Cloned constructs

For the final Colisweeper circuit we plan a four plasmid system. The mine cells constitutively express LuxI and NagZ. In the Non-Mine cells LuxR and PhoA are expressed constitutively whereas Aes and GusA are expressed from pLux promoters with different sensitivities. To get to this system we tested different versions of the circuit with GFP. In the following table we list all the biobricks we used, the plasmids we cloned and what experiments we used them for. In general we used standard biobrick cloning techniques as described in the methods section. Whenever we used PCR gene amplification for cloning, we list the primers used in the following table. To be able to co-transform different plasmids we used backbones with compatible origins of replication and resistance genes. In the table you can find which backbone versions we used for which constructs.

Figure 1. Plasmids in mine and non-mine cells

GFP constructs
	Description	Cloning	Maps
1	Receiver cell construct for GFP diffusion experiments	[http://parts.igem.org/Part:BBa_J09855 BBa_J09855] backbone (SpeI, PstI) and [http://parts.igem.org/Part:BBa_E0840 BBa_E0840] insert (XbaI, PstI)
2	Library of the Receiver cell constructs	Using the BBa_J09855-E0840 construct a library with mutated pLux promoters was created through site-saturation mutagenesis to screen for promoters with changed sensitivities for OHHL:
3	Receiver cell construct for GFP experiments without the LuxR generating part	[http://parts.igem.org/Part:BBa_R0062 BBa_R0062] backbone (SpeI, PstI) and [http://parts.igem.org/Part:BBa_E0840 BBa_E0840] insert (XbaI, PstI)

LuxI generating constructs
	Description	Cloning	Maps
4	Sender cell construct with a very strong constitutive promoter from the BBa_J23100 promoter library for GFP and Hydrolase experiments	[http://parts.igem.org/Part:BBa_J23100 BBa_J23100] backbone (SpeI, PstI) and [http://parts.igem.org/Part:BBa_K805016 BBa_K805016] insert (XbaI, PstI)
5	Sender cell construct with an intermediate constitutive promoter from the BBa_J23100 promoter library for GFP and Hydrolase experiments	[http://parts.igem.org/Part:BBa_J23118 BBa_J23118] backbone (SpeI, PstI) and [http://parts.igem.org/Part:BBa_K805016 BBa_K805016] insert (XbaI, PstI)
6	Sender cell construct with an intermediate constitutive promoter from the BBa_J23100 promoter library for GFP and Hydrolase experiments	[http://parts.igem.org/Part:BBa_J23110 BBa_J23110] backbone (SpeI, PstI) and [http://parts.igem.org/Part:BBa_K805016 BBa_K805016] insert (XbaI, PstI)
7	Sender cell construct with a weak constitutive promoter from the BBa_J23100 promoter library for GFP and Hydrolase experiments	[http://parts.igem.org/Part:BBa_J23114 BBa_J23114] backbone (SpeI, PstI) and [http://parts.igem.org/Part:BBa_K805016 BBa_K805016] insert (XbaI, PstI)

LuxR generating constructs
	Description	Cloning	Maps
8	constitutive LuxR generating biobrick	BBa_J09855
9	constitutive LuxR generating biobrick, with negative feedback-loop at high OHHL concentrations	BBa_F2621
10	constitutive LuxR generating construct, repressible through LacI	BBa_R0010 backbone (SpeI, PstI) and BBa_I0462 insert (XbaI, PstI)
11	constitutive LuxR generating construct, with negative feedback-loop at high OHHL concentrations	BBa_R0063 backbone (SpeI,PstI) and BBa_I0462 insert (XbaI, PstI)
12	auto-inducible LuxR generating construct with positive feedback loop	BBa_R0062 backbone (SpeI, PstI) and BBa_I0462 insert (XbaI, PstI)
13	negatively regulated pLuxL-LacI construct to improve leakiness of LuxR system	BBa_R0063 backbone (SpeI, PstI) and BBa_C0012 insert (SpeI,PstI)

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