The transfer of light energy from phycobilisomes (PBS) to photosystem II (PSII) reaction centers is vital for photosynthesis in cyanobacteria and red algae. To investigate the relationship between PBS and PSII and to optimize the energy transfer efficiency from PBS to PSII, isolation of the PBS-PSII supercomplex is necessary. SPC (sucrose/phosphate/citrate) is a conventional buffer for isolating PBS-PSII supercomplex in cyanobacteria. However, the energy transfer occurring in the supercomplex is poor. Here, we developed a new buffer named SGB by adding 1M glycinebetaine and additional sucrose to SPC buffer. Compared to SPC, the newly developed SGB buffer greatly enhanced the associated populations of PBS with thylakoid membranes and PSII and further improved the energy transfer efficiency from PBS to PSII reaction centers in cyanobacteria in vitro. Therefore, we conclude that SGB is an excellent buffer for isolating the PBS-PSII supercomplex and for enhancing the energy transfer efficiency from PBS to PSII reaction centers in cyanobacteria in vitro., L. P. Chen, Q. X. Wang, W. M. Ma., and Obsahuje bibliografii
Based on the crystal structure and spectral properties of C-phycocyanin (C-PC) from cyanobacteria, models for complexes with 2 and 3 C-PC hexamer disks were built and the energy transfer dynamic properties were studied by the use of stochastic computer simulation approach. In addition, an experimental parameter of 0.056 ps-1, corresponding to a time constant of 18 ps, derived from the previous time-resolved measurement, was used for simulation of the energy transfer process from the three terminal symmetrically equivalent β84 chromophores of the core-linked disk to an α84 chromophore of the allophycocyanin (APC) core. The simulation showed: (1) The disk-to-disk energy transfer can be as fast as several picoseconds. (2) The energy transfer efficiencies from the first disk to the core would depend on the length of the rod (i.e. the number of disks). Efficiencies of 0.95, 0.87, and 0.75 were found for the rods with 1, 2 and 3 hexamer disks, respectively. (3) The energy transfer along a rod in a native phycobilisome (PBS) is probably very close to the one-way manner. It is the core of PBS that makes the excitation energy be transferred fast in a nearly one-way manner. and Jie Xie, Jing-quan Zhao, Chenghang Peng.
Fluorescence spectroscopy at 77 K showed that the application of glucose lead to the depletion of phycobilisomes (PBS) and photosystems (PS) 2 and 1, and that PS2 was more sensitive to glucose than PS1. The application of sodium thiosulfate, an effective scavenger of reactive oxygen intermediates, counteracted the effects of glucose. Sodium thiosulfate effectively protected photosynthetic apparatus, PS2, PS1, and PBS against glucose-induced depletion. Sodium thiosulfate showed strong capability to inhibit the disappearance of chlorophyll induced by glucose. At a relatively low concentration of glucose, the application of sodium thiosulfate can even be helpful for the assembly of photosynthetic apparatus. Hence the reactive oxygen species might be involved in the depletion of the photosynthetic apparatus in the cyanobacterium Synechocystis sp. PCC 6803 cells grown in the presence of glucose. and Zeneng Wang ... [et al.].
Plants have developed various photoprotective mechanisms to resist irradiation stress. One of the photoprotective mechanisms described in the literature for LHC2-containing organisms involves a down-regulation of photosystem (PS) 2 occurring simultaneously with the build-up of a proton gradient across the thylakoid membrane (ΔpH). It is often correlated with deepoxidation of xanthophylls located in LHC2. In Rhodophyta instead of LHC2, the peripheral antenna of PS2 consists of a large extramembrane complex, the phycobilisome (PBS), which transfers its excitation to the core antennae of PS2 composed of the CP43 and CP47 protein-chlorophyll complexes and there is no xanthophyll cycle. In the red alga Rhodella violacea a ΔpH-dependent chlorophyll (Chl) a fluorescence quenching can be formed. We characterised this quenching, studied the effects of various irradiances and inhibitors. Under photoinhibitory conditions, the ΔpH-dependent Chl fluorescence quenching exerts a photoprotective role and delays the kinetics of photoinhibition. It is the first time that such a photoprotective mechanism is described in PBS-containing organisms. and M. Ritz, K. V. Neverov, A.-L. Etienne.