Part:BBa_K2036031

PP2CA-TTADH1-pCyc

It is one of the Basic Part in the eukaryotic version of signal filter (BBa_K2036030)and it is constructed by In-Fusion method.

Protein expression

Pichia pastoris are typical Eukaryotic expression host, but expressing plant genes are still a big challenge. So we firstly tested whether our three interest genes can be efficient expressed. We measured the secretion expression of PP2CA, ABF2 and SnRK2.2. We ran a SDS-PAGE of the culture supernatants of induced cells to identify the three recombinant proteins (Fig1). Compared to vector trasnfected cells, 3 kinds of recombinant protein plasmids trasnfected cells all expressed proteins at ~80kD under induction. The shift of protein bands suggested potential glycosylation modification.

Fig1: SDS PAGE

Bi-stable function:

We constructed expression plasmid and submitted this part (BBa_K2036030) to the registry. But due to the limited time, its function characterization is still under testing. However, our modeling simulation showed promising switch functions. ([http://2016.igem.org/Team:HUST-China/Model/model-euk See more details in our Eukaryote circuit modeling]).

Sequence and Features

Assembly Compatibility:

• 10
  COMPATIBLE WITH RFC[10]
• 12
  COMPATIBLE WITH RFC[12]
• 21
  INCOMPATIBLE WITH RFC[21]

  Illegal BglII site found at 90
  Illegal BamHI site found at 661
  Illegal BamHI site found at 806
  Illegal BamHI site found at 918
  Illegal XhoI site found at 65
  Illegal XhoI site found at 875
  
• 23
  COMPATIBLE WITH RFC[23]
• 25
  INCOMPATIBLE WITH RFC[25]

  Illegal AgeI site found at 48
  
• 1000
  COMPATIBLE WITH RFC[1000]