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Effect of novel compound, 1-methyl-1-piperidino methane sulfonate (MPMS), on the osmoprotectant activity of glycine betaine, cholien and l-proline in Escherichia coli

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Abstract

A novel compound, 1-methyl-1-piperidino methane sulfonate (MPMS), was found to block the osmoprotectant activity of choline and L-proline, but not glycine betaine in Escherichia coli. MPMS was more active against salt-sensitive than salt-resistant strains, but had no effect on the salt tolerance of a mutant which was unable to transport choline, glycine betaine and proline. Growth of E. coli in NaCl was inhibited by MPMS and restored by glycine betaine, but not by choline or L-proline. Uptake of radiolabeled glycine betaine, choline or L-proline by cells grown at high osmolarity was not inhibited when MPMS and the radioactive substrates were added simultaneously. Preincubation for 5 min with MPMS reduced the uptake of choline and L-proline, but not glycine betaine. Similar incubation with MPMS had no effect on the uptake of radiolabeled glucose or succinate. The toxicity of MPMS was much lower than that of the L-proline analogues L-azetidine-2-carboxylic acid and 3,4-dehydro-DL-proline. The exact mechanism by which MPMS exerts its effect is not entirely clear. MPMS or a metabolite may interfere with the activity of several independent permeases involved in the uptake of osmoprotective compounds, or the conversion of choline to glycine betaine, or effect the expression of some of the osmoregulatory genes.

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Abbreviations

MPMS:

1-methyl-1-piperidino-methane sulfonate

References

  • Abdel-Ghany Y, Miller DD, Kunin CM, Tong HH (1993) Structure activity relationship of glycine betaine analogs on osmotolerance of enteric bacteria. J Med Chem 36: 784–789

    Google Scholar 

  • Booth IR, Higgins CF (1990) Enteric bacteria and osmotic stress: intracellular potassium glutamate as a secondary signal of osmotic stress? FEMS Microbiol Rev 75: 239–246

    Google Scholar 

  • Cairney J, Higgins CF, Booth IR (1984) Proline uptake through the major transport systems of Salmonella typhimurium is coupled to sodium ions. J Bacteriol 160: 22–27

    Google Scholar 

  • Cairney J, Booth IR, Higgins CF (1985) Osmoregulation of gene expression in Salmonella typhimurium: proU encodes an osmotically induced betaine transport system. J Bacteriol 164: 1224–1232

    Google Scholar 

  • Cairney J, Booth IR, Higgins CF (1985) Salmonella typhimurium proP gene encodes a transport system for the osmoprotectant betaine. J Bacteriol 164: 1218–1223

    Google Scholar 

  • Chambers ST, Kunin CM (1985) The osmoprotective properties of urine for bacteria: The protective effect of betaine and human urine against low pH and high concentrations of electrolytes, sugars and urea. J Infect Dis 152: 1308–1315

    Google Scholar 

  • Chambers ST, Kunin CM (1987) Osmoprotective activity for E. coli in mammalian renal inner medulla and urine: correlation of glycine and proline betaines and sorbitol with response to osmotic stress. J Clin Invest 80: 1255–1260

    Google Scholar 

  • Chambers ST, Kunin CM, Miller D, Hamada A (1987) Dimethylthetin can substitute for glycine betaine as an osmoprotectant molecule for Escherichia coli. J Bacteriol 169: 4845–4847

    Google Scholar 

  • Csonka LA (1989) Physiology and genetic responses of bacteria to osmotic stress. Microbiol Rev 53: 121–147

    Google Scholar 

  • Davis BD, Dulbecco DR, Eisen HN, Ginsburg HS, Wood WBJr (1973) Microbiology, 2nd ed. Harper and Row, Hagerstown Maryland

    Google Scholar 

  • Dunlap JA, Csonka LN (1985) Osmotic regulation of L-proline transport in Salmonella typhimurium. J Bacteriol 163: 296–304

    Google Scholar 

  • Epstein W (1986) Osmoregulation by potassium transport in Escherichia coli. FEMS Microbiol Rev 39: 73–78

    Google Scholar 

  • Eshoo MW (1988) lac Fusion analysis of the bet genes of Escherichia coli: regulation by osmolarity, temperature, oxygen, choline and glycine betaine. J Bacteriol 170: 5208–5215

    Google Scholar 

  • Faatz E, Middendorf A, Bremer E (1988) Cloned structural genes for the osmotically regulated binding-protein-dependent glycine betaine transport system (ProU) of Escherichia coli K-12. Mol Microbiol 2: 265–279

    Google Scholar 

  • Grothe S, Krogsrund RL; McClellan DJ, Millner JL, Wood JM (1986) Proline transort and osmotic stress response in Escherichia coli K-12. J Bacteriol 166: 253–259

    Google Scholar 

  • Kunin CM, Rudy J (1991) Effect of NaCl-induced osmotic stress on intracellular concentrations of glycine betaine and potassium in Escherichia coli, Enterococcus faecalis, and Staphylococci. J Lab Clin Med 188: 217–224

    Google Scholar 

  • Kunin CM, Tong HH, White LVA, Villarejo M (1992) Growth of Escherichia coli in human urine: role of salt tolerance and accumulation of glycine betaine. J Infect Dis 166: 1311–1315

    Google Scholar 

  • Landfald B, Strom AR (1986) Choline-glycine betaine path-way confers a high level osmotic tolerance in Escherichia coli. J Bacteriol 165: 849–855

    Google Scholar 

  • Lamark T, Kaasen I, Eshoo MW, Falkenberg P, McDougall J, Strom AR (1991) DNA sequence and analysis of the bet genes encoding the osmoregulatory choline-glycine betaine pathway of Escherichia coli. Mol Microbiol 5: 1049–1064

    Google Scholar 

  • LeRudulier D, Strom AR, Dandekar AM, Smith LT, Valentine RC (1984) Molecular biology of osmoregulation. Science 224: 1064–1068

    Google Scholar 

  • May G, Faatz E, Villarejo M, Bremer E (1986) Binding protein dependent transport of glycine betaine and its osmotic regulation in Escherichia coli K12. Mol Gen Genet 205: 225–233

    Google Scholar 

  • Perroud B, LeRudulier D (1985) Glycine betaine transport in Escherichia coli: osmotic modulation. J Bacteriol 161:393–401

    Google Scholar 

  • Stalmach ME, Grothe S, Wood JM (1983) Two proline porters in Escherichia coli K-12. J Bacteriol 156: 481–486

    Google Scholar 

  • Styrvold OB, Falkenberg P, Landfald B, Eshoo MW, Bjornsen T, Strom AR (1986) Selection, mapping, and characterization of osmoregulatory mutants of Escherichia coli blocked in the choline-glycine betaine pathway. J Bacteriol 165: 856–863

    Google Scholar 

  • Styrvold OB, Strom AR (1991) Synthesis, accumulation, and excretion of trehalose in osmotically stresses Escherichia coli K-12 strains: influence of amber suppressors and function of the periplasmic trehalase. J Bacteriol 173: 1187–1192

    Google Scholar 

  • Sutherland L, Cairney J, Elmore MJ, Booth IR, Higgins CF (1986) Osmotic regulation of transcription: induction of the proU betaine transport gene is dependent on accumulation of intracellular potassium. J Bacteriol 168: 805–814

    Google Scholar 

  • Wood JM (1981) Genetics of L-proline utilization in Escherichia coli. J Bacteriol 146: 895–901

    Google Scholar 

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Kunin, C.M., Tong, H.H., Miller, D.D. et al. Effect of novel compound, 1-methyl-1-piperidino methane sulfonate (MPMS), on the osmoprotectant activity of glycine betaine, cholien and l-proline in Escherichia coli . Arch. Microbiol. 160, 81–86 (1993). https://doi.org/10.1007/BF00288707

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  • DOI: https://doi.org/10.1007/BF00288707

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