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Temperature‐dependent changes in Photosystem II heterogeneity of attached leaves under high light
Author(s) -
Aro EvaMari,
Tyystjärvi Esa,
Nurmi Arja
Publication year - 1990
Publication title -
physiologia plantarum
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.351
H-Index - 146
eISSN - 1399-3054
pISSN - 0031-9317
DOI - 10.1111/j.1399-3054.1990.tb00029.x
Subject(s) - photoinhibition , thylakoid , cucurbita pepo , photosystem ii , biophysics , membrane , light intensity , electron transport chain , chemistry , photosynthesis , fluorescence , electron microscope , botany , chloroplast , biology , biochemistry , optics , gene , physics
Attached leaves of pumpkin ( Cucurbita pepo L. cv. Jattiläismeloni) were exposed to high light intensity at room temperature (ca 23°C) and at 1°C. Fluorescence parameters and electron transport activities measured from isolated thylakoids indicated faster photoinhibition of PSII at low temperature. Separation of the α and β components of the complementary area above the fluorescence induction curve of dichlorophenyl‐dimethylurea‐poisoned thylakoids revealed that at low temperature only the α‐centers declined during exposure to high light intensity while the content of functional β‐centers remained constant. Freeze‐fracture electron microscopy showed no decrease in the density of particles on the appressed exoplasmic fracture face, indicating that the photoinhibited α‐centers remained in the appressed membranes at 1°C. Because of the function of the repair and protective mechanisms of PSII, strong light induced less photoinhibition at room temperature, but more complicated changes occurred in the α/β‐heterogeneity of PSII. During the first 30 min at high light intensity the decrease in α‐centers was almost as large as at 1°C, but in contrast to the situation at low temperature the decrease in α‐centers was compensated for by a significant increase in PSIIβ‐centers. Changes in the density and size of freeze‐fracture particles suggest that this increase in β‐centers was due to migration of phosphorylated light‐harvesting complex from appressed to non‐appressed thylakoid membranes while the PSII core remained in the appressed membranes. This situation, however, was only transient and was followed by a rapid decrease in the functionalβ‐centers.