Difference between revisions of "Part:BBa K553003"
 
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<partinfo>BBa_K553003 short</partinfo>
 
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This part produces constitutively the LasR trans-activator.
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This part produces constitutively the ''P. aeruginosa'' LasR trans-activator.
  
 
The generated protein binds OC12 HLA and regulates positively PromLasB promoter
 
The generated protein binds OC12 HLA and regulates positively PromLasB promoter
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===Download Datasheet===
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<partinfo>BBa_K553003 parameters</partinfo>
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<html><div class="table_cell"><center><a title="BBa_K553003" target="_blank" href="https://static.igem.org/mediawiki/parts/9/98/K553003_lasRcost_V.pdf"><img src="https://static.igem.org/mediawiki/parts/6/66/Units-BBa_K553003.jpg"></a></center></div></html>
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<!-- Add more about the biology of this part here
 
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===Functional Parameters===
 
===Functional Parameters===
 
<partinfo>BBa_K553003 parameters</partinfo>
 
<partinfo>BBa_K553003 parameters</partinfo>
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==Functional Parameters: Austin_UTexas==
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<html>
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<body>
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<h3><center>Burden Imposed by this Part:</center></h3>
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<figure>
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<div class = "center">
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<center><img src = "https://static.igem.org/mediawiki/parts/4/43/T--Austin_Utexas--Low_significant_burden.png" style = "width:200px;height:120px"></center>
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</div>
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<figcaption><center><b>Burden Value: 5.7 ± 3.1% </b></center></figcaption>
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</figure>
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<p> Burden is the percent reduction in the growth rate of <i>E. coli</i> cells transformed with a plasmid containing this BioBrick (± values are 95% confidence limits). This part exhibited a significant burden. Users should be aware that BioBricks with a burden of >20-30% may be susceptible to mutating to become less functional or nonfunctional as an evolutionary consequence of this fitness cost. This risk increases as they used for more bacterial cell divisions or in larger cultures. Users should be especially careful when combining multiple burdensome parts, as plasmids with a total burden of >40% are expected to mutate so quickly that they become unclonable. Refer to any one of the
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<a href="https://parts.igem.org/Part:BBa_K3174002">BBa_K3174002</a> - <a href="https://parts.igem.org/Part:BBa_K3174007">BBa_K3174007</a> pages for more information on the methods and other conclusions from a large-scale measurement project conducted by the <a href="https://2019.igem.org/Team:Austin_UTexas">2019 Austin_UTexas team.</a></p>
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<p>This functional parameter was added by the <a href="https://2020.igem.org/Team:Austin_UTexas/Contribution">2020 Austin_UTexas team.</a></p>
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Latest revision as of 00:13, 4 September 2020

constitutive production of LasR trans-activator

This part produces constitutively the P. aeruginosa LasR trans-activator.

The generated protein binds OC12 HLA and regulates positively PromLasB promoter

Download Datasheet


Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 7
    Illegal NheI site found at 30
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal NgoMIV site found at 383
    Illegal AgeI site found at 580
  • 1000
    COMPATIBLE WITH RFC[1000]


Functional Parameters



Functional Parameters: Austin_UTexas

Burden Imposed by this Part:

Burden Value: 5.7 ± 3.1%

Burden is the percent reduction in the growth rate of E. coli cells transformed with a plasmid containing this BioBrick (± values are 95% confidence limits). This part exhibited a significant burden. Users should be aware that BioBricks with a burden of >20-30% may be susceptible to mutating to become less functional or nonfunctional as an evolutionary consequence of this fitness cost. This risk increases as they used for more bacterial cell divisions or in larger cultures. Users should be especially careful when combining multiple burdensome parts, as plasmids with a total burden of >40% are expected to mutate so quickly that they become unclonable. Refer to any one of the BBa_K3174002 - BBa_K3174007 pages for more information on the methods and other conclusions from a large-scale measurement project conducted by the 2019 Austin_UTexas team.

This functional parameter was added by the 2020 Austin_UTexas team.