibly, by increased maturity at the stem end, leading to cracking and increased ABS development.     

Effect of hyperbaric pressure and temperature on respiration rates and quality attributes of tomato

Previous work with hyperbaric treatment of tomato focused on application at lower temperature (13 °C). In this work, hyperbaric treatment at varying pressure levels (i.e., 0.1, 0.3, 0.5, 0.7 and 0.9 MPa) at ambient temperature (20 °C) was tested as a potential alternative to conventional refrigerated storage (0.1 MPa at 13 °C) to preserve tomato quality. The experiments were divided into 3 phases: (1) 4 day of hyperbaric treatment, (2) 5 day of post-treatment ripening, and (3) 10 day of post-treatment ripening. Respiration rate (RR) of the tomatoes was continuously monitored during the course of the hyperbaric treatments. Quality attributes were assessed immediately after removal from the hyperbaric treatments and after 5 and 10 day ripening at 20 °C after removal from the treatments. Hyperbaric treatments at ≥0.3 MPa resulted in RR equal or higher than the RR in control fruit (0.1 MPa at 20 °C). The lowest RR was obtained from tomato stored at 0.1 MPa at 13 °C. Hyperbaric treatment at 0.5, 0.7 and 0.9 MPa significantly reduced weight loss, retained color, firmness, total soluble solid (TSS), titratable acidity (TA) and TSS:TA ratio at similar levels as the tomato treated at 13 °C and 0.1 MPa. Firmness after treatment was highest for fruit from 0.1 MPa at 13 °C and from 0.5, 0.7 and 0.9 MPa at 20 °C. The higher firmness advantage declined by 5 day of ripening after treatment, with higher firmness only being retained for fruit from the 0.9 MPa at 20 °C and the 0.1 MPa at 13 °C treatments. After 10 day ripening, firmness was similar for all treatments. Lightness (L*) and hue angle were greater for all treatments compared with the 0.1 MPa at 20 °C treatment. However, only the greater hue angle difference was maintained after 5 day of ripening. After 10 day ripening, no significant differences were found in color attributes. Only 0.1 MPa at 13 °C retained higher soluble solids, lower titratable acidity and higher TSS:TA ratios after treatment and after 5 day ripening. At 10 day of ripening none of the quality attribute differences noted were retained for any of the treatments. These results show that the only consistent effect of hyperbaric treatment at 0.5, 0.7 and 0.9 MPa was to reduce weight loss and enhance firmness retention up to 5 day ripening after treatment.     

Efficacy of 1-MCP treatment in tomato fruit: 1. Duration and concentration of 1-MCP treatment to gain an effective delay of postharvest ripening

‘Raf’ tomato fruit were harvested at the mature-green stage and treated with 1-methylcyclopropene (1-MCP) at 0.5 (for 3, 6, 12 or 24 h) or 1 μl l⁻¹ for 3 or 6 h. Fruit were stored at 10 °C for 7 days and a further 4 days at 20 °C for a shelf life period. All 1-MCP treatments reduced both ethylene production and respiration rate and in turn retarded the changes in parameters related to fruit ripening, such as fruit softening, colour (a^*) change, and increase in ripening index (TSS/TA ratio). These effects were significantly higher when 1-MCP was applied at 0.5 μl l⁻¹ for 24 h. In order to obtain the maximum benefit from 1-MCP, this treatment would be the most suitable for commercial purposes.     

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.     

Effect of gamma irradiation on the physico-chemical and visual properties of mango (Mangifera indica L.), cv. ‘Dushehri’ and ‘Fazli’ stored at 20 °C

The effect of γ-irradiation doses (0.3, 0.5, 0.7, 1.0, 6.0, 10.0 kGy) on different physico-chemical and visual properties of two Indian cultivars of mango, cv. ‘Dushehri’ and ‘Fazli’ was observed during storage at 20 °C for the evaluation of delayed ripening and extension of shelf-life. Visually all the irradiated fruit showed greener peel and lighter pulp throughout the storage, however, radiation injuries were present in ‘Dushehri’ treated with 6–10 kGy and in ‘Fazli’ with 1–10 kGy. Loss of fruit due to rotting was less in the irradiated samples, treated up to 1 kGy of both the cultivars. Irradiated fruit of both the cultivars at high doses (6–10 kGy) showed increased sugar content from 0 d, however, all the treated fruit registered a slower rate of increase of sugars with storage compared to the respective controls and those treated with the lower doses of 0.5 and 0.7 kGy attained peak sugar concentration later. Significant (p ≤ 0.05) textural deterioration could be detected immediately after irradiation, in ‘Dushehri’ at doses ≥1 kGy and in ‘Fazli’ at doses ≥0.7 kGy. However, low dose treated fruit (0.3–1 kGy) of both the cultivars softened at a considerably slower rate during storage and registered significantly greater fruit firmness (compression strength) throughout the storage period. Similarly, ‘Dushehri’ treated with 0.3–0.7 kGy and Fazli treated with 0.7 kGy registered significantly greater flesh firmness (shear strength). ‘Dushehri’ treated with 0.3–1 kGy and ‘Fazli’ with 0.5–1 kGy also registered significantly harder and tougher peel, as determined by puncture test, throughout the storage. Scanning electron microscopy (SEM) performed on 3rd and 2nd d of storage of ‘Dushehri’ and ‘Fazli’ respectively, revealed microstructural breakdown at and above 1 kGy in both cultivars. Cell separation could be observed in ‘Fazli’ even at 0.7 kGy. SEM also revealed that the control fruit were in a more advanced stage of ripening than the low dose treated fruit. The study showed the feasibility of low dose γ-irradiation on ‘Dushehri’ (0.3–0.7 kGy) and ‘Fazli’ (0.5 and 0.7 kGy) that induced useful delay in ripening and extension of shelf-life by a minimum of 3 and 4 d, respectively.     

Effects of postharvest treatments on gene expression in Prunus persica fruit: Normal and altered ripening

Peach (Prunus persica) fruit have a short shelf-life, and the most common method employed to delay ripening and increase their postharvest life is cold storage. However, after extended storage at low temperature some cultivars have alterated ripening processes, resulting in a lack of juice and a woolly texture. To improve our understanding of the molecular mechanisms involved in the responses of peach fruit to cold storage we determined gene expression changes of fruit (cv. O’Henry) under different postharvest conditions: ripening (5 days at 21 °C), cold storage (21 days at 4 °C) and induction of woolliness (21 days at 4 °C followed by 5 days at 21 °C).Cluster analyses of genes differentially expressed between treatments revealed unique patterns associated with biological processes that operate during postharvest treatments. Genes up-regulated during postharvest ripening and woolliness include components of ethylene, and aroma biosynthesis as well as oxidative stress response. During cold storage treatment and woolliness, several genes linked to the oxidative stress response increased in abundance, suggesting changes in redox status. Quantitative RT-PCR analysis showed a sequential increase levels of mRNAs encoding key components of cellular stress response. Moreover, after 21 days of cold storage, expression of genes encoding oxidoreductase, catalase, superoxide dismutase and gluthatione reductase was still significantly higher than before cold treatment, suggesting that fruit cells were able to respond to the increased production of ROS that was induced by extended cold storage. In the woolly fruit, up-regulation of stress response genes was accompanied by down-regulation of key components of metabolic pathways that are active during peach ripening. The altered expression pattern of these genes might account for the abnormal ripening of woolly fruit.     

Role of putrescine in regulating fruit softening and antioxidative enzyme systems in ‘Samar Bahisht Chaunsa’ mango

The role of putrescine (PUT) in regulating fruit softening, antioxidative enzymes and biochemical changes in fruit quality was investigated during ripening and cold storage of mango (Mangifera indica cv. Samar Bahisht Chaunsa). Fruit were treated with various PUT concentrations (0.0, 0.1, 1.0 and 2.0 mM) and were allowed to ripen at 32 ± 2 °C for 7 days, or stored at 11 ± 1 °C for up to 28 days. Respiration rate and ethylene production were measured daily during ripening and cold storage. Cell wall degrading enzymes such as exo-polygalacturonase (exo-PG), endo-polygalacturonase (endo-PG), pectin esterase (PE), endo-1,4-β-d-glucanase (EGase), antioxidative enzymes including superoxide dismutase (SOD), peroxidase (POX), and catalase (CAT), fruit firmness as well as biochemical fruit quality characteristics were estimated during ripening and cold storage at 2 and 7 day intervals, respectively. PUT treatments reduced respiration rate, ethylene production and maintained higher fruit firmness during ripening as well as cold storage. PUT-treated fruit exhibited significantly suppressed activities of cell wall enzymes (exo-, endo-PG and EGase), but retained higher PE activity during ripening and cold storage. Total phenolic and antioxidant contents were significantly higher in PUT-treated fruit during ripening as well in the cold storage period than in the controls. Activities of antioxidative enzymes (CAT, POX and SOD) were also significantly higher in PUT-treated fruit during ripening as well as cold storage. SSC and SSC:TA were lower in PUT-treated fruit, while TA and ascorbic acid content showed the reverse trend. In conclusion, pre-storage 2.0 mM PUT treatment inhibited ethylene production and suppressed the activities of cell wall enzymes, while resulting in higher activities of antioxidative enzymes and maintaining better fruit quality during ripening and cold storage.     

Ripening-related defense proteins in Annona fruit

In order to obtain a better understanding of the active defense strategy of cherimoya (Annona cherimola Mill.) fruit, hydrolytic and antifungal activity, as well as expression of proteins functionally and immunogenically related to the pathogenesis-related proteins chitinase (PR-Q) and 1,3-β-glucanase (PR-2), were estimated in fruit at different ripening stages. Increase in expression of the 27 kDa constitutive chitinase and the induction of two new proteins, a 26 kDa chitinase and a 51 kDa 1,3-β-glucanase were associated with enhanced in vitro hydrolytic and antifungal activity of the acidic protein extract in ripe fruit. Ripening modified the expression of constitutive basic isoenzymes, with a sharp decrease in both relative accumulation and hydrolytic activity. Likewise, a new basic 33 kDa chitinase was induced in the over-ripe fruit, concomitant with accumulation of a basic constitutive 76 kDa 1,3-β-glucanase. At this stage, the basic protein extract modified in vitro growth inhibition of Botrytis cinerea. Short-term high CO₂ treatment delayed fruit ripening and maintained a similar distribution of activity and isoenzymatic pattern in both protein fractions to that in unripe fruit. These results indicate that the changes in the pattern of defense proteins and hydrolytic activity in cherimoyas appear to be associated with ripening. Moreover, unlike the constitutively expressed isoenzymes, only the transitorily induced chitinases and 1,3-β-glucanases were associated with an active defense-related response.     

Response of climacteric-type guava (Psidium guajava L.) to postharvest treatment with 1-MCP

Guava (Psidium guajava L. cv. ‘Allahabad Safeda’) fruit harvested at the mature light-green stage were exposed to 300 and 600 nL L⁻¹ 1-methylcyclopropene (1-MCP) for 6, 12 and 24 h at 20 ± 1 °C, and held in either cold storage (10 °C) for 25 days or ambient conditions (25–29 °C) for 9 days. Most of the physiological and biochemical changes during storage and ripening were affected by 1-MCP in a dose dependent manner. Ethylene production and respiratory rates were significantly suppressed during storage as well as ripening under both the storage conditions depending upon 1-MCP concentration and exposure duration. 1-MCP treatment had a pronounced effect on fruit firmness changes during storage under both the conditions. The reduced changes in the soluble solids contents (SSC), titratable acidity (TA) and vitamin C content showed the effectiveness of 1-MCP in retarding fruit ripening. Vitamin C content in 1-MCP-treated fruit was significantly higher than in non-treated fruit, and those treated with 300 nL L⁻¹ 1-MCP for 6 h. The development of chilling injury symptoms was ameliorated to a greater extent in 1-MCP-treated fruit during cold storage and ripening. A significant reduction in the decay incidence of 1-MCP-treated fruit was observed under both the storage conditions. 1-MCP at 600 nL L⁻¹ for 12 h, in combination with cold storage (10 °C) seems a promising way to extend the storage life of guava cv. ‘Allahabad Safeda’ while 1-MCP at 300 nL L⁻¹ for 12 and 24 h or 600 nL L⁻¹ for 6 h, may be used to provide 4–5 days extended marketability of fruit under ambient conditions.     

Low dose gamma irradiation does not affect the quality,proximate or nutritional profile of ‘Brigitta’ blueberry and ‘Maravilla’ raspberry fruit

Blueberry (Northern Highbush, cv ‘Brigitta’) and raspberry (cv ‘Maravilla’) fruit were subject to low dose gamma irradiation (0, 150, 400 and 1000 Gy) and stored at 0 °C for three or ten days (blueberry) and two or seven days (raspberry) to determine the effects of irradiation on fruit quality and nutritional and proximate contents. In general, none of the irradiation doses (≤1000 Gy) significantly affected blueberry or raspberry fruit quality (overall fruit quality, colour, firmness, weight loss, TSS, TA levels or TSS/TA ratio), or the nutritional or proximate content (ash, carbohydrate, dietary fibre, energy, moisture, protein, sodium, potassium, total sugars, fructose, ascorbic acid, monomeric anthocyanin, citric and malic acids). The length of time in storage affected some fruit quality and nutritional and proximate content parameters (such as overall fruit quality, firmness, weight loss, TA levels, dietary fibre, potassium, ascorbic acid, citric and malic acids), with longer storage periods resulting in lower quality fruit, irrespective of irradiation treatment. No interaction was detected between the effects of irradiation treatment and storage time, indicating that the storage effect was consistent for all irradiation doses on both blueberry and raspberry fruit quality.     

Treatment with 1-MCP and the role of ethylene in aroma development of mountain papaya fruit

Mountain or highland papaya (Vasconcellea pubescens) is a climacteric fruit which develops a strong and characteristic aroma during ripening. The dynamics of aroma volatile production during ripening of whole papaya fruit were analysed by headspace-SPME. The main compounds produced by the fruit were esters (aliphatic and branched) and alcohols: the most abundant esters were ethyl acetate, ethyl butanoate, methyl butanoate and butyl acetate, comprising 88% of the volatiles in fully ripe fruit; butanol was the most abundant alcohol. Among the volatiles produced, ethyl butanoate, ethyl acetate, ethyl hexanoate and ethyl 2-methylbutanoate were found to be the most potent odour compounds. During ripening of mountain papaya fruit there was an increase in the total content of both esters and alcohols. In order to clarify the role of ethylene in aroma formation, mature fruit were treated with 0.3 μL L⁻¹ of 1-MCP (16 h at 20 °C) or with 2 g L⁻¹ Ethrel, and then allowed to ripen at 20 °C. The treatment of the fruit with 1-MCP inhibited the rise in ethylene production in the fruit, while Ethrel advanced the development of the climacteric phase. Most esters identified in mountain papaya were dependent on ethylene, showing an increase in production during ripening and in response to Ethrel treatment, and a strong reduction in response to 1-MCP treatment. The data presented provide evidence that most esters produced by mountain papaya are derived from fatty acids and amino acid metabolic pathways, both of them being affected by ethylene.