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Updated: May 6, 2026

Analysis of Arabidopsis thaliana Growth Behavior in Different Light Qualities
Published on: February 2, 2018
Mechanistic differences in photoinhibition of sun and shade plants
G Oquist1, J M Anderson, S McCaffery
1Division of Plant Industry, CSIRO, GPO Box 1600, ACT 2601, Canberra, Australia.
Abstract:
Leaf discs of the shade plant Tradescantia albiflora Kunth grown at 50 μmol · m(-2) · s(-1), and the facultative sun/shade plant Pisum sativum L. grown at 50 or 300 μmol · m(-2), s(-1), were photoinhibited for 4 h in 1700 μmol photons m(-2) · s(-1) at 22° C. The effects of photoinhibition on the following parameters were studied: i) photosystem II (PSII) function; ii) amount of D1 protein in the PSII reaction centre; iii) dependence of photoinhibition and its recovery on chloroplast-encoded protein synthesis; and, iv) the sensitivity of photosynthesis to photoinhibition in the presence or absence of the carotenoid zeaxanthin. We show that: i) despite different sensitivities to photoinhibition, photoinhibition in all three plants occurred at the reaction centre of PSII; ii) there was no correlation between the extent of photoinhibition and the degradation of the D1 protein; iii) the susceptibility to photoinhibition by blockage of chloroplas-tencoded protein synthesis was much less in shade plants than in plants acclimated to higher light; and iv) inhibition of zeaxanthin formation increased the sensitivity to photoinhibition in pea, but not in the shade plant Tradescantia. We suggest that there are mechanistic differences in photoinhibition of sun and shade plants. In sun plants, an active repair cycle of PSII replaces photoinhibited reaction centres with photochemically active ones, thereby conferring partial protection against photoinhibition. However, in shade plants, this repair cycle is less important for protection against photoinhibition; instead, photoinhibited PSII reaction centres may confer, as they accumulate, increased protection of the remaining connected, functional PSII centres by controlled, nonphotochemical dissipation of excess excitation energy.
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