ArticlePhotosynthesis research2019
Photosynthesis supported by a chlorophyll f-dependent, entropy-driven uphill energy transfer in Halomicronema hongdechloris cells adapted to far-red light.
Article in Photosynthesis research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.
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15 citing papers in PubMed, 70 citations in OpenAlex.
- Driving Electron Transfer in Photosystem I Using Far-Red Light: Overall Perspectives.Plants (Basel, Switzerland) · 2025Review
- Far-red light-driven photoautotrophy of chlorophyll f-producing cyanobacterium without red-shifted phycobilisome core complex.Photosynthesis research · 2025Article
- Strain-Compensated Quantum Well Asymmetric Waveguide Edge-Emitting Laser Operating at 730 nm.Sensors (Basel, Switzerland) · 2025Article
- How electron tunneling and uphill excitation energy transfer support photochemistry in Halomicronema hongdechloris.Photosynthesis research · 2024Article
- Adaptation processes inFrontiers in plant science · 2024Review
- The antenna of far-red absorbing cyanobacteria increases both absorption and quantum efficiency of Photosystem II.Nature communications · 2022Article
- The PshX subunit of the photochemical reaction center from Heliobacterium modesticaldum acts as a low-energy antenna.Photosynthesis research · 2022Article
- Structure of the far-red light utilizing photosystem I of Acaryochloris marina.Nature communications · 2021Article
- Quantitative assessment of chlorophyll types in cryo-EM maps of photosystem I acclimated to far-red light.BBA advances · 2021Article
- Femtosecond visible transient absorption spectroscopy of chlorophyll-Proceedings of the National Academy of Sciences of the United States of America · 2020Article
- Far-red absorption and light-use efficiency trade-offs in chlorophyll f photosynthesis.Nature plants · 2020Article
- Structural basis for the adaptation and function of chlorophyll f in photosystem I.Nature communications · 2020Article
- Energy transfer from chlorophyll f to the trapping center in naturally occurring and engineered Photosystem I complexes.Photosynthesis research · 2019Article
- Spectral signatures of five hydroxymethyl chlorophyll a derivatives chemically derived from chlorophyll b or chlorophyll f.Photosynthesis research · 2019Article
- Genome and proteome of the chlorophyll f-producing cyanobacterium Halomicronema hongdechloris: adaptative proteomic shifts under different light conditions.BMC genomics · 2019Article
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9 authors at 5 institutions in 5 countries.
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No grant is acknowledged in the PubMed record.
Abstract
The phototrophic cyanobacterium Halomicronema hongdechloris shows far-red light-induced accumulation of chlorophyll (Chl) f, but the involvement of the pigment in photosynthetic energy harvesting by photosystem (PS) II is controversially discussed. While H. hongdechloris contains negligible amounts of Chl f in white-light culture conditions, the ratio of Chl f to Chl a is reversibly changed up to 1:8 under illumination with far-red light (720-730 nm). We performed UV-Vis absorption spectroscopy, time-integrated and time-resolved fluorescence spectroscopy for the calculation of decay-associated spectra (DAS) to determine excitation energy transfer (EET) processes between photosynthetic pigments in intact H. hongdechloris filaments. In cells grown under white light, highly efficient EET occurs from phycobilisomes (PBSs) to Chl a with an apparent time constant of about 100 ps. Charge separation occurs with a typical apparent time constant of 200-300 ps from Chl a. After 3-4 days of growth under far-red light, robust Chl f content was observed in H. hongdechloris and EET from PBSs reached Chl f efficiently within 200 ps. It is proposed based on mathematical modeling by rate equation systems for EET between the PBSs and PSII and subsequent electron transfer (ET) that charge separation occurs from Chl a and excitation energy is funneled from Chl f to Chl a via an energetically uphill EET driven by entropy, which is effective because the number of Chl a molecules coupled to Chl f is at least eight- to tenfold larger than the corresponding number of Chl f molecules. The long lifetime of Chl f molecules in contact to a tenfold larger pool of Chl a molecules allows Chl f to act as an intermediate energy storage level, from which the Gibbs free energy difference between Chl f and Chl a can be overcome by taking advantage from the favorable ratio of degeneracy coefficients, which formally represents a significant entropy gain in the Eyring formulation of the Arrhenius law. Direct evidence for energetically uphill EET and charge separation in PSII upon excitation of Chl f via anti-Stokes fluorescence in far-red light-adapted H. hongdechloris cells was obtained: Excitation by 720 nm laser light resulted in robust Chl a fluorescence at 680 nm that was distinctly temperature-dependent and, notably, increased upon DCMU (3-(3,4-dichlorophenyl)-1,1-dimethylurea) treatment in far-red light-adapted cells. Thus, rather than serving as an excitation energy trap, Chl f in far-red light-adapted H. hongdechloris cells is directly contributing to oxygenic photosynthesis at PSII.
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