2022
DOI: 10.1016/j.foodchem.2021.131849
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Identification of three novel antioxidative peptides from Auxenochlorella pyrenoidosa protein hydrolysates based on a peptidomics strategy

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Cited by 27 publications
(9 citation statements)
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“…As a hydrogen donor, the peptide pairs with the single electron of DPPH that exists in the form of free radicals in solution to complete the free radical scavenging [ 47 ]. The six identified peptides are rich in amino acid residues such as Pro, Tyr and Ala, which are reported to be effective hydrogen donors and play an important role in the antioxidant capacity of peptides [ 48 , 49 ]. Based on the simulation results, the identified peptides and DPPH molecules had strong hydrophobic interactions and hydrogen bonds, so the peptides had strong DPPH free radical scavenging activity.…”
Section: Resultsmentioning
confidence: 99%
“…As a hydrogen donor, the peptide pairs with the single electron of DPPH that exists in the form of free radicals in solution to complete the free radical scavenging [ 47 ]. The six identified peptides are rich in amino acid residues such as Pro, Tyr and Ala, which are reported to be effective hydrogen donors and play an important role in the antioxidant capacity of peptides [ 48 , 49 ]. Based on the simulation results, the identified peptides and DPPH molecules had strong hydrophobic interactions and hydrogen bonds, so the peptides had strong DPPH free radical scavenging activity.…”
Section: Resultsmentioning
confidence: 99%
“…The hydrolysate was prepared using a previously described method by Zhu et al with slight modifications . The 5 g of dry GBSC protein isolate was mixed with 500 mL of water (w/v), and the pH was adjusted to 7.50 using 1 M NaOH.…”
Section: Methodsmentioning
confidence: 99%
“…The sequence analysis of the sample was performed with reference to the previous method . In brief, the fraction P3 was dissolved in 0.1% aqueous trifluoroacetic acid and loaded onto an activated (50% acetonitrile) and equilibrated (0.1% aqueous trifluoroacetic acid) ZipTip C18 column, desalted with H 2 O (0.1% trifluoroacetic acid), eluted with 50% acetonitrile (0.1% trifluoroacetic acid), and then freeze-dried.…”
Section: Methodsmentioning
confidence: 99%
“…The sequence analysis of the sample was performed with reference to the previous method. 13 In brief, the fraction P3 was dissolved in 0.1% aqueous trifluoroacetic acid and loaded onto an activated (50% acetonitrile) and equilibrated (0.1% aqueous trifluoroacetic acid) ZipTip C18 column, desalted with H 2 O (0.1% trifluoroacetic acid), eluted with 50% acetonitrile (0.1% trifluoroacetic acid), and then freeze-dried. LC−MS/MS analysis was performed by using an Ultimate 3000 UPLC system (Thermo, Waltham, MA, USA) equipped with an ACQUITY UPLC Peptide CSH C18 column (1 mm × 150 mm, 1.7 μm) coupled to a Q Exactive mass spectrometer.…”
Section: Purification Of Scihmentioning
confidence: 99%