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In silico Analysis and Molecular Modeling of RNA Polymerase, Sigma S (RpoS) Protein in Pseudomonas aeruginosa PAO1

Authors :
Mansour Sedighi
Mohsen Moghoofei
Ebrahim Kouhsari
Abazar Pournajaf
Behzad Emadi
Masoud Tohidfar
Mehrdad Gholami
Source :
Reports of Biochemistry and Molecular Biology, Vol 4, Iss 1, Pp 32-42 (2015)
Publication Year :
2015
Publisher :
Varastegan Institute for Medical Sciences, 2015.

Abstract

Background: Sigma factors are proteins that regulate transcription in bacteria. Sigma factors can be activated in response to different environmental conditions. The rpoS (RNA polymerase, sigma S) gene encodes sigma-38 (σ38, or RpoS), a 37.8 kDa protein in Pseudomonas aeruginosa (P. aeruginosa) strains. RpoS is a central regulator of the general stress response and operates in both retroactive and proactive manners; not only does it allow the cell to survive environmental challenges; it also prepares the cell for subsequent stresses (cross-protection). Methods: The significance of RpoS for stress resistance and protein expression in stationary-phase P. aeruginosa cells was assessed. The goal of the current study was to characterize RpoS of P. aeruginosa PAO1 using bioinformatics tools. Results: The results showed that RpoS is an unstable protein that belongs to the sigma-70 factor family. Secondary structure analysis predicted that random coil is the predominant structure followed by extended alpha helix. The three-dimensional (3D) structure was modeled using SWISS-MODEL Workspace. Conclusion: Determination of sequence, function, structure, and predicted epitopes of RpoS is important for modeling of inhibitors that will help in the design of new drugs to combat multi-drug-resistant (MDR) strains. Such information may aid in the development of new diagnostic tools, drugs, and vaccines for treatment in endemic regions.

Details

Language :
English
ISSN :
23223480
Volume :
4
Issue :
1
Database :
Directory of Open Access Journals
Journal :
Reports of Biochemistry and Molecular Biology
Publication Type :
Academic Journal
Accession number :
edsdoj.9a3fda78775447cc86e3077b01110795
Document Type :
article