Monitoring Photosynthesis in Individual Cells of Synechocystis sp. PCC 6803 on a Picosecond Timescale

Autor: Sashka Krumova, G. Ajlani, Zoltán Gombos, Sergey P. Laptenok, H. van Amerongen, Bettina Ughy, Jan Willem Borst
Přispěvatelé: Système membranaires, photobiologie, stress et détoxication (SMPSD), Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Centre National de la Recherche Scientifique (CNRS), Institut de Biologie Intégrative de la Cellule (I2BC), Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université Paris-Saclay-Centre National de la Recherche Scientifique (CNRS)
Rok vydání: 2010
Předmět:
0106 biological sciences
spectroscopy
Time Factors
Photosystem II
Kinetics
Spectroscopy
Imaging
and Other Techniques

Biophysics
Biochemie
synechococcus 6301
macromolecular substances
Biology
Photosynthesis
Photosystem I
Photochemistry
01 natural sciences
Biochemistry
intact photosystem-ii
03 medical and health sciences
excitation-energy transfer
Phycobilisomes
chlorophyll
time
030304 developmental biology
0303 health sciences
Photosystem I Protein Complex
Synechocystis
Photosystem II Protein Complex
food and beverages
[SDV.BBM.BM]Life Sciences [q-bio]/Biochemistry
Molecular Biology/Molecular biology

thylakoid membrane
biology.organism_classification
[SDV.MP.BAC]Life Sciences [q-bio]/Microbiology and Parasitology/Bacteriology
phycobilisome
fluorescence emission-spectra
Biofysica
Microscopy
Fluorescence

kinetics
Thylakoid
Picosecond
Mutation
Phycobilisome
010606 plant biology & botany
Zdroj: Biophysical Journal
Biophysical Journal, 2010, 99 (6), pp.2006-2015. ⟨10.1016/j.bpj.2010.07.015⟩
Biophysical Journal 99 (2010) 6
Biophysical Journal, 99(6), 2006-2015
ISSN: 0006-3495
1542-0086
DOI: 10.1016/j.bpj.2010.07.015
Popis: Picosecond fluorescence kinetics of wild-type (WT) and mutant cells of Synechocystis sp. PCC 6803, were studied at the ensemble level with a streak-camera and at the cell level using fluorescence-lifetime-imaging microscopy (FLIM). The FLIM measurements are in good agreement with the ensemble measurements, but they (can) unveil variations between and within cells. The BE mutant cells, devoid of photosystem II (PSII) and of the light-harvesting phycobilisomes, allowed the study of photosystem I (PSI) in vivo for the first time, and the observed 6-ps equilibration process and 25-ps trapping process are the same as found previously for isolated PSI. No major differences are detected between different cells. The PAL mutant cells, devoid of phycobilisomes, show four lifetimes: similar to 20 Ps (PSI and PSII), similar to 80 ps, similar to 440 ps, and 2.8 ns (all due to PSII), but not all cells are identical and variations in the kinetics are traced back to differences in the PSI/PSII ratio. Finally, FLIM measurements on WT cells reveal that in some cells or parts of cells, phycobilisomes are disconnected from PSI/PSII. It is argued that the FLIM setup used can become instrumental in unraveling photosynthetic regulation mechanisms in the future.
Databáze: OpenAIRE