Coding

Part:BBa_K3015006

Designed by: Valentina Stuchlik   Group: iGEM19_BOKU-Vienna   (2019-10-14)
Revision as of 12:32, 19 October 2019 by Lenti (Talk | contribs)


T7 RNA Polymerase (No BbsI/BpiI)

Since BbsI/BpiI can be a very important restriction enzyme for golden gate cloning in some labs, we decided to remove those recognition sites by codon swapping from the Part BBa_K14001 to improve the applicability. The

Usage and Biology

The T7-polymerase will start transcription from a T7-promotor
We Mutated the following basepairs to delete BbsI/BpiI recognition sites
1) S202 changed from TCT to TCC (bp 604-606)
2) E207 changed from GAA to GAG (bp 619-621)
3) E309 changed from GAA to GAG (bp 925-927)
4) E365 changed from GAA to GAG (bp 1093-1095)
5) K714 changed from AAG to AAA (bp 2140-21429

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]


[edit]
Categories
Parameters
None