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The Quenching of Long-Wavelength Fluorescence by the Closed Reaction Center in Photosystem I in Thermostichus vulcanus at 77 K

Akhtar, Parveen and van, Stokkum I.H.M. and Lambrev, Petar (2024) The Quenching of Long-Wavelength Fluorescence by the Closed Reaction Center in Photosystem I in Thermostichus vulcanus at 77 K. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 25 (22). No.-12430. ISSN 1661-6596

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Abstract

Photosystem I in most organisms contains long-wavelength or “Red” chlorophylls (Chls) absorbing light beyond 700 nm. At cryogenic temperatures, the Red Chls become quasi-traps for excitations as uphill energy transfer is blocked. One pathway for de-excitation of the Red Chls is via transfer to the oxidized RC (P700+), which has broad absorption in the near-infrared region. This study investigates the excitation dynamics of Red Chls in Photosystem I from the cyanobacterium Thermostichus vulcanus at cryogenic temperatures (77 K) and examines the role of the oxidized RC in modulating their fluorescence kinetics. Using time-resolved fluorescence spectroscopy, the kinetics of Red Chls were recorded for samples with open (neutral P700) and closed (P700+) RCs. We found that emission lifetimes in the range of 710–720 nm remained unaffected by the RC state, while more red-shifted emissions (>730 nm) decayed significantly faster when the RC was closed. A kinetic model describing the quenching by the oxidized RC was constructed based on simultaneous fitting to the recorded fluorescence emission in Photosystem I with open and closed RCs. The analysis resolved multiple Red Chl forms and variable quenching efficiencies correlated with their spectral properties. Only the most red-shifted Chls, with emission beyond 730 nm, are efficiently quenched by P700+, with rate constants of up to 6 ns−1. The modeling results support the notion that structural and energetic disorder in Photosystem I can have a comparable or larger effect on the excitation dynamics than the geometric arrangement of Chls. © 2024 by the authors.

Item Type: Article
Additional Information: HUN-REN Biological Research Centre, Temesvári krt. 62, Szeged, 6726, Hungary Department of Physics and Astronomy and LaserLaB, Faculty of Science, Vrije Universiteit Amsterdam, De Boelelaan 1081, Amsterdam, 1081 HV, Netherlands Export Date: 17 December 2024 Correspondence Address: Lambrev, P.H.; HUN-REN Biological Research Centre, Temesvári krt. 62, Hungary; email: akhtar.parveen@brc.hu Chemicals/CAS: chlorophyll, 1406-65-1, 15611-43-5; Chlorophyll; Photosystem I Protein Complex Funding details: Nemzeti Kutatási, Fejlesztési és Innovaciós Alap, NKFIA Funding details: Nemzeti Kutatási Fejlesztési és Innovációs Hivatal, NKFIH, FK-139067, ANN-144012, 2018-1.2.1-NKP-2018-00009 Funding details: Nemzeti Kutatási Fejlesztési és Innovációs Hivatal, NKFIH Funding details: Hungarian Research Network, HUN-REN, HUN-REN SA-76/2021 Funding details: Hungarian Research Network, HUN-REN Funding text 1: The work was supported by grants from the National Research, Development, and Innovation Fund (NKFI FK-139067 to P.A. and ANN-144012 and 2018-1.2.1-NKP-2018-00009 to P.L.) and the Hungarian Research Network (HUN-REN SA-76/2021 to P.A.).
Uncontrolled Keywords: chlorophyll; cyanobacteria; energy transfer; light harvesting; Thermosynechococcus vulcanus; time-resolved fluorescence
Subjects: Q Science / természettudomány > QH Natural history / természetrajz > QH301 Biology / biológia
Q Science / természettudomány > QH Natural history / természetrajz > QH301 Biology / biológia > QH3015 Molecular biology / molekuláris biológia
Q Science / természettudomány > QR Microbiology / mikrobiológia
SWORD Depositor: MTMT SWORD
Depositing User: MTMT SWORD
Date Deposited: 23 Jan 2025 14:00
Last Modified: 23 Jan 2025 14:00
URI: https://real.mtak.hu/id/eprint/214231

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