Difference between revisions of "Part:BBa K3475008"

 
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<div style="text-align:center">[[Image:T--Tongji_China--202_6.jpg | 750px]]</div>
 
<div style="text-align:center">[[Image:T--Tongji_China--202_6.jpg | 750px]]</div>
 
<p style="width:600px; margin-left:150px; margin-bottom:60px;
 
<p style="width:600px; margin-left:150px; margin-bottom:60px;
text-align:justify "><em><strong>FIGURE 4.</strong> '''The relative fluorescence of HrtR- (E.coli-pSB1K3-HrtO-cI-pA1c-R0051-mRFP-I12007-GFP), HrtR+ (E.coli-pHSB-cI-pA1c-R0051-mRFP-I12007-GFP) and WT (E.coli-wildtype).'''<br/> Measured by excitation wavelength of 475 nm, emission wavelength of 515 nm for GFP; and by excitation wavelength of 588 nm, emission wavelength of 635 nm for mRFP. Relative fluorescence is calculated by the formula below, LB medium as blank.As shown in the figure, when heme is sufficient (simulated by KO of HrtR), the expression of GFP (promoter: I12007) is activated and the expression of RFP (promoter: R0051) is repressed; when heme lacks, the expression of GFP (promoter: I12007) is repressed and the expression of RFP (promoter: R0051) is activated. This can to some extent prove the engineering success of the connection between heme biosensor system and bilateral ARG system.
+
text-align:justify "><em><strong>FIGURE 6.</strong> '''The relative fluorescence of HrtR- (E.coli-pSB1K3-HrtO-cI-pA1c-R0051-mRFP-I12007-GFP), HrtR+ (E.coli-pHSB-cI-pA1c-R0051-mRFP-I12007-GFP) and WT (E.coli-wildtype).'''<br/> Measured by excitation wavelength of 475 nm, emission wavelength of 515 nm for GFP; and by excitation wavelength of 588 nm, emission wavelength of 635 nm for mRFP. Relative fluorescence is calculated by the formula below, LB medium as blank.As shown in the figure, when heme is sufficient (simulated by KO of HrtR), the expression of GFP (promoter: I12007) is activated and the expression of RFP (promoter: R0051) is repressed; when heme lacks, the expression of GFP (promoter: I12007) is repressed and the expression of RFP (promoter: R0051) is activated. This can to some extent prove the engineering success of the connection between heme biosensor system and bilateral ARG system.
  
 
  </em> </p>
 
  </em> </p>
 
<div style="text-align:center">[[Image:T--Tongji_China--202_t.jpg | 750px]]</div>
 
<div style="text-align:center">[[Image:T--Tongji_China--202_t.jpg | 750px]]</div>
 
<p style="width:600px; margin-left:150px; margin-bottom:60px;
 
<p style="width:600px; margin-left:150px; margin-bottom:60px;
text-align:justify "><em><strong>FIGURE 5.</strong> '''Calculating formula.'''<br/>  
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text-align:justify "><em><strong>FIGURE 7.</strong> '''Calculating formula.'''<br/>  
 
  </em> </p>
 
  </em> </p>
  

Latest revision as of 01:05, 28 October 2020


Prm+ RBS GFP Ter

GFP activated by cI

Usage and Biology

T--Tongji China--202 6.jpg

FIGURE 6. The relative fluorescence of HrtR- (E.coli-pSB1K3-HrtO-cI-pA1c-R0051-mRFP-I12007-GFP), HrtR+ (E.coli-pHSB-cI-pA1c-R0051-mRFP-I12007-GFP) and WT (E.coli-wildtype).
Measured by excitation wavelength of 475 nm, emission wavelength of 515 nm for GFP; and by excitation wavelength of 588 nm, emission wavelength of 635 nm for mRFP. Relative fluorescence is calculated by the formula below, LB medium as blank.As shown in the figure, when heme is sufficient (simulated by KO of HrtR), the expression of GFP (promoter: I12007) is activated and the expression of RFP (promoter: R0051) is repressed; when heme lacks, the expression of GFP (promoter: I12007) is repressed and the expression of RFP (promoter: R0051) is activated. This can to some extent prove the engineering success of the connection between heme biosensor system and bilateral ARG system.

T--Tongji China--202 t.jpg

FIGURE 7. Calculating formula.

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
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI.rc site found at 738