Effect of Pre-Treatments on Biochemical and Microbial Parameters of Guava Fruit during storage
U. L. Nandaniya1, D. K. Gojiya*2, R. D. Bandhiya3 And Dr. D. K. Antala4
1,3P.G Scholar
2,4Assistant Professor
Department of Processing and Food Engineering, College of Agricultural Engineering and Technology, Junagadh Agricultural University, Junagadh-362001, India
Abstract:
Freshly harvested and fully matured guava fruits (Lucknow-49) were hydro-cooled at 2 ±1 °C for 10 min and pretreated with different
treatments viz., calcium chloride (2 %), hydrogen peroxide (1 %), benomyl (0.1 %), neem oil (2 %), lemon grass oil (0.2 %), cinnamon
oil (4 %) and ozone (150 mg/h). Fruits were packed in 50 µm LDPE bags and stored at 10 ± 1 o
C. Control fruits without any pre-treatment
were stored at low as well as room temperature. The biochemical, sensory and microbial parameters of the guava fruit were recorded at
5 days interval during storage. Minimum TSS (14.1 o
Brix) and total sugar (8.94 %) were observed in ozone treatment while maximum
titratable acidity (1.13 %) and ascorbic acid (236 mg/100 g) was observed in ozone treatment on 30 days of storage. Maximum sensory
score was found in ozone and in cinnamon oil treatments. Microbial parameters viz., total plate count, E.coli, salmonella and yeast and
mould in the fruit were found absent for ozone, cinnamon oil, neem oil and hydrogen peroxide treatments. Maximum changes in biochemical,
sensory and microbial parameters were found in control at room temperature followed by control at low temperature. Shelf
life of guava fruit could be increased up to 30 days with minimum changes in biochemical, sensory and microbial parameters when the
fruits pretreated with ozone (150 mg/h) followed by packaging in 50 µm LDPE bags at 10 ± 1 o
C storage temperature.
Keywords: Guava, Pre-Treatments, Chemical, Essential Oil, Ozone, Packaging and Storage
Introduction:
India is the largest producer of the guava fruit (Psidium Guajava
L.) in the world. Guava being climacteric fruit, it has very short
shelf life and marketing of fresh fruits to distant places is very
difficult. The short harvesting season, limited domestic demand
and improper storage facility creates glut in the market and consequently
loss to the fruit growers. Due to its short shelf-life, as
much as 18-20 % of fruits perish as post-harvest losses during
different post-harvest operations (Anon., 2014). Pre-storage treatments
viz., pre-cooling, certain chemicals, plant extracts (essential
oils), inhibitors, ozonation or combination prior to packaging and
storage play an important role to control insect pests, yeast and
mould on the food surface; prevent bacterial and fungal rots; destroy
pesticides and chemical residues which ultimately leads to
improve the shelf life of fruits.
Chemicals have been widely used to reduce the incidence of
post-harvest disease. Although effective, many of these materials
have been removed from the market in recent years because of
economic, environmental or health concerns. These problems associated
with the use of chemicals have stimulated the produce
industry to identify alternative treatments equivalent to chlorine
in antimicrobial effectiveness. The plant extracts are generally
assumed to be more acceptable and less hazardous than synthetic
compounds for preventing fungal decay in organic fruits after
harvest which is a novel preservation approaches. Ozonation is a
noble technology that can be used to sanitize produce. A naturally
occurring molecule, ozone is a powerful disinfectant. The potential
utility of ozone in the produce industry depends on the fact
that as an oxidizing agent, it is 1.5 times stronger than chlorine and
is effective over a much wider spectrum of microorganisms than
chlorine and other disinfectants.
At present no specific pre-treatment technique is followed for guava
fruit to control insect pests, bacterial and fungal rots on the food surface as well as destruction of pesticides and chemical residues
prior to packaging and storage. However good pre-treatment
before storage reduces post-harvest losses, preserves quality and
prolongs the shelf life of fresh guava fruit to fulfill the consumers
and market demand. International markets reject fruits and vegetables
containing unauthorized pesticides, with pesticide residues
exceeding permissible limits and with inadequate labeling and
packaging. Obviously, post-harvest management determines food
quality and safety, competitiveness in the market and the profits
earned by producers.
Materials and Methods:
Raw Material:
Freshly harvested and fully matured guava fruit cv Lucknow-49 at
colour breaker stage were procured and brought to the laboratory
in plastic crates to avoid any physical damage. The fruits were
graded on the basis of weight (120-150 g) to maintain homogeneity
and damaged fruits were sorted out. The fruits were thoroughly
washed with clean water to remove dust and dirt particles. Then,
the fruits were hydro-cooled (2 ± 1 o
C) using ice water for 10 minutes
to remove field heat. The pre-cooled fruits were pre-treated
with different treatments viz., calcium chloride (2 %), hydrogen
peroxide (1 %), benomyl (0.1 %), neem oil (2 %), lemon grass oil
(0.2 %), cinnamon oil (4 %) and ozone (150 mg/h). The fruits were
kept in different solutions for 10 minutes while for ozone treated
the fruits were kept for 8 minutes in ozone purifier.
Storage study:
After application of pre-treatments, the fruits were dried under
shade to remove surface moisture. Two fruits together were packed
in a 150 x 225 mm size of 50 µm thick LDPE bag with 80-100 mm
headspace. The samples were stored at 10 ± 1 o
C with 80-85 %
Rh in cold chamber. There were two control treatments. Control
fruits were not treated with pre-treatments. Control fruits packed
in LDPE bags were stored at 10 ± 1 o
C storage temperature. The
control fruits without packaging were stored at room temperature
(22 ± 7 o
C) with Rh range of 35-60 %.
Details of treatments:
A. Independent parameters :
1. Calcium chloride (CaCl2
, 2%) for 10 minutes
2. Hydrogen peroxide (H2 O2
, 1%) for 10 minutes
3. Neem oil (2%) for 10 minutes
4. Lemon grass oil (0.2%) for 10 minutes
5. Cinnamon oil (4%) for 10 minutes
6. Benomyl (0.1%) for 10 minutes
7. Ozone (150 mg/h) for 8 minutes
8. Control at 10 ± 1 oC storage temperature (with packaging)
9. Control at room temperature storage (22 ± 7 o
C) (without packaging)
B. Treatments : 09
C. No. of replications : 04
Biochemical parameters:
Total soluble solids (TSS) was measured by hand refractometer (range 0-90 %) and corrected at 20o
C. Total sugar was determined by phenol sulphuric acid method as reported by Sadasivam and Manikam, while ascorbic acid and titratable acidity was estimated as reported by Ranganna.
Sensory analysis:
Sensory characteristic in terms of overall acceptability of guava
fruit was evaluated on the basis of appearance, pulp colour and
taste after ripening of the fruits at room temperature (30 ± 2 o
C) for
two days by covering gunny bag. Sensory characteristics of ripe
fruits were evaluated by a panel of semi trained 10 judges using 9
point hedonic scale (Amerine et al., 1965).
Microbial parameters:
Total plate counts was measured using N-agar method,
E.coli was measured using EMB-agar method, Salmonella using
SS-agar method and Yeast and mould was measured using PDAagar
method as suggested by Downes and Ito (2001).
Statistical analysis:
The observations taken for various parameters of guava fruits at 5
days interval during storage were subjected to analysis of variance
technique considering Completely Randomized Design with four replications. All the treatments of the experiment were compared
at 5 per cent level of significance. The analysis of variance (ANOVA), standard error of mean (SEM), critical difference (CD), coefficient of variance (CV) and mean values were tabulated and the level of significance was reported as suggested by Panse and Sukhatme (1985).
Results and discussion:
Biochemical parameters:
Total soluble solids (oBrix):
TSS of the fruit enhanced with increase in storage period. The increase in TSS with storage period might be due to the increase in concentration of organic solutes as a consequence of water loss in the fruit. It is evident from the Figure 1 that TSS was observed minimum in ozone (14.1 o Brix) and maximum TSS was found in control at room temperature (16.5 o Brix) followed by control at low temperature (16.2 o Brix) at the end of storage period. The increase in TSS during storage was also reported by Wijewardane and Guleria (2009) in apple.

Figure 1 Effect of different pre-treatments on TSS of guava fruit
Total sugar (%):
The total sugars of the fruit increased with increase in storage period. The increase in total sugars with storage period might be due to the
release of sugars by the hydrolysis of polysaccharides. From the Figure 2, it is clear that total sugars was observed minimum in ozone
(8.94 %) and maximum total sugar was found in control at room temperature (13.28 %) followed by control at low temperature (12.11
%) at the end of storage period. The increase in total sugars with storage period was also reported by Eman et al. (2013) in mango.

Figure 2 Effect of different pre-treatments on total sugars of guava fruit
Titratable acidity (%):
Titratable acidity of the fruit decreased with increase in storage period. The decrease in titratable acidity might be due to the conversion
of acids into sugars and also use of organic acids as respiratory substrate during storage. From the Figure 3, it can be observed that titratable
acidity was observed maximum in ozone (1.13 %) and minimum titratable acidity was recorded in control at low temperature (0.76
%) at the end of storage period. Similar results for titratable acidity were also reported by Eman et al. (2013) in mango.

Figure 3 Effect of different pre-treatments on titratable acidity of guava fruit
Ascorbic acid (mg/100g):
Ascorbic acid of the fruit declined with advancement of storage period. The decrease in ascorbic acid might be due to the process of
oxidation of ascorbic acid. From the Figure 4, it is clear that ascorbic acid was found maximum in ozone (236 mg/100 g) and minimum
ascorbic acid was recorded in control at room temperature (162 mg/100 g) followed by control at low temperature (165 mg/100 g) at the
end of the storage period. These results for ascorbic acid are in agreement with the results reported by Monaco et al. (2014) in mango.

Figure 4 Effect of different pre-treatments on ascorbic acid of guava fruit
Sensory evaluation:
From the Table 1, it is clear that maximum sensory score of guava fruit (7.6) was observed in ozone and cinnamon oil treatments while
minimum score of overall acceptability was recorded in control at room temperature (4.5) followed by control at low temperature (5.3)
at the end of the storage period. These results are in conformity with the results reported by Antala et al. (2014) in guava.

Table 1 Effect of different pre-treatments on overall acceptability of guava fruit during storage
Microbial parameters:
Total plate counts:
Total plate counts was found absent after pre-treatments of guava fruit at initial stage. The mean value of total plate count of control fruits
at initial stage after hydro-cooling was 2×102 cfu/g. From the table 2, it is clear that total plate counts of the fruit increased with increase
in storage period in benomyl, calcium chloride, lemon grass oil and control. However, it was found absent in the fruits treated with
ozone, cinnamon oil, neem oil and hydrogen peroxide throughout storage period. Minimum total plate counts was recorded in benomyl
(8×102 cfu/g) and maximum total plate counts was recorded in control at room temperature (14×104 cfu/g) followed by control at low
temperature (11×104 cfu/g) at the end of storage period. These results for total plate counts are in agreement with Bialka and Demirci
(2007) in raspberry and strawberry.

Table 2 Effect of different pre-treatments on total plate counts (cfu/g) of guava fruits during storage
E.coli:
The effect of different pre-treatments on E.coli of guava fruit during storage is presented in Table 3. E.coli was not observed after and
before pre-treatments at an initial stage including control. E.coli was found present in lemon grass oil (1×102 cfu/g) and control at low
temperature (3×102 cfu/g) on 30 days of storage. It was also found in control at room temperature (2×104 cfu/g) on 10 days of storage.
Similar findings for E.coli were also reported by Achen and Yousef (2001) in apple.

Table 3 Effect of different pre-treatments on E.coli (cfu/g) of guava fruits during storage
Yeast and Mould:
Yeast and mould in guava fruits were found absent after pre-treatments at initial stage. From the Table 4, it is apparent that yeast and
mould was found absent in the fruits for ozone, cinnamon oil, neem oil and hydrogen peroxide treatments during entire storage period.
Yeast and mould in calcium chloride, benomyl and lemon grass oil was observed 8×102 cfu/g, 11×102 cfu/g and 2×104 cfu/g, respectively
at the end of storage period. Maximum yeast and mould was recorded in control at room temperature (16×104 cfu/g) followed
by control at low temperature (3×104 cfu/g) at the end of storage period. These results for yeast and mould are in conformity with the
results reported by Aday et al. (2014) in strawberry and Abd-El-Latif (2016) in apple.

Table 4 Effect of different pre-treatments on yeast and mould (cfu/g) of guava fruits during storage
Conclusions:
It may be concluded that ozone treatment (150 mg/h) followed
by packaging in 50 µm LDPE bags at low temperature storage
retained shelf life of fresh guava fruit up to 30 days with minimum
change in biochemical, sensory and microbial parameters of the
fruit.
Acknowledgement:
The authors are thankful to Dr. A. R. Pathak, Honorable Vice-chancellor,
Junagadh Agricultural University, Junagadh, Dr. V. P.
Chovatiya, Director of Research & Dean P.G. Studies Junagadh
Agricultural University, Junagadh, Dr. N. K, Gontia, Principal
and Dean, College of Agricultural Engineering and Technology,
Junagadh Agricultural University, Junagadh, Dr. B. A. Golakiya,
Professor and Head, Department of Biochemistry, College of
Agriculture, Junagadh, Dr. P. M. Chauhan, Professor and Head,
Renewable Energy and Rural Engineering Department, Junagadh
Agricultural University, Junagadh. Our thanks are also to Dr. P.
J. Rathod, Assistant Professor, Department of Biochemistry, JAU,
Junagadh, Prof. D. M. Vyas, Professor and Head, Dr. V. P. Sangani,
Assistant Professor, Dr. S. P. Cholera, Assistant Professor and
Prof. A. M. Joshi, Assistant Food Microbiologist, Processing and
food Engineering Department, College of Agricultural Engineering
and Technology, Junagadh Agricultural University, Junagadh.
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