Correlations between the temperature dependence of chlorophyll fluorescence and the fluidity of thylakoid membranes

To monitor changes in membrane fluidity in Arabidopsis leaves and thylakoid membranes, we investigated the temperature dependence of a chlorophyll fluorescence parameter, minimum fluorescence (Fo), and calculated the threshold temperature [T(Fo)] at which the rise of the fluorescence level Fo was considered to be started. For the modification of membrane fluidity we took three different approaches: (1) an examination of wild-type leaves initially cultured at room temperature (22 degrees C), then exposed to either a lower (4 degrees C) or higher (35 degrees C) temperature for 5days; (2) measurements of the shift in T(Fo) by two mutants deficient in fatty acid desaturase genes fad7 and fad7fad8 and (3) an evaluation of the performance of wild-type plants when leaves were infiltrated with chemicals that modify fluidity. When wild-type plants were grown at 22 degrees C, the T(Fo) was 48.3 +/- 0.3 degrees C. Plants that were then transferred to a chamber set at 4 or 35 degrees C showed a shift in their T(Fo) to 42.7 +/- 0.9 degrees C or 48.9 +/- 0.1 degrees C, respectively. Under low-temperature acclimation, the decline in this putative transition temperature was significantly less in fad7 and fad7fad8 mutants compared with the wild-type. In both leaf and thylakoid samples, values for T(Fo) were reduced in samples treated with benzyl alcohol, a membrane fluidizer, whereas T(Fo) rose in samples treated with dimethylsulfoxide, a membrane rigidifier. These results indicate that the heat-induced rise of chlorophyll fluorescence is strongly correlated with the fluidity of thylakoid membranes.