TY - JOUR
T1 - Irreversible photoinhibition of photosystem II is caused by exposure of Synechocystis cells to strong light for a prolonged period
AU - Allakhverdiev, Suleyman I.
AU - Tsvetkova, Nelly
AU - Mohanty, Prasanna
AU - Szalontai, Balász
AU - Byoung, Yong Moon
AU - Debreczeny, Mónika
AU - Murata, Norio
N1 - Funding Information:
The authors are grateful to Prof. Kimiyuki Satoh of Okayama University and Prof. Eva-Mari Aro of Turku University for their generous gifts of antibodies against the D1 and D2 proteins, respectively. This work was supported, in part, by an Invitation Fellowship for Research in Japan from the Japan Society for the Promotion of Science (to S.I.A.), and by grants from the Hungarian Science Foundation (OTKA O31973 and 043425) to M.D. and B.S.
PY - 2005/7/15
Y1 - 2005/7/15
N2 - Irreversible photoinhibition of photosystem II (PSII) occurred when Synechocystis sp. PCC 6803 cells were exposed to very strong light for a prolonged period. When wild-type cells were illuminated at 20°C for 2 h with light at an intensity of 2,500 μmol photons m-2 s-1, the oxygen-evolving activity of PSII was almost entirely and irreversibly lost, whereas the photochemical reaction center in PSII was inactivated only reversibly. The extent of irreversible photoinhibition was enhanced at lower temperatures and by the genetically engineered rigidification of membrane lipids. Western and Northern blotting demonstrated that, after cells had undergone irreversible photoinhibition, the precursor to D1 protein in PSII was synthesized but not processed properly. These observations may suggest that exposure of Synechocystis cells to strong light results in the irreversible photoinhibition of the oxygen-evolving activity of PSII via impairment of the processing of pre-D1 and that this effect of strong light is enhanced by the rigidification of membrane lipids.
AB - Irreversible photoinhibition of photosystem II (PSII) occurred when Synechocystis sp. PCC 6803 cells were exposed to very strong light for a prolonged period. When wild-type cells were illuminated at 20°C for 2 h with light at an intensity of 2,500 μmol photons m-2 s-1, the oxygen-evolving activity of PSII was almost entirely and irreversibly lost, whereas the photochemical reaction center in PSII was inactivated only reversibly. The extent of irreversible photoinhibition was enhanced at lower temperatures and by the genetically engineered rigidification of membrane lipids. Western and Northern blotting demonstrated that, after cells had undergone irreversible photoinhibition, the precursor to D1 protein in PSII was synthesized but not processed properly. These observations may suggest that exposure of Synechocystis cells to strong light results in the irreversible photoinhibition of the oxygen-evolving activity of PSII via impairment of the processing of pre-D1 and that this effect of strong light is enhanced by the rigidification of membrane lipids.
KW - D1 protein
KW - Photodamage
KW - Photosystem II
KW - Synechocystis
UR - http://www.scopus.com/inward/record.url?scp=21744436441&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=21744436441&partnerID=8YFLogxK
U2 - 10.1016/j.bbabio.2005.05.006
DO - 10.1016/j.bbabio.2005.05.006
M3 - Article
C2 - 15950925
AN - SCOPUS:21744436441
SN - 0005-2728
VL - 1708
SP - 342
EP - 351
JO - Biochimica et Biophysica Acta - Bioenergetics
JF - Biochimica et Biophysica Acta - Bioenergetics
IS - 3
ER -