The PsbH protein belongs to a group of small protein subunits of photosystem II (PSII) complex. This protein is predicted to have a single transmembrane helix and it is important for the assembly of the PSII complex as well as for the proper function at the acceptor side of PSII. To identify the location of the PsbH subunit, the PSII complex with His-tagged PsbH protein was isolated from the cyanobacterium Synechocystis sp. PCC 6803 and labeled by Ni(2+)-nitrilo triacetic acid Nanogold. Electron microscopy followed by single particle image analysis identified the location of the labeled His-tagged PsbH protein at the periphery of the dimeric PSII complex. These results indicate that the N terminus of the PsbH protein is located at the stromal surface of the PSII complex and close to the CP47 protein.
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http://dx.doi.org/10.1016/j.jsb.2005.08.001 | DOI Listing |
Proc Natl Acad Sci U S A
January 2025
State Key Laboratory of Protein and Plant Genetic Engineering, School of Life Science, Peking University, Beijing 100871, People's Republic of China.
Phycobilisomes (PBS) are the major photosynthetic light-harvesting complexes in cyanobacteria and red algae. While the structures of PBS have been determined in atomic resolutions, how PBS are attached to the reaction centers of photosystems remains less clear. Here, we report that a linker protein (LcpA) is required for the attachment of PBS to photosystem II (PSII) in the cyanobacterium sp.
View Article and Find Full Text PDFPhysiol Plant
January 2025
Department of Plant Anatomy, Institute of Biology, Faculty of Science, ELTE Eötvös Loránd University, Budapest, Hungary.
Investigating the effects of drought stress and subsequent recovery on the structure and function of chloroplasts is essential to understanding how plants adapt to environmental stressors. We investigated Ctenanthe setosa (Roscoe) Eichler, an ornamental plant that can tolerate prolonged drought periods (40 and 49 days of water withdrawal). Conventional biochemical, biophysical, physiological and (ultra)structural methods combined for the first time in a higher plant with in vivo small-angle neutron scattering (SANS) were used to characterize the alterations induced by drought stress and subsequent recovery.
View Article and Find Full Text PDFPhotosynth Res
January 2025
State Key Laboratory of Forage Breeding-by-Design and Utilization, Key Laboratory of Photobiology, Institute of Botany, Chinese Academy of Sciences, Beijing, 100093, China.
Maize (Zea mays L.) performs highly efficient C photosynthesis by dividing photosynthetic metabolism between mesophyll and bundle sheath cells. In vivo physiological measurements are indispensable for C photosynthesis research as photosynthetic activities are easily interrupted by leaf section or cell isolation.
View Article and Find Full Text PDFInorg Chem
January 2025
Research School of Chemistry, Australian National University, Canberra, ACT 2601, Australia.
In this study, we apply TD-DFT and DFT calculations to explore the mechanistic details of O evolution in an artificial system that closely resembles Photosystem II (PSII). The reaction involves mononuclear Mn(III) complex [Mn(salpd)(OH)] and -benzoquinone under light-driven conditions. Our calculations reveal that the Schiff-base ligand salpd plays a crucial role in several key steps of the reaction, including the light-mediated oxidation of [Mn(salpd)(OH)] to [Mn(salpd)(OH)] by -benzoquinone, the subsequent oxidation of [Mn(salpd)(OH)] to the key Mn(V) intermediate [Mn(salpd)(O)], and the critical O-O bond formation step.
View Article and Find Full Text PDFPhysiol Plant
January 2025
Department of Horticulture, University of Georgia, Athens, GA, USA.
Optimizing photosynthetic lighting is essential for maximizing crop production and minimizing electricity costs in controlled environment agriculture (CEA). Traditional lighting methods often neglect the impact of environmental factors, crop type, and light acclimation on photosynthetic efficiency. To address this, a chlorophyll fluorescence-based biofeedback system was developed to adjust light-emitting diode (LED) intensity based on real-time plant responses, rather than using a fixed photosynthetic photon flux density (PPFD).
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