Effect of duck egg white peptide-ferrous chelate on iron bioavailability in vivo and structure characterization

J Sci Food Agric. 2019 Mar 15;99(4):1834-1841. doi: 10.1002/jsfa.9377. Epub 2018 Oct 31.

Abstract

Background: In order to utilize the industrial by-product 'salted duck egg white' as novel iron additives, the effects of desalted duck egg white peptides-ferrous chelate (DPs-Fe) on the promotion of iron uptake and the structure were investigated.

Results: Different doses of DPs-Fe were given and iron sulfate (FeSO4 ) was used as a positive control. After three weeks, hemoglobin (Hb), hematocrit (HCT), red blood cells (RBCs), mean corpuscular volume (MCV), serum iron (SI) and serum ferritin (SF) in iron-deficiency anemia (IDA) rats could be significantly (P < 0.05) increased to the normal levels by DPs-Fe. The gene expressions of divalent metal transporter 1 (DMT1), ferroportin 1 (FPN1) and Hepcidin could be regulated by DPs-Fe. Additionally, DPs-Fe was formed during the chelation process and the structure was characterized. Eight crucial iron-chelating peptides of duck egg white peptides (DPs) were identified by HPLC-ESI-MS/MS, such as Pro-Val-Glu-Glu and Arg-Ser-Ser. It indicated that Glu, Asp, Lys, His, Ser, Cys residues might play crucial roles in the chelating of DPs with iron.

Conclusion: DPs-Fe could be a potential iron supplement, and the Glu, Asp, Lys, His played important roles in binding iron and promoting iron uptake. This research expands the understanding of iron uptake by DPs and provides an opportunity for recycling a discarded processing byproduct. © 2018 Society of Chemical Industry.

Keywords: anemia; characterization; duck egg white peptides-ferrous chelate (DPs-Fe); hemoglobin; iron-regulated genes.

MeSH terms

  • Anemia, Iron-Deficiency / blood
  • Anemia, Iron-Deficiency / diet therapy*
  • Anemia, Iron-Deficiency / metabolism
  • Animals
  • Biological Availability
  • Cation Transport Proteins / metabolism
  • Ducks
  • Egg White / chemistry
  • Eggs / analysis
  • Erythrocyte Count
  • Humans
  • Iron / chemistry
  • Iron / metabolism*
  • Iron Chelating Agents / chemistry
  • Iron Chelating Agents / metabolism*
  • Male
  • Peptides / chemistry
  • Peptides / metabolism*
  • Rats
  • Rats, Sprague-Dawley
  • Tandem Mass Spectrometry

Substances

  • Cation Transport Proteins
  • Iron Chelating Agents
  • Peptides
  • metal transporting protein 1
  • solute carrier family 11- (proton-coupled divalent metal ion transporters), member 2
  • Iron