6ONT

Structure of the Francisella response regulator 1452 receiver domain

6ONT の概要

• エントリーDOI: 10.2210/pdb6ont/pdb
• 分子名称: Two-component response regulator 1452 receiver, CALCIUM ION, SODIUM ION, ... (5 entities in total)
• 機能のキーワード: response regulator, transcription regulator, transcription
• 由来する生物種: Francisella tularensis subsp. novicida (strain U112)
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 15060.65

構造登録者

Milton, M.E.,Cavanagh, J. (登録日: 2019-04-22, 公開日: 2020-03-25, 最終更新日: 2023-10-11)

主引用文献

Dean, S.N.,Milton, M.E.,Cavanagh, J.,van Hoek, M.L.
Francisella novicidaTwo-Component System Response Regulator BfpR Modulates iglC Gene Expression, Antimicrobial Peptide Resistance, and Biofilm Production.
Front Cell Infect Microbiol, 10:82-82, 2020

PubMed Abstract: Response regulators are a critical part of the two-component system of gene expression regulation in bacteria, transferring a signal from a sensor kinase into DNA binding activity resulting in alteration of gene expression. In this study, we investigated a previously uncharacterized response regulator in , FTN_1452 that we have named BfpR (Biofilm-regulating protein Regulator, ). In contrast to another Francisella response regulator, QseB/PmrA, BfpR appears to be a negative regulator of biofilm production, and also a positive regulator of antimicrobial peptide resistance in this bacterium. The protein was crystallized and X-ray crystallography studies produced a 1.8 Å structure of the BfpR N-terminal receiver domain revealing interesting insight into its potential interaction with the sensor kinase. Structural analysis of BfpR places it in the OmpR/PhoP family of bacterial response regulators along with WalR and ResD. Proteomic and transcriptomic analyses suggest that BfpR overexpression affects expression of the critical virulence factor iglC, as well as other proteins in the bacterium. We demonstrate that mutation of is associated with an antimicrobial peptide resistance phenotype, a phenotype also associated with other response regulators, for the human cathelicidin peptide LL-37 and a sheep antimicrobial peptide SMAP-29. with mutated replicated better than WT in intracellular infection assays in human-derived macrophages suggesting that the down-regulation of iglC expression in mutant may enable this intracellular replication to occur. Response regulators have been shown to play important roles in the regulation of bacterial biofilm production. We demonstrate that biofilm formation was highly increased in the mutant, corresponding to altered glycogen synthesis. Waxworm infection experiments suggest a role of BfpR as a negative modulator of iglC expression with de-repression by Mg. In this study, we find that the response regulator BfpR may be a negative regulator of biofilm formation, and a positive regulator of antimicrobial peptide resistance in .

PubMed: 32232010
DOI: 10.3389/fcimb.2020.00082

実験手法

X-RAY DIFFRACTION (1.803 Å)