Identification of a Ferric uptake regulator from Microcystis aeruginosa PCC7806

FEMS Microbiol Lett. 2006 Jan;254(1):63-70. doi: 10.1111/j.1574-6968.2005.00015.x.

Abstract

Ferric uptake regulator (Fur) proteins are widely recognized as repressors that in many prokaryotes regulate a large number of genes involved in iron homeostasis and oxidative stress response. In our study, we were able to identify the complete sequence of the fur gene from Microcystis aeruginosa using inverse-polymerase chain reaction. DNA sequence analysis confirmed the presence of a 183 amino-acid open reading frame that showed high identity with Fur proteins reported for cyanobacteria. The recombinant Fur protein has been purified and electrophoretical mobility shift assays shown to be active. Mn2+ and dithiothreitol enable Fur to bind to its promoter, with dithiothreitol being more potent. The expression of Fur in Microcystis was induced about twofold in iron-deficient conditions.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Bacterial Proteins
  • Base Sequence
  • Cloning, Molecular
  • Ferric Compounds / metabolism
  • Gene Expression Regulation, Bacterial
  • Iron / metabolism*
  • Microcystis / metabolism
  • Molecular Sequence Data
  • Recombinant Proteins / genetics
  • Recombinant Proteins / metabolism
  • Repressor Proteins
  • Sequence Alignment
  • Sequence Analysis, DNA

Substances

  • Bacterial Proteins
  • Ferric Compounds
  • Recombinant Proteins
  • Repressor Proteins
  • ferric uptake regulating proteins, bacterial
  • Iron