Part:BBa_K1412014
Characterize the efficiency of pTetR (R0040) with chemotaxis
BBa_K1412014: pTetR-RBS(1.0)-CheZ-TT
This part consists of [http://en.wikipedia.org/wiki/Chemotaxis cheZ] gene which can express CheZ protein make E. coli tumbling or swimming straight. In this light, we linked different promoters before cheZ gene. Then we can characterize the efficiency of promoter via measuring the migration distance positively associated with the expression strength of CheZ protein.
Usage
When we want to characterize the efficiency of promoter, we usually connect the promoter with GFP, then measuring the fluorescence intensity of GFP. In our part, you just need connect RBS(1.0) after a pTetR promoter and before CheZ gene, ending with double terminator(pTetR-RBS(1.0)-CheZ-TT). Then transfer this gene circuit into E.coli (CheZ knocked out), and coat plates, culuture on semi-solid medium to measure the migration diameter of E.coli.
Relevant parts
BBa_K1412000: pLac-RBS(1.0)-CheZ-TT CheZ generator under pLac promoter
BBa_K1412005: RBS(1.0)-CheZ-TT
BBa_K1412006: RBS(0.01)-CheZ-TT
BBa_K1412007: RBS(0.3)-CheZ-TT
BBa_K1412614: pBAD-RBS(1.0)-CheZ-TT Characterize the efficiency of promoters with chemotaxis
BBa_K1412801: pLac-RBS(0.01)-CheZ-TT Characterize the efficiency of RBS with chemotaxis
BBa_K1412829: pLac-RBS(0.3)-CheZ-TT Characterize efficiency of RBS with chemotaxis
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Reference
[1] [http://www.jbioleng.org/content/3/1/4 Kelly J R, Rubin A J, Davis J H, et al. Measuring the activity of BioBrick promoters using an in vivo reference standard[J]. Journal of biological engineering, 2009, 3(1): 4].
[2] https://parts.igem.org/Part:BBa_R0010:Experience
More information, click here: [http://2014.igem.org/Team:XMU-China# XMU-China]
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