Enzyme redesign and interactions of substrate analogues with sterol methyltransferase to understand phytosterol diversity, reaction mechanism and the nature of the active site

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Abstract

Several STM (sterol methyltransferase) genes have been cloned, sequenced and expressed in bacteria recently, making it possible to address questions of the relationship between sterol structure and function. The active site and mechanism of action of a set of phylogenetically diverse SMTs have been probed by site-directed mutagenesis as well as by using substrate and related analogues of the SMT-catalysed reaction. An active-site model has been developed that is in accord with the results presented, which is consistent with the hypothesis that SMTs are bifunctional enzymes kinetically responsible to bind Δ24-acceptor sterols of specific steric and electronic character and rigid orientation imposed by multiple hydrophobic active site contacts exacted from a common waxy core. Functional divergence influenced by the architectural role of sterols in membranes is considered to govern the evolution of product distribution and specificity of individual SMTs as discussed.

Original languageEnglish
Pages (from-to)1189-1196
Number of pages8
JournalBiochemical Society Transactions
Volume33
Issue number5
DOIs
StatePublished - Nov 2005

Keywords

  • Enzyme redesign
  • Ergosterol
  • Phytosterol diversity
  • Site-directed mutagenesis
  • Sterol biosynthesis inhibitor
  • Sterol methyltransferase

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