W. Einig et al., OZONE-INDUCED ACCUMULATION OF CARBOHYDRATES CHANGES ENZYME-ACTIVITIESOF CARBOHYDRATE-METABOLISM IN BIRCH LEAVES, New phytologist, 137(4), 1997, pp. 673-680
Birch cuttings (Betula pendula Roth) were grown in a sand-culture syst
em with two concentrations (0.05, HF and 0.005%, LF) of fertilizer con
taining macronutrients and micronutrients, and were exposed to 90/40 n
l l(-1) O-3 (day/night) and < 3 nl l(-1) O-3 (control) for one growing
season in the field fumigation chambers at Birmensdorf (Switzerland).
Leaves of different ages were analysed for gas exchange, contents of
chlorophyll, protein, and for metabolites as well as enzyme activities
of carbohydrate metabolism. Ozone reduced net photosynthesis and chlo
rophyll contents in mature leaves of both fertilization treatments, wh
ereas that of protein was only reduced in high-fertilized plants (HF).
However, net photosynthesis, chlorophyll, and protein increased in yo
ung leaves of low-fertilized plants (LF). The effects of ozone on enzy
me activities of carbohydrate metabolism were most pronounced in leave
s of LF plants. Specific activities of the sucrose-cleaving enzymes, s
ucrose synthase and alkaline invertase, were induced, whereas acid inv
ertase was unchanged. Extractable activity of sucrose phosphate syntha
se, which is a key enzyme of sucrose synthesis, was reduced. Levels of
fructose 2,6-bisphosphate, an inhibitor of sucrose synthesis, were in
creased in leaves of O-3/LF plants, but reduced in O-3/HF plants. In a
ddition, activities of enzymes involved in starch metabolism, ADP-gluc
ose pyrophosphorylase and starch phosphorylase, were lowered in ozone-
treated samples and the ratio of ATP:ADP was increased. It is conclude
d that chronic ozone exposure leads to an inhibition of sucrose synthe
sis and favours sucrose degradation. This effect is modulated by the n
utrient status of the plants, indicating higher O-3 tolerance in HF pl
ants. Furthermore, as the metabolic responses in the ozone-treated sam
ples resemble very closely those observed under end-product inhibition
of photosynthesis, we assume that the O-3 effect is mainly due to red
uced photosynthate export.