Part:BBa_K4770022

IPT_Isopentenyltransferase_Level_1

Description and Biology

Level 1 vectors are single transcriptional units. This Level 1 contains a constitutive promoter PPSAD, a coding sequence for isopentenyltransferase in Chlamydomonas reinhardtii linked through F2A (a self-cleaving peptide) to a NanoLuc reporter. With this vector we aim to enhance IPT expression, making the first step of the cytokines synthesis pathway constitutive by using the PPSAD promoter and being able to measure this expression through the NanoLuc signal.

How can this part be used

This Level 1 is aimed to later be assembled in a level M in position 5 through MoClos assembly. Should you use this part and need advice on how to use it, please do not hesitate to contact us at algagenix@gmail.com

Source of this part

Original PPSAD sequence: BBa_K4770007 Original IPT sequence: BBa_K4770005 Original F2A sequence: BBa_K4770012 Original NanoLuc sequence: BBa_K4770011 Original TPSAD sequence: BBa_K4770008

Design considerations

We performed Chlamydomonas reinhardtii's domestication for GS sequence. This process includes a reduction of the GC% content to make the sequence suitable for commercial synthesis while maintaining it high enough to fit Chlamydomonas reinhardtii's codon usage. This was done using our optimizing software (see AlgaGenix's wiki for additional information). Moreover, recognition sites for BbsI and BsaI were eliminated, changing said codons with synonymous ones. Besides, we also added an intron to perform what is known as intron-mediated enhancement (IME), which studies show aids with stable high-level expression of a foreign gene (Lumbreras et al., 1998) AlgaGenix’s Level 1s are designed to have the same structure and not having to build different pieces with different positions for each gene.

Assembly Compatibility:

• 10
  INCOMPATIBLE WITH RFC[10]

  Illegal PstI site found at 958
  Illegal PstI site found at 2090
  Illegal PstI site found at 2511
  Illegal PstI site found at 2535
  
• 12
  INCOMPATIBLE WITH RFC[12]

  Illegal PstI site found at 958
  Illegal PstI site found at 2090
  Illegal PstI site found at 2511
  Illegal PstI site found at 2535
  Illegal NotI site found at 838
  Illegal NotI site found at 2471
  
• 21
  INCOMPATIBLE WITH RFC[21]

  Illegal BglII site found at 3202
  Illegal BamHI site found at 1830
  
• 23
  INCOMPATIBLE WITH RFC[23]

  Illegal PstI site found at 958
  Illegal PstI site found at 2090
  Illegal PstI site found at 2511
  Illegal PstI site found at 2535
  
• 25
  INCOMPATIBLE WITH RFC[25]

  Illegal PstI site found at 958
  Illegal PstI site found at 2090
  Illegal PstI site found at 2511
  Illegal PstI site found at 2535
  Illegal NgoMIV site found at 888
  Illegal NgoMIV site found at 1902
  Illegal NgoMIV site found at 2168
  Illegal NgoMIV site found at 2572
  Illegal NgoMIV site found at 2584
  Illegal NgoMIV site found at 3018
  
• 1000
  COMPATIBLE WITH RFC[1000]