2014
DOI: 10.1016/j.jprot.2014.08.003
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Egg-yolk protein by-product as a source of ACE-inhibitory peptides obtained with using unconventional proteinase from Asian pumpkin (Cucurbita ficifolia)

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Cited by 50 publications
(34 citation statements)
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“…The peptides obtained by hydrolysis with unconventional aspartyl proteinase from Y. lipolytica JII1c were characterized by much lower free radical scavenging activity (about 4.5-5.5 times lower than activity of other hydrolysates) and ACE-inhibitory activity. Similarly to our results, hydrolysis of the egg-yolk protein by-product with using various proteases including neutrase, porcine pepsin and protease from C. ficifolia, led to the production of peptides with varied antioxidant and antihypertensive activity (Zambrowicz et al 2015a, b;Eckert et al 2014;Pokora et al 2013). In addition, simultaneous ability of enzymatic hydrolysates to scavenge of DPPH radicals and to inhibit of ACE have been demonstrated in other study (Davalos et al 2004;Lu et al 2010;Zambrowicz et al 2015b).…”
Section: Preparation Of Peptides With Biological Activity From the Egsupporting
confidence: 84%
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“…The peptides obtained by hydrolysis with unconventional aspartyl proteinase from Y. lipolytica JII1c were characterized by much lower free radical scavenging activity (about 4.5-5.5 times lower than activity of other hydrolysates) and ACE-inhibitory activity. Similarly to our results, hydrolysis of the egg-yolk protein by-product with using various proteases including neutrase, porcine pepsin and protease from C. ficifolia, led to the production of peptides with varied antioxidant and antihypertensive activity (Zambrowicz et al 2015a, b;Eckert et al 2014;Pokora et al 2013). In addition, simultaneous ability of enzymatic hydrolysates to scavenge of DPPH radicals and to inhibit of ACE have been demonstrated in other study (Davalos et al 2004;Lu et al 2010;Zambrowicz et al 2015b).…”
Section: Preparation Of Peptides With Biological Activity From the Egsupporting
confidence: 84%
“…Furthermore, we have proven that peptides: LAPSLPGKPKPD and VTGRFAGHPAAQ possessed antidiabetic activity, as demonstrated by significant inhibition of α-glucosidase activity in vitro (Zambrowicz et al 2015a, b). We confirmed the multidirectional biological activity of synthetic analogs of YP-derived peptides (Zambrowicz et al 2015a, b;Eckert et al 2014).…”
Section: Introductionsupporting
confidence: 81%
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“…21 Finally, it is very important to determine the cytotoxic activity of potential nutraceuticals or/and pharmacological substances to establish their safety and proper impact on the body. 21 Finally, it is very important to determine the cytotoxic activity of potential nutraceuticals or/and pharmacological substances to establish their safety and proper impact on the body.…”
Section: Resultsmentioning
confidence: 99%