Affiliation:
1. Department of Microbiology, University of Illinois, B103 Chemical and Life Sciences Laboratory, 601 S. Goodwin Ave, Urbana, IL 61801, USA
Abstract
Summary: Wild-type Salmonella typhimurium expresses three proline transport systems: a high-affinity proline transport system encoded by the putP gene, and two glycine betaine transport systems with a lower affinity for proline encoded by the proP and proU genes. Although proline uptake by the ProP and ProU transport systems is sufficient to supplement a proline auxotroph, it is not efficient enough to allow proline utilization as a sole source of carbon or nitrogen. Thus, the PutP transport system is required for utilization of proline as a carbon or nitrogen source. In this study, an overexpression suppressor, designated proY, which allows proline utilization in a putP genetic background and does not require the function of any of the known proline transport systems, was cloned and characterized. The suppressor gene, designated proY, maps at 8 min on the S. typhimurium linkage map, distant from any of the other characterized proline transport genes. The DNA sequence of the proY gene predicts that it encodes a hydrophobic integral membrane protein, with strong similarity to a family of amino acid transporters. The suppressor phenotype requires either a multicopy clone of the proY
+ gene or both a single copy of the proY
+ gene and a proZ mutation. These results indicate that the proY gene is the structural gene for a cryptic proline transporter that is silent unless overexpressed on a multicopy plasmid or activated by a proZ mutation.
Reference45 articles.
1. Basic local alignment search tool;Altschul;J MolBiol,1990
2. Plasmid insertion mutagenesis and lac gene fusion with mini-Mu bacteriophage transposons;Beatriz;Proc Natl Acad Sci USA,1984
3. Isolation and characterization of a mutation that alters the substrate specificity of the Escherichia coli glucose permease;Begley;J Bacteriol,1996
4. Identification and characterization of recD, a gene affecting plasmid maintenance and recombination in Escherichia coli;Biek;J Bacteriol,1986
5. Curing bacterial cells of lysogenic viruses by using UCB indicator plates;Bochner;BioTechniques,1984
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