Difference between revisions of "Part:BBa K143033:Design"

Revision as of 14:10, 17 September 2008

LacI (Lva^-, N-terminal deletion) regulatory protein

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]

Design Notes

LacI was located in the sequence of the B. subtilis shuttle vector pDR111. This version of LacI lacks a Lva degradation sequence and has a small N-terminal deletion that is observed in many LacI used in studies on B.subtilis. In particular, this LacI protein is used in pDR111 to regulate expression of the inducible Phyper-spank protein (BBa_K143015) (also used in the pDR111 vector). The BioBrick prefix and suffix were applied to the gene.

Source

The LacI gene was cloned fromB. subtilis shuttle vector pDR111 using Pfu DNA polymerase PCR

References

1 pmid=16166525

</biblio>

@@ Line 6: / Line 6: @@
 ===Design Notes===
-LacI was located in the sequence of the ''B. subtilis'' shuttle vector pDR111. This version of LacI lacks a Ltva degradation sequence and has a small N-terminal deletion that is observed in many LacI used in studies on ''B.subtilis''. In particular, this LacI protein is used in pDR111 to regulate expression of the inducible Phyper-spank protein (<bbpart>BBa_K143015</bbpart>) (also used in the pDR111 vector). The BioBrick prefix and suffix were applied to the gene
+LacI was located in the sequence of the ''B. subtilis'' shuttle vector pDR111. This version of LacI lacks a Lva degradation sequence and has a small N-terminal deletion that is observed in many LacI used in studies on ''B.subtilis''. In particular, this LacI protein is used in pDR111 to regulate expression of the inducible Phyper-spank protein (<bbpart>BBa_K143015</bbpart>) (also used in the pDR111 vector). The BioBrick prefix and suffix were applied to the gene.
 ===Source===