Fruits 75(2), 71–77 | ISSN 0248-1294 print, 1625-967X online | https://doi.org/10.17660/th2020/75.2.

2 | © ISHS 2020

Original article

Characterization of ascorbic acid and phenolic compounds for

identification of nutritionally rich cultivars and accessions of
Indian gooseberry
A.K. Bhattacherjee1,a, A. Dikshit1, D. Pandey1 and Achal Singh2
1
ICAR – Central Institute for Subtropical Horticulture, Rehmankhera, Lucknow, India
2
ICAR – National Bureau of Fish Genetic Resources, Canal Ring Road, Lucknow, India

Summary Significance of this study

Introduction  –  Indian gooseberry (Emblica offici- What is already known on this subject?
nalis Gaertn.) is a therapeutically important underuti- • Indian gooseberry (aonla) is a fruit well-known for its
lized fruit due to the presence of high amount of two therapeutic value and traditionally used in Ayurvedic
well-known antioxidants, ascorbic acid and polyphe- medicine system in India. It is very rich in ascorbic
nols. The present study aimed at identification and acid and polyphenols which have antioxidant potential
quantification of different phenolic compounds and against many human ailments.
ascorbic acid in fresh fruits of seven cultivars and two
promising accessions of Indian gooseberry. Materials What are the new findings?
and methods   –   Ascorbic acid was estimated by titri- • The present study provides an original description of
metric method and individual phenolic compounds the profiling of seven phenolic compounds and ascor-
were identified and quantified by RP-HPLC method bic acid in fruits of seven Indian aonla cultivars and
with PDA detector. Multivariate method and ANOVA two promising accessions identified by this institute
were applied for statistical evaluation. Results  –  The at edible stage. ‘Desi’ aonla and two accessions pos-
content of ascorbic acid varied from 335.24 mg 100 g-1 sessed very good amounts of ascorbic acid and phe-
(‘NA-7’) to 1278.31 mg 100 g-1 (‘Desi’) among the cul- nolic compounds.
tivars, whereas it ranged between 418.12 mg 100 g-1
(CISH A-31) and 490.13 mg 100 g-1 (CISH A-33) among What is the expected impact on horticulture?
the accessions. Seven phenolic compounds were • Being a therapeutically important but underutilized
identified and quantified at various proportions in fruit crop in the world, it is important to identify
different aonla cultivars and their variations among and quantify various phenolic compounds in differ-
the cultivars were assessed. Among the cultivars/ ent aonla cultivars and accessions. Characterization
accessions studied, ‘Desi’ aonla possessed maximum of polyphenols will be useful for the future breeding
amount of total polyphenols (58.207 mg g-1) followed activities also. A deep knowledge of useful phenolic
by CISH A-31 (40.708 mg g-1) and ‘NA-6’ (35.081 compounds in fruit can also have impact on process-
mg g-1). Multivariate evaluation revealed that gallic ing and phyto-pharmaceutical industries as aonla is
acid, p-coumaric acid, total polyphenols and ascor- extensively used for these purposes. Aonla accessions
bic acid were the major variables in aonla and ‘Desi’ with good antioxidant potential can be released as
and ‘NA-6’ were the most important cultivars. Conclu- varieties so that their health benefit can be availed by
sion   –   ‘Desi’ aonla fruits were the richest source of the consumers.
ascorbic acid and phenolic compounds among the
cultivars. Two accessions along with cultivars ‘NA-6’,
‘Krishna’ and ‘Lakshmi 52’ were also rich in both the
quench lipid peroxidation, prevent DNA oxidative damage,
nutraceuticals. These cultivars and accessions are not
scavenge free radicals and prevent inhibition of cell com-
only beneficial for human health but can also be used
munication (Cao and Cao, 1999) which are all indication of
in processing and phyto-pharmaceutical industries.
antioxidant properties. The antioxidant activity of phenolic
compounds is due to the reactivity of phenol moiety (hydrox-
Keywords
yl group) on aromatic ring, which has the ability to scavenge
‘Desi’ aonla, gallic acid, p-coumaric acid, ascorbic acid,
free radicals via hydrogen or electron donation (Shahidi and
HPLC characterization, multivariate evaluation
Wanasundara, 1992). Gallic acid has anti-inflammatory, anti-
microbial, antimutagenic, anticancer and radical scavenging
activities (Madsen and Bertelsen, 1995); ellagic acid exhibits
antimutagenic, anticancer and antiviral abilities and stim-
Introduction ulates the activities of detoxifying enzymes (Mandal et al.,
Polyphenols or phenolic compounds are secondary me- 1988); catechin and epicatechin protect against congestive
tabolites of plants and are widely distributed in plant-based heart failure, myoglobinuric acute renal failure and myo-
food products. Phenolic compounds have the capacities to cardial ischemia, have anticancer and anti-aging properties
(Augustyniak et al., 2005); ellagic acid, chlorogenic acid and
a
Corresponding author: [email protected]. catechin also show α-glucosidase inhibitory activity (Čakar

Volume 75 | Issue 2 | March-April 2020 71

Bhattacherjee et al. | Profiling of ascorbic acid and phenolic compounds in aonla

et al., 2018b). Ascorbic acid (vitamin C) is known to be a po- of seven Indian aonla cultivars and two promising accessions
tent antioxidant having capacity to eliminate reactive oxygen conserved at ICAR-CISH, Lucknow, India, using reverse phase
species, keep the membrane-bound antioxidant α–tocoph- HPLC technique and multivariate evaluation methods.
erol in the reduced state, act as a cofactor maintaining the
activity of a number of enzymes (by keeping metal ions in the Materials and methods
reduced state), appears to be substrate for oxalate and tarta-
rate biosynthesis and has a role in stress resistance (Davey et Plant materials
al., 2000; Arrigoni and De Tullio, 2002). Many fruits are rich Panna district of Madhya Pradesh, India, is rich in aon-
source of phenolic compounds and ascorbic acid. Phenolic la diversity and many accessions are collected from Panna
compounds are the main cause of astringency in many fruits and grown at the institute as accessions. Freshly harvested
and also contribute to the taste, colour, odour and preserva- mature aonla fruits of seven cultivars (‘Krishna’, ‘Kanchan’,
tion of fruits and their processed products. ‘NA-6’, ‘NA-7’, ‘Chakaiya’, ‘Lakshmi-52’ and ‘Desi’) and two
Indian gooseberry or aonla (Emblica officinalis Gaertn.) promising accessions (CISH A-31 and CISH A-33) were col-
belongs to the family Euphorbiaceae and is grown in many lected from the Institute farm at Rehmankhera, Lucknow.
countries like Indonesia, India, Philippines, Brazil, Sri Lan- After washing of fruits in water to remove any dirt and air
ka, Mexico, Thailand, Malaysia, Vietnam, Ghana, Nigeria, etc. drying to remove surface water, segments were separated
A single aonla fruit contains almost 20 times more ascorbic and macerated in a mixer-grinder. One gram pulp sample
acid than two oranges (Yadav et al., 2011). Due to the pres- (in triplicate) was collected for the analysis of both phenolic
ence of high amount of phenolic compounds, fruits are as- compounds and ascorbic acid.
tringent in taste and difficult to consume fresh, resulting
in its main use in processing and Ayurvedic medicine. The Chemicals
value-added products prepared from aonla are juice, pre- Reference standards of various phenolic compounds like
serve (murabba), candy, pickle, segments-in-syrup, pow- gallic acid, chlorogenic acid, catechin, epicatechin, caffeic
der, laddoo, etc. (Rakesh et al., 2004). Many popular aonla acid, ellagic acid and p-coumaric acid along with L-ascor-
cultivars are grown in central and northern India. Informa- bic acid were purchased from Sigma-Aldrich, India Branch,
tion on the content of ascorbic acid and total polyphenols Mumbai. HPLC grade solvents (methanol and water) were
in various aonla cultivars is plenty and few attempts have procured locally. Stock solutions of 1,000 μg mL-1 were pre-
also been made to identify and quantify individual phenolic pared by dissolving 25 mg of each reference standard in
compounds in some aonla cultivars (Liu et al., 2008; Kumar 25 mL of HPLC grade methanol. Working solutions of 5, 10
and Rao, 2010; Parveen et al., 2019; Parveen and Khatkar, and 50 μg mL-1 for each reference standard (phenolic com-
2019). As the proportion of ascorbic acid and polyphenols pounds) were prepared by subsequent dilution in metha-
varies as per variety as well as location, the present study nol. Chemical structures of ascorbic acid and phenolic com-
was, therefore, undertaken to identify and quantify various pounds are presented in Figure 1.
phenolic compounds and ascorbic acid present in fresh fruits

L-Ascorbic acid Gallic acid Ellagic acid

Chlorogenic acid Caffeic acid p-Coumaric acid

Figure 1.  Chemical struc-

tures of ascorbic acid and
seven phenolic compounds
(+) Catechin (–) Epicatechin identified in aonla culti-
vars/accessions.

FIGURE 1. Chemical structures of ascorbic acid and seven phenolic compounds identified in aonla
cultivars/accessions.

72 International Journal of Tropical and Subtropical Horticulture

Bhattacherjee et al. | Profiling of ascorbic acid and phenolic compounds in aonla

Extraction

phenolic compounds
One gram pulp sample was extracted with 20 mL of
Total of selected

12.25 ± 0.467g
31.65 ± 0.950d

18.09 ± 0.318e
30.97 ± 0.521d
58.21 ± 3.973a
40.71 ± 1.558b
31.85 ± 0.469d
35.08 ± 0.620c
15.00 ± 0.860f
80 per cent methanol by centrifugation at 10,000 rpm for

(mg g-1 fw)

quantified 10 min for phenolic compounds. The process was repeated
twice and pooled supernatant were collected, methanol was
evaporated completely in a rotary vacuum evaporator and
residue was dissolved in 5 mL of HPLC grade methanol. Final
volume was made up to 10 mL with the same solvent.

HPLC analysis
1.30 ± 0.130g
4.19 ± 0.257e
8.88 ± 0.339a
7.27 ± 0.620b
4.53 ± 0.199e

9.28 ± 0.048a

5.97 ± 0.303d
6.73 ± 0.302c
3.42 ± 0.167f
Epicatechin
(mg g-1 fw)

High performance liquid chromatography (HPLC) is the

most favourable tool to estimate and quantify phenolic com-
pounds in aonla fruits, juice and spray-dried powder (Kumar
and Rao, 2010; Bhattacherjee et al., 2011a; Bhattacherjee et
al., 2011b; Parveen and Khatkar, 2019; Parveen et al., 2019).
Here also phenolic compounds were estimated with the help
of a Shimadzu, Japan make HPLC (model SCL 10 AVP) cou-
6.67 ± 0.329e

6.62 ± 0.412e

18.54 ± 1.537a
14.22 ± 0.592b
8.67 ± 0.493d
11.12 ± 0.489c
10.88 ± 0.394c

11.78 ± 0.930c
0.89 ± 0.109f
(mg g-1 fw)

pled with rheodyne manual injector and photodiode array

Catechin

(PDA) detector. The method suggested by Bhattacherjee et

Table 1.  The contents of quantified phenolic compounds in different cultivars/accessions of Indian gooseberry (fresh weight basis).

al. (2011b) has been employed with slight modifications in

mobile phase combination and its flow-rate. The linear gra-
dient of mobile phase [potassium dihydrogen orthophos-
phate solution (0.01M) (A) : acetonitrile-water (75:25, v/v)
(B) = 80:20] was carried out at a flow-rate of 1.0 mL min-1
p-Coumaric acid

0.11 ± 0.013ef
0.16 ± 0.021d

0.18 ± 0.008d

0.13 ± 0.003e
1.51 ± 0.007a
0.40 ± 0.025b
0.24 ± 0.029c

0.25 ± 0.034c
0.09 ± 0.001f

at 280 nm. The stationary phase consisted of reverse phase

(mg g-1 fw)

Phenomenex® Luna C-18 column (250 × 4.6 mm i.d., 100 Å,

5 µ film thickness). Before injecting to HPLC, all the samples
were filtered through a sample clarification kit with nylon
membrane filter (Axiva, 13 mm diameter, 0.45 μ thickness).
The content of ascorbic acid was estimated by titrimetric
method using 2,6-dichlorophenol indophenol dye solution
0.78 ± 0.009de
0.61 ± 0.039e
0.80 ± 0.041d
8.28 ± 0.077a

4.47 ± 0.041b

0.96 ± 0.040d
1.41 ± 0.069c
1.35 ± 0.291c

1.39 ± 0.064c

(Ranganna, 2000). Total amount of selected quantified phe-

Caffeic acid
(mg g-1 fw)

nolic compounds were calculated by adding the amounts of

individual polyphenols detected by HPLC.

Statistical analysis
The statistical analysis was carried out for analysis of vari-
ance (ANOVA) using completely randomized design with three
Chlorogenic acid

replications by Web Agri Stat Package (WASP) v. 2.0 software

9.01 ± 0.216b
2.56 ± 0.305e
3.28 ± 0.149d
2.65 ± 0.431e
8.54 ± 0.387b

9.77 ± 0.332a
7.41 ± 0.250c
1.41 ± 0.065f
(mg g-1 fw)

through student’s t-test (LSD) at p≤0.05. Coefficient of varia-

ND

tion (CV) was also presented to show the variation among the
cultivars. The multivariate methods – principal component
Data with different number in column as superscript are statistically significant.

analysis and canonical discriminant function analysis – were

performed using SPSS v. 16 and SAS 9.3 software.

Results
0.37 ± 0.029de
0.64 ± 0.021cd
1.16 ± 0.033b

0.19 ± 0.008e
1.34 ± 0.144b
1.15 ± 0.193b

0.24 ± 0.024e
1.93 ± 0.404a
0.75 ± 0.121c

Seven phenolic compounds (gallic acid, chlorogenic acid,

Ellagic acid
(mg g-1 fw)

The values are expressed as mean ± SD; ND = Not detected.

catechin, epicatechin, caffeic acid, ellagic acid and p-couma-

ric acid) were simultaneously detected and quantified in
seven cultivars and two accessions of aonla by RP-HPLC. The
data are presented in Table 1. Ascorbic acid was also estimat-
ed in these cultivars and accessions.
5.21 ± 0.083cd

5.18 ± 0.214cd

7.96 ± 0.752bc
1.41 ± 0.088e

3.59 ± 0.486d
1.78 ± 0.228e
1.50 ± 0.156e

24.05 ± 2.445b

6.83 ± 1.343a

Ascorbic acid
(mg g-1 fw)
Gallic acid

Ascorbic acid is the predominant vitamin present in aon-

la fruit and the main reason for its therapeutic activity. Both
the accessions and cultivars were found very good source
of ascorbic acid. Accession CISH A-33 possessed maximum
amount of ascorbic acid (490.13 mg 100 g-1) among the ac-
cessions followed by CISH A-31 (418.12 mg 100 g-1). How-
ever, among the cultivars ‘Desi’ aonla was the richest source
Lakshmi-52

of ascorbic acid. Though it was smaller in size (14–18 g

accessions

Desi aonla
CISH A-31
CISH A-33
Cultivars/

Chakaiya
Kanchan

fruit weight), it contained 1278.31 mg 100 g-1 of ascorbic

Krishna
NA-6
NA-7

acid, which was quite high compared to other cultivars and

accessions (Figure 2). Variation in ascorbic acid content in

Volume 75 | Issue 2 | March-April 2020 73

Bhattacherjee et al. | Profiling of ascorbic acid and phenolic compounds in aonla

Ascorbic acid (mg/100g) 1400

1200
1000
800
600 b
d c
400
200
0

Figure 2. Ascorbic acid content

(fresh weight basis) in different
aonla cultivars/accessions.

other aonla cultivars was also prominent (CV = 2.158) where Epicatechin
‘Krishna’ contained 390.34 mg 100 g-1 of ascorbic acid and It also belongs to flavans category of phenolic compounds
‘NA-7’ the lowest (335.24 mg 100 g-1). Two accessions were from flavonoids group. Variation in the content of epicate-
found slightly richer in ascorbic acid content than popular chin was significant between the cultivars (LSD = 0.523 and
cultivars except ‘Desi’ aonla. A highly significant difference CV = 5.336). HPLC data revealed that Desi aonla fruits were
(LSD = 18.287) was noticed in ascorbic acid content among the richest source of this compound (9.28 mg g-1) closely fol-
the cultivars and accessions. lowed by NA-6 (8.88 mg g-1) (Table 1). Other cultivars and
accessions rich in epicatechin were NA-7 (7.26 mg g-1), CISH
Gallic acid A-31 (6.73 mg g-1) and CISH A-33 (5.79 mg g-1). Minimum
Gallic acid is one of the most important phenolic com- amount of epicatechin was noticed in Kanchan (1.30 mg g-1).
pounds present in aonla fruits. Maximum gallic acid content
(24.05 mg g-1) was recorded in ‘Desi’ aonla which was dis- Ellagic acid
tantly seconded by CISH A-31 (7.96 mg g-1) and CISH A-33 Ellagic acid is another important phenolic compound
(6.83 mg g-1). Lower gallic acid content was observed in three identified in aonla fruits which is being popular because of
cultivars, i.e., ‘Kanchan’ (1.41 mg g-1), ‘Chakaiya’ (1.50 mg g-1) its anti-cancer activity. The content of ellagic acid varied sig-
and ‘NA-7’ (1.77 mg g-1) (Table 1). A highly significant dif- nificantly between 0.19 mg g-1 (‘NA-7’) and 1.93 mg g-1 (CISH
ference (LSD = 1.689 and CV = 15.405) was observed in gallic A-33). Cultivars ‘Chakaiya’ (1.34 mg g-1), ‘Krishna’ (1.16
acid content between cultivars and accessions. mg g-1) and ‘Lakshmi-52’ (1.15 mg g-1) were the other good
sources of ellagic acid (Table 1). The LSD value for this com-
Chlorogenic acid pound is 0.28 and CV value is 18.88, indicating highly signifi-
The content of chlorogenic acid varied significant- cant variation among the cultivars tested.
ly among the cultivars and accessions tested (LSD = 0.503
and CV = 5.207). Accession CISH A-31 contained maximum Caffeic acid
amount of chlorogenic acid (9.77 mg g-1) closely followed A significantly higher amount of caffeic acid (8.28 mg g-1)
by ‘Krishna’ (9.01 mg g-1), whereas ‘Kanchan’ contained was quantified in ‘NA-6’ by HPLC analysis (Table 1). ‘Desi’
minimum amount of this phenolic acid (1.41 mg g-1) (Ta- aonla contained next best amount of this phenolic acid (4.47
ble 1). Cultivar ‘Lakshmi-52’ and accession CISH A-33 also mg g-1), while minimum amount of caffeic acid was detect-
possessed a good amount of chlorogenic acid (8.54 and 7.41 ed in ‘Kanchan’ (0.61 mg g-1). Other cultivars and accessions,
mg g-1, respectively). Interestingly, chlorogenic acid was not which were good source of caffeic acid, were ‘NA-7’ (1.41
detected in ‘Desi’ aonla. mg g-1), ‘Chakaiya’ (1.35 mg g-1) and CISH A-31 (1.39 mg g-1).
A highly significant difference (LSD = 0.187 and CV = 4.888)
Catechin was observed between the cultivars and accessions regard-
Catechin belongs to flavans group of phenolic com- ing the content of caffeic acid.
pounds and is the major phenolic compound detected in all
aonla cultivars and accessions except ‘NA-7’, where epicate- p-Coumaric acid
chin was recorded as major phenolic compound. Maximum Among the phenolic compounds detected, p-coumaric
amount of catechin (18.54 mg g-1) was detected in ‘Desi’ aon- acid was quantified least in aonla cultivars. The content of
la (Table 1). Other cultivars like ‘Lakshmi-52’ (11.78 mg g-1), p-coumaric acid ranged between 0.085 mg g-1 (minimum
‘Krishna’ (11.12 mg g-1) and ‘NA-6’ (10.88 mg g-1) as well as in ‘Kanchan’) to 1.51 mg g-1 (maximum in ‘Desi’) among the
accessions CISH A-31 (14.22 mg g-1) and CISH A-33 (8.67 cultivars (Table 1). Other cultivars/accessions with good to
mg g-1) were the other very good source of this antioxidant. moderate amount of p-coumaric acid were CISH A-31 (0.40
However, ‘NA-7’ contained minimum amount of catechin mg g-1), CISH A-33 (0.25 mg g-1) and ‘NA-6’ (0.24 mg g-1).
(0.89 mg g-1), which is quite low compared to other cultivars. A significant variation was noticed in the content of p-cou-
Here also a highly significant difference (LSD = 1.214 and maric acid among the cultivars (LSD = 0.033 and CV = 5.681).
CV = 7.124) was noticed among the cultivars studied.

74 International Journal of Tropical and Subtropical Horticulture

Bhattacherjee et al. | Profiling of ascorbic acid and phenolic compounds in aonla

Total of selected quantified phenolic compounds high surface area, which might be the reason for the pres-
After adding all the individual phenolic compounds de- ence of maximum ascorbic acid and total polyphenols in it.
tected, it was found that ‘Desi’ aonla contained maximum Several other literatures have also highlighted high vitamin
amount of total quantified phenolic compounds (58.21 C content in ‘Desi’ aonla fruits. Parveen and Khatkar (2015)
mg g-1), distantly followed by accession CISH A-31 (40.71 have reported that ‘Desi’’ aonla had minimum fruit weight
mg g-1). Fruits of cultivars ‘NA-6’, ‘Krishna’, ‘Lakshmi-52’ and (14.27 g) but maximum ascorbic acid content (3.29 g 100 g-1
accession CISH A-33 also contained good amount of total dry weight basis) among the five varieties studied. Mishra et
quantified phenolic compounds (35.08, 31.65, 30.97 and al. (2009) have reported higher ascorbic acid content (560
31.85 mg g-1, respectively) (Table 1). Other three cultivars mg 100 g-1) in ‘Desi’/wild aonla variety as compared to ‘Cha-
contained less than 20 mg g-1 of total quantified phenolic kiya’ variety (463 mg 100 g-1). Ascorbic acid content in aonla
compounds with Kanchan having the minimum amount is varietal as well as location-specific trait which is evident
(12.25 mg g-1). Here also a significant variation (LSD = 2.624 in various literatures. Among the five cultivars grown under
and CV = 5.027) in total quantified phenolic compounds con- semi-arid conditions of Faizabad, UP, India, ascorbic acid var-
tent was recorded between the cultivars. ied from 613.64 mg 100 g-1 in ‘Kanchan’ to 730.63 mg 100 g-1
in ‘NA-7’ (Singh et al., 2016) which is quite high compared
Multivariate evaluation to present findings. High ascorbic acid content in four aonla
Seven aonla cultivars (‘Kanchan’, ‘Krishna’, ‘NA-6’, ‘NA-7’, cultivars grown at Faizabad, UP, India has also been reported
‘Chakaiya’, ‘Lakshmi-52’, ‘Desi’) and two accessions (CISH by Mishra et al. (2018). Similarly, higher ascorbic acid con-
A-31 and CISH A-33) were evaluated over nine variables as tent (> 700 mg 100 g-1 of pulp) has been recorded in eight
seven phenolic compounds, total of selected quantified phe- aonla cultivars cultivated in Raipur, Chattisgarh, India (Singh
nolic compounds and ascorbic acid through multivariate et al., 2009). Slightly higher amount of ascorbic acid (451.2
analysis – principal component analysis (PCA) and canonical to 564.4 mg 100 g-1) was noticed in six aonla varieties grown
discriminant function analysis. Principal component analy- under Bengaluru, Karnataka, India conditions where fluctu-
sis suggested that p-coumaric acid (0.96), gallic acid (0.94), ation in temperature during winter season is minimal (Chi-
total polyphenols (0.91) and ascorbic acid (0.91) had high- ranjeevi et al., 2018). Kumar et al. (2009) have mentioned a
er contribution in controlling variation through correlation significant variation in ascorbic acid content (690.9 to 881.8
with principal component one (PC1) which accounted for mg 100 g-1) among the eight aonla cultivars studied by them.
highest (57.8%) variation in 27 × 9 data matrix as observed In the present study, two accessions collected from Panna,
from highly significant Eigen value (5.20) (Table 2) and also Madhya Pradesh, India contained > 400 mg 100 g-1 of ascor-
had a significant role in cultivar identification. The result of bic acid and was found very promising.
canonical discriminant function (CDF) analysis revealed five Phenolic compounds are another important antioxidant
significant functions controlling 99.92 per cent of total vari- present in aonla fruits. Aonla is very rich in phenolic com-
ation in data matrix 27 × 9 (Table 3). Regardless of positive pounds which also vary from cultivar to cultivar. Even the
or negative values, CDF indicated that ‘Desi’ and ‘NA-6’ were amount of individual phenolic compounds also varied sig-
the most important cultivars in terms of nutraceuticals com- nificantly from cultivar to cultivar. In the present investiga-
position, followed by ‘Krishna’, ‘Lakshmi-52’ and CISH A-31. tion, catechin was found as the most dominant phenolic com-
pound in eight out of nine cultivars followed by epicatechin,
Discussion chlorogenic acid, and gallic acid. Like ascorbic acid, ‘Desi’
Ascorbic acid is the most important antioxidant found aonla was also found as a rich source of phenolic compounds
in aonla fruits. ‘Desi’ aonla contained maximum amount of with maximum amounts of gallic acid, catechin, epicatechin,
ascorbic acid and phenolic compounds in the present inves- p-coumaric acid and total polyphenols. Accessions CISH A-31
tigation. ‘Desi’ aonla fruits are smaller in size (14–20 g) with and CISH A-33 and cultivars ‘NA-6’, ‘Krishna’ and ‘Laksh-
mi-52’ were also a very good source of phenolic compounds.
Parveen et al. (2019) have identified four phenolic com-
Table 2.  The principal component loading of nine variables pounds, viz. gallic acid, ellagic acid, ethyl gallate, and quer-
(phenolic compounds and ascorbic acid) in fruits of nine cetin in aonla extract by RP-HPLC at 270 nm. They have also
aonla cultivars. observed significant variations in the amount of individual
phenolic compounds among the five aonla varieties where
Principal components (PC) with loading of ‘Desi’ variety contained the highest level of phenolic com-
Variables each variable pounds. Gallic acid and ellagic acid were the most abundant
PC1 PC2 PC3 phenolic compounds in aonla varieties as mentioned by the
Gallic acid 0.94 0.23 -0.2 authors. Six phenolic compounds namely geraniin, quercetin
Chlorogenic acid -0.32 0.73 0.53 3-b-d-glucopyranoside, kaempferol 3-b-d-glucopyranoside,
Catechin 0.78 0.47 0.14 quercetin, kaempferol and isocorilagin were identified in
Chinese emblica fruit by chromatographic and spectroscopic
Epicatechin 0.72 0.34 0.42
methods (Liu et al., 2008). Ethyl gallate, methyl gallate, ellag-
Caffeic acid 0.56 -0.53 0.45 ic acid, quercetin 3-O-rhamnoside, isocorilagin, mucic acid-1,
Ellagic acid -0.38 0.52 0.13 4-lactone-3-O-gallate and hamamelitannin were identified in
p-Coumaric acid 0.96 0.02 0.24 another Chinese emblica fruit using HPLC coupled with mass
Total polyphenols 0.91 0.34 0.23 spectroscopy after microwave-assisted extraction (Li et al.,
Ascorbic acid 0.91 0.07 0.38 2019). Singh et al. (2016) have also noticed a significant
Eigen value 5.2 1.62 1.01 variation in total polyphenols content in five aonla varieties
grown under semi-arid conditions at Faizabad, India. Kumar
Per cent of variation 57.8 18.1 11.22
and Rao (2010) have identified nine phenolic acids (gallic
Cumulative per cent 57.8 75.9 87.12 acid, protocatechuic acid, p-hydroxybenzoic acid, vanillic

Volume 75 | Issue 2 | March-April 2020 75

Bhattacherjee et al. | Profiling of ascorbic acid and phenolic compounds in aonla

Table 3.  The canonical discriminant functions (unstandardized score) evaluated at group means of nine aonla cultivars with
nine variables.
Functions at group centroids
Cultivars
1 2 3 4 5
Kanchan -14.55 0.63 -17.44 11.39 -5.28
Krishna -31.08 -17.40 8.82 2.03 1.02
NA-6 17.97 78.70 12.06 1.01 -0.14
NA-7 -8.05 10.23 -18.71 -15.29 0.32
Chakaiya -9.22 6.78 -11.69 3.77 2.09
Lakshmi-52 -32.33 -15.87 8.26 5.57 0.32
CISH A-31 -24.17 -20.85 13.92 -8.50 -7.22
CISH A-33 -10.91 -15.61 3.15 -0.77 9.60
Desi 112.34 -26.60 1.63 0.79 -0.71
Per cent of variance 60.97 31.53 4.90 1.85 0.67
Cumulative variance 60.97 92.50 97.40 99.25 99.92
Canonical correlation 0.99 0.99 0.99 0.99 0.98

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Supplemental Information  –  Figure S1.  Canonical discriminant function (Function-1 and Function-2) for evaluation of
nine varieties: 1: ‘Kanchan’, 2: ‘Krishna’, 3: ‘NA-6’, 4: ‘NA-7’, 5: ‘Chakaiya’, 6: ‘Lakshmi-52’, 7: CISH A-31, 8: CISH A-33, 9: ‘Desi’.
These nine centroids for nine varieties have performance (score) over nine variables as gallic acid, catechin, epicatechin,
SUPPLEMENTAL
caffeic acid, ellagicINFORMATION – Facid,
acid, chlorogenic S1. Canonical
IGUREp-coumaric discriminant
acid, total function
polyphenols and (Function-1
ascorbic acid. and Function-2) for
evaluation of nine varieties: 1: ‘Kanchan’, 2: ‘Krishna’, 3: ‘NA-6’, 4: ‘NA-7’, 5: ‘Chakaiya’, 6: ‘Lakshmi-52’, 7. CISH A-
31, 8. CISH A-33, 9. ‘Desi’. These nine centroids for nine varieties have performance (score) over nine variables as
gallic acid, catechin, epicatechin, caffeic acid, ellagic acid, chlorogenic acid, p-coumaric acid, total polyphenols and
V ascorbic
o l u m e acid.
75 | Issue 2 | March-April 2020 77