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Fig. 2 | Biotechnology for Biofuels and Bioproducts

Fig. 2

From: Efficient biosynthesis of (R)-mandelic acid from styrene oxide by an adaptive evolutionary Gluconobacter oxydans STA

Fig. 2

a FPKM value of 10 top strongly transcribed genes of G. oxydans 621H. b Strength of screened promoters evaluated with eGFP as reporter and the microscope pictures of P02805, P09400, P04650 and P12780. c Relative activity of SpEH. SpEH were expressed with screened and reported promoters. The enzyme activity of SpEH controlled by Plac was set to 100% and its enzyme activity was 5.69 ± 0.26 U/mL. ****P < 0.0001. d SDS–PAGE of SpEH expression strains with the screened promoters. Lane M: protein marker; Lane 1: whole cell protein of G. oxydans 621H without overexpressing SpEH; Lanes 2–11: whole cell protein of recombinant G. oxydans strains with SpEH expressed by Plac, Pdnak, PtufB, P12780, P04000, P04750, P10190, P09400, P02805, P04650. e Biotransformation time course of styrene oxide to R-MA of WT-speh and WT-control-speh cells. f Growth curves for G. oxydans 621H under 0, 1, 2, 3 and 4 g/L R-MA

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