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. 1983 Jan;153(1):134–139. doi: 10.1128/jb.153.1.134-139.1983

Experimental evolution of a metabolic pathway for ethylene glycol utilization by Escherichia coli.

A Boronat, E Caballero, J Aguilar
PMCID: PMC217350  PMID: 6336729

Abstract

Spontaneous mutants of Escherichia coli able to grow on ethylene glycol as a sole source of carbon and energy were obtained from mutants that could grow on propylene glycol. Attempts to obtain ethylene glycol-utilizing mutants from wild-type E. coli were unsuccessful. The two major characteristics of the ethylene glycol-utilizing mutants were (i) increased activities of propanediol oxidoreductase, an enzyme present in the parental strain (a propylene glycol-positive strain), which also converted ethylene glycol into glycolaldehyde; and (ii) constitutive synthesis of high activities of glycolaldehyde dehydrogenase, which converted glycolaldehyde to glycolate. Glycolate was metabolized via the glycolate pathway, which was present in the wild-type cells; this was indicated by the induction in ethylene glycol-grown cells of glycolate oxidase, the first enzyme in the pathway. Glycolaldehyde dehydrogenase was partially characterized as an enzyme of this new metabolic pathway in E. coli, and glycolate was identified as the product of the reaction. This enzyme used NAD and NADP as coenzymes, although the NADP-dependent activity was about 10 times lower than the NAD-dependent activity. Uptake of [14C]ethylene glycol was dependent on the presence of the enzymes capable of metabolism of ethylene glycol. Glycolaldehyde and glycolate were identified as intermediate metabolites in the pathway.

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Selected References

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  1. Bachmann B. J. Pedigrees of some mutant strains of Escherichia coli K-12. Bacteriol Rev. 1972 Dec;36(4):525–557. doi: 10.1128/br.36.4.525-557.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Boronat A., Aguilar J. Experimental evolution of propanediol oxidoreductase in Escherichia coli. Comparative analysis of the wild-type and mutant enzymes. Biochim Biophys Acta. 1981 Jan 7;672(1):98–107. doi: 10.1016/0304-4165(81)90283-x. [DOI] [PubMed] [Google Scholar]
  3. Boronat A., Aguilar J. Rhamnose-induced propanediol oxidoreductase in Escherichia coli: purification, properties, and comparison with the fucose-induced enzyme. J Bacteriol. 1979 Nov;140(2):320–326. doi: 10.1128/jb.140.2.320-326.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Child J., Willetts A. Microbial metabolism of aliphatic glycols. Bacterial metabolism of ethylene glycol. Biochim Biophys Acta. 1978 Jan 18;538(2):316–327. doi: 10.1016/0304-4165(78)90359-8. [DOI] [PubMed] [Google Scholar]
  5. Cocks G. T., Aguilar T., Lin E. C. Evolution of L-1, 2-propanediol catabolism in Escherichia coli by recruitment of enzymes for L-fucose and L-lactate metabolism. J Bacteriol. 1974 Apr;118(1):83–88. doi: 10.1128/jb.118.1.83-88.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Dunstan P. M., Anthony C., Drabble W. T. Microbial metabolism of C 1 and C 2 compounds. The involvement of glycollate in the metabolism of ethanol and of acetate by Pseudomonas AM1. Biochem J. 1972 Jun;128(1):99–106. doi: 10.1042/bj1280099. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. FURUYA A., HAYASHI J. A. GLYCOLIC ACID OXIDATION BY ESCHERICHIA COLI ADAPTED TO GLYCOLATE. J Bacteriol. 1963 May;85:1124–1131. doi: 10.1128/jb.85.5.1124-1131.1963. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Gonzalez C. F., Taber W. A., Zeitoun M. A. Biodegradation of ethylene glycol by a salt-requiring bacterium. Appl Microbiol. 1972 Dec;24(6):911–919. doi: 10.1128/am.24.6.911-919.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. HANSEN R. W., HAYASHI J. A. Glycolate metabolism in Escherichia coli. J Bacteriol. 1962 Mar;83:679–687. doi: 10.1128/jb.83.3.679-687.1962. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Hacking A. J., Aguilar J., Lin E. C. Evolution of propanediol utilization in Escherichia coli: mutant with improved substrate-scavenging power. J Bacteriol. 1978 Nov;136(2):522–530. doi: 10.1128/jb.136.2.522-530.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. JAKOBY W. B. Aldehyde oxidation. I. Dehydrogenase from Pseudomonas fluorescens. J Biol Chem. 1958 May;232(1):75–87. [PubMed] [Google Scholar]
  12. KORNBERG H. L., SADLER J. R. The metabolism of C2-compounds in micro-organisms. VIII. A dicarboxylic acid cycle as a route for the oxidation of glycollate by Escherichia coli. Biochem J. 1961 Dec;81:503–513. doi: 10.1042/bj0810503. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. LeBlanc D. J., Mortlock R. P. Metabolism of D-arabinose: a new pathway in Escherichia coli. J Bacteriol. 1971 Apr;106(1):90–96. doi: 10.1128/jb.106.1.90-96.1971. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Ornston L. N., Ornston M. K. Regulation of glyoxylate metabolism in Escherichia coli K-12. J Bacteriol. 1969 Jun;98(3):1098–1108. doi: 10.1128/jb.98.3.1098-1108.1969. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. STOUTHAMER A. H., VAN BOOMJ, BASTIAANSE A. J. METABOLISM OF C2 COMPOUNDS IN ACETOBACTER ACETI. Antonie Van Leeuwenhoek. 1963;29:393–406. doi: 10.1007/BF02046092. [DOI] [PubMed] [Google Scholar]
  16. Sridhara S., Wu T. T., Chused T. M., Lin E. C. Ferrous-activated nicotinamide adenine dinucleotide-linked dehydrogenase from a mutant of Escherichia coli capable of growth on 1, 2-propanediol. J Bacteriol. 1969 Apr;98(1):87–95. doi: 10.1128/jb.98.1.87-95.1969. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Sridhara S., Wu T. T. Purification and properties of lactaldehyde dehydrogenase from Escherichia coli. J Biol Chem. 1969 Oct 10;244(19):5233–5238. [PubMed] [Google Scholar]
  18. Vanderwinkel E., De Vlieghere M. Physiologie et génétique de l'isocitritase et des malate synthases chez Escherichia coli. Eur J Biochem. 1968 Jun;5(1):81–90. doi: 10.1111/j.1432-1033.1968.tb00340.x. [DOI] [PubMed] [Google Scholar]
  19. Wu T. T. Experimental evolution in bacteria. CRC Crit Rev Microbiol. 1978 Sep;6(1):33–51. doi: 10.3109/10408417809090619. [DOI] [PubMed] [Google Scholar]

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