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Structural Entities Associated with Different Lipid Phases of Plant Thylakoid Membranes—Selective Susceptibilities to Different Lipases and Proteases

It is well established that plant thylakoid membranes (TMs), in addition to a bilayer, contain two isotropic lipid phases and an inverted hexagonal (H(II)) phase. To elucidate the origin of non-bilayer lipid phases, we recorded the (31)P-NMR spectra of isolated spinach plastoglobuli and TMs and test...

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Detalles Bibliográficos
Autores principales: Dlouhý, Ondřej, Karlický, Václav, Javornik, Uroš, Kurasová, Irena, Zsiros, Ottó, Šket, Primož, Kanna, Sai Divya, Böde, Kinga, Večeřová, Kristýna, Urban, Otmar, Gasanoff, Edward S., Plavec, Janez, Špunda, Vladimír, Ughy, Bettina, Garab, Győző
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9454902/
https://www.ncbi.nlm.nih.gov/pubmed/36078087
http://dx.doi.org/10.3390/cells11172681
Descripción
Sumario:It is well established that plant thylakoid membranes (TMs), in addition to a bilayer, contain two isotropic lipid phases and an inverted hexagonal (H(II)) phase. To elucidate the origin of non-bilayer lipid phases, we recorded the (31)P-NMR spectra of isolated spinach plastoglobuli and TMs and tested their susceptibilities to lipases and proteases; the structural and functional characteristics of TMs were monitored using biophysical techniques and CN-PAGE. Phospholipase-A1 gradually destroyed all (31)P-NMR-detectable lipid phases of isolated TMs, but the weak signal of isolated plastoglobuli was not affected. Parallel with the destabilization of their lamellar phase, TMs lost their impermeability; other effects, mainly on Photosystem-II, lagged behind the destruction of the original phases. Wheat-germ lipase selectively eliminated the isotropic phases but exerted little or no effect on the structural and functional parameters of TMs—indicating that the isotropic phases are located outside the protein-rich regions and might be involved in membrane fusion. Trypsin and Proteinase K selectively suppressed the H(II) phase—suggesting that a large fraction of TM lipids encapsulate stroma-side proteins or polypeptides. We conclude that—in line with the Dynamic Exchange Model—the non-bilayer lipid phases of TMs are found in subdomains separated from but interconnected with the bilayer accommodating the main components of the photosynthetic machinery.