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1.
J Biotechnol ; 158(4): 215-23, 2012 Apr 30.
Artigo em Inglês | MEDLINE | ID: mdl-21740932

RESUMO

The effects of reduced efficiency of proton-motive force (pmf) generation on glucose metabolism were investigated in Escherichia coli respiratory-chain mutants. The respiratory chain of E. coli consists of two NADH dehydrogenases and three terminal oxidases, all with different abilities to generate a pmf. The genes for isozymes with the highest pmf-generating capacity (NADH dehydrogenase-1 and cytochrome bo3 oxidase) were knocked out singly or in combination, using a wild-type strain as the parent. Analyses of glucose metabolism by jar-fermentation revealed that the glucose consumption rate per cell increased with decreasing efficiency of pmf generation, as determined from the growth parameters of the mutants. The highest rate of glucose metabolism was observed in the double mutant, and the lowest was observed in the wild-type strain. The respiration rates of the single-knockout mutants were comparable to that of the wild-type strain, and that of the double mutant was higher, apparently as a result of the upregulation of the remaining respiratory chain enzymes. All of the strains excreted 2-oxoglutaric acid as a product of glucose metabolism. Additionally, all of the mutants excreted pyruvic acid and/or acetic acid. Interestingly, the double mutant excreted L-glutamic acid. Alterations of the fermentation profiles provide clues regarding the metabolic regulation in each mutant.


Assuntos
Escherichia coli/enzimologia , Escherichia coli/genética , Glucose/metabolismo , Ácido Acético/metabolismo , Transporte de Elétrons , Escherichia coli/metabolismo , Proteínas de Escherichia coli/genética , Proteínas de Escherichia coli/metabolismo , Fermentação , Glucose/genética , Ácido Glutâmico/genética , Ácido Glutâmico/metabolismo , Ácidos Cetoglutáricos/metabolismo , Mutação/genética , NADH Desidrogenase/genética , NADH Desidrogenase/metabolismo , Oxirredutases/genética , Oxirredutases/metabolismo , Consumo de Oxigênio/genética , Força Próton-Motriz/genética , Ácido Pirúvico/metabolismo
2.
J Bacteriol ; 188(19): 6869-76, 2006 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-16980490

RESUMO

The physiological changes in an F1-ATPase-defective mutant of Escherichia coli W1485 growing in a glucose-limited chemostat included a decreased growth yield (60%) and increased specific rates of both glucose consumption (168%) and respiration (171%). Flux analysis revealed that the mutant showed approximately twice as much flow in glycolysis but only an 18% increase in the tricarboxylic acid (TCA) cycle, owing to the excretion of acetate, where most of the increased glycolytic flux was directed. Genetic and biochemical analyses of the mutant revealed the downregulation of many TCA cycle enzymes, including citrate synthase, and the upregulation of the pyruvate dehydrogenase complex in both transcription and enzyme activities. These changes seemed to contribute to acetate excretion in the mutant. No transcriptional changes were observed in the glycolytic enzymes, despite the enhanced glycolysis. The most significant alterations were found in the respiratory-chain components. The total activity of NADH dehydrogenases (NDHs) and terminal oxidases increased about twofold in the mutant, which accounted for its higher respiration rate. These changes arose primarily from the increased (3.7-fold) enzyme activity of NDH-2 and an increased amount of cytochrome bd in the mutant. Transcriptional upregulation appeared to be involved in these phenomena. As NDH-2 cannot generate an electrochemical gradient of protons and as cytochrome bd is inferior to cytochrome bo3 in this ability, the mutant was able to recycle NADH at a higher rate than the parent and avoid generating an excess proton-motive force. We discuss the physiological benefits of the alterations in the mutant.


Assuntos
Escherichia coli/genética , Escherichia coli/metabolismo , Mutação , Fosforilação Oxidativa , ATPases Translocadoras de Prótons/genética , Ácido Acético/metabolismo , Ciclo do Ácido Cítrico , Proteínas de Escherichia coli/genética , Regulação Bacteriana da Expressão Gênica , Glucose/metabolismo , Glicólise , Immunoblotting , NADH Desidrogenase/metabolismo , Oxirredutases/metabolismo , Consumo de Oxigênio , Transcrição Gênica
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