In bacteria the initiation of protein synthesis is a complex phenomenon in which specific proteins, termed initiation factors (IFs) IF1, IF2, and IF3, are involved. Notwithstanding the progress made in understanding their functions, the precise molecular mechanisms of action of these factors remain somewhat obscure. One reason for this lack of knowledge is the difficulty involved in purifying sufficient quantities of these proteins. We have developed a new procedure for purification of IFs from recombinant Escherichia coli strains producing high levels of E. coli IF3 and Bacillus stearothermophilus IF2. This new procedure is quicker than previous methods, easily scaled up to large volumes, and can be used, with only minor modifications, for different IFs. This new purification method consists essentially of one chromatographic (FPLC) separation on an ion-exchange resin (S-Sepharose fast-flow or Mono-S HR). Using this procedure we have been able to obtain chromatographically pure and biologically active preparations of both IF2 and IF3.
Purification procedure for bacterial translational initiation factors IF2 and IF3.
SPURIO, Roberto;
1994-01-01
Abstract
In bacteria the initiation of protein synthesis is a complex phenomenon in which specific proteins, termed initiation factors (IFs) IF1, IF2, and IF3, are involved. Notwithstanding the progress made in understanding their functions, the precise molecular mechanisms of action of these factors remain somewhat obscure. One reason for this lack of knowledge is the difficulty involved in purifying sufficient quantities of these proteins. We have developed a new procedure for purification of IFs from recombinant Escherichia coli strains producing high levels of E. coli IF3 and Bacillus stearothermophilus IF2. This new procedure is quicker than previous methods, easily scaled up to large volumes, and can be used, with only minor modifications, for different IFs. This new purification method consists essentially of one chromatographic (FPLC) separation on an ion-exchange resin (S-Sepharose fast-flow or Mono-S HR). Using this procedure we have been able to obtain chromatographically pure and biologically active preparations of both IF2 and IF3.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
