Part:BBa_K4361202
BlcR BTB primer F1.2 D37V
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). A single amino acid substitution is built-in in the forward primer to introduce a point mutation in the BlcR production plasmid (Part:BBa_K4361106).
The mutations are built-in with a site-directed mutagenesis technique. A DNA polymerase is used to lengthen the single-strand primer. After PCR, a Kinase, Ligase, and DpnI (KLD) mix reaction can be performed. The KLD mix contains three enzymes: kinase, for phosphorylation, ligase for ligation, and DpnI for removal of the plasmid template (Figure 1). DNA sequencing is used to identify mutants and determine whether they carry the desired mutation. To know more about the methods we used, see the protocols page ( Figure 1 ).
The primer sets are divided as follows:
- Set 1, residues 36 to 39
- Part:BBa_K4361200: R1
- Part:BBa_K4361201: F1.1 D37R
- Part:BBa_K4361202: F1.2 D37V
- Part:BBa_K4361203: F1.3 L38V
- Set 4, residues 40 to 41
- Part:BBa_K4361204: R4
- Part:BBa_K4361205: F4.1 A40V
- Set 5, residues 47 to 49
- Part:BBa_K4361206: R5
- Part:BBa_K4361207: F5.1 T47S
- Part:BBa_K4361208: F5.2 T47V
- Part:BBa_K4361209: F5.3 A48V
- Set 7, residues 61 to 63
- Part:BBa_K4361210: R7
- Part:BBa_K4361211: F7.1 S61V
- Part:BBa_K4361212: F7.2 A62V
- Part:BBa_K4361213: F7.3 A62I
- Part:BBa_K4361214: F7.4 A62K
- Part:BBa_K4361215: F7.5 A62T
- Part:BBa_K4361216: F7.6 H63V
- Part:BBa_K4361217: F7.7 H63Y
- Set 3, residues 65 to 68
- Part:BBa_K4361218: R3
- Part:BBa_K4361219: F3.1 L66V
- Part:BBa_K4361220: F3.2 L66A
- Part:BBa_K4361221: F3.3 L66I
- Part:BBa_K4361222: F3.4 A67Q
- Part:BBa_K4361223: F3.5 A67V
- Part:BBa_K4361224: F3.6 A67H
- Part:BBa_K4361225: F3.7 V68T
- Part:BBa_K4361226: F3.8 V68K
- Part:BBa_K4361227: F3.9 V68S
This primer contains a mutation that changes the codon for aspartic acid (D, GAC) in position 37 to that of valine (V, GTG).
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
None |