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1.
Microsc Microanal ; 19(3): 513-24, 2013 Jun.
Article in English | MEDLINE | ID: mdl-23551883

ABSTRACT

The effect of lead and copper on apical segments of Gracilaria domingensis was examined. Over a period of 7 days, the segments were cultivated with concentrations of 5 and 10 ppm under laboratory conditions. The samples were processed for light, confocal, and electron microscopy, as well as histochemistry, to evaluate growth rates, mitochondrial activity, protein levels, chlorophyll a, phycobiliproteins, and carotenoids. After 7 days of exposure to lead and copper, growth rates were slower than control, and biomass loss was observed on copper-treated plants. Ultrastructural damage was primarily observed in the internal organization of chloroplasts and cell wall thickness. X-ray microanalysis detected lead in the cell wall, while copper was detected in both the cytoplasm and cell wall. Moreover, lead and copper exposure led to photodamage of photosynthetic pigments and, consequently, changes in photosynthesis. However, protein content and glutathione reductase activity decreased only in the copper treatments. In both treatments, decreased mitochondrial NADH dehydrogenase activity was observed. Taken together, the present study demonstrates that (1) heavy metals such as lead and copper negatively affect various morphological, physiological, and biochemical processes in G. domingensis and (2) copper is more toxic than lead in G. domingensis.


Subject(s)
Copper/toxicity , Gracilaria/drug effects , Lead/toxicity , Biomass , Carotenoids/analysis , Cell Wall/chemistry , Cell Wall/drug effects , Cell Wall/ultrastructure , Chlorophyll/analysis , Chlorophyll A , Chloroplasts/drug effects , Chloroplasts/ultrastructure , Copper/analysis , Cytoplasm/chemistry , Electron Probe Microanalysis , Gracilaria/growth & development , Gracilaria/metabolism , Gracilaria/ultrastructure , Lead/analysis , Microscopy , Mitochondria/drug effects , Mitochondria/metabolism , Mitochondria/ultrastructure , NADH Dehydrogenase/metabolism , Photosynthesis/drug effects , Phycobiliproteins/analysis
2.
Microsc Microanal ; 18(6): 1467-79, 2012 Dec.
Article in English | MEDLINE | ID: mdl-23153514

ABSTRACT

We undertook a study of Porphyra acanthophora var. brasiliensis to determine its responses under ambient conditions, photosynthetically active radiation (PAR), and PAR+UVBR (ultraviolet radiation-B) treatment, focusing on changes in ultrastructure, and cytochemistry. Accordingly, control ambient samples were collected in the field, and two different treatments were performed in the laboratory. Plants were exposed to PAR at 60 µmol photons m-2 s-1 and PAR + UVBR at 0.35 W m-2 for 3 h per day during 21 days of in vitro cultivation. Confocal laser scanning microscopy analysis of the vegetative cells showed single stellate chloroplast in ambient and PAR samples, but in PAR+UVBR-exposed plants, the chloroplast showed alterations in the number and form of arms. Under PAR+UVBR treatment, the thylakoids of the chloroplasts were disrupted, and an increase in the number of plastoglobuli was observed, in addition to mitochondria, which appeared with irregular, disrupted morphology compared to ambient and PAR samples. After UVBR exposure, the formation of carpospores was also observed. Plants under ambient conditions, as well as those treated with PAR and PAR+UVBR, all showed different concentrations of enzymatic response, including glutathione peroxidase and reductase activity. In summary, the present study demonstrates that P. acanthophora var. brasiliensis shows the activation of distinct mechanisms against natural radiation, PAR and PAR+UVBR.


Subject(s)
Chloroplasts/metabolism , Chloroplasts/radiation effects , Porphyra/metabolism , Porphyra/radiation effects , Ultraviolet Rays , Carotenoids/analysis , Cell Shape/radiation effects , Cell Wall/metabolism , Chlorophyll/analysis , Chlorophyll A , Cytoplasm/metabolism , Enzyme Activation , Enzyme Assays , Glutathione Peroxidase/metabolism , Microscopy, Confocal/methods , Mitochondria/metabolism , Mitochondria/radiation effects , NADH Dehydrogenase , Organelle Shape/radiation effects , Photons , Photosynthesis , Plant Cells/metabolism , Porphyra/enzymology , Porphyra/growth & development , Time Factors
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