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

Cells. 2022 Aug 28;11(17):2681. doi: 10.3390/cells11172681.

Abstract

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

Keywords: 31P-NMR spectroscopy; lipid polymorphism; lipocalins; membrane fusion; membrane models; non-bilayer lipids; plastoglobuli; structural and functional plasticity; thylakoid membrane.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Lipase / metabolism
  • Lipid Bilayers* / metabolism
  • Magnetic Resonance Spectroscopy
  • Peptide Hydrolases / metabolism
  • Thylakoids* / metabolism

Substances

  • Lipid Bilayers
  • Lipase
  • Peptide Hydrolases

Grants and funding

This work was supported by grants from Czech Science Foundation (GAČR 19-13637S, to G.G.), National Research Development and Innovation Office of Hungary (OTKA K 128679, to G.G., and GINOP-2.3.2-15-2016-00058, to B.U.), the Ministry of Education, Youth and Sports of the Czech Republic (project “SustES—Adaptation strategies for sustainable ecosystem services and food security under adverse environmental conditions”; CZ.02.1.01/0.0/0.0/16_019/0000797, to V.Š., K.V., O.U., I.K., and V.K.), Silesian Region (07359/2019/RRC, to O.D.), European Union‘s Horizon 2020 Research and Innovation Program (No. 101000501, to B.U. and S.D.K), University of Ostrava (SGS11/PřF/2022, to O.D.) and Slovenian Research Agency (ARRS, grant P1-242 to J.P.). The authors acknowledge Central European Research Infrastructure (CERIC-ERIC) Consortium for the access to experimental facilities and financial support. The 31P-NMR measurements were performed in Slovenian NMR Center of CERIC-ERIC Consortium at National Institute of Chemistry in Ljubljana (project No. 20217148).