The Biosynthesis of the Benzoxazole in Nataxazole Proceeds via an Unstable Ester and has Synthetic Utility

Angew Chem Int Ed Engl. 2020 Apr 6;59(15):6054-6061. doi: 10.1002/anie.201915685. Epub 2020 Feb 11.

Abstract

Heterocycles, a class of molecules that includes oxazoles, constitute one of the most common building blocks in current pharmaceuticals and are common in medicinally important natural products. The antitumor natural product nataxazole is a model for a large class of benzoxazole-containing molecules that are made by a pathway that is not characterized. We report structural, biochemical, and chemical evidence that benzoxazole biosynthesis proceeds through an ester generated by an ATP-dependent adenylating enzyme. The ester rearranges via a tetrahedral hemiorthoamide to yield an amide, which is a shunt product and not, as previously thought, an intermediate in the pathway. A second zinc-dependent enzyme catalyzes the formation of hemiorthoamide from the ester but, by shuttling protons, the enzyme eliminates water, a reverse hydrolysis reaction, to yield the benzoxazole and avoids the amide. These insights have allowed us to harness the pathway to synthesize a series of novel halogenated benzoxazoles.

Keywords: benzoxazole; enzyme catalysis; heterocycles; structural biology; structure-activity relationships.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphate / metabolism
  • Benzoxazoles / chemistry*
  • Benzoxazoles / metabolism*
  • Enzymes / chemistry
  • Enzymes / metabolism
  • Esters / chemistry*
  • Halogenation
  • Models, Molecular
  • Protein Conformation

Substances

  • Benzoxazoles
  • Enzymes
  • Esters
  • nataxazole
  • Adenosine Triphosphate