Abstract

ABSTRACTThe fluorescence yield of chlorophyll(ide) (Chl[ide]) excited by weak modulated light was recorded at room temperature during a 2 h period after a short actinic light pulse that transformed all photoactive protochlorophyllide in dark‐grown barley leaves. A typical pattern of fluorescence yield variations was found whatever the age of the leaf but with age‐dependent changes in rates. Its successive phases were related to the Chl(ide) spectral shifts observed in low‐temperature emission spectra. The fluorescence yield started at a high level and strongly declined during the formation of Chlide695 from Chlide668 within a few seconds. It increased to a transient maximum during the Shibata shift (15–25 min) that resulted in Chl(ide)682. A final, slow decrease to a steady state occurred during the final red shift to Chl685. Pretreatments with δ‐aminolevulinic acid, chloramphenicol or 1, 10‐phenanthroline resulted in correlated modifications of Chl(ide) fluorescence yield transients and shifts of the low‐temperature Chl(ide) emission band. The complex response of the final decrease phase of the fluorescence yield to these compounds suggests that it results both from the assembly of photosynthetic Chl proteins and from the reorganization of the etioplast membrane system. From these results it is concluded that continuous recordings of Chl(ide) fluorescence yield after a short light pulse represent a useful tool to monitor the kinetics of pigment–protein organization and primary thylakoid assembly triggered by Pchlide photoreduction.

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