thiBPQ encodes an ABC transporter required for transport of thiamine and thiamine pyrophosphate in Salmonella typhimurium

J Biol Chem. 1998 Apr 10;273(15):8946-50. doi: 10.1074/jbc.273.15.8946.

Abstract

In Salmonella typhimurium, thiamine pyrophosphate (TPP) is a required cofactor for several enzymes in central metabolism. Herein we identify a new thi operon, thiBPQ (designated sfuABC in Escherichia coli), required for the transport of thiamine and TPP into the cell. Insertions in the operon result in strains that are phenotypically and biochemically defective in thiamine and TPP transport. Data presented herein show that this operon is transcriptionally repressed in the presence of exogenous thiamine, with TPP the likely regulatory molecule. This work represents the first identification of thiamine transport genes in bacteria and demonstrates the function of a proposed ABC transporter in E. coli.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • ATP-Binding Cassette Transporters / biosynthesis*
  • ATP-Binding Cassette Transporters / genetics*
  • Escherichia coli / genetics
  • Gene Expression Regulation, Bacterial
  • Kinetics
  • Mutagenesis, Insertional
  • Operon*
  • Recombinant Fusion Proteins / biosynthesis
  • Salmonella typhimurium / genetics
  • Salmonella typhimurium / metabolism*
  • Thiamine / metabolism*
  • Thiamine Pyrophosphate / metabolism*
  • Transcription, Genetic
  • beta-Galactosidase / biosynthesis

Substances

  • ATP-Binding Cassette Transporters
  • Recombinant Fusion Proteins
  • beta-Galactosidase
  • Thiamine Pyrophosphate
  • Thiamine