World J. Cur. Sci. Res. (2021) 1:3
World Journal of Current Scientific Research
Journal Homepage: www.wjcsr.com
Cipadessa baccifera Fruit- an Unexplored Store House of Nutrient Kavitha, K.R., Jyothsna, B.S., Arpita De* Nrupathunga University (Formerly, Government Science College, Autonomous)Department of Botany, Nrupathunga Rd, Sampangi Rama Nagar, Ambedkar Veedhi, Bengaluru, Karnataka 560001, India
A R T I C L E I N F O ABSTRACT
Keywords: Traditional practice of ethnobotany bridges the gap between plant resources and man. This will not only Bioprospecting help to sustain the exponentially rising population but will also upgrade the economic condition of tribal Cipadessa baccifera Ethnobotany folk. Cipadessa baccifera fruit is one those wild grown treasures that is generously loaded with medicinal as indigenous fruit well as nutritional values. Literature is overflowing with reports on the chemical composition and medicinal proximate analysis properties of the leaves. This ignited a completely different spark of interest in evaluating the proximate, chemical and vitamin composition of the fruit of Cipadessa baccifera. The present study was undertaken to *Corresponding author. evaluate the bioactive potentials of this fruit through proximate analysis. The results of analysis clearly E-mail addresses: [email protected] depict that Cipadessa baccifera fruits are fortified with incredibly important minerals (calcium, phosphorus, m potassium) and nutrients (carbohydrate, fibre) that are indispensable for healthy growth of our body. Since these plants grow in the wilderness, bioprospecting of this indigenous fruit will serve as a cost effective method to combat food insecurity and malnutrition.
with tetratriterpenoid (Li et al., 2007), trepenoids (Lin et al., 1. Introduction 2008) and limonids (Yu et al., 2020). Methanolic leaf extracts of Cipadessa baccifera have antimicrobial, anticancer as well as Medicinal plants are Nature’s gift to mankind. Cipadessa antioxidant properties (Thirunavukarasu et al., 2014; Rajani et baccifera, an ethnomedicinal shrub, is widely distributed in al., 2015). Bhakshu et al., in 2016 evaluated the anti candidal tropical forests of Asia, especially in the Western Ghats (Chetty properties of Cipadessa baccifera. These edible globose drupes et al., 2008). The monotypic genus Cipadessa belongs to family (fruits) of Cipadessa baccifera are reported to have radical Meliaceae and comprises of a single species viz., Cipadessa scavenging properties (Valve et al., 2011), hence assessing its baccifera, which is commonly known by the English names, nutritional content is a promising area of research that may help 'Black- oil tree', 'Intellect tree' and 'Climbing-staff plant'. The in contributing to the food constituent data repository of wild fruits and leaves of this Meliacean member is loaded with species for the development of new food products and dietary medicinal properties. The leaves are a storehouse of essential supplements. oils that has immense application in drug manufacturing industry (Kavitha et al., 2016). It is extensively used in the Thorough evaluation of the nutritional aspects of a plant treatment of hypertension (Jebarubi et al., 2018), diabetes, necessitates proximate analysis of the edible parts of that plant. dysentery, rheumatism, malarial fever, piles, dermatological The proximate system of analysis, originally developed by problems like pruritus (itchy skin), headache, psoriasis, burns, Hennerber and Stohmann of Germany way back in the mid19th scalds and to heal wounds (Zhu, 1998; Luo et al., 2000; Jeevan century (1860), is a qualitative method used to determine the et al., 2004; Amit and Shailendra, 2006; Malarvannan et al., macronutrients present in an edible material (Greenfield and 2009). Smoke toxicity of Cipadessa baccifera was proven to be Southgate, 1992; Gafar and Itodo, 2011). In this method, the effective against mosquitoes. Ramkumar et al., (2015) relative amounts of nutrients which are partitioned into 6 major demonstrated that leaf extract of this plant can be used as an categories based on the chemical properties viz., moisture, ash, ecofriendly mosquito repellent. protein, fat, crude fibre and carbohydrates are estimated (Bender, 2009) thereby rendering a vivid picture of nutritional This ethnopharmacologically important shrub is fortified
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Cite this article as Kavitha, K.R., Jyothsna, B.S., Arpita De. 2021. Cipadessa baccifera Fruit- an Unexplored Store House of Nutrient World J.Cur. Sci. Res.,1(3):164-171. Cipadessa baccifera Fruit- an Unexplored Store House of Nutrient Kavitha et al composition of the plant part in study. air oven at 70°C for about 8 hours keeping the lid of the petri dish open. Thereafter it as cooled at room temperature for an hour Despite being an ethnopharmacologically important plant, and final weight was recorded (W3). The dish with dried sample literature study shows that Cipadessa baccifera fruit has not was allowed to cool in a desiccator and its weight was noted been subjected to systematic and comprehensive scientific (W3). Difference in the dried weight after 1 hour should not evaluation for its bioactive potential. Prior to the present exceed 10 mg (Ranganna, 1986). The moisture content in the investigation the chemical compositions of the essential oils in fruit sample was calculated using following formula: the leaves of this plant were evaluated. The current study is an [( ) ( )] attempt to evaluate the bioactive potential and validate the Percentage of moisture content = X 100 pharmacological properties of this ethnobotanically important ( ) medicinal plant. Where, W1 = weight of clean and dry empty petri dish
The fruits were thus thoroughly screened for its W2 = weight of petri dish + wet sample nutraceutical potentials to see whether this can be W3 = weight of petri dish + dry sample recommended for inclusion in regular diet as a nutrient alternative. 2.4. Total ash content 2. Material and Methods Ash is the inorganic residue remaining after water and organic matter have been removed by heating and refers to the 2.1. Collection of plant material total mineral content. The ash content is determined by The plant samples for investigation were collected from incinerating the sample in Muffle furnace at a high temperature Thavarekere and Savandurga, Magadi Taluk, Bengaluru Rural of 550°C until all carbon has been removed and a light gray or district and outskirts of Bengaluru. They were identified white powder remains. as Cipadessa baccifera (Roth) Miq using Flora of Hassan (1976) 5 g of fruit sample was taken in a clean, dry silica crucible and Flora of Karnataka (1996) by Saldana. Further, and pre-ignited at 550°C for about 4 hours to remove the identification was authenticated by National Ayurveda and carbonaceous matter. The ash thus obtained was cooled in Dietetics Research Institute, Bangalore; vide voucher specimen desiccator and weighed (W3). The weight of the dish was noted number, RRCBI-8971 (Appendix 1). A separate voucher as W3. The ash was allowed to stand for another 1 hour to specimen BOT/Dec/11 is deposited in the herbarium of PG achieve constant weight. Difference in dried weight should not Department of Botany and Research Centre, St. Joseph's exceed 10 mg (Ranganna, 1986). The ash content in the fruit College, Bengaluru. The samples such as leaves, bark, fruits, sample was calculated using following formula: seeds and roots were collected in clean and sterile polythene bags for various analyses. Percentage of Ash = X 100
2.2. Proximate analysis of fruits 2.5. Total fat content
Proximate analysis is the quantitative evaluation of food 5 g of the fruit sample was taken in a dry, empty 250 ml to determine the percentage of the six fractions it divides food beaker and weight was recorded. 50 ml of distilled water and 5 materials into viz., moisture, total ash, fat or ether extractives, ml of concentrated HCl were added to the sample and the protein, crude fibre and carbohydrates. Carbohydrates could solution was warmed for about 10 minutes in water bath at 60°C. include additional compounds like dietary fibres, sugars and The contents were then transferred to a separating funnel by sugar alcohol, but are not limited by them. Ash content filtering with Whattman No.1 filter paper. 100 ml of petroleum includes, but is not limited to dietary minerals (sodium, ether was added to the separating funnel, swirled slowly and the potassium, iron, calcium) and vitamins (β-carotene, retinol, pressure released. Saturated solution of NaCl was then added to vitamin D3, vitamin D2 and vitamin B). Proximate parameters separate the emulsion and shaken vigorously. The layers were do not give the entire nutritional content, nevertheless it is an allowed to separate and the ether layer was collected. The important assay used today to assess the nutritional separation of aqueous solution was continued similarly with 100 significance of edible fruits and vegetables (Pandey et al., ml petroleum ether. Petroleum ether was collected; 100 ml of 2006) and monitor deviations from the quality of food. Today water was added to it for washing, until it is neutral to acid. The edible plants and their derived food products are assessed sample was passed through sodium sulphate and the petroleum qualitatively and quantitatively for the minerals and vitamins ether fraction was collected in a pre-dried 250 ml beaker. The using proximate parameters (Gafar and Itodo, 2011). petroleum ether was evaporated to near dryness and kept in an 2.3. Moisture content oven for about 1 hour. The beaker was cooled in desiccator and the weight of fat was calculated (Ranganna, 1986). The total fat A clean, oven dried petri dish was cooled (in a desiccator) content in the fruit sample was determined by following formula: and weighed (W1). 5 g of fruit sample was weighed on it and Percentage of Fat = X 100 total weight was recorded (W2). The sample was dried in hot
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Cipadessa baccifera Fruit- an Unexplored Store House of Nutrient Kavitha et al
2.6. Protein content Carbohydrate are determined as follows:
The total protein content of C. baccifera fruits was Percentage of N.F.E = 100 – (% Moisture + % Ash + % Crude fibre calculated from the nitrogen content in the fruit following + % Fat + % Protein) Kjeldahl method with minor modifications.1 g of fruit sample Percentage of Total Carbohydrate = % Nitrogen Free Extract was weighed into Kjeldahl flask and 1 g of CuSO4, 10 g of (N.F.E) + % Crude fibre. Na2SO4 and 25 ml of H2SO4 were added to it. The sample was heated for digestion on a heating mantle until the appearance 2.9. Determination of metals and minerals in fruits of green or blue colour. Thereafter it was cooled and the Sample digestion contents were transferred to a round bottomed distillation flask. On the receiver end, a beaker containing 25 ml of 0.1N Sample preparation for metal estimation was done H2SO4 with 2 drops of methyl red indicator was placed. The according to the guidelines of US-EPA 3050b. 0.3 g of C. baccifera acid in the beaker was neutralized by adding 40% NaOH. fruits was weighed in a 250 ml Erlenmeyer flask and 5 ml of 1:1 Distillation process was continued till about 50 ml of distillate HNO3 was added to it. The solution was heated on a hot plate to was collected. The distillate was titrated with 0.1N NaOH till 95ºC, refluxed for 15 minutes without boiling. After cooling, 2.5 the appearance of a persistent yellow colour. The titre volume ml of concentrated HNO3 was added; the sample was then in ml was recorded. 25 ml of 0.1N H2SO4 was used as a blank refluxed for 30 minutes at 95ºC without boiling and this step was (Ranganna, 1986). The protein content in the fruit sample was repeated. Thereafter, the sample was evaporated to 5 ml without calculated using the following formula: boiling. After cooling, 2 ml of double distilled water was added to the sample. This was followed by slow addition of 3 ml of 30% Percentage of Protein H2O2. The solution was then heated until the effervescence ( ) . = 푋 1000 subsided. About 6 ml of 30% H2O2 in 1 ml aliquots was added and then solution was refluxed. After allowing it to cool, 2.5 ml of 2.7. Crude fibre concentrated HCl was added and the sample was refluxed for 15 minutes without boiling. After cooling to room temperature, the 2.5 g of fruit sample, taken in a dried round bottom flask sample was filtered using Whattman No.1 filter paper and then was weighed. 200 ml of 2.5% w/v H2SO4 was added to it and diluted to 50 ml with double distilled water. All samples were the mixture was boiled for 30 minutes with a condenser analyzed in triplicates by ICP-OES; Inductively Coupled Plasma– attached. The residue was cooled, filtered through linen cloth Optical Emission Spectrometer (AOAC, 2005). The measurements and washed with water and transferred into the same round were performed using the Perkin Elmer Optima ICP-OES bottomed flask. To the residue 2.5% w/w NaOH was added and instrument, ICP version; 4.0 software for simultaneous boiled for 30 minutes with condenser attached. The residue measurement of all analyte wavelengths of interest. was allowed to cool, filtered, given a water wash and transferred to a pre-weighed silica crucible. The residue was then dried at 110°C for 12 hours to obtain a constant mass and ICP–OES parameters Wavelengths the weight was noted. The crucible with dried residue was placed in a muffle furnace set at 550°C temperature for 3 Calcium (Ca) 315.887 nm hours, till constant mass was achieved and the weight was Copper (Cu) 324.752 nm recorded. The crude fibre present in the fruits was calculated as follows: Iron (Fe) 259.939 nm