Team:Wageningen UR/Notebook/OptogeneticKillSwitch
These experiments were performed primarily by Marijn Uitenbroek, with significant contributions by Tianhe Wang during the final phase. Unless otherwise indicated, protocols were done according to the Protocols page.
May 16 - June 6: Obtaining Parts
Both MazE and MazF have been registered as BioBricks (parts BBa_K1096001 and BBa_K302033, respectively). However, as of the creation period of the kill switch, neither are available from the iGEM registry. For this reason, we chose to isolate both genes directly from E. coli genomic DNA via PCR amplification. In order to simplify the construction process, the forward primers we synthesized included BBa_K592006: FixK2 (Promoter triggered by YF1-FixJ)
Accounting for the possibility that natively produced MazE could interfere with the kill switch, we also obtained a MazEF-deficient strain (MC4100ΔmazEFrelA+, or ΔmazEF for short)1 for potential use as a chassis organism. A culture of these cells was made chemically competent.
4 July - 1 August: pDawn Construction
Our target constructs were put together piece by piece via standard 3A ligation. Isolated constructs were confirmed through sequencing.
- CP-YF1-FixJ-tt: Light sensing part, including promoter and terminator.
- FixK2-mRFP: Reporter (intended to assess exact response)
- FixK2-MazF:
8 August - 3 October: pDusk Construction
The greatest obstacle to creating a working kill switch was the fact that it proved impossible to create a part actively expressing MazF; the ligation-transformation process for this part failed consistently. The possibility was considered that the MazF produced under a constitutive promoter was simply too much for even non-deficient cells to handle properly. We therefore created a cloning strain that overproduces MazE. In order to do so, we made use of the ASKA cloning library2, a collection of E. coli strains that overexpress specific native genes when induced by IPTG. We grew a culture of the ASKA MazE strain (registered in the library under its synonym, chpR), then isolated the chloramphenicol-resistance plasmid and transformed it into a DH5α cloning strain as per standard protocols. The resulting strain (AE) was made chemically competent. During the final growth phase, the culture was induced by 0.1 mM IPTG. The ligation mixture of CP-MazF was transformed into these competent cells, which were then grown on IPTG-containing plates. However, no colonies containing the desired plasmid were found.
During this period, we also tested the response of our constructed pDusk-RFP by way of the light response protocol detailed on the Protocols page. A complete lack of distinguishable expression from this part prompted us to make use of the original pDawn- and pDusk-mCherry parts as created by Möglich et al.
References
1. Sat, B., Reches, M., Engelberg-Kulka, H. (2003)
The Escherichia coli mazEF Suicide Module Mediates Thymineless Death. Journal of Bacteriology vol. 185 no. 6, 1803-1807.
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2.Kitagawa, M., Ara, T., Arifuzzaman, M,, Ioka-Nakamichi, T., Inamoto, E., Toyonaga, H., Mori, H. (2005) Complete set of ORF clones of Escherichia coli ASKA library (a complete set of E. coli K-12 ORF archive): unique resources for biological research. DNA Research 12(5):291-9.↩
