DOES THE FORMATION OF THE S-3-STATE IN CA2-DEPLETED PHOTOSYSTEM-II CORRESPOND TO AN OXIDATION OF TYROSINE-Z DETECTABLE BY CW-EPR AT ROOM-TEMPERATURE()

Citation
A. Boussac et Aw. Rutherford, DOES THE FORMATION OF THE S-3-STATE IN CA2-DEPLETED PHOTOSYSTEM-II CORRESPOND TO AN OXIDATION OF TYROSINE-Z DETECTABLE BY CW-EPR AT ROOM-TEMPERATURE(), Biochimica et biophysica acta. Bioenergetics, 1230(3), 1995, pp. 195-201
Citations number
31
Categorie Soggetti
Biology,Biophysics
ISSN journal
00052728
Volume
1230
Issue
3
Year of publication
1995
Pages
195 - 201
Database
ISI
SICI code
0005-2728(1995)1230:3<195:DTFOTS>2.0.ZU;2-S
Abstract
The tyrosine EPR signal(s) have been investigated at room temperature in Ca2+-depleted Photosystem II. It was found that at low, non-saturat ing microwave powers, the tyrosine signal present after flash illumina tion decayed monophasically in about 40% of the centers with a t(1/2) of 780 s. This decay is attributed to TyD degrees reduction. The radic al formed as the formal S-3 state and detected as a split EPR signal a t helium temperature, decayed monophasically at room temperature with a t(1/2) of 110 s. When the tyrosine EPR signals were monitored at roo m temperature using a high, saturating microwave power, in addition to the 780 s phase, a faster phase of 110 s was observed. This additiona l phase is attributed to TyrD degrees, the amplitude of which is enhan ced by dipolar coupling to the fast relaxing S-3 state. Its decay corr esponds to the loss of the fast relaxing S-3 species. Similar effects reported earlier and attributed to the formation of TyrZ degrees are r einterpreted as a relaxation enhancement of TyD degrees. No evidence w as found from this approach to attribute the split S-3 EPR signal to a TyrZ degrees signal which is detectable at room temperature.