Theoretical Model of the Far-Red-Light-Adapted Photosystem I Reaction Center of Cyanobacterium Acaryochloris marina Using Chlorophyll d and the Effect of Chlorophyll Exchange.

A theoretical model of the far-red-light-adapted photosystem I (PSI) reaction center (RC) complex of a cyanobacterium, Acaryochloris marina (AmPSI), was constructed based on the exciton theory and the recently identified molecular structure of AmPSI by Hamaguchi et al. (Nat. Commun., 2021, 12, 2333). A. marina performs photosynthesis under the visible to far-red light (400-750 nm), which is absorbed by chlorophyll d (Chl-d). It is in contrast to the situation of all the other oxygenic photosynthetic processes of cyanobacteria and plants, which contains chlorophyll a (Chl-a) that absorbs only 400-700 nm visible light. AmPSI contains 70 Chl-d, 1 Chl-d', 2 pheophytin a (Pheo-a), and 12 carotenoids in the currently available structure. A special pair of Chl-d/Chl-d' acts as the electron donor (P740) and two Pheo-a act as the primary electron acceptor A0 as the counterparts of P700 and Chl-a, respectively, of Chl-a-type PSIs. The exciton Hamiltonian of AmPSI was constructed considering the excitonic coupling strength and site energy shift of individual pigments using the Poisson-TrESP (P-TrESP) and charge density coupling (CDC) methods. The model was constructed to fit the experimentally measured spectra of absorption and circular dichroism (CD) spectra during downhill/uphill excitation energy transfer processes. The constructed theoretical model of AmPSI was further compared with the Chl-a-type PSI of Thermosynechococcus elongatus (TePSI), which contains only Chl-a and Chl-a'. The functional properties of AmPSI and TePSI were further examined by the in silico exchange of Chl-d by Chl-a in the models.

[1]  Jimin Wang,et al.  Structure of a monomeric photosystem II core complex from a cyanobacterium acclimated to far-red light reveals the functions of chlorophylls d and f , 2021, The Journal of biological chemistry.

[2]  N. Nelson,et al.  Two-Dimensional Electronic Spectroscopy of a Minimal Photosystem I Complex Reveals the Rate of Primary Charge Separation. , 2021, Journal of the American Chemical Society.

[3]  Jian-Ren Shen,et al.  A unique photosystem I reaction center from a chlorophyll d-containing cyanobacterium Acaryochloris marina. , 2021, Journal of integrative plant biology.

[4]  Y. Shigeta,et al.  Comparison between the Light-Harvesting Mechanisms of Type-I Photosynthetic Reaction Centers of Heliobacteria and Photosystem I: Pigment Site Energy Distribution and Exciton State. , 2021, The journal of physical chemistry. B.

[5]  J. Ogilvie,et al.  Excitonic structure and charge separation in the heliobacterial reaction center probed by multispectral multidimensional spectroscopy , 2021, Nature Communications.

[6]  K. Shinzawa-Itoh,et al.  Structure of the far-red light utilizing photosystem I of Acaryochloris marina , 2020, Nature Communications.

[7]  Jian-Ren Shen,et al.  Architecture of the photosynthetic complex from a green sulfur bacterium , 2020, Science.

[8]  Su Lin,et al.  The structure of a red-shifted photosystem I reveals a red site in the core antenna , 2020, Nature Communications.

[9]  Jimin Wang,et al.  Opportunities and challenges for assigning cofactors in cryo-EM density maps of chlorophyll-containing proteins , 2020, Communications Biology.

[10]  H. Oh-oka,et al.  Energy transfer and primary charge separation upon selective femtosecond excitation at 810 nm in the reaction center complex from Heliobacterium modesticaldum , 2020 .

[11]  N. Miyazaki,et al.  Structural basis for assembly and function of a diatom photosystem I-light-harvesting supercomplex , 2020, Nature Communications.

[12]  T. Kondo,et al.  Cryogenic Single-Molecule Spectroscopy of the Primary Electron Acceptor in Photosynthetic Reaction Center. , 2020, The journal of physical chemistry letters.

[13]  D. Bryant,et al.  Evidence that Chlorophyll f Functions Solely as an Antenna Pigment in Far-Red-Light Photosystem I from Fischerella thermalis PCC 7521. , 2020, Biochimica et biophysica acta. Bioenergetics.

[14]  P. Fromme,et al.  The structure of Photosystem I acclimated to far-red light illuminates an ecologically important acclimation process in photosynthesis , 2020, Science Advances.

[15]  N. Miyazaki,et al.  Structural basis for the adaptation and function of chlorophyll f in photosystem I , 2020, Nature Communications.

[16]  Y. Shigeta,et al.  Excitonic Coupling on Heliobacterial Symmetrical Type-I Reaction Center: Comparison with Photosystem I. , 2019, The journal of physical chemistry. B.

[17]  M. Ikeuchi,et al.  Structure of a cyanobacterial photosystem I tetramer revealed by cryo-electron microscopy , 2019, Nature Communications.

[18]  N. Miyazaki,et al.  Structure of the green algal photosystem I supercomplex with a decameric light-harvesting complex I , 2019, Nature Plants.

[19]  Jian-Ren Shen,et al.  Structure of a green algal photosystem I in complex with a large number of light-harvesting complex I subunits , 2019, Nature Plants.

[20]  D. Bryant,et al.  Energy transfer from chlorophyll f to the trapping center in naturally occurring and engineered Photosystem I complexes , 2019, Photosynthesis Research.

[21]  S. Itoh,et al.  Theoretical Model of Exciton States and Ultrafast Energy Transfer in Heliobacterial Type I Homodimeric Reaction Center. , 2018, The journal of physical chemistry. B.

[22]  N. Nelson,et al.  Structure and function of wild-type and subunit-depleted photosystem I in Synechocystis. , 2018, Biochimica et biophysica acta. Bioenergetics.

[23]  T. Friedrich,et al.  Photosynthesis supported by a chlorophyll f-dependent, entropy-driven uphill energy transfer in Halomicronema hongdechloris cells adapted to far-red light , 2018, Photosynthesis Research.

[24]  S. Santabarbara,et al.  Photochemistry beyond the red limit in chlorophyll f–containing photosystems , 2018, Science.

[25]  Jian-Ren Shen,et al.  Unique organization of photosystem I–light-harvesting supercomplex revealed by cryo-EM from a red alga , 2018, Proceedings of the National Academy of Sciences.

[26]  S. Itoh,et al.  Light-Induced Electron Spin-Polarized (ESP) EPR Signal of the P800+ Menaquinone- Radical Pair State in Oriented Membranes of Heliobacterium modesticaldum: Role/Location of Menaquinone in the Homodimeric Type I Reaction Center. , 2018, The journal of physical chemistry. B.

[27]  Hiroshi Ishikita,et al.  Absorption-energy calculations of chlorophyll a and b with an explicit solvent model , 2017 .

[28]  R. Fromme,et al.  Structure of a symmetric photosynthetic reaction center–photosystem , 2017, Science.

[29]  Gabriel F. Dorlhiac,et al.  Femtosecond Visible Transient Absorption Spectroscopy of Chlorophyll f-Containing Photosystem I , 2017, Biophysical journal.

[30]  M. Pessarakli Handbook of Photosynthesis, Third Edition , 2016 .

[31]  C. Simmerling,et al.  ff14SB: Improving the Accuracy of Protein Side Chain and Backbone Parameters from ff99SB. , 2015, Journal of chemical theory and computation.

[32]  N. Nelson,et al.  Structure and energy transfer in photosystems of oxygenic photosynthesis. , 2015, Annual review of biochemistry.

[33]  Jian-Ren Shen,et al.  Structural basis for energy transfer pathways in the plant PSI-LHCI supercomplex , 2015, Science.

[34]  D. Bryant,et al.  Extensive remodeling of a cyanobacterial photosynthetic apparatus in far-red light , 2014, Science.

[35]  Alán Aspuru-Guzik,et al.  Advances in molecular quantum chemistry contained in the Q-Chem 4 program package , 2014, Molecular Physics.

[36]  H. Miyashita,et al.  Discovery of Chlorophyll d in Acaryochloris marina and Chlorophyll f in a Unicellular Cyanobacterium, Strain KC1, Isolated from Lake Biwa , 2014 .

[37]  Jian-Ren Shen,et al.  Photosystem II Does Not Possess a Simple Excitation Energy Funnel: Time-Resolved Fluorescence Spectroscopy Meets Theory , 2013, Journal of the American Chemical Society.

[38]  T. Renger,et al.  Theory of excitonic couplings in dielectric media , 2011, Photosynthesis Research.

[39]  Keisuke Kawakami,et al.  Crystal structure of oxygen-evolving photosystem II at a resolution of 1.9 Å , 2011, Nature.

[40]  H. Scheer,et al.  A Red-Shifted Chlorophyll , 2010, Science.

[41]  S. Itoh,et al.  Kinetically distinct three red chlorophylls in photosystem I of Thermosynechococcus elongatus revealed by femtosecond time-resolved fluorescence spectroscopy at 15 K. , 2010, The journal of physical chemistry. B.

[42]  T. Renger,et al.  Structure-based calculations of optical spectra of photosystem I suggest an asymmetric light-harvesting process. , 2010, Journal of the American Chemical Society.

[43]  S. Mukamel,et al.  Exciton delocalization and transport in photosystem I of cyanobacteria Synechococcus elongates: simulation study of coherent two-dimensional optical signals. , 2009, The journal of physical chemistry. B.

[44]  H. Miyashita,et al.  Unique photosystems in Acaryochloris marina , 2008, Photosynthesis Research.

[45]  Thomas Renger,et al.  Light harvesting in photosystem II core complexes is limited by the transfer to the trap: can the core complex turn into a photoprotective mode? , 2008, Journal of the American Chemical Society.

[46]  Tatsuya Uzumaki,et al.  Function of chlorophyll d in reaction centers of photosystems I and II of the oxygenic photosynthesis of Acaryochloris marina. , 2007, Biochemistry.

[47]  L. Valkunas,et al.  Red Chlorophylls in the Exciton Model of Photosystem I , 2005, Photosynthesis Research.

[48]  N. Handy,et al.  A new hybrid exchange–correlation functional using the Coulomb-attenuating method (CAM-B3LYP) , 2004 .

[49]  A. Larkum,et al.  Excitation dynamics in the core antenna in the photosystem I reaction center of the chlorophyll d-containing photosynthetic prokaryote acaryochloris marina , 2003 .

[50]  P. Fyfe,et al.  Type I photosynthetic reaction centres: structure and function. , 2003, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

[51]  K. Schulten,et al.  Robustness and Optimality of Light Harvesting in Cyanobacterial Photosystem I , 2002, physics/0207070.

[52]  Thomas Renger,et al.  On the relation of protein dynamics and exciton relaxation in pigment–protein complexes: An estimation of the spectral density and a theory for the calculation of optical spectra , 2002 .

[53]  Nathan A. Baker,et al.  Electrostatics of nanosystems: Application to microtubules and the ribosome , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[54]  Petra Fromme,et al.  Three-dimensional structure of cyanobacterial photosystem I at 2.5 Å resolution , 2001, Nature.

[55]  Q. Hu,et al.  A photosystem I reaction center driven by chlorophyll d in oxygenic photosynthesis. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[56]  Hideaki Miyashita,et al.  Chlorophyll d as a major pigment , 1996, Nature.

[57]  Mark S. Gordon,et al.  General atomic and molecular electronic structure system , 1993, J. Comput. Chem..

[58]  Alfred G. Redfield,et al.  On the Theory of Relaxation Processes , 1957, IBM J. Res. Dev..