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PMID: 8071213 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Osmoregulation in Bacillus subtilis: synthesis of the osmoprotectant glycine betaine from exogenously provided choline.

Journal of bacteriology ·Vol. 176 ·No. 17 ·1994-09-00 ·Pages 5364-71

Boch J, Kempf B, Bremer E

Abstract

Exogenously provided glycine betaine functions as an efficient osmoprotectant for Bacillus subtilis in high-osmolarity environments. This gram-positive soil organism is not able to increase the intracellular level of glycine betaine through de novo synthesis in defined medium (A. M. Whatmore, J. A. Chudek, and R. H. Reed, J. Gen. Microbiol. 136:2527-2535, 1990). We found, however, that B. subtilis can synthesize glycine betaine when its biosynthetic precursor, choline, is present in the growth medium. Uptake studies with radiolabelled [methyl-14C]choline demonstrated that choline transport is osmotically controlled and is mediated by a high-affinity uptake system. Choline transport of cells grown in low- and high-osmolarity media showed Michaelis-Menten kinetics with Km values of 3 and 5 microM and maximum rates of transport (Vmax) of 10 and 36 nmol min-1 mg of protein-1, respectively. The choline transporter exhibited considerable substrate specificity, and the results of competition experiments suggest that the fully methylated quaternary ammonium group is a key feature for substrate recognition. Thin-layer chromatography revealed that the radioactivity from exogenously provided [methyl-14C]choline accumulated intracellularly as [methyl-14C]glycine betaine, demonstrating that B. subtilis possesses enzymes for the oxidative conversion of choline into glycine betaine. Exogenously provided choline significantly increased the growth rate of B. subtilis in high-osmolarity media and permitted its proliferation under conditions that are otherwise strongly inhibitory for its growth. Choline and glycine betaine were not used as sole sources of carbon or nitrogen, consistent with their functional role in the process of adaptation of B. subtilis to high-osmolarity stress.

MeSH Terms
Bacillus subtilis/drug effects,metabolism,physiology Betaine/metabolism Biological Transport Choline/metabolism Cloning, Molecular Culture Media Escherichia coli Kinetics Osmolar Concentration Sodium Chloride/pharmacology Time Factors
Chemicals
Culture Media Betaine Sodium Chloride Choline
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Boch J
Max-Planck Institute for Terrestrial Microbiology, Marburg, Federal Republic of Germany.
Kempf B
Bremer E
References (27)
27 references, click to expand
  1. Osmoregulation in Rhodobacter sphaeroides.
    J Bacteriol. 1990 Jan;172(1):149-54 PMID: 2294084
  2. Characterization of three choline transport activities in Rhizobium meliloti: modulation by choline and osmotic stress.
    J Bacteriol. 1989 Jan;171(1):531-7 PMID: 2914855
  3. Binding protein dependent transport of glycine betaine and its osmotic regulation in Escherichia coli K12.
    Mol Gen Genet. 1986 Nov;205(2):225-33 PMID: 2949137
  4. Choline transport in Fusarium graminearum A 3/5.
    FEMS Microbiol Lett. 1992 May 1;71(3):247-51 PMID: 1624123
  5. DNA sequence and analysis of the bet genes encoding the osmoregulatory choline-glycine betaine pathway of Escherichia coli.
    Mol Microbiol. 1991 May;5(5):1049-64 PMID: 1956285
  6. The aerobic decomposition of choline by microorganisms. I. The ability of aerobic organisms, particularly coryneform bacteria, to utilize choline as the sole carbon and nitrogen source.
    Arch Mikrobiol. 1970;71(3):235-44 PMID: 4918912
  7. Osmotic control of glycine betaine biosynthesis and degradation in Rhizobium meliloti.
    J Bacteriol. 1988 Jul;170(7):3142-9 PMID: 3290197
  8. Stress proteins and cross-protection by heat shock and salt stress in Bacillus subtilis.
    J Gen Microbiol. 1992 Oct;138(10):2125-35 PMID: 1362210
  9. Prokaryotic osmoregulation: genetics and physiology.
    Annu Rev Microbiol. 1991;45:569-606 PMID: 1741624
  10. Betaine is the main compatible solute of halophilic eubacteria.
    J Bacteriol. 1984 Oct;160(1):478-9 PMID: 6148337
  11. The stabilization of proteins by osmolytes.
    Biophys J. 1985 Mar;47(3):411-4 PMID: 3978211
  12. 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. 1991 Sep;118(3):217-24 PMID: 1919294
  13. Living with water stress: evolution of osmolyte systems.
    Science. 1982 Sep 24;217(4566):1214-22 PMID: 7112124
  14. Roles of N-acetylglutaminylglutamine amide and glycine betaine in adaptation of Pseudomonas aeruginosa to osmotic stress.
    Appl Environ Microbiol. 1993 Feb;59(2):473-8 PMID: 8434912
  15. Molecular biology of osmoregulation.
    Science. 1984 Jun 8;224(4653):1064-8 PMID: 16827211
  16. lac fusion analysis of the bet genes of Escherichia coli: regulation by osmolarity, temperature, oxygen, choline, and glycine betaine.
    J Bacteriol. 1988 Nov;170(11):5208-15 PMID: 3141381
  17. Choline-glycine betaine pathway confers a high level of osmotic tolerance in Escherichia coli.
    J Bacteriol. 1986 Mar;165(3):849-55 PMID: 3512525
  18. Trehalose metabolism in Escherichia coli: stress protection and stress regulation of gene expression.
    Mol Microbiol. 1993 Apr;8(2):205-10 PMID: 8391102
  19. Stress-induced activation of the sigma B transcription factor of Bacillus subtilis.
    J Bacteriol. 1993 Dec;175(24):7931-7 PMID: 8253681
  20. TRANSFORMATION OF BIOCHEMICALLY DEFICIENT STRAINS OF BACILLUS SUBTILIS BY DEOXYRIBONUCLEATE.
    Proc Natl Acad Sci U S A. 1958 Oct 15;44(10):1072-8 PMID: 16590310
  21. Analysis of the induction of general stress proteins of Bacillus subtilis.
    Microbiology. 1994 Apr;140 ( Pt 4):741-52 PMID: 8012595
  22. Choline transport activity in Staphylococcus aureus induced by osmotic stress and low phosphate concentrations.
    J Bacteriol. 1993 Apr;175(8):2400-6 PMID: 8468298
  23. Staphylococcus aureus osmoregulation: roles for choline, glycine betaine, proline, and taurine.
    J Bacteriol. 1992 Apr;174(8):2711-6 PMID: 1556089
  24. Determination of turgor pressure in Bacillus subtilis: a possible role for K+ in turgor regulation.
    J Gen Microbiol. 1990 Dec;136(12):2521-6 PMID: 2127801
  25. The effects of osmotic upshock on the intracellular solute pools of Bacillus subtilis.
    J Gen Microbiol. 1990 Dec;136(12):2527-35 PMID: 2127802
  26. Choline oxidase, a catabolic enzyme in Arthrobacter pascens, facilitates adaptation to osmotic stress in Escherichia coli.
    J Bacteriol. 1991 Jan;173(2):472-8 PMID: 1987142
  27. Selection, mapping, and characterization of osmoregulatory mutants of Escherichia coli blocked in the choline-glycine betaine pathway.
    J Bacteriol. 1986 Mar;165(3):856-63 PMID: 3512526
Article Info
Journal
Journal of bacteriology
Abbr.
J Bacteriol
ISSN
0021-9193
Published
1994-09-00
Pages
5364-71
Language
English
Region
United States
NLM ID
2985120R
PMCID
PMC196722
Subset
IM
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