CHANGES OF CHLOROPHYLL(IDE) FLUORESCENCE YIELD INDUCED BY A SHORT LIGHT-PULSE AS A PROBE TO MONITOR THE EARLY STEPS OF ETIOPLAST PHOTOTRANSFORMATION IN DARK-GROWN LEAVES
P. Eullaffroy et al., CHANGES OF CHLOROPHYLL(IDE) FLUORESCENCE YIELD INDUCED BY A SHORT LIGHT-PULSE AS A PROBE TO MONITOR THE EARLY STEPS OF ETIOPLAST PHOTOTRANSFORMATION IN DARK-GROWN LEAVES, Photochemistry and photobiology, 67(6), 1998, pp. 676-682
The fluorescence yield of chlorophyll(ide) (ChI[ide]) excited by weak
modulated light was recorded at room temperature during a 2 h period a
fter a short actinic light pulse that transformed all photoactive prot
ochlorophyllide in dark-grown barley leaves. A typical pattern of fluo
rescence yield variations was found whatever the age of the leaf but w
ith 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 d
eclined during the formation of Chlide(695) from Chlide(688) within a
few seconds. It increased to a transient maximum during the Shibata sh
ift (15-25 min) that resulted in ChI(ide)(682). A final, slow decrease
to a steady state occurred during the final red shift to ChI(685). Pr
etreatments with delta-aminolevulinic acid, chloramphenicol or 1,10-ph
enanthroline resulted in correlated modifications of Chl(ide) fluoresc
ence yield transients and shifts of the low-temperature Chl(ide) emiss
ion band. The complex response of the final decrease phase of the fluo
rescence yield to these compounds suggests that it results both from t
he assembly of photosynthetic Chi proteins and from the reorganization
of the etioplast membrane system. From these results it is concluded
that continuous recordings of CN(ide) fluorescence yield after a short
light pulse represent a useful tool to monitor the kinetics of pigmen
t-protein organization and primary thylakoid assembly triggered by Pch
lide photoreduction.