Skip to main content
. 2017 Sep 14;8:1714. doi: 10.3389/fmicb.2017.01714

Figure 6.

Figure 6

Determination of promoter activities by β-galactosidase. (A) Determination of promoter activities of pnpC operons induced by different substance. The β-galactosidase activity was determined in the strain PaW340 containing constructs pCMgfp-lpClacZ and pBBR1-tacexpnpM. The cells were induced by the following substrates: p-nitrophenol (PNP), m-nitrophenol (MNP), o-nitrophenol (ONP), hydroquinone (HQ), benzoquinone (BQ) and catechol, respectively. There was a significant difference in promoter activity between PNP and HQ as well as other substrates as inducers (p < 0.05). (B) Expression of promoter pnpA-lacZ translational fusions in strain PaW340. The β-galactosidase activities were determined in the strains: 1. PaW340 (pCMgfp-lpAlacZ+pBBR1-mcs2); 2. PaW340 (pCMgfp-lpAlacZ+pBBR1-tacpnpR); 3. PaW340 (pCMgfp-lpAlacZ+pBBR1-tacexpnpM); 4. PaW340 (pCMgfp-lpAlacZ+pBBR1-tacpnpMpnpR). There was a significant difference in the promoter activity of pnpA operon between regulator PnpR and PnpM with or without PNP (p < 0.05, Paired-samples test). (C) Expression of promoter pnpC-lacZ translational fusions in strain PaW340. The β-galactosidase activities were determined in the above strains: 1. PaW340 (pCMgfp-lpClacZ+pBBR1-mcs2); 2. PaW340 (pCMgfp-lpClacZ+pBBR1-tacpnpR); 3. PaW340 (pCMgfp-lpClacZ+pBBR1-tacexpnpM); 4. PaW340 (pCMgfp-lpClacZ+pBBR1-tacpnpMpnpR). There was a significant difference in the promoter activity of pnpC operon among different inducer (p < 0.05, Paired-samples test). Light gray columns stand for gene expression level without inducer. Gray columns stand for gene expression level induced by PNP. Black columns stand for gene expression level induced by HQ.