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. 2024 Oct 19;22(10):479. doi: 10.3390/md22100479

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© 2024 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 (https://creativecommons.org/licenses/by/4.0/).

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Purification of Protamex hydrolysate (STP). (A) ABTS radical scavenging activities of hydrolysate both inside (STPI, ≥3500 Da) and outside (STPO, <3500 Da) the 3500 Da dialysis membrane. (B) The FPLC pattern on the GPC column of the STPO active fraction and the ABTS radical scavenging activities of the fractions. (C) The reversed-phase HPLC pattern of the STPO-B active fraction and the ABTS radical scavenging activities of the fractions. (D) The HPLC pattern with a GPC column of the STPO-B-II active fraction. Each value is the mean ± SD (n ≥ 3). Different superscripts (a–l) in the same column are significantly different at p < 0.05, using Duncan’s multiple range test.

Purification of Protamex hydrolysate (STP). (A) ABTS radical scavenging activities of hydrolysate both inside (STPI, ≥3500 Da) and outside (STPO, <3500 Da) the 3500 Da dialysis membrane. (B) The FPLC pattern on the GPC column of the STPO active fraction and the ABTS radical scavenging activities of the fractions. (C) The reversed-phase HPLC pattern of the STPO-B active fraction and the ABTS radical scavenging activities of the fractions. (D) The HPLC pattern with a GPC column of the STPO-B-II active fraction. Each value is the mean ± SD (n ≥ 3). Different superscripts (a–l) in the same column are significantly different at p < 0.05, using Duncan’s multiple range test.