Hl. Macintyre et al., ACTIVATION AND DEACTIVATION OF RIBULOSE-1,5-BISPHOSPHATE CARBOXYLASE OXYGENASE (RUBISCO) IN 3 MARINE MICROALGAE/, Photosynthesis research, 51(2), 1997, pp. 93-106
The activity of ribulose-1,5-bisphosphate carboxylase/oxygenase (Rubis
co) was examined in three marine microalgae: the chlorophyte Dunaliell
a tertiolecta and the chromophytes Pavlova lutheri and Thalassiosira p
seudonana. The three species differed in the sensitivity of Rubisco ac
tivity in crude extracts to magnesium ion concentration, the presence
of protease inhibitors, the duration of the incubation on activity, an
d the potential for full activation of Rubisco with 20 mM magnesium ch
loride and 20 mM bicarbonate in vitro. D. tertiolecta had responses th
at were similar to those described in vascular plants: regulation of i
nitial activity on a gradient of irradiances; maximum initial activiti
es that were 80-90% of light-saturated photosynthesis; total activitie
s that exceeded light-saturated photosynthesis by 30-100%; and deactiv
ation of Rubisco in darkness. Both initial and total activity declined
in darkness and increased on a return to growth irradiance. First-ord
er time constants were about 9 min for deactivation and 3 min for reac
tivation of initial activity. The decline in total activity after a tr
ansition into darkness could not be reversed in vitro but could be rev
ersed by exposing D. tertiolecta to light, a characteristic of regulat
ion by CA1P. The responses of T pseudonana were qualitatively similar,
except that recovery of initial activity was low and could only accou
nt for 30-40% of light-saturated photosynthesis. Rubisco from T pseudo
nana exposed to low irradiance could be activated in vitro but at grow
th irradiance and higher, total activity was lower than initial activi
ty. The time constants for deactivation and reactivation of initial ac
tivity after reciprocal switches between growth irradiance and darknes
s were 12-18 min and 3 min in T pseudonana. T! lutheri showed no regul
ation of Rubisco activity in response to changes in irradiance or ligh
t-dark transitions. This may have been an artifact of the conditions c
hosen to measure activity.