Localization of protochlorophyll(ide) (Pchlide) forms and chlorophyllide (Chlide) transformation process were studied by using comparative analyses of de-convoluted 77 K fluorescence spectra of barley etioplast stroma and different membrane fractions obtained by sucrose gradient centrifugation. Non-photoactive 633 nm Pchlide form was mainly located in the envelope-prothylakoid membrane mixture while the photoactive 657 nm Pchlide was dominant pigment in the prolamellar body membrane and in the soluble etioplast fraction (stroma). When these fractions were exposed to a saturating flash, conversion of photoactive Pchlide into 697 nm Chlide was preferential in the prolamellar body and in the stroma, while the 676 nm Chlide was dominant pigment form in the envelope-prothylakoid fraction. These spectral characteristics are considered to reflect molecular composition and organization of the pigment-protein complexes specific for each etioplast compartment. and D. Kovacevic, D. Dewez, R. Popovic.
The changes in thermoluminescence (TL) signals induced by short-term ozone exposure of leaves are characterized by a down-shift of the peak-temperature of the TLB-band and an increase of a TL band at 55°C. We investigated the relationship of these changes to photosystem 2 (PS2) photochemistry. The changes were not only detectable in the presence of ozone, but also after irradiation of dark-adapted leaves and after aging of irradiated detached leaf segments. The opposite effect on TL, an up-shift of the peak-temperature of the B-band and the decrease of the intensity of the band at 55°C were found after infiltration of leaves with nigericin, antimycin A, and diphenyleneiodonium chloride (DPI). Propyl gallate down-shifted the peak-temperature of the B-band. 2,5-dimethyl-1,4-benzoquinone up-shifted the peak-temperature of the B-band and decreased the intensity of the 55°C band. The intensity of the 55°C band did not change significantly in the presence of oxygen in comparison to that in nitrogen atmosphere. It decreased with time of dark adaptation (50% intensity was observed after 3 h of dark adaptation at room temperature), however, it was reactivated to its initial value (at 5 min of dark adaptation) after 1 single-turnover flash. The 55°C band was not significantly changed in the presence of DCMU. Thus the ozone-induced band at 55°C is assigned to charge recombination in PS2. Changes in the electron transport chain at the acceptor side of PS2, probably related to the cyclic electron transport around photosystem 1 and/or chlororespiration, could play an important role in the increase of the 55°C band and the down-shift of the B-band. The changes at the acceptor side indicated by TL can be an ex pression of a physiological regulatory mechanism functional under stress conditions. and J. Skotnica ... [et al.].
UV screening by plant surfaces can be determined by exposing plant organs to UV radiation and measuring the chlorophyll (Chl) fluorescence elicited. From this fluorescence, the UV transmittance can be derived: the more intense the screening the lower the reporter Chl fluorescence and the lower the UV transmittance. The relationships between UV screening at 375 nm, as determined in the field by a portable UV-A-PAM fluorimeter, and UV screening at 314 and 360 nm, measured in the laboratory with the non-portable XE-PAM fluorimeter, were investigated in leaves of grapevine (Vitis vinifera L. cv. Bacchus) and barley (Hordeum vulgare cv. Ricarda), as well as in white grape berries. With leaves, linear trends were observed between XE-PAM measurements at 314 nm and UV-A-PAM measurements at 375 nm but the relationship between transmittance at 360 and 375 nm in barley was curved: a simple model calculation suggests that this curvi-linearity arises from particularly weak absorbance of barley flavonoids at 375 nm relative to absorbance at 360 nm. Transmittance values at 314 nm plotted against 375 nm yielded a much smaller slope in grapevine leaves than in barley leaves, which was attributed to screening in the short-wavelength UV by hydroxycinnamic acids in the former but not in the latter species. With grape berries, a poor correlation was detected between transmittances at 314 and 375 nm which might arise from high scattering of UV radiation at the berry surface. Such artefacts appear to be confined to the UV-B region, as berry transmittance at 360 nm correlated very well with that at 375 nm. Thus, assessment of UV screening in the field at short UV wavelengths using 375 nm readings from a UV-A-PAM fluorimeter is possible provided that information is available on the relationship between the transmittance at the UV wavelength of interest and at 375 nm for the sample tissue being investigated. and C. A. Kolb ... [et al.].