# Donor- and Acceptor-Side Protection Against Photosystem I Photoinhibition in Arabidopsis thaliana

**Authors:** Marina Kozuleva

PMC · DOI: 10.3390/ijms27010009 · International Journal of Molecular Sciences · 2025-12-19

## TL;DR

This study shows that two types of light stress affect Photosystem I differently in plants, with distinct protective mechanisms.

## Contribution

The study reveals that donor- and acceptor-side protection mechanisms against PSI photoinhibition differ under pulsed and fluctuating light.

## Key findings

- Pulsed illumination and fluctuating light cause distinct types of PSI photoinhibition.
- The tap38/pph1 mutant shows contrasting sensitivity to wild-type plants under different light treatments.
- Different mutants highlight varied protective mechanisms against photoinhibition.

## Abstract

Photosystem I (PSI) photoinhibition (PI(I)) is gaining traction as a potentially more significant threat to plant performance than photoinhibition of photosystem II (PSII). The increased focus is facilitated by the implementation of specific protocols that induce PI(I), such as artificial fluctuating light (FL) and repetitive short saturating pulses (rSPs). rSPs were long considered a specific sub-case of FL. However, recent evidence suggests that PI(I) proceeds via at least two distinct, treatment-dependent mechanisms, leading to damage at the donor or acceptor side of PSI. This discovery suggests that rSPs and FL represent distinct photoinhibitory stresses and that different mechanisms protect PSI against FL and rSPs. This study comparatively analyzed the effects of FL and rSPs on PSI activity in Arabidopsis thaliana wild-type plants and a selection of mutants (pgr5, pgrl1, stn7, tap38/pph1, and pgr1), previously noted or hypothesized to have altered PI(I) sensitivity relative to the wild type. The results of this work, particularly the contrasting sensitivity of tap38/pph1 compared to the wild type under FL and rSP conditions, strongly suggest that pulsed illumination and fluctuating light are distinct photoinhibitory treatments, and different mechanisms protect PSI against them.

## Linked entities

- **Genes:** GPR152 (G protein-coupled receptor 152) [NCBI Gene 390212], STN7 (Serine/Threonine kinase domain protein) [NCBI Gene 843215], TAP38 (thylakoid-associated phosphatase 38) [NCBI Gene 828893], BMPR2 (bone morphogenetic protein receptor type 2) [NCBI Gene 659], PTGR1 (prostaglandin reductase 1) [NCBI Gene 22949]
- **Species:** Arabidopsis thaliana (taxon 3702)

## Full-text entities

- **Genes:** TAP38 (thylakoid-associated phosphatase 38) [NCBI Gene 828893] {aka PPH1, PROTEIN PHOSPHATASE 1, T27E11.40, T27E11_40, thylakoid-associated phosphatase 38}, PETC (photosynthetic electron transfer C) [NCBI Gene 827996] {aka F4C21.21, F4C21_21, PGR1, PROTON GRADIENT REGULATION 1, RIESKE IRON-SULFUR PROTEIN PRECURSOR, photosynthetic electron transfer C}, STN7 (Serine/Threonine kinase domain protein) [NCBI Gene 843215] {aka STT7 homolog STN7, T6L1.2, T6L1_2}, PGR5 (proton gradient regulation 5) [NCBI Gene 815111] {aka AtPGR5, T20G20.3, T20G20_3, proton gradient regulation 5}
- **Diseases:** PSI (MESH:D006969)
- **Chemicals:** rSP (-)
- **Species:** Arabidopsis thaliana (mouse-ear cress, species) [taxon 3702]

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12786166/full.md

## References

68 references — full list in the complete paper: https://tomesphere.com/paper/PMC12786166/full.md

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Source: https://tomesphere.com/paper/PMC12786166