Cloning, mapping and gene product identification of rhaT from Escherichia coli K12

FEMS Microbiol Lett. 1990 Oct;60(1-2):103-7. doi: 10.1016/0378-1097(90)90353-r.

Abstract

Rhamnose utilization requires the function of a specific rhamnose transport system. Rhamnose transport mutants have been isolated and characterized. The structural gene, rhaT, encoding the rhamnose permease has been cloned from Escherichia coli. rhaT has been mapped in the rha locus (87.7 min) by analysis of cotransduction with glpK and other rha markers. The precise location of the gene has been determined by complementation analysis of rhamnose transport mutants transformed with recombinant plasmids containing different fragments of the cloned region. Gene order (counterclockwise) is established as glpK . . . rhaT-rhaR-rhaS-rhaB-rhaA-rhaD. The gene product has been identified by expression of rhaT in a T7 RNA polymerase/promoter system. This 23 kDa protein has been assigned to the rhaT product and has been shown to be located in the cell membrane.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biological Transport
  • Chromosome Mapping
  • Cloning, Molecular
  • Escherichia coli / enzymology
  • Escherichia coli / genetics*
  • Escherichia coli Proteins*
  • Genes, Bacterial*
  • Genetic Complementation Test
  • Kinetics
  • Membrane Transport Proteins / genetics*
  • Membrane Transport Proteins / metabolism
  • Mutation
  • Restriction Mapping
  • Rhamnose / metabolism*
  • Symporters*
  • Transduction, Genetic
  • Transformation, Bacterial

Substances

  • Escherichia coli Proteins
  • Membrane Transport Proteins
  • RhaT protein, E coli
  • Symporters
  • Rhamnose