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Investigation of the Potential of Selected Food-Derived Antioxidants to Bind and Stabilise the Bioactive Blue Protein C-Phycocyanin from Cyanobacteria Spirulina.

Authors :
Gligorijević, Nikola
Jovanović, Zorana
Cvijetić, Ilija
Šunderić, Miloš
Veličković, Luka
Katrlík, Jaroslav
Holazová, Alena
Nikolić, Milan
Minić, Simeon
Source :
International Journal of Molecular Sciences; Jan2024, Vol. 25 Issue 1, p229, 15p
Publication Year :
2024

Abstract

Blue C-phycocyanin (C-PC), the major Spirulina protein with innumerable health-promoting benefits, is an attractive colourant and food supplement. A crucial obstacle to its more extensive use is its relatively low stability. This study aimed to screen various food-derived ligands for their ability to bind and stabilise C-PC, utilising spectroscopic techniques and molecular docking. Among twelve examined ligands, the protein fluorescence quenching revealed that only quercetin, coenzyme Q<subscript>10</subscript> and resveratrol had a moderate affinity to C-PC (K<subscript>a</subscript> of 2.2 to 3.7 × 10<superscript>5</superscript> M<superscript>–1</superscript>). Docking revealed these three ligands bind more strongly to the C-PC hexamer than the trimer, with the binding sites located at the interface of two (αβ)<subscript>3</subscript> trimers. UV/VIS absorption spectroscopy demonstrated the changes in the C-PC absorption spectra in a complex with quercetin and resveratrol compared to the spectra of free protein and ligands. Selected ligands did not affect the secondary structure content, but they induced changes in the tertiary protein structure in the CD study. A fluorescence-based thermal stability assay demonstrated quercetin and coenzyme Q<subscript>10</subscript> increased the C-PC melting point by nearly 5 °C. Our study identified food-derived ligands that interact with C-PC and improve its thermal stability, indicating their potential as stabilising agents for C-PC in the food industry. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
16616596
Volume :
25
Issue :
1
Database :
Complementary Index
Journal :
International Journal of Molecular Sciences
Publication Type :
Academic Journal
Accession number :
174716987
Full Text :
https://doi.org/10.3390/ijms25010229