Skip to main content
Applied and Environmental Microbiology logoLink to Applied and Environmental Microbiology
. 1996 Dec;62(12):4405–4409. doi: 10.1128/aem.62.12.4405-4409.1996

Physiologic Mechanisms Involved in Accumulation of 3-Hydroxypropionaldehyde during Fermentation of Glycerol by Enterobacter agglomerans

F Barbirato, P Soucaille, A Bories
PMCID: PMC1388999  PMID: 16535461

Abstract

When grown in 700 mM glycerol within the pH range 6.0 to 7.5, anaerobic pH-regulated cultures of Enterobacter agglomerans exhibited an extracellular accumulation of 3-hydroxypropionaldehyde (3-HPA). This phenomenon, which causes fermentation cessation, occurred earlier when pH was low. In contrast, substrate consumption was complete at pH 8. Levels of glycerol-catabolizing enzymes, i.e., glycerol dehydrogenase and dihydroxyacetone kinase for the oxidative route and glycerol dehydratase and 1,3-propanediol dehydrogenase for the reductive route, as well as the nucleotide pools were determined periodically in the pH 7- and pH 8-regulated cultures. A NAD/NADH ratio of 1.7 was correlated with the beginning of the production of the inhibitory metabolite. Further accumulation was dependent on the ratio of glycerol dehydratase activity to 1,3-propanediol dehydrogenase activity. For a ratio higher than 1, 3-HPA was produced until fermentation ceased, which occurred for the pH 7-regulated culture. At pH 8, a value below 1 was noticed and 3-HPA accumulation was transient, while the NAD/NADH ratio decreased. The low rate of glycerol dissimilation following the appearance of 3-HPA in the culture medium was attributed to the strong inhibitory effect exerted by 3-HPA on glycerol dehydrogenase activity.

Full Text

The Full Text of this article is available as a PDF (198.6 KB).

Selected References

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

  1. ABELES R. H., BROWNSTEIN A. M., RANDLES C. H. beta-Hydroxypropionaldehyde, an intermediate in the formation of 1,3-propanediol by Aerobacter aerogenes. Biochim Biophys Acta. 1960 Jul 15;41:530–531. doi: 10.1016/0006-3002(60)90054-8. [DOI] [PubMed] [Google Scholar]
  2. Barbirato F., Grivet J. P., Soucaille P., Bories A. 3-Hydroxypropionaldehyde, an inhibitory metabolite of glycerol fermentation to 1,3-propanediol by enterobacterial species. Appl Environ Microbiol. 1996 Apr;62(4):1448–1451. doi: 10.1128/aem.62.4.1448-1451.1996. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Bouvet O. M., Lenormand P., Carlier J. P., Grimont P. A. Phenotypic diversity of anaerobic glycerol dissimilation shown by seven enterobacterial species. Res Microbiol. 1994 Feb;145(2):129–139. doi: 10.1016/0923-2508(94)90006-x. [DOI] [PubMed] [Google Scholar]
  4. Chevalier M., Lin E. C., Levine R. L. Hydrogen peroxide mediates the oxidative inactivation of enzymes following the switch from anaerobic to aerobic metabolism in Klebsiella pneumoniae. J Biol Chem. 1990 Jan 5;265(1):42–46. [PubMed] [Google Scholar]
  5. Daniel R., Gottschalk G. Growth temperature-dependent activity of glycerol dehydratase in Escherichia coli expressing the Citrobacter freundii dha regulon. FEMS Microbiol Lett. 1992 Dec 15;100(1-3):281–285. doi: 10.1111/j.1574-6968.1992.tb14053.x. [DOI] [PubMed] [Google Scholar]
  6. Forage R. G., Foster M. A. Glycerol fermentation in Klebsiella pneumoniae: functions of the coenzyme B12-dependent glycerol and diol dehydratases. J Bacteriol. 1982 Feb;149(2):413–419. doi: 10.1128/jb.149.2.413-419.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Forage R. G., Lin E. C. DHA system mediating aerobic and anaerobic dissimilation of glycerol in Klebsiella pneumoniae NCIB 418. J Bacteriol. 1982 Aug;151(2):591–599. doi: 10.1128/jb.151.2.591-599.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Honda S., Toraya T., Fukui S. In situ reactivation of glycerol-inactivated coenzyme B12-dependent enzymes, glycerol dehydratase and diol dehydratase. J Bacteriol. 1980 Sep;143(3):1458–1465. doi: 10.1128/jb.143.3.1458-1465.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Johnson B. C., Stroinski A., Schneider Z. Glycerol dehydratase from Aerobacter aerogenes. Methods Enzymol. 1975;42:315–323. doi: 10.1016/0076-6879(75)42134-6. [DOI] [PubMed] [Google Scholar]
  10. Johnson E. A., Burke S. K., Forage R. G., Lin E. C. Purification and properties of dihydroxyacetone kinase from Klebsiella pneumoniae. J Bacteriol. 1984 Oct;160(1):55–60. doi: 10.1128/jb.160.1.55-60.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Johnson E. A., Levine R. L., Lin E. C. Inactivation of glycerol dehydrogenase of Klebsiella pneumoniae and the role of divalent cations. J Bacteriol. 1985 Oct;164(1):479–483. doi: 10.1128/jb.164.1.479-483.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. 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]
  13. LIN E. C., MAGASANIK B. The activation of glycerol dehydrogenase from Aerobacter aerogenes by monovalent cations. J Biol Chem. 1960 Jun;235:1820–1823. [PubMed] [Google Scholar]
  14. Lin E. C. Glycerol dissimilation and its regulation in bacteria. Annu Rev Microbiol. 1976;30:535–578. doi: 10.1146/annurev.mi.30.100176.002535. [DOI] [PubMed] [Google Scholar]
  15. MAGASANIK B., BROOKE M. S., KARIBIAN D. Metabolic pathways of glycerol dissimilation; a comparative study of two strains of Aerobacter aerogenes. J Bacteriol. 1953 Nov;66(5):611–619. doi: 10.1128/jb.66.5.611-619.1953. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. RUSH D., KARIBIAN D., KARNOVSKY M. L., MAGASANIK B. Pathways of glycerol dissimilation in two strains of Aerobacter aerogenes; enzymatic and tracer studies. J Biol Chem. 1957 Jun;226(2):891–899. [PubMed] [Google Scholar]
  17. Ruch F. E., Jr, Lin E. C., Kowit J. D., Tang C. T., Goldberg A. L. In vivo inactivation of glycerol dehydrogenase in Klebsiella aerogenes: properties of active and inactivated proteins. J Bacteriol. 1980 Mar;141(3):1077–1085. doi: 10.1128/jb.141.3.1077-1085.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. 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]
  19. Ruch F. E., Lin E. C. Independent constitutive expression of the aerobic and anaerobic pathways of glycerol catabolism in Klebsiella aerogenes. J Bacteriol. 1975 Oct;124(1):348–352. doi: 10.1128/jb.124.1.348-352.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Talarico T. L., Casas I. A., Chung T. C., Dobrogosz W. J. Production and isolation of reuterin, a growth inhibitor produced by Lactobacillus reuteri. Antimicrob Agents Chemother. 1988 Dec;32(12):1854–1858. doi: 10.1128/aac.32.12.1854. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Toraya T., Ushio K., Fukui S., Hogenkamp P. C. Studies on the mechanism of the adenosylcobalamin-dependent diol dehydrase reaction by the use of analogs of the coenzyme. J Biol Chem. 1977 Feb 10;252(3):963–970. [PubMed] [Google Scholar]
  22. Vasconcelos I., Girbal L., Soucaille P. Regulation of carbon and electron flow in Clostridium acetobutylicum grown in chemostat culture at neutral pH on mixtures of glucose and glycerol. J Bacteriol. 1994 Mar;176(5):1443–1450. doi: 10.1128/jb.176.5.1443-1450.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Applied and Environmental Microbiology are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES