In this article, the effects of increased light intensities on antioxidant metabolism during ex vitro establishment of Ulmus minor micropropagated plants are investigated. Three month old in vitro plants were acclimatized to ex vitro conditions in a climate chamber with two different light intensities, 200 μmol m-2 s-1 (high light, HL) and 100 μmol m-2 s-1 (low light, LL) during 40 days. Immediately after ex vitro transfer, the increase of both malondialdehyde (MDA) and electrolyte leakage in persistent leaves is indicative of oxidative stress. As the acclimatization continues, an upregulation of the superoxide dismutase (SOD), catalase (CAT), and glutathione reductase (GR) enzyme activities were also observed. Simultaneously, MDA content and membrane permeability stabilized, suggesting that the antioxidant enzymes decrease the deleterious effects of reactive oxygen species (ROS) generation. Unexpectedly, newly formed leaves presented a different pattern of antioxidative profile, with high levels of MDA and membrane leakage and low antioxidant enzyme activity. Despite these differences, both leaf types looked healthy (e.g. greenish, with no necrotic spots) during the whole acclimatization period. The results indicate that micropropagated U. minor plantlets develop an antioxidant enzyme system after ex vitro transfer and that, in general, LL treatment leads to lower oxidative stress. Moreover, new leaves tolerate higher levels of ROS without the need to activate the antioxidative pathway, which suggests that the environment at which leaves are exposed during its formation determinate their ability to tolerate ROS. and M. C. Dias, G. Pinto, C. Santos.
In vivo chlorophyll fluorescence analysis reflecting the photosystem II functionality was investigated in the cyanobacterium Anabaena variabilis PCC 7937 under simulated solar radiation in a combination with various cut-off filters (WG 280, WG 295, WG 305, WG 320, WG 335, WG 345, and GG 400) to assess the effects of photosynthetically active radiation (PAR), ultraviolet-A (UV-A), and ultraviolet-B (UV-B) radiations on photosynthesis. The photosynthetic activity (PA) was severely inhibited immediately after 10 min of exposure to high PAR, UV-A, and UV-B radiations compared with low PAR grown control samples. After 1 h of exposure, PA of 17.5 ± 2.9% was detected in the high PAR exposed samples compared with the control, while only a trace or no PA was observed in the presence of ultraviolet radiation (UVR). A recovery of PA was recorded after 2 h of the exposure, which continued for next 4, 8, 12, and 24 h. After 24 h of the exposure, PA of 57.5 ± 1.9%, 36.1 ± 11.7%, 23.5 ± 3.3%, 22.3 ± 5.2%, 20.8 ± 6.7%, 13.2 ± 6.6%, and 21.6 ± 9.5% was observed compared with the control sample in 400, 345, 335, 320, 305, 295, and 280 nm cut-off filters-covered samples, respectively. The relative electron transport rate, measured after 24 h exposure, showed also a disturbance in electron transfer between the two photosystems under the high PAR and UVR treatments relative to the control samples, suggesting the inhibition of photosynthesis. This study suggests that both high PAR and UVR inhibited the photosynthetic performance of A. variabilis PCC 7937 by damaging the photosynthetic apparatus, however, photoprotective mechanisms evolved by the organism allowed an immediate repair of ecologically important machinery, and enabled its survival., S. P. Singh ... [et al.]., and Obsahuje bibliografii