Bioactive films based on cuttlefish (Sepia officinalis) skin gelatin incorporated with cuttlefish protein hydrolysates: Physicochemical characterization and antioxidant properties

被引:54
作者
Kchaou, Hela [1 ]
Jridi, Mourad [1 ,2 ]
Benbettaieb, Nasreddine [3 ,4 ]
Debeaufort, Frederic [3 ,4 ]
Nasri, Moncef [1 ]
机构
[1] Univ Sfax, Natl Sch Engn Sfax, Lab Enzyme Engn & Microbiol, POB 1173, Sfax 3038, Tunisia
[2] Univ Jendouba, Higher Inst Biotechnol Beja, Ave Habib Bourguiba Beja 9000,BP 382, Beja, Tunisia
[3] Univ Bourgogne Franche Comte AgroSup Dijon, UMR PAM A 02 102, 1 Esplanade Erasme, F-21000 Dijon, France
[4] IUT Dijon Auxerre, Bioengn Dept, 7 Blvd Docteur Petitjean, F-20178 Dijon, France
关键词
Cuttlefish skin proteins and hydrolysates; Edible films; Functional properties; Antioxidant activity; FISH GELATIN; FUNCTIONAL-PROPERTIES; EDIBLE FILMS; BLEND FILMS; ISOLATE; ACE; ELABORATION; PLASTICIZER; EXTRACTS; OIL;
D O I
10.1016/j.fpsl.2020.100477
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
The objective of this study was to apply cuttlefish (Sepia officinalis) skin protein isolate (CSPI) and hydrolysates (CSPH), using commercial Savinase (R) and Purafect (R) enzymes, as bioactive additives in the elaboration of gelatin-based films. CSPH and CSPI enriched films were colored and exhibited a higher UV-barrier properties compared to gelatin film. In addition, compared to CSPI added film, an increase of the glass transition temperature by 20 % and 4 %, respectively, for Purafect and Savinase hydrolysates enriched films was noted. However, elongation at break decreased significantly for CSPH incorporated films by 2.5-fold. The tensile strength was reduced by 28.2 % and 44.4 % for Purafect and Savinase hydrolysates added films, respectively. Furthermore, a decrease of water contact angle by 45 % and 51 % for films added with Purafect and Savinase hydrolysates, respectively, was displayed compared to gelatin film. Interestingly, CSPH enriched films also displayed higher antioxidant potential than control gelatin films evaluated by several in vitro assays.
引用
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页数:11
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