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1.
Protoplasma ; 261(6): 1185-1206, 2024 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-38864933

RESUMO

Microalgae are considered promising sustainable sources of natural bioactive compounds to be used in biotechnological sectors. In recent years, attention is increasingly given to the search of microalgae-derived compounds with antioxidant and anti-inflammatory properties for nutraceutical or pharmacological issues. In this context, attention is usually focused on the composition and bioactivity of algae or their extracts, while less interest is driven to their biological features, for example, those related to morphology and cultivation conditions. In addition, specific studies on the antioxidant and anti-inflammatory properties of microalgae mainly concern Chlorella or Spirulina. The present work was focused on the characterization of the Chlorophyta Neochloris oleoabundans under two combinations of cultivation modes: autotrophy and glucose-induced mixotrophy, each followed by starvation. Biomass for morphological and biochemical characterization, as well as for extract preparation, was harvested at the end of each cultivation phase. Analyses indicated a different content of the most important classes of bioactive compounds with antioxidant/anti-inflammatory properties (lipids, exo-polysaccharides, pigments, total phenolics, and proteins). In particular, the most promising condition able to prompt the production of antioxidant algal biomass with anti-inflammatory properties was the mixotrophic one. Under mixotrophy, beside an elevated algal biomass production, a strong photosynthetic metabolism with high appression of thylakoid membranes and characteristics of high photo-protection from oxidative damage was observed and linked to the overproduction of exo-polysaccharides and lipids rather than pigments. Overall, mixotrophy appears a good choice to produce natural bioactive extracts, potentially well tolerated by human metabolism and environmentally sustainable.


Assuntos
Anti-Inflamatórios , Antioxidantes , Clorófitas , Microalgas , Antioxidantes/farmacologia , Antioxidantes/metabolismo , Anti-Inflamatórios/farmacologia , Anti-Inflamatórios/química , Microalgas/química , Microalgas/efeitos dos fármacos , Microalgas/metabolismo , Clorófitas/química , Clorófitas/metabolismo , Biomassa
2.
Plant Biol (Stuttg) ; 11(4): 631-41, 2009 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-19538401

RESUMO

Thylakoid dismantling is one of the most relevant processes occurring when chloroplasts are converted to non-photosynthetically active plastids. The process is well characterised in senescing leaves, but other systems could present different features. In this study, thylakoid dismantling has been analysed in dividing cells of the unicellular alga, Euglena gracilis, cultured in darkness. Changes in photosynthetic pigments and in the abundance of LHC and PSII core proteins (D2 and CP43) showed that: (i) during the 0-24 h interval, the decline in LHCII was faster than that in the PSII core; (ii) during the 24-48 h interval, PSII and LHCII were strongly degraded to nearly the same extent; (iii) in the 48-72 h interval, the PSII core proteins declined markedly, while LHCII was maintained. These changes were accompanied by variations in room temperature fluorescence emission spectra recorded from single living cells with a microspectrofluorimeter (excitation, 436 nm; range 620-780 nm). Emission in the 700-715 nm range was proposed to derive from LHCI-II assemblages; changes in emission at 678 nm relative to PSII matched PSII core degradation phases. Overall, the results suggest that, in degreening E. gracilis, thylakoid dismantling is somewhat different from that associated with senescence, because of the early loss of LHCII. Moreover, it is proposed that, in this alga, disruption of the correct LHCI-II stoichiometry alters the energy transfer to photosystems and destabilises membrane appression leading to the thylakoid destacking observed using transmission electron microscopy.


Assuntos
Cloroplastos/metabolismo , Euglena gracilis/metabolismo , Espectrometria de Fluorescência/métodos , Tilacoides/metabolismo , Animais , Western Blotting , Cloroplastos/ultraestrutura , Eletroforese em Gel de Poliacrilamida , Euglena gracilis/ultraestrutura , Microscopia Confocal , Microscopia Eletrônica de Transmissão , Complexo de Proteína do Fotossistema II/metabolismo , Temperatura , Tilacoides/ultraestrutura
3.
Chemosphere ; 145: 98-105, 2016 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-26688244

RESUMO

Along with cadmium, lead, mercury and other heavy metals, chromium is an important environmental pollutant, mainly concentrated in areas of intense anthropogenic pressure. The effect of potassium dichromate on Lemna minor populations was tested using the growth inhibition test. Cyto-histological and physiological analyses were also conducted to aid in understanding the strategies used by plants during exposure to chromium. Treatment with potassium dichromate caused a reduction in growth rate and frond size in all treated plants and especially at the highest concentrations. At these concentrations the photosynthetic pathway was also altered as shown by the decrease of maximum quantum yield of photosystem II and the chlorophyll b content and by the chloroplast ultrastructural modifications. Starch storage was also investigated by microscopic observations. It was the highest at the high concentrations of the pollutant. The data suggested a correlation between starch storage and reduced growth; there was greater inhibition of plant growth than inhibition of photosynthesis, resulting in a surplus of carbohydrates that may be stored as starch. The investigation helps to understand the mechanism related to heavy metal tolerance of Lemna minor and supplies information about the behavior of this species widely used as a biomarker.


Assuntos
Araceae , Cromo/toxicidade , Poluentes Ambientais/toxicidade , Araceae/efeitos dos fármacos , Araceae/fisiologia , Araceae/ultraestrutura , Clorofila/biossíntese , Cromo/metabolismo , Poluentes Ambientais/metabolismo , Fotossíntese/efeitos dos fármacos , Folhas de Planta/efeitos dos fármacos , Folhas de Planta/fisiologia , Folhas de Planta/ultraestrutura , Amido/biossíntese
4.
Plant Biol (Stuttg) ; 6(5): 578-89, 2004 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-15375729

RESUMO

Plant tolerance to heavy metals requires morpho-physiological mechanisms that are still poorly understood, especially in hydrophytes. This study focuses on the young floating lamina of the rhyzophyte Trapa natans exposed for 10 d to 130 microM Mn. The lamina has the ability to bioaccumulate Mn (> 3000 microg g(-1)). X-ray microanalysis of Mn cellular distribution revealed accumulation in the upper epidermis, in the first palisade layer, and in the idioblasts of the spongy tissue, which were shown with electron microscopy to contain osmiophilic vacuolar deposits, also observed to a minor extent in the control leaves. On the basis of biochemical and histochemical tests, these deposits were attributed to phenolic compounds that were probably able to chelate Mn. Net photosynthesis, photosynthetic pigments, room temperature microspectrofluorimetric analyses, and ultrastructural studies of plastids were performed to evaluate the status of the photosynthetic apparatus. A greater development of thylakoid membranes was observed in plastids of the second palisade and spongy tissue, which, however, did not accumulate Mn. Only the spongy tissue experienced inadequate assembly of PS II, but this did not significantly influence the photosynthetic yield of the whole lamina. It was concluded that T. natans can optimise productivity in the presence of Mn by means of specific intra-tissue responses within the framework of the floating lamina.


Assuntos
Lythraceae/efeitos dos fármacos , Manganês/farmacologia , Microanálise por Sonda Eletrônica , Complexos de Proteínas Captadores de Luz/metabolismo , Lythraceae/metabolismo , Lythraceae/ultraestrutura , Manganês/farmacocinética , Microscopia Eletrônica , Microscopia Eletrônica de Varredura , Fotossíntese/efeitos dos fármacos , Complexo de Proteína do Fotossistema II/metabolismo , Folhas de Planta/efeitos dos fármacos , Folhas de Planta/metabolismo , Folhas de Planta/ultraestrutura , Espectrometria de Fluorescência , Distribuição Tecidual
5.
Protoplasma ; 231(1-2): 65-82, 2007.
Artigo em Inglês | MEDLINE | ID: mdl-17602280

RESUMO

The present study focuses on the responses of floating laminae of the Mn-tolerant hydrophyte Trapa natans L. to 1 mM Mn and their ability to accumulate the metal. Studies were carried out first on young floating laminae belonging to the second verticil of 30-day-old plants which originated from fruits that had been maintained in a 1 mM Mn-treated environment and again on the young floating laminae after 10 days of further treatment with 1 mM Mn. Mn storing was observed from the first days after germination, but only 10-day-treated laminae showed the capability to hyperaccumulate the element inside specialised cells (>20000 microg/g [dry weight]). Electron microscopy and the Folin-Ciocalteu reaction for phenolics revealed deposits of chelated material inside vacuoles of the first palisade layer and of idioblasts in the spongy tissue. X-ray microanalysis indicated that the deposits were Mn chelated with phenolic compounds. Numerous trichomes were observed at the lower epidermis of 10-day-treated laminae. They were rich in phenolics and characterised by Mn concretions at their base. As they are associated with a high concentration of the metal in culture water and sediments, trichomes may constitute a morphological differentiation for the secretion of Mn-chelating molecules into the culture water, as a probable "avoidance" mechanism. Finally, monitoring of the photosynthetic apparatus showed that photosynthetic function was not impaired, though differences in development occurred.


Assuntos
Lythraceae , Manganês , Antocianinas/metabolismo , Bioensaio , Biomassa , Microanálise por Sonda Eletrônica , Manganês/metabolismo , Manganês/farmacologia , Fenóis/metabolismo , Fotossíntese/efeitos dos fármacos , Plastídeos/ultraestrutura , Espectrometria de Fluorescência , Espectrofotometria Atômica , Lythraceae/efeitos dos fármacos , Lythraceae/metabolismo , Lythraceae/ultraestrutura
6.
Protoplasma ; 226(3-4): 125-35, 2005 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-16333571

RESUMO

The response of the plastid was studied, with a special emphasis on thylakoid structure and function, in a snow filamentous xanthophycean alga (Xanthonema sp.) incubated in darkness for two months. Microspectrofluorimetric analyses were performed on single living cells to study the variations in the assembly of the chlorophyll-protein complexes of photosystem II, in comparison with cells grown in light. In parallel, changes in micro- and submicroscopic plastid morphology and in photosynthetic pigment content were monitored. Throughout the experiment, the lamellar architecture of thylakoids in the alga was relatively well preserved, whereas photosystem II underwent disassembly and degradation triggered by prolonged darkness. Conversely, the light-harvesting complex of photosystem II proved to be relatively stable for long periods in darkness. Moreover, a role of the peripheral antennae in determining thylakoid arrangement in xanthophycean algae is implied. Although the responses observed in Xanthonema sp. can be considered in terms of acclimation to darkness, the progressive destabilisation of the light-harvesting complex of photosystem II testifies to incipient ageing of the cells after 35 days.


Assuntos
Eucariotos/metabolismo , Tilacoides/metabolismo , Eucariotos/crescimento & desenvolvimento , Eucariotos/ultraestrutura , Luz , Complexos de Proteínas Captadores de Luz/metabolismo , Microscopia Eletrônica de Transmissão , Microscopia de Fluorescência , Microespectrofotometria , Fotossíntese , Complexo de Proteína do Fotossistema II/metabolismo , Plastídeos/metabolismo , Plastídeos/ultraestrutura , Espectrometria de Fluorescência/métodos , Tilacoides/ultraestrutura , Fatores de Tempo
7.
Protoplasma ; 224(3-4): 167-77, 2004 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-15614477

RESUMO

Asynchronous cultures of wild-type Euglena gracilis were tested for their morphophysiological response to 10 mM MnSO4. Growth was only moderately slowed (15%), while oxygen evolution was never compromised. Inductively coupled plasma analyses indicated that the Mn cell content doubled with respect to controls, but no signs of localised accumulation were detected with X-ray microanalysis. Evident morphological alterations were found at the plastid level with transmission electron microscopy and confocal laser scanning microscopy. An increase in the plastid mass, accompanied by frequent aberrations of chloroplast shape and of the organisation of the thylakoid system, was observed. These aspects paralleled a decrease in the molar ratio of chlorophyll a to b and an increase in the fluorescence emission ratio of light-harvesting complex II to photosystem II, the latter evaluated by in vivo single-cell microspectrofluorimetry. These changes were observed between 24 and 72 h of treatment. However, the alterations in the pigment pattern and photosystem II fluorescence were no longer observed after 96 h of Mn exposure, notwithstanding the maintenance of the large plastid mass. The response of the photosynthetic apparatus probably allows the alga to limit the photooxidative damage linked to the inappropriately large peripheral antennae of photosystem II. On the whole, the resistance of Euglena gracilis to Mn may be due to an exclusion-tolerance mechanism since most Mn is excluded from the cell, and the small amount entering the organism is tolerated by means of morphophysiological adaptation strategies, mainly acting at the plastid level.


Assuntos
Adaptação Fisiológica/fisiologia , Cloroplastos/metabolismo , Euglena gracilis/metabolismo , Manganês/metabolismo , Complexo de Proteínas do Centro de Reação Fotossintética/metabolismo , Plastídeos/metabolismo , Adaptação Fisiológica/efeitos dos fármacos , Animais , Clorofila/metabolismo , Clorofila A , Cloroplastos/efeitos dos fármacos , Cloroplastos/ultraestrutura , Resistência a Medicamentos/fisiologia , Euglena gracilis/efeitos dos fármacos , Euglena gracilis/ultraestrutura , Complexos de Proteínas Captadores de Luz/efeitos dos fármacos , Complexos de Proteínas Captadores de Luz/metabolismo , Manganês/farmacologia , Compostos de Manganês/farmacologia , Microscopia Confocal , Microscopia Eletrônica de Transmissão , Estresse Oxidativo/efeitos dos fármacos , Estresse Oxidativo/fisiologia , Fotossíntese/efeitos dos fármacos , Fotossíntese/fisiologia , Complexo de Proteínas do Centro de Reação Fotossintética/efeitos dos fármacos , Complexo de Proteínas do Centro de Reação Fotossintética/ultraestrutura , Complexo de Proteína do Fotossistema II/efeitos dos fármacos , Complexo de Proteína do Fotossistema II/metabolismo , Plastídeos/efeitos dos fármacos , Plastídeos/ultraestrutura , Sulfatos/farmacologia , Tilacoides/efeitos dos fármacos , Tilacoides/metabolismo , Tilacoides/ultraestrutura
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