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Probing the structural stability of R-phycocyanin under pressure.
Minic, Simeon; Velickovic, Luka; Annighöfer, Burkhard; Thureau, Aurélien; Gligorijevic, Nikola; Jovanovic, Zorana; Brûlet, Annie; Combet, Sophie.
Afiliación
  • Minic S; Faculty of Chemistry, Center of Excellence for Molecular Food Sciences & Department of Biochemistry, University of Belgrade, Belgrade, Serbia.
  • Velickovic L; Faculty of Chemistry, Center of Excellence for Molecular Food Sciences & Department of Biochemistry, University of Belgrade, Belgrade, Serbia.
  • Annighöfer B; Laboratoire Léon-Brillouin (LLB), UMR12 CEA, CNRS, Université Paris-Saclay, CEA-Saclay, F-91191 Gif-sur-Yvette CEDEX, Gif-sur-Yvette, France.
  • Thureau A; SWING beamline, Synchrotron SOLEIL, Gif-sur-Yvette, France.
  • Gligorijevic N; Department of Chemistry, University of Belgrade-Institute of Chemistry, Technology, and Metallurgy, National Institute of the Republic of Serbia, Belgrade, Serbia.
  • Jovanovic Z; Faculty of Chemistry, Center of Excellence for Molecular Food Sciences & Department of Biochemistry, University of Belgrade, Belgrade, Serbia.
  • Brûlet A; Laboratoire Léon-Brillouin (LLB), UMR12 CEA, CNRS, Université Paris-Saclay, CEA-Saclay, F-91191 Gif-sur-Yvette CEDEX, Gif-sur-Yvette, France.
  • Combet S; Laboratoire Léon-Brillouin (LLB), UMR12 CEA, CNRS, Université Paris-Saclay, CEA-Saclay, F-91191 Gif-sur-Yvette CEDEX, Gif-sur-Yvette, France.
Protein Sci ; 33(9): e5145, 2024 Sep.
Article en En | MEDLINE | ID: mdl-39150070
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.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Ficocianina / Presión / Estabilidad Proteica Idioma: En Revista: Protein Sci Asunto de la revista: BIOQUIMICA Año: 2024 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Ficocianina / Presión / Estabilidad Proteica Idioma: En Revista: Protein Sci Asunto de la revista: BIOQUIMICA Año: 2024 Tipo del documento: Article