Regulation of compatible solute accumulation in Salmonella typhimurium: evidence for a glycine betaine efflux system.

The regulation of glycine betaine accumulation has been investigated in Salmonella typhimurium. The size of the glycine betaine pool in the cells is determined by the external osmotic pressure and is largely independent of the external glycine betaine concentration. Analysis of the activity of the ProP and ProU transport systems suggests that other systems must be active in the regulation of the glycine betaine pool. Addition of p-chloromercuribenzoate (PCMB) or p-chloromercuribenzene sulphonate (PCMBS) to cells that have accumulated glycine betaine provokes rapid loss of glycine betaine. The route of glycine betaine efflux under the influence of PCMB is independent of either the ProP or ProU transport systems. Rapid loss of the accumulated pool of glycine betaine in the presence of PCMB is specific to glycine betaine and proline; accumulated pools of serine and lysine are not significantly affected by the -SH reagent. A specific glycine betaine/proline efflux system is postulated on the basis of these data and its role in the regulation of glycine betaine and proline accumulation is discussed.

[1]  A. Strøm,et al.  Synthesis, accumulation, and excretion of trehalose in osmotically stressed Escherichia coli K-12 strains: influence of amber suppressors and function of the periplasmic trehalase , 1991, Journal of bacteriology.

[2]  D. le Rudulier,et al.  Osmoregulation in Azospirillum brasilense: glycine betaine transport enhances growth and nitrogen fixation under salt stress. , 1990, Journal of general microbiology.

[3]  I. Booth,et al.  Activation potassium efflux from Escherichia coli by glutathione metabolites , 1990, Molecular microbiology.

[4]  C. Higgins,et al.  Molecular characterization of the proU loci of Salmonella typhimurium and Escherichia coli encoding osmoregulated glycine betaine transport systems , 1989, Molecular microbiology.

[5]  L N Csonka,et al.  Physiological and genetic responses of bacteria to osmotic stress. , 1989, Microbiological reviews.

[6]  J. Cairney,et al.  Enteric bacteria and osmotic stress: an integrated homeostatic system. , 1988, Society for Applied Bacteriology symposium series.

[7]  L. Csonka Regulation of cytoplasmic proline levels in Salmonella typhimurium: effect of osmotic stress on synthesis, degradation, and cellular retention of proline , 1988, Journal of bacteriology.

[8]  A. Middendorf,et al.  Cloned structural genes for the osmotically regulated binding‐protein‐dependent glycine betaine transport system (ProU) of Escherichia coli K‐12 , 1988, Molecular microbiology.

[9]  I. Booth,et al.  Evidence for multiple K+ export systems in Escherichia coli , 1987, Journal of bacteriology.

[10]  J. Imhoff Osmoregulation and compatible solutes in eubacteria , 1986 .

[11]  W. Epstein Osmoregulation by potassium transport in Escherichia coli , 1986 .

[12]  J. Cairney,et al.  Osmoregulation of Gene Expression in Salmonella typhimurium: proU Encodes an Osmotically Induced Betaine Transport System , 1986, Journal of bacteriology.

[13]  J. Cairney,et al.  Salmonella typhimurium proP gene encodes a transport system for the osmoprotectant betaine , 1985, Journal of bacteriology.

[14]  J. Meury,et al.  Turgor-controlled K+ fluxes and their pathways in Escherichia coli. , 1985, European journal of biochemistry.

[15]  D. Dietzler,et al.  Osmotic stress drastically inhibits active transport of carbohydrates by Escherichia coli. , 1985, Biochemical and biophysical research communications.

[16]  D. le Rudulier,et al.  Glycine betaine transport in Escherichia coli: osmotic modulation , 1985, Journal of bacteriology.

[17]  L. Csonka A third L-proline permease in Salmonella typhimurium which functions in media of elevated osmotic strength , 1982, Journal of bacteriology.

[18]  W. Hamilton,et al.  Quantitative analysis of proton-linked transport system. beta-Galactoside exit in Escherichia coli. , 1980, The Biochemical journal.

[19]  W. Epstein,et al.  Cation transport in Escherichia coli. IX. Regulation of K transport , 1978, The Journal of general physiology.

[20]  I. West,et al.  Stoicheiometry of lactose–proton symport across the plasma membrane of Escherichia coli , 1973 .

[21]  D. Clark,et al.  Synthesis , Accumulation , and Excretion of Trehalose in Osmotically Stressed Escherichia coli K-12 Strains : Influence of Amber Suppressors and Function of the Periplasmic Trehalase , 2022 .