ReviewPlanta2026
Understanding plant resilience by putting photosynthesis and photorespiration in the metabolic context.
Review in Planta, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors.
Funding
Abstract
MAIN
conclusionPhotorespiration is a dynamic metabolic process that contributes to energy balance, stress resilience, and nutrient flux, warranting its integration into genome-scale models to enhance plant productivity and climate adaptation. Photorespiration, sometimes referred to as a wasteful byproduct of rubisco's oxygenation activity, is increasingly recognized as a vital and multifaceted component of plant metabolism. This perspective explores three underappreciated roles of photorespiration: as an alternative energy sink, a marker of stress resilience, and a metabolic hub. Photorespiration consumes significant ATP and reducing equivalents, potentially serving as a photoprotective mechanism under environmental stress. However, its role in energy dissipation remains debated, particularly in relation to non-photochemical quenching. Stress conditions such as drought and heat elevate photorespiratory flux due to Rubisco kinetics and stomatal responses, yet the link between photorespiration and resilience is complex and species-dependent. Metabolites like serine and glycine, key intermediates in photorespiration, correlate with stress responses and may exit the canonical pathway, contributing to one-carbon metabolism and amino acid biosynthesis. Calculations suggest that serine export from photorespiration could explain nitrate assimilation rates, yet protein synthesis alone cannot account for this flux, indicating unknown metabolic sinks. Genome-scale metabolic models (GSMMs) and resource allocation models (RAMs) offer promising tools to integrate photorespiration into broader metabolic frameworks. These models can simulate open-loop versus closed-loop photorespiration, assess energy dissipation capacity, and track amino acid fate. Future research should focus on refining GSMMs to include accurate photorespiratory pathways and leveraging them to understand photorespiration's role in plant resilience and nutrition, especially under realistic field conditions. This integrated approach is essential for reimagining photorespiration not as a metabolic burden, but as a central player in plant adaptation and productivity.
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What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.