An investigation into the butyrylcholinesterase-catalyzed hydrolysis of formylthiocholine using heavy atom kinetic isotope effects

Bioorg Chem. 2016 Apr:65:57-60. doi: 10.1016/j.bioorg.2016.01.006. Epub 2016 Feb 2.

Abstract

Heavy atom kinetic isotope effects (KIEs) were determined for the butyrylcholinesterase-catalyzed hydrolysis of formylthiocholine (FTC). The leaving-S, carbonyl-C, and carbonyl-O KIEs are (34)k=0.994±0.004, (13)k=1.0148±0.0007, and (18)k=0.999±0.002, respectively. The observed KIEs support a mechanism for both acylation and deacylation where the steps up to and including the formation of the tetrahedral intermediate are at least partially rate determining. These results, in contrast to previous studies with acetylthiocholine, suggest that the decomposition of a tetrahedral intermediate is not rate-determining for FTC hydrolysis. Structural differences between the two substrates are likely responsible for the observed mechanism change with FTC.

Keywords: Butyrylcholinesterase; Kinetic isotope effects; Thioester hydrolysis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biocatalysis*
  • Butyrylcholinesterase / metabolism*
  • Humans
  • Hydrolysis
  • Isotopes / chemistry
  • Isotopes / metabolism*
  • Kinetics
  • Molecular Structure
  • Thiocholine / analogs & derivatives*
  • Thiocholine / chemistry
  • Thiocholine / metabolism

Substances

  • Isotopes
  • formylthiocholine
  • Thiocholine
  • Butyrylcholinesterase