KINETICS OF S-2 AND S-3 REDUCTION BY TYROSINE-Y-D AND OTHER ENDOGENOUS DONORS AS A FUNCTION OF TEMPERATURE IN SPINACH PS-II MEMBRANE-FRAGMENTS WITH A RECONSTITUTED PLASTOQUINONE POOL
Ag. Seeliger et al., KINETICS OF S-2 AND S-3 REDUCTION BY TYROSINE-Y-D AND OTHER ENDOGENOUS DONORS AS A FUNCTION OF TEMPERATURE IN SPINACH PS-II MEMBRANE-FRAGMENTS WITH A RECONSTITUTED PLASTOQUINONE POOL, Biochemistry, 36(9), 1997, pp. 2459-2464
The characteristic period four oscillation patterns of oxygen evolutio
n induced by a train of single-turnover flashes were measured as a fun
ction of temperature in dark-adapted photosystem II (PS II) membrane f
ragments that were reconstituted with native plastoquinone-9 (PQ-9) by
a recently developed procedure [Kurreck, J., Seeliger, A. G., Reifart
h, F., Karge, M., & Renger, G. (1995) Biochemistry 34, 15721-15731]. T
he following results were obtained: (a) within the range 0-35 degrees
C, the probabilities of misses (alpha) and double-hits (beta) and the
dark population of redox state S-1 exhibit similar dependencies on the
temperature; (b) below a characteristic temperature upsilon(c) these
parameters remain virtually independent of temperature, above upsilon(
c) (upsilon(c) = 20 degrees C for alpha, and beta; upsilon(c) = 30 deg
rees C for S-1) the values of alpha and beta increase whereas S-1 decr
eases; and (c) the dark decay of S-2 and S-3 via fast and slow kinetic
s owing to reduction of the water oxidase by Y-D and other endogenous
electron donor(s), respectively, exhibits comparatively strong tempera
ture dependencies with the following activation energies: E(A)(S-2(fas
t)) = 60 +/- 10 kJ/mol, E(A)(S-3(fast)) = 55 +/- 10 kJ/mol, E(A)(S-2(s
low)) = 80 +/- 5 kJ/mol, and E(A)(S-3(slow)) = 75 +/- 5 kJ/mol. These
values of PQ-9 reconstituted PS II membrane fragments are very similar
to those that were previously reported for thylakoids [Messinger, J.,
Schroder, W. P., & Renger, G. (1993) Biochemistry 32, 7658-7668]. The
se findings reveal that the reaction coordinates of feeding electrons
by endogenous electron donors into the water oxidizing complex (WOC) t
hat attains the redox states S-2 and S-3 is virtually invariant to Tri
ton X-100 treatment used in the isolation procedure of PS II membrane
fragments from thylakoids. Implications of these findings are discusse
d.