Difference between revisions of "Part:BBa K4229033"
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[[File:IndigoLaborBild.jpg|300px|thumb|left|[Fig.1]:  A: Left Erlenmeyer flasks with 200 mL culture after Indigo-production, right Erlenmeyer flasks with 200 mL culture after Indirubin-production; B: Pellet of 1.5 mL bacterial culture after Indigo-production in 200 mL culture followed by centrifugation; C: Pellet of 1.5 mL bacterial culture after Indirubin-production in 200 mL culture followed by centrifugation. For Indirubin production, L-Cysteine was added to shift the reaction. ]]
 
[[File:IndigoLaborBild.jpg|300px|thumb|left|[Fig.1]:  A: Left Erlenmeyer flasks with 200 mL culture after Indigo-production, right Erlenmeyer flasks with 200 mL culture after Indirubin-production; B: Pellet of 1.5 mL bacterial culture after Indigo-production in 200 mL culture followed by centrifugation; C: Pellet of 1.5 mL bacterial culture after Indirubin-production in 200 mL culture followed by centrifugation. For Indirubin production, L-Cysteine was added to shift the reaction. ]]
  
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[[File:IndigoAbsorbance.jpg|500px|thumb|right|[Fig.2]:  A: Indigo-concentration measured via fluorescence (excitation 612 nm, emission 670 nm), B: Indirubin-concentration measured via absorbance at 540 nm. Production with 200 mL cultures in 500 mL Erlenmeyer-flasks, at 25 °C after IPTG-induction at OD = 0.8, with L-Tryptophan-concentration of 5 mM. Photometric readout using a plate reader. ]]
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[[File:IndigoAbsorbance.jpg|550px|thumb|right|[Fig.2]:  A: Indigo-concentration measured via fluorescence (excitation 612 nm, emission 670 nm), B: Indirubin-concentration measured via absorbance at 540 nm. Production with 200 mL cultures in 500 mL Erlenmeyer-flasks, at 25 °C after IPTG-induction at OD = 0.8, with L-Tryptophan-concentration of 5 mM. Photometric readout using a plate reader. ]]
  
 
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Revision as of 12:09, 11 October 2022


TnaA fused with SnoopCatcher N-terminal and Fre under T7v promoter and LacOperator

We had this BioBrick together with BBa_K4229034 on our Plasmid, which was transformed into BL21(DE3) E.Coli. We successfully produced Indigo and Indirubin with our transformed bacteria. The production of the compounds was shown visibly by the colour change of the culture[Fig.1].

[Fig.1]: A: Left Erlenmeyer flasks with 200 mL culture after Indigo-production, right Erlenmeyer flasks with 200 mL culture after Indirubin-production; B: Pellet of 1.5 mL bacterial culture after Indigo-production in 200 mL culture followed by centrifugation; C: Pellet of 1.5 mL bacterial culture after Indirubin-production in 200 mL culture followed by centrifugation. For Indirubin production, L-Cysteine was added to shift the reaction.
[Fig.2]: A: Indigo-concentration measured via fluorescence (excitation 612 nm, emission 670 nm), B: Indirubin-concentration measured via absorbance at 540 nm. Production with 200 mL cultures in 500 mL Erlenmeyer-flasks, at 25 °C after IPTG-induction at OD = 0.8, with L-Tryptophan-concentration of 5 mM. Photometric readout using a plate reader.

Sequence and Features


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal PstI site found at 1064
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal PstI site found at 1064
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal PstI site found at 1064
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal PstI site found at 1064
    Illegal AgeI site found at 229
    Illegal AgeI site found at 315
    Illegal AgeI site found at 1687
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal SapI.rc site found at 2224
    Illegal SapI.rc site found at 2344