# Preparative isolation and preliminary characterization of LHCII trimers and PSII monomers from Posidonia oceanica L

**Authors:** Stefano Francesco Farci, Luca Iesu, Domenica Farci, Dario Piano

PMC · DOI: 10.1007/s11120-026-01196-3 · 2026-01-29

## TL;DR

This paper describes a new method to isolate and study key photosynthetic components from the marine plant Posidonia oceanica.

## Contribution

A novel chromatography-based workflow for isolating LHCII trimers and PSII monomers from P. oceanica is developed.

## Key findings

- A procedure for thylakoid solubilization was developed to isolate LHCII trimers and PSII monomers.
- Mass spectrometry and peptide homology analysis identified the isolated proteins despite the lack of a curated proteome.
- The workflow enables functional and structural studies of P. oceanica's photosynthetic apparatus.

## Abstract

Posidonia oceanica L. is a vascular marine plant that represents a relevant case study in plant physiology due to its phylogenetic position, ecological adaptations, and, in particular, the specialization of its photosynthetic apparatus. Here, we present a procedure for fractional thylakoid solubilization, in which a crude leaf extract obtained by blending is preliminarily depleted of the polyphenolic fraction and subsequently subjected to stepwise solubilization. The resulting thylakoid extracts, processed through a chromatographic workflow, enable the preparative isolation of trimeric Light-Harvesting Complex II and monomeric Photosystem II core complex. Protein identification was supported by mass spectrometry, with peptide homology analysis used for the assignment due to the absence of a curated proteome for P. oceanica. The resulting fractions enable downstream characterization, establishing the first chromatography-based preparative workflow for functional and structural investigations of the photosynthetic apparatus of this ecologically unique species.

The online version contains supplementary material available at 10.1007/s11120-026-01196-3.

## Linked entities

- **Proteins:** LOC100682487 (chlorophyll a-b binding protein of LHCII type 1), psiI (PA14 domain-containing protein)

## Full-text entities

- **Genes:** PSBE [NCBI Gene 3677466], PSBA [NCBI Gene 3677462], PSBD [NCBI Gene 3677465], PSBL [NCBI Gene 3677472], PSBH [NCBI Gene 3677468], PSBC [NCBI Gene 3677464], PSBB [NCBI Gene 3677463]
- **Diseases:** necrotic (MESH:D009336)
- **Chemicals:** iodoacetamide (MESH:D007460), SDS (MESH:D012967), formic acid (MESH:C030544), sodium fluoride (MESH:D012969), PEG (MESH:D011092), CaCl2 2H2O (-), methionine (MESH:D008715), Polyphenols (MESH:D059808), acetonitrile (MESH:C032159), tannins (MESH:D013634), Cys (MESH:D003545), pheophytin (MESH:D010674), PEG 4000 (MESH:C000595214), peptide (MESH:D010455), ascorbic acid (MESH:D001205), carotenoid (MESH:D002338), 13C (MESH:C000615229), NaHCO3 (MESH:D017693), Lys (MESH:D008239), sorbitol (MESH:D013012), Urea (MESH:D014508), LiDS (MESH:C028913), sucrose (MESH:D013395), heme (MESH:D006418), chlorophyll b (MESH:C037184), quinones (MESH:D011809), DTT (MESH:D004229), PEG 6000 (MESH:C000595215), chlorophyll (MESH:D002734), MES (MESH:C004550), Polyacrylamide (MESH:C016679), hydrogen (MESH:D006859), CBB (MESH:C004692), Hydroxyl (MESH:D017665), water (MESH:D014867), NaCl (MESH:D012965), aminocaproic acid (MESH:D015119), His (MESH:D006639)
- **Species:** Arabidopsis thaliana (mouse-ear cress, species) [taxon 3702], Posidonia oceanica (species) [taxon 55489], conifers [taxon 3312], Picea abies (Norway spruce, species) [taxon 3329], Pinus sylvestris (Scotch pine, species) [taxon 3349]

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12855319/full.md

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Source: https://tomesphere.com/paper/PMC12855319