Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 1 de 1
Filtrar
Mais filtros










Base de dados
Intervalo de ano de publicação
1.
Biochem Biophys Res Commun ; 341(2): 494-9, 2006 Mar 10.
Artigo em Inglês | MEDLINE | ID: mdl-16430864

RESUMO

The previous report from our laboratory has recently identified a new trpE gene (termed trpE2) which exists independently in Azospirillum brasilense Yu62. In this study, amplification of trpE(G) (termed trpE1(G) here) confirmed that there are two copies of trpE gene, one trpE being fused into trpG while the other trpE existed independently. This is the first report to suggest that two copies of the trpE gene exist in this bacterium. Comparison of the nucleotide sequence demonstrated that putative leader peptide, terminator, and anti-terminator were found upstream of trpE1(G) while these sequence features did not exist in front of trpE2. The beta-galactosidase activity of an A. brasilense strain carrying a trpE2-lacZ fusion remained constant at different tryptophan concentrations, but the beta-galactosidase activity of the same strain carrying a trpE1(G)-lacZ fusion decreased as the tryptophan concentration increased. These data suggest that the expression of trpE1(G) is regulated at the transcriptional level by attenuation while trpE2 is constantly expressed. The anthranilate synthase assays with trpE1(G)- and trpE2- mutants demonstrated that TrpE1(G) fusion protein is feedback inhibited by tryptophan while TrpE2 protein is not. We also found that both trpE1(G) and trpE2 gene products were involved in IAA synthesis.


Assuntos
Antranilato Sintase/genética , Azospirillum brasilense/enzimologia , Motivos de Aminoácidos , Sequência de Aminoácidos , Antranilato Sintase/biossíntese , Clonagem Molecular , Relação Dose-Resposta a Droga , Regulação Bacteriana da Expressão Gênica , Marcadores Genéticos , Genótipo , Óperon Lac , Dados de Sequência Molecular , Mutação , Peptídeos/química , Plasmídeos/metabolismo , Sinais Direcionadores de Proteínas , Subunidades Proteicas/biossíntese , Subunidades Proteicas/genética , Proteínas Recombinantes de Fusão/química , Análise de Sequência de DNA , Homologia de Sequência de Aminoácidos , Transcrição Gênica , beta-Galactosidase/metabolismo
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA
...