Response Factorial Design Analysis on Papain-Generated Hydrolysates from Actinopyga lecanora for Determination of Antioxidant and Antityrosinase Activities

被引:25
|
作者
Bahari, Aqilah Noor [1 ,2 ]
Saari, Nazamid [3 ]
Salim, Norazlinaliza [1 ,2 ,4 ]
Ashari, Siti Efliza [2 ,4 ]
机构
[1] Univ Putra Malaysia, Halal Prod Res Inst, Putra Infoport, Upm 43400, Selangor, Malaysia
[2] Univ Putra Malaysia, Fac Sci, Integrated Chem BioPhys Res, Upm 43400, Selangor, Malaysia
[3] Univ Putra Malaysia, Fac Food Sci & Technol, Dept Food Sci, Serdang 43400, Selangor, Malaysia
[4] Univ Putra Malaysia, Ctr Fdn Studies Agr Sci, Upm 43400, Selangor, Malaysia
来源
MOLECULES | 2020年 / 25卷 / 11期
关键词
factorial design optimization; hydrolysates; antioxidant; antityrosinase; Actinopyga lecanora; FUNCTIONAL-PROPERTIES; PROTEIN HYDROLYSATE; BIOACTIVE PEPTIDES; OPTIMIZATION; MODEL; SKIN; DYE;
D O I
10.3390/molecules25112663
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Actinopyga lecanora (A. lecanora) is classified among the edible species of sea cucumber, known to be rich in protein. Its hydrolysates were reported to contain relatively high antioxidant activity. Antioxidants are one of the essential properties in cosmeceutical products especially to alleviate skin aging. In the present study, pH, reaction temperature, reaction time and enzyme/substrate ratio (E/S) have been identified as the parameters in the papain enzymatic hydrolysis of A. lecanora. The degree of hydrolysis (DH) with antioxidant activities of 2,2-diphenyl-1-picrylhydrazyl (DPPH) and ferric-reducing antioxidant power (FRAP) assays were used as the responses in the optimization. Analysis of variance (ANOVA), normal plot of residuals and 3D contour plots were evaluated to study the effects and interactions between parameters. The best conditions selected from the optimization were at pH 5.00, 70 degrees C of reaction temperature, 9 h of hydrolysis time and 1.00% enzyme/substrate (E/S) ratio, with the hydrolysates having 51.90% of DH, 42.70% of DPPH activity and 109.90 Fe2+mu g/mL of FRAP activity. The A. lecanora hydrolysates (ALH) showed a high amount of hydrophobic amino acids (286.40 mg/g sample) that might be responsible for antioxidant and antityrosinase activities. Scanning electron microscopy (SEM) image of ALH shows smooth structures with pores. Antityrosinase activity of ALH exhibited inhibition of 31.50% for L-tyrosine substrate and 25.40% for L-DOPA substrate. This condition suggests that the optimized ALH acquired has the potential to be used as a bioactive ingredient for cosmeceutical applications.
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页数:20
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