Abstract
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.
Highlights
To be able to survive in ever-changing environments is a critical biological need, and survival/acclimation strategies rely on complex regulatory processes
During longterm light acclimation cells optimize their light-harvesting antenna size and composition, and photosystem II (PSII)/photosystem I (PSI) ratios according to incident light conditions to poise the redox state of the electron transport chain, and especially of the PQ pool that transports electrons from PSII to downstream carriers (Fujita et al, 1994; Fujita, 1997; Dietzel et al, 2008)
Specific form of long-term light acclimation is cyanobacterial chromatic acclimation (CA), in which CA-capable cyanobacteria adjust the pigment composition in their PBS according to light quality (Tandeau de Marsac, 1977; Sanfilippo et al, 2019; see Introduction)
Summary
To be able to survive in ever-changing environments is a critical biological need, and survival/acclimation strategies rely on complex regulatory processes. Chromatic acclimation occurs in various freshwater and marine habitats and classified into six different types according to the changes in the pigment composition of the of the cyanobacterial light-harvesting antennae, the phycobilisomes (PBS) (Tandeau de Marsac, 1977; Gutu and Kehoe, 2012). We interpreted these properties as a signature of substantial excitonic decoupling induced by continuous weak light under certain physiological conditions This suggests that suboptimal photosynthetic performance of C. gracile cells grown under near far-red light is due to a solid redox- and/or signal-imbalance, which leads to the activation of this light acclimation process. We found wavelength-specific changes in cell morphology, pigment content, photoprotection, and photosynthetic efficiency, suggesting a high level of light utilization plasticity and previously unrecognized light acclimation strategies in C. gracile
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