Difference between revisions of "Part:BBa K2570019:Design"
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===References=== | ===References=== | ||
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+ | 1. Soma, Y., Fujiwara, Y., Nakagawa, T., Tsuruno, K., & Hanai, T. (2017). Reconstruction of a metabolic regulatory network in Escherichia coli for purposeful switching from cell growth mode to production mode in direct GABA fermentation from glucose. Metabolic Engineering, 43(August), 54–63. | ||
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+ | 2. Soma, Y., Tsuruno, K., Wada, M., Yokota, A., Hanai, T., 2014. Metabolic flux redirection from a central metabolic pathway toward a synthetic pathway using a metabolic toggle switch. Metab. Eng. 23, 175–184. |
Latest revision as of 15:55, 16 October 2018
tetR+GFP+mazF+PLtetO1+RFP
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal AgeI site found at 2590
Illegal AgeI site found at 2702 - 1000COMPATIBLE WITH RFC[1000]
Design Notes
We have added an enzyme cutting site in the design to facilitate BIOBRICK.
anhydrotetracycline (ATc) is a tetracycline analog, showing increased (30x) affinity for tet repressor. 42 ng/mL gives induction at half maximum according to an in vitro assay.
Source
We ordered the part DNA from a synthesis company and had codon optimization of the sequence.
References
1. Soma, Y., Fujiwara, Y., Nakagawa, T., Tsuruno, K., & Hanai, T. (2017). Reconstruction of a metabolic regulatory network in Escherichia coli for purposeful switching from cell growth mode to production mode in direct GABA fermentation from glucose. Metabolic Engineering, 43(August), 54–63.
2. Soma, Y., Tsuruno, K., Wada, M., Yokota, A., Hanai, T., 2014. Metabolic flux redirection from a central metabolic pathway toward a synthetic pathway using a metabolic toggle switch. Metab. Eng. 23, 175–184.