Part:BBa_K2082151
Stop Beta-Lactamase (K30*)
This Part contains a promoter, a ribosomal binding site, a modified beta-lactamse (K30*) and a terminator. This device may be used for characterization and quantification of in vivo mutagenesis systems. Functionality of this part was proven using an error prone DNA-polymerase I. The stop codon in concern was created by a point mutation (A149T). A beta-lactamase containing a stop codon further downstream in the coding sequence can be found here.
Usage and Biology
After transformation the cells in concern are enabled to grow in chloramphenicol to sustain segregative stability. When mutagenesis has been performed, bacteria is harvested and plated on ampicillin agar. When a mutation reverted the stop codon
colonies are formed. The quantity of revertants compared to the total cell number determines the mutation rate. An exact protocol for reversion assays to determine in vivo mutation rates can be found here.
In the first step the beta-lactamase cds of pSB1AK3 was cloned in pSB1C3 containing the other parts of the device by gibson cloning. After verification by plating on ampicillin and chloramphenicol containing agar, one clone was picked and amplified. The plasmid DNA was mutated by using primers containing a mismatch leading to a single point mutation after the first amplification round and a 20 bp overlap similar to the other end of the linear DNA. The DNA has been closed by a one part gibson cloning and transformed to screen for a loss of function (Fig. 1). Single point mutation was verified by sanger sequening.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 7
Illegal NheI site found at 30 - 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 777
None |