Category:Team PSU 2

Fig 5 shows in vitro transcription from wild type bipA promoter with increasing concentrations of Phosphorylated BvgA. Low concentrations are sufficient to activate bipA transcription, while higher concentrations inhibit transcription.

Figure 3C. shows that large clusters of CheW chemotaxis protein predominately assemble at the cell poles of the cellular membrane.

Figure 2H. demonstrates that the largest clusters of the TAR chemotaxis proteins are predominately localized at the cell poles.

Figure 3F. shows predominant CheY chemotaxis protein localization to the cellular poles of the cell membrane.

Fig. 1B, MinC constructed under arabinose promoter control results in elongation in the presence of arabinose via inhibition of FtsZ polymerization (Fig. 4A)

ATc- strain shows MalF-mCerulean protein aggregation at mid cell indicating that the DnaK chaperone system is vital for proper membrane protein localization (Figure 1D).

Figure 1. Shows strong Dnak chaperone system localization to the inclusion body surfaces of fusion protein VP1LAC while low levels were detected in the cytoplasm.

Fig 5 shows in vitro transcription from wild type bipA promoter with increasing concentrations of Phosphorylated BvgA. Low concentrations are sufficient to activate bipA transcription, while higher concentrations inhibit transcription.

Figure 5A Immunoelectron microscopy with antibodies directed against BipA C-terminus reveals outer cell membrane localization.

Figure 5D confirms localization when cell extract treated with proK.

Figure 5E confirms localization when cell extract treated with proK and protease inhibitor.

FIG 3, midcell MinE rings result in detectable oscillation of GFP-MinD between periphery, inhibiting FtsZ assembly in aberrant locations

FIG 1A and 1B, expression of sulA inhibits FtsZ localization at division site and induces filamentation

Table 3 Localization of GFP-FtsQ in fts mutants, shows how denaturation of temperature-sensitive FtsZ at 42°C prevents FtsQ localization and results in no cytokinetic ring formation.

Figure 5. SEM Analysis

CagA positive H. pylori cells induced morphological changes to human gastric cells junctions.