Difference between revisions of "Part:BBa K5133000"

Line 5: Line 5:
 
Group: <b>GEC-China (iGEM 2024, team number: #5133)</b>
 
Group: <b>GEC-China (iGEM 2024, team number: #5133)</b>
  
This basic part is derived from plasmid pJL1 (Addgene: #69496)<sup>[1]</sup>, including a conserved DNA sequence of T7 promoter as <b>5'-taatacgactcactatagggaga-3'</b><sup>[2]</sup>. The plasmid pJL1 is commonly used for the sfGFP expression for cell-free protein synthesis (CFPS). Hence, this part is used for the construction of three composite parts: BBa_K5133004 (sfGFP generator for CFPS), BBa_K5133006 (Microcin H47 generator for CFPS), and BBa_K5133008 (Microcin M generator for CFPS), respectively.
+
 
 +
This basic part is derived from plasmid pJL1 (Addgene: #69496)<sup>[1]</sup>, including a conserved DNA sequence of T7 promoter as <b>5'-taatacgactcactatagggaga-3'</b><sup>[2]</sup>. The plasmid pJL1 is commonly used for the sfGFP expression for cell-free protein synthesis (CFPS). Hence, this part is used for the construction of three composite parts: <bbpart>BBa_K5133004</bbpart> (sfGFP generator), <bbpart>BBa_K5133006</bbpart> (Microcin H47 generator), and <bbpart>BBa_K5133008</bbpart> (Microcin M generator), for CFPS in our project.
  
  

Revision as of 02:46, 27 July 2024


T7 promoter (from plasmid pJL1)

Group: GEC-China (iGEM 2024, team number: #5133)


This basic part is derived from plasmid pJL1 (Addgene: #69496)[1], including a conserved DNA sequence of T7 promoter as 5'-taatacgactcactatagggaga-3'[2]. The plasmid pJL1 is commonly used for the sfGFP expression for cell-free protein synthesis (CFPS). Hence, this part is used for the construction of three composite parts: BBa_K5133004 (sfGFP generator), BBa_K5133006 (Microcin H47 generator), and BBa_K5133008 (Microcin M generator), for CFPS in our project.



Sequence and Features


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal XbaI site found at 51
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal XbaI site found at 51
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal XbaI site found at 51
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI.rc site found at 32