Biosynthesis of the macrolide oleandomycin by Streptomyces antibioticus. Purification and kinetic characterization of an oleandomycin glucosyltransferase

J Biol Chem. 1995 Aug 4;270(31):18234-9. doi: 10.1074/jbc.270.31.18234.

Abstract

The oleandomycin (OM) producer, Streptomyces antibioticus, possesses a mechanism involving two enzymes for the intracellular inactivation and extracellular reactivation of the antibiotic. Inactivation takes place by transfer of a glucose molecule from a donor (UDP-glucose) to OM, a process catalyzed by an intracellular glucosyltransferase. Glucosyltransferase activity is detectable in cell-free extracts concurrent with biosynthesis of OM. The enzyme has been purified 1,097-fold as a monomer, with a molecular mass of 57.1 kDa by a four-step procedure using three chromatographic columns. The reaction operates via a compulsory-order mechanism. This has been shown by steady-state kinetic studies using either OM or an alternative substrate (rosaramycin) and dead-end inhibitors, and isotopic exchange reactions at equilibrium. OM binds first to the enzyme, followed by UDP-glucose. A ternary complex is thus formed prior to transfer of glucose. UDP is then released, followed by the glycosylated oleandomycin (GS-OM).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Erythromycin / pharmacology
  • Glucosyltransferases / isolation & purification*
  • Glucosyltransferases / metabolism*
  • Glycosylation
  • Kinetics
  • Oleandomycin / biosynthesis*
  • Streptomyces antibioticus / enzymology
  • Streptomyces antibioticus / metabolism*
  • Uridine Diphosphate Glucose / pharmacology

Substances

  • Erythromycin
  • Glucosyltransferases
  • Oleandomycin
  • Uridine Diphosphate Glucose