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Fig. 5 | Microbial Cell Factories

Fig. 5

From: Exacerbation of substrate toxicity by IPTG in Escherichia coli BL21(DE3) carrying a synthetic metabolic pathway

Fig. 5

Summarized effects of IPTG concentration on gene expression levels, pathway output, and cell viability in pre-induced Escherichia coli deg31 cells. Viability was determined by plating pre-induced deg31 cells resuspended in phosphate buffer before incubation with TCP. Pathway output was expressed as the theoretical conversion of TCP into glycerol at the end of 5 h degradation experiments with pre-induced, resting deg31 cells (see also Additional file 1: Fig. S5). The content of TCP pathway enzymes was estimated by analyzing cell-free extracts obtained from pre-induced cells by sodium dodecyl sulfate polyacrylamide gel electrophoresis (Additional file 1: Fig. S7 and Table S1). Two gels were analysed by densitometry and mean values are shown. Error bars represent standard deviations calculated from three independent experiments. Values determined for deg31 pre-induced with 1 mM lactose are indicated by squares

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