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1.
J Exp Bot ; 58(10): 2661-71, 2007.
Artigo em Inglês | MEDLINE | ID: mdl-17586607

RESUMO

It has been known that leaves exposed to high light contain more L-ascorbic acid (AsA) than those in the shade. However, the mechanism of the light regulation of the AsA pool size in plants is largely unknown. In this work, the relationship between gene expression levels related to AsA biosynthesis and photosynthesis have been studied. When 2-week-old Arabidopsis plants grown under a 16 h daily photoperiod were moved into the dark, the AsA level in the leaves was decreased by 91% in 72 h, whereas it increased by 171% in the leaves of plants exposed to continuous light during the same period. Among the several enzymes of the AsA biosynthesis pathway, the transcript levels of GDP-D-mannose pyrophosphorylase, L-galactose 1-P phosphatase, L-galactono-1,4-lactone dehydrogenase, and the VTC2 gene were down-regulated in the dark. Treatment with inhibitors of photosynthesis, 3-(3,4-dichlorophenyl)-1,1-dimethylurea and atrazine, arrested a rise in the AsA pool size accompanying the decrease in the transcript levels of the genes of the above enzyme in the leaves. When the plants were transferred to a medium containing 0.5% (w/v) sucrose, the photosynthesis activities and the leaf AsA levels were lowered even under exposure to light compared with those in plants on the medium without sucrose. In contrast, the AsA level in leaves of the sugar-insensitive Arabidopsis mutant abi4/sun6 was unaffected by external sucrose. No significant difference in the expression profiles for AsA biosynthesis enzymes was observed between the wild-type and mutant plants by sucrose feeding. The results suggest that photosynthetic electron transport of chloroplasts is closely related to AsA pool size regulation in leaves.


Assuntos
Arabidopsis/metabolismo , Ácido Ascórbico/biossíntese , Transporte de Elétrons , Luz , Fotossíntese , Arabidopsis/efeitos dos fármacos , Arabidopsis/genética , Proteínas de Arabidopsis/genética , Proteínas de Arabidopsis/metabolismo , Atrazina/farmacologia , Diurona/farmacologia , Regulação da Expressão Gênica de Plantas/efeitos da radiação , Mutação , Nucleotidiltransferases/genética , Nucleotidiltransferases/metabolismo , Oxirredutases/genética , Oxirredutases/metabolismo , Monoéster Fosfórico Hidrolases/genética , Monoéster Fosfórico Hidrolases/metabolismo , Fotoperíodo , Sacarose/farmacologia
2.
Yakugaku Zasshi ; 125(2): 177-85, 2005 Feb.
Artigo em Japonês | MEDLINE | ID: mdl-15684572

RESUMO

To establish guidelines for avoiding the side effects of mycophenolate mofetil (MMF) in renal transplant recipients with tacrolimus (TAC)-based immunosuppression, the relationship between the daily dose of MMF and the occurrence of side effects was analyzed in this study. The frequency of side effects was investigated retrospectively in 28 renal transplant recipients treated with immunosuppression (men 14 : women 14, age: 33.0+/-12.4 years, weight: 50.9+/-10.7 kg). Cytomegalovirus (CMV) infection and diarrhea were the most frequent side effects in the early transplant phase (from transplantation to 3-month biopsy) in the recipients. In 18 recipients, excluding the recipients with risk factors for CMV infection (ABO-incompatible transplantation, donor (+)/recipient (-) CMV serostatus, etc.), no significant correlation was shown between the daily dose of MMF and the occurrence of CMV infection in the two-sample t-test. On the other hand, the daily dose in the diarrhea group (33.2+/-4.3 mg/kg/day, n = 5) was significantly higher than that in the no-diarrhea group at 30 days (28.4+/-3.7 mg/kg/day, n = 23, p < 0.05) and 90 days (25.7+/-4.4 mg/kg/day, n = 21, p < 0.005) after transplantation, respectively. The receiver-operating characteristic (ROC) curve also revealed that the risk of diarrhea increased with a daily MMF dose higher than 30 mg/kg/day. In conclusion, to decrease the risk of diarrhea in the early transplant phase in renal transplant recipients with TAC-based immunosuppression, the daily dose of MMF should not be more than 30 mg/kg/day.


Assuntos
Infecções por Citomegalovirus/etiologia , Diarreia/etiologia , Imunossupressores/administração & dosagem , Imunossupressores/efeitos adversos , Transplante de Rim , Ácido Micofenólico/análogos & derivados , Ácido Micofenólico/administração & dosagem , Ácido Micofenólico/efeitos adversos , Adolescente , Adulto , Criança , Infecções por Citomegalovirus/epidemiologia , Infecções por Citomegalovirus/prevenção & controle , Diarreia/epidemiologia , Diarreia/prevenção & controle , Relação Dose-Resposta a Droga , Feminino , Humanos , Transplante de Rim/efeitos adversos , Masculino , Pessoa de Meia-Idade , Curva ROC , Estudos Retrospectivos
3.
Plant Cell Physiol ; 45(9): 1271-9, 2004 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-15509850

RESUMO

We have studied the enzymological properties of L-galactose dehydrogenase (l-GalDH), a key enzyme in the biosynthetic pathway of l-ascorbate (AsA) in plants. L-GalDH was purified approximately 560-fold from spinach leaves. The enzyme was a homodimer with a subunit mass of 36 kDa. We also cloned the full-length cDNA of spinach L-GalDH, which contained an open reading frame encoding 322 amino acid residues with a calculated molecular mass of 35,261 Da. The deduced amino acid sequence of the cDNA showed 82, 79 and 75% homology to L-GalDH from kiwifruit, apple and Arabidopsis, respectively. Recombinant enzyme expressed from the cDNA in Escherichia coli showed L-GalDH activity. Southern blot analysis revealed that the spinach L-GalDH gene occurs in a single copy. Northern blot analysis suggests that L-GalDH is expressed in different organs of spinach. The purified native L-GalDH showed high specificity for L-galactose with a Km of 116.2+/-3.2 microM. Interestingly, spinach L-GalDH exhibited reversible inhibition by AsA, the end-product of the biosynthetic pathway. The inhibition kinetics indicated a linear-competitive inhibition with a Ki of 133.2+/-7.2 microM, suggesting feedback regulation in AsA synthesis in the plant.


Assuntos
Ácido Ascórbico/farmacologia , Inibidores Enzimáticos/farmacologia , Galactose Desidrogenases/antagonistas & inibidores , Spinacia oleracea/enzimologia , Sequência de Aminoácidos , Sequência de Bases , Southern Blotting , Primers do DNA , DNA Complementar , Eletroforese em Gel de Poliacrilamida , Galactose Desidrogenases/química , Galactose Desidrogenases/genética , Cinética , Dados de Sequência Molecular , Fases de Leitura Aberta , Folhas de Planta/enzimologia , Homologia de Sequência de Aminoácidos
4.
Plant J ; 32(6): 915-25, 2002 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-12492834

RESUMO

To evaluate the physiological importance of thylakoid membrane-bound ascorbate peroxidase (tAPX) in the active oxygen species-scavenging system of chloroplasts, the level of tAPX in tobacco plants was altered by expression of the tAPX cDNA in both sense and antisense orientation. The tobacco plants transformed with constructs of antisense tAPXs from spinach and tobacco could not be obtained, suggesting that the suppression of tAPX in higher plants had a severe effect on the growth even under normal conditions. In contrast, the transgenic tobacco plants (TpTAP-12) overexpressing tAPX, which had approximately 37-fold higher activity than that of the wild-type plants, were generated. The TpTAP-12 plants showed increased tolerance to oxidative stress caused by application of methylviologen (MV, 50 microm) under light intensity (300 and 1600 microE m(-2) sec(-1)) and by chilling stress with high light intensity (4 degrees C, 1000 microE m(-2) sec(-1)). At 24 h after the MV treatment under illumination at 300 microE m-2 sec-1, destruction of chlorophyll was observed in the wild-type plants, but not in the TpTAP-12 plants. The activities of thiol-modulated enzymes in the Calvin cycle, the level and redox status of ascorbate (AsA), and the activity of tAPX in the wild-type plants significantly decreased, while those in the TpTAP-12 plants were hardly changed. These observations suggest that tAPX is a limiting factor of antioxidative systems under photo-oxidative stress in chloroplasts, and that the enhanced activity of tAPX functions to maintain the AsA content and the redox status of AsA under stress conditions.


Assuntos
Nicotiana/enzimologia , Peroxidases/metabolismo , Espécies Reativas de Oxigênio/metabolismo , Tilacoides/enzimologia , Antioxidantes/metabolismo , Ascorbato Peroxidases , Ácido Ascórbico/metabolismo , Proteínas de Transporte/metabolismo , Clorofila/antagonistas & inibidores , Clorofila/metabolismo , Temperatura Baixa , DNA Complementar/genética , Regulação Enzimológica da Expressão Gênica , Regulação da Expressão Gênica de Plantas , Luz , Proteínas de Membrana/metabolismo , Oxirredução , Estresse Oxidativo/efeitos dos fármacos , Paraquat/farmacologia , Peroxidases/genética , Fotossíntese/efeitos dos fármacos , Fotossíntese/fisiologia , Plantas Geneticamente Modificadas , Nicotiana/genética
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