Skip to main content
Journal of Bacteriology logoLink to Journal of Bacteriology
. 1976 Aug;127(2):747–754. doi: 10.1128/jb.127.2.747-754.1976

Phosphorylation of glycerol and dihydroxyacetone in Acetobacter xylinum and its possible regulatory role.

H Weinhouse, M Benziman
PMCID: PMC232980  PMID: 956117

Abstract

Extracts of Acetobacter xylinum catalyze the phosphorylation of glycerol and dihydroxyacetone (DHA) by adenosine 5'-triphosphate (ATP) to form, respectively, L-alpha-glycerophosphate and DHA phosphate. The ability to promote phosphorylation of glycerol and DHA was higher in glycerol-grown cells than in glucose- or succinate-grown cells. The activity of glycerol kinase in extracts is compatible with the overall rate of glycerol oxidation in vivo. The glycerol-DHA kinase has been purified 210-fold from extracts, and its molecular weight was determined to be 50,000 by gel filtration. The glycerol kinase to DHA kinase activity ratio remained essentially constant at 1.6 at all stages of purification. The optimal pH for both reactions was 8.4 to 9.2. Reaction rates with the purified enzyme were hyperbolic functions of glycerol, DHA, and ATP. The Km for glycerol is 0.5 mM and that for DHA is 5 mM; both are independent of the ATP concentration. The Km for ATP in both kinase reactions is 0.5 mM and is independent of glycerol and DHA concentrations. Glycerol and DHA are competitive substrates with Ki values equal to their respective Km values as substrates. D-Glyceraldehyde and l-Glyceraldehyde were not phosphorylated and did not inhibit the enzyme. Among the nucleotide triphosphates tested, only ATP was active as the phosphoryl group donor. Fructose diphosphate (FDP) inhibited both kinase activities competitively with respect to ATP (Ki= 0.02 mM) and noncompetitively with respect to glycerol and DHA. Adenosine 5'-diphosphate (ADP) and adenosine 5'-monophosphate (AMP) inhibited both enzymic activities competitively with respect to ATP (Ki (ADP) = 0.4 mM; Ki (AMP) =0.25 mM). A. xylinum cells with a high FDP content did not grow on glycerol. Depletion of cellular FDP by starvation enabled rapid growth on glycerol. It is concluded that a single enzyme from A. xylinum is responsible for the phosphorylation of both glycerol and DHA. This as well as the sensitivity of the enzyme to inhibition by FDP and AMP suggest that it has a regulatory role in glycerol metabolism.

Full text

PDF
748

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. BENZIMAN M., ABELIOVITZ A. METABOLISM OF DICARBOXYLIC ACIDS IN ACETOBACTER XYLINUM. J Bacteriol. 1964 Feb;87:270–277. doi: 10.1128/jb.87.2.270-277.1964. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. BENZIMAN M., BURGER-RACHAMIMOV H. Synthesis of cellulose from pyruvate by succinate-grown cells of Acetobacter xylinum. J Bacteriol. 1962 Oct;84:625–630. doi: 10.1128/jb.84.4.625-630.1962. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Benziman M., Palgi A. Characterization and properties of the pyruvate phosphorylation system of Acetobacter xylinum. J Bacteriol. 1970 Oct;104(1):211–218. doi: 10.1128/jb.104.1.211-218.1970. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. GROMET Z., SCHRAMM M., HESTRIN S. Synthesis of cellulose by Acetobacter Xylinum. 4. Enzyme systems present in a crude extract of glucose-grown cells. Biochem J. 1957 Dec;67(4):679–689. doi: 10.1042/bj0670679. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Grunnet N., Lundquist F. Kinetics of glycerol kinases from mammalian liver and Candida mycoderma. Eur J Biochem. 1967 Dec;3(1):78–84. doi: 10.1111/j.1432-1033.1967.tb19500.x. [DOI] [PubMed] [Google Scholar]
  6. HAUGE J. G., KING T. E., CHELDELIN V. H. Alternate conversions of glycerol to dihydroxyacetone in Acetobacter sub-oxydans. J Biol Chem. 1955 May;214(1):1–9. [PubMed] [Google Scholar]
  7. HAYASHI S., LIN E. C. CAPTURE OF GLYCEROL BY CELLS OF ESCHERICHIA COLI. Biochim Biophys Acta. 1965 Mar 29;94:479–487. doi: 10.1016/0926-6585(65)90056-7. [DOI] [PubMed] [Google Scholar]
  8. LIN E. C., LEVIN A. P., MAGASANIK B. The effect of aerobic metabolism on the inducible glycerol dehydrogenase of Aerobacter aerogenes. J Biol Chem. 1960 Jun;235:1824–1829. [PubMed] [Google Scholar]
  9. LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
  10. MONOD J., CHANGEUX J. P., JACOB F. Allosteric proteins and cellular control systems. J Mol Biol. 1963 Apr;6:306–329. doi: 10.1016/s0022-2836(63)80091-1. [DOI] [PubMed] [Google Scholar]
  11. Newsholme E. A., Robinson J., Taylor K. A radiochemical enzymatic activity assay for glycerol kinase and hexokinase. Biochim Biophys Acta. 1967 Mar 15;132(2):338–346. doi: 10.1016/0005-2744(67)90153-2. [DOI] [PubMed] [Google Scholar]
  12. Opheim D., Bernlohr R. W. Purification and regulation of glucose-6-phosphate dehydrogenase from Bacillus licheniformis. J Bacteriol. 1973 Dec;116(3):1150–1159. doi: 10.1128/jb.116.3.1150-1159.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Robinson J., Newsholme E. A. Some properties of hepatic glycerol kinase and their relation to the control of glycerol utilization. Biochem J. 1969 May;112(4):455–464. doi: 10.1042/bj1120455. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Ruch F. E., Lengeler J., Lin E. C. Regulation of glycerol catabolism in Klebsiella aerogenes. J Bacteriol. 1974 Jul;119(1):50–56. doi: 10.1128/jb.119.1.50-56.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. SCHRAMM M., GROMET Z., HESTRIN S. Synthesis of cellulose by Acetobacter Xylinum. 3. Substrates and inhibitors. Biochem J. 1957 Dec;67(4):669–679. doi: 10.1042/bj0670669. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. SCHRAMM M., HESTRIN S. Factors affecting production of cellulose at the air/liquid interface of a culture of Acetobacter xylinum. J Gen Microbiol. 1954 Aug;11(1):123–129. doi: 10.1099/00221287-11-1-123. [DOI] [PubMed] [Google Scholar]
  17. SCHRAMM M., KLYBAS V., RACKER E. Phosphorolytic cleavage of fructose-6-phosphate by fructose-6-phosphate phosphoketolase from Acetobacter xylinum. J Biol Chem. 1958 Dec;233(6):1283–1288. [PubMed] [Google Scholar]
  18. Swissa M., Weinhouse H., Benziman M. Activities of citrate synthase and other enzymes of Acetobacter xylinum in situ and in vitro. Biochem J. 1976 Feb 1;153(2):499–501. doi: 10.1042/bj1530499. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Thorner J. W., Paulus H. Catalytic and allosteric properties of glycerol kinase from Escherichia coli. J Biol Chem. 1973 Jun 10;248(11):3922–3932. [PubMed] [Google Scholar]
  20. Weinhouse H., Benziman M. Proceedings: Factors affecting glycerol and dihydroxyacetone phosphorylation in Acetobacter xylinum. Isr J Med Sci. 1975 Nov;11(11):1179–1180. [PubMed] [Google Scholar]

Articles from Journal of Bacteriology are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES