TY - JOUR ID - 47019 TI - The Increase in Protein and Plasmid Yields of E. coli with Optimized Concentration of Ampicillin as Selection Marker JO - Iranian Journal of Biotechnology JA - IJB LA - en SN - 1728-3043 AU - Feizollahzadeh, Sadegh AU - Kouhpayeh, Shirin AU - Rahimmansh, Ilnaz AU - Khanahmad, Hossein AU - Sabzehei, Faezeh AU - Ganjalikhani-hakemi, Mazdak AU - Andalib, Alireza AU - Hejazi, Zahra AU - Rezaei, Abbas AD - Department of Immunology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, 81746-73461 Iran AD - Department of Molecular Biology and Genetics, School of Medicine, Isfahan University of Medical Sciences, Isfahan, 81746-73461 Iran Y1 - 2017 PY - 2017 VL - 15 IS - 2 SP - 128 EP - 134 KW - Ampicillin KW - Escherichia coli KW - Plasmid KW - Protein DO - DOI:10.15171/ijb.1467 N2 - Background: Escherichia coli is still the common host for ing and heterologous protein expression. Various strategies have been employed to increase protein expression in E. coli, but, it seems that external factors such as selection marker concentration can drastically aff ect the yield of protein and plasmid.Objectives: Alterations of protein expression and plasmid yields of E. coli in diff erent concentrations of ampicillin, as selection marker, will be determined. In order to improve heterologous expression, the system will be redesigned and optimized.Materials and Methods: The expression cassette of codon optimized EGFP for E. coli was synthesized in pUC57. The pUC57-GFP was transformed into E. coli Top10F’. The expression of GFP was verifi ed by SDS-PAGE and fl ow cytometry after induction by IPTG (0.5 mM) and incubation with 0, 100, 200 and 300 μg.mL-1 ampicillin. Plasmid copy numbers of samples were determined by Real-Time PCR on AMP gene using regression line of diluted standard curve.Results: GFP expressing clones formed fair green colonies on LB agar supplemented with 0.5 mM IPTG and showed fluorescence in FL1 fi lter of fl ow cytometry and an extra protein band on SDS-PAGE gel. The fl uorescent intensity of GFP in 0, 100, 200 and 300 μg.mL-1 ampicillin in medium were 549.83, 549.78, 1443.52, 684.87, and plasmid copy numbers were 6.07×109, 3.21×109, 2.32×1010 , 8.11×108, respectively. The plasmid yields were 55 ng.μL-1, 69 ng.μL-1, 164 ng.μL-1 and 41 ng.μL-1, respectively.Conclusion: Protein and plasmid yields of E. coli are variable in diff erent concentrations of ampicillin and need to be optimized in newly designed expression systems. Protein and plasmid yield in the optimized concentration (200 μg.mL-1) was signifi cantly (p < 0.01) higher than other doses. UR - https://www.ijbiotech.com/article_47019.html L1 - https://www.ijbiotech.com/article_47019_d2d0e812287ff2bcc9f52389c4411c33.pdf ER -