Measurement of photosynthesis in vivo with a leaf disc electrode: correlations between light dependence of steady-state photosynthetic O 2 evolution and chlorophyll a fluorescence transients

1986 ◽  
Vol 227 (1248) ◽  
pp. 267-280 ◽  

The application of a leaf disc electrode to the measurement of the quantum yield of photosynthetic oxygen evolution (in saturating carbon dioxide concentrations) is described. The technique was also used to characterize the light-saturation curves for photosynthesis in leaves of spinach plants grown in relatively low (‘shade’) and high (‘sun’) light intensities. It was found that the flux of a blue excitation light required to elicit oscillations in chlorophyll a fluorescence corresponded, approximately, to the flux of (white) light required to saturate photosynthetic oxygen evolution. The requirement was higher for leaves of sun-grown plants (approximately 800 μmol m -2 s -1 ) than for shade-grown plants (approximately 200 μmol m -2 s -1 ). Brief pretreatment of leaf discs from sun-grown plants with D-mannose did not change the quantum yield, but lowered the light saturated rate and the photon flux density required to saturate photosynthesis. Oscillations in fluorescence could then be observed at lower fluxes of blue excitation light, similar to those required by leaves from shade-grown plants. Photoinhibition of shade-grown plants (exposed to full sunlight for 5 h) reduced quantum yield and increased the light flux required for saturation of photosynthesis. Oscillations in fluorescence, normally observed at low fluxes of blue light in these leaves, could not be detected after photoinhibition. These correlations are interpreted and applications of the techniques described are discussed.

2020 ◽  
Author(s):  
Azeez Beebo ◽  
Ahmad Zia ◽  
Christopher R. Kinzel ◽  
Andrei Herdean ◽  
Karim Bouhidel ◽  
...  

SUMMARYPhotosynthetic oxygen evolution by photosystem II requires water supply into the chloroplast to reach the thylakoid lumen. A rapid water flow is also required into the chloroplast for optimal oxygen evolution and to overcome osmotic stress. The mechanisms governing water transport in chloroplasts are largely unexplored. Previous proteomics indicated the presence of three aquaporins from the tonoplast intrinsic protein (TIP) family, TIP1;1, TIP1;2 and TIP2;1, in chloroplast membranes of Arabidopsis thaliana. Here we revisited their location and studied their role in chloroplasts. Localization experiments indicated that TIP2;1 resides in the thylakoid, whereas TIP1;2 is present in both thylakoid and envelope membranes. Mutants lacking TIP1;2 and/or TIP2;1 did not display a macroscopic phenotype when grown under standard conditions. The mutant chloroplasts and thylakoids underwent less volume changes than the corresponding wild type preparations upon osmotic treatment and in the light. Significantly reduced rates of photosynthetic electron transport were obtained in the mutant leaves, with implications on the CO2 fixation rates. However, electron transport rates did not significantly differ between mutants and wild type when isolated thylakoids were examined. Less acidification of the thylakoid lumen was measured in mutants thylakoids, resulting in a slower induction of delta pH-dependent photoprotective mechanisms. These results identify TIP1;2 and TIP2;1 as chloroplast proteins and highlight their importance for osmoregulation and optimal photosynthesis. A third aquaporin, TIP1;1, is present in the chloroplast envelope, and may play role in photosynthesis under excessive light conditions, as based on the weak photosynthetic phenotype of its mutant.


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