Development of Garcinia Atroviridis (Asam Gelugur) During Fruit Growth
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Journal of Advanced Research in Materials Science 73, Issue 1 (2020) 12-20 Journal of Advanced Research in Materials Science Journal homepage: www.akademiabaru.com/arms.html ISSN: 2289-7992 Development of Garcinia Atroviridis (Asam Gelugur) during Open Access Fruit Growth O. Nur Allisha1,*, O. Zaulia1, M. A. I. Mohd Shukri2, M. N. Suriani1, G. Nur Syafini2, M. N. Azhar2, R. Khdijah2, A. R. Razali2, R. Mohd Azhar1, M. Nur Izzati2, A. Siti Nur Raihan2, M. Razali2, I. Salma1, A. Khadijah1, G. Mohd Nor Faizal3 1 Industrial Crop Research Centre, Persiaran MARDI-UPM Headquaters, 43000 Serdang, Selangor, Malaysia 2 Horticulture Research Center, Persiaran MARDI-UPM Headquaters, 43000 Serdang, Selangor, Malaysia 3 Biodiversity and Environment Research Center, Persiaran MARDI-UPM Headquaters, 43000 Serdang, Selangor, Malaysia ABSTRACT Asam gelugur (Garcinia atroviridis Griff ex. T. Anderson) in Malaysia normally used as dried fruit for ingredients in the food. Dried G. atroviridis also used for medicinal and health benefits food. Recently, G. atroviridis become more popular when RandD found that this fruit has high hydroxy acetic acid (HCA) (to reduce cholesterol and fat, slimming agent), high antioxidant content, anti- bacteria, anti-tumour, manage high blood pressure etc. This fruit was processed as health benefit foods and also as supplement and healthy drink. This traditional plant also proven can be planted on a commercial scale and give promising income to entrepreneurs. Therefore, a study on this plant also given priority. Study on different maturity stages is important to understand the development of fruit and to determine suitable harvesting stage as a guideline for harvesting and processing. Therefore, this study were carried out by tagging the fruit from flowering until the fruit set, matured and ripen stage. From the observation, fruit at age 85 days after flowering seem started matured and they were picked at every 5 days and analysed until day 125 when fruit were overripe and drop from tree. Fruit were analysed on physical (visual appearance, firmness, lightness, chroma, hue) and chemical (pH, total titratable acidity (TTA), ascorbic acid, soluble solid content (SSC) changes. Result showed that SSC of G. atroviridis were range from 6.13 – 7.73. SSC of G. atroviridis maintain during development and significantly increased after 120 days. Acidity (TTA) of G. atroviridis were very high (3.83 – 4.60 mg/100g). TTA significantly low at day 90 and 120 after fruit set, compare to other stages. Ascorbic acid content of G. atroviridis is considered low (0.77 – 1.35 mg/100g). pH of G. atroviridis is very low at 2.41 -2.60. This considered too low compared to other fruits. pH and ascorbic acid of G. atroviridis is fluctuated during the development of fruit from 85 to 125 day after flowering. Skin lightness increased significantly from day 85 to 100, maintain until day 110 and significantly decreased until day 125. Flesh lightness maintain during fruit development. Skin chroma maintain from day 85 to day 105, significantly increased after day 105 to 110, maintain until day 115 and significantly decreased thereafter. Flesh chroma remain un-change during fruit development from day 85 to day 120, but slightly increased from day 120 to until day 125. Skin hue maintain from day 85 to day 95, significantly decreased after day 100 to 110, significantly increased until day 115 and maintain thereafter. Flesh hue remain un-change during fruit development from day 85 to day 125. Firmness of G. atroviridis maintain during development, 19.35 – 23.25 N, but significantly higher at 125 days after flowering, 25.32 N. Keywords: Chemical, physical, visual, flowering, visual appearance Copyright © 2020 PENERBIT AKADEMIA BARU - All rights reserved Received: 15 August 2020 Revised: 3 October 2020 Accepted: 5 October 2020 Published: 31 October 2020 * Corresponding author. E-mail address: [email protected] https://doi.org/10.37934/arms.73.1.1220 12 Journal of Advanced Research in Materials Science Volume 73, Issue 1 (2020) 12-20 1. Introduction The dried rind of G. atroviridis has been used for centuries throughout this part of the world as a food preservative, flavouring agent and carminative [17]. Recently, demand for more studies for G. atroviridis has increase for health or food purposes. Postharvest physiology stage of "matured" in commodity when it reached an adequate stage of development that after harvesting and postharvest handling, its quality will be no least than a minimum acceptable quality to consumer" [4,16]. The studies on information of development of maturity gives the techniques to measure maturity and matured fruit at preferred eating quality for consumer. As a fruit ripens, acidity declines and usually are sweeter, but not for fruit like G. atroviridis. It gives certain volatile compounds its characteristic aroma [10,18]. Knowledge of maturity will help our ability to see ripening process, leading to improved procedures for the production and post-harvest handling of fruits [16]. G. atroviridis is categorize as seasonal fruit as flowering occur after raining season entering dry season in March-April and ended in July. G. atroviridis is a non-climacteric fruit as it ripen while attached to the tree. None climacteric fruits does not link to ethylene production during ripening however other hormone such as auxin and abscisic acid (ABA) thus the alteration of chlorophyll, anthocyanin and carotenoid. Hormones play important roles in both climacteric and non-climacteric fruits [2]. The cell wall modification and degradation enzymes during ripening seems to be responsible for excessive tissue softening of a number of fruits [3]. Pectins major components of primary cell wall and middle lamella, contributing to the firmness and quality of G. atroviridis. Ripen G. atroviridis does not alter it's flavour much to eatable palette due to high acidity taste although sweeter in Brix reading compared to unripen ones. G. atroviridis has inner core around its seed which turned into orange colour and the cell turgor lessor and cell wall structure has become softer. These changes in colour, flavour, firmness, and aroma make fruit ripening a complex process, which must be very tightly regulated. A study based on biochemical analysis were conducted to read the different stages of maturity during fruit development of G. atroviridis. Samples obtained from female tree in Taman Botani, Putrajaya were tagged since budding, blooming and becoming fruit. The evaluation comprises of biochemical analysis (SSC, pH, total titratable acidity and ascorbic acid content), physical analysis (visual appearance, firmness, fruit size, colour) and antioxidant properties. 2. Materials and Methods 2.1 Tagging Buds of Flowers Buds of flower were tagged when it started to appear. This stage buds were marked using plant tagging paper and carbon pencil. Date and name of individual buds flower is recorded in log book by week for width and length. Process end until the buds become a matured fruit (breaker stage when fruit start to yellowing) and ready to harvest. 2.2 Measurement of Fruit Development Measurement using venire calliper MITUYO were carried out from fruit set until ripen. Setting began from 0.00 for width of buds opening (red colour) and width of fruit. From the record, week and size of fruit were gathered for average and stages were identified. 13 Journal of Advanced Research in Materials Science Volume 73, Issue 1 (2020) 12-20 2.3 Postharvest Quality Assessment From the observation, fruit at age 85 days after flowering seem started to matured and they were picked at every 5 days and analysed until day 125, when fruit were over ripe and drop from tree. Fruits were harvested, transported to packinghouse, sorting, washing, drip dried and analysed. Quality observation and analysis were carried out on physiology (appearance, disease, freshness, colour, firmness), chemical (pH, SSC, TTA, ascorbic acid content) and physical (firmness, colour (L, hue, chroma). The quality of G. atroviridis fruits was judged visually and the characteristics of fruit such as colour, freshness and diseases were evaluated. The L, hue, chroma values were measured with a Chromameter (CR-300 Minolta, Japan). Soluble solids concentration (SSC) were determined with a digital refractometer (Atago, CO., LTD, Japan and Model DBX-55). The pH values were measured using a pH meter (Hanna Instruments pH 211 Inc. RI-USA, Microprocessor pH Meter). The total titratable acidity (TTA) was determined by titrating 20 ml of extraction with 0.1 mol l-1NaOH to pH 8.1. Ascorbic acid was determined by extraction of 10 gm of sample with added 100 ml 3% of metaphosphoric acid. Then, 5 ml of extraction was titrating immediately with standard dye solution to first permanent pink endpoint. Hue and chroma are measured by a* and b* coordinates a* and b* and correspond to basic tint of colour and the saturation or vividness of colour. The location of colour on a rectangular-coordinate grid perpendicular to the L* axis. The colour at the grid origin (a*=0, b*= 0) is achromatic (gray). On the horizontal axis, positive a* indicates a hue of red purple and negative a* of bluish-green. On vertical axis, positive b* indicates yellow and negative b* blue. Hue is tan-1 (b*/a*) [11].. Chroma formulae for calculation derived from a* and b* [9]; C* ab = (a*2 + b*2 ) ½ (1) The skin and flesh firmness of G. atroviridis was measured using texture meter TA.XTplus Stable Micro System with 2 mm probe attachment. Load cell of full scale ranges from 5 – 50 kg. A maximum load of 5 kg was used for penetration of the flesh and 20 kg load was used for penetration through the skin. The drive speed to determine the yield force used were 100 mm/min. The results of texture measurement were reported in using N and N*area. All data were analysed by analysis of variance (ANOVA) using SAS from Statistical Analysis.