Part:BBa_K2572025

pTac

pTac promoter is a hybrid of Lac promoter and Trp promoter, and shows much stronger expression when induce by IPTG than either. However in our experiments we found the promoter ineffective.

Characterization and Improvements by GENAS_China 2019

• Group: GENAS_China 2019
• This part can be seen as an improved version of the original Ptac promoter (BBa_K864400). The main improvement point is this version applyed a symmetrical lacO site to get a more tightly regulation.
• The page of a twin part was created for a full annotation (BBa_K3254014).
• We used this part to construct an IPTG inducible transcriptional device by combining with a lacI expression cassette(BBa_K3254022) on a P15A plamisd. An insulated sfgfp reporter translational unit (BBa_K3254024) was applied for quantitative assay the dynamic response curve. The full structure of this operon was described on the page of BBa_K3254025.
• Furthermore, we improved this part by mutant the -10 region of this promoter and successfully achieved a series of IPTG inducible promoters(Ptac-M1, Ptac-M2, Ptac-M3) with different dynamic ranges and lower non-induced activities.

Genetic Design

• The sequence detail was described on the page of BBa_K3254025.
• The host cell is E.coli DH5α.

Experimental Setup

• All incubations were carried out using a Digital Thermostatic Shaker maintained at 37 °C and 1000 rpm, using Corning flat-bottom 96-well plates sealed with sealing film. For characterization the circuit response functions, a previously developed quantitative method that measures gene expression at steady state was used(Zhang, Chen et al. 2016). Briefly, bacteria harboring the parts/circuits of interest were first inoculated from single colonies into a flat-bottom 96-well plate for overnight growth, after which the cell cultures were diluted 196-fold with M9 medium. After 3 h of growth, the cultures were further diluted 700-fold with M9 medium containing gradient concentrations of IPTG, and incubated for another 6 h. Finally, 20-μL samples of each culture were transferred to a new plate containing 180 μL per well of PBS supplemented with 2 mg/mL kanamycin to terminate protein expression. The fluorescence distribution of each sample was assayed using a flow cytometer with appropriate voltage settings; each distribution contained >20,000 events. Each sample was experimentally assayed at least three times. The arithmetical mean of each sample was determined using FlowJo software.
• M9 medium (supplemented）: 6.8 g/L Na₂HPO₄, 3 g/L KH₂PO₄, 0.5 g/L NaCl, 1 g/L NH₄Cl, 0.34 g/L thiamine, 0.2% casamino acids, 0.4% glucose, 2mM MgSO₄, and 100 μM CaCl₂.

Results

• Background: Cells without any FP genes.
• Ptac with normal lacO: BBa_K864400
• Ptac with symmetrical lacO: BBa_K2572025
• Ptac-M1: BBa_K3254015
• Ptac-M2: BBa_K3254016
• Ptac-M3: BBa_K3254017

References

• Zhang HM, et al. Measurements of Gene Expression at Steady State Improve the Predictability of Part Assembly. ACS Synthetic Biology 5, 269-273 (2016).
• Zong Y, et al. Insulated transcriptional elements enable precise design of genetic circuits. Nature communications 8, 52 (2017).

Sequence and Features

Assembly Compatibility:

• 10
  COMPATIBLE WITH RFC[10]
• 12
  COMPATIBLE WITH RFC[12]
• 21
  COMPATIBLE WITH RFC[21]
• 23
  COMPATIBLE WITH RFC[23]
• 25
  COMPATIBLE WITH RFC[25]
• 1000
  COMPATIBLE WITH RFC[1000]