Part:BBa_K3733005
J23106a:Improved promoter of J23106
J23106a is a constitutive promoter obtained by mutating <a url="https://parts.igem.org/Part:BBa_J23106"> J23106</a>. The strength of this promoter is much weaker than J23106.
Functional Parameters
To characterize this part, J23106a and J23106 were cloned into pSC101 vector separately. We chose <a url="https://parts.igem.org/Part:BBa_K3733012">neGFP </a> as the reporter. Plasmids were transferred into E.coli DH5α. The E. coli strain was cultured overnight, and the relative intensity of J23106a was evaluated by measuring RFU/OD600 under the control of two different promoters. The relative fluorescence unit (RFU) was determined by Synergy H1 microplate reader.
Figure 2. Comparison of relative strength between J23106 and J23106a.The microplate reader gain adopts 50
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 7
Illegal NheI site found at 30 - 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
biology | Escherichia coli |