Substitution of a conserved aspartate allows cation-induced polymerization of FtsZ

FEBS Lett. 2001 Apr 6;494(1-2):34-7. doi: 10.1016/s0014-5793(01)02310-9.

Abstract

The prokaryotic tubulin homologue FtsZ polymerizes in vitro in a nucleotide dependent fashion. Here we report that replacement of the strictly conserved Asp212 residue of Escherichia coli FtsZ by a Cys or Asn, but not by a Glu residue results in FtsZ that polymerizes with divalent cations in the absence of added GTP. FtsZ D212C and D212N mutants co-purify with GTP as bound nucleotide, providing an explanation for the unusual phenotype. We conclude that D212 plays a critical role in the coordination of a metal ion and the nucleotide at the interface of two FtsZ monomers.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Substitution
  • Aspartic Acid / genetics
  • Aspartic Acid / metabolism
  • Aspartic Acid / physiology*
  • Bacterial Proteins / genetics
  • Bacterial Proteins / metabolism*
  • Cations, Divalent
  • Cytoskeletal Proteins*
  • Guanosine Triphosphate / metabolism
  • Mutagenesis, Site-Directed
  • Polymers*

Substances

  • Bacterial Proteins
  • Cations, Divalent
  • Cytoskeletal Proteins
  • FtsZ protein, Bacteria
  • Polymers
  • Aspartic Acid
  • Guanosine Triphosphate