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Synthesis and Structure Determination of µ-Conotoxin PIIIA Isomers with Different Disulfide Connectivities
Published on: October 2, 2018
ACE-inhibitory and antioxidant peptides from coconut cake albumin hydrolysates: purification, identification and
Yajun Zheng1,2, Yan Li1,2, Guifeng Li1
1College of Food Science, Shanxi Normal University Linfen 041004 China zyj_coconut@163.com +86-0357-2051482 +86-13976563642.
Abstract:
Coconut cake albumin was hydrolysed by sequential digestion with alcalase, flavourzyme, pepsin and trypsin to purify bioactive peptides with ACE-inhibitory and antioxidant activities. Following fractionation with sequential ultrafiltration, Sephadex gel chromatography and RP-HPLC, three novel peptides KAQYPYV, KIIIYN and KILIYG were identified. KAQYPYV, KIIIYN and KILIYG provided an IC50 value of 37.06 μM, 58.72 μM and 53.31 μM on ACE-inhibitory activity, respectively. For hydroxyl radical scavenging activity, KAQYPYV, KIIIYN and KILIYG demonstrated an IC50 value of 70.84 μM, 77.62 μM and 95.23 μM, respectively. All the three peptides exhibited a mixed modality of noncompetitive and uncompetitive inhibition on ACE and KAQYPYV showed good stability against gastrointestinal enzymes digestion. Moreover, these peptides could effectively lower intracellular endothelin-1 content without significant cytotoxicity, and protected vascular endothelial cells from reactive oxygen species mediated damage. Furthermore, KAQYPYV, KIIIYN and KILIYG also demonstrated high ion chelating ability (62.13% ± 4.21%, 64.66% ± 5.51% and 69.82% ± 7.24% at 0.1 mg mL-1, respectively) and considerable superoxide radical scavenging activity (39.30% ± 2.72%, 46.79% ± 1.70% and 51.16% ± 3.23% at 1.0 mg mL-1, respectively). These results indicate that coconut cake albumin is a potential source of bioactive peptides possessing ACE-inhibitory and antioxidant activities.

