Reaction mechanism of Escherichia coli dihydrodipicolinate synthase investigated by X-ray crystallography and NMR spectroscopy

Biochemistry. 1997 Jan 7;36(1):24-33. doi: 10.1021/bi962272d.


Dihydrodipicolinate synthase (DHDPS) catalyzes the condensation of pyruvate with L-aspartate beta-semialdehyde. It is the first enzyme unique to the diaminopimelate pathway of lysine biosynthesis. Here we present the crystal structures of five complexes of Escherichia coli DHDPS with substrates, substrate analogs, and inhibitors. These include the complexes of DHDPS with (1) pyruvate, (2) pyruvate and the L-aspartate beta-semialdehyde analog succinate beta-semialdehyde, (3) the inhibitor alpha-ketopimelic acid, (4) dipicolinic acid, and (5) the natural feedback inhibitor L-lysine. The kinetics of inhibition were determined, and the binding site of the L-lysine was identified. NMR experiments were conducted in order to elucidate the nature of the product of the reaction catalyzed by DHDPS. By this method, (4S)-4-hydroxy-2,3,4,5-tetrahydro-(2S)-dipicolinic acid is identified as the only product. A reaction mechanism for DHDPS is proposed, and important features for inhibition are identified.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacterial Proteins / chemistry
  • Binding Sites
  • Crystallization
  • Crystallography, X-Ray
  • Escherichia coli / enzymology*
  • Hydro-Lyases / chemistry*
  • Hydro-Lyases / metabolism
  • Lysine / chemistry
  • Lysine / metabolism
  • Magnetic Resonance Spectroscopy
  • Models, Chemical
  • Models, Molecular
  • Molecular Structure
  • Picolinic Acids / chemistry
  • Picolinic Acids / metabolism
  • Protein Conformation
  • Pyruvates / chemistry
  • Pyruvates / metabolism
  • Schiff Bases / metabolism
  • Succinates / chemistry
  • Succinates / metabolism


  • Bacterial Proteins
  • Picolinic Acids
  • Pyruvates
  • Schiff Bases
  • Succinates
  • Hydro-Lyases
  • 4-hydroxy-tetrahydrodipicolinate synthase
  • Lysine
  • dipicolinic acid