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1. Exciton-Condensate-Like Energy Transport in Light-Harvesting Complex 2

   https://doi.org/10.1103/PRXEnergy.4.013004  

   Schouten, Anna O; Mazziotti, David A (February 2025, PRX Energy)

   Bose-Einstein condensation of excitons, with its potential for frictionless energy transport, has recently been observed in materials at low temperatures. Here, we show that partial exciton condensation plays a significant role in the 18-chromophore B850 ring of the light-harvesting complex 2 (LH2) in purple bacteria. Even in the single-excitation regime, we observe that excitonic entanglement across multiple sites exhibits signatures of exciton condensation in the particle-hole reduced density matrix—a partial exciton condensate. Crucially, we find that, by distributing the exciton across multiple sites of the ring, the exciton-condensate-like state sets favorable conditions for enhanced energy transfer, both before and after decoherence. Surprisingly, this discovery reveals that excitonic condensation, previously thought to require extreme conditions, can occur in a partial form in biological systems under ambient conditions, providing new insight into energy transport. These results additionally bring new insight into the long-standing debate on quantum versus classical mechanisms in photosynthetic light harvesting by showing that quantum coherence, in the form of a partial exciton condensate, indirectly initializes subsequent classical transfer. Our findings not only deepen our understanding of quantum coherence in light harvesting but also suggest design principles for materials capable of leveraging excitonic entanglement for efficient energy transport. Published by the American Physical Society2025 

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2. DNA scaffold supports long-lived vibronic coherence in an indodicarbocyanine (Cy5) dimer

   https://doi.org/10.1039/D0SC01127D  

   Sohail, Sara H.; Otto, John P.; Cunningham, Paul D.; Kim, Young C.; Wood, Ryan E.; Allodi, Marco A.; Higgins, Jacob S.; Melinger, Joseph S.; Engel, Gregory S. (August 2020, Chemical Science)

   null (Ed.)

   Vibronic coupling between pigment molecules is believed to prolong coherences in photosynthetic pigment–protein complexes. Reproducing long-lived coherences using vibronically coupled chromophores in synthetic DNA constructs presents a biomimetic route to efficient artificial light harvesting. Here, we present two-dimensional (2D) electronic spectra of one monomeric Cy5 construct and two dimeric Cy5 constructs (0 bp and 1 bp between dyes) on a DNA scaffold and perform beating frequency analysis to interpret observed coherences. Power spectra of quantum beating signals of the dimers reveal high frequency oscillations that correspond to coherences between vibronic exciton states. Beating frequency maps confirm that these oscillations, 1270 cm −1 and 1545 cm −1 for the 0-bp dimer and 1100 cm −1 for the 1-bp dimer, are coherences between vibronic exciton states and that these coherences persist for ∼300 fs. Our observations are well described by a vibronic exciton model, which predicts the excitonic coupling strength in the dimers and the resulting molecular exciton states. The energy spacing between those states closely corresponds to the observed beat frequencies. MD simulations indicate that the dyes in our constructs lie largely internal to the DNA base stacking region, similar to the native design of biological light harvesting complexes. Observed coherences persist on the timescale of photosynthetic energy transfer yielding further parallels to observed biological coherences, establishing DNA as an attractive scaffold for synthetic light harvesting applications. 

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3. Quieting a noisy antenna reproduces photosynthetic light-harvesting spectra

   https://doi.org/10.1126/science.aba6630  

   Arp, Trevor B.; Kistner-Morris, Jed; Aji, Vivek; Cogdell, Richard J.; van Grondelle, Rienk; Gabor, Nathaniel M. (June 2020, Science)

   null (Ed.)

   Photosynthesis achieves near unity light-harvesting quantum efficiency yet it remains unknown whether there exists a fundamental organizing principle giving rise to robust light harvesting in the presence of dynamic light conditions and noisy physiological environments. Here, we present a noise-canceling network model that relates noisy physiological conditions, power conversion efficiency, and the resulting absorption spectra of photosynthetic organisms. Using light conditions in full solar exposure, light filtered by oxygenic phototrophs, and light filtered under seawater, we derived optimal absorption characteristics for efficient solar power conversion. We show how light-harvesting antennae can be tuned to maximize power conversion efficiency by minimizing excitation noise, thus providing a unified theoretical basis for the observed wavelength dependence of absorption in green plants, purple bacteria, and green sulfur bacteria. 

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4. Nonphotochemical quenching kinetics GWAS in sorghum identifies genes that may play conserved roles in maize and Arabidopsis thaliana photoprotection

   https://doi.org/10.1111/tpj.16967  

   Sahay, Seema; Shrestha, Nikee; Dias, Henrique_Moura; Mural, Ravi_V; Grzybowski, Marcin; Schnable, James_C; Głowacka, Katarzyna (August 2024, The Plant Journal)

   SUMMARY Photosynthetic organisms must cope with rapid fluctuations in light intensity. Nonphotochemical quenching (NPQ) enables the dissipation of excess light energy as heat under high light conditions, whereas its relaxation under low light maximizes photosynthetic productivity. We quantified variation in NPQ kinetics across a large sorghum (Sorghum bicolor) association panel in four environments, uncovering significant genetic control for NPQ. A genome‐wide association study (GWAS) confidently identified three unique regions in the sorghum genome associated with NPQ and suggestive associations in an additional 61 regions. We detected strong signals from the sorghum ortholog ofArabidopsis thaliana Suppressor Of Variegation 3(SVR3) involved in plastid–nucleus signaling. By integrating GWAS results for NPQ across maize (Zea mays) and sorghum‐association panels, we identified a second gene,Non‐yellowing 1(NYE1), originally studied by Gregor Mendel in pea (Pisum sativum) and involved in the degradation of photosynthetic pigments in light‐harvesting complexes. Analysis ofnye1insertion alleles inA. thalianaconfirmed the effect of this gene on NPQ kinetics in eudicots. We extended our comparative genomics GWAS framework across the entire maize and sorghum genomes, identifying four additional loci involved in NPQ kinetics. These results provide a baseline for increasing the accuracy and speed of candidate gene identification for GWAS in species with high linkage disequilibrium. 

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5. Photosynthesis tunes quantum-mechanical mixing of electronic and vibrational states to steer exciton energy transfer

   https://doi.org/10.1073/pnas.2018240118  

   Higgins, Jacob S.; Lloyd, Lawson T.; Sohail, Sara H.; Allodi, Marco A.; Otto, John P.; Saer, Rafael G.; Wood, Ryan E.; Massey, Sara C.; Ting, Po-Chieh; Blankenship, Robert E.; et al (March 2021, Proceedings of the National Academy of Sciences)

   Photosynthetic species evolved to protect their light-harvesting apparatus from photoxidative damage driven by intracellular redox conditions or environmental conditions. The Fenna–Matthews–Olson (FMO) pigment–protein complex from green sulfur bacteria exhibits redox-dependent quenching behavior partially due to two internal cysteine residues. Here, we show evidence that a photosynthetic complex exploits the quantum mechanics of vibronic mixing to activate an oxidative photoprotective mechanism. We use two-dimensional electronic spectroscopy (2DES) to capture energy transfer dynamics in wild-type and cysteine-deficient FMO mutant proteins under both reducing and oxidizing conditions. Under reducing conditions, we find equal energy transfer through the exciton 4–1 and 4–2-1 pathways because the exciton 4–1 energy gap is vibronically coupled with a bacteriochlorophyll-avibrational mode. Under oxidizing conditions, however, the resonance of the exciton 4–1 energy gap is detuned from the vibrational mode, causing excitons to preferentially steer through the indirect 4–2-1 pathway to increase the likelihood of exciton quenching. We use a Redfield model to show that the complex achieves this effect by tuning the site III energy via the redox state of its internal cysteine residues. This result shows how pigment–protein complexes exploit the quantum mechanics of vibronic coupling to steer energy transfer. 

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