2023
DOI: 10.1016/j.psj.2023.102680
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The elastase and melanogenesis inhibitory and anti-inflammatory activities of phosvitin phosphopeptides produced using high-temperature and mild-pressure (HTMP) pretreatment and enzyme hydrolysis combinations

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Cited by 8 publications
(3 citation statements)
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“…Yap et al (2020) reported that the monophenolase and diphenolase activity inhibition values of EWPPs were 45.9% and 48.1%, respectively, at the optimized conditions (55% trypsin, 45% chymotrypsin, S/E 10:1 w/w, 2 h; 100% trypsin, S/E 22.13:1 w/w and 3.18 h), and EWPPs were able to bind to H85, H94, H259, H263, and H296 (hotspots for active residues) as well as F92, M280, and F292 (stabilizing residues) of tyrosinase based on the structure-activity relationship analysis [128]. PPPs prepared with HTMP-T-S (HTMP pretreatment-trypsin-sterilization hydrolysis) showed the most potent inhibition of tyrosinase and elastase, with the inhibition rates of 88.09% and 70.67% in sequence, respectively, which reduced the melanin content in B16F10 melanoma cells [82].…”
Section: Enzyme Inhibitorsmentioning
confidence: 99%
“…Yap et al (2020) reported that the monophenolase and diphenolase activity inhibition values of EWPPs were 45.9% and 48.1%, respectively, at the optimized conditions (55% trypsin, 45% chymotrypsin, S/E 10:1 w/w, 2 h; 100% trypsin, S/E 22.13:1 w/w and 3.18 h), and EWPPs were able to bind to H85, H94, H259, H263, and H296 (hotspots for active residues) as well as F92, M280, and F292 (stabilizing residues) of tyrosinase based on the structure-activity relationship analysis [128]. PPPs prepared with HTMP-T-S (HTMP pretreatment-trypsin-sterilization hydrolysis) showed the most potent inhibition of tyrosinase and elastase, with the inhibition rates of 88.09% and 70.67% in sequence, respectively, which reduced the melanin content in B16F10 melanoma cells [82].…”
Section: Enzyme Inhibitorsmentioning
confidence: 99%
“…Similarly, some peptides harbor the ability to forestall damages orchestrated by reactive nitrogen species (RNS), encompassing peroxynitrite and nitric oxide, the latter recognized as the most potent oxidant [ 117 ]. It is imperative to note that ROS/RNS have garnered infamy as culprits behind a gamut of chronic ailments, spanning diabetes, renal impairment, Parkinson’s disease, cardiovascular events, and an array of inflammatory disorders, skin aging, cancers, cardiovascular maladies, osteoporosis, and gastrointestinal afflictions [ 118 , 119 ]. The vista that unfolds before us beckons toward the horizon of bioactive peptides as therapeutic forerunners.…”
Section: The Implications Of Research On Bioactive Peptides and Gut M...mentioning
confidence: 99%
“…In a model of H 2 O 2 -induced Caco-2 cells, PPPs could upregulate the expression of antioxidant genes and promote the secretion of antioxidant enzymes, reducing oxidative stress and protecting cells from oxidative damage [114−115] . Lee et al [116] found that PPP obtained by enzymatic hydrolysis (trypsin) after high temperature and light pressure pretreatment had the efficacy of reducing elastase and tyrosinase activities in B16F10 melanoma cells. In addition, melanin levels in melanoma cells decreased from 31.18% to 38.58% after the intervention of PPP.…”
Section: Enhancement Of Bone Density and Antioxidant Effect Of Pvmentioning
confidence: 99%