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Published online 2010 Oct 28. doi: 10.1007/s13197-010-0133-y

A legislative aspect of artificial fruit ripening. The PDF file you selected should load here if your Web browser has a PDF reader. Ethylene effects include fruit ripening, loss of chlorophyll, abortion of plant parts, stem shortening, abscission of plant parts, and epinasty (bending of stems). Eating artificially ripened fruits is harmful. B., Artificial ripening of fruits and vegetables. GET pdf × Close Log In. Ripening of fruits by artificial heat. In ripe fruits the chemical transformations are proceeding at a high rate, while in green fruits digestion and respiration are comparatively slow. Even if the processes of 'respiration and. Also, a greater amount of banana oil is app::irently produced in the fruits.

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Abstract

Banana (Musa sp var ‘Robusta’) fruits harvested at 75–80% maturity were dip treated with different concentrations of ethrel (250–1,000 ppm) solution for 5 min. Ethrel at 500 ppm induced uniform ripening without impairing taste and flavour of banana. Untreated control banana fruits remained shriveled, green and failed to ripen evenly even after 8 days of storage. Fruits treated with 500 ppm of ethrel ripened well in 6 days at 20 ± 1 °C. Changes in total soluble solids, acidity, total sugars and total carotenoids showed increasing trends up to 6 days during ripening whereas fruit shear force values, pulp pH and total chlorophyll in peel showed decreasing trends. Sensory quality of ethrel treated banana fruits (fully ripe) were excellent with respect to external colour, taste, flavour and overall quality.

Keywords: Robusta banana, Musa sp, 2-Chloro ethyl phosphonic acid, Ripening

Introduction

India is the largest producer of banana (Musa sp) in the world with an annual production of 23.205 million MT from an area of 0.647 million ha (NHB 2009). Banana var. ‘Robusta’ is one of the important tropical fruits grown commercially in India and is produced in large quantities throughout the year. Banana is a climacteric fruit and after harvest it exhibits a respiratory peak during natural ripening at 20 °C. Most of the banana bunches are harvested at complete maturity while they are green and unripe and subsequently allowed to ripen at ambient conditions. To meet the regular domestic requirement, green banana bunches are artificially ripened. Smoke treatment is one of the most common methods adopted to induce ripening (Ram et al. 1979). In this method, banana bunches are exposed to smoke generated by burning kerosene stove inside the airtight chambers for 24 h. As a result, the temperature inside the chamber also increases besides evolving ethylene gas with traces of other gases like acetylene and carbon monoxide. The ethylene gas triggers the enzymatic reactions in banana fruits causing early and uniform ripening with development of yellow colour on the skin along with its flavour. However, this type of smoke treatment is crude and ineffective as controlled ethylene treatment and also evolution of carbon monoxide is hazardous to health. Improper smoke treatment leads to uneven ripening and also poor external colour (yellow) development since the optimum temperature and relative humidity (RH) are not maintained in the ripening chamber. Otherwise generally, bananas are artificially ripened in local markets by the use of banned chemical calcium carbide. The use of this chemical is prohibited due to health reasons (PFA 2003). Extensive work has been done to study the effect of chemical substances to induce ripening (Singh et al. 1977; Nicholas and Thompson 1987). Commercially ethylene gas is used to ripen banana. But ethylene gas may be prove explosive when it reaches higher concentration. Hence, it has to be used very carefully. Commercial liquid like ethrel releases ethylene. It has been reported that exogenous application of ethylene in the form of ethrel accelerates ripening, increases colour and eating quality with reduced spoilage in different varieties of mango (Saltveit 1999; Singh and Janes 2001). The present study was taken up to evaluate the effect of ethrel dip treatment on ripening and sensory quality characteristics banana var. ‘Robusta’ at room temperature (20 °C).

Materials and methods

Twelve banana (var. ‘Robusta’) bunches were harvested at optimum stage of maturity from an orchard near Mysore and were immediately transported to the laboratory. Banana hands were separated from each bunch and delatexed for about 2 h to drain latex from cut portion. Banana hands present in the top and bottom of each bunch were discarded as these were not suitable for ripening studies. Selected banana hands were washed thoroughly with potable water to remove dirt and foreign materials present.

Post-harvest treatments and ripening conditions

Banana hands were dipped in different concentrations of ethrel (2-chloro ethyl phosphonic acid) solution ranging from 250 to 1,000 ppm for 5 min. One group of banana hands was used as untreated control fruits. Treated fruits were air dried to remove surface moisture. Five hands of each treatment (5 replicate for each treatment) were packed in ventilated round shaped plastic baskets and covered with polyethylene sheet to create high RH (80%) and kept for ripening at 20 ± 1 °C (Saeed et al. 2001). At each time of sampling, 6 fruits from 2 hands from each treatment were used for recording physical and textural characteristics periodically on 2, 4 and 6 days of storage at 20 ± 1 °C.

Physical attributes

The changes in cumulative physiological loss in weight (PLW) in both treated and control fruits were recorded during storage. Pulp to peel ratio of fruits for each treatment was determined by dividing weight of pulp by peel weight. The fruit colour was measured using UV–visible spectrophotometer (Shimadzu UV 2100, Japan) at wave length of 360–800 nm and expressed as L, a, b Hunter colour values (Hunter 1975). Fruit firmness (shear) of whole fruit was determined by using Instron Instrument (Model 4301, High Wycombe, UK) and values are expressed as Newton required to shear the fruit into two parts with speed 50 mm/min (Rushing and Huber 1983).

Chemical composition

Five fruits were randomly selected from each treatment at each stage and peel was removed, pulp was homogenized in warring blender. Moisture content in peel and pulp of banana fruits at each stage was determined by drying in oven at 70 °C for 24 h. The total soluble solids (TSS) of fruit pulp was measured with the help of Erma hand refractometer, while titratable acidity (% malic acid), pH and total sugars, starch and chlorophyll content were analyzed as per Ranganna (1986) methods. Total carotenoids of fruit pulp was extracted (by repeated extraction) with petroleum ether and acetone (3:2 v/v ratio, 60–80 °C) according to the method of Roy (1973).

Sensory quality characteristics

Descriptive sensory quality of ripe fruits viz., colour and appearance, texture (finger feel), taste, flavour and overall quality were assessed by a panel of 10 judges.

Statistical analysis

All the determinations were made in three different batches. The data were subjected to analysis of variance using the method of Snedecor and Cochran (1967).

Results and discussion

Physiological loss in weight (PLW)

Data on the cumulative loss in weight due to transpiration and respiration processes indicated that banana fruits kept in open condition without ethrel dip treatment lost weight up to 6.7% on 8th day of storage (Table 1). Fruits treated with ethrel solution of different concentrations showed increasing PLW ranging from 2.1 to 8.8%. Results showed that increase in PLW was directly proportional to increase in ethrel concentration. Maximum PLW (8.8%) was recorded in fruits treated with 1,000 ppm of ethrel at the end of 6 days. This increase in PLW of ethrel treated banana fruits during ripening could be due to upsurge in respiration rate leading to faster and uniform ripening compared to untreated fruits. Similar results were reported by Singh et al. (1977) and Mahajan et al. (2008).

Table 1

Changes in physical characteristics in banana (var. ‘Robusta’) fruits during storage (20 ± 1 °C) and ripening

Ethrel, ppmStorage period, days
246
Physiological loss in weight (PLW),%
02.2 ± 0.43dw4.3 ± 0.25cy5.9 ± 0.25by
2502.1 ± 0.22cw5.0 ± 0.16bx7.5 ± 0.29ax
5002.7 ± 0.14cw5.0 ± 0.16bx8.6 ± 0.25aw
1,0002.4 ± 0.16cw5.7 ± 0.37bw8.8 ± 0.46aw
Pulp/peel ratio (1.2 ± 0.14a)
01.3 ± 0.16aw1.3 ± 0.08aw1.4 ± 0.14ax
2501.1 ± 0.14bw1.5 ± 0.22abw1.6 ± 0.22ax
5001.3 ± 0.16bw1.7 ± 0.28abw2.2 ± 0.33aw
1,0001.3 ± 0.22cw1.8 ± 0.22bw2.3 ± 0.22aw
Hunter colour, L (48.4 ± 1.23a)
048.4 ± 1.73ay47.2 ± 1.20ay45.5 ± 1.59ay
25056.5 ± 1.63ax56.4 ± 1.56ax57.3 ± 1.15ax
50063.5 ± 1.97bw68.0 ± 1.27aw62.7 ± 1.78bw
1,00054.0 ± 1.63bx65.3 ± 1.10aw64.4 ± 1.42aw
Hunter colour, a (−12.8 ± 1.88a)
0−2.8 ± 1.71aw−12.8 ± 1.93aw−11.7 ± 1.02aw
250−0.3 ± 0.90bx−4.8 ± 0.46cx−2.2 ± 0.28dx
500−8.7 ± 0.46bx−3.7 ± 0.36cx−1.2 ± 0.42dx
1,000−9.5 ± 0.86bx−2.6 ± 0.28cx−1.6 ± 0.16cx
Hunter colour, b (20.9 ± 1.49a)
020.8 ± 1.61ay21.2 ± 1.02ay20.1 ± 1.53ay
25026.3 ± 1.20ax27.6 ± 1.49ax28.6 ± 1.58ax
50030.8 ± 1.73aw31.5 ± 0.99aw33.4 ± 1.42aw
1,00026.3 ± 1.02cx30.6 ± 1.56bw34.4 ± 1.70aw
Shear force, N (79.1 ± 2.21a)
074.4 ± 1.73abw70.2 ± 1.66bw63.6 ± 1.84cw
25064.4 ± 1.73bx56.3 ± 2.49cx32.4 ± 1.73dx
50061.4 ± 2.41bx53.2 ± 2.36cx26.5 ± 2.48dy
1,00060.3 ± 2.33bx46.1 ± 2.12cy25.0 ± 1.41dy

Means with different superscripts (a, b, c, d, e) for ethrel treatments and (w, x, y, z) for storage period differ significantly (p ≤ 0.05), (n = 3). Initial values are given in parenthesis

Pulp/peel ratio

In ethrel treated banana fruits, weight of the fruit pulp increased with decrease in peel weight during ripening. Fruits treated with 1,000 ppm ethrel attained maximum increase in pulp to peel ratio of 2.3 followed by 2.2 in 500 ppm of treated fruits at the full ripe stage. Little change in pulp/peel ratio was recorded in control during storage. The results indicated that pulp to peel ratio of ethrel treated banana fruits during ripening increased with the increase in the ethrel concentration.

Changes in fruit colour

The intensity of greenness in the peel of all ethrel treated fruits decreased with fruit ripening and attained least ‘a’ values of −2.2, −1.2 and −1.63 in 250, 500 and 1,000 ppm of ethrel treated fruits, respectively on 6 days of storage. Fruits treated with ethrel also attained improvement in yellow colour of fruit peel as indicated by their respective ‘b’ values at the end of storage at 20 ± 1 °C. Tandon and Kalra (1995) also observed uniform yellow colour development in mango fruits treated by dipping in ethrel solution after harvest. There was no definite trend in the change of ‘L’ values.

Fruit firmness

Gas Used For Artificial Ripening Of Fruits

The rapid decline in fruit firmness (shear force) values were recorded from 79.1 N at 0 day to 25.0 and 26.5 N in 1,000 and 500 ppm ethrel treated fruits, respectively at full ripe stage of 6 days (Table 1). Texture of fruits decreased at faster rate in treated fruits with increase in ethrel concentration. The decrease in texture of treated fruits during ripening could be due to breakdown of insoluble protopectin into soluble pectin or by cellular disintegration leading to membrane permeability (Brinston et al. 1988). In control fruits, texture of fruits decreased slowly from 79.1 N (at harvest day) to 63.6 N and remained unripe and shriveled even after 6 days. Similar observations were reported in banana by Peleg (1977) and Thompson and Burden (1995).

Chemical changes

Artificial Ripening Of Fruits And Vegetables

Moisture content in fruit pulp gradually increased during ripening while in peel there was a gradual decrease in all samples (Table 2). Ethrel treatment had mariginal effect on moisture content (Table 2). The increase in pulp moisture content during ripening is due to carbohydrate breakdown and osmotic transfer from the peel to pulp (John and Marchal 1995). The pH of pulp in all ethrel treated banana fruits decreased gradually during ripening whereas, in untreated samples, not much changes were observed. The decrease in pH of ethrel treated fruit pulp could be due to increase in total acidity during ripening. Banana fruits treated with 500 and 1,000 ppm of ethrel solution could reach optimum stage of ripening in 6 days of storage when pulp pH decreased to 4.8. Total acidity of ethrel treated fruits (500 ppm) increased gradually and reached a maximum of 0.54% at the optimum ripe stage. Control fruits developed total acidity of 0.34% on 6th day, as the fruits were still in unripe condition. TSS increased with increase in the concentration of ethrel during ripening. The TSS of pulp during ripening increased from 3.2° B (Brix) to 18.0° B in 250 ppm, 24.0° B in 500 ppm and 23.8° B in 1,000 ppm ethrel treated fruits at the end of 6 days storage. In untreated fruits, the change in TSS content in the pulp was slow and reached to a maximum of 7° Brix after 6 days of storage. The increase in TSS of fruit pulp could be due to the breakdown of starch into soluble sugars.

Table 2

Changes in chemical composition of banana (var. ‘Robusta’) fruits during storage (20 ± 1 °C) ripening

Ethrel, ppmStorage period, days
246
Moisture (%), peel (91.8 ± 3.46aw)
091.6 ± 3.37aw89.5 ± 1.22aw89.3 ± 0.91aw
25090.7 ± 2.12aw88.9 ± 1.48aw86.5 ± 1.23aw
50090.7 ± 1.90aw89.3 ± 1.71aw88.8 ± 2.23aw
1,00090.00 ± 2.16aw88.9 ± 0.91aw88.8 ± 2.23aw
Moisture (%), pulp (72.1 ± 1.52b)
072.41 ± 1.78bw72.1 ± 1.49bw78.46 ± 1.76aw
25071.03 ± 0.82aw72.0 ± 1.61aw73.06 ± 1.46aw
50072.26 ± 1.63aw72.6 ± 1.94aw73.88 ± 2.30aw
1,00073.68 ± 3.70aw73.9 ± 2.82aw75.76 ± 3.79aw
pH (5.4 ± 0.14a)
05.4 ± 0.14aw5.4 ± 0.22aw5.3 ± 0.22aw
2505.0 ± 0.16awx4.9 ± 0.22ax4.8 ± 0.43aw
5004.6 ± 0.28bx4.7 ± 0.16bx4.8 ± 0.29bw
1,0004.6 ± 0.22bx4.7 ± 0.14bx4.8 ± 0.37bw
Total soluble solids (TSS), °Brix (3.2 ± 0.08c)
04.3 ± 0.46cz5.9 ± 0.57by7.0 ± 0.78by
25010.2 ± 0.14cy15.0 ± 0.22bx18.0 ± 0.94ax
50014.4 ± 0.16bx23.5 ± 1.08aw24.0 ± 1.41aw
1,00016.0 ± 0.41bw24.0 ± 0.82aw23.8 ± 1.88aw
Total acidity,% (0.24 ± 0.02c)
00.27 ± 0.02bcz0.32 ± 0.03abx0.34 ± 0.01ay
2500.41 ± 0.02by0.48 ± 0.01aw0.50 ± 0.02ax
5000.47 ± 0.01bx0.50 ± 0.04abw0.54 ± 0.02awx
1,0000.53 ± 0.01aw0.54 ± 0.01aw0.56 ± 0.02aw
Total sugars,% (1.5 ± 0.22b)
01.5 ± 0.14by1.8 ± 0.08bz2.0 ± 0.16by
2504.4 ± 0.22cx9.5 ± 0.22by11.0 ± 1.20ax
5007.2 ± 0.16cw13.5 ± 1.08bx17.6 ± 1.45aw
1,0007.4 ± 0.29bw15.6 ± 1.22aw17.4 ± 0.99aw
Starch in pulp,% (15.9 ± 0.29a)
012.6 ± 0.16bw8.6 ± 0.36cw7.4 ± 0.22dw
2508.4 ± 0.50bx3.7 ± 0.64cx1.6 ± 0.36dx
5004.8 ± 0.71by2.2 ± 0.16cy1.0 ± 0.43dx
1,0004.1 ± 0.29by2.0 ± 0.43cy0.98 ± 0.08dx
Total chlorophyll in peel, mg/100 g (3.6 ± 0.14a)
03.6 ± 0.08aw2.4 ± 0.14bw1.8 ± 0.14cx
2503.3 ± 0.08aw2.4 ± 0.16bw2.2 ± 0.14bw
5003.1 ± 0.14bw1.4 ± 0.16cx0.3 ± 0.08dy
1,0002.4 ± 0.43bx0.4 ± 0.08cy0.2 ± 0.08cy
Total carotenoids in pulp, μg/200 g (411 ± 1.41e)
0433 ± 5.72dy457 ± 2.2cz468 ± 2.2bz
250481 ± 7.87cx583 ± 2.2by647 ± 2.8ay
500522 ± 2.16cw623 ± 3.6bw726 ± 2.4ax
1,000523 ± 2.16cw610 ± 3.7bx752 ± 2.8aw

Means with different superscripts a, b, c, d, e for ethrel treatments and w, x, y, z for storage period differ significantly (p ≤ 0.05, n = 3). Initial values are given in parenthesis

The total sugars in mature green fruits was 1.5% at harvest time. No appreciable difference was observed in the development of total sugars in control sample at the end of 6 days of ripening (2%). Total sugars accumulation was 17.6 and 17.4% in fruit pulp with 500 and 1,000 ppm of ethrel treated fruits, respectively at the end of 6 days of ripening. Starch contents were lower with higher levels of ethrel concentration and gradually decreased during ripening. The results indicated that the conversion of starch into sugars was rapid in ethrel treated fruits than in untreated fruits. This could be due to the rapid induction of pre-climacteric and climacteric phases and onset of climacteric peak in respiratory metabolic pathways in starch hydrolysis (Marriot ).

Chlorophyll content in peels of 500 and 1,000 ppm ethrel treated fruits decreased from 3.6 to 0.3 and to 0.2 mg/100 g, respectively after 6 days of ripening. Whereas in control fruits the total chlorophyll content decreased from 3.6 to 1.8 mg/100 g after 6 days of ripening. The results indicated that the degradation of chlorophyll pigments in fruit peel in ethrel treated fruits was more rapid than in untreated fruits. This could be due to accelerated rate of diffusion of exogenous ethylene in peel of ethrel treated fruits which triggered the degradation of chlorophyll pigments (Terai et al. 1973). In untreated fruits, there was less chlorophyll degradation in the peel tissues in the absence of exogenous ethylene treatment which probably depends on ethylene produced by pulp (Vendrell and McGlasson 1971). Similar results were reported by Srinivasan et al. (1973). The total carotenoids in ethrel treated fruits increased from 411 to 726 and 752 μg/100 g in 500 and 1,000 ppm of ethrel treated fruits, respectively after 6 days of ripening, whereas control fruits pulp developed 468 mg/100 g even after 6 days of ripening. The improper development of total carotenoid pigments in pulp of control samples could be due to delayed ethylene biogenesis.

Sensory quality characteristics

The descriptive sensory quality evaluation revealed that the fruits treated with ethrel solution of 500 and 1,000 ppm could reach optimum ripe stage on 6th day of storage with excellent overall organoleptic characteristics with respect to external colour, sweet taste, flavour and overall quality characteristics of ripe fruits. However, control fruits remained unripe and shriveled even after 6 days of storage.

Conclusion

It may be concluded that 500 ppm of ethrel solution was optimum for inducing uniform ripening of 75–80% mature banana fruits in 6 days at 20 ± 1 °C. The ethrel treated fruits ripened in 6 days at 20 ± 1 °C. At full ripe stage fruits had excellent sensory quality characteristics with respect to external yellow colour, sweetness, taste, flavour and overall quality. This method may be adapted by the small traders as replacement to calcium carbide treatment.

Acknowledgement

Authors are grateful to Prakash V, Director, CFTRI, Mysore for his keen interest, constant encouragement and support during the course of investigation. Authors extend their sincere thanks to Rajarathnam S, Head, and Ramana KVR, Former Head, Department of Fruit and Vegetable Technology for their constant encouragement and guidance during the course of investigation.

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Ripening is a normal phase in the maturation process of fruits and vegetables. Upon its onset, it only takes about a few days before the fruit or vegetable is considered inedible. This unavoidable process brings significant losses to both farmers and consumers alike.

Ripening of fruits

Scientists have been working to delay fruit ripening so that farmers will have the flexibility in marketing their goods and ensure consumers of “fresh-from-the-garden” produce.

The Fruit Ripening Process

Ethylene is a natural plant hormone associated with growth, development, ripening and aging of many plants. This phytohormone is said to promote ripening in a variety of fruits including bananas, pineapples, tomatoes, mangoes, melons, and papayas. It is produced in varying quantities depending on the type of fruit. But when the concentration of ethylene reaches 0.1-1.0 ppm (parts per million), the ripening process in climacteric fruits is considered irreversible.
Climacteric fruits are usually harvested once they have reached maturity which then undergoes rapid ripening during transit and storage. Important tropical fruits such as banana, mango, papaya, pineapple and guava are examples of these fruits. Non-climacteric fruits do not ripen after harvest. Thus, in order to attain full ripeness and flavor, these fruits such as strawberries and oranges, are often harvested once they have fully ripened.

In tomatoes, it takes about 45-55 days for the fruit to reach full maturity. After which, it starts to undergo the ripening process. The production of ethylene within the fruit in turn signals the activity of different enzymes resulting in physiological changes such as change of color from green to red, softening of the fruit, and development of its distinct taste and aroma.

Normally, farmers pick their produce while they are still green. The ripening process is then induced by spraying the fruits or vegetables with ethylene gas when they reach their destination. For long hauls, fruits and vegetables are refrigerated to prevent damage and delay ripening.

However, there are drawbacks to these post harvest practices. Fruits that have been harvested prematurely may result in poor taste and quality despite appearing as fully ripened ones. Fruits transported for long periods under refrigeration also have the tendency to lose their quality.

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Controlling the Ripening Process

There are several ways by which scientists can control the ripening process by genetic modification.

Regulation of Ethylene Production

The amount of ethylene produced can be controlled primarily by “switching off” or decreasing the production of ethylene in the fruit and there are several ways to do this. They include:

a. Suppression of ACC synthase gene expression.ACC (1-aminocyclopropane-1-carboxylic acid) synthase is the enzyme responsible for the conversion of S-adenosylmethionine (SAM) to ACC; the second to the last step in ethylene biosynthesis. Enzyme expression is hindered when an antisense (“mirror-image”) or truncated copy of the synthase gene is inserted into the plant’s genome.
b. Insertion of the ACC deaminase gene.The gene coding for the enzyme is obtained from Pseudomonas chlororaphis, a common nonpathogenic soil bacterium. It converts ACC to a different compound thereby reducing the amount of ACC available for ethylene production.
c. Insertion of the SAM hydrolase gene.This approach is similar to ACC deaminase wherein ethylene production is hindered when the amount of its precursor metabolite is reduced; in this case, SAM is converted to homoserine. The gene coding for the enzyme is obtained from E. coli T3 bacteriophage.
d. Suppression of ACC oxidase gene expression.ACC oxidase is the enzyme which catalyzes the oxidation of ACC to ethylene, the last step in the ethylene biosynthetic pathway. Through anti-sense technology, down regulation of the ACC oxidase gene results in the suppression of ethylene production, thereby delaying fruit ripening.

Control of Ethylene Perception

Since ethylene signals the onset of fruit ripening, delayed ripening on some plants can be achieved by modifying their ethylene receptors. The gene ETR1 is one example, and it has been shown to encode an ethylene binding protein. Plants with modified ETR1 lack the ability to respond to ethylene.

Suppression of Polygalacturonase Activity

Polygalacturonase (PG) is the enzyme responsible for the breakdown of pectin, the substance that maintains the integrity of plant cell walls. Pectin breakdown occurs at the start of the ripening process resulting in the softening of the fruit. To produce a fruit with DR trait using this method, scientists insert an anti-sense or a truncated copy of the PG gene into the plant’s genome resulting in a dramatic reduction of the amount of PG enzyme produced thereby delaying pectin degradation.

Advantages of DR Technology

The increased shelf life of products offers several advantages to both producers and consumers:

  1. Assurance of top quality fruits and vegetables on the market. Farmers can now wait for the fruits and vegetables to attain full maturity before they are plucked from their vines thereby allowing the fruits to exude full quality. Consumers will get value for their money.
  2. Widening of market opportunities for farmers as their produce can now be transported for longer periods of time, some of which would not even require refrigeration.
  3. Reduction in postharvest losses. DR fruits do not go soft easily compared to conventional ones and are therefore more resilient to damage during handling and transportation. This ensures a significant percentage of the harvested fruits to end up on the market shelves.
  4. Extension in shelf life as fruits or vegetables as they stay fresher and nutritious for longer periods. These fruits will not easily go “over the hill”.


Safety Aspects of DR Technology

The first ever GM crop approved for marketing was the Flavr-SavrTM tomato produced by Calgene, Inc. (U.S.) in 1994. After thoroughly studying DR technology and its products, US regulatory agencies concluded that the DR technology is safe, it produces tomatoes that have the same nutritional composition as the conventional ones and that show no difference in levels of allergens or toxins compared to normal fruit. In addition, field trials have shown that the DR tomatoes do not pose any threat to other plants nor to any non-target organisms.

Other DR tomatoes that followed thereafter have also been granted deregulated status by regulatory agencies in several countries including the U.S., Canada, and Mexico. In 1996, the UK’s food safety regulators also gave their thumbs up to a DR tomato developed by Zeneca Seeds but it is not currently being sold in supermarkets.

A European First

On February 5, 1996, branches of Safeway and Sainsbury’s supermarkets throughout the UK started to sell tomato pureé made from genetically-modified tomatoes. This was the first time that food made from a GM organism had been sold in Europe.

Labels on the cans clearly stated that the product had been made with GM tomatoes. Although there was no legal requirement to label the product, both supermarkets adopted an ‘open’ information policy from the start. For the inquisitive customer there was no shortage of information: leaflets were available describing the product, its benefits to the environment and consumer, the technology, and the regulatory processes through which the product had to pass.

According to the supermarkets, sales in around 80 stores in which supplies were initially available were brisk. Figures indicated that once they bought the product, shoppers came back for more. In November 1997, Safeway Stores announced that they had sold three quarters of a million cans of the product, and that average sales per store of the modified tomato purée exceeded those of the conventional equivalent. One reason might have been the price: the new purée cost 29 pence for 170 grams while the traditional form cost slightly more: 29 pence for a mere 142 grams.

Both supermarket chains pledged that the new product would always be offered alongside its old-fashioned counterpart. This move pleased consumer groups, which had no objection to the purée, provided that it was safe to eat and that consumers were always given a choice.

However, commercial pressures generated by public concern about GM foods early in 1999 forced Sainsbury’s to announce that it would withdraw the product from sale. Stocks were exhausted by July 1999.

Source: http://www.ncbe.reading.ac.uk/NCBE/GMFOOD/tomato.html

Current Status of DR Technology

Delayed Ripening (DR) Technology has been applied for use in tomatoes, melons, and papaya. An interesting application of DR technology is in floriculture where experiments are underway to apply the technology to delay the withering of flowers.

In Southeast Asia, DR technology is being applied for use in papayas, a popular subsistence food and part of the general diet in the region. This technology could significantly increase the availability of this nutritious fruit to consumers and to small-scale and mostly resource-poor farmers in the region.

Regulatory approval of countries for crops with the DR trait.

CropCountriesType of Approval
CarnationAustralia
Norway
Cultivation
Cultivation
MelonUSAFood
TomatoChina
Canada
Mexico
USA
Food, feed, cultivation
Food
Food
Food, feed, cultivation

Source: ISAAA GM Approval Database. http://www.isaaa.org/gmapprovaldatabase.

References

Artificial Ripening Of Fruits Pdf Readers

  • Bleecker, A.B. and H. Kende. 2000. Ethylene: A Gaseous Signal Molecule in Plants. Annual Review Cell and Development Biology 16: 1-18.
  • Catalytic Generators, Inc. n.d. Ethylene. http://catalyticigenerators/com/whatisethylene.html.
    Essential Biosafety. 2002. Agriculture and Biotechnology Strategies, Inc.
  • Hautea, R., Y.K.Chan, S. Attathom, and A.F. Krattiger. 1999. The Papaya Biotechnology Network of Southeast Asia: Biosafety Considerations and Papaya Background Information. ISAAA Brief No. 11. ISAAA: Ithaca, NY.
  • ISAAA. 2003. Papaya Biotechnology Network of South East Asia Report.
  • PBS and ABSP II. 2004. Agricultural Biotechnology: Brief #3: What are GE Crops? http://absp2.cornell.edu/resources/briefs/documents/warp_briefs_eng_scr.pdf.

*Updated October 2018

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