MAPPING, CLONING, EXPRESSION, AND SEQUENCING OF THE RHAT GENE, WHICH ENCODES A NOVEL L-RHAMNOSE-H-TYPHIMURIUM AND ESCHERICHIA-COLI( TRANSPORT PROTEIN IN SALMONELLA)

Citation
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
Citations number
46
ISSN journal
00219258
Volume
267
Issue
10
Year of publication
1992
Pages
6923 - 6932
Database
ISI
SICI code
0021-9258(1992)267:10<6923:MCEASO>2.0.ZU;2-3
Abstract
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.