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Fig. 2 | Microbial Cell Factories

Fig. 2

From: Two-step conversion of polyethylene into recombinant proteins using a microbial platform

Fig. 2

a Growth of P. aeruginosa RR1 RK2-GFPuv at 24 and 48 h post inoculation with and without kanamycin supplementation. b P. aeruginosa RR1 RK2-GFPuv plasmid maintenance at 24 and 48 h post inoculation in the presence of 50 µg/ml kanamycin. c Growth of P. oleovorans RK2-GFPuv at 24 and 48 h post inoculation with and without kanamycin supplementation. d P. oleovorans RK2-GFPuv plasmid maintenance at 24 and 48 h post inoculation in the presence of 50 µg/ml kanamycin. For both strains, culture conditions that yielded the best growth on hexadecane were used. Namely 0.46% w/v hexadecane with 1.9 g/L NH4NO3 for P. aeruginosa RR1 and 0.46% w/v hexadecane with 2.5 g/L NH4Cl for P. oleovorans. Error bars represent standard deviations from the mean values of three replicates

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