Crystallization and preliminary crystallographic analysis of hygromycin B phosphotransferase from Escherichia coli

Acta Crystallogr Sect F Struct Biol Cryst Commun. 2007 Aug 1;63(Pt 8):685-8. doi: 10.1107/S1744309107032757. Epub 2007 Jul 21.

Abstract

Aminoglycoside antibiotics, such as hygromycin, kanamycin, neomycin, spectinomycin and streptomycin, inhibit protein synthesis by acting on bacterial and eukaryotic ribosomes. Hygromycin B phosphotransferase (Hph; EC 2.7.1.119) converts hygromycin B to 7''-O-phosphohygromycin using a phosphate moiety from ATP, resulting in the loss of its cell-killing activity. The Hph protein has been crystallized for the first time using a thermostable mutant and the hanging-drop vapour-diffusion method. The crystal provided diffraction data to a resolution of 2.1 A and belongs to space group P3(2)21, with unit-cell parameters a = b = 71.0, c = 125.0 A. Crystals of complexes of Hph with hygromycin B and AMP-PNP or ADP have also been obtained in the same crystal form as that of the apoprotein.

MeSH terms

  • Cinnamates / metabolism
  • Crystallization
  • Crystallography, X-Ray
  • Escherichia coli Proteins / chemistry*
  • Escherichia coli Proteins / metabolism
  • Hygromycin B / analogs & derivatives
  • Hygromycin B / metabolism
  • Phosphotransferases (Alcohol Group Acceptor) / chemistry*
  • Phosphotransferases (Alcohol Group Acceptor) / metabolism
  • Protein Synthesis Inhibitors / chemistry
  • Protein Synthesis Inhibitors / metabolism

Substances

  • Cinnamates
  • Escherichia coli Proteins
  • Protein Synthesis Inhibitors
  • Hygromycin B
  • hygromycin A
  • Phosphotransferases (Alcohol Group Acceptor)
  • hygromycin-B kinase