Most cited article - PubMed ID 29090427
On the origin of the slow M-T chlorophyll a fluorescence decline in cyanobacteria: interplay of short-term light-responses
Cyanobacteria play a key role in primary production in both oceans and fresh waters and hold great potential for sustainable production of a large number of commodities. During their life, cyanobacteria cells need to acclimate to a multitude of challenges, including shifts in intensity and quality of incident light. Despite our increasing understanding of metabolic regulation under various light regimes, detailed insight into fitness advantages and limitations under shifting light quality remains underexplored. Here, we study photo-physiological acclimation in the cyanobacterium Synechocystis sp. PCC 6803 throughout the photosynthetically active radiation (PAR) range. Using light emitting diodes (LEDs) with qualitatively different narrow spectra, we describe wavelength dependence of light capture, electron transport and energy transduction to main cellular pools. In addition, we describe processes that fine-tune light capture, such as state transitions, or the efficiency of energy transfer from phycobilisomes to photosystems (PS). We show that growth was the most limited under blue light due to inefficient light harvesting, and that many cellular processes are tightly linked to the redox state of the plastoquinone (PQ) pool, which was the most reduced under red light. The PSI-to-PSII ratio was low under blue photons, however, it was not the main growth-limiting factor, since it was even more reduced under violet and near far-red lights, where Synechocystis grew faster compared to blue light. Our results provide insight into the spectral dependence of phototrophic growth and can provide the foundation for future studies of molecular mechanisms underlying light acclimation in cyanobacteria, leading to light optimization in controlled cultivations.
- Keywords
- Cyanobacteria, Light harvesting, Light quality, Photomorphogenesis, Photosynthesis, State transitions,
- MeSH
- Acclimatization * MeSH
- Photosynthesis * physiology MeSH
- Photosystem I Protein Complex metabolism MeSH
- Photosystem II Protein Complex metabolism MeSH
- Light * MeSH
- Synechocystis * physiology radiation effects metabolism growth & development MeSH
- Electron Transport MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Photosystem I Protein Complex MeSH
- Photosystem II Protein Complex MeSH
Winter oilseed rape (Brassica napus L.), the principal oilseed crop in Europe, is notably vulnerable to spring frosts that can drastically reduce yields in ways that are challenging to predict with standard techniques. Our research focused on evaluating the efficacy of photosynthetic efficiency analysis in this crop and identifying specific chlorophyll fluorescence parameters severely impacted by frost, which could serve as noninvasive biomarkers for yield decline. The experiments were carried out in semi-controlled conditions with several treatments: a control, one day at -3°C, three days at -3°C, one day at -6°C, and three days at -6°C. We employed continuous-excitation and pulse-amplitude-modulation chlorophyll fluorescence measurements to assess plant sensitivity to frost. Also, plant gas exchange and chlorophyll content index measurements were performed. Certain parameters strongly correlated with final yield losses, thereby establishing a basis for developing new agricultural protocols to predict and mitigate frost damage in rapeseed crops accurately.
- Keywords
- abiotic stresses, bioindicator, chlorophyll a fluorescence, noninvasive biomarkers, plant gas exchange, plant traits,
- Publication type
- Journal Article MeSH
Photomorphogenesis is a process by which photosynthetic organisms perceive external light parameters, including light quality (color), and adjust cellular metabolism, growth rates and other parameters, in order to survive in a changing light environment. In this study we comprehensively explored the light color acclimation of Cyanobium gracile, a common cyanobacterium in turbid freshwater shallow lakes, using nine different monochromatic growth lights covering the whole visible spectrum from 435 to 687 nm. According to incident light wavelength, C. gracile cells performed great plasticity in terms of pigment composition, antenna size, and photosystem stoichiometry, to optimize their photosynthetic performance and to redox poise their intersystem electron transport chain. In spite of such compensatory strategies, C. gracile, like other cyanobacteria, uses blue and near far-red light less efficiently than orange or red light, which involves moderate growth rates, reduced cell volumes and lower electron transport rates. Unfavorable light conditions, where neither chlorophyll nor phycobilisomes absorb light sufficiently, are compensated by an enhanced antenna size. Increasing the wavelength of the growth light is accompanied by increasing photosystem II to photosystem I ratios, which involve better light utilization in the red spectral region. This is surprisingly accompanied by a partial excitonic antenna decoupling, which was the highest in the cells grown under 687 nm light. So far, a similar phenomenon is known to be induced only by strong light; here we demonstrate that under certain physiological conditions such decoupling is also possible to be induced by weak light. This suggests that suboptimal photosynthetic performance of the near far-red light grown C. gracile cells is due to a solid redox- and/or signal-imbalance, which leads to the activation of this short-term light acclimation process. Using a variety of photo-biophysical methods, we also demonstrate that under blue wavelengths, excessive light is quenched through orange carotenoid protein mediated non-photochemical quenching, whereas under orange/red wavelengths state transitions are involved in photoprotection.
- Keywords
- cyanobacteria, imbalance, light-quality acclimation, photosynthesis, pigment composition,
- Publication type
- Journal Article MeSH
Cold acclimation modifies the photosynthetic machinery and enables plants to survive at sub-zero temperatures, whereas in warm habitats, many species suffer even at non-freezing temperatures. We have measured chlorophyll a fluorescence (ChlF) and CO2 assimilation to investigate the effects of cold acclimation, and of low temperatures, on a cold-sensitive Arabidopsis thaliana accession C24. Upon excitation with low intensity (40 µmol photons m- 2 s- 1) ~ 620 nm light, slow (minute range) ChlF transients, at ~ 22 °C, showed two waves in the SMT phase (S, semi steady-state; M, maximum; T, terminal steady-state), whereas CO2 assimilation showed a linear increase with time. Low-temperature treatment (down to - 1.5 °C) strongly modulated the SMT phase and stimulated a peak in the CO2 assimilation induction curve. We show that the SMT phase, at ~ 22 °C, was abolished when measured under high actinic irradiance, or when 3-(3, 4-dichlorophenyl)-1, 1- dimethylurea (DCMU, an inhibitor of electron flow) or methyl viologen (MV, a Photosystem I (PSI) electron acceptor) was added to the system. Our data suggest that stimulation of the SMT wave, at low temperatures, has multiple reasons, which may include changes in both photochemical and biochemical reactions leading to modulations in non-photochemical quenching (NPQ) of the excited state of Chl, "state transitions," as well as changes in the rate of cyclic electron flow through PSI. Further, we suggest that cold acclimation, in accession C24, promotes "state transition" and protects photosystems by preventing high excitation pressure during low-temperature exposure.
- Keywords
- 3-(3, 4-dichlorophenyl)-1, 1- dimethylurea, Chlorophyll fluorescence transients, Cold acclimation, Gas-exchange measurements, Low-temperature effect, Methyl viologen, Slow SMT fluorescence phase, State transition,
- MeSH
- Acclimatization MeSH
- Arabidopsis metabolism MeSH
- Chlorophyll A metabolism MeSH
- Photosynthesis physiology MeSH
- Cold Temperature MeSH
- Temperature MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Chlorophyll A MeSH