Difference between revisions of "Part:BBa K3832001:Design"

(→‎Design Notes)
(→‎Design Notes)
 
(3 intermediate revisions by the same user not shown)
Line 14: Line 14:
 
Reverse: T7Te terminator, rrnB T1 terminator, lacI(CDS), eSD, BBaJ23100(promoter)
 
Reverse: T7Te terminator, rrnB T1 terminator, lacI(CDS), eSD, BBaJ23100(promoter)
  
−
[[File:T--XJTU-China--Part aroG.png|1000px|thumb|left|Features of BBa_K3832001 text]]]
+
[[File:T--XJTU-China--Part aroG.png|920px|thumb|left|Click to view features of BBa_K3832001 text]]
  
 
===Source===
 
===Source===

Latest revision as of 07:45, 26 September 2021


Induced expression circuit of aroG (Mutant s211f)


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 2554
    Illegal NheI site found at 2577
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BglII site found at 2541
    Illegal XhoI site found at 1146
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal SapI.rc site found at 453


Design Notes

This part can be directly linked to the vector plasmid. No extra Promoter and Repressor gene(lacI) are required.

The following subparts are included in order：

Forward: lacUV5 promoter， lac operator， BBa_B0034(RBS), aroG-s211f(CDS), T7 terminator; Reverse: T7Te terminator, rrnB T1 terminator, lacI(CDS), eSD, BBaJ23100(promoter)

Click to view features of BBa_K3832001 text

Source

The sequence of the parts used in the device are gained from iGEM parts collections. Partial of the subparts are de-novo synthesized. All the subparts are assembled into this device by using GoldenGate assembly.

References