Part:BBa_K2057004:Design
LasR under the regulation of the promoter BtI-BtII
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 715
Illegal AgeI site found at 912 - 1000COMPATIBLE WITH RFC[1000]
Design Notes
As promoter is not available in the biobricks, we amplified, sequenced and characterized using the cry1Ac gene as template.
Source
Promoter BtI-BtII is harbor in a megaplasmid of B. thuringiensis, lasR was obtained from a biobrick.
References
(i) VON TERSCH MA, Robbins HL, Jany CS, Johnson TB (1991) Insecticidal toxins from Bacillus thuringiensis subsp. kenyae: gene cloning and characterization and comparison with B. thuringiensis subsp. kurstaki CryIA(c) toxins Appl. Environ. Microbiol. 57: 349-358.2. (II) SEDLAK M, Walter T, Aronson A (2000) Regulation by overlapping promoters of the rate of synthesis and deposition into crystalline inclusions of Bacillus thuringiensis delta-endotoxins. J Bacteriol. 182(3):734-41.