Photosynthesis in dynamic light: systems biology of unconventional chlorophyll fluorescence transients in Synechocystis sp. PCC 6803

2005 ◽  
Vol 84 (1-3) ◽  
pp. 99-106 ◽  
Author(s):  
Ladislav Nedbal ◽  
Vítězslav Březina ◽  
Jan Červený ◽  
Martin Trtílek
2016 ◽  
Vol 12 (8) ◽  
pp. 2552-2561 ◽  
Author(s):  
Reza Mohammadi ◽  
Jalil Fallah-Mehrabadi ◽  
Gholamreza Bidkhori ◽  
Javad Zahiri ◽  
Mohammad Javad Niroomand ◽  
...  

Metabolic network models can be optimized for the production of desired materials like biofuels.


1993 ◽  
Vol 35 (3) ◽  
pp. 305-310 ◽  
Author(s):  
Ren� K. Juhler ◽  
Mette Miller ◽  
David Simpson ◽  
Raymond P. Cox

1987 ◽  
Vol 84 (3) ◽  
pp. 748-752 ◽  
Author(s):  
Kenji Omasa ◽  
Ken-Ichiro Shimazaki ◽  
Ichiro Aiga ◽  
Walter Larcher ◽  
Morio Onoe

2016 ◽  
Vol 6 (1) ◽  
pp. 54-65 ◽  
Author(s):  
Michaela Marečková ◽  
Miloš Barták

Chlorophyll fluorescence is an effective tool for investigating characteristics of any photosynthesizing organisms and its responses due to different stressors. Here, we have studied a short-term temperature response on two Antarctic green algal lichen species: Umbilicaria antarctica, and Physconia muscigena. We measured slow chlorophyll fluorescence transients in the species during slow a cooling of thallus temperature from 20°C to 5°C with a 10 min. acclimation at each temperature in dark. The measurements were supplemented with saturation pulses for the analysis of chlorophyll fluorescence parameters: maximum yield of PS II photochemistry (FV/FM), effective quantum yield of PS II photochemistry (FPSII) and non-photochemical quenching (NPQ). In response to decreasing thallus temperature, we observed species-specific changes in chlorophyll fluorescence levels P, S, M, T reached during chlorophyll fluorescence transient as well as in the shape of the chlorophyll fluorescence transients. With a decrease in temperature, the time at which M and T chlorophyll fluorescence levels were reached, increased. These changes were attributed to redox state of plastoquinon pool, changes in Calvin-Benson cycle activity, non-photochemical quenching components, state transition in particular. In this study, we present some chlorophyll fluorescence ratios (P/M, M/T, P/T) and chlorophyll fluorescence increase rates (FR1, i.e. O to P, and FR2 - i.e. S to M) as the parameters reflecting direct temperature effects on chloroplastic apparatus of lichen alga sensitively. We proposed that species-specific changes in the slow phase of chlorophyll fluorescence transients could be potentially used as indicators of low temperature effects in photosynthetic apparatus of lichen algal photobionts. Interspecific differences in response to low temperature might be evaluated using the approach as well.


Life ◽  
2021 ◽  
Vol 11 (4) ◽  
pp. 279
Author(s):  
Hao Zhang ◽  
Haitao Ge ◽  
Ye Zhang ◽  
Yingchun Wang ◽  
Pengpeng Zhang

Upon exposure of photosynthetic organisms to high light (HL), several HL acclimation responses are triggered. Herein, we identified a novel gene, slr0320, critical for HL acclimation in Synechocystis sp. PCC 6803. The growth rate of the Δslr0320 mutant was similar to wild type (WT) under normal light (NL) but severely declined under HL. Net photosynthesis of the mutant was lower under HL, but maximum photosystem II (PSII) activity was higher under NL and HL. Immunodetection revealed the accumulation and assembly of PSII were similar between WT and the mutant. Chlorophyll fluorescence traces showed the stable fluorescence of the mutant under light was much higher. Kinetics of single flash‐induced chlorophyll fluorescence increase and decay revealed the slower electron transfer from QA to QB in the mutant. These data indicate that, in the Δslr0320 mutant, the number of functional PSIIs was comparable to WT even under HL but the electron transfer between QA and QB was inefficient. Quantitative proteomics and real‐time PCR revealed that expression profiles of psbL, psbH and psbI were significantly altered in the Δslr0320 mutant. Thus, Slr0320 protein plays critical roles in optimizing PSII activity during HL acclimation and is essential for PSII electron transfer from QA to QB.


Sign in / Sign up

Export Citation Format

Share Document