Probing the structural stability of R‐phycocyanin under pressure

The red macroalgae Porphyra, commonly known as Nori, is widely used as food around the world due to its high nutrient content, including the significant abundance of colored phycobiliproteins (PBPs). Among these, R-phycocyanin (R-PC) stands out for its vibrant purple color and numerous bioactive properties, making it a valuable protein for the food industry. However, R-PC's limited thermal stability necessitates alternative processing methods to preserve its color and bioactive properties. Our study aimed to investigate the in-situ stability of oligomeric R-PC under high pressure (HP) conditions (up to 4000 bar) using a combination of absorption, fluorescence, and small-angle X-ray scattering (SAXS) techniques. The unfolding of R-PC is a multiphase process. Initially, low pressure induces conformational changes in the R-PC oligomeric form (trimers). As pressure increases above 1600 bar, these trimers dissociate into monomers, and at pressures above 3000 bar, the subunits begin to unfold. When returned to atmospheric pressure, R-PC partially refolds, retaining 50% of its original color absorbance. In contrast, heat treatment causes irreversible and detrimental effects on R-PC color, highlighting the advantages of HP treatment in preserving both the color and bioactive properties of R-PC compared to heat treatment.

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Publication Details

Journal
Protein Science
Published
2024-08-16
DOI
https://doi.org/10.1002/pro.5145
Citations
2
Primary Topic
Algal biology and biofuel production
Type
article
Field-Weighted Citation Impact
0.20

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article

Probing the structural stability of R‐phycocyanin under pressure

Nikola Gligorijević, Annie Brûlet, Burkhard Annighöfer, Sophie Combet et al.
2 citations
Protein Science
Algal biology and biofuel production
0.20
article

Probing the structural stability of R‐phycocyanin under pressure

Nikola Gligorijević, Annie Brûlet, Burkhard Annighöfer, Sophie Combet, Simeon Minić, Aurélien Thureau, Luka Veličković, Zorana Jovanovic
article en
2 citations

Abstract

The red macroalgae Porphyra, commonly known as Nori, is widely used as food around the world due to its high nutrient content, including the significant abundance of colored phycobiliproteins (PBPs). Among these, R-phycocyanin (R-PC) stands out for its vibrant purple color and numerous bioactive properties, making it a valuable protein for the food industry. However, R-PC's limited thermal stability necessitates alternative processing methods to preserve its color and bioactive properties. Our study aimed to investigate the in-situ stability of oligomeric R-PC under high pressure (HP) conditions (up to 4000 bar) using a combination of absorption, fluorescence, and small-angle X-ray scattering (SAXS) techniques. The unfolding of R-PC is a multiphase process. Initially, low pressure induces conformational changes in the R-PC oligomeric form (trimers). As pressure increases above 1600 bar, these trimers dissociate into monomers, and at pressures above 3000 bar, the subunits begin to unfold. When returned to atmospheric pressure, R-PC partially refolds, retaining 50% of its original color absorbance. In contrast, heat treatment causes irreversible and detrimental effects on R-PC color, highlighting the advantages of HP treatment in preserving both the color and bioactive properties of R-PC compared to heat treatment.

Protein ScienceVol. 33(9)
Centre National de la Recherche Scientifique (FR), Commissariat à l'Énergie Atomique et aux Énergies Alternatives (FR), Université Paris-Saclay (FR), Synchrotron soleil (FR), University of Belgrade (RS), Laboratoire Léon Brillouin (FR), CEA Paris-Saclay (FR)
Federation of European Biochemical Societies, Alliance of International Science Organizations
Responsible consumption and production
Openalex Percentile: Top 59%
Algal biology and biofuel production
0.20
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