The pH optimum of native uracil-DNA glycosylase of Archaeoglobus fulgidus compared to recombinant enzyme indicates adaption to cytosolic pH

Acta Biochim Pol. 2014;61(2):393-5. Epub 2014 Jun 16.

Abstract

Uracil-DNA glycosylase of Archaeoglobus fulgidus (Afung) in cell extracts exhibited maximal activity around pH 6.2 as compared to pH 4.8 for the purified recombinant enzyme expressed in Escherichia coli. Native Afung thus seems to be adapted to the intracellular pH of A. fulgidus, determined to be 7.0±0.1. Both recombinant and native Afung exhibited a broad temperature optimum for activity around 80°C, reflecting the A. fulgidus optimal growth temperature of 83°C. Adaption to the neutral conditions in the A. fulgidus cytoplasm might be due to covalent modifications or accessory factors, or due to a different folding when expressed in the native host.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptation, Physiological
  • Archaeal Proteins / genetics
  • Archaeal Proteins / metabolism*
  • Archaeoglobus fulgidus / enzymology*
  • Cytosol / enzymology*
  • Escherichia coli / genetics
  • Escherichia coli / metabolism
  • Gene Expression
  • Hot Temperature
  • Hydrogen-Ion Concentration
  • Kinetics
  • Recombinant Proteins / genetics
  • Recombinant Proteins / metabolism
  • Substrate Specificity
  • Uracil-DNA Glycosidase / genetics
  • Uracil-DNA Glycosidase / metabolism*

Substances

  • Archaeal Proteins
  • Recombinant Proteins
  • Uracil-DNA Glycosidase