Difference between revisions of "Part:BBa J119375"

Revision as of 20:25, 2 March 2015

81 Mutated Ptac Promoters with Varying Strengths

Mutations were introduced into the Ptac promoter using NNNNNN in place of the TTGACA of the -35 region. Synthetic oligonucleotides carry the 4096 possible sequences were cloned via Golden Gate Assembly into pClone Red. A total of 81 different promoters were picked from clone library plates like the one shown below. The DNA sequence of the 81 mutant promoters was determined and their strength was measured by fluorometry.

Below is the DNA sequence of the 81 mutant promoters. The strength of the promoters was measured using the RFP reporter gene in pClone Red. In the table below, strength is reported in the column labeled RFP as the ratio of the red fluorescence of each clone to that of Ptac.

Consensus sequences from data sets such as the one shown in Figure 4 are usually determined by analyzing the top 5-20% of the promoters. In order to use the information collected for all of the 81 promoter sequences, a weighted method of consensus building was developed that assigned a score to each base in each -35 region based on the RFP expression of the mutant promoter that contained it. The consensus produced is shown below.

Sequence and Features