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Métodos Terapêuticos e Terapias MTCI
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1.
Mol Microbiol ; 38(4): 750-9, 2000 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-11115110

RESUMO

In nitrogen-poor soils, rhizobia elicit nodule formation on legume roots, within which they differentiate into bacteroids that fix atmospheric nitrogen. Protection against reactive oxygen species (ROS) was anticipated to play an important role in Rhizobium-legume symbiosis because nitrogenase is extremely oxygen sensitive. We deleted the sodA gene encoding the sole cytoplasmic superoxide dismutase (SOD) of Sinorhizobium meliloti. The resulting mutant, deficient in superoxide dismutase, grew almost normally and was only moderately sensitive to oxidative stress when free living. In contrast, its symbiotic properties in alfalfa were drastically affected. Nitrogen-fixing ability was severely impaired. More strikingly, most SOD-deficient bacteria did not reach the differentiation stage of nitrogen-fixing bacteroids. The SOD-deficient mutant nodulated poorly and displayed abnormal infection. After release into plant cells, a large number of bacteria failed to differentiate into bacteroids and rapidly underwent senescence. Thus, bacterial SOD plays a key protective role in the symbiotic process.


Assuntos
Fabaceae/microbiologia , Fabaceae/fisiologia , Plantas Medicinais , Rhizobium/fisiologia , Superóxido Dismutase/fisiologia , Simbiose/fisiologia , Proteínas de Bactérias/fisiologia
2.
Plant Physiol ; 112(2): 525-35, 1996 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-8883376

RESUMO

In eukaryotes, manganese superoxide dismutase is a nuclear-encoded protein that scavenges superoxide radicals in the mitochondrial matrix. We have isolated two manganese superoxide dismutase genes from Nicotiana plumbaginifolia L. and fused the 5' upstream regulatory region of these genes to the beta-glucuronidase reporter gene. The two gene fusions displayed a differential tissue specificity in transgenic tobacco (Nicotiana tabacum). Promoter activity of the SodA1 gene fusion was found in the pollen, middle layer, and stomium of anthers, but was usually undetectable in vegetative organs of mature plants. The SodA2 gene fusion was expressed in the leaves, stems, roots, and flowers. SodA2 promoter activity was most prominent in the vascular bundles, stomata, axillary buds, pericycle, stomium, and pollen. Histochemical analysis of succinate dehydrogenase activity suggested that the spatial expression of the two gene fusions is generally correlated with mitochondrial respiratory activity.


Assuntos
Regulação da Expressão Gênica de Plantas , Genes de Plantas , Nicotiana/genética , Plantas Tóxicas , Regiões Promotoras Genéticas , Superóxido Dismutase/genética , Transporte Biológico , Compartimento Celular , Genes Reporter , Glucuronidase/genética , Histocitoquímica , Mitocôndrias/metabolismo , Dados de Sequência Molecular , Consumo de Oxigênio , Raízes de Plantas/enzimologia , Brotos de Planta/enzimologia , Pólen/enzimologia , RNA Mensageiro/análise , RNA de Plantas/análise , Succinato Desidrogenase/análise , Superóxido Dismutase/biossíntese , Distribuição Tecidual , Nicotiana/enzimologia
3.
Planta Med ; 54(1): 14-7, 1988 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-17265195

RESUMO

Anther culture of DATURA INNOXIA Mill, has permitted the obtention of spontaneous diploid androgenic plants which produced the tropane alkaloids. The source plants (zygotic diploid) showed no significant variations in the leaf alkaloid content. On the contrary, androgenic diploid plants obtained after the first cycle of androgenesis showed important quantitative and qualitative variations in the leaf alkaloid content. Thus, androgenesis was found to induce a large variation in the accumulation of these secondary metabolites in the leaves. It has also permitted the obtention of tropane alkaloid-overproductive plants, particularly rich in scopolamine. The analyses of zygotic plants obtained from seed germination of the first cycle androgenic plants have shown that this variability is transmissible by simple cross-pollination. The analyses of androgenic diploid plants obtained after the second cycle of androgenesis also showed variations in the leaf alkaloid content. IN VITRO androgenesis, therefore, clearly induced variability in the leaf alkaloid content of the androgenic plants. The role of IN VITRO androgenesis in inducing variability has been discussed.

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