MAPPING, CLONING, EXPRESSION, AND SEQUENCING OF THE RHAT GENE, WHICH ENCODES A NOVEL L-RHAMNOSE-H-TYPHIMURIUM AND ESCHERICHIA-COLI( TRANSPORT PROTEIN IN SALMONELLA)
Cg. Tate et al., MAPPING, CLONING, EXPRESSION, AND SEQUENCING OF THE RHAT GENE, WHICH ENCODES A NOVEL L-RHAMNOSE-H-TYPHIMURIUM AND ESCHERICHIA-COLI( TRANSPORT PROTEIN IN SALMONELLA), The Journal of biological chemistry, 267(10), 1992, pp. 6923-6932
A L-rhamnose transport-negative strain of Escherichia coli was generat
ed by Mu d(Ap(R),lac)I mutagenesis. This strain was used to isolate a
clone of Salmonella typhimurium DNA that encoded L-rhamnose-H+ transpo
rt activity, the gene for which, rhaT, was sequenced. The rhaT gene wa
s mapped on the E. coli chromosome between rhaR and sodA at 87.9 min,
initially by Southern blot analysis and then by the isolation, express
ion, and sequencing of the rhaT gene. Both rhaT genes encoded a hydrop
hobic protein of 344 amino acids (91% identical) that contained 10 put
ative transmembrane regions. The RhaT protein represents a novel class
of sugar transport protein.