Structural characterization of Escherichia coli sialic acid synthase

Biochem Biophys Res Commun. 2002 Jul 5;295(1):167-73. doi: 10.1016/s0006-291x(02)00620-4.

Abstract

Sialic acid synthase encoded by the neuB gene of Escherichia coli catalyzes the condensation of N-acetylmannosamine and phosphoenolpyruvate to form N-acetylneuraminic acid. This report demonstrates the first structural information on sialic acid synthase by CD, MALDI-TOF, and chemical cross-linking studies. Also, a specific cleavage by endogenous protease(s) has been identified at Lys(280) of the enzyme (40 kDa) by LC-MS and N-terminal sequencing analyses. The cleavage results in the formation of two inactive fragments of 33 and 7 kDa. The structural analysis indicates that the fragmentation is associated with a significant change of the enzyme from a tetrameric to trimeric form, and alterations in both secondary and native quaternary structures.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aldehyde-Lyases / chemistry
  • Circular Dichroism
  • Escherichia coli / enzymology*
  • Oxo-Acid-Lyases / chemistry*
  • Oxo-Acid-Lyases / metabolism
  • Protein Conformation
  • Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization

Substances

  • 2-dehydro-3-deoxyphosphooctonate aldolase
  • N-acetylneuraminate synthase
  • Aldehyde-Lyases
  • Oxo-Acid-Lyases
  • N-acetylneuraminate lyase