Difference between revisions of "Part:BBa K190015:Design"

 
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__NOTOC__
 
__NOTOC__
 
<partinfo>BBa_K190015 short</partinfo>
 
<partinfo>BBa_K190015 short</partinfo>
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===Design Notes===
 
===Design Notes===
−
None
 
  
 +
The ArsR regulated promoter has been cloned into the [https://parts.igem.org/Part:BBa_J61002 BBa_J61002-R0040] plasmid for construction of promoter basic parts and their derivatives. Insertion of a promoter element between the XbaI and SpeI sites resulted in a RFP reporter while retaining the ability to do biobrick assembly.
  
 +
[[Image:PBca1020-r0040.jpg|200px]]
 +
 +
===Modelling===
 +
 +
{{GraphHeader}}
 +
<html>
 +
<script type="text/javascript" src="/Groningen2009/Model.js?action=raw"></script>
 +
<script type="text/javascript" src="/Groningen2009/Arsenic.js?action=raw"></script>
 +
</html>
 +
 +
The three graphs below illustrate the promoter response after induction with arsenic (directly in the cell, with the equivalent of 1&micro;M in the solution) with and without constitutive expression of ArsR (the first two graphs) and with slower production and degradation of ArsR (the two left graphs). Also, each graph has a line showing the formation of a product behind the ars promoter that does not degrade (and has production rate 1), subtracting the production that would have occurred without induction to show the effect of adding arsenic. Some conclusions:
 +
 +
* Constitutive expression of ArsR greatly reduces (and slows) the promoter response.
 +
* On the other hand, if we divide the production and degradation rates of ArsR by ten the promoter response is ten times slower, producing ten times as much product.
 +
* In the bottom-right graph the induction is done gradually (the amount of arsenic increases linearly during the first five minutes), showing the high-pass behaviour of the promoter and that this can negatively impact product formation.
 +
 +
<html>
 +
<script type="text/javascript">
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addOnloadHook(computePromoterActivation);
 +
 +
function computePromoterActivation() {
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  // Set up constants
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  var maxt = 600;
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  var c = arsenicModelConstants();
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  var cNP = {}, cS = {}, cG = {};
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  c.v5 = 0;
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  c.k8 = 0;
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  c.pro = 0;
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  c.ars2T = 0;
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  for(var a in c) {
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    cNP[a] = c[a];
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    cS[a] = c[a];
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    cG[a] = c[a];
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  }
 +
 +
  var Vcell = 1 * 1e-15; // micrometer^3/cell -> liter/cell
 +
  var avogadro = 6.02214179e23; // 1/mol
 +
  c.pro = 2/(avogadro*Vcell); // 1/cell -> mol/L
 +
  cS.tauR *= 10;
 +
  cS.beta1 /= 10;
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  cS.beta3 /= 10;
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  cG.ars2T = 100*cG.ars1T;
 +
 +
  // Initialize
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  var x0 = arsenicModelInitialization(c,0);
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  var xNP0 = arsenicModelInitialization(cNP,0);
 +
  var xS0 = arsenicModelInitialization(cS,0);
 +
  var x20 = arsenicModelInitialization(c,0);
 +
  var xG0 = arsenicModelInitialization(cG,0);
 +
  var AsT = 1e-6*c.Vs;
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  x0.AsinT = AsT/c.Vc;
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  xNP0.AsinT = AsT/c.Vc;
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  xS0.AsinT = AsT/c.Vc;
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  x20.AsinT = 0;
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  xG0.AsinT = AsT/c.Vc;
 +
 +
  // Simulate
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  var x = simulate(x0,maxt,function(t,d){return arsenicModelGradient(c,d);});
 +
  var xNP = simulate(xNP0,maxt,function(t,d){return arsenicModelGradient(cNP,d);});
 +
  var xS = simulate(xS0,maxt*10,function(t,d){return arsenicModelGradient(cS,d);});
 +
  var xG = simulate(xG0,maxt,function(t,d){return arsenicModelGradient(cG,d);});
 +
  var x2 = simulate(x0,maxt,function(t,d){
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                              var Dx = arsenicModelGradient(c,d);
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                              if (t<maxt/2) Dx.AsinT += (AsT/c.Vc)*2/maxt;
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                              return Dx;
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                            });
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 +
  // Output
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  function convertToSeries(c,x0,x) {
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    var bAsin, cAsin, ArsR, ars, arsP, arsE;
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    var arsInt = 0;
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    var series = [[],[]];
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    var preTime = -x.time[x._arsF.length-1]/(60*20);
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    arsE = x0._arsF;
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    series[0].push({x:preTime,y:100*arsE});
 +
    series[0].push({x:0,y:100*arsE});
 +
    series[1].push({x:preTime,y:0});
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    for(var i=0; i<x._arsF.length; i++) {
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      ars = x._arsF[i];
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      if (i>0) arsInt += (x.time[i]-x.time[i-1])*(ars+arsP)/2;
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      series[0].push({x:x.time[i]/60,y:100*ars});
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      series[1].push({x:x.time[i]/60,y:(arsInt-x.time[i]*arsE)});
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      arsP = ars;
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    }
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    return series;
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  }
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  document.getElementById("promoterActivationData").data = {
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    ars:convertToSeries(c,x0,x),
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    arsNP:convertToSeries(cNP,xNP0,xNP),
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    arsS:convertToSeries(cS,xS0,xS),
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    arsG:convertToSeries(cG,xG0,xG),
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    ars2:convertToSeries(c,x20,x2)};
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  var graphNodes = [document.getElementById("promoterActivationGraph"),
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                    document.getElementById("promoterActivationGraphNP"),
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                    document.getElementById("promoterActivationGraphS"),
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                    document.getElementById("promoterActivationGraphG"),
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                    document.getElementById("promoterActivationGraph2")];
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  for(var i in graphNodes) if (graphNodes[i]) graphNodes[i].refresh();
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}
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</script>
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</html>
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<span id="promoterActivationData"></span>
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{|
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|{{graph|Part:BBa K190015:Graphs/PromoterActivationNP|promoterActivitationGraphNP}}
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|{{graph|Part:BBa K190015:Graphs/PromoterActivation|promoterActivitationGraph}}
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|{{graph|Part:BBa K190015:Graphs/PromoterActivationG|promoterActivitationGraphG}}
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|-
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|{{graph|Part:BBa K190015:Graphs/PromoterActivationSlow|promoterActivitationGraphS}}
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|{{graph|Part:BBa K190015:Graphs/PromoterActivation2|promoterActivitationGraph2}}
 +
|}
  
 
===Source===
 
===Source===
  
−
E.coli TOP10
+
The arsRp promoter is present in most ''E. coli'' strains, and is regulated by ArsR dimer complex. Using the sequence of the promoter in our own ''E. coli'' TOP10 cells, oligo's were designed and annealed to produce the promoter with EcoRI and SpeI (prefix and suffix) overhangs.
 +
 
 +
'''Other organisms'''
 +
 
 +
''Bacillus subtilis''
 +
 
 +
In <i>B. subtilis</i>, an ArsR family repressor (ArsR<sub>BS</sub>) responds to As(III) and Sb(III) and regulates the ars operon encoding itself (ArsR), and arsenate reductase (ArsC), an arsenite efflux pump (ArsB) and a protein of unknown function (YqcK). The order in which ArsR<sub>BS</sub> recognises metals is as follows: As(III)>As(V)>Cd(II)~Ag(I).
 +
 
 +
A second protein, AseR, negatively regulates itself and AseA, an As(III) efflux pump which contributes to arsenite resistance in cells lacking a functional ars operon. The order in which AseR recognises metals is as follows: As(III)>As(V).
  
 
===References===
 
===References===
 +
 +
1) C. Xu, W. Shi, and B.P. Rosen (1996) The Chromosomal ''arsR'' Gene of ''Escherichia coli'' Encodes a ''trans''-acting Metalloregulatory Protein, ''The Journal of Biological Chemistry'', Vol. 271, No. 5, Issue of February 2, pp. 2427–2432.
 +
 +
2) Jason R. Kelly, Adam J. Rubin, Joseph H. Davis, et al (March 2009). "Measuring the activity of BioBrick promoters using an in vivo reference standard". Journal of Biological Engineering 3: 4
 +
 +
3) Anne O. Summers (April 2009). "Damage control: regulating defenses against toxic metals and metalloids". Current Opinion in Microbiology 12(2): 138-144

Latest revision as of 19:05, 21 October 2009

Arsenic Promoter (ArsR regulated)


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]


Design Notes

The ArsR regulated promoter has been cloned into the BBa_J61002-R0040 plasmid for construction of promoter basic parts and their derivatives. Insertion of a promoter element between the XbaI and SpeI sites resulted in a RFP reporter while retaining the ability to do biobrick assembly.

PBca1020-r0040.jpg

Modelling

The three graphs below illustrate the promoter response after induction with arsenic (directly in the cell, with the equivalent of 1µM in the solution) with and without constitutive expression of ArsR (the first two graphs) and with slower production and degradation of ArsR (the two left graphs). Also, each graph has a line showing the formation of a product behind the ars promoter that does not degrade (and has production rate 1), subtracting the production that would have occurred without induction to show the effect of adding arsenic. Some conclusions:

  • Constitutive expression of ArsR greatly reduces (and slows) the promoter response.
  • On the other hand, if we divide the production and degradation rates of ArsR by ten the promoter response is ten times slower, producing ten times as much product.
  • In the bottom-right graph the induction is done gradually (the amount of arsenic increases linearly during the first five minutes), showing the high-pass behaviour of the promoter and that this can negatively impact product formation.

Loading graph...
Loading graph...
Loading graph...
Loading graph...
Loading graph...

Source

The arsRp promoter is present in most E. coli strains, and is regulated by ArsR dimer complex. Using the sequence of the promoter in our own E. coli TOP10 cells, oligo's were designed and annealed to produce the promoter with EcoRI and SpeI (prefix and suffix) overhangs.

Other organisms

Bacillus subtilis

In B. subtilis, an ArsR family repressor (ArsRBS) responds to As(III) and Sb(III) and regulates the ars operon encoding itself (ArsR), and arsenate reductase (ArsC), an arsenite efflux pump (ArsB) and a protein of unknown function (YqcK). The order in which ArsRBS recognises metals is as follows: As(III)>As(V)>Cd(II)~Ag(I).

A second protein, AseR, negatively regulates itself and AseA, an As(III) efflux pump which contributes to arsenite resistance in cells lacking a functional ars operon. The order in which AseR recognises metals is as follows: As(III)>As(V).

References

1) C. Xu, W. Shi, and B.P. Rosen (1996) The Chromosomal arsR Gene of Escherichia coli Encodes a trans-acting Metalloregulatory Protein, The Journal of Biological Chemistry, Vol. 271, No. 5, Issue of February 2, pp. 2427–2432.

2) Jason R. Kelly, Adam J. Rubin, Joseph H. Davis, et al (March 2009). "Measuring the activity of BioBrick promoters using an in vivo reference standard". Journal of Biological Engineering 3: 4

3) Anne O. Summers (April 2009). "Damage control: regulating defenses against toxic metals and metalloids". Current Opinion in Microbiology 12(2): 138-144