The concerted inactivation of Escherichia coli uridine diphosphate galactose 4-epimerase by sugar nucleotide together with a free sugar

Biochem J. 1976 May 1;155(2):225-9. doi: 10.1042/bj1550225.

Abstract

1. The combined effect of the sugar nucleotides UDP-D-fucose or UDP-D-glucuronic acid together with the free sugars D-fucose or L-arabinose is the inactivation of the Escherichia coli enzyme UDP-galactose 4-epimerase (EC 5.1.3.2). The sugar nucleotide or the free sugar alone or the sugar nucleotide plus 5'-Ump do not inactivate the enzyme. 2. The inactivation of the enzyme by its substrate UDP-D-glucose was not affected by the presence of free sugar. 3. In all cases the inactivation observed follows pseudo-first-order kinetics. 4. A comparison of various sugar nucleotides indicates that the hydroxymethyl group at position 6 of the sugar moiety of the natural substrates is important for substrate binding.

MeSH terms

  • Arabinose / pharmacology*
  • Binding Sites
  • Carbohydrate Epimerases / antagonists & inhibitors*
  • Escherichia coli / enzymology*
  • Fucose / pharmacology*
  • Kinetics
  • UDPglucose 4-Epimerase / antagonists & inhibitors*
  • Uracil Nucleotides / pharmacology
  • Uridine Diphosphate Sugars / pharmacology*

Substances

  • Uracil Nucleotides
  • Uridine Diphosphate Sugars
  • Fucose
  • Arabinose
  • Carbohydrate Epimerases
  • UDPglucose 4-Epimerase