Photoinhibition of photosynthesis in intact kiwifruit (Actinidia deliciosa) leaves: Effect of light during growth on photoinhibition and recovery

Planta ◽  
1988 ◽  
Vol 175 (3) ◽  
pp. 355-363 ◽  
Author(s):  
D. H. Greer ◽  
W. A. Laing
1988 ◽  
Vol 15 (2) ◽  
pp. 195 ◽  
Author(s):  
DH Greer

Photoinhibition of photosynthesis was induced in intact leaves of kiwifruit (Actinidia deliciosa) grown in natural light not exceeding a photon irradiance (PI) of 300 �mol m-2 s-1 by exposing them to a PI of 1500 �mol m-2 s-1. The temperature was held constant during the high-light exposure between 5 and 35°C. Recovery was followed at temperatures between 10 and 35°C, after photoinhibition was induced by a 240 min exposure to high light. The kinetics of photoinhibition and recovery were followed by chlorophyll fluorescence at 692 nm and 77K. Photoinhibition occurred at all temperatures but was greatest at low temperatures. Temperature affected the severity of photoinhibitory damage but not the kinetics of photoinhibition. Recovery was also temperature-dependent with little or no recovery occurring below about 20°C and rapid recovery at 30-35°C. The extent of photoinhibition also affected the rates of recovery which were reduced as the severity of photoinhibition increased. An analysis of the rate constants for energy transfer within photosystem II indicated that kiwifruit leaves have some capacity to prevent photoinhibition by increasing the amount of non-radiative energy dissipation. However, the analysis also indicates that this protection mechanism was not wholly effective since the primary photochemical reactions apparently become inactivated during exposure of these leaves to high light.


1986 ◽  
Vol 126 (2-3) ◽  
pp. 195-205 ◽  
Author(s):  
Dagfrid Skogen ◽  
Rekha Chaturvedi ◽  
Fredrik Weidemann ◽  
Stein Nilsen

1993 ◽  
Vol 20 (1) ◽  
pp. 33 ◽  
Author(s):  
DH Greer ◽  
WA Laing ◽  
DJ Woolley

Photoinhibition of photosynthesis in kiwifruit [Actinidia deliciosa (A. Chev.) C. F. Liang et A. R. Ferguson] leaves in high light and its subsequent recovery in low light was assessed in the presence of chloramphenicol (CAP), an inhibitor of chloroplast-encoded protein synthesis. Rooted cuttings were grown in a controlled environment at a photosynthetic irradiance of 700 μmol m-2 s-1 and a day/night temperature of 25/20�C. Time-courses of photoinhibition and recovery treatments were followed by measuring CO2 exchange and chlorophyll fluorescence at 77K and 692 nm. CAP both exacerbated photoinhibition and blocked recovery for at least 150 min, especially at high temperatures. The close conformation of these two effects affirm that photoinhibition and recovery occur concomitantly. There was no apparent effect of CAP on the xanthophyll cycle, either during photoinhibition or recovery, indicating that zeaxanthin-mediated non-radiative energy (thermal) dissipation was unaffected by CAP. Because the CAP-induced increase in photoinhibition was not matched by an increase in the ratio of zeaxanthin to violaxanthin and antheraxanthin, the capacity of this photoprotective mechanism was apparently saturated. The primary effect of CAP on chlorophyll fluorescence was to affect Fm, the maximum fluorescence. There was only a minor effect on the initial fluorescence, Fo, during the photoinhibition and recovery treatments. The calculation of the rate constants for non-radiative dissipation (kD) and photochemistry (kp) from the fluorescence measurements indicated that an increase in kD occurred during high-light exposures and this was stimulated by CAP. However, since zeaxanthin was not mediating this, an alternative quencher in kiwifruit leaves, perhaps damaged PSII centres, is proposed. This would be consistent with an increased inactivation of PSII, as indicated by the changes in kp.


Author(s):  
C. S. Bricker ◽  
S. R. Barnum ◽  
B. Huang ◽  
J. G. Jaworskl

Cyanobacteria are Gram negative prokaryotes that are capable of oxygenic photosynthesis. Although there are many similarities between eukaryotes and cyanobacteria in electron transfer and phosphorylation during photosynthesis, there are two features of the photosynthetic apparatus in cyanobacteria which distinguishes them from plants. Cyanobacteria contain phycobiliproteins organized in phycobilisomes on the surface of photosynthetic membrane. Another difference is in the organization of the photosynthetic membranes. Instead of stacked thylakolds within a chloroplast envelope membrane, as seen In eukaryotes, IntracytopIasmlc membranes generally are arranged in three to six concentric layers. Environmental factors such as temperature, nutrition and light fluency can significantly affect the physiology and morphology of cells. The effect of light Intensity shifts on the ultrastructure of Internal membrane in Anabaena variabilis grown under controlled environmental conditions was examined. Since a major constituent of cyanobacterial thylakolds are lipids, the fatty acid content also was measured and correlated with uItrastructural changes. The regulation of fatty acid synthesis in cyanobacteria ultimately can be studied if the fatty acid content can be manipulated.


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