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Quantification of electron transport-related oxidative signals by time and wavelength-resolved redox biosensors and chlorophyll fluorescence

bioRxiv · 12 Sept 2024 · 10.1101/2024.09.09.611861

Abstract

Reductive and oxidative signals transmitted from the photosynthetic electron chain to target proteins through the redox signaling network are key regulators of carbon assimilation and downstream metabolism. However, despite their crucial role in activating and inhibiting photosynthetic activity, their relation to photosynthetic efficiency is hardly quantified due to the methodological gap between traditional spectroscopic approaches for investigating photosynthesis and biochemical analyses used in the redox regulation field. Here, we simultaneously quantified redox signals and photosynthetic activity by exploring time and wavelength-resolved fluorescence spectra that capture biosensor and chlorophyll fluorescence signals. Using a set of potato plants expressing genetically encoded redox biosensors, we demonstrated how reductive and oxidative signals are amplified with elevated light intensities and revealed the tight connection between electron transport rate (ETR) and the generation of peroxiredoxin-related oxidative signals. These results demonstrate how full spectrum analysis can pave the way for the integration of genetically encoded biosensors in photosynthesis research and demonstrate light-dependent activation of inhibitory oxidative signals in major crop plants.

Plant phenotyping relevance

時間・波長分解蛍光スペクトルを用いて、植物のレドックスシグナルと光合成活性を同時定量する測定法を開発・実証しており、植物生理状態の取得が研究の中心です。

abstractHere, we simultaneously quantified redox signals and photosynthetic activity by exploring time and wavelength-resolved fluorescence spectra that capture biosensor and chlorophyll fluorescence signals.
abstractThese results demonstrate how full spectrum analysis can pave the way for the integration of genetically encoded biosensors in photosynthesis research

Code and data availability

The paper describes custom-written MATLAB scripts for image preprocessing and ChloroKin/ChloroSoft analysis, but no public deposit, availability statement, or URL for data or code is provided in the supplied blocks. No public phenotype datasets, images, or author code repositories are identified.

No evidence-backed public reproduction asset is currently recorded.

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