Difference between revisions of "Part:BBa K4361203"
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       <li>[[Part:BBa_K4361201]]: F1.1 D37R</li>
 
       <li>[[Part:BBa_K4361201]]: F1.1 D37R</li>
 
       <li>[[Part:BBa_K4361202]]: F1.2 D37V</li>
 
       <li>[[Part:BBa_K4361202]]: F1.2 D37V</li>
−
       <li><i><u>Part:BBa_K4361203]]</u>: F1.3 L38V</i></li>
+
       <li><i><u>Part:BBa_K4361203</u>: F1.3 L38V</i></li>
 
     </ul>
 
     </ul>
 
   </li>
 
   </li>

Revision as of 13:29, 14 September 2022


BlcR BTB primer F1.3 L38V

For the site-directed mutagenesis (SDM) of our protein of interest, BlcR, multiple sets of back-to-back (BTB) primers were designed. The 5' ends of these primers anneal to adjacent nucleotides such that the full plasmid containing the protein (Part:BBa_K4361106) can be replicated. Each of these numbered sets of primers contains a single reverse primer (denoted as Rn with n being the number of the set) and a varying number of forward primers (denoted as Fn.m followed by the induced substitution). Every set covers a small range of amino acids in the DNA-binding domain of BlcR, with each position being mutated to different residues by different forward-facing primers. Do note, however, that while a large number of primers have been designed, sequencing showed that the mutagenesis protocol was not successful for all variants. Therefore, only the primers that resulted in the desired mutants will be described in our collection of BioBricks.

The primer sets are divided as follows:

This primer contains a mutation that changes the codon for leucine (L, TTG) in position 37 to that of valine (V, GTG).

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]