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.
Biochim Biophys Acta ; 1769(3): 194-203, 2007 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-17337072

RESUMO

PNPase is a phosphate-dependent exonuclease of Escherichia coli required for growth in the cold. In this work we explored the effect of specific mutations in its two RNA binding domains KH and S1 on RNA binding, enzymatic activities, autoregulation and ability to grow at low temperature. We removed critical motifs that stabilize the hydrophobic core of each domain, as well as made a complete deletion of both (DeltaKHS1) that severely impaired PNPase binding to RNA. Nevertheless, a residual RNA binding activity, possibly imputable to catalytic binding, could be observed even in the DeltaKHS1 PNPase. These mutations also resulted in significant changes in the kinetic behavior of both phosphorolysis and polymerization activities of the enzyme, in particular for the double mutant Pnp-DeltaKHS1-H. Additionally, PNPases with mutations in these RNA binding domains did not autoregulate efficiently and were unable to complement the growth defect of a chromosomal Deltapnp mutation at 18 degrees C. Based on these results it appears that in E. coli the RNA binding domains of PNPase, in particular the KH domain, are vital at low temperature, when the stem-loop structures present in the target mRNAs are more stable and a machinery capable to degrade structured RNA may be essential.


Assuntos
Escherichia coli/enzimologia , Regulação Bacteriana da Expressão Gênica , Polirribonucleotídeo Nucleotidiltransferase/metabolismo , RNA Bacteriano/metabolismo , Sequência de Aminoácidos , Sítios de Ligação/genética , Ensaio de Desvio de Mobilidade Eletroforética , Escherichia coli/genética , Escherichia coli/crescimento & desenvolvimento , Teste de Complementação Genética , Homeostase , Dados de Sequência Molecular , Mutação/genética , Polirribonucleotídeo Nucleotidiltransferase/genética , Ligação Proteica , Estrutura Terciária de Proteína/genética , RNA Mensageiro/genética , Deleção de Sequência , Homologia de Sequência de Aminoácidos , Temperatura
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA