Protein Expression and Purification, Vol.92, No.2, 190-194, 2013
Cloning, expression, purification and characterization of an iron-dependent regulator protein from Thermobifida fusca
Iron-dependent regulators (IdeRs) control the transcription of a variety of genes associated with iron homeostasis in Gram-positive bacteria. In this study we report the cloning of a putative IdeR gene from the moderate thermophile Thermobifida fusca into the pET-21a(+) expression vector. The expressed protein, Tf-IdeR, was purified using immobilized metal affinity and size-exclusion chromatography, and yielded approximately 12-16 mg of protein per liter of culture. The purified Tf-IdeR protein binds the fox operator sequence in the presence of divalent metal ions. Two Tf-IdeR binding sites were identified in the T. fusca genome upstream of a putative enterobactin exporter and a putative ABC-type multidrug transporter. (C) 2013 Elsevier Inc. All rights reserved.
Keywords:DtxR;IdeR;Thermobifida fusca;Iron-dependent regulator protein;Protein purification;DNA-binding