Difference between revisions of "Part:BBa K1084406"

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<partinfo>BBa_K1084406 short</partinfo>
 
<partinfo>BBa_K1084406 short</partinfo>
  
This parts is promoter 1 assembled with mRFP1 expression color generator.
+
This parts is promoter 6 assembled with mRFP1 expression color generator.
  
 
iGEM HokkaidoU Japan 2013 original promoter family is constructed from consensus promoter (BBa_K1084001) by adding mutation at -35 region. Other region is same among family members, and similar with promoter consensus sequence.
 
iGEM HokkaidoU Japan 2013 original promoter family is constructed from consensus promoter (BBa_K1084001) by adding mutation at -35 region. Other region is same among family members, and similar with promoter consensus sequence.
  
 
https://static.igem.org/mediawiki/2013/c/c1/HokkaidoU2013_promoter_Result-fig1.png
 
https://static.igem.org/mediawiki/2013/c/c1/HokkaidoU2013_promoter_Result-fig1.png
 +
<div>Fig. 1  Randomized promoter family sequences</div>
  
 
Correspondence of sequence and parts number is below.
 
Correspondence of sequence and parts number is below.
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   TCTCGG    K1084010    10
 
   TCTCGG    K1084010    10
  
t. e. = transcription efficyency
+
t. e. = theoretical transcription efficyency
 +
 
 
Promoter transcription efficiency was measured with mRFP1, LacZ and Kanamycine resistance.
 
Promoter transcription efficiency was measured with mRFP1, LacZ and Kanamycine resistance.
 
https://static.igem.org/mediawiki/2013/7/73/HokkaidoU2013_promoter_Result-fig2.png
 
https://static.igem.org/mediawiki/2013/7/73/HokkaidoU2013_promoter_Result-fig2.png

Revision as of 08:40, 29 September 2013

promoter6-B0034-RFP-dT

This parts is promoter 6 assembled with mRFP1 expression color generator.

iGEM HokkaidoU Japan 2013 original promoter family is constructed from consensus promoter (BBa_K1084001) by adding mutation at -35 region. Other region is same among family members, and similar with promoter consensus sequence.

HokkaidoU2013_promoter_Result-fig1.png

Fig. 1 Randomized promoter family sequences

Correspondence of sequence and parts number is below.

  -35        BBa_         t. e. rank
  TTGACA     K1084001     1   
  TAGGTC     K1084002     2
  CTGAAG     K1084003     6
  GGGGTG     K1084004     3
  GAGGAT     K1084005     5
  GCAATA     K1084006     7
  GGGGGG     K1084007     8
  TGTGTG     K1084008     4
  AGTGGG     K1084009     9
  TCTCGG     K1084010     10

t. e. = theoretical transcription efficyency

Promoter transcription efficiency was measured with mRFP1, LacZ and Kanamycine resistance. HokkaidoU2013_promoter_Result-fig2.png

Fig. 2 mRFP1 assay result

HokkaidoU2013_promoter_Result-fig4.png

Fig. 3 β-Galactosidase assay result

HokkaidoU2013_promoter_Result-fig5.png

Fig. 4 Comparison of assay results and modeling data

Theoretical promoter modeling also has done (see promoter Background page in HokkaidoU 2013 wiki). According to protein, these promoters show relatively another protein activity revel. Choose your best promoter by promoter optimization kit (POK).

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
    INCOMPATIBLE WITH RFC[25]
    Illegal AgeI site found at 621
    Illegal AgeI site found at 733
  • 1000
    COMPATIBLE WITH RFC[1000]