Journal of Sustainability Science and Management
Volume 10 Number 1, June 2015: 66-75
ISSN: 1823-8556
© Penerbit UMT
PHYSIOLOGICAL AND BIOCHEMICAL PROPERTIES OF THREE
CULTIVARS OF WAX APPLE (Syzygium samarangense [Blume] Merrill
& L.M. Perry) FRUITS
MOHAMMAD MONERUZZAMAN KHANDAKER
1
*, A. I. ALEBIDI
2
, ABM SHARIF HOSSAIN
3
,
NASHRIYAH MAT
1
AND AMRU NASRULHAQ BOYCE
4
1
School of Agriculture Science and Biotechnology, Faculty of Bioresource and Food Industry, Universiti Sultan Zainal Abidin,
Tembila Campus, 22200 Besut, Terengganu, Malaysia.
2
Department of Pomology, College of Food and Agricultural Sciences,
King Saud University, KSA, Saudi Arabia.
3
Biotechnology Program, Biological Sciences, Faculty of Science, University of Hail,
Hail, KSA.
4
nstitute of Biological Sciences, Faculty of Science, University of Malaya, 50603, Kuala Lumpur, Malaysia.
*Corresponding author: moneruzzaman@unisza.edu.my
Introduction
The wax apple (Syzygium samarangense) is
a non-climacteric tropical fruit species. It is
also known as wax apple, rose apple or java
apple. Its pear-shaped fruits are usually pink,
light-red, red, green, sometimes greenish-
white, or cream-colored and are generally
crisp, with a subtly sweet taste or aromatic
flavor (Morton, 1987). The species presumably
originated in Malaysia and other South-east
Asian countries. It is widely cultivated and
grown throughout Malaysia and in neighboring
countries such as Thailand, Indonesia and
Taiwan (Moneruzzaman et al., 2011).
Currently in Malaysia it is cultivated mainly as
a smallholding business ranging from 1 to 5 ha
for each farmer. The cultivated area throughout
the country is estimated at about 2000 ha
in 2005 (Shu et al., 2006). In Malaysia, the
species shows a great potential to develop as
an export fruit industries.
There are three species of Syzygium,
namely the water apple (Syzygium aquem),
Malay apple (Syzygium malaccense) and wax
apple (Syzygium samaragense) bear edible
fruits. Wax apple contains fruit with more round
and oblong in shape and less watery compare to
the other Syzygium species and the fruits are
eaten raw with salt or cooked as sauce. The wax
apple fruit has a very low respiration rate, with
10–20 mg CO
2
/kg h at 20°C, although they are
highly perishable fruits (Akamine and Goo,
1979). The composition of wax apple per 100
g edible portion is water with more than 90%
portion, protein 0.7 g, fat 0.2 g, carbohydrates
4.5 g, fibre 1.9 g, vitamin A 253 IU, vitamin
B1 and B2 with traces amount, vit-C 8 mg, and
energy with 80 kJ/100 g (Wills et al., 1986).
Fruit growth and development are associated
with the morphological, anatomical and
physiological changes of the plant (El-Otmani
et al., 1987). Fruit maturation is associated
with changes in rind texture, juice composition
and taste (El-Otmani et al., 1987). Felker et
al., (2002) reported that the major variation in
fruit quality is not related to the environment
Abstract: A study under field condition was carried out to evaluate physiological and biochemical
properties of three cultivars of wax apple (Syzygium samarangense) namely ‘Jambu Madu Red’,
‘Masam Manis Pink’ and ‘Giant Green’. Physicochemical parameters, such as stomatal conductance,
fruit development, pigmentation, fruit shape, yield, total soluble solids (TSS), titratable acidity
(TA), sugar acid ratio, vitamin-C (vit-C), chlorophyll, carotene and anthocyanin content, in three
cultivars of wax apple were investigated. The highest stomatal conductance, color development
and yield were recorded in ‘Jambu Madu Red’ cultivar. Lowest amount of TA, highest TSS, sugar
acid ratio and carotene content were also observed in this cultivar. Earlier color development, fruit
maturity, good shape, highest vit-C and anthocyanin content were found in ‘Masam Manis Pink’.
Meanwhile, the highest chlorophyll a, b and total chlorophyll (chl
ab
) content and late maturation
fruit were recorded in ‘Giant Green’ Cultivar. Stomatal conductance showed positive correlation
with yield and fruit biomass. It is concluded that ‘Jambu Madu Red’ and ‘Masam Manis Pink’
cultivars are comparatively better yield than those of ‘Giant Green’ cultivar grown under tropical
field conditions.
Keywords: Wax apple, yield, TSS, TA, chlorophyll, carotene, fruit development.
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J. Sustain. Sci. Manage. Volume 10 (1) 2015: 66-75
or edaphic factors but rather ascribed to genetic
factors. Color is probably the most important
quality factor depending on light, temperature,
position on the tree, growing stage, leaf: fruit
ratio number (Shu et al., 2001). Chang et
al., (2003) stated that sucrose, glucose and
fructose are important quality parameters
that influence the anthocyanin biosynthesis in
wax apple fruits. The flowers, which contain
tannins, desmethoxymatteucinol, 5-O-methyl-
40-desmethoxymatteucinol, oleanic acid,
and b-sitosterol, are used in Taiwan to treat
fever and halt diarrhea (Morton, 1987).
Ethanolic leaf extract of wax apple exhibited
immunostimulant activity (Srivastava et
al., 1995), the hexane extract was found to
relax the hyper motility of the gut (Ghayur
et al., 2006), while the alcoholic extract of
the stem bark showed antibacterial activity
(Chattopadhayay et al., 1998). The fruit of
wax apple can also be used to treat high blood
pressure and several inflammatory conditions,
including sore throat. It was also reported
as useful fruits antimicrobial, antiscorbutic,
carminative, diuretic, and astringent (Rivera
and Obón, 1995). The fruit pulp of Masam
Manis Pink cultivar of wax apple is a rich
sources of phenolics content, flavonoids and
several antioxidant compounds (Simirgiotis
et al., 2007). It was also reported that edible
fruits of wax apple may have potential benefits
for human health because the presence of
polyphenolic antioxidants in it.
For the commercial purpose, the
difference in fruit quality among the cultivars
is important in order to grade the fruit. Since
there are no report that has been published on
the physiological and biochemical quality on
the cultivars of wax apple, this project was
conducted with the aims to evaluate the fruit
development, pigmentation and quality on
different cultivars of wax apple based on the
physiological and biochemical measurements
of the three cultivars Jambu Madu Red, Masam
Manis Pink and Giant Green of wax apple.
Methodology
Experimental Site
The experiments were carried out in an orchard
located at a commercial farm in Banting,
Selangor (2
0
30N, 112
0
30E and 1
0
28 N, 111
0
20E) at an elevation of about 45 m above
sea level. The area was covered by hot and
humid tropical climatic condition. The soil
in the orchards is peat with pH 4.6 (Ismail et
al., 1995). The experiments were conducted
in between the year of 2009 to 2010. The
experiments were carried out in the first season
from October 2009 to February 2010, and in
the second seasons from April to August 2010.
Plant Material
Twelve years old wax apple plants in the field
were selected for the study. The planted trees
were in a 4.5 ft × 4.5 ft hexagonal arrangement
and received the same intercultural operation;
fertilization, irrigation and insecticide
application. Three wax apple cultivars namely;
‘Giant Green’, ‘Masam Manis Pink’ and ‘Jambu
Madu Red’ were used in the study. Three trees
per cultivar were selected and used for fruit
sampling for each season. Thirty six uniform
branches (four branches per tree) of about the
same length, and diameter, and approximately
the same number of leaves from nine trees were
selected for fruit harvesting. The experiments
consist of 3 treatments (cultivar), with twelve
replications and four uniform branch was taken
as an experimental unit. The selected uniform
branches were tagged properly at the beginning
of flower opening until fruit maturation. The
experiments were arranged in a complete
randomized design.
Measurement of Physiological Parameters
(Stomatal Conductance, Fruit Development,
Fruit Biomass and Color Development).
Leaves of selected uniformed branches were
used for stomatal conductance measurement
that was done at 11.00 am under fully sunshine
condition during fruit developmental stage.
Stomatal conductance was measured by using a
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Mohammad Moneruzzaman Khandaker et al.
68
J. Sustain. Sci. Manage. Volume 10 (1) 2015: 66-75
Titrable Acidity (TA)
The fruit juice was extracted by using a Phillips
HR1833 Juicer Extractor. The fruit juice was
titrated with 0.1 M NaOH and the results were
expressed in terms of percentage of citric acid
which was calculated by using the Bhattarai and
Gautam (2006) formula. Thus TA percentage
can be calculated as following,
N
b
× V
b
×E
a
× d f× 100
TA (%) =------------------------------
V
s
Where N
b
= normality of the base, V
b
= volume
of the base, E
a
= mill equivalent weight of citric
acid, V
S
= volume of sample and df = dilution
factor.
Total Soluble Solids (TSS) and Acidity Ratio
Total soluble solids (TSS) of fruit is one of
the parameters that strongly affect consumer
acceptability of a variety. The total soluble
solids (TSS) value was determined at 25°C
by using portable hand refractometer, 8469
(Atago Co. LTD., Tokyo, Japan) and expressed
the value as °Brix. The pulp of the fruit was
homogenized by using a blender. A small
fraction of the homogenous fruit pulp was
centrifuged at 4000 ×g for 10 min, and the
clear supernatant was analyzed chemically for
determinate the TSS. The sugar acid ratio of
the fruit juice is given as the ratio of TSS/TA.
Total Ascorbic Acid (Vitamin-C) Content
Total ascorbic acid (vit-C) content was
determined by adopting the method modified
by Hashimoto and Yamafuji (2006). Five g
of fruit pulp was homogenized with cold 5%
metaphosphoric acid and then filtered through
the cloth sheet. A 0.8 mL of filtrate was then
reacted with the mixture of 0.4 mL of 2% di-
indophenol, 0.4 mL of 2% thiourea and 0.4 mL
of 1% dinitrophenol hydrazine. After that the
mixture was incubated at 37 °C for 3 hours and
then 2 mL of 85% sulphuric acid was added.
The solution was again left at room temperature
for 30 minutes and the absorbance at 540 nm
was then recorded using spectrophotometer.
portable Leaf Porometer, (Modal SC-1, USA).
Fruit shape (length and diameter ratio) is an
important component of the visual fruit quality
and can be influenced by several factors. Fruit
shape was classified by visual inspection
as round, round-flattened, oblate [spheroid;
length: diameter ratio (L: D) ˃1.5], oblong
(blossom end larger than stem-end; L: D 1.5–
2), pyriform (having a secondary constriction;
L: D 1.5–2), elliptical (blossom- and stem-
end equal size; L: D 2–3), and elongate (L:
D˃ 3) (Miriam et al., 2008). Fruit length, fruit
diameter and fruit growth was measured with
the Vernier caliper. Total yield were determined
by total number and weighing mature fruits
per individual plant. Fruit dry biomass was
determined by weighing the pulp mass at 0%
moister content. The skin color of the fruits
was measured by using a Minolta colorimeter,
CR-300, Konica, (Japan). Color parameters
such as “L” (lightness), “a” (greenness to
redness) and “b” (blueness to yellowness) were
determined at three different spots at the top,
middle and end of the fruits. The changing in
color of the tagging fruits was measured at the
stage of fruit development from pit stage until
harvest. Fruit sample colors were calculated
and expressed in L*, a*, b* Hunter parameter,
by using the formula (L* x a*) / b*. Fruit length
and diameter ratio was measured immediately
after harvested from the tree.
Measurement of Biochemical Parameters
Fruits of different cultivars were randomly
harvested from the selected outside branches at
fully ripening stage during the first and second
fruiting seasons of the trees. Fruit maturity was
measured by observing the skin color of wax
apple cultivars. Harvesting was carried out
manually in the early morning with a minimum
mechanical injury. Fully ripened fruits were
kept in a refrigerator at 4ºC with 80-90% RH
for used in biochemical analysis. A total of 24
fruits were taken randomly from each cultivar
for use in the analysis.
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J. Sustain. Sci. Manage. Volume 10 (1) 2015: 66-75
Table 1: Fruit development of different cultivars of Syzygium samarangense
Cultivar
Stomatal
Conductance (Gs)
Bud
development
Flower opening
& anthesis
Fruit
development
.........................................................................................
mol H
2
Om
-2
s
-1
Fruit set, Cell division, Cell expansion & Maturation
‘Giant Green’
0.031± 05b
24±5 day
3±2 day
50±5DAA
‘Masam Manis Pink’
0.036 ±11b
18±4 day
3±2 day
38±4DAA
‘Jambu Madu Red’
0.039±13a
20±5 day
3±2 day
45±5DAA
**
ns
ns
**
Total vit-C content was expressed as mg vit-C
per 100 g fresh weight.
Chlorophyll, Carotene and Anthocyanin Content
In this study, the chlorophyll in the fruits skin
was measured at the fully ripening stage.
The chlorophyll of fruits was determined
by methods described by Hendry and Price
(1993). The total carotene and anthocyanin
contents of the hydrophilic extracts were
measured by using the pH-differential method
with cyanidin-3-glucoside used as a standard
(Rodriguez-Saona et al., 2001).
Statistical Analysis
The experimental design was a completely
randomized design (CRD) with twelve
replicates. The data from the two seasons were
pooled and analyzed using MSTAT-C statistical
software. One way ANOVA was applied to
evaluate the significant difference between
cultivars for each parameters studied. Least
significant difference (Fisher’s protected LSD)
was calculated, and F-test at (p = 0.05) was
determined as the significant level.
Results and Discussion
Physiological Measurement
Stomatal Conductance
Stomatal conductance affects the photosynthesis
rate by regulating CO
2
fixation in leaf mesophyll
tissue. Accumulation of dry matter content in the
plants depends on the stomatal conductance.
With regard to the stomatal conductance of the
leaves, ‘Jambu Madu Red’ cultivar produced a
significantly difference from the ‘Giant Green’
and ‘Masam Manis Pink’ cultivars. The result of
this study indicated that, stomatal conductance
measured in a sunny day at 11.00 am was
highest (0.039 mol H
2
O m
-2
s
-1
) in ‘Jambu Madu
Red’, followed by conductance of 0.036 mol
H
2
O m
-2
s
-1
in ‘Masam Manis Pink’. The lowest
stomatal conductance 0.031 mol H
2
O m
-2
s
-1
was
recorded in ‘Giant Green’ cultivar (Table1).
Stomatal conductance also depends on cultural
conditions. Nahar and Takeshi (2002) observed
that the using of synthetic auxin (figaron) with a
lower concentration had increased the stomatal
conductance but with a higher concentration
had decreased the conductance in soybean.
Fruit Development (Number of Day Flowering
Opening to Maturity)
The variations for bloom to maturity time
of apple cultivars have been reported by
Westwood (1978) and it was 135 and 150 days
in ‘McIntosh’ and ‘Golden Delicious’ apple
cultivars respectively. In this study, for bud
development, ‘Masam Manis Pink’ cultivar
requires 18 ± 4 days small tiny bud to open
and ‘Jambu Madu Red’ requires 20 ± 5 days,
whereas, ‘Giant Green’ cultivars requires 24 ±
5 days (Figure 1). There were no differences
among the cultivars from flower opening to
anthesis periods. It takes more or less 3 days.
The fruit developmental period after anthesis
varied significantly with different cultivars of
Syzygium samarangense. Results showed that
Means ( ± S.E) within the same column followed by the same letter, do not differ significantly according to
LSD test at ά=0.01 ns, non-significant * Significant at 0.05 levels, ** Significant at 0.01 levels
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J. Sustain. Sci. Manage. Volume 10 (1) 2015: 66-75
‘Masam Manis Pink’ cultivar had the earliest
fruit development and maturity approximately
38 days after anthesis followed by ‘Jambu
Madu Red’ cultivar with nearly 45 days (Figure
1). On the other hand, ‘Giant Green’ cultivar
had late maturity which about 50 days to reach
harvest stage from anthesis.
Our findings supported the results of
Morton (1987) who reported that the average
period from anthesis to berry maturity in wax
apple cultivars is about 35 to 50 days.
Fruit Development (Length Diameter Ratio of
the Fruit)
Length and diameter ratio of the wax apple
varied significantly among the three cultivars.
The highest length diameter ratio (1.78) was
recorded in “Jambu Madu Red” cultivar,
followed by ‘Giant Green’ with a L/D ratio of
1.21, whereas, the lowest (1.0) length diameter
ratio was recorded in ‘Masam Manis pink’
cultivar (Figure 1 & Table 2).
Color Development
Color is an important aspect of both fresh and
processed fruits particularly for commercial
reasons. Colors in the fruits reflect the presence
of certain biologically active phytochemical
compounds and antioxidants that reportedly can
promote good health. The development of red
pigmentation in the skin of maturing wax apple
fruits is the result of a massive accumulation
of anthocyanin content and chlorophyll
degradation during the maturation period
(Zhang et al., 2008). Positive values of a* and
b*, as observed in this work, are attributed to
carotenoids or anthocyanins present in the skin.
Fruits of wax apple produced the
significance difference of skin color among
the three cultivars. Figure 2 shows that fruit
Figure 1: Photograph showing fruit development and ripening of different cultivars of Syzygium samarangense
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J. Sustain. Sci. Manage. Volume 10 (1) 2015: 66-75
color development was drastically change in
the fruits of ‘Masam Manis Pink’ cultivar by
exhibiting the greatest percentage of skin color
between 14 and 35 DAA. It was also observed
that on day seven the pink and red color of the
fruits of the ‘Masam Manis Pink’ and ‘Jambu
Madu Red’ cultivar; beginning to appear, but
in ‘Giant Green’ cultivar, the color begins to
develop at three weeks after anthesis. At the
35
th
day of observation, the ‘Masam Manis
Pink’ cultivar fruits displayed at most 99%
pink color and fruits of ‘Jambu Madu Red’
cultivar showed about 95% color development,
whereas, ‘Giant Green’ cultivar was only 14%
(Figure 2). Figure 1, showed that ‘Masam
Manis Pink’ and ‘Jambu Madu Red’ cultivar
fruits produced significantly different in skin
color development from the fruit of ‘Giant
Green’ cultivar.
Fruit Biomass Development (Yield)
The results of this study showed that ‘Masam
Manis Pink’ and ‘Jambu Madu Red’ cultivar
produced the highest number of fruits per
plants than the ‘Giant Green’ cultivar (data not
shown). The total yield (kg/tree) was highest
(76.66 kg) in the ‘Jambu Madu Red’ cultivar
followed by ‘Masam Manis Pink’ cultivar with
a yield of 74.67 kg/tree, whereas minimum
yield (58 kg/ tree) was recorded in ‘Giant
Green’ cultivar (Figure 3). These differences
were found to be statistically significant
(P>0.05) among the different cultivars of wax
apple.
The results were in agreement with that
of Shu et al., (1998) who observed that trees
of S. samarangense yielded about 700 fruits
per plant with the fruit weight varies among
cultivars. Chiu (2003) reported that wax
apple (pink) is a heavy producer plant on well
fertilized good soils that can produce more than
200 fruit clusters per trees, with 4-5 fruits per
cluster when reach maturity. They also reported
that average fruit weight of ‘Masam Manis
Pink’ variety is about 100 g per fruit.
Correlation between Stomatal Conductance
and Biomass
Stomatal conductance affects the photosynthesis
rate by regulating CO
2
fixation in leaf
mesophyll tissue, that’s ultimately affects
the photosynthesis and yield of the crops.
Accumulation of dry matter content in plants
depends on stomatal conductance. The results
of this study showed that stomatal conductance
had a strong correlation (R
2
= 0.88) with the
fruit biomass development of wax apple.
Highest stomatal conductance (Gs) and fruit
biomass yield were observed in ‘Jambu Madu
Red’ cultivar followed by ‘Giant Green’
cultivar, whilst ‘Masam Manis Pink’ cultivar
had the lowest photosynthetic and dry fruit
biomass yields (Figure 4). The results of this
study were in line with the result of Nahar and
Takeshi (2002) which found that the stomatal
conductance of leaf regulates the dry matter
accumulation and yield in soybean.
Figure 2: Colour development in the fruit skin of three
cultivars of Syzygium samarangense. DAA = Day
After Anthesis
Figure 3: Fruit weight (kg/tree) of three cultivars of
Syzygium samarangense under field conditions
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J. Sustain. Sci. Manage. Volume 10 (1) 2015: 66-75
Biochemical Analysis
Titratable Acidity (TA)
Various organic acids have been reported
present in fruits and these include citric, malic,
acetic, fumaric, tartaric and lactic acids. The
main acid accounting for titratable acidity in
fruits is citric acid (Melgarejo et al., 2000). It
was reported that the decrease in fruit acidity
was coincided with an increase in sugar content
of the fruits. The results for the TA analysis is
shown in Table 2. Our results clearly indicated
that TA was significantly affected by genetic
of different cultivars. The lowest amount of
TA (0.78%) was observed in the ‘Jambu Madu
Red’ cultivar, followed by ‘Giant Green’ (0.83
%) and ‘Masam Manis Pink’ (0.90%). Our
results are in agreement with the results of
Supapvanich et al., (2011) which reported that
the range of TA in fresh cut wax apple was 0.75
-0.80 % of citric acid.
Total Soluble Solids (TSS) and TSS/TA Ratio
TSS content of fruit was not statistically
different among the cultivars of wax apple
(Table 2). It can be seen that the soluble solids
content in ‘Jambu Madu Red’ was wide-
ranging from 5.63 to 12.5% Brix. From this
study, it was observed that TSS content of the
fruits did not varied significantly among the
fruits within the same cultivar (Table 2).
The significant changes of sugar acid
ratio is the key factor affecting quality of the
wax apple cultivars. As shown in Table 2, the
sweetness index (sugar acid ratio) of fruits was
significantly affected by the different cultivars
of wax apple. The ‘Jambu Madu Red’ cultivar
increased the sugar acid ratio by 18%, followed
by the ‘Giant Green’ with increases of 5%
relative to the ‘Masam Manis Pink’.
Vitamin-C Content
Vit-C content in fruits varies among crop
species and is affected by environmental
factors, maturity, plant vigor and the age of the
plant. Figure 5 shows that Vit-C content varied
significantly among of different cultivars of
wax apple. The highest amount of vit-C content
(5.7 mg/100g) was recorded in ‘Masam Manis
Pink’ cultivar followed by ‘Jambu Madu Red’
and ‘Giant Green’ cultivar with a vit-C content
of 5.53 and 5.45 mg/100g respectively (Figure
5). Similar range of vitamin-C in fresh cut wax
apple fruit was observed by Supapvanich et al.,
(2011).
Table 2: Content of different pigments in ripening fruit of three cultivars of Syzygium samarangense
Cultivar
L/D
ratio
Titratable
acidity (TA) (%)
TSS
(% Brix)
TSS/TA
ratio
‘Giant Green’
1.21 ±0.01b
0.83 ± 0.05b
8.56±0.23a
10.31± 1.10a
‘Masam Manis Pink’
1.0 ±0.040c
0.90 ± 0.04a
8.89±1.18a 09.88± 0.98b
‘Jambu Madu Red’
1.78 ±0.07b
**
0.78 ± 0.04b
*
9.06±0.17a
ns
11.61±1.15a
*
Means (±S.E) within the same column followed by the same letter, do not differ significantly according to
LSD test at ά=0.01 ns, non-significant * Significant at 0.05 levels, ** Significant at 0.01 levels
Figure 4: Correlation between the stomatal conductance
and dry biomass yield of cultivars of wax apple
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J. Sustain. Sci. Manage. Volume 10 (1) 2015: 66-75
Chlorophyll Content
It is well documented in the literature that during
ripening, the skin of fruits changes from green
to a different brighter color. The most obvious
change which take place is the degradation
of chlorophyll content and accompanied by
the synthesis of other pigments usually either
anthocyanin or carotenoids. It was observed that
the chlorophyll content reduce loss gradually
according to the color turning changes of the
fruits. The results showed that ‘Giant Green’
cultivar had a significantly difference of
chlorophyll (a, b and ab) content compared
to the ‘Jambu Madu Red’ and ‘Masam Manis
Pink’ cultivars. The highest (3.43 mg/L) total
chlorophyll content in fruit skin was recorded
in ‘Giant Green’ cultivar followed by ‘Jambu
Madu Red’ and ‘Masam Manis Pink’ cultivar
with a chlorophyll content of 1.33 mg/L and
0.31 mg/L respectively.
Carotene Content
Carotenoids are the precursors of vitamin A, and
those commonly occurring in nature include α,
and γ carotene, lycopene and cryptoxanthin
(Goodwin, 1986). Among these, β-carotene
precursors, a major proportion of vitamin A
activity is analysed to represent the content of
carotene in the fruits. The results of this study
showed that the cultivars of S. samarangense
produced the significant difference of carotene
content among themselves. Table 3, showed
that ‘Jambu Madu Red’ cultivar fruits has
the highest (6.23 mg/L) carotene content as
compared with ‘Masam Manis pink’ and
‘Giant Green’ cultivar with carotene content of
3.16 and 1.83 mg/L respectively.
Anthocyanin Content
Anthocyanin pigments are responsible for the
red, purple, and blue colors of many fruits,
vegetables, cereal grains, and flowers. As a
result, research on anthocyanin pigments has
intensified recently because of their possible
health benefits as dietary antioxidants (Ronald,
2001). The anthocyanin content in ‘Masam
Manis Pink’ and ‘Jambu Madu Red’ cultivars
were significantly different from Giant Green
cultivar. ‘Masam Manis Pink’ and ‘Jambu
Madu Red’ cultivars produced 3.05 and 2.78
mg/L of anthocyanin respectively, meanwhile
‘Giant Green’ cultivar produced 0.95 mg/L
which is the lowest amount of anthocyanin
contents in the species. Khandaker et al., (2012)
also reported similar amount of anthocyanin
Table 3: Content of various pigments in ripening fruit of three cultivars of Syzygium samarangense
Cultivar
Chlorophyll-a
(mg/L)
Chlorophyll-b
(mg/L)
Total
chlorophyll
(mg/L)
Carotene
(µg/g)
Anthocyanin
(mg/100g)
‘Giant Green’
2.12±0.05a
1.31±0.13 a
3.43±0.18a
3.83±0.15c
9.5±0.15b
‘Masam Manis
Pink’
0.13±0.04c
0.16±0.08c 0.31±0.09c
5.16±0.31b
30.5±0.20a
‘Jambu Madu
Red’
0.72±0.07b
**
0.61±0.05b
**
1.33±0.09b
**
6.23±0.78a
**
27.8±0.15a
**
Means (±S.E) within the same column followed by the same letter, do not differ significantly according to
LSD test at ά=0.01 ns, non-significant * Significant at 0.05 levels, ** Significant at 0.01 levels
Figure 5: Vit-C content in different cultivars of
Syzygium samarangense
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Mohammad Moneruzzaman Khandaker et al.
74
J. Sustain. Sci. Manage. Volume 10 (1) 2015: 66-75
content in jambu madu with hydrogen peroxide
treatments. Anthocyanin content in the
fruits also varies within the cultivar which is
depending on the conditions of the environment
like light, temperature, growth substances etc.
The observations recorded in the present
investigation suggested that the three cultivars
of wax apple varied markedly with respect to
physiological and biochemical characteristics
under field conditions. These differences
appeared due to their genetic variations among
the cultivars and the ‘Jambu Madu Cultivar’
showed the better quality.
Acknowledgements
This research was supported by grants from the
University of Malaya, 50603, Kuala Lumpur,
Malaysia (Project No.RG002/09BIO) and
Universiti Sultan Zainal Abidin, Tembila
Campus, 22200 Besut, Terengganu (Project
No. UniSZA/14/GU/024).
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