Optimization of enzymatic hydrolysis for the production of antioxidative peptide from Nannochloropsis gaditana using response surface methodology

In the present research, microalgae protein hydrolysate of Nannochloropsis gaditana (MPH) was extracted via enzymatic hydrolysis using alcalase enzyme. Hydrolysis conditions like (pH, temperature, enzyme concentration and substrate concentration) were optimized by Response Surface Methodology (RSM)...

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Main Authors: Md Saleh, Nur Izzati, Wan Ab. Karim Ghani, Wan Azlina, Harun, Mohd Razif, Mustapa Kamal, Siti Mazlina
Format: Article
Language:English
Published: Universiti Putra Malaysia Press 2019
Online Access:http://psasir.upm.edu.my/id/eprint/69692/
http://psasir.upm.edu.my/id/eprint/69692/1/04%20JST-S0500-2019.pdf
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author Md Saleh, Nur Izzati
Wan Ab. Karim Ghani, Wan Azlina
Harun, Mohd Razif
Mustapa Kamal, Siti Mazlina
author_facet Md Saleh, Nur Izzati
Wan Ab. Karim Ghani, Wan Azlina
Harun, Mohd Razif
Mustapa Kamal, Siti Mazlina
author_sort Md Saleh, Nur Izzati
building UPM Institutional Repository
collection Online Access
description In the present research, microalgae protein hydrolysate of Nannochloropsis gaditana (MPH) was extracted via enzymatic hydrolysis using alcalase enzyme. Hydrolysis conditions like (pH, temperature, enzyme concentration and substrate concentration) were optimized by Response Surface Methodology (RSM) using Central Composite Design (CCD). Four range of independent variables namely; pH (7-9), temperature (45-55°C), substrate concentration (2-6 g/L) and enzyme concentration (0.2-0.4 g/L) were used to study the influence of these parameters on the degree of hydrolysis. The CCD consisted of twenty-four experimental points and six replicates of central points with the optimum conditions obtained from this experiment were at pH 8.14, a temperature 51.4°C, a substrate concentration 5.48 g/L and an enzyme concentration 0.26 g/L with maximum degree hydrolysis of 55.76%. All experiments were fixed at 24 hours reaction time. The degree of hydrolysis of MPH was analysed using O-phthaldehyde (OPA) method to quantify the cleavage of peptide bond. The optimized sample was evaluated for its antioxidant activity using 1,1-Diphenyl-2-picrylhydrazyl (DPPH) assay with 52.19% and 2, 2'- azino-bis (ethylbenzthiazoline-6-sulfonic acid (ABTS) assay with 14.13%. The bioactive peptides contained in Nannochloropsis gaditana have the ability to scavenge free radicals and act as good antioxidants.
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spelling upm-696922019-07-08T03:58:18Z http://psasir.upm.edu.my/id/eprint/69692/ Optimization of enzymatic hydrolysis for the production of antioxidative peptide from Nannochloropsis gaditana using response surface methodology Md Saleh, Nur Izzati Wan Ab. Karim Ghani, Wan Azlina Harun, Mohd Razif Mustapa Kamal, Siti Mazlina In the present research, microalgae protein hydrolysate of Nannochloropsis gaditana (MPH) was extracted via enzymatic hydrolysis using alcalase enzyme. Hydrolysis conditions like (pH, temperature, enzyme concentration and substrate concentration) were optimized by Response Surface Methodology (RSM) using Central Composite Design (CCD). Four range of independent variables namely; pH (7-9), temperature (45-55°C), substrate concentration (2-6 g/L) and enzyme concentration (0.2-0.4 g/L) were used to study the influence of these parameters on the degree of hydrolysis. The CCD consisted of twenty-four experimental points and six replicates of central points with the optimum conditions obtained from this experiment were at pH 8.14, a temperature 51.4°C, a substrate concentration 5.48 g/L and an enzyme concentration 0.26 g/L with maximum degree hydrolysis of 55.76%. All experiments were fixed at 24 hours reaction time. The degree of hydrolysis of MPH was analysed using O-phthaldehyde (OPA) method to quantify the cleavage of peptide bond. The optimized sample was evaluated for its antioxidant activity using 1,1-Diphenyl-2-picrylhydrazyl (DPPH) assay with 52.19% and 2, 2'- azino-bis (ethylbenzthiazoline-6-sulfonic acid (ABTS) assay with 14.13%. The bioactive peptides contained in Nannochloropsis gaditana have the ability to scavenge free radicals and act as good antioxidants. Universiti Putra Malaysia Press 2019 Article PeerReviewed text en http://psasir.upm.edu.my/id/eprint/69692/1/04%20JST-S0500-2019.pdf Md Saleh, Nur Izzati and Wan Ab. Karim Ghani, Wan Azlina and Harun, Mohd Razif and Mustapa Kamal, Siti Mazlina (2019) Optimization of enzymatic hydrolysis for the production of antioxidative peptide from Nannochloropsis gaditana using response surface methodology. Pertanika Journal of Science & Technology, 27 (S1). pp. 41-55. ISSN 0128-7680; ESSN: 2231-8526 http://www.pertanika.upm.edu.my/Pertanika%20PAPERS/JST%20Vol.%2027%20(S1).%202019/04%20JST-S0500-2019.pdf
spellingShingle Md Saleh, Nur Izzati
Wan Ab. Karim Ghani, Wan Azlina
Harun, Mohd Razif
Mustapa Kamal, Siti Mazlina
Optimization of enzymatic hydrolysis for the production of antioxidative peptide from Nannochloropsis gaditana using response surface methodology
title Optimization of enzymatic hydrolysis for the production of antioxidative peptide from Nannochloropsis gaditana using response surface methodology
title_full Optimization of enzymatic hydrolysis for the production of antioxidative peptide from Nannochloropsis gaditana using response surface methodology
title_fullStr Optimization of enzymatic hydrolysis for the production of antioxidative peptide from Nannochloropsis gaditana using response surface methodology
title_full_unstemmed Optimization of enzymatic hydrolysis for the production of antioxidative peptide from Nannochloropsis gaditana using response surface methodology
title_short Optimization of enzymatic hydrolysis for the production of antioxidative peptide from Nannochloropsis gaditana using response surface methodology
title_sort optimization of enzymatic hydrolysis for the production of antioxidative peptide from nannochloropsis gaditana using response surface methodology
url http://psasir.upm.edu.my/id/eprint/69692/
http://psasir.upm.edu.my/id/eprint/69692/
http://psasir.upm.edu.my/id/eprint/69692/1/04%20JST-S0500-2019.pdf