Extraction of Crude Bone Collagen from Yellowfin Tuna (Thunnus albacares) and Determination of Anti-oxidative Activity of Its Hydrolysates

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dc.contributor.authorWijekoon, W.M.M.P.
dc.contributor.authorAruppala, A.L.Y.H.
dc.contributor.authorKariyawasam, M.G.T.R.
dc.contributor.authorAbeyrathne, E.D.N.S.
dc.date.accessioned2019-07-09T05:29:00Z
dc.date.available2019-07-09T05:29:00Z
dc.date.issued2018
dc.description.abstractFish bones are significant part of fish processing by-product and rich source of collagen proteins. Utilization of yellowfin tuna bones are important economically as well as environmentally. Objective of this research was to extract crude collagen from yellowfin tuna bones and to identify the anti-oxidative activities of its hydrolysates which can be a potential natural anti-oxidative agent in food industry. Acid-pepsin soluble collagens were extracted from fresh yellowfin tuna bones. As with the pre-treatment process EDTA and citric acid were tested to decalcify. Extracted collagens from two treatments were subjected to the hydrolysis using protease enzyme with different time combinations (0, 3, 6, 9, 12, 24 h) at 37 °C followed with heat inactivation at 100 °C for 15 minutes. Antioxidant activity of the best hydrolysates were evaluated using thiobarbituric acid reactive substances (TBARS) assay and 2,2-dipheny1-1-picrylhydrazyl (DPPH) free radical scavenging activity method. All treatments were replicated (n = 3). Resulting extracts with citric acid treatment (1.23±0.05%) showed higher yield compared to the EDTA treatment (0.62±0.18%) (p < 0.05). Both treatments showed similar band patterns with 08% SDS-PAGE gel electrophoresis confirming the extracted collagen are same. Hydrolysates produced after incubating for 3 hours at 37 °C followed with heat inactivation was selected as the best (p < 0.05). The results showed that collagen hydrolysate of yellowfin tuna bones inhibited lipid oxidation in oil emulsion system and also control free radicals (DPPH). TBARS results of EDTA and citric acid treatment showed no significance difference with the control(p > 0.05). EDTA (86.14±1.88%) and citric acid (87.92±7.72%) treatments showed DPPH free radical scavenging activity compared with ascorbic acid (89.10±0.64%). These results suggest that hydrolysates produced from yellowfin tuna bones with citric acid can be used as a potential natural antioxidant agent in food industry.en_US
dc.identifier.isbn9789550481194
dc.identifier.urihttp://erepo.lib.uwu.ac.lk/bitstream/handle/123456789/1412/86-2018-Extraction%20of%20Crude%20Bone%20Collagen%20from%20Yellowfin%20Tuna%20%28Thunnus%20.pdf?sequence=1&isAllowed=y
dc.language.isoenen_US
dc.publisherUva Wellassa University of Sri Lankaen_US
dc.subjectBiotechnologyen_US
dc.subjectBioprocess Technologyen_US
dc.subjectBio Chemicals Engineeringen_US
dc.titleExtraction of Crude Bone Collagen from Yellowfin Tuna (Thunnus albacares) and Determination of Anti-oxidative Activity of Its Hydrolysatesen_US
dc.title.alternativeInternational Research Conference 2018en_US
dc.typeOtheren_US
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International Research Symposium of UWU-2018