P4 Artikel 2
P4 Artikel 2
To cite this article: H. Rymbai, M. Srivastav, R. R. Sharma, C. R. Patel & A. K. Singh (2013) Bio-
active compounds in mango (Mangifera indica L.) and their roles in human health and plant
defence – a review, The Journal of Horticultural Science and Biotechnology, 88:4, 369-379, DOI:
10.1080/14620316.2013.11512978
Article views: 22
Download by: [University of Nebraska, Lincoln] Date: 09 June 2016, At: 11:48
Journal of Horticultural Science & Biotechnology (2013) 88 (4) 369–379
SUMMARY
Downloaded by [University of Nebraska, Lincoln] at 11:48 09 June 2016
Mango (Mangifera indica L.) is one of the most important tropical fruits in the World. Mango leaves, bark, and fruit
(pulp, peel, and stone) are rich sources of bio-active compounds (BaCs) such as proteins [0.36 – 0.40 g 100 g–1 fresh
weight (FW) of pulp; 1.76 – 2.05% (w/w) of peel; 66.1 g kg–1 of kernel flour; and 3.0% (w/w) of leaves], vitamin A [0.135
– 1.872 mg 100 g–1 FW pulp; 15.27 International Units (IU) in kernels; 1,490 IU in leaves], vitamin C [7.8 – 172.0 mg
100 g–1 FW of pulp; 188 – 349 µg g–1 FW of peel; 0.17 g kg–1 DW of kernel flour; 53 mg 100 g–1 dry matter (DM) in
leaves], carotenoids (0.78 – 29.34 µg g–1 FW of pulp; 493 – 3,945 µg g–1 FW of peel), mangiferin (1,690.4 mg kg–1 DM
in peel; 4.2 mg kg–1 DW of kernel extract), phenolic compounds, dietary fibre (DF), carbohydrates, minerals, and other
anti-oxidants known to have medicinal, nutritional, and industrial benefits. Bio-active compounds exist in functional
foods and can protect us against diseases via several mechanisms. The anti-oxidant properties of several BaCs are
important to protect against diseases related to oxidative stress. Fruit intake provides us with anti-oxidants that may
act in a synergistic way to offer protection. In mango fruit, only the pulp is used, while all other parts are discarded
and cause environmental pollution. The importance of all the different parts of mango fruit and trees should not be
disregarded. With a global increase in health issues there is an increasing demand for natural foods. Hence, there is
need to study all the bio-active constituents in mango to provide greater insights into their medical, nutritional, and
industrial applications, as well as their role(s) in defending of the plant. This review aims to assist in the proper
utilisation of mangoes to improve nutrition and health, as well as to improve our understanding of the defence
mechanisms in plants that depend on these compounds.
pronounced differences in the concentrations of the concentrations can be inhibited by delaying ripening
different BaCs in pulp, peel, and seed (stone; Masibo and using controlled atmospheric storage treatments (Kim
He, 2008). Therefore, the pulp, peel, and stones of mango et al., 2007). The PP present in mango pulp can have
fruit may also be of interest from an industrial point-of- several roles. Ellagi-tannins (ET) and EA have been
view (Masibo and He, 2009a). shown to inhibit cancer cell proliferation in vitro
(Sreeram et al., 2005). Carotenoids and polyphenols
Bio-active compounds in mango pulp enrich the anti-oxidant property of mango fruit. These
Mango pulp is a valuable dietary source of many BaCs anti-oxidants are important as neutraceuticals,
which also impart the characteristic colour and flavour of preventing the occurrence of several diseases such as
mango fruit (Grundhofer et al., 2001; Haard and Chism, coronary atherosclerosis caused by elevated cholesterol,
1996). Pulp is also the starting material for the beverage lowering the levels of low density lipoprotein-cholesterol
industry, for flavouring ingredients in the dairy industry, (LDL-C), triglycerides, apolipoproteins B and C-III, and
and for baby food formulations (FAO, 2007). The increasing the levels of high density lipoprotein-
contents of BaCs in the pulp vary with cultivar, locality, cholesterol (HDL-C) and apolipoprotein A-I (Castelli,
climate, and the stage of fruit maturity. The various BaCs 1986). It is also known that nutritional anti-oxidants such
present in mango pulp are discussed below. as GA, mangiferin, myricetin, and flavan-3-ols (e.g.,
catechin and epicatechin) can prevent membrane lipid
Polyphenolics (PP): Among the many BaCs present in peroxidation (Kappus, 1985) and thereby protect cells
pulp, polyphenolics (PP) are the most widely-distributed and tissues from several disorders such as Parkinson’s
secondary metabolites and serve as the dominant anti- disease.
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lower risk of degenerative diseases such as cancer, heart tri-terpene (FAO, 2007). It is a biologically-active
disease, inflammation, arthritis, immune system decline, compound that has been reported to possess numerous
brain dysfunction, and cataracts (Michels et al., 2000). pharmacological properties, acting as a strong anti-
oxidant, anti-mutagenic, anti-inflammatory, and anti-
Carotenoids: Natural carotenoids are a diverse group of arthritic agent (Moriarity et al., 1998; Nagaraj et al., 2000;
over 600 structurally-related isoprenoids synthesised by Saleem et al., 2004). Lupeol also prevented 7, 12-
plants, fungi, and bacteria (Ben-Amotz and Fishler, dimethylbenz(a)anthracene-induced strand breaks in
1998). Chena et al. (2004) reported that mango fruit pulp DNA (Nigam et al., 2007), thereby reducing the
contained high concentrations of total carotenoids [0.9 – incidence of tumours, lowering the tumour body burden,
9.2 mg 100 g–1 fresh weight (FW)] and that their and causing a significant delay in the latency period of
composition and quantity depended on cultivar, tumour appearance (Saleem et al., 2004). Lupeol showed
geographical location, and stage of maturity (Pott et al., a similar trend to that of silymarin, a well-known hepato-
2003). Chena et al. (2004) identified a total of 25 protective agent, in protecting the liver from AFB1-
carotenoids in mango pulp, of which all-trans -carotene induced toxicity (Preetha et al., 2006).
was present at the highest concentration (29.34 µg g–1
FW; Table III). Codoy and Rodriguez-Amaya (1989) Bio-active compounds in mango peel
reported that -carotene was the dominant carotenoid in Mango peel is a major by-product of the mango
mango, representing 48 – 84% of total carotenoids. processing industry. Mango peel represents approx. 15 –
Carotenoids are associated with the climacteric increase 20% of the total weight of fresh fruit (Beerh et al., 1976).
in respiration in mango fruit that is initiated by the action It is a good source of several valuable BaCs such as
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of ethylene (Saltveit, 1999). Hence, -carotene is known polyphenols, carotenoids, vitamin, enzymes, and dietary
to predominate over xanthophylls in the later stages of fibre (DF; Ajila et al., 2007a; Berardini et al., 2005b;
ripening of mango fruit (Bhaskarachary et al., 1995), Ashoush and Gadallah, 2011) which, if extracted, can
which becomes apparent as the yellow-to-orange colour provide a source of health-promoting medicines. The
of ripe mango pulp. Green, unripe mango pulp does not AOC of mango peel extract was also higher than that of
contain any trace of carotenoids (Masibo and He, 2009a). mangiferin and quercetin 3-O-glucoside (Berardini et al.,
During ripening, the increase in carotenoids content was 2005a).
accompanied by a decrease in total organic acids content
and increases in sugars and mevalonic acid, the precursor Polyphenolics: The PP content of mango peel was higher
of carotenoids (Modi and Patwa, 1960). than that of the pulp at all stages of fruit development
Mango possesses high vitamin A activity and AOC, (Lakshminarayana et al., 1970). The polyphenolics
which is beneficial for human health (Mercadante et al., content of peel ranged from 55 – 110 mg GA equivalents
1998). Vitamin A is essential for vision and a variety of g–1 peel dry weight (DW) and was higher in ripe peel
metabolic functions. The AoA of carotenoids plays a than in unripe peel (Ajila et al., 2007a). The predominant
vital role against degenerative diseases such as cancer, substrate for PPC in mango peel is EA (Prabha and
CD, cataracts, and muscular diseases, as well as Patwardhan, 1986). Mango peel also contains two major
neurological, inflammatory, and immune disorders polyphenols, mangiferin and quercetin 3-O-galactoside.
(Bendich, 1993). The abundance of 9-cis--carotene and The mangiferin content of peel was 1,690.4 mg kg–1 DM,
a wide variety of carotenoids and their stereo-isomers in which decreased slightly at elevated temperatures, while
mango pulp should shift nutritional and medicinal the concentrations of other xanthone derivatives
attention from the synthetic all-trans -carotene towards increased significantly (Berardini et al., 2005b). These
natural carotenoids as potential candidates for the changes may be attributed to the formation of xanthones
prevention of degenerative diseases (Albanes et al., from benzophenone derivatives in mango peel
1996). (Berardini et al., 2004), which are considered to be the
Mango pulp also contains small amounts of lycopene precursors of xanthone C-glycosides (Larrauri, 1999;
(353 µg 100 g–1 FW; Budi et al., 2001). Lycopene has been Table IV).
reported to exhibit the highest AoA among various plant
carotenoids, followed by -cryptoxanthin, -carotene,
lutein, and zeaxanthin which possess pro-vitamin A TABLE IV
activity (Miller et al., 1996; Erdman et al., 1998). Phenolic compounds in mango peel
Component Concentration (mg kg–1 DM)
Lupeol: Mango pulp also contains lupeol, a pentacyclic Mangiferin 1,690.4
Iso-mangiferin 134.5
Mangiferin gallate 321.9
Iso-mangiferin gallate 82.0
TABLE III Quercetin 3-O-galactoside 651.2
Carotenoid composition of mango pulp Quercetin 3-O-glucoside 557.7
Component Concentration (µg g–1 DM) Quercetin 3-O-xyloside 207.3
Quercetin 3-O-rhamnoside 20.1
All-trans--carotene 29.34 Quercetin 3-O-arabinofuranoside 103.6
cis--Carotene 9.86 Quercetin 3-O-arabinopyranoside 101.5
cis-Violaxanthin 6.40 Kaempferol 3-O-glucoside 36.0
Neochrome 5.03 Rhamnetin 3-O galactoside 94.4
Luteoxanthin 3.60 Quercetin 65.3
cis-Neoxanthin 1.88 Ellagic acid nd
Zeaxanthin 1.16 Total phenolics 4,066.0
9- or 9'-cis-Lutein 0.78
Data are from Berardini et al. (2005b). DM, dry matter of peel (at 90ºC
Data are from Chena et al. (2004). DM, dry matter. for 90 min). nd, not determined. All data are means ± SD (n = 2).
372 Bio-active compounds in mango and their roles
content of ripe mango peel ranged from 3,400 – 3,945 µg AoA and phenolics contents of the stone was > 70%
g–1 DW ripe peel, while it was only 493 – 547 µg g–1 in (Soong and Barlow, 2004). The MK also contains a higher
unripe mango peel. Mango peel also contains vitamin C overall AoA than the fruit of longan, jack fruit, avocado,
(188 – 349 µg g–1 DW) and an appreciable quantity of and tamarind, thus providing a rationale for the
vitamin E (205 – 509 µg g–1 DW; Ajila et al., 2007a). commercial use of MK as an ingredient in functional
Carotenoid and vitamin concentrations were higher in foods.
ripe mango peel than in unripe peel (Table V).
Polyphenolics: Mango stones are rich in PP with potent
Anthocyanins: Anthocyanins are a group of phenolic anti-oxidant activity (values are given in Table VI).
compounds in plants that impart colour to fruit, exhibit Puravankara et al. (2000) reported that GA and EA exist
anti-oxidant properties, and have health benefits. Ripe as GT and ET, respectively, either in a free or bound
mango peel contained higher concentrations of form (Okuda, 1996) in MK. Abdalla et al. (2007) reported
anthocyanins (360 – 565 mg 100 g–1 FW) than unripe peel higher amounts of tannin and vanillin than GA, caffeic
(203 – 326 mg 100 g–1 FW; Ajila et al., 2007a). However, acid, and mangiferin in a MK powder. GA is known to
anti-oxidant extracts of green peel showed higher have anti-inflammatory, anti-mutagenic, anti-cancer, and
inhibition of lipoxygenase (LO) activities than extracts high AoA (Inoue et al., 1995; Kroes et al., 1992), while
from ripe peel (Ajila et al., 2007b). Lipoxygenases are EA is known to exhibit anti-mutagenic, anti-viral, anti-
responsible for many diseases such as asthma, tumour, and anti-oxidant properties (Khanduja et al.,
atherosclerosis, cancer (Mogul and Holman, 2001), and 1999; Wood et al., 1982; Huang et al., 2006). MK powder
tumour angiogenesis (Nie and Honn, 2002). can also be used as a functional food in the food industry
Lipoxygenases consist of a family of non-haem-containing due to its high anti-oxidant potential and associated
dioxygenase enzymes that are widely-distributed in plants stability, even at 160ºC (Soong and Barlow, 2004). The
and animals. In mammalian cells these enzymes have key polyphenols in MK exhibit a broad anti-microbial
roles in the biosynthesis of a variety of bio-regulatory spectrum, but are more active against Gram-positive
compounds such as hydroxy-eicosatetraenoic acid, than Gram-negative bacteria (Kabuki et al., 2000). MK
leukotrienes, lipoxins, and hepoxylines (Lands, 1985). extracts have been reported to be effective in the
Lipoxygenases are therefore potential targets for rational reduction of total bacterial counts in unpasteurised cow
drug design and the discovery of mechanism-based milk by retarding the development of acidity (Abdalla et
inhibitors to treat a variety of disorders and autoimmune al., 2007) and in the complete inhibition of coli-form
diseases. Anti-oxidants interact non-specifically with LO bacterial growth (Kabuki et al., 2000). The anti-microbial
by scavenging radical intermediates and/or by reducing activity of MK extracts was stable under conditions
the active haem-site (Cao et al., 1996).
TABLE VI
Phenolic compounds in mango seed kernel extract
Dietary fibre (DF): Mango peel has also been found to be
Component Concentration (mg 100 g–1 DM)
a source of nutritionally-rich DF having wide
Tannin 20.7
functionality (Table V). The crude fibre content of peel Gallic acid 6.0
(3.8 – 5.8 mg g–1 FW) represents mainly the cellulose Coumarin 12.6
fraction [a major part of the insoluble dietary fibre (IDF); Caffeic acid 7.7
Vanillin 20.2
Ajila et al. (2007a)]. Mango peel also contains high Mangiferin 4.2
quantities of soluble dietary fibre (SDF), IDF, and total Ferulic acid 10.4
dietary fibre (TDF), as indicated in Table V. DF is a Cinamic acid 11.2
Unknown compounds 7.1
functional food component and is known to have
Data are from Abdalla et al. (2007). DM, dry matter.
beneficial effects in reducing the risk of obesity, Mango seed kernel extract contained 112 mg total polyphenols 100 g–1
atherosclerosis, coronary heart disease, colorectal cancer, dry seed kernel powder. All data are means ± SD (n = 4).
H. RYMBAI, M. SRIVASTAV, R. R. SHARMA, C. R. PATEL and A. K. SINGH 373
TABLE VII edible oils including sunflower oil, ghee, and cheese
Nutrient composition of processed mango kernel flour
–1
(Dinesh et al., 2000). Tocopherols, carotenoids, and
Component Concentration (g kg PKF) mineral micronutrients such as Se, Cu and Zn may also be
Moisture 91.0 involved in the anti-oxidant activity of MK (Nunez-Selles
Protein 66.1
Fat 94.0 et al., 2002). Lipids extracted from the kernels of different
Fibre 28.0 mango varieties were found to be free from toxic
Ash 10.8 materials such as hydrocyanic acid (Rashwan, 1990), as
Sucrose 27.5
Starch 500.0 shown by the traditional used of MK flour for making
Carbohydrate 182.6 chapatti in India, roasted and eaten by tribal peoples, and
Ascorbic acid 0.17
processed into an edible flour in Nigeria (Arogba, 1999).
Data are from Arogba (1999). PKF, processed kernel flour. Therefore, Sims et al. (1972) and Gordon and Magos
The calorific value of processed mango kernel flour was 19.6 kJ kg–1
PKF. All data are means ± SD (n = 4). (1983) suggested that MK may be used as a natural food
supplement.
normally used during food processing; for example, Kernel vitamins and minerals: The MK contains several
heating (121ºC, 15 min), freezing (–20ºC, 16 h), and/or vitamins and dietary minerals (Table X). The major
pH treatment (pH 3 – 9; Kabuki et al., 2000). vitamins present in MK are vitamin A, vitamin E,
vitamin K, vitamins B1, B2, B6, B12, and vitamin C; while,
Nutritional compounds: The MK also contains Ca, Mg, K, Na, Fe, Zn, Mn, Se, and Cu are the main
phytosterols such as campesterol, -sitosterol, minerals present (Fowomola, 2010; Ashoush and
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stigmesterol, tocopherols, and several other nutritional Gadallah, 2011). The vitamins found in MKs are
compounds in varying proportions (Arogba, 1999; powerful anti-oxidants that neutralise free-radicals,
Ashoush and Gadallah, 2011; Table VII). which helps to protect against CD, cancers, and other
ailments (Anon, 2012b). Vitamin E from MK can help
Kernel proteins: MK are rich in proteins, essential amino the endocrine system to function more efficiently. It is
acids (EAAS), and non-essential amino acids (NEAAs). also reported that the high mineral content of MK may
Among the EAAS, leucine, lysine, and valine are present prevent anaemia, relieve clogged pores in the skin, and
at the highest concentrations (6.9, 5.8, and 4.3 g 100 g–1 reduce the risk of high blood pressure (Anon, 2012b). In
protein, respectively), with a total of 32.1 g EAAS 100 g–1 fact, MKs were shown to be as effective as the glucose-
protein. Among the NEAAS, glutamic acid was the lowering drug, rosiglitazone, and lipid-lowering drug,
highest (18.2 g 100 g–1 protein), with a total of 52.2 g fenofibrate, in reducing adipose tissue in an animal
NEAAS 100 g–1 protein (Abdalla et al., 2007; Arogba, model (Anon, 2012a).
1999; Table VIII).
Kernel anti-nutrients: Anti-nutrient substances generally
Kernel lipids: MKs are also rich in fats and fatty acids interfere with the absorption of nutrients when
(FAs; Table IX; Anon, 2010). Kernel oil has been reported consumed in excess amounts. Although, MKs contain
to be rich in saturated FAs and mono-unsaturated oleic several anti-nutrients, their levels are low enough not to
acid, as well as sterols such as D-avenasterol, fructosterol, cause any adverse effects (Table XI; Fowomola, 2010).
phytosterols, and squalene. The phospholipids and Moreover, during the processing of MKs by soaking,
phenolic compounds in MK extracts are known to have a boiling, autoclaving, irradiation, and roasting, there is a
synergistic effect in extending the shelf-life of various drastic reduction in these anti-nutritional factors
TABLE VIII
Amino acid composition of dry mango kernels
EAA Concentration (g 100 g–1 protein) NEAA Concentration (g 100 g–1 protein)
Leucine 6.9 ± 0.2 Aspartic acid 6.5 ± 0.4
Isoleucine 4.4 ± 0.2 Glutamic acid 18.2 ± 0.8
Methionine 1.2 ± 0.1 Serine 3.3 ± 0.1
Phenylalanine 3.4 ± 0.1 Proline 3.5 ± 0.2
Lysine 4.3 ± 0.2 Glycine 4.0 ± 0.4
Threonine 3.4 ± 0.2 Alanine 4.2 ± 0.4
Tyrosine 2.7 ± 0.1 Histidine 5.5 ± 0.6
Valine 5.8 ± 0.3 Arginine 7.3 ± 0.8
Total EAAs 32.1 ± 2.2 Total NEAAs 52.2 ± 2.1
Data are from Abdalla et al. (2007). EAAs, essential amino acids; NEAAs, non-essential amino acids. All data are means ± SD (n = 4).
TABLE IX
Lipid composition of dry mango kernels
Lipid Concentration [% (w/w)] Fatty acid Concentration [% (w/w)]
Fully saturated glycerides 14.2 Myristic 0.69
Mono-oleoglycerides 24.2 Palmitic 4.40 – 8.83
Di-oleoglycerides 60.8 Stearic 33.96 – 47.8
Tri-unsaturated glycerides 0.8 Arachidonic 2.70 – 6.74
Oleic 38.20 – 49.78
Linoleic 4.40 – 5.40
Linolenic 0.5
Data are from Anon (2010). Values are expressed on a % (w/w) dry weight basis.
374 Bio-active compounds in mango and their roles
TABLE X
Vitamin and mineral composition of dry mango seed
Vitamin Concentration (mg 100 g–1 DW) Mineral Concentration (mg 100 g–1 DW)
E 1.30 Na 21.00
K 0.59 K 22.30
B1 0.08 Ca 111.30
B2 0.03 Mg 94.80
B6 0.19 Fe 11.90
B12 0.12 Zn 1.10
C 0.56 Mn 0.04
Data are from Fowomola (2010). DW, dry weight. Dry mango seeds also contained 15.27 IU vitamin A. All the data are means ± SEM (n = 3).
(Agunbiade and Olanlokun, 2006). Therefore, MK populations for the treatment of gastritis and gastric
powder can be consumed safely after processing. ulcers (Robineau et al., 1996).
PP fraction represents > 50% of all constituents, and is the various BaCs present, including AsA, -tocopherols,
rich in mangiferin, catechin, and epicatechin (Scartezzini carotenoids, polyphenols, and micro-elements (Olsson et
and Speroni, 2000; Nunez-Selles et al., 2002). Similarly, al., 2004; Masibo and He, 2009a). These BaCs are
the main BaC in mango leaves is mangiferin (Stoilova effective electron donors which reduce Fe3+ or
et al., 2008). The BaCs of mango bark and leaves have ferricyanide complexes to their ferrous form, thereby
pharmacologically-active ingredients and health- indicating their AoA (Chung et al., 2002; Yen and Chen,
promoting effects. This was indicated through their use in 1995). Similarly, phenol moieties (hydroxyl groups) on
traditional medicine over many centuries (Stoilova et al., aromatic rings scavenge free-radicals through their
2008) to treat conditions such as menorrhagia, diarrhoea, hydrogen or electron donating ability, which contributes
syphilis, diabetes, scabies, cutaneous infections, and to the AoA of PP (Shahidi and Wanasundara, 1992; Van
anaemia (Scartezzini and Speroni, 2000), malignant Gadow et al., 1971). Synthetic anti-oxidants such as
tumours (Tamayo et al., 2001), benign prostate butylated hydroxytoluene and butylated hydroxyanisole
hyperplasia, dermatitis, and lupus erythematosus are used in food processing to reduce deterioration,
(Alberto et al., 2007), as well as having analgesic, anti- rancidity, and oxidative discolouration, but are volatile
inflammatory, immuno-modulatory, and anti-HIV (Ichiki and decompose easily at high temperatures (Branien,
et al., 1998; Ojewole, 2005; Guha et al., 1996), spasmolytic 1975). In contrast, the natural anti-oxidants from mango
(Tona et al., 2000), and immuno-stimulatory (Garcia are safe and have potential nutritional and therapeutic
et al., 2003) properties. values. BaCs in mango such as quercetin, the aglycone
‘Vimang’ is an extract of mango bark that contains derivative of mangiferin, and norathyriol have also been
numerous polyphenols with anti-oxidant properties, and shown to modulate the transactivation of isoforms of
improves the lives of people with HIV/AIDS. It is also peroxisome proliferator-activated receptors (PPARs;
used as an effective complement to anti-retroviral Huang et al., 2006; Wilkinson et al., 2008). PPARs are
treatments (Anon, 2011; Grogg, 2012). The mango tree transcription factors implicated in the control of
was listed for the treatment of various ailments in pathways relevant to many human diseases such as
“TRAMIL”, a research project on medicinal plant dyslipidemia, diabetes, obesity, inflammation,
resources in the Caribbean countries (Robineau et al.,
1996). Immature mango leaves also contain several TABLE XII
Bio-active chemical constituents in mango stem bark extracts
nutrients (Table XIV; Anon, 2010) and have medicinal
Component Component Component
properties. For example, a leaf decoction prevented
bleeding dysentery (Quisumbing, 1978) and an aqueous Polyphenols Polyalcohols Mineral elements
Mangiferin Sorbitol Calcium
leaf extract possessed hypoglycaemic activity (+) Catechin Myo-inositol Potassium
(Aderibigbe et al., 2001). An aqueous decoction from (–) Epicatechin Xylitol Magnesium
Gallic acid, propyl ester Iron
mango flowers has also been used by Caribbean Benzoic acid, propyl ester Terpenoids Selenium
3, 4-Dihydroxybenzoic acid -Elemene Copper
TABLE XI Benzoic Acid Aromandrene Zinc
Anti-nutrient composition of mango seed Gallic Acid -Guaiene Lead
Lignans -Selinene
Component Concentration (mg 100 g–1 DW) Hinesol Phytosterols
Alkaloids 0.01 ± 0.00 Fatty & dicarboxylic acids -Eudesmol -Sitosterol
Tannins 1.03 ± 0.01 Myristic Cyclo-artanols -Campesterol
Phytate 1.44 ± 0.01 Palmitic
Cyanide 0.00 Linoleic Free sugars
Saponin 0.04 ± 0.00 Estearic Glucose
Oxalate 1.49 ± 0.01 Eicosatrienoic Galactose
Succinic Arabinose
Data are from Fowomola (2010). DW, dry weight. Mean trypsin inhibitor Malonic
activity = 18.42 ± 2.54 trypsin inhibitor units mg–1 DW. All data are
means ± SEM (n = 3). Data are from Nunez-Selles et al. (2002) and Masibo and He (2009a,b).
H. RYMBAI, M. SRIVASTAV, R. R. SHARMA, C. R. PATEL and A. K. SINGH 375
occurrence of malformation (Sharma et al., 2001b; possibly by modulating the ROS used for signalling
Sharma, 2003). (Ben-Amor et al., 1999). Singh et al. (2012) underlined
Flavonoids possess anti-bacterial properties, as shown the significance of the enzymatic ROS scavenging system
by Kanwal et al. (2009) who isolated and evaluated five in the resistance or susceptibility of mango plants to
flavonoids: epicatechin-3-O--glucopyranoside; 5- disease and also indicated that leaf PPO, LOX, and anti-
hydroxy-3-(4-hydroxylphenyl) pyrano [3,2-g] chromene- oxidant enzyme activities can be used as biochemical
4 (8H)-one; 6-(p-hydroxybenzyl) taxifolin-7-O--D- indicators with which to screen mango germplasm
glucoside (tricuspid); quercetin-3-O--glucopyranosyl- against the malformation disorder. They also suggested
(1-2)--glucopyranoside; and (–)-epicatechin [2- (3, 4- that manipulation of the anti-oxidant system in plants
dihydroxyphenyl]-3, 4-dihydro-2H-chromene-3,5,7-triol] through over-expression of the enzymes involved in
from mango leaves. They found that all five flavonoids ROS-scavenging may help to maintain or improve plant
significantly reduced the growth of all four bacterial productivity under stress.
species tested (Lactobacillus sp., Escherichia coli, This review concludes that many parts of mango trees
Azospirillium lipoferum, and Bacillus sp.). However, such as the bark, leaves, fruit pulp, peel, and stone, are
among these five flavonoids, the last listed was the most rich sources of BaCs, including polyphenols,
effective against bacteria. Similarly, Masibo and He carotenoids, AsA, carbohydrates, proteins, minerals, and
(2009b) found that mangiferin from mango leaf extracts DF. The levels of these substances varies according to
inhibited the growth of all four pathogenic bacterial mango genotype and growing environment. These
species tested (Salmonella typhimurium, E. coli, substances can have new applications in functional
Staphylococcus aureus, and Bacillus cereus) and two non- foods, pharmaceuticals, and industrial products. The
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pathogenic bacteria (Streptococcus thermophilus and overall anti-oxidant activity (AoA) of mango fruit
Lactobacillus acidophilus). results from a synergism between the various BaCs and
The BaCs from mango also have important roles in ROS scavenging intermediates. The BaCs in mango
protecting the plant against oxidative stress by activating may be considered a potential source for rational drug
various anti-oxidant enzymes including superoxide design and the discovery of mechanism-based inhibitors
dismutase (SOD), catalase (CAT), and peroxidase for the treatment of a wide variety of disorders and
(POX; Niranjana et al., 2009). During post-harvest autoimmune diseases. The information provided here
chilling and heating, POX activity increased, which offers a valuable guide for the use and consumption of
degraded any accumulated H2O2 in mango fruit mango products in human and animal diets. It also
(Niranjana et al., 2009). CAT is also involved in the illustrates the protective roles of BaCs and their
removal of excess H2O2 during stress in plants; however, potential use to develop natural defence mechanisms
other peroxidases such as ascorbate peroxidase, have against pests, diseases, and environmental stresses by
been shown to be among the most important anti- accumulating anti-pathogenic and ROS-scavenging
oxidant defence enzymes during low-temperature injury, compounds.
REFERENCES
ABDALLA, A. E. M., DARWISH, S. M., AYAD, E. H. E. and EL- ALBERTO, J. N., REN, E. D., GARRIDO-GARRID, D. G., MARIELA, G.
HAMAHMY, R. M. (2007). Egyptian mango by-product 1. G. and GILBERTO, L. P. A. (2007). The paradox of natural prod-
Compositional quality of mango seed kernel. Food Chemistry, ucts as pharmaceuticals. experimental evidences of a mango
103, 1141–1152. stem bark extract. Pharmacology Research, 55, 351–358.
ADERIBIGBE, A. O., EMUDIANUGHE, T. S. and LOWAL, B. A. (2001). ANON (2010). Mango Mangifera indica L., and mango leaves:
Evaluation of anti-diabetic action of Mangifera indica in mice. health benefits and interesting facts. Mango leaf extract.
Phytotherapy Research, 15, 456–458. www.mdidea.com/products/herbextract/mangiferin/data.html.
AGUNBIADE, S. O. and OLANLOKUN, J. O. (2006). Studies on the ANON (2011). Nutrients and phytochemicals of mango.
nutritive value of the seed kernels of exotic and local mangoes www.mangoes.in/nutrients-andphytochemicals-of-mango.html.
(Mangifera indica L.). Biosciences and Biotechnology Research ANON (2012a). The effects of mango on glucose and lipid parame-
Asia, 3, 81–86. ters in high fat diet-induced obesity. http://www.mango.org/
AJILA, C. M., BHAT, S. G. and PRASADA RAO, U. J. S. (2007a). media/47759/mango%20modulates%20glucose
Valuable components of raw and ripe peels from two Indian %20and%20lipid%20parameters%20exec%20summary.pdf.
mango varieties. Food Chemistry, 102, 1006–1011. ANON (2012b). Health benefits of mango. http://www.balanced-
AJILA, C. M., NAIDU, K. A., BHAT, S. G. and PRASADA RAO, U. J. S. concepts.net/health_benefits mango.pdf.
(2007b). Bio-active compounds and anti-oxidant potential of AROGBA, S. S. (1997). Physical, chemical and functional properties
mango peel extract. Food Chemistry, 105, 982–988. of Nigerian mango kernel and its processed flour. Journal of the
ALBANES, D., HEINONEN, P., TAYLOR, P. R., VIRTAMO, J., EDWARDS, B. Science of Food and Agriculture, 73, 321–328.
K., RAUTALAHTI, M., HARTMAN, A. M., PALMGREN, J., FREED- AROGBA, S. S. (1999). The performance of processed mango kernel
MAN, L. S., HAAPAKOSKI, J., BARRET, M. J., PIETINEN, P., MALILA, flour in a model food system. Bioresource Technology, 70,
N., TALA, E., LIIPPO, K., SALOMAA, E. R., TANGREA, J. A., TEPPO, 277–281.
L., ASKIN, F. B., TASKINEN, E., EROZAN, Y., GREENWALD, P. and ARRIGONI, O. and DE TULLIO, M. C. (2002). Ascorbic acid: much
HUTTUNEN, J. K. (1996). -Tocopherol and -carotene supple- more than just an anti-oxidant. Biochimica et Biophysica Acta,
ments and lung cancer incidence in the -tocopherol, - 1569, 1–9.
carotene cancer prevention study: Effect of base-line ARUOMA, O. I. (1998). Free radicals, oxidative stress and anti-oxi-
characteristics and study compliance. Journal of the National dants in human health and diseases. Journal of the American Oil
Cancer Institute, 88, 1568–1570. Chemistry Society, 75, 199–212.
H. RYMBAI, M. SRIVASTAV, R. R. SHARMA, C. R. PATEL and A. K. SINGH 377
ARUOMA, O. I. (2003). Methodological considerations for character- CLUGSTON, G. A. and SMITH, T. E. (2002). Global nutrition problems
izing potential anti-oxidant actions of bio-active compounds in and novel foods. Asia Pacific Journal of Clinical Nutrition, 11,
plant foods. Mutation Research, 9, 523–524. 100–111.
ASHOUSH, I. S. and GADALLAH, M. G. E. (2011). Utilization of COATES, L. (2007). Management of postharvest diseases of sub-
mango peels and seed kernels powders as sources of phyto- tropical and tropical fruit using their natural resistance mecha-
chemicals in biscuit. World Journal of Dairy and Food Sciences, nisms. Host defence mechanisms in mango and avocado fruit
6, 35–42. (Sri Lanka and Australia). Project ID: HORT/1997/094.
BEERH, O. P., RAGHURAMAIAH, B., KRISHNAMURTHY, G. V. and http://aciar. gov.au/project/ HORT/1997/094.
GIRIDHAR, N. (1976). Utilization of mango waste: recovery of CODOY, H. T. and RODRIGUEZ-AMAYA, D. B. (1989). Carotenoid
juice from waste pulp and peel. Journal of Food Science and composition of commercial mangoes from Brazil. Lebensmittel-
Technology, 13, 138–141. Wissenschaft & Technologie, 22, 100–103.
BEN-AMOR, M., FLORES, B., LATCHE, A., BOUZAYEN, M., PECH, J. C. DAVEY, M. W., VAN MONTAGU, M., INZE, D., SANMARTIN, M.,
and ROMOJARO, F. (1999). Inhibition of ethylene biosynthesis of KANELLIS, A., SMIRNOFF, N., BENZIE, I. F. F., STRAIN, J. J.,
by antisense ACC oxidase RNA prevents chilling injury in FAVELL, D. and FLETCHER, J. (2000). Plant L-ascorbic acid:
‘Charentais cantaloupe’ melons. Plant Cell and Environment, chemistry, function, metabolism, bioavailability and effects of
22, 1579–1586. processing. Journal of the Science of Food and Agriculture, 80,
BEN-AMOTZ, A. and FISHLER, R. (1998). Analysis of carotenoids 825–860.
with emphasis on 9--carotene in vegetables and fruits com- DINESH, P., BOGHRA, V. R. and SHARMA, R. S. (2000). Effect of anti-
monly consumed in Israel. Food Chemistry, 62, 515–520. oxidant principles isolated from mango (Mangifera indica L.)
BENDICH, A. (1993). Biological functions of dietary carotenoids. In: seed kernels on oxidative stability of ghee (butter fat). Journal
Carotenoids in Human Health. (Canfield, L. M., Krinsky, N. I. of Food Science and Technology, 37, 6–10.
and Olson, J. A., Eds.). Annals of the New York Academy of ERDMAN, J. W., POOT, C. L. and DIETZ, J. M. (1998). Factors affect-
Sciences, New York, NY, USA. 61–67. ing the bioavailability of vitamin A, carotenoids and vitamin E.
BERARDINI, N., CARLE, R. and SCHIEBER, A. (2004). Food Technology, 42, 214–219.
Downloaded by [University of Nebraska, Lincoln] at 11:48 09 June 2016
Characterization of gallotannins and benzophenone derivatives FAO (2007). Food and Agriculture Organization of the United
from mango (Mangifera indica L. cv. Tommy Atkins) peels, pulp Nations. http://faostat.fao.org.
and kernels by high-performance liquid chromatography/elec- FOWOMOLA, M. A. (2010). Some nutrients and anti-nutrients con-
trospray ionization mass spectrometry. Rapid Communications tents of mango (Magnifera indica L.) seed. African Journal of
in Mass Spectrometry, 18, 2208–2216. Food Science, 4, 472–476.
BERARDINI, N., FEZER, R., CONRAD, J., BEIFUSS, U., CARLE, R. and GARCIA, D., LEIRO, J., DELGADO, R., SANMARTIN, M. L. and UBEIRA,
SCHIEBER, A. (2005a). Screening of mango (Mangifera indica F. M. (2003). Mangifera indica L. extract (Vimang) and
L.) cultivars for their contents of flavonol O- and xanthone C- mangiferin modulate mouse humoral immune responses.
glycosides, anthocyanins and pectin. Journal of Agricultural and Phytotherapy Research, 17, 1182–1187.
Food Chemistry, 53, 1563–1570. GARDNER, P. T., WHITE, T. A. C., MCPHAIL, D. B. and DUTHIE, G. G.
BERARDINI, N., KNODLER, M., SCHIEBER, A. and CARLE, R. (2005b). (2000). The relative contribution of vitamin C, carotenoids and
Utilization of mango peel as a source of pectin and polypheno- phenolics to the anti-oxidant potential of fruit juices. Food
lics. Innovative Food Science and Emerging Technologies, 6, Chemistry, 68, 471–474.
442–452. GORDON, M. and MAGOS, P. (1983). The effect of sterols on the oxi-
BERGER, J. P., AKIYAMA, T. E. and MEINKE, P. T. (2005). PPARs: ther- dation of edible oils. Food Chemistry, 10, 141–147.
apeutic targets for metabolic disease. Trends in GORINSTEIN, S., ZEMSER, M., HARUENKIT, R., CHUTHAKORN, R.,
Pharmacological Sciences, 26, 244–251. GRAUER, F., MARTIN-BELLOSO, O. and TRAKHTENBERG, S.
BEST, D. (1991). Whatever happened to fibre. Prepared Foods, 160, (1999). Comparative content of total polyphenols and dietary
54–58. fibre in tropical fruits and persimmon. Journal of Nutritional
BHASKARACHARY, K., SANKAR RAO, D. S., DEOSTHALE, Y. G. and Biochemistry, 10, 367–371.
REDDY, V. (1995). Carotene content of some common and less GROGG, P. (2012). Mango bark used in HIV/AIDS fight.
familiar foods of plant origin. Food Chemistry, 54, 189–193. Tierremerica. http://www.tierramerica.info/nota.php?lang=eng
BINGHAM, S. A., DAY, N. E. and LUBEN, R. (2003). Dietary fibre in &idnews=2483.
food and protection against colorectal cancer in the European GRUNDHOFER, P., NIEMETZ, R., SCHILLING, G. and GROSS, G. G.
prospective investigation into cancer and nutrition (EPIC): An (2001). Biosynthesis and subcellular distribution of
observational study. The Lancet, 361, 1496–1499. hydrolysable tannins. Phytochemistry, 57, 915–927.
BRANIEN, A. L. (1975). Toxicology and biochemistry of butylated GUHA, S., GHOSAL, S. and CHATTOPADHYAY, U. (1996). Anti-tumour,
hydroxy anisole and butylated hydroxy toluene. Journal of the immunomodulatory and anti-HIV effect of mangiferin, a natu-
American Oil Chemists’ Society, 52, 59–63. rally occurring glucosylxanthone. Chemotherapy, 42, 443–451.
BUDI, S., AHMAD, S., DAVID, W. G. and JUDY, A. D. (2001). HAARD, N. F. and CHISM, G. W. (1996). Characteristics of edible
Carotenoid content of selected Indonesian fruits. Journal of plant tissues. In: Food Chemistry Inc. 3rd Edition. (Fennema, O.
Food Composition and Analysis, 14, 169–176. R., Ed.). Marcel Dekker, New York, NY, USA. 943–951.
CAO, G., SOFIE, E. and PRIOR, R. L. (1996). Anti-oxidant activity of HASLAM, E. (1996). Natural polyphenols (vegetable tannins) as
tea and common vegetables. Journal of Agricultural and Food drugs: possible mode of action. Journal of Natural Products, 59,
Chemistry, 44, 3426–3431. 205–215.
CASTELLI, W. P., GARRISON, R. J., WILSON, P. W. F., ABBOTT, R. D., HUANG, T. H., PENG, G., LI, G. Q., YAMAHARA, J., ROUFOGALIS, B. D.
KALOUSDIAN, S. and KANNEL, W. B. (1986). Incidence of coro- and LI, Y. (2006). Salacia oblonga root improves postprandial
nary heart disease and lipoprotein cholesterol levels. The hyperlipidemia and hepatic steatosis in zucker diabetic fatty
Framingham study. Journal of the American Medical rats: activation of PPAR-alpha. Toxicology and Applied
Association, 256, 2835–2838. Pharmacology, 210, 225–235.
CASTILLO, F., HERNÁNDEZ, D., GALLEGOS, G., RODRÍGUEZ, R. and ICHIKI, H., MIURA, T., KUBO, M., ISHIHARA, E., KOMATSU, Y., TANI-
AGUILAR, C. N. (2011). Antifungal properties of bio-active com- GAWA, K. and OKADA, M. (1998). New anti-diabetic compounds,
pounds from plants. In: Fungicides for Plant and Animal mangiferin and its glucoside. Biology and Pharmaceutical
Diseases. Chapter 4. Tech-Open Access Company, Hotel Bulletin, 21, 1389–1390.
Equatorial, Shanghai, P. R. China. 81–84. INGEBRIGTSEN, K. (2010). Main plant poisonings in livestock in the
CHENA, J. P., TAI, C. Y. and CHEN, B. H. (2004). Improved liquid Nordic countries. In: Bio-Active Compounds in Plants –
chromatographic method for determination of carotenoids in Benefits and Risks for Man and Animals. Proceedings of the
Taiwanese mango (Mangifera indica L.). Journal of Norwegian Academy of Science and Letters. 13–14th
Chromatography, 1054, 261–268. November 2008. Oslo, Norway. 31.
CHUNG, Y. C., CHANG, C. T., CHAO, W. W., LIN, C. F. and CHOU, S. T. INOUE, M., SUZUKI, R., SAKAGUCHI, N., ZONG, L., TAKEDA, T.,
(2002). Anti-oxidant activity and safety of the 50% ethanolic OGIHARA, Y., JIANG, B. Y. and CHEN, Y. (1995). Selective induc-
extract from red bean fermented by Bacillus subtilis IMR-NK1. tion of cell death in cancer cells by gallic acid. Biology and
Journal of Agricultural and Food Chemistry, 50, 2454–2458. Pharmaceutical Bulletin, 18, 1526–1530.
378 Bio-active compounds in mango and their roles
JASNA, S. D., BRUNET, C. and CETKOVIC, G. (2009). By-products of MORIARITY, D. M., HUANG, J., YANCEY, C. A., ZHANG, P., SETZER, W.
fruits processing as a source of phytochemicals. Chemical N., LAWTON, R. O., BATES, R. B. and CALDERA, S. (1998). Lupeol
Industry & Chemical Engineering, 15, 1–12. is the cytotoxic principle in the leaf extract of Dendropanax
KABUKI, T., NAKAJIMA, H., ARAI, M., UEDA, S., KUWABARA, Y. and querceti. Planta Medica, 64, 370–372.
DOSAKO, S. (2000). Characterization of novel antimicrobial NABARD (2011). Model Bankable Scheme for Organic Cultivation of
compounds from mango (Mangifera indica L.) kernel seeds. Mango in Tamil Nadu. http://www.nabard.org/modelbankprojects/
Food Chemistry, 71, 61–66. mango.asp.
KANWAL, Q., HUSSAIN, I., SIDDIQUI, H. L. and JAVAID, A. (2009). NAGARAJ, M., SUNITHA, S. and VARALAKSHMI, P. (2000). Effect of
Flavonoids from mango leaves with antibacterial activity. lupeol, a pentacyclic triterpene, on the lipid peroxidation and
Journal of the Serbian Chemical Society, 74, 1389–1399. anti-oxidant status in rat kidney after chronic cadmium expo-
KAPPUS, H. (1985). Lipid peroxidation: mechanisms, analysis, enzy- sure. Journal of Applied Toxicology, 20, 413–417.
mology and biological relevance. In: Oxidative Stress. (Sies, H., NARASIMHA, C. B. L. and AZEEMODDIN, G. (1989). Edible fat from
Ed.). Academic Press, New York, NY, USA. 273–310. mango stones. Acta Horticulturae, 231, 744–748.
KHANDUJA, K. L., GANDHI, R. K., PATHANIA, V. and SHAL, N. (1999). NHB (2011). National Horticulture Board. Indian Horticulture
Prevention of N-nitrosodiethylamine-induced lung tumorigen- Database. Ministry of Agriculture, New Delhi, India. 4 pp.
esis by ellagic acid and quercetin in mice. Food and Chemical NIE, D. and HONN, K. V. (2002). Cyclo-oxygenase, lipoxygenase and
Toxicology, 37, 313–318. tumor angiogenesis. Cellular and Molecular Life Science, 59,
KIM, Y, BRECHT, K. J. and TALCOTT, S. T. (2007). Anti-oxidant phy- 799–807.
tochemical and fruit quality changes in mango (Mangifera NIGAM, N., PRASAD, S. and SHUKLA, Y. (2007). Preventive effects of
indica L.) following hot-water immersion and controlled lupeol on DMBA-induced DNA alkylation. Food Chemistry
atmosphere storage. Food Chemistry, 10, 1016. and Toxicology, 10, 1016.
KROES, B. H., VAN DEN BERG, A. J. J., UFFORD, H. C. Q., VAN DIJK, NIRANJANA, P., GOPALAKRISHNA, K. P. R., SUDHAKAR, D. V. R. and
H. and LABADIE, R.P. (1992). Anti-inflammatory activity of MADHUSUDHAN, B. (2009). Effect of pre-cooling and heat treat-
gallic acid. Planta Medica, 58, 499–504. ment on anti-oxidant enzymes profile of mango and banana.
Downloaded by [University of Nebraska, Lincoln] at 11:48 09 June 2016
LAKSHMINARAYANA, S., SUBHADRA, N. V. and SUBRAMANYAM, H. African Journal of Food, Agriculture, Nutrition and
(1970). Some aspects of developmental physiology of mango Development, 9, 1211–1225.
fruit. Journal of Horticultural Science, 45, 133–142. NUNEZ-SELLES, A. J. (2005). Anti-oxidant therapy: myth or reality?
LANDS, W. E. M. (1985). Mechanism of action of anti-inflammatory Journal of the Brazilian Chemistry Society, 6, 699–710.
drugs. Advances in Drug Research, 14, 157–167. NUNEZ-SELLES, A. J., VELEZ-CASTRO, H. T., AGUERO-AGUERO, J.,
LARRAURI, J. A. (1999). New approaches in the preparation of high GONZALEZ-GONZALEZ, J., NADDEO, F., DE SIMONE, F. and RAS-
TRELI, L. (2002). Isolation and quantitative analysis of phenolic
dietary fibre powders from fruit by-products. Trends in Food
Science and Technology, 10, 3–8. anti-oxidants, free sugars, and polyols from mango (Mangifera
LIRA, S. R. H., HERNÁNDEZ, S. M., CHAVÉZ, B. C., HERNÁNDEZ, C. F. indica L.) stem bark aqueous decoction used in Cuba as a nutri-
D. and CUELLAR, V .E. (2007). Bioplaguicidas de origen vegetal: tional supplement. Journal of Agricultural and Food Chemistry,
50, 762–766.
El caso de los extractos y productos derivados de la gobe-
madora (Larrea tridentata). In: Biopesticides and Biological OJEWOLE, J. A. (2005). Anti-inflammatory, analgesic and hypo-
Control. Centro de Investigación en Química Aplicada glycemic effects of Mangifera indica Linn. (Anacardiaceae)
(CIQA), Monterrey, México. 13–29. stem-bark aqueous extract. Clinical Pharmacology, 27, 547–554.
OKUDA, T. (1996). Tannins, a new family of bio-active natural
LOELILLET, D. (1994). The European mango market: a promising
organic compounds. Yakugaku Zasshi, 115, 81–100.
tropical fruit. Fruits, 49, 332–334.
OLSSON, M. E., GUSTAVSSON, K. E., ANDERSSON, S., NILSSON, A. and
LOUNDS-SINGLETON, A. J. (2003). Influence of Thermal Postharvest
DUAN, R. D. (2004). Inhibition of cancer cell proliferation in
Stress on Mango (Magnifera indica) Polyphenolics During
vitro by fruit and berry extracts and correlations with anti-
Ripening. M.Sc. Thesis. University of Florida, FL, USA. 14 pp.
oxidant levels. Journal of Agricultural and Food Chemistry, 52,
MASIBO, M. and HE, Q. (2008). Major mango polyphenols and their 7264–7271.
potential significance to human health. Comprehensive Reviews
POOVARODOM, S., HARUENKIT, R., VEARASILP, S., NAMIESNIK, J.,
on Food Science and Food Safety, 7, 309–319.
CVIKROV, M., MARTINCOVA, O., EZRA, A., SUHAJ, M., RUAM-
MASIBO, M. and HE, Q. (2009a). Mango bio-active compounds and SUKE, P. and GORINSTEIN, S. (2010). Comparative characterisa-
related nutraceutical properties: a review. Food Reviews tion of durian, mango and avocado. International Journal of
International, 25, 346–370. Food Science and Technology, 45, 921–929.
MASIBO, M. and HE, Q. (2009b). In-vitro antimicrobial activity and POTT, I., MARX, M., NEIDHART, S., MÜHLBAUER, W. and CARLE, R.
the major polyphenol in leaf extract of mango (Mangifera (2003). Quantitative determination of -carotene stereoiso-
indica L.). Malaysian Journal of Microbiology, 5, 73–80. mers in fresh, dried and solar-dried mangoes (Mangifera indica
MAYER, A. M. and HAREL, E. (1979). Polyphenol oxidase in higher L.). Journal of Agricultural and Food Chemistry, 51, 4527–4531.
plants: a review. Phytochemistry, 18, 193–215. PRABHA, T. N. and PATWARDHAN, M. V. (1986). Endogenously oxi-
MECKES, M, RIVERA, A. D., NAVA, V. and JIMENEZ, A. (2004). dizable polyphenols of mango, sapota and banana. Acta
Activity of some Mexican medicinal plant extracts on car- Alimentaria, 15, 123–128.
rageenan-induced rat paw edema. Phytomedicine, 11, 446–451. PREETHA, S. P., KANNIAPPAN, M., SELVAKUMAR, E., NAGARAJ, M.
MERCADANTE, A. Z. and RODRIGUEZ-AMAYA, D. B. (1998). Effects and VARALAKSHMI, P. (2006). Lupeol ameliorates aflatoxin B1-
of ripening, cultivar differences and processing on the induced peroxidative hepatic damage in rats. Comparative
carotenoid compositing of mango. Journal of Agricultural and Biochemistry & Physiology – Part C: Toxicology &
Food Chemistry, 46, 128–130. Pharmacology, 143, 333–339.
MICHELS, K. B., GIOVANNUCCI, E., JOSHIPURA, K. J., ROSNER, B. A., PURAVANKARA, D., BOHGRA, V. and SHARMA, R. S. (2000). Effect of
STAMPFER, M. J., FUCHS, C. S., COLDITZ, G. A., SPEIZER, F. E. and anti-oxidant principles isolated from mango (Mangifera indica
WILLETT, W. C. (2000). Prospective study of fruit and vegetable L.) seed kernels on oxidative stability of buffalo ghee (butter-
consumption and incidence of colon and rectal cancers. Journal fat). Journal of Agricultural and Food Chemistry, 80, 522–526.
of the National Cancer Institute, 92, 1740–1752. QUISUMBING, E. (1978). Medicinal Plants of the Philippines. Katha
MILLER, H. E., RIGELHOF, F., MARQUART, L., PRAKASH, A. and Publishing Co. & JMC Press, Quezon, The Phillipines. 538–541.
KANTER, M. (2000). Whole grain products and anti-oxidants. RAM, S. (1991). Horticultural aspects of mango malformation. Acta
Cereal Food World, 45, 59–63. Horticulturae, 291, 235–252.
MILLER, N. J., SAMPSON, J., CANDEIAS, L. P., BRAMLEY, P. M. and RASHWAN, M. R.A. (1990). Fatty acids composition, neutral lipids and
RICE-EVANS, C. A. (1996). Anti-oxidant activities of carotenes phospholipids fractionation in the kernel lipids of the mango
and xanthophylls. FEBS Letters, 384, 240–246. varieties. Assiut Journal of Agricultural Science, 21, 105–117.
MODI, V. and PATWA, D. (1960). Enzymatic synthesis and destruc- ROBINEAU, L. G., SOEJARTO, D. D. and TRAMIL, A. (1996). Research
tion of carotenoids in mango extracts. Experientia, 16, 352. project on the medicinal plant resources of the Caribbean. In:
MOGUL, R. and HOLMAN, T. R. (2001). Inhibition studies of soybean Resources of the Tropical Forest. (Balick, M.J., Elisabetsky, E.
and human 15-lipoxygenase with long chain alkenyl sulfate sub- and Laird, S.A., Eds.). Columbia University Press, New York,
strates. Biochemistry, 49, 4391–4396. NY, USA. 318–325.
H. RYMBAI, M. SRIVASTAV, R. R. SHARMA, C. R. PATEL and A. K. SINGH 379
SALEEM, M., AFAQ, F., ADHAMI, V. M. and MUKHTAR, H. (2004). STOILOVA, I., JIROVETZ, L. and STOYANOVA, A. (2008). Anti-oxidant
Lupeol modulates NF-(kappa) B and PI3K/Akt pathways and activity of the polyphenol mangiferin. EJEAF Chemistry, 7,
inhibits skin cancer in CD-1 mice. Oncogene, 23, 5203–5214. 2706–2716.
SALEH, N. A. M. and L-ANSARI, M. A. I. (1975). Polyphenolics of SZETO, Y. T., TOMLINSON, B. and BENZIE, I. F. F. (2007). Total antiox-
twenty local varieties of Mangifera indica L. Planta Medica, 28, idant and ascorbic acid content of fresh fruits and vegetables:
124–130. implications for dietary planning and food preservation. British
SALTVEIT, M. E. (1999). Effect of ethylene on quality of fresh fruits Journal of Nutrition, 87, 55-59.
and vegetables. Postharvest Biology and Technology, 15, 279–292. TAMAYO, D., MARI, E., GONZALEZ, S., GUEVARA, M., GARRIDO, G.
SCARTEZZINI, P. and SPERONI, E. (2000). Review on some plants of and DELGADO, R. E. A. (2001). Vimang as natural anti-oxidant
Indian traditional medicine with anti-oxidant activity. Journal supplementation in patients with malignant tumors. Minerva
of Ethnopharmacology, 71, 23–43. Medica, 92, 95–97.
SCHIEBER, A., ULLRICH, W. and CARLE, R. (2000). Characterization TONA, L., KAMBU, K., NGIMBI, N., MESIA, K., PENGE, O., LUSAK-
of polyphenols in mango purée concentrate by HPLC with IBAZA, M., CIMANGA, K., DE BRUYNE, T., APERS, S., TOTTE, J.,
diode array and mass spectrometric detection. Innovative Food PIETERS, L. and VLIETINCK, A. (2000). Anti-amoebic and spas-
Science and Emerging Technology, 1, 161–166. molytic activities of extracts from some anti-diarrhoeal tradi-
SHAHIDI, F. and WANASUNDARA, P. K. J. P. D. (1992). Phenolic anti-oxi- tional preparations used in Kinshasa, Congo. Phytomedicine, 7,
dants. Critical Reviews in Food Science and Nutrition, 32, 67–103. 31, 38.
SHARMA, R. R. (2003). Catecholase and cresolase activity as a bio- TYAGI, S., GUPTA, P., SAINI, A. S., KAUSHAL, C. and SHARMA, C.
chemical index for screening mango (Mangifera indica L.) (2011). The peroxisome proliferator-activated receptor: A
seedlings at nursery stage for bearing behaviour in their future family of nuclear receptors role in various diseases. Journal of
reproductive life. Plant Genetic Resources Newsletter, 133, 31–34. Advanced Pharmaceutical Technological Research, 2, 236–240.
SHARMA, R. R., GOSWAMI, A. M., SINGH, C. N., CHHONKAR, O. P. and VAN GADOW, A., JOUBERT, E. and HANNSMAN, C. T. (1997).
SINGH, G. (2001a). Catecholase and cresolase activities and phe- Comparison of the anti-oxidant activity of aspalathin with that
nolic content in mango (Mangifera indica L.) at panicle initia- of other plant phenols of roolbos tea (Aspalathus linearis), -
Downloaded by [University of Nebraska, Lincoln] at 11:48 09 June 2016
tion. Scientia Horticulturae, 87, 147–151. tocopherol, BHT, and BHA. Journal of Agricultural and Food
SHARMA, R. R., SINGH, C. N. and GOSWAMI, A. M. (2001b). Chemistry, 45, 632–638.
Polyphenol oxidase activity in mango (Mangifera indica L.) in VAUGHAN, K. C. and DUKE, S. O. (1984). Function of polyphenol
relation to flowering behaviour and the malformation inci- oxidase in higher plants. Physiologia Plantarum, 60, 106-112.
dence. Fruits, 56, 219–224. WANG, H., CAO, G. and PRIOR, R. L. (1996). Total anti-oxidant
SIMS, R., FIORITI, J. and KANUK, M. (1972). Sterol additives as poly- capacity of fruits. Journal of Agricultural and Food Chemistry,
merization inhibitors for frying oils. Journal of the American Oil 44, 701–705.
Chemists’ Society, 49, 298–301. WILKINSON, A. S., MONTEITH, G. R., SHAW, P. N., LIN, C. N., GIDLEY,
SINGH, Z. and DHILLON, B. S. (1991). Mango malformation: possible M. J. and ROBERTS-THOMSON, S. J. (2008). Effects of mango
involvement of malformin-like substance (s) and control. Acta components mangiferin and quercetin and the putative
Horticulturae, 291, 253–264. mangiferin metabolite norathyriol on the transactivation of
SINGH, O. P., USHA, K., SABOKI, E., SRIVASTAV, M., DAHUJA, A. and peroxisome proliferator-activated receptor isoforms. Journal of
SINGH, B. (2012). Enzymatic reactive oxygen species scavenging Agricultural and Food Chemistry, 56, 3037–3042.
system in mango varieties resistant and susceptible to mango WOOD, A. W., HUANG, M. T., CHANG, R. L., NEWMARK, H. L., LEHR,
malformation. Scientia Horticulturae, 138, 81–89. R. E., YAGI, H., SAYER, J. M., JERINA, D. M. and CONNEY, A. H.
SOONG, Y. and BARLOW, J. (2004). Anti-oxidant activity and pheno- (1982). Inhibition of the mutagenicity of bay-region diol epox-
lic content of selected fruit seeds. Food Chemistry, 88, 411–417. ides of polycyclic aromatic hydrocarbons by naturally occur-
SREERAM, N. P., ADAMS, L. S., HENNING, S. M., NIU, Y., ZHANG, Y., ring plant phenols: exceptional activity of ellagic acid.
NAIR, M. G. and HEBER, D. (2005). In-vitro anti-proliferative, Proceedings of the National Academy of Sciences of the USA,
apoptotic and anti-oxidant activities of punicalagin, ellagic acid 79, 5513–5517.
and a total pomegranate tannin extract are enhanced in combi- YEN, G. C. and CHEN, H. Y. (1995). Anti-oxidant activity of various
nation with other polyphenols as found in pomegranate juice. tea extracts in relation to their anti-mutagenicity. Journal of
Journal of Nutrition and Biochemistry, 16, 360–367. Agricultural and Food Chemistry, 43, 27–32.