Difference between revisions of "Part:BBa K4201019"

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<partinfo>BBa_K4201019 short</partinfo>
 
<partinfo>BBa_K4201019 short</partinfo>
  
This composite part is made using a Kan BsaI backbone. The B/W selection was excised during Golden Gate synthesis and replaced with a sequence containing CrtE-cytoTDS-MBP, T5aOH, and RUBY genes. Each inserted gene is flanked by a Gmubi promoter and AtHSP terminator. This construct was made to be transfected into agrobacterium and then into Glycine max.  
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This composite part is made using a Kan BsaI backbone. The B/W selection was excised during Golden Gate synthesis and replaced with a sequence containing CrtE-cytoTDS-MBP, T5aOH, and RUBY genes. Each inserted gene is flanked by a Gmubi promoter and AtHSP terminator. This construct was made to be transfected into agrobacterium and then into <i>Glycine max</i>.  
The Crte-cytoTDS-MBP is a fusion protein that codes for the first two enzymes in the paclitaxel biosynthesis pathway. The T5aOH encodes for the third step in the biosynthesis of paclitaxel. The RUBY reporter was added to visualize the construct when integrated into the G. max genome.  
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The Crte-cytoTDS-MBP is a fusion protein that codes for the first two enzymes in the paclitaxel biosynthesis pathway. The T5aOH encodes for the third step in the biosynthesis of paclitaxel. The RUBY reporter was added to visualize the construct when integrated into the <i>G. max</i> genome.  
  
 
<!-- Add more about the biology of this part here
 
<!-- Add more about the biology of this part here

Revision as of 10:24, 12 October 2022


crtE-cytoTDS-MBP_T5αOH_RUBY

This composite part is made using a Kan BsaI backbone. The B/W selection was excised during Golden Gate synthesis and replaced with a sequence containing CrtE-cytoTDS-MBP, T5aOH, and RUBY genes. Each inserted gene is flanked by a Gmubi promoter and AtHSP terminator. This construct was made to be transfected into agrobacterium and then into Glycine max. The Crte-cytoTDS-MBP is a fusion protein that codes for the first two enzymes in the paclitaxel biosynthesis pathway. The T5aOH encodes for the third step in the biosynthesis of paclitaxel. The RUBY reporter was added to visualize the construct when integrated into the G. max genome.

Sequence and Features


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal EcoRI site found at 6826
    Illegal PstI site found at 994
    Illegal PstI site found at 4792
    Illegal PstI site found at 5632
    Illegal PstI site found at 8365
    Illegal PstI site found at 13549
  • 12
    INCOMPATIBLE WITH RFC[12]
    Unknown
  • 21
    INCOMPATIBLE WITH RFC[21]
    Unknown
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal EcoRI site found at 6826
    Illegal PstI site found at 994
    Illegal PstI site found at 4792
    Illegal PstI site found at 5632
    Illegal PstI site found at 8365
    Illegal PstI site found at 13549
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal EcoRI site found at 6826
    Illegal PstI site found at 994
    Illegal PstI site found at 4792
    Illegal PstI site found at 5632
    Illegal PstI site found at 8365
    Illegal PstI site found at 13549
    Illegal NgoMIV site found at 6975
    Illegal NgoMIV site found at 9705
    Illegal NgoMIV site found at 10284
    Illegal NgoMIV site found at 11997
    Illegal AgeI site found at 937
    Illegal AgeI site found at 2313
    Illegal AgeI site found at 5429
    Illegal AgeI site found at 5701
    Illegal AgeI site found at 6640
    Illegal AgeI site found at 8162
    Illegal AgeI site found at 8434
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI site found at 1
    Illegal BsaI site found at 940
    Illegal BsaI site found at 5432
    Illegal BsaI site found at 5704
    Illegal BsaI site found at 6643
    Illegal BsaI site found at 8165
    Illegal BsaI site found at 8437
    Illegal BsaI.rc site found at 934
    Illegal BsaI.rc site found at 5426
    Illegal BsaI.rc site found at 5698
    Illegal BsaI.rc site found at 6637
    Illegal BsaI.rc site found at 8159
    Illegal BsaI.rc site found at 8431
    Illegal BsaI.rc site found at 9370
    Illegal SapI.rc site found at 3369
    Illegal SapI.rc site found at 3575