Fillet

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  • 文章类型: Journal Article
    使用Protamex和Alcalase制备Bighe鱼(Aristichthysnobilis)的骨水解产物,水解度(DH)为5%,10%和15%。在体外评估了骨水解物的抗氧化活性,然后将具有更好抗氧化活性的水解物用于通过真空浸渍工艺以1%和2%的浓度浸入big鱼片。在六种水解产物中,用Protamex水解的鱼骨在DH10%时表现出最高的清除1,1-二苯基-2-吡啶酰肼(DPPH)的能力(88.79%),2,2'-偶氮-双-3-乙基苯并噻唑啉-6-磺酸(ABTS)(57.76%)和羟基(62.72%),以及螯合亚铁离子(91.46%)。水解产物有效地延缓了冻结和解冻诱导的蛋白质/脂质氧化。与未经处理的鱼片相比,浸渍的鱼片具有较高的巯基含量,更高的Ca2+-ATPase活性,低级羰基和低级硫代巴比妥酸反应性物质(TBARS)。骨水解产物对冻融鱼片的质地和保水能力也有积极影响。Protamex的鱼骨水解产物可以作为潜在的抗氧化剂来保存鱼片。
    Bone hydrolysates from bighead carp (Aristichthys nobilis) were prepared using Protamex and Alcalase with degrees of hydrolysis (DH) of 5%, 10% and 15%. The antioxidant activity of bone hydrolysates was evaluated in vitro and then the hydrolysates with better antioxidant activity were used to immerse bighead carp fillets through a vacuum impregnation process at concentrations of 1% and 2%. Among the six hydrolysates, fish bone hydrolyzed with Protamex at DH 10% exhibited the highest ability to scavenge 1, 1-diphenyl-2-picrylhydrazyl (DPPH) (88.79%), 2, 2\'-azino-bis-3-ethylbenzthiazoline-6-sulphonic acid (ABTS) (57.76%) and hydroxyl radicals (62.72%), as well as to chelate ferrous ions (91.46%). The hydrolysates effectively postponed freezing- and thawing-induced protein/lipid oxidation. Compared with the fillets without treatment, the impregnated fillets had higher sulfhydryl contents, greater Ca2+-ATPase activity, lower carbonyls and lower thiobarbituric acid-reactive substances (TBARS). Bone hydrolysates also have a positive effect on the texture and water-holding ability of freeze-thawed fish fillets. Fish bone hydrolysates of Protamex could serve as potential antioxidants to preserve fish fillets.
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  • 文章类型: Journal Article
    The present study studied the effects of fish gelatin (FG) incorporated with grape seed extract (GSE) through vacuum impregnation (VI) on refrigerated tilapia (Oreochromis niloticus) fillets over 12 days. The VI of FG-GSE significantly improved the quality of the fish by decreasing drip loss, texture changes, and microbial survival. It also delayed protein oxidation by inhibiting the formation of disulphide bonds and carbonyl groups, and maintaining a higher sulfhydryl content and Ca2+-ATPase activity. Regarding myofibril degradation, FG-GSE maintained their secondary structure by increasing the ratio of α-helices and β-sheets (70.88-75.51%). Atomic force microscopy further revealed that the FG-GSE coating preserved the myofibril nanostructure by maintaining their length, width, and height. Overall, the synergistic effects of VI with 3% FG and 0.9% GSE suggested a promising approach for fillet preservation.
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