Difference between revisions of "Part:BBa K4283013:Design"
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Here we report an improved version of sulAp UV-inducible promoter, the double LexA Binding Unit RadiatioN Exercisable Regulator (dLexburner,). SulAp has been used for regulatory purposes and was initially designed and submitted by team UT-Tokyo in 2011 (iGEM11_UT-Tokyo, Part:BBa_K518010). | Here we report an improved version of sulAp UV-inducible promoter, the double LexA Binding Unit RadiatioN Exercisable Regulator (dLexburner,). SulAp has been used for regulatory purposes and was initially designed and submitted by team UT-Tokyo in 2011 (iGEM11_UT-Tokyo, Part:BBa_K518010). | ||
− | + | For detailed part infomation, please navigate: Part:BBa K4283013 | |
− | + | ||
===Source=== | ===Source=== | ||
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===References=== | ===References=== | ||
+ | Lewis, L. K., Harlow, G. R., Gregg-Jolly, L. A., & Mount, D. W. (1994). Identification of high affinity binding sites for LexA which define new DNA damage-inducible genes in Escherichia coli. Journal of molecular biology, 241(4), 507-523. | ||
+ | |||
+ | Oertel-Buchheit, P., Porte, D., Schnarr, M., & Granger-Schnarr, M. (1992). Isolation and characterization of LexA mutant repressers with enhanced DNA binding affinity. Journal of molecular biology, 225(3), 609-620. | ||
+ | |||
+ | Little, J. W., & Gellert, M. (1983). The SOS regulatory system: control of its state by the level of RecA protease. Journal of molecular biology, 167(4), 791-808. | ||
+ | |||
+ | Sandler, S. J. (1994). Studies on the mechanism of reduction of W-inducible sulAp expression by recF overexpression in Escherichia coli K-12. Molecular and General Genetics MGG, 245(6), 741-749. |
Latest revision as of 10:12, 13 October 2022
dLexburner SulAp
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
Here we report an improved version of sulAp UV-inducible promoter, the double LexA Binding Unit RadiatioN Exercisable Regulator (dLexburner,). SulAp has been used for regulatory purposes and was initially designed and submitted by team UT-Tokyo in 2011 (iGEM11_UT-Tokyo, Part:BBa_K518010).
For detailed part infomation, please navigate: Part:BBa K4283013
Source
biosynthesis
References
Lewis, L. K., Harlow, G. R., Gregg-Jolly, L. A., & Mount, D. W. (1994). Identification of high affinity binding sites for LexA which define new DNA damage-inducible genes in Escherichia coli. Journal of molecular biology, 241(4), 507-523.
Oertel-Buchheit, P., Porte, D., Schnarr, M., & Granger-Schnarr, M. (1992). Isolation and characterization of LexA mutant repressers with enhanced DNA binding affinity. Journal of molecular biology, 225(3), 609-620.
Little, J. W., & Gellert, M. (1983). The SOS regulatory system: control of its state by the level of RecA protease. Journal of molecular biology, 167(4), 791-808.
Sandler, S. J. (1994). Studies on the mechanism of reduction of W-inducible sulAp expression by recF overexpression in Escherichia coli K-12. Molecular and General Genetics MGG, 245(6), 741-749.