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J. Bacteriol., 01 1996, 61-67, Vol 178, No. 1
P Klemm, S Tong, H Nielsen and T Conway
The gntP gene, located between the fim and uxu loci in Escherichia coli
K-12, has been cloned and characterized. Nucleotide sequencing of a region
encompassing the gntP gene revealed an open reading frame of 447 codons
with significant homology to the Bacillus subtilis gluconate permease.
Northern (RNA) blotting indicated that the gntP gene was monocistronic and
was transcribed as an mRNA with an apparent molecular size of 1.54 kb. The
transcriptional start point was determined by primer extension analysis.
The gntP gene was found to be under catabolite repression and was not
induced by gluconate. Also, expression seemed to be stringently controlled.
Several observations indicated that the GntP protein is an inner membrane
protein; it contains characteristic membrane-spanning regions and was
isolated predominantly from the inner-membrane fraction of fractionated
host cells. A topology analysis predicted a protein with 14 membrane-
spanning segments. The inability of a mutant strain to grow on gluconate
minimal medium could be relieved by introduction of a plasmid encoding the
gntP gene. Finally, the kinetics of GntP-mediated gluconate uptake were
investigated, indicating an apparent Km for gluconate of 25 microM.
Copyright © 1996, American Society for Microbiology
The gntP gene of Escherichia coli involved in gluconate uptake
Department of Microbiology, Technical University of Denmark, Lyngby, Denmark.
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