Part:BBa_K2008006

pVeg->sec-TD1-KSCI-BBI

This part is an improvement on the comK gene with the intent to make it more accessible to future iGEM teams. Internal restriction enzyme sites (one SpeI site located at base pairs 170-175 and two EcoRI sites located at base pairs 557-562 & 572-577 in the comK part submitted by UofC_Calgary 2014) have been removed. In our version of comK, the SpeI site (ACTAGT) was deleted entirely, as the site was contained within a spacer region between the xylose-inducible promoter and RBS. To remove EcoRI sites, the DNA bases of the new comK construct were changed, and codons were optimized for B. subtilis:

553 A>G 556 C>T 568 A>G 571 C>T

As the UofC_Calgary 2014 iGEM team discusses in their comK part (BBa_K1444018), comK is the master transcription factor involved in the competency of B. subtilis. ComK further affects the other competence factors (comC, comE, comF, comG and comK) to increase B. subtilis’ ability to be transformed (van Sinderen et al., 1995). As such, when additional comK is transcribed, it increases B. subtilis transformation efficiency.

Also like the UofC_Calgary 2014 iGEM team, we included a xylose-inducible promoter upstream of the comK coding sequence. This allows for induction of competency upon the addition of xylose, which is beneficial as the usual starvation method for transformation of B. subtilis is typically time-consuming and costly.

Note: This part is a composite part, not a basic part, but it could not be added as composite at the time of entry.

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]