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Construction and characterization of recombinant systems for stress response analysis in pollutant-degrading rhodococci
Křenková, Lucie ; Štěpánek, Václav (advisor) ; Marešová, Helena (referee)
Genus Rhodococcus is represented by Gram-positive, mycolate-containing non- sporulating actinobacteria that excel in their ability to withstand effects of various physical and chemical stressors. Their enormous metabolic capacity allows them to efficiently degrade a wide range of toxic compounds. To benefit from these capabilities, it is essential to know the molecular basis of their response to the stresses, the regulation of which is primarily controlled by σ factors of RNA polymerase. These σ factors are still poorly described in rhodococci. This thesis aims to explore the potential of Rhodococcus erythropolis CCM2595 as a model organism for studying stress responses in rhodococci. R. erythropolis ΔsigH mutant and single-plasmid strains have been constructed which allow studying promoter activities of genes responding to osmotic, heat, and oxidative stress by measurement of GFP fluorescence intensity, in the cells of R. erythropolis. Further, homologous two- plasmid strains, which support induced overproduction of s factors, were also constructed. Comparison with analogous Corynebacterium glutamicum host-based systems showed that the use of rhodococci themselves as hosts for plasmid systems is still very limited, probably due to the plasmid instability in rhodococcal cells. Thus, for routine...
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Domain 1.1 of the primary sigma factor and a new expression system for Bacillus subtilis RNA polymerase.
Kálalová, Debora ; Krásný, Libor (advisor) ; Cvačková, Zuzana (referee)
RNA polymerase (RNAP) is a key multi-subunit enzyme of gene expression that, together with the σ factor, forms a holoenzyme and transcribes genetic information from DNA to RNA. RNAP from Bacillus subtilis and its primary factor σA were studied in this thesis. The σA factor determines the specificity for the promoters to which the holoenzyme binds. Part of its structure is domain 1.1, which is likely to prevent binding of σA to the promoter by itself (unless it is part of the holoenzyme) by binding to domains 2 and 4. The first part of the thesis verifies the hypothesis that domain 1.1 binds domains 2 and 4 and thus prevents binding of σA to the promoter. To this end, various domain constructs have been created and their interactions have been tested. Domain interaction was tested by Nitrocellulose Filter Binding Assay, EMSA, and in vitro transcription. The results did not show significant interaction between domains. The second part of the thesis deals with the creation of a tool for the study of the enzymatology of RNAP from B. subtilis - recombinant RNAP (rRNAP). First, a plasmid construct for expression of rRNAP in Escherichia coli was constructed by a series of cloning steps, followed by protein isolation and characterization. Isolation was achieved without contamination by σ factors (this...
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