Payel Ghosh1, Rama Chandra Pradhan2, Sabyasachi Mishra1. 1. Department of Food Process Engineering, National Institute of Technology, Rourkela, Rourkela, 769008, Odisha, India. 2. Department of Food Process Engineering, National Institute of Technology, Rourkela, Rourkela, 769008, Odisha, India. pradhanrc@nitrkl.ac.in.
Abstract
Jamun fruit comprises of seed and thick pulp. The pectin-protein bond of the thick pulp creates difficulty in making juice. Clear Jamun juice is not available in the market, so there is a need for extraction of juice with maximum yield. The goal of this research is to obtain high yield of clarified juice with the help of Pectinase (Aspergillus aculeatus) enzyme. The study was conducted at different enzyme concentration (0.01-0.1%), time duration (40-120 min), and temperature (30-50 °C). Various physical and chemical parameters, such as yield, turbidity, viscosity, clarity, colour, polyphenol, protein, TSS, and total solid, were measured as dependent variables. Process optimization has been done using Box-Behnken design. Optimization has been done for maximum yield percentage, L* value, a* value, protein, and polyphenol content, and minimum values for turbidity, viscosity, clarity, b* value, TSS, and total solid content. The suggested parameters for extraction of juice were at 0.05% enzyme concentration at 44 °C for 80 min. In a large-scale production, extraction of juice by Pectinase (Aspergillus aculeatus) has a significance importance due to its high yield as well as nutritional values.
Jamun fruit comprises of seed and thick pulp. The pectin-protein bond of the thick pulp creates difficulty in making juice. Clear Jamun juice is not available in the market, so there is a need for extraction of juice with maximum yield. The goal of this research is to obtain high yield of clarified juice with the help of Pectinase (Aspergillus aculeatus) enzyme. The study was conducted at different enzyme concentration (0.01-0.1%), time duration (40-120 min), and temperature (30-50 °C). Various physical and chemical parameters, such as yield, turbidity, viscosity, clarity, colour, polyphenol, protein, TSS, and total solid, were measured as dependent variables. Process optimization has been done using Box-Behnken design. Optimization has been done for maximum yield percentage, L* value, a* value, protein, and polyphenol content, and minimum values for turbidity, viscosity, clarity, b* value, TSS, and total solid content. The suggested parameters for extraction of juice were at 0.05% enzyme concentration at 44 °C for 80 min. In a large-scale production, extraction of juice by Pectinase (Aspergillus aculeatus) has a significance importance due to its high yield as well as nutritional values.
Fruits are known for their excellent antioxidant properties,
therapeutic value, and nutrient enrichment. Jamun (Indian Blackberry) is a tropical
natural product, with its antidiabetic properties, which helps in the transformation
of starch or sugar into vitality. It is rich in iron and subsequently helps in the
purification of blood (Sehwag and Das 2015; Mahesh and Satish 2008; Jabeen and Javaid 2010). Preservation of fresh produced samples over long time is
energy consuming and expensive. After harvest, the nutritional and quality
attributes of fresh juicy fruit, such as Jamun, get deteriorate as it comes in
contact with surrounding of physical and microbial environment. Low yield and low
extraction efficiency of Jamun juice have been attributed to chemical structure of
the fruit system. Exploration of the structural make up of Jamun fruit has indicated
that the presence of higher pectin and tannin content and storage linkage between
protein and pectin molecules has resulted in hindrance for extraction efficiency. In
case of perishable fruit system, such as Jamun, there is a need for the development
of novel strategies for proper processing to get higher juice yield so as to achieve
continuous supply. Meanwhile, the application of enzymes for enhancing the yield and
extraction efficiency has been given wide range of commercial importance.In the beverage industry, enzymatic juice extraction process followed
by clarification and membrane separation is considered as an advanced step for
concentration of juice. However, a very few studies have been done on clarification
of natural product with enzymatic pre-treatment particularly for tropical fruit
juices (Rai et al. 2004; Sin et al.
2006). In the process of enzymatic
pre-treatment for juice clarification, hydrolysis of pectic substances is impacted
by few components, for example, enzyme concentration, incubation time, and
incubation temperature (Rai et al. 2004; Sin et al. 2006).In case of fruit juice depectinization and to increase the product
yield, several enzymes have been used as a pre-treatment. Several studies have
reported on pectinases enzyme for depectinization which could effectively clarify
the fruit juices (Tastan and Baysal 2015; Domingues et al. 2012; Tu et al. 2013;
Maktouf et al. 2014). A particular
enzyme with various strains also acts differently. For example, pectinase obtained
from Aspergillus Niger will act on a biological
system in a certain manner where pectinase obtained from Aspergillus aculeatus will work in differently. Therefore, many
studies with different strains also reported for various fruits (Ghosh et al.
2016; Sharma et al. 2015; Tapre and Jain 2014; Landbo et al. 2007; Pinelo et al. 2010; Lee et al. 2006;
Landbo and Meyer 2004; Sandri et al.
2014).Response surface Methodology (RSM) is a statistical and mathematical
tool valuable for breaking down the total impacts of several independent variables
and responses (Box and Draper 1987). One
of the types for RSM is known as Box–Behnken design (does not contain an embedded
factorial or fractional factorial design) which do not have axial points, thus, can
be sure that all design points fall within your safe operating zone. Box–Behnken
designs also ensure that all factors are not set at their high levels at the same
time. This procedure is more functional contrasted with hypothetical models. It
emerges from trial approach which incorporates intelligent impacts of the variables,
and inevitably, it portrays the general impacts of the parameters on the procedure
(Bas and Boyaci 2007). The most ideal
approach to picture the impact of the independent variables on the reliant ones is
to draw response surface plots of the model. In this manner, a response surface
trial plan was esteemed to be most suitable method for the present
examination.The objectives of this study is to optimize the enzyme concentration,
incubation time, and temperature for juice extraction and clarification from Jamun
fruit with the help of commercial pectinase (Aspergillus
aculeatus) using the response surface methodology (RSM). The second
objective is to characterise the physico-chemical properties, such as viscosity,
turbidity, yield, clarity, colour, total polyphenol, protein concentration, TSS, and
total solid in the fresh product, as well as the treated samples.
Materials and methods
Jamun fruit sample
Fresh ripen Jamun (locally called as Ram
Jamun) was obtained from Rourkela, Odisha, India. Due to high
perishable nature of Jamun fruits, the samples were manually washed (water with 2%
CaCl2), cleaned, and then packed in polythene bags. The
cleaned samples were stored at −20 ± 1 °C for further study (Benherlal
2010).
Pectinase enzyme and chemicals
The enzyme pectinase (Commercial Name: Pectinex Ultra SPL; activity
3800 units/ml) from Aspergillus aculeatus, and
Folin–Ciocalteu reagent was procured from Sigma-Aldrich, Bangalore, India.
Hydrazine sulphate, potassium sodium tartrate, and hexamine LR grade were
purchased from HiMediaPvt. Ltd., Mumbai, India. Copper (II) sulphate pentahydrate
was collected from Merck, Mumbai, India. Bovine serum albumin (BSA) and Gallic
acid standard were purchased from Otto Chemie Pvt. Ltd, Mumbai, India.
Method of Jamun juice extraction
The cleaned Jamun samples from deep freezer were taken out and
washed and clean to avoid microbial contaminations, and other foreign particles,
if any. Then, the samples were allowed to warm up at room temperature for 3 h. To
avoid bitterness of juice, seeds were manually removed from the samples. Collected
pulp of the fruit sample then mixed using a grinder (Bajaj Mixer, India).
Afterwards, the grinded pulp was poured in beakers. As per the experimental
design, the pectinase enzyme was added with the mentioned temperature and
time.
Enzymatic treatment
As mentioned in Table 1
(experimental design), 100 g of homogenised pulp was treated with enzyme. The
independent parameters, such as incubation temperature X
1 (30–50 °C), enzyme concentration, X
2 (0.01–0.1 w/v, %), and incubation time, X
3 (40–120 min), were considered. An incubated orbital
shaker (REMI Laboratory Instrument, Mumbai, India) at 120 rpm was used for
vigorous mixing of enzymatic treated pulp at particular temperature and time.
Then, the suspension was kept at −2 °C for 5 min for inactivation of the enzyme
(Molinari and Silva 1997; Sandri et
al. 2011). A muslin cloth was used
to filtrate the juice. The filtrate was taken for further analysis of different
physico-chemical properties. One sample was kept without any enzymatic treatment,
known as control sample.
Table 1
Properties of raw Jamun juice without enzymatic
treatment
Property
Yield (%)
Viscosity (mPaS)
Turbidity (NTU)
Clarity (%T)
L
a*
b*
Protein (mg/g)
Polyphenol (mg GAE/g)
TSS (°B)
Total solid (%)
Raw Juice
65
1.21
116
0.165
5.76
2.65
−1.61
132.70
89.08
13
12.94
Properties of raw Jamun juice without enzymatic
treatment
Characterisation of juice
Physical parameters, such as viscosity, turbidity, yield, clarity,
and colour, and chemical parameters, such as protein, polyphenol, TSS, and total
solid, were determined as response parameters. A viscometer and a digital
turbidity-meter were used to measure the viscosity and turbidity of juice,
respectively (Sin et al. 2006). The
treated pulp was passed through muslin cloth (Shahnawaz and Sheikh 2011). The percent juice content of Jamun was
given as:Clarity of the juice was determined by transmittance (%T) at 660 nm
(Rai et al. 2006) and total phenolic
substance was measured by the Folin–Ciocalteu method at 650 nm (% absorbance)
(Singleton et al. 1999) using a
spectrophotometer (Systronics India Ltd). A Hunter colorimeter (Colorflex EZ, USA)
was used for measurements of juice colour {L*
(brightness/darkness), a*(redness/greenness),
b* (yellowness/blueness)} (Rai et al.
2006). Protein concentration was
measured with Bovine Serum Albumin (BSA) as the standard according to method
described by Lowry et al. (1951). An
Abbe-type refractometer (°B) was used to measure the total soluble sugar (TSS) in
the sample. Total solid was measured by weight difference (Sagu et al.
2014).
Experimental setup
Box–Behnken Design was considered to optimise the treatment and
extraction conditions for Jamun juice. The Design Expert Software (Version
8.0.7.1) was used for optimisation of independent variables.For the enzymatic treatment of juice, the key elements are
incubation temperature, enzyme concentration, and incubation time, which coded as
X1, X2, and X3, respectively. Box-Behnken Design setup was taken to analyse on the
combined impact of these three variables. Total 17 experiments with 5 replications
at the center point were designed through software. Tables 2 and 3 show
the real and coded values of the experiments, respectively. The effects of
variables in terms of linear, quadratic, and interaction terms can be explain by
mathematical model as shown below:where Y the experimental responses;
X
1 and X
2 the levels of variables; b
0 the constant; b
1 the linear coefficient; b
11 the quadratic term; and b
12 the coefficient of the interaction terms.
Table 2
Box–Behnken design: real variables and experimental responses
(physical parameters)
Exp. no.
Real variables
Experimental responses
X1 (°C)
X2 (%)
X3 (min)
Yield (%)
Clarity (%T)
Turbidity (NTU)
Viscosity (mPaS)
L* value
a* value
b* value
Act
Pre
Act
Pre
Act
Pre
Act
Pre
Act
Pre
Act
Pre
Act
Pre
1
30
0.01
80
76
75.75
78.33
76.84
14.9
14.70
1.086
1.08
1.17
1.11
0.81
0.83
−0.37
−0.32
2
50
0.01
80
77
76.75
66.40
67.99
46.8
46.74
1.092
1.09
0.53
0.45
1.11
1.11
−0.20
−0.19
3
30
0.10
80
78
78.25
72.97
71.38
20.65
20.71
1.100
1.11
0.68
0.77
1.01
1.01
−0.18
−0.19
4
50
0.10
80
79
79.25
68.63
70.13
45.30
45.50
1.077
1.08
0.55
0.61
1.02
1.00
−0.21
−0.27
5
30
0.06
40
79
79.50
68.60
70.70
19.65
19.61
1.086
1.10
0.93
0.92
0.93
0.90
−0.16
−0.18
6
50
0.06
40
81
81.50
70.33
69.15
46.80
46.62
1.071
1.08
0.55
0.56
1.15
1.14
−0.18
−0.16
7
30
0.06
120
80
79.50
74.30
75.48
18.95
19.13
1.100
1.09
1.00
0.99
0.98
0.99
−0.19
−0.21
8
50
0.06
120
80
79.50
68.83
66.93
48.90
48.94
1.100
1.09
0.52
0.53
0.99
1.03
−0.21
−0.19
9
40
0.01
40
82
81.75
77.30
76.89
13.50
13.74
1.071
1.07
0.89
0.96
0.69
0.71
−0.15
−0.18
10
40
0.10
40
85
84.25
77.13
76.82
12.90
12.88
1.086
1.07
0.92
0.84
0.64
0.67
−0.16
−0.13
11
40
0.01
120
80
80.75
79.43
79.75
11.40
11.42
1.041
1.06
0.87
0.95
0.66
0.62
−0.15
−0.18
12
40
0.10
120
83
83.25
76.10
76.51
17.30
17.06
1.071
1.08
0.97
0.89
0.75
0.73
−0.21
−0.18
13
40
0.06
80
74
73.80
29.47
29.29
32.10
32.36
1.101
1.10
2.13
2.31
3.22
3.21
−1.40
−1.21
14
40
0.06
80
74
73.80
29.43
29.29
32.40
32.36
1.100
1.10
2.18
2.31
3.24
3.21
−1.15
−1.21
15
40
0.06
80
74
73.80
29.03
29.29
32.10
32.36
1.086
1.10
2.51
2.31
3.13
3.21
−1.10
−1.21
16
40
0.06
80
74
73.80
29.33
29.29
32.60
32.36
1.100
1.10
2.54
2.31
3.24
3.21
−1.27
−1.21
17
40
0.06
80
73
73.80
29.17
29.29
32.60
32.36
1.100
1.10
2.19
2.31
3.21
3.21
−1.13
−1.21
Table 3
Box–Behnken design: real variables and experimental responses
(chemical parameters)
Exp. no.
Coded variables
Experimental responses
x1
x2
x3
Protein (mg/g)
Polyphenol (mg GAE/g)
TSS (°B)
Total solid (%)
Act
Pre
Act
Pre
Act
Pre
Act
Pre
1
−1
−1
0
368.02
375.47
111.34
110.08
13.00
13.02
15.64
15.59
2
1
−1
0
139.40
142.25
130.58
128.68
13.20
13.23
15.96
15.44
3
−1
1
0
394.99
392.14
119.25
121.14
13.30
13.17
15.42
15.45
4
1
1
0
179.19
171.74
121.92
123.18
13.10
13.17
15.64
15.69
5
−1
0
−1
409.30
403.89
113.81
111.68
13.20
13.15
14.66
14.65
6
1
0
−1
127.70
126.89
118.31
116.82
13.00
12.98
14.51
14.47
7
−1
0
1
356.16
356.97
116.02
117.52
13.00
13.03
14.63
14.68
8
1
0
1
174.94
180.35
130.88
133.01
13.40
13.43
14.93
14.98
9
0
−1
−1
159.09
157.05
99.44
102.83
12.40
12.40
13.99
14.07
10
0
1
−1
166.59
174.84
112.90
113.13
12.60
12.65
14.11
14.10
11
0
−1
1
163.29
155.03
121.60
121.37
12.80
12.75
14.29
14.30
12
0
1
1
181.37
183.41
120.02
116.63
12.60
12.60
14.45
14.37
13
0
0
0
108.18
106.12
121.47
118.19
12.40
12.46
14.05
14.29
14
0
0
0
105.31
106.12
118.35
118.19
12.30
12.46
14.03
14.29
15
0
0
0
107.81
106.12
117.29
118.19
12.60
12.46
14.58
14.29
16
0
0
0
104.30
106.12
116.47
118.19
12.60
12.46
14.55
14.29
17
0
0
0
104.99
106.12
117.38
118.19
12.40
12.46
14.23
14.29
Box–Behnken design: real variables and experimental responses
(physical parameters)Box–Behnken design: real variables and experimental responses
(chemical parameters)Analysis of variance (ANOVA) was considered to validate the model.
Three-dimensional plots were obtained by changing the variables, i.e., one
variable constant at the center point and changing the other two variables within
the experimental range. Different responses namely viscosity, turbidity, yield,
clarity, colour, protein concentration, polyphenol, TSS, and total solid were
selected. The model equations with the help of contour plots are used to describe
the individual and cumulative effects on the responses.
Results and discussions
Properties of fresh Jamun juice (with no treatment) are tabulated in
Table 1. Response Surface Methodology
(RSM) Box–Behnken outline was considered for enhancing the parameter for
physico-chemical properties of Jamun juice. Effect of three variables (incubation
time, temperature, and concentration) on the exploratory variables, i.e., physical
properties (yield, viscosity, turbidity, clarity, and colour) and chemical
properties (protein, polyphenol, TSS and total solid) is mentioned in
Tables 2 and 3, separately. The analysis of variance (ANOVA) for every reactions
demonstrated that the proposed models can clarify more than 90% trial perceptions as
a component of independent variables. The proposed model was sufficient with
agreeable estimations of R
2.The yield of the juice ranges from 73 to 85 ml. Table 2 represents the actual and predicted values of the
juice yield. As mentioned in Table 4
temperature (A) (p < 0.0001) and concentration (B) (p < 0.0001) have a positive
linear effect, whereas time (C) (p < 0.0001) has a negative linear effect. All the
quadratic parameters possess positive effect (p < 0.001). The quadratic model obtained for regression analysis for
yield in terms of coded levels of variables or the Jamun juice is given
below
Table 4
Regression coefficients and R
2 value for all dependent variables for enzymatic
clarified Jamun Juice
Regression coefficient
Yield (%)
Viscosity (mPaS)
Turbidity (NTU)
Clarity (%T)
L
a*
b*
Protein (mg/g)
Polyphenol (mgGAE/g)
TSS (°B)
Total solid (%)
b0
73.80
1.10
32.36
29.29
2.31
3.21
−1.21
106.12
118.19
12.46
14.29
A (Temp.)
0.50
−4.6 × 10−3
14.21
−2.53
−0.21
0.069
0.012
−113.40
5.16
0.050
0.022
B (Conc.)
1.25
5.59 × 10−3
1.19
−0.83
−0.043
0.018
0.014
11.54
1.39
0.025
0.027
C (Time)
−0.50
0.001
0.46
0.64
0.10
−5 × 10−3
−0.014
1.64
5.51
0.075
0.13
A2
0.06
6.71 × 10−3
9.68
17.69
−0.87
−0.95
0.48
131.86
4.42
0.62
0.86
B2
3.10
−0.016
−10.12
24.61
−0.71
−1.28
0.49
32.42
−1.84
0.07
0.39
C2
5.60
−0.015
−8.46
23.59
−0.69
−1.25
0.55
29.04
−2.86
0.07
−0.47
AB
0.011
−7.4 × 10−3
−1.81
1.90
0.13
−0.073
−0.051
3.20
−4.14
−0.05
0.099
AC
−0.50
3.71 × 10−3
0.70
−1.75
−0.025
−0.052
−8.33 × 10−4
25.09
2.59
0.15
0.11
BC
0.002
3.72 × 10−3
1.62
−0.79
0.016
0.037
−0.013
2.65
−3.76
−0.10
9.75 × 10−3
R2
0.984
0.870
0.99
0.997
0.976
0.999
0.98
0.998
0.9231
0.959
0.941
Regression coefficients and R
2 value for all dependent variables for enzymatic
clarified Jamun JuiceThe fit model was also expressed by coefficient of determination
(R
2) and found to be 98.4% with an adjusted R
2 value of 96.35%. From the above equation as well as
Fig. 1a, it is observed that with increase
in concentration of enzyme dosage yield will also increase as it degrades the
binding pectinase and protein bonding. Figure 1b represents that the interaction effect of time and concentration
has the highest effect on the yield of the Jamun juice. With a highest concentration
of 0.1% and nominal time, i.e., 40 min gives the highest yield at 40 °C. Similar
trend of data obtained by Surajbhan et al. (2012).
Fig. 1
3D Response surface plots for yield, clarity, and turbidity as a
function of temperature and enzyme concentration (a, c, e) and enzyme concentration and time (b, d, f)
3D Response surface plots for yield, clarity, and turbidity as a
function of temperature and enzyme concentration (a, c, e) and enzyme concentration and time (b, d, f)The clarity of the juice ranges from 30 to 80% (%T).
Table 2 represents the actual as well as
predicted values of clarity of the clarified juice. It can be observed that the
juice clarity is minimum at the centre point of experiments. Clarity is one of the
most important parameters for the clarified juice. Market trends shows that the
maximum the value of the clarity, the more acceptability of the juice by the
consumer. From Table 4, it is seen that the
temperature (A) and enzyme concentration
(B) have a linear negative effect, whereas time
(C) as a positive linear effect. All the
quadratic effects are positive in nature, but interaction terms have a negative
effect. The regression equation for clarity of juice with respect to temperature
(A), concentration (B), and time (C) in terms of their
real value is given as follows:The coefficient of determination (R
2) for the above equation is 0.99 which implies that the
regression model can analyse 99% of data variability. The same trend has been
followed where changes in the interaction affect temperature—enzyme concentration
Fig. 1c and time—temperature first
decrease the clarity and then increase. Figure 1d shows the time–concentration interaction helped to obtain the
maximum clarity as with the increasing concentration. At a certain temperature when
the time increases, the clarification of juices will be more than the less time. At
a lower concentration of enzyme dosage and maximum time, clarity is maximum. Similar
trend has been noticed by Lee et al. (2006) and Shah and Nath (2007) for clarification of banana and litchijuice, respectively.
Whereas Abdullah et al. (2007) observed
a different trend in clarity of carambola juice.Turbidity ranges from 12 to 47 NTU. Turbidity is considered as one of
the major parameter for the clarification process. The lower the value of the
turbidity, the acceptability will be more. From Table 4, it is clearly observed that three factors temperature (A) (p < 0.0001),
enzyme concentration (B) (p < 0.0001), and time (C)
(p < 0.0001) all have a positive linear
effect, but in case of quadratic terms except temperature (p < 0.001), concentration and time have negative effect (p < 0.001). The regression equation for turbidity with
respect to temperature (A), concentration
(B), and time (C) can be represented as:The interaction term has no significant value. The R
2 value for the above equation is 0.99 which implies that
the model can analyse 99% of data variability. From Fig. 1e, it is observed that positive slope is obtained with the
interaction effect of concentration and temperature. With the increase in
temperature and concentration, turbidity also increases. In case of
Fig. 1f, interaction effect of time and
concentration has a different trend. With respect to time as the concentration of
enzyme increased, turbidity value also increases, but after a certain period, it
started decreasing. Similar trend had obtained by Abdullah et al. (2007) and Lee et al. (2006) for clarification of carambola juice and
bananajuice with a positive linear coefficient and negative quadratic coefficients.
Pinelo et al. (2010) descried that the
turbidity of the cherry juice clarification has a similar trend with the values of
the recent data. The results for clarity and turbidity are supporting the data with
each other. From the centre point, clarity is low which represents that turbidity
will be high at that point.It is seen from Table 4 that
the viscosity was affected by all the three parameters, such as temperature
(A) (p < 0.0001) has a negative linear effect, and concentration
(B) (p < 0.001) and time (C) (p < 0.001) have a positive linear effect. Quadratic
effect is positive in case of temperature. The regression model for viscosity with
respect to temperature (A), concentration
(B), and time (C) can be represented as:The R
2 value for the above equation is 0.87 which implies that
the regression model can analyse 87% of data variability for viscosity.
Figure 2a represents that as temperature
and concentration decreases, viscosity decreases and become constant at its maximum
level. Again from Fig. 2a, it is seen that
enzyme concentration is directly proportional to viscosity. Pectin forms gel
structure which increases the viscosity at high temperature. However, at temperature
between 30 and 40 °C, the water holding capacity of pectin is reduced which results
in lower viscosity (Kittur et al. 2003).
Figure 2b gave a perfect concave nature of
the graph which implies that concentration of the enzyme has the main effect on the
viscosity of the juice.
Fig. 2
3D Response surface plots for viscosity and protein as a function
of temperature and enzyme concentration (a,
c) and enzyme concentration and time
(b, d)
3D Response surface plots for viscosity and protein as a function
of temperature and enzyme concentration (a,
c) and enzyme concentration and time
(b, d)Colour is divided into three different parameters where L* value represents the lightness and darkness of the
juice, positive a* value represents the redness
and negative b* value represents the blueness of
the juice. The negative the colour of the b*
value characteristics, colour of the jamun juice can be obtained. From
Table 4, in case of L*, temperature (A)
(p < 0.0001) and concentration (B) (p < 0.0001)
have a negative linear and quadratic value, whereas interaction terms (p < 0.05) are positive in nature. For a* value, temperature (A) (p < 0.0001) and
concentration (B) (p < 0.0001) have a positive
value, but time (C) (p < 0.0001) has a
negative slope. The quadratic values for all the parameter (p < 0.001) possess negative value. In case of b* value, temperature (A) (p < 0.0001) and
concentration (B) (p < 0.0001) have a positive linear effect, but time (C) (p < 0.0001) has
a negative linear effect. All the quadratic effects (p < 0.001) are positive, but the interaction terms are (p < 0.05) are negative in nature. The regression model
for colour is given asThe R
2 value for L*,
a*, and b*
equations is 0.97, 0.99, and 0.98, respectively which implies that the model can
analyse 97, 99, and 98% of data variability. From Fig. 3a, as the increase in concentration and temperature, there is no
significant changes in value, but in a combined effect, L* value decreases
significantly. The same trend is observed from Fig. 3b, so it can be concluded that time has a positive trend which can
increase lightness of the clarified juice. This result can be justified by the
results obtained from the clarity values. Similar trend in the L* value is obtained by Abdullah et al. (2007). In case of a* value from Fig. 3c, as the
temperature and concentration increased at first, the value of a* will increase and then it hinders. With the
combination of both the value decreases. The highest value for the redness obtained
at the centre point with a value of 3.24. For b*
value Fig. 3e, f shows that with respect of
independent variables, the value decreases up to 0.06% concentration, 40 °C
temperature, and 80 min, and then the value shoots up. The more negative the value,
the original colour of Jamun juice can be obtained. The most negative value obtained
at the centre point with −1.4.
Fig. 3
3D Response surface plots for colour values (L*, a*,
b*) as a function of temperature and
enzyme concentration (a, c, e) and enzyme
concentration and time (b, d, f)
3D Response surface plots for colour values (L*, a*,
b*) as a function of temperature and
enzyme concentration (a, c, e) and enzyme
concentration and time (b, d, f)Denaturation of protein–pectin bond is one of the major process
mechanisms for the clarification of the juice. Increase of the amount of protein in
the clarified juice signifies a proper clarification process. Ranges of protein
content is in between 105 and 409 mg/g. Table 4 signifies that only temperature (A) (p < 0.0001) has a linear
negative effect, whereas time (C) and enzyme
concentration (B) (p < 0.0001) have positive linear slope. The quadratic terms
(p < 0.001) also have a positive effect with
a positive interaction effect. The regression model representing the effect of
temperature, enzymatic concentration, and time on Jamun juice in terms of their real
value is given asThe coefficient of determination (R
2) for the fit model was determined as 0.99 which
indicates that the regression model is able to explain 99% of the variability of the
data. Figure 2c shows that as the
temperature increases, amount of protein decreases but when the concentration of
enzymatic dosage goes up amount of protein content increases. As the enzyme used in
this study obtained from a strain, Aspergillus
aculeatus has a particular effective time zone where it can give its
best result. Figure 2d shows that time has a
positive slope but not significant. Therefore, it can be concluded that
concentration of the enzyme has the maximum effect on the protein amount and then
time also has a significant role. At lowest temperature 30 °C with 0.06%
concentration with 40 min treatment time, maximum retention of the protein content
409.30 mg/g had obtained.Phenol is one of the major components in Jamun with the effect of
enzyme concentration and time–temperature effect. Extraction of phenol content
increases in the clarified juice. As the clarification process varies with the
parameters, the amount of polyphenol ranges between 99 and 130 mgGAE/g. In case of
polyphenol, all the independent parameter temperature (A) (p < 0.0001), enzyme
concentration (B), and time (C) (p < 0.0001)
have positive linear effect with a negative quadratic effect for enzyme
concentration (B) and time (C) (p < 0.001). The
interaction effects are also negative (p < 0.05). The regression model for polyphenol with the coded value
can be represented asThe values for coefficient of determination (R
2) are 0.92, which indicates that the regression model is
able to explain 92% of variability of the polyphenol concentration of the Jamun
juice. Figure 4a shows that enhancing of
concentration and temperature will also enhance the polyphenol value, but in
combined interaction, the value increases up to a level and then follows the
decreasing trend. From Fig. 4b, combined
effect of enzyme concentration and time has negative effect. Increasing of time and
temperature will increase the polyphenol content and interaction effect will
increase the polyphenol value at its maximum which signifies the coefficient of
interaction value of A and C is positive. Therefore, it can be conclude that
time–temperature effect is playing the major role in case of polyphenol activities.
At 50 °C with 0.06% concentration and 120 min incubation time, highest polyphenol
content can be obtained 130.8 mgGAE/g.
Fig. 4
3D Response surface plots for polyphenol, TSS, and total solid as
a function of temperature and enzyme concentration (a, c, e) and enzyme concentration and time (b, d, f)
3D Response surface plots for polyphenol, TSS, and total solid as
a function of temperature and enzyme concentration (a, c, e) and enzyme concentration and time (b, d, f)Total soluble solid or sugar present in the juice will be another
important nutritional parameter for the clarified process. Table 4 clearly shows that temperature (A), enzyme concentration (B), and time (C) (p < 0.0001) have positive linear effect with a
positive quadratic effect. The interaction effects are negative (p < 0.05) at significant level. The regression model
for TSS with the coded value can be represented asThe values for coefficient of determination (R
2) are 0.95, which indicates that the model can explain
95% of variability of the TSS of the Jamun juice. From Fig. 4c, a perfect convex quadratic curve has obtained where
increase in concentration enhances the values of the TSS, but temperature acts first
in a decreasing trend, then it increases up. From Fig. 4d, it can conclude that time has a positive inclination on TSS
values, whereas interaction effect of time and concentration of enzyme has almost a
linear trend. Concentration and temperature play the major roles in changing the TSS
value. At a temperature of 40 °C with 0.01% concentration, TSS value is minimum
12.4 °B.Clarified juice should contain less amount of total solid. Therefore,
measurement of total solid can quantify the process of clarification. The ranges of
total solid content in the experimental setup were 13.9–15.6%. From
Table 4, it is clearly visible that
temperature (A), enzyme concentration (B), and time (C)
(p < 0.0001) have positive linear effect,
and in case of quadratic effect, time (C)
(p < 0.0001) has negative trend. Interaction
effects also have positive impact. The regression model for total solid with the
coded value can be represent asThe coefficient of determination (R
2) is 0.94, which indicates that the model can explain
94% of variability of the total solid content of the Jamun juice. From
Fig. 4e, it can be said that concentration
of enzyme has a direct positive approach where in case of temperature, total solid
value decreases up to 40 °C and then it increases again. As the time increases, the
value of TS enhances, but interaction of time–temperature combination decreases the
total solid in the mid ranges. Coagulation of protein polyphenol takes place at this
time. From Fig. 4f, it can be concluded that
interaction effect of time and concentration has a negative approach to the TS. The
least value for the TS (13.9%) obtained at 40 °C with 0.01% concentration at 40 min
of time.
Conclusion
The optimum conditions for clarification and extractions were
determined on the basis of high yield percent, L*
value, a* value, protein, and polyphenol content
and lower values for turbidity, viscosity, clarity, b* value, TSS, and total solid content. According to the
optimised-dependent parameters, the incubation temperature should be 40 °C with
80 min and the concentration of enzyme will be 0.05% (w/v). At the optimised
condition, the value of major parameters was turbidity: 32.21 NTU; clarity: 74.39%
T; viscosity: 1.07 mPaS; polyphenol: 115.31 mg GAE/g; protein: 102.43 mg/g; yield:
75%; TSS: 12.4 °B; total solid: 13.97%; L*: 2.34;
a*: 3.25, b*: −1.30. For the clarification process, 3D contour plots with the help
of RSM signify better understanding of the results.