Difference between revisions of "Part:BBa K3040006"

Line 1: Line 1:
==Description==
+
__NOTOC__
 +
<partinfo>BBa_K3040013 short</partinfo>
 +
 
 
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.
 
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.
 
According to the previous research [1], there is improvement in expression for pFadBA with consensus sequence.  
 
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.
 
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.
 +
 +
 +
<!-- Add more about the biology of this part here
 +
===Usage and Biology===
 +
 +
<!-- -->
 +
<span class='h3bb'>Sequence and Features</span>
 +
<partinfo>BBa_K3040013 SequenceAndFeatures</partinfo>
 +
 +
 +
<!-- Uncomment this to enable Functional Parameter display
 +
===Functional Parameters===
 +
<partinfo>BBa_K3040013 parameters</partinfo>
 +
<!-- -->
 +
  
 
==Reference==
 
==Reference==
 
JENSEN, Peter Ruhdal; HAMMER, Karin. The sequence of spacers between the consensus sequences modulates the strength of prokaryotic promoters. Appl. Environ. Microbiol., 1998, 64.1: 82-87.
 
JENSEN, Peter Ruhdal; HAMMER, Karin. The sequence of spacers between the consensus sequences modulates the strength of prokaryotic promoters. Appl. Environ. Microbiol., 1998, 64.1: 82-87.

Revision as of 13:05, 19 October 2019

Native pFadD promoter regulating downstream RFP

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. 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.


Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Unknown
  • 21
    INCOMPATIBLE WITH RFC[21]
    Unknown
  • 23
    INCOMPATIBLE WITH RFC[23]
    Unknown
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal AgeI site found at 755
    Illegal AgeI site found at 867
  • 1000
    COMPATIBLE WITH RFC[1000]



Reference

JENSEN, Peter Ruhdal; HAMMER, Karin. The sequence of spacers between the consensus sequences modulates the strength of prokaryotic promoters. Appl. Environ. Microbiol., 1998, 64.1: 82-87.