Photosystem I photoinhibition induced by fluctuating light depends on background low light irradiance

2021 ◽  
Vol 181 ◽  
pp. 104298
Author(s):  
Shun-Ling Tan ◽  
Jia-Lin Huang ◽  
Feng-Ping Zhang ◽  
Shi-Bao Zhang ◽  
Wei Huang
Plants ◽  
2020 ◽  
Vol 9 (3) ◽  
pp. 316 ◽  
Author(s):  
Elias Kaiser ◽  
Dirk Walther ◽  
Ute Armbruster

The capacity of photoautotrophs to fix carbon depends on the efficiency of the conversion of light energy into chemical potential by photosynthesis. In nature, light input into photosynthesis can change very rapidly and dramatically. To analyze how genetic variation in Arabidopsis thaliana affects photosynthesis and growth under dynamic light conditions, 36 randomly chosen natural accessions were grown under uniform and fluctuating light intensities. After 14 days of growth under uniform or fluctuating light regimes, maximum photosystem II quantum efficiency (Fv/Fm) was determined, photosystem II operating efficiency (ΦPSII) and non-photochemical quenching (NPQ) were measured in low light, and projected leaf area (PLA) as well as the number of visible leaves were estimated. Our data show that ΦPSII and PLA were decreased and NPQ was increased, while Fv/Fm and number of visible leaves were unaffected, in most accessions grown under fluctuating compared to uniform light. There were large changes between accessions for most of these parameters, which, however, were not correlated with genomic variation. Fast growing accessions under uniform light showed the largest growth reductions under fluctuating light, which correlated strongly with a reduction in ΦPSII, suggesting that, under fluctuating light, photosynthesis controls growth and not vice versa.


2008 ◽  
Vol 191 (5) ◽  
pp. 1581-1586 ◽  
Author(s):  
Yurie Seino ◽  
Tomoko Takahashi ◽  
Yukako Hihara

ABSTRACT The coordinated high-light response of genes encoding subunits of photosystem I (PSI) is achieved by the AT-rich region located just upstream of the core promoter in Synechocystis sp. strain PCC 6803. The upstream element enhances the basal promoter activity under low-light conditions, whereas this positive regulation is lost immediately after the shift to high-light conditions. In this study, we focused on a high-light regulatory 1 (HLR1) sequence included in the upstream element of every PSI gene examined. A gel mobility shift assay revealed that a response regulator RpaB binds to the HLR1 sequence in PSI promoters. Base substitution in the HLR1 sequence or decrease in copy number of the rpaB gene resulted in decrease in the promoter activity of PSI genes under low-light conditions. These observations suggest that RpaB acts as a transcriptional activator for PSI genes. It is likely that RpaB binds to the HLR1 sequence under low-light conditions and works for positive regulation of PSI genes and for negative regulation of high-light-inducible genes depending on the location of the HLR1 sequence within target promoters.


Botany ◽  
2009 ◽  
Vol 87 (7) ◽  
pp. 712-721 ◽  
Author(s):  
Chuanjiu He ◽  
Fred T. Davies ◽  
Ronald E. Lacey

There are important engineering and crop production advantages in growing plants under hypobaric (reduced atmospheric pressure) conditions for extraterrestrial base or spaceflight environments. The objectives of this research were to determine the influence of hypobaria and reduced partial pressure of oxygen (pO2) (hypoxia) under low and high light irradiance on carbon dioxide (CO2) assimilation (CA), dark-period respiration (DPR), and the CO2 compensation and CO2 saturation points of lettuce (Lactuca sativa L. ‘Buttercrunch’). Plants were grown under variable total gas pressures [25 and 101 kPa (ambient)] at 6, 12, or 21 kPa pO2 (approximately the partial pressure in air at normal pressure). Light irradiance at canopy level of the low-pressure plant growth system (LPPG) was at 240 (low) or 600 (high) µmol·m–2·s–1. While hypobaria (25 kPa) had no effect on CA or the CO2 compensation point, it reduced the DPR and the CO2 saturation point, and increased the CA / DPR ratio. Hypoxia (6 kPa pO2) and low light reduced CA, DPR, and the CA / DPR ratio. Hypoxia decreased the CO2 compensation point regardless of total pressure. Hypoxia also decreased the the CO2 saturation point of ambient-pressure plants, but had no effect on hypobaric plants. While low light reduced the CO2 saturation point, it increased the CO2 compensation point, compared with high-light plants. The results show that hypobaric conditions of 25 kPa do not adversely affect gas exchange compared with ambient-pressure plants, and may be advantageous during hypoxic stress.


Plant Science ◽  
2021 ◽  
Vol 303 ◽  
pp. 110795
Author(s):  
Ying-Jie Yang ◽  
Shun-Ling Tan ◽  
Hu Sun ◽  
Jia-Lin Huang ◽  
Wei Huang ◽  
...  

2007 ◽  
Vol 189 (7) ◽  
pp. 2750-2758 ◽  
Author(s):  
Masayuki Muramatsu ◽  
Yukako Hihara

ABSTRACT Genes encoding subunits of photosystem I (PSI genes) in the cyanobacterium Synechocystis sp. strain PCC 6803 are actively transcribed under low-light conditions, whereas their transcription is coordinately and rapidly down-regulated upon the shift to high-light conditions. In order to identify the molecular mechanism of the coordinated high-light response, we searched for common light-responsive elements in the promoter region of PSI genes. First, the precise architecture of the psaD promoter was determined and compared with the previously identified structure of the psaAB promoter. One of two promoters of the psaAB genes (P1) and of the psaD gene (P2) possessed an AT-rich light-responsive element located just upstream of the basal promoter region. These sequences enhanced the basal promoter activity under low-light conditions, and their activity was transiently suppressed upon the shift to high-light conditions. Subsequent analysis of psaC, psaE, psaK1, and psaLI promoters revealed that their light response was also achieved by AT-rich sequences located at the −70 to −46 region. These results clearly show that AT-rich upstream elements are responsible for the coordinated high-light response of PSI genes dispersed throughout Synechocystis genome.


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