J. Brulfert et al., ENZYMATIC RESPONSES TO WATER-STRESS IN DETACHED LEAVES OF THE CAM PLANT KALANCHOE-BLOSSFELDIANA POELLN, Plant physiology and biochemistry, 31(4), 1993, pp. 491-497
Total extractable activity (''capacity'') of phosphoenolpyruvate carbo
xylase (EC 4.1.1.31, PEPC), phosphofructokinase (EC 2.7.1.1, PKF), ald
olase (EC 4.1.2.7), phosphoglycerate mutase (EC 5.4.2.1, PGM), enolase
(EC 4.2.1.11), glucose-6-phosphate dehydrogenase (EC 1.1.1.49, G-6-PD
H) and phenylalanine ammonia lyase (EC 4.3.1.5, PAL) was measured in l
eaves detached from the CAM plant Kalanchoe blossfeldiana grown under
long days (C3-performing). The isolated leaves were maintained 36 h un
der 280 mumol m-2 s-1 PAR, at 27-degrees-C, under drought (50% relativ
e air humidity). A 50% water deficit was brought about in the leaves b
y the treatment. Control leaves were kept with petioles immersed in wa
ter. Under water stress but not in the control leaves, the capacities
of PEPC, PGM and enolase showed a short-term and correlative increase.
Immunotitration techniques established that the increase in PEPC was
due to de novo synthesis of the enzyme. The capacity of PAL dropped un
der drought, following a kinetic inverse of that of PEPC. No effect of
the treatment could be demonstrated on PFK, aldolase and G-6-PDH. The
responses did not occur in darkness or under red light. Stomatal clos
ure in the water-stressed leaves resulted in depletion of the small ma
late pool present in the C3-performing leaves at the beginning of the
treatment. The increase in enzyme capacities was not followed by induc
tion of CAM operation. The results are a further demonstration that en
zymatic responses upon stress are triggered in the CAM pathway and in
the surrounding network as early steps preceding the actual CAM syndro
me.