The role of the pigment–protein complex LHCBM1 in nonphotochemical quenching in Chlamydomonas reinhardtii

Xin Liu, Wojciech J. Nawrocki, Roberta Croce*

*Corresponding author for this work

Research output: Contribution to JournalArticleAcademicpeer-review

Abstract

Nonphotochemical quenching (NPQ) is the process that protects photosynthetic organisms from photodamage by dissipating the energy absorbed in excess as heat. In the model green alga Chlamydomonas reinhardtii, NPQ is abolished in the knock-out mutants of the pigment–protein complexes LHCSR3 and LHCBM1. However, while LHCSR3 is a pH sensor and switches to a quenched conformation at low pH, the role of LHCBM1 in NPQ has not been elucidated yet. In this work, we combined biochemical and physiological measurements to study short-term high-light acclimation of npq5, the mutant lacking LHCBM1. In low light in the absence of this complex, the antenna size of PSII was smaller than in its presence; this effect was marginal in high light (HL), implying that a reduction of the antenna was not responsible for the low NPQ. The mutant expressed LHCSR3 at the wild-type level in HL, indicating that the absence of this complex is also not the reason. Finally, NPQ remained low in the mutant even when the pH was artificially lowered to values that can switch LHCSR3 to the quenched conformation. We concluded that both LHCSR3 and LHCBM1 are required for the induction of NPQ and that LHCBM1 is the interacting partner of LHCSR3. This interaction can either enhance the quenching capacity of LHCSR3 or connect this complex with the PSII supercomplex.

Original languageEnglish
Pages (from-to)936-944
Number of pages9
JournalPlant physiology
Volume194
Issue number2
Early online date17 Oct 2023
DOIs
Publication statusPublished - Feb 2024

Bibliographical note

Publisher Copyright:
© The Author(s) 2023. Published by Oxford University Press on behalf of American Society of Plant Biologists.

Funding

This work is partially supported by the Human Frontier Science Program (HRSP) grant RGP0005/2021. X.L. was supported by the Chinese Scholarship Council 201606910042.

FundersFunder number
Human Frontier Science ProgramRGP0005/2021
China Scholarship Council201606910042

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