Genetic reconstitution of the high-affinity L-arabinose transport system

J Bacteriol. 1989 Jun;171(6):3053-9. doi: 10.1128/jb.171.6.3053-3059.1989.

Abstract

Expression plasmids containing various portions of araFGH operon sequences were assayed for their ability to facilitate the high-affinity L-arabinose transport process in a strain lacking the chromosomal copy of this operon. Accumulation studies demonstrated that the specific induction of all three operon coding sequences was necessary to restore high-affinity L-arabinose transport. Kinetic analysis of this genetically reconstituted transport system indicated that it functions with essentially wild-type parameters. Therefore, L-arabinose-binding protein-mediated transport appears to require only two inducible membrane-associated components (araG and araH) in addition to the binding protein (araF).

Publication types

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

MeSH terms

  • Arabinose / metabolism*
  • Biological Transport, Active
  • Blotting, Southern
  • Carrier Proteins / genetics*
  • Cloning, Molecular
  • DNA Mutational Analysis
  • DNA, Bacterial / genetics
  • Escherichia coli / genetics
  • Escherichia coli / metabolism*
  • Escherichia coli Proteins
  • Genes, Bacterial
  • Kinetics
  • Membrane Proteins / metabolism*
  • Membrane Transport Proteins / genetics
  • Membrane Transport Proteins / metabolism*
  • Plasmids
  • Restriction Mapping

Substances

  • AraF protein, E coli
  • Carrier Proteins
  • DNA, Bacterial
  • Escherichia coli Proteins
  • Membrane Proteins
  • Membrane Transport Proteins
  • Arabinose