Iranian Research Organization for Science and Technology (IROST) Microbiology, Metabolites and Biotechnology 2980-8855 2 2 2019 11 01 Antioxidant activity of alcalase hydrolysates of Spirulina proteins 109 118 998 10.22104/armmt.2020.4280.1041 EN Mina Mehdi Shishavan Department of Biotechnology, Iranian Research Organization for Science & Technology (IROST), Tehran, Iran. Saeed Mirdamadi Department of Biotechnology, Iranian Research Organization for Science & Technology (IROST), Tehran, Iran. 0000-0002-8356-771X Hamideh Ofoghi Department of Biotechnology, Iranian Research Organization for Science & Technology (IROST), Tehran, Iran. 0000-0003-2163-2448 Journal Article 2020 07 11 <span style="font-size: 10.0pt; line-height: 107%; font-family: 'Times New Roman',serif; mso-fareast-font-family: Calibri; color: #1c1e29; mso-ansi-language: EN-US; mso-fareast-language: EN-US; mso-bidi-language: AR-SA;">Spirulina <span style="font-size: 10.0pt; line-height: 107%; font-family: 'Times New Roman',serif; mso-fareast-font-family: Calibri; color: #1c1e29; mso-ansi-language: EN-US; mso-fareast-language: EN-US; mso-bidi-language: AR-SA;">microalgae are gaining increasing consideration for its pharmaceutical and nutritional (60–70% protein) virtues. Protein can be further processed to produce peptides that have functional and nutritional properties such as antihypertensive, immunomodulatory, antioxidant, hypocholesterolemic, and metal chelating activity.The purpose of this study is to investigate the relevance between antioxidant properties and the degree of hydrolysis (DH)of hydrolysates resulting from the effect of the alcalase enzyme on Spirulina protein at different times and the effect of time on the DH. For this purpose, Spirulina cells were disrupted with ultrasonication, bead milling, and water suspension methods. The resulting cell extract was hydrolyzed with serine proteases like the Alcalase enzyme. The sampling was taken every hour for up to 6 hours. DH of the samples was measured by the ortho-phthalaldehyde (OPA) method. Antioxidant activities of the hydrolysates were evaluated by assessing 2,2-diphenyl-1-picrylhydrazy (DPPH) and 2, 2′-azinobis (3-ethyl- benzothiazoline-6-sulphonate) (ABTS) radical scavenging activity. The ultrasonication method was selected for cell wall disruption. Results demonstrate that the highest increase in DH occurred in the first hour of hydrolysis. Then DH increased gradually with a low slope. The highest DH with an enzyme/substrate ratio of 1% (v/v) was 33.45% after 6 hours. Maximum DPPH radical scavenging activity occurred precisely at 120 minutes (22.71 ± 1.18 µM TE/mg protein, DH=28.29 ± 0.58). The scavenging activity of the DPPH radical increased by more than 2-fold after 2 hours of hydrolysis. The antioxidant activity of ABTS radicalscavenging increased and reached 862.09 ± 22.26 µM TE/mg protein after 5 hours of hydrolysis (DH%=32.83 ± 0.87). This research indicates that along with the increase of DH, the ABTS radical scavenging activity also increases. Therefore, hydrolysis produces peptides that can scavenge DPPH and ABTS radicals at certain times. These results can be used to determine both DH and the time it occurs; therefore, the probability creation and isolation of bioactive peptides increase with high antioxidant activities. So, the hydrolysates or peptides derivative from Spirulina can be used as a functional food to improve and even prevent various diseases and disorders.

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