Regulatory

Part:BBa_K3040105

Designed by: Lai, Si-Ying   Group: iGEM19_NTHU_Taiwan   (2019-10-15)


pFadBA_NTHU

It is pointed out by the previous iGEM team, UPF CRG Barcelona_2018 iGEM, that the native promoter pFadBA has great leakage and is a weak promoter that isn’t ideal enough for our system. Therefore, to enhance the sensitivity and reduce the leakage of the promoter pFadBA for making it more suitable for our system, we modified the native promoter pFadBA with a mutant in its consensus sequence of -10 and -35 region.

Usage and Biology

According to the previous research [1], there is improvement in expression for pFadBA with consensus sequence. Furthermore, the improved in expression portion enhance greatly if there’s a point of mutant in consensus sequence. Therefore, we designed our promoter pFadBA with a mutant in its consensus sequence of -10 and -35 region, to promote its strength.

[Ref] The-Sequence-of-Spacers-between-the-Consensus-Sequences-Modulates-the-Strength-of-Prokaryotic-Promoters


Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]


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Categories
Parameters
None