Team:Cambridge/Parts

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Previous iGEM teams have charaterised an impressive array of inducible promoters, along with other elements of biosensing circuitry... Read More






Parts designed and constructed

[http://partsregistry.org/wiki/index.php?title=Part:BBa_K9110031.Fluoride Sensitive Riboswitch (Part:BBa_K911003) ]

Riboswitch that is highly sensitive to the F- ion. We have characterized this part in three different chassis: TOP10 e.coli, Laboratory strain bacillus subtilis and a strain of bacillus subtilis with its normal fluoride riboswitch knocked out (kindly provided by the Breaker lab in Yale). Results of Miller assays for these three chassis are also provided.


[http://partsregistry.org/wiki/index.php?title=Part:BBa_K9110042.Synthesised Ratiometric Luciferase construct in non-standard plasmid (Part:BBa_K911004) ]

This part was designed as a ratiometric luciferase reporter. The first promoter, hyperSpank, is LacI - repressed and controls the transcription of a (vibrio harveyi) luxA gene that has been fused at the N-terminus to an mOrange gene via a flexible linker. This was described by Dachuan Ke and Shiao-Chun Tu (2011) as having an additional peak in its emission spectrum at 560 nm, whereas the normal peak is at 490 nm. This is terminated by b0015. Downstream, pVEG controls the translation of the entire normal lux operon, which is again terminated by b0015. The idea is that the normal luciferase output acts as an internal control signal, to which the output of the induced luciferase with the spectral shift can be normalised. We designed this to be compatible with our cheap open-source sensing hardware. We contacted the registry about this part and were granted exemption from the pSB1C3 standard for this part.


<groupparts>iGEM012 Cambridge</groupparts>