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

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          Abstract

          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 °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 Fe 2+μg/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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          Improved Method for Determining Food Protein Degree of Hydrolysis

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            A comprehensive review on tyrosinase inhibitors

            Abstract Tyrosinase is a multi-copper enzyme which is widely distributed in different organisms and plays an important role in the melanogenesis and enzymatic browning. Therefore, its inhibitors can be attractive in cosmetics and medicinal industries as depigmentation agents and also in food and agriculture industries as antibrowning compounds. For this purpose, many natural, semi-synthetic and synthetic inhibitors have been developed by different screening methods to date. This review has focused on the tyrosinase inhibitors discovered from all sources and biochemically characterised in the last four decades.
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              Antioxidant peptides from marine by-products: Isolation, identification and application in food systems. A review

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                Author and article information

                Journal
                Molecules
                Molecules
                molecules
                Molecules
                MDPI
                1420-3049
                08 June 2020
                June 2020
                : 25
                : 11
                : 2663
                Affiliations
                [1 ]Halal Products Research Institute, Putra Infoport, Universiti Putra Malaysia, Serdang 43400 UPM, Selangor, Malaysia; aqilahnoorbahari@ 123456gmail.com
                [2 ]Integrated Chemical BioPhysics Research, Faculty of Science, Universiti Putra Malaysia, Serdang 43400 UPM, Selangor, Malaysia; ctefliza@ 123456upm.edu.my
                [3 ]Department of Food Science, Faculty of Food Science and Technology, Universiti Putra Malaysia, Serdang 43400, Selangor, Malaysia
                [4 ]Centre of Foundation Studies for Agricultural Science, Universiti Putra Malaysia, Serdang 43400 UPM, Selangor, Malaysia
                Author notes
                Author information
                https://orcid.org/0000-0002-8879-2780
                https://orcid.org/0000-0002-4185-9415
                https://orcid.org/0000-0001-5295-8390
                Article
                molecules-25-02663
                10.3390/molecules25112663
                7321370
                32521731
                c826601c-0115-422d-a54e-65df5ba3849f
                © 2020 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 12 March 2020
                : 14 April 2020
                Categories
                Article

                factorial design optimization,hydrolysates,antioxidant,antityrosinase,actinopyga lecanora

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