Properties of the Glutamate Transport System in Escherichia coli
AUTOR(ES)
Halpern, Yeheskel S.
RESUMO
The properties of the glutamate transport system in two glutamate-utilizing mutants of Escherichia coli K-12 were investigated. Growth in the presence of glutamate enhanced the capacity of the bacteria for glutamate uptake. Accumulation of glutamate was found to be an energy-linked highly temperature-dependent process. Nonlinear double reciprocal plots of uptake were obtained in the absence of an exogenous energy source and in the presence of glucose or glycerol. Addition of γ-aminobutyrate, succinate, ketoglutarate, or aspartate accelerated glutamate uptake and brought about “normalization” of its kinetics. Straight-line kinetics of uptake was also observed when succinate served as the source of energy. Under these conditions, aspartate and α-ketoglutarate inhibited glutamate uptake in a noncompetitive fashion, whereas γ-aminobutyrate activated the system. A number of other amino acids were found to act as “noncompetitive” inhibitors. d-glutamate and some derivatives of glutamate with an unsubstituted α-carboxylic and α-amino group inhibited l-glutamate uptake in a strictly competitive fashion. An allosteric permease model, consistent with all of these findings, is proposed.
ACESSO AO ARTIGO
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=276548Documentos Relacionados
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