scholarly journals Chloroplast Movement in the Shade Plant Tradescantia albiflora Helps Protect Photosystem II against Light Stress

1996 ◽  
Vol 111 (3) ◽  
pp. 867-875 ◽  
Author(s):  
Y. I. Park ◽  
W. S. Chow ◽  
J. M. Anderson
2017 ◽  
Vol 114 (38) ◽  
pp. E8110-E8117 ◽  
Author(s):  
Jun Liu ◽  
Robert L. Last

Despite our increasingly sophisticated understanding of mechanisms ensuring efficient photosynthesis under laboratory-controlled light conditions, less is known about the regulation of photosynthesis under fluctuating light. This is important because—in nature—photosynthetic organisms experience rapid and extreme changes in sunlight, potentially causing deleterious effects on photosynthetic efficiency and productivity. Here we report that the chloroplast thylakoid lumenal protein MAINTENANCE OF PHOTOSYSTEM II UNDER HIGH LIGHT 2 (MPH2; encoded byAt4g02530) is required for growth acclimation ofArabidopsis thalianaplants under controlled photoinhibitory light and fluctuating light environments. Evidence is presented thatmph2mutant light stress susceptibility results from a defect in photosystem II (PSII) repair, and our results are consistent with the hypothesis that MPH2 is involved in disassembling monomeric complexes during regeneration of dimeric functional PSII supercomplexes. Moreover,mph2—and previously characterized PSII repair-defective mutants—exhibited reduced growth under fluctuating light conditions, while PSII photoprotection-impaired mutants did not. These findings suggest that repair is not only required for PSII maintenance under static high-irradiance light conditions but is also a regulatory mechanism facilitating photosynthetic adaptation under fluctuating light environments. This work has implications for improvement of agricultural plant productivity through engineering PSII repair.


2002 ◽  
Vol 357 (1426) ◽  
pp. 1441-1450 ◽  
Author(s):  
Wah Soon Chow ◽  
Hae–Youn Lee ◽  
Youn–Il Park ◽  
Yong–Mok Park ◽  
Yong–Nam Hong ◽  
...  

Photoinactivation of photosystem II (PSII), the light–induced loss of ability to evolve oxygen, is an inevitable event during normal photosynthesis, exacerbated by saturating light but counteracted by repair via new protein synthesis. The photoinactivation of PSII is dependent on the dosage of light: in the absence of repair, typically one PSII is photoinactivated per 10 7 photons, although the exact quantum yield of photoinactivation is modulated by a number of factors, and decreases as fewer active PSII targets are available. PSII complexes initially appear to be photoinactivated independently; however, when less than 30% functional PSII complexes remain, they seem to be protected by strongly dissipative PSII reaction centres in several plant species examined so far, a mechanism which we term ‘inactive PSII–mediated quenching‘. This mechanism appears to require a pH gradient across the photosynthetic membrane for its optimal operation. The residual fraction of functional PSII complexes may, in turn, aid in the recovery of photoinactivated PSII complexes when conditions become less severe. This mechanism may be important for the photosynthetic apparatus in extreme environments such as those experienced by over–wintering evergreen plants, desert plants exposed to drought and full sunlight and shade plants in sustained sunlight.


1973 ◽  
Vol 12 (2) ◽  
pp. 391-401
Author(s):  
R. MACHE ◽  
S. LOISEAUX

The growth rate of the shade plant Marchantia was at its maximum for a low illumination, 2-3 x 103 lx, and was inhibited by an excess of light. Photosynthesis by intact thalli and by isolated chloroplasts of Marchantia was saturated by a light intensity of 2-3 x 103 lx. These isolated chloroplasts were able to carry on satisfactory rates of photosynthesis, up to 35 µM CO2/h/mg chlorophyll. The Hill reaction and photosystem II were also saturated by the same light intensities, demonstrating that the factor limiting the light saturation of photosynthesis is located in the chloroplast. The structure of chloroplasts was strongly modified by an excess of light, small grana and fret membranes being replaced by continuous grana.


2010 ◽  
Vol 61 (10) ◽  
pp. 2707-2717 ◽  
Author(s):  
K. S. Gould ◽  
D. A. Dudle ◽  
H. S. Neufeld

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