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1.
PLoS One ; 11(7): e0159629, 2016.
Artigo em Inglês | MEDLINE | ID: mdl-27462710

RESUMO

In the present studies, we focused on substrate specificity of tocopherol cyclase, the key enzyme in the biosynthesis of the tocopherols and plastochromanol-8, the main plant lipid antioxidants, with special emphasis on the preference for tocopherols and plastochromanol-8 precursors, taking advantage of the recombinant enzyme originating from Arabidopsis thaliana and isolated plastoglobules, thylakoids and various model systems like micelles and thylakoids. Plastoglobules and triacylglycerol micelles were the most efficient reaction environment for the cyclase. In various investigated systems, synthesis of γ-tocopherol proceeded considerably faster than that of plastochromanol-8, probably mainly due to different localization of the corresponding substrates in the analyzed lipid structures. Moreover, our study was complemented by bioinformatics analysis of the phylogenetic relations of the cyclases and sequence motifs, crucial for the enzyme activity, were proposed. The analysis revealed also a group of tocopherol cyclase-like proteins in a number of heterotrophic bacterial species, with a conserved region common with photosynthetic organisms, that might be engaged in the catalytic activity of both groups of organisms.


Assuntos
Proteínas de Arabidopsis/metabolismo , Arabidopsis/enzimologia , Transferases Intramoleculares/metabolismo , Arabidopsis/genética , Proteínas de Arabidopsis/química , Proteínas de Arabidopsis/genética , Cromanos/metabolismo , Transferases Intramoleculares/química , Transferases Intramoleculares/genética , Filogenia , Especificidade por Substrato , Tilacoides/metabolismo , Tocoferóis/metabolismo , Vitamina E/análogos & derivados , Vitamina E/metabolismo
2.
Physiol Plant ; 157(2): 147-60, 2016 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-27174597

RESUMO

In this study, 25 accessions of Arabidopsis thaliana originating from a variety of climate conditions were grown under controlled circumstances of different light intensity and temperature. The accessions were analyzed for prenyllipids content and composition, as well as expression of the genes involved in tocochromanol biosynthesis (vte1-5). It was found that the applied conditions did not strongly affect total tocochromanols content and there was no apparent correlation of the tocochromanol content with the origin of the accessions. However, the presented results indicate that the temperature, more than the light intensity, affects the expression of the vte1-5 genes and the content of some prenyllipids. An interesting observation was that under low growth temperature, the hydroxy-plastochromanol (PC-OH) to plastochromanol (PC) ratio was considerably increased regardless of the light intensity in most of the accessions. PC-OH is known to be formed as a result of singlet oxygen stress, therefore this observation indicates that the singlet oxygen production is enhanced under low temperature. Unexpectedly, the highest increase in the PC-OH/PC ratio was found for accessions originating from cold climate (Shigu, Krazo-1 and Lov-5), even though such plants could be expected to be more resistant to low temperature stress.


Assuntos
Antioxidantes/metabolismo , Arabidopsis/fisiologia , Cromanos/metabolismo , Regulação da Expressão Gênica de Plantas , Antioxidantes/análise , Arabidopsis/genética , Arabidopsis/efeitos da radiação , Proteínas de Arabidopsis , Cromanos/análise , Temperatura Baixa , Geografia , Luz , Lipídeos/biossíntese , Lipídeos/química , Prenilação , Oxigênio Singlete/metabolismo , Temperatura
3.
N Biotechnol ; 33(5 Pt B): 636-643, 2016 Sep 25.
Artigo em Inglês | MEDLINE | ID: mdl-26970272

RESUMO

Isoprenoid quinones and chromanols in plants fulfill both signaling and antioxidant functions under oxidative stress. The redox state of the plastoquinol pool (PQ-pool), which is modulated by interaction with reactive oxygen species (ROS) during oxidative stress, has a major regulatory function in both short- and long-term acclimatory responses. By contrast, the scavenging of ROS by prenyllipids affects signaling pathways where ROS play a role as signaling molecules. As the primary antioxidants, isoprenoid quinones and chromanols are synthesized under high-light stress in response to any increased production of ROS. During photo-oxidative stress, these prenyllipids are continuously synthesized and oxidized to other compounds. In turn, their oxidation products (hydroxy-plastochromanol, plastoquinol-C, plastoquinone-B) can still have an antioxidant function. The oxidation products of isoprenoid quinones and chromanols formed specifically in the face of singlet oxygen, can be indicators of singlet oxygen stress.


Assuntos
Cromanos/metabolismo , Plantas/metabolismo , Terpenos/metabolismo , Antioxidantes/metabolismo , Biotecnologia , Oxirredução , Estresse Oxidativo , Plastoquinona/metabolismo , Quinonas/metabolismo , Espécies Reativas de Oxigênio/metabolismo , Transdução de Sinais , Tocoferóis/metabolismo
4.
Plant Cell Environ ; 38(12): 2698-706, 2015 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-26013323

RESUMO

In the present study, we have identified new prenyllipid metabolites formed during high light stress in Arabidopsis thaliana, whose origin and function remained unknown so far. It was found that plastoquinone-C accumulates mainly in the reduced form under high light conditions, as well as during short-term excess light illumination both in the wild-type and tocopherol biosynthetic vte1 mutant, suggesting that plastoquinone-C, a singlet oxygen-derived prenyllipid, is reduced in chloroplasts by photosystem II or enzymatically, outside thylakoids. Plastoquinone-B, a fatty acid ester of plastoquinone-C, was identified for the first time in Arabidopsis in high light grown wild-type plants and during short-time, excess light illumination of the wild-type plants and the vte1 mutant. The gene expression analysis showed that vte2 gene is most pronouncedly up-regulated among the prenyllipid biosynthetic genes under high light and induction of its expression is mainly caused by an increased level of singlet oxygen, as was demonstrated in experiments with D2 O-treated plants under excess light conditions.


Assuntos
Alquil e Aril Transferases/genética , Proteínas de Arabidopsis/genética , Arabidopsis/metabolismo , Regulação Enzimológica da Expressão Gênica/efeitos da radiação , Transferases Intramoleculares/genética , Plastoquinona/metabolismo , Oxigênio Singlete/metabolismo , Alquil e Aril Transferases/metabolismo , Arabidopsis/química , Arabidopsis/genética , Arabidopsis/efeitos da radiação , Proteínas de Arabidopsis/metabolismo , Cloroplastos/metabolismo , Regulação da Expressão Gênica de Plantas/efeitos da radiação , Transferases Intramoleculares/metabolismo , Luz , Mutação , Estresse Oxidativo , Complexo de Proteína do Fotossistema II/metabolismo , Plastoquinona/análise , Tilacoides/metabolismo , Tocoferóis/metabolismo
5.
Physiol Plant ; 154(2): 194-209, 2015 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-25214438

RESUMO

During their lifetime, plants need to adapt to a changing environment, including light and temperature. To understand how these factors influence plant growth, we investigated the physiological and antioxidant responses of two Arabidopsis accessions, Shahdara (Sha) from the Shahdara valley (Tajikistan, Central Asia) in a mountainous area and Lovvik-5 (Lov-5) from northern Sweden to different light and temperature conditions. These accessions originate from different latitudes and have different life strategies, both of which are known to be influenced by light and temperature. We showed that both accessions grew better in high-light and at a lower temperature (16°C) than in low light and at 23°C. Interestingly, Sha had a lower chlorophyll content but more efficient non-photochemical quenching than Lov-5. Sha, also showed a higher expression of vitamin E biosynthetic genes. We did not observe any difference in the antioxidant prenyllipid level under these conditions. Our results suggest that the mechanisms that keep the plastoquinone (PQ)-pool in more oxidized state could play a role in the adaptation of these accessions to their local climatic conditions.


Assuntos
Antioxidantes/metabolismo , Arabidopsis/fisiologia , Aclimatação , Arabidopsis/genética , Arabidopsis/efeitos da radiação , Arabidopsis/ultraestrutura , Clorofila/metabolismo , Luz , Oxirredução , Folhas de Planta/genética , Folhas de Planta/fisiologia , Folhas de Planta/efeitos da radiação , Folhas de Planta/ultraestrutura , Plastoquinona/metabolismo , Suécia , Temperatura
6.
Physiol Plant ; 141(3): 289-98, 2011 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-21114674

RESUMO

In this study, we have compared three isolation methods of cytochrome b6f complex, obtained from spinach (Spinacia oleracea), differing in the preservation of the cytochrome b6f-associated ferredoxin:NADP+ oxidoreductase (FNR). Although the complexes isolated by all the methods showed the presence of the FNR peptide(s), when incorporated into liposome membranes, the NADPH-PQ (plastoquinone) oxidoreductase activity was not detected for the cytochrome b6f complex isolated with the original method including a NaBr wash. Some activity was found for the complex isolated with the omission of the wash, but the highest activity was detected for the complex isolated with the use of digitonin. The reaction rate of PQ reduction of the investigated complexes in liposomes was not significantly influenced by the addition of free FNR or ferredoxin. The reaction was inhibited by about 60% in the presence of 2 µM 2-n-nonyl-4-hydroxyquinoline N-oxide, an inhibitor of the cytochrome b6 f complex at the Q(i) site, while it was not affected by triphenyltin or isobutyl cyanide that interacts with the recently identified heme c(i) . The obtained data indicate that FNR associated with the cytochrome b6 f complex can participate in the cyclic electron transport as PSI-PQ or NADPH-PQ oxidoreductase. Moreover, we have shown that PQ can be non-enzymatically reduced by ascorbate in liposomes and this reaction might be involved in non-photochemical reduction pathways of the PQ-pool in chloroplasts.


Assuntos
Complexo Citocromos b6f/metabolismo , Ferredoxina-NADP Redutase/metabolismo , Plastoquinona/química , Spinacia oleracea/enzimologia , Complexo Citocromos b6f/isolamento & purificação , Transporte de Elétrons , Ferredoxina-NADP Redutase/análise , Flavina-Adenina Dinucleotídeo/análise , Lipossomos/química , NADH NADPH Oxirredutases/metabolismo , Oxirredução , Proteínas de Plantas/metabolismo
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