| Literature DB >> 29945971 |
Juan L Teran-Melo1, Gabriela R Peña-Sandoval2, Hortencia Silva-Jimenez3, Claudia Rodriguez1, Adrián F Alvarez1, Dimitris Georgellis4.
Abstract
The Arc (anoxic redox control) two-component system of Escherichia coli, comprising ArcA as the response regulator and ArcB as the sensor histidine kinase, modulates the expression of numerous genes in response to respiratory growth conditions. Under reducing growth conditions, ArcB autophosphorylates at the expense of ATP, and transphosphorylates ArcA via a His292 → Asp576 → His717 → Asp54 phosphorelay, whereas under oxidizing growth conditions, ArcB catalyzes the dephosphorylation of ArcA-P by a reverse Asp54 → His717 → Asp576 → Pi phosphorelay. However, the exact phosphoryl group transfer routes and the molecular mechanisms determining their directions are unclear. Here, we show that, during signal propagation, the His292 → Asp576 and Asp576 → His717 phosphoryl group transfers within ArcB dimers occur intra- and intermolecularly, respectively. Moreover, we report that, during signal decay, the phosphoryl group transfer from His717 to Asp576 takes place intramolecularly. In conclusion, we present a mechanism that dictates the direction of the phosphoryl group transfer within ArcB dimers and that enables the discrimination of the kinase and phosphatase activities of ArcB.Entities:
Keywords: ArcB/A two-component system; bacteria; bacterial signal transduction; conformation; histidine kinase; intermolecular phosphotransfer; intramolecular phosphotransfer; phosphorelay; phosphoryl transfer; phosphorylation; sensor kinase
Mesh:
Substances:
Year: 2018 PMID: 29945971 PMCID: PMC6109937 DOI: 10.1074/jbc.RA118.003910
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157