Separation by FPLC chromatofocusing of UDP-glucosyltransferases from three developmental stages of Drosophila melanogaster

Arch Insect Biochem Physiol. 1997;34(3):347-58. doi: 10.1002/(SICI)1520-6327(1997)34:3<347::AID-ARCH8>3.0.CO;2-R.

Abstract

Variation of UDP-glucosyltransferase activity, during Drosophila melanogaster development, was analyzed. The endogenous metabolite xanthurenic acid and the xenobiotic compounds 1-naphthol and 2-naphthol were used as substrates. Developmentally regulated differences were observed for the three substrates, suggesting the presence of UDP-glucosyltransferase isoenzymes. This was further confirmed by FPLC chromatofocusing on a Mono P column: seven peaks of UDP-glucosyltransferase activity (pHs: > or = 6.3, 5.8, 5.5, 4.9, 4.5, 4.2, < or = 4.0) with either single or overlapping substrate specificity were detected. A single xanthurenic acid:UDP-glucosyltransferase activity (pl 5.8) was found throughout development. In contrast, a gradual increase in the number of 2-napthol:UDP-glucosyltransferase-isoenzymes (pl from 6.3 to 4.0) was observed during development, whereas no isoenzymes specific for 1-naphthol were resolved. Based on the distribution and substrate specificity of the eluted peaks in the three developmental stages analyzed, the presence of seven or possibly eight UDP-glucosyltransferase isoenzymes is proposed.

MeSH terms

  • Animals
  • Chromatography, Gel
  • Chromatography, High Pressure Liquid
  • Drosophila melanogaster / enzymology*
  • Drosophila melanogaster / growth & development
  • Female
  • Gene Expression Regulation, Developmental*
  • Gene Expression Regulation, Enzymologic
  • Glucosyltransferases / biosynthesis*
  • Glucosyltransferases / isolation & purification
  • Isoenzymes / biosynthesis*
  • Isoenzymes / isolation & purification
  • Oviposition
  • Substrate Specificity

Substances

  • Isoenzymes
  • Glucosyltransferases