Loading…

Spectroscopic Methods in Photosynthesis: Photosystem Stoichiometry and Chlorophyll Antenna Size

Light-induced absorbance change and fluorescence measurements were employed in the quantitation of photosystem stoichiometry and in the measurement of the chlorophyll (Chl) antenna size in thylakoid membranes. Results with thylakoid membranes from diverse photosynthetic tissues indicated a PSII/PSI...

Full description

Saved in:
Bibliographic Details
Published in:Philosophical transactions of the Royal Society of London. Series B, Biological sciences Biological sciences, 1989-04, Vol.323 (1216), p.397-409
Main Author: Melis, A.
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Light-induced absorbance change and fluorescence measurements were employed in the quantitation of photosystem stoichiometry and in the measurement of the chlorophyll (Chl) antenna size in thylakoid membranes. Results with thylakoid membranes from diverse photosynthetic tissues indicated a PSII/PSI reaction-centre stoichiometry that deviates from unity. Cyanobacteria and red algae have a PSII/PSI ratio in the range of 0.3 to 0.7. Chloroplasts from spinach and other vascular-plant species grown under direct sunlight have PSII/PSI = 1.8-t-0.3. Chlorophyll b-deficient and Chl b-lacking mutants have PSII/PSI > 2. The observation that PSII/PSI. ratios are not unity and show a large variation among different photosynthetic membranes appears to be contrary to the conventional assumption derived from the Z-scheme. However, the photosystem stoichiometry is not the only factor that needs to be taken into account to explain the coordination of the two photosystems in the process of linear electron transport. The light-harvesting capacity of each photosystem must also be considered. In cyanobacterial thylakoids (from Synechococcus 6301, PsII/PSI = 0.5 $\pm$ 0.2), the phycobilisome-PSII complexes collectively harvest as much light as the PSI complexes. In vascular plant chloroplasts, the light-harvesting capacity of a PSII complex (250 molecules, Chl a/Chl b = 1.7) is lower than that of a PSI complex (230 Chl, Chl a/Chl b = 8.0) because Chl b has a lower extinction coefficient than Chl a. A differential attenuation of light intensity through the grana further reduces the light absorbed by PSII. Hence, a PSII/PSI ratio greater than one in vascular-plant chloroplasts compensates for the lower absorption of light by individual PSII complexes and ensures that, on average, PSII will harvest about as much light as PSI. In conclusion, distinct light-harvesting strategies among diverse plant species complement widely different photosystem stoichiometries to ensure a balanced absorption of light and a balanced electron flow between the two photoreactions, thereby satisfying the requirement set forth upon the formulation of the Z-scheme by Hill & Bendall (Nature, Lond. 186, 136-137 (1960)) and by Duysens, Amesz & Kamp (Nature, Lond. 190, 510-511 (1961)).
ISSN:0962-8436
0080-4622
1471-2970
2054-0280
DOI:10.1098/rstb.1989.0019