A. Laisk et Ge. Edwards, OXYGEN AND ELECTRON FLOW IN C-4 PHOTOSYNTHESIS - MEHLER REACTION, PHOTORESPIRATION AND CO2 CONCENTRATION IN THE BUNDLE-SHEATH, Planta, 205(4), 1998, pp. 632-645
The photosynthetic linear electron transport rate in excess of that us
ed for CO2 reduction was evaluated in Sorghum bicolor Moench. [:NADP-m
alic enzyme (ME)-type C-4 plant], Amaranthus cruentus L. (NAD-ME-type
C-4 plant) and Helianthus annuus L. (C-3 plant) leaves at different CO
2 and O-2 concentrations. The electron transport rate (J(F)) was calcu
lated from fluorescence using the light partitioning factor (relative
PSII cross-section) determined under conditions where excess electron
transport was assumed to be negligible: low light intensities, 500 mu
mol CO2 mol(-1) and 2% O-2 Under high light intensities there was a la
rge excess of J(F)/4 at 10-100% O-2 in the C-3 plant due to photorespi
ration, but very little in sorghum and somewhat more in amaranth, show
ing that photorespiration is suppressed, more in the NADP-ME- and less
in the NAD-ME-type species. It is concluded that when C-4 photosynthe
sis is limited by supply of atmospheric CO2 to the C-4 cycle, the C3 c
ycle becomes limited by regeneration of ribulose 1,5-bisphosphate (RuB
P) which in turn limits RuBP oxygenase activity and photorespiration.
The rate of excess electron transport over that consumed for CO2 fixat
ion in C-4 plants was very sensitive to the presence of O-2 in the gas
phase, rapidly increasing between 0.01 and 0.1% O-2, and at 2% O-2 it
was about two-thirds of that at 21% O-2 This shows the importance of
the Mehler O-2 reduction as an electron sink, compared with photorespi
ration in C-4 plants. However, the rate of the Mehler reaction is stil
l too low to fully account for the extra ATP which is needed in C-4 ph
otosynthesis.