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. 1985 Jan;161(1):435–437. doi: 10.1128/jb.161.1.435-437.1985

Fermentation mechanism of fucose and rhamnose in Salmonella typhimurium and Klebsiella pneumoniae.

J Badía, J Ros, J Aguilar
PMCID: PMC214891  PMID: 3918008

Abstract

An equimolar amount of 1,2-propanediol was detected in the medium when Salmonella typhimurium or Klebsiella pneumoniae fermented L-fucose or L-rhamnose. These metabolic conditions induced a propanediol oxidoreductase that converted the lactaldehyde formed in the dissimilation of either sugar into the diol. The enzyme was further identified by cross-reaction with antibodies against Escherichia coli propanediol oxidoreductase. This indicates that L-fucose and L-rhamnose fermentation takes place in these species by 1,2-propanediol production and excretion.

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Selected References

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  1. Al-Zarban S., Heffernan L., Nishitani J., Ransone L., Wilcox G. Positive control of the L-rhamnose genetic system in Salmonella typhimurium LT2. J Bacteriol. 1984 May;158(2):603–608. doi: 10.1128/jb.158.2.603-608.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Boronat A., Aguilar J. Metabolism of L-fucose and L-rhamnose in Escherichia coli: differences in induction of propanediol oxidoreductase. J Bacteriol. 1981 Jul;147(1):181–185. doi: 10.1128/jb.147.1.181-185.1981. [DOI] [PMC free article] [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. Chiu T. H., Feingold D. S. L-rhamnulose 1-phosphate aldolase from Escherichia coli. Crystallization and properties. Biochemistry. 1969 Jan;8(1):98–108. doi: 10.1021/bi00829a015. [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. GHALAMBOR M. A., HEATH E. C. The metabolism of L-fucose. II. The enzymatic cleavage of L-fuculose 1-phosphate. J Biol Chem. 1962 Aug;237:2427–2433. [PubMed] [Google Scholar]
  7. GREEN M., COHEN S. S. Enzymatic conversion of L-fucose to L-fuculose. J Biol Chem. 1956 Apr;219(2):557–568. [PubMed] [Google Scholar]
  8. Gasser F., Gasser C. Immunological relationships among lactic dehydrogenases in the genera Lactobacillus and Leuconostoc. J Bacteriol. 1971 Apr;106(1):113–125. doi: 10.1128/jb.106.1.113-125.1971. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. HEATH E. C., GHALAMBOR M. A. The metabolism of L-fucose. I. The purification and properties of L-fuculose kinase. J Biol Chem. 1962 Aug;237:2423–2426. [PubMed] [Google Scholar]
  10. 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]
  11. OUCHTERLONY O. Antigen-antibody reactions in gels. IV. Types of reactions in coordinated systems of diffusion. Acta Pathol Microbiol Scand. 1953;32(2):230–240. [PubMed] [Google Scholar]
  12. Old D. C., Dawes P. F., Barker R. M. Transduction of inositol-fermenting ability demonstrating phylogenetic relationships among strains of Salmonella typhimurium. Genet Res. 1980 Apr;35(2):215–224. doi: 10.1017/s0016672300014063. [DOI] [PubMed] [Google Scholar]
  13. Ros J., Aguilar J. Genetic and structural evidence for the presence of propanediol oxidoreductase isoenzymes in Escherichia coli. J Gen Microbiol. 1984 Mar;130(3):687–692. doi: 10.1099/00221287-130-3-687. [DOI] [PubMed] [Google Scholar]
  14. SANDERSON K. E., DEMEREC M. THE LINKAGE MAP OF SALMONELLA TYPHIMURIUM. Genetics. 1965 Jun;51:897–913. doi: 10.1093/genetics/51.6.897. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Saint Martin E. J., Mortlock R. P. Natural and altered induction of the L-fucose catabolic enzymes in Klebsiella aerogenes. J Bacteriol. 1976 Jul;127(1):91–97. doi: 10.1128/jb.127.1.91-97.1976. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Sanderson K. E., Roth J. R. Linkage map of Salmonella typhimurium, Edition VI. Microbiol Rev. 1983 Sep;47(3):410–453. doi: 10.1128/mr.47.3.410-453.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. TAKAGI Y., SAWADA H. THE METABOLISM OF L-RHAMNOSE IN ESCHERICHIA COLI. I. L-RHAMNOSE ISOMERASE. Biochim Biophys Acta. 1964 Oct 23;92:10–17. doi: 10.1016/0926-6569(64)90263-9. [DOI] [PubMed] [Google Scholar]
  18. TAKAGI Y., SAWADA H. THE METABOLISM OF L-RHAMNOSE IN ESCHERICHIA COLI. II. L-RHAMNULOSE KINASE. Biochim Biophys Acta. 1964 Oct 23;92:18–25. doi: 10.1016/0926-6569(64)90264-0. [DOI] [PubMed] [Google Scholar]

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