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Latest revision as of 12:50, 22 October 2011

UNIPV TEAM 2011

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Results

Parts assembly

All the parts have been cloned with success. The part name, plasmids and quality controls are reported in the Freezer section.

^top

Characterization of basic modules

Characterization of promoters pTet and pLux

Inducible promoters pLux and pTet were assembled upstream of mRFP coding sequences containing an RBS from the Community collection.

The assembled RBSs are:

BioBrick code	Declared efficiency
BBa_B0030	0,6
BBa_B0031	0,07
BBa_B0032	0,3
BBa_B0034	1

The RBS variation has the purpose to stretch the induction curve, thus modulating the PoPs-OUT range of the inducible device.

The complex RBS-promoter acts as a whole regulatory element and determines the amount of translated protein. RBSs have been reported to have an un-modular behavior, since the translational efficiency is not independent on the coding sequences, but variates as an effect of different mRNA structure stability [Salis et al., Nat Biotec, 2009]. It is not possible to separate the effects of the sole promoter and of the sole RBS on the total amount/activity of gene product (in this case study, mRFP).

For this reason, every combination 'Promoter+RBS' was studied as a different regulatory element. Regulatory elements were characterized using mRFP reporter protein for different RBSs in terms of Synthesis rate per Cell (S_cell) and R.P.U.s (Relative Promoter Units) as explained in measurements section.

Operative parameters of the promoter are derived from the estimated Hill equations obtained by nonlinear least squares fitting (lsqnonlin Matlab routine) of the Hill function expressed in RPUs:

RPU_max is equal to the α and represents the maximum promoter activity

RPU_min is equal to the α * δ represents the minimum promoter activity

Switch point is computed as the abscissa of the inflection point of the Hill curve and it is representative of the position of linear region

Linearity boundaries are determined as the intersection between the tangent line to the inflection point and the upper and lower horizontal boundaries of the Hill curve.

The estimated parameters for the Hill functions of pLux are summarized in the table below. For more details on parameter estimation, see the model section.

RBS	α_{p_Lux} [(AUr/min)/cell]	δ_{p_Lux} [-]	η_{p_Lux} [-]	k_{p_Lux} [ng/ml]
BBa_B0030	438 [10]	0.05 [>100]	2 [47]	1.88 [27]
BBa_B0031	9.8 [7]	0.11 [57]	1.2 [29]	1.5 [26]
BBa_B0032	206 [3]	0 [>>100]	1.36 [10]	1.87 [9]
BBa_B0034	1105 [6]	0.02 [>100]	1.33 [19]	2.34 [18]

Data are provided as average [CV%].

The operative parameters of pLux are summarized in the table below:

RBS	RPU_max	RPU_min	Switch point [nM]	Linear boundaries [MIN; MAX] [nM]
B0030	4.28	0.20	1.08	[0.36; 3.27]
B0031	4.93	0.55	0.25	[0.03; 2.30]
B0032	9.49	0.02	0.47	[0.07; 3.07]
B0034	21.53	0.51	0.53	[0.08; 3.77]

The protocols for the characterization of p_Tet promoter are reported in the p_Tet measurement section.

Here we have characterized its transcriptional strength as a function of aTc induction (ng/ml) for different RBSs. Three different induction curves were obtained and are reported in figure:

The estimated parameters of the Hill curves described in the figures are summarized in the table below:

RBS	α_{p_Tet} [(AUr/min)/cell]	δ_{p_Tet} [-]	η_{p_Tet} [-]	k_{p_Tet} [nM]
BBa_B0030	230.67 [3.7]	0.028 [91.61]	4.61 [23.73]	8.75 [4.16]
BBa_B0031	ND	ND	ND	ND
BBa_B0032	55.77 [12]	1.53E-11 [>>100]	4.98 [57.62]	7.26 [14.98]
BBa_B0034	120 [5.95]	0.085 [40.6]	24.85 [47.6]	9 [5.43]

Data are provided as average [CV%]

The operative parameters are summarized in the table below:

RBS	RPU_max	RPU_min	Switch point [ng/ml]	Linear boundaries [MIN; MAX] [ng/ml]
B0030	1.53	~0	7.95	[4.66;11.99]
B0031	ND	ND	ND	ND
B0032	3.16	~0	6.7	[4.45;10.05]
B0034	2.73	0.23	8.96	[8.27;9.71]

^top

Characterization of enzymes AiiA and LuxI

LuxI has been characterized through the Biosensor BBa_T9002 (see modelling section) using the p_Tet-RBSx-LuxI-TT measurement systems.
The parameters V_max, k_M,LuxI and α_RBSx were estimated with a simultaneous fitting of the data collected as described in measurement section for the four measurement parts p_Tet-RBSx-LuxI-TT assayed by BBa_T9002 biosensor section.

The estimated parameters for the enzymatic activity of LuxI are reported in the table below:

V_max	k_M,LuxI	α_B0030	α_B0031	α_B0032	α_B0034
3.56*10^-9	6.87*10³	87	8.5	ND	252

The provided parameters k_M and V_max represent the enzymatic activity of LuxI, described by our model. They must not be confused with the operative parameters of the Michaelis-Menten relation. These synthetic parameters have a great importance, since they can be used in more complicated models in order to predict the behavior of complex circuits.

The AiiA enzyme activity has been characterized under the regulation of p_tet promoter, assaying its enzymatic activity.

The parameters k_cat, k_M,AiiA and α_RBSx would have been estimated with a simultaneous fitting of the data collected as described in measurement section for the four measurement parts p_Tet-RBSx-AiiA-TT assayed by BBa_T9002 biosensor section. Unfortunately, their estimation revealed difficult.
In the first experiments with the measurement system p_Tet-RBSx-AiiA-TT in LOW-COPY at pH=7 no degradation of HSL was observed. The collected data are shown in the figure below. HSL degradation is identical in the measurement system and in the negative control after 21 hours.

Experiments on these parts gave us the opportunity to characterize only the activity of the enzyme in E. COLI TOP10 in high copy number plasmid, providing only some information about the order of magnitude of the model parameters, which has been designed to work in E. COLI MGZ1 in low copy number plasmid.

^top

Characterization of the efficiency of RBSs from the community collection

RBSs were used for the fine tuning of CTRL+E. Different experimental conditions were assayed.

Estimated efficiencies in pSB4C5 plasmid with -RBSx-mRFP-TT coding sequence under the control of the specified promoter:

RBS	eff_{p_Lux}	eff_{p_Tet}	eff_J23101	Declared efficiency
B0030	0.40	1.6814	2.45	0,6
B0031	0.01	ND	0.04	0,07
B0032	0.19	0.4193	0.40	0,3
B0034	1	1	1	1

Estimated efficiencies in pSB4C5 plasmid with pTet-RBSx-GeneX-TT, with GeneX=mRFP, AiiA or LuxI:

RBS	eff_mRFP	eff_AiiA	eff_LuxI	Declared efficiency
B0030	1.72	0.53	0.45	0,6
B0031	0.03	0.83	0.028	0,07
B0032	0.37	0.50	N.D.	0.3
B0034	1	1	1	1

^top

Identification of bacterial growth parameters

The bacterial growth curve has been modelled as a logistic curve and is represented by the following equation:

dN/dt=N*μ*(N_max-N)/N_max
N(0)=n₀

where μ represents the growth rate of the cells (E. coli MGZ1 in M9 supplemented medium) and N_max represents the maximum number of cells in the well. For a detailed description of the parameters, see modelling section. For details on parameters identification, see identification section. The growth curves in all the performed experiments are measured in O.D.₆₀₀. Since the N species in the model is expressed in cell number, a conversion factor has been estimated. The conversion factor K_O.D.toC.F.U. has been estimated as follows.

Two cultures C1 and C2 (MGZ1 cells) were grown in 1ml M9 medium till saturation (ON liquid culture, 37°C, 220 rpm).
Next morning, both C1 and C2 were diluted in M9 medium with a final volume of 1ml with the following dilution factors:
- 1:1
- 1:10
- 1:100
- 1:1000
in fresh M9 medium. These cultures were grown for further 1 hour at 37°C, 220 rpm.
After 1 hour, O.D.₆₀₀ was measured using TECAN microplate reader (don't forget to measure a M9 sample for blanking!)
NB: from now on, cultures must be placed in ice to stop cell growth.
At the same time, proper dilution of the cultures were plated on LB agar plates.
NB: All the dilutions are performed moving 100 μl of culture in previously ice-chilled 900 μl fresch M9. 100 μl of the final dilution are plated (It still represents a 1:10 dilution!)
Plates were grown overnight and next morning C.F.U. were counted.
C.F.U. values were corrected by the dilution factor and a linear regression (N vs O.D.₆₀₀) was performed in order to evaluate the conversion factor K_O.D.toC.F.U..
K_O.D.toC.F.U. was used as conversion factor to multiply the O.D.₆₀₀ value of saturation in the growth curves (~0,5).

The results are summarized in the table and in the figure below:

Culture	O.D.₆₀₀ TECAN	O.D.₆₀₀ Spectrophotometer	C.F.U.	Dilution Factor (10^)	N
C1	0,367950002	0,758004416	990	5	990000000
C1	0,044649998	0,091982322	141	6	1410000000
C1	0,004799999	0,009888356	136	5	136000000
C1	0,000549998	0,001133037	20	6	200000000
C2	0,54840003	1,129744917	165	4	16500000
C2	0,058200002	0,119896339	23	5	23000000
C2	0,008700002	0,017922652	251	3	2510000
C2	0,000100002	0,000206011	24	4	2400000

The estimation of μ parameter was performed by determining the slope of the logarithmic curve of O.D.₆₀₀ in exponential phase. Exponential phase was determined by visual inspection as the linear phase of the logarithmic curve of O.D.₆₀₀.

The estimated parameters are summarized in the table below:

N_max [cell number]	μ [min^-1]
1*10⁹	0.004925

The reported value of μ corresponds to a doubling time of 142 minutes.

^top

Estimation of the spontaneous degradation of HSL in M9 medium and in cultures at different pH values

In order to estimate the spontaneous degradation rate of HSL in M9 medium and in a culture of MGZ1 cells as a function of pH, two simple tests have been performed.
Two different M9 media were prepared, one with the nominal pH (7.0) and one with pH=6.0.
These media, now named respectively M9_{pH 7} and M9_{pH 6}, were added with a known concentration of HSL (100 nM) and then incubated at 37°C, 220 rpm (NB: the media were not infected with any culture but the standard growth conditions were reproduced). The amount of HSL present in the medium was assayed through the BBa_T9002 biosensor at 4 time points:

t=0 h;
t=1 h;
t=2 h;
t=4 h;
t=8 h;

The obtained time series of HSL amounts were processed to evaluate the time constant governing the dynamic of HSL degradation, supposing an exponential decay. The results are reported in the table below:

	*t_1/2^ [h]**	γ_HSL^ [h^-1]**
M9_{pH 6}	32	0.022
M9_{pH 7}	8	0.087

The described experiment was repeated with a MGZ1 culture in order to evaluate the effect of culture on HSL stability. The estimated values are reported in the table below:

	*t_1/2^ [h]**	γ_HSL^ [h^-1]**
Culture_{pH 6}	∞	0
Culture_{pH 7}	19	0.037

It is evident from the reported data that the spontaneous degradation of HSL is negligible when CTRL+E is implemented in MGZ1 cells grown in M9 medium with pH=6.0 and pH=7.0.
Thus in the simulations we set γ_HSL=0;

^top

Characterization of BBa_T9002 biosensor

As described in the modelling section, BioBrick BBa_T9002 is an HSL biosensor, which provides a non linear relationship between HSL input and S_cell output. More precisely, the characteristic sigmoidal curve requires synthetic parameters for its accurate identification. These are the minimum and maximum values, the swtich point (i.e., the curve inflection point), and the upper and lower boundaries of linearity. This biosensor revealed greatly reliable, providing measurement repeatability and minimal experimental noise. Referring to its activation formula, the calibration curve is shown below.

Minimum [S_cell]	Maximum [S_cell]	Switch point [nM]	Lower boundary of linearity [nM]	Upper boundary of linearity [nM]
17.31	739.4	1.39	0.38	5.07

In order to determine the threshold sensitivity of T9002 biosensor, experiments were performed with several HSL inductions minimally interspaced in the region of low detectability. Hypothesizing that the inducer is 1:20 diluted (as for all of our tests), the minimum detectable HSL concentration is 3 nM.

^top

Conclusions

To sum up the results of our project, we have characterized several basic parts and documented all of our experiments in the experience pages. All the data collected have been reported and synthetic parameters to describe the behavior of promoters, RBSs and genes have been provided. Such parameters can be used for the in silico simulation of mathematical models of complex circuits.
For what concerns CTRL+E, that is a proof of concept of the modular behavior of systems in synthetic biology, all the parameters of pTet, pLux and LuxI have been estimated. AiiA parameters revealed difficult to estimate.
Reasonable values for AiiA parameters have been derived from experiments in different contexts. These values were used to simulate the behavior of CTRL+E.
Further experiments are necessary to evaluate the consistence of the derived parameters for AiiA.
Once the most promising module combinations will be evaluated, a library of differently tuned controller will be built and characterized in order to assess the correspondence between the model predictions and the real data.

Team:UNIPV-Pavia/Project/Results

From 2011.igem.org

Latest revision as of 12:50, 22 October 2011

Results

Contents

Parts assembly

Characterization of basic modules

Characterization of promoters pTet and pLux

Characterization of enzymes AiiA and LuxI

Characterization of the efficiency of RBSs from the community collection

Identification of bacterial growth parameters

Estimation of the spontaneous degradation of HSL in M9 medium and in cultures at different pH values

Characterization of BBa_T9002 biosensor

Conclusions

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-                                <h2 class="art-postheader">
+<h2 class="art-postheader"> Results </h2>
-                Results
-                                </h2>
-                <div class="cleared"></div>
-                                <div class="art-postcontent">
-<!-------------------------------->
-<!-------------------------------->
-<!-------------------------------->
-<!-----------MENU----------------->
-<!-------------------------------->
-<!-------------------------------->
-<!-------------------------------->
-<br>
-<a name='indice'></a>
 <div class="cleared"></div>
 <div class="art-postcontent">
-<table id="toc" class="toc"><tr><td><div id="toctitle"><h2>Contents</h2></div>
+  <!-------------------------------->
-<ul>
+  <!-------------------------------->
-<li class="toclevel-1"><a href="#assembly"><span class="tocnumber">1</span> <span class="toctext">Part assembly</span></a>
+  <!-------------------------------->
-<li class="toclevel-1"><a href="#characterization"><span class="tocnumber">1</span> <span class="toctext">Characterization of basic modules</span></a>
+  <!-----------MENU----------------->
-<ul>
+  <!-------------------------------->
-<li class="toclevel-2"><a href="#promoters"><span class="tocnumber">2.1</span> <span class="toctext">Promoter characterization</span></a></li>
+  <!-------------------------------->
-<li class="toclevel-2"><a href="#enzymes"><span class="tocnumber">2.2</span> <span class="toctext">Characterization of the activity of the enzymes AiiA and LuxI</span></a></li>
+  <!-------------------------------->
-<li class="toclevel-2"><a href="#rbs"><span class="tocnumber">2.3</span> <span class="toctext">Characterization of RBS efficiency</span></a></li>
+  <br>
-</ul>
+  <a name='indice'></a>
-<li class="toclevel-1"><a href="#growth"><span class="tocnumber">3</span> <span class="toctext">Identification of bacterial growth parameters</span></a></li>
+  <div class="cleared"></div>
-<li class="toclevel-1"><a href="#HSL"><span class="tocnumber">4</span> <span class="toctext">Estimation of the spontaneous degradation of HSL in M9 medium and in cultures at different pH values</span></a></li>
+  <div class="art-postcontent">
-<li class="toclevel-1"><a href="#t9002"><span class="tocnumber">5</span> <span class="toctext">Characterization of BBa_T9002 biosensor</span></a></li>
+    <table id="toc" class="toc">
-</ul></td></tr></table>
+      <tr>
+        <td><div id="toctitle">
+            <h2>Contents</h2>
+          </div>
+          <ul>
+            <li class="toclevel-1"><a href="#assembly"><span class="tocnumber">1</span> <span class="toctext">Part assembly</span></a>
+            <li class="toclevel-1"><a href="#characterization"><span class="tocnumber">1</span> <span class="toctext">Characterization of basic modules</span></a>
+              <ul>
+                <li class="toclevel-2"><a href="#promoters"><span class="tocnumber">2.1</span> <span class="toctext">Promoter characterization</span></a></li>
+                <li class="toclevel-2"><a href="#enzymes"><span class="tocnumber">2.2</span> <span class="toctext">Characterization of the activity of the enzymes AiiA and LuxI</span></a></li>
+                <li class="toclevel-2"><a href="#rbs"><span class="tocnumber">2.3</span> <span class="toctext">Characterization of RBS efficiency</span></a></li>
+              </ul>
+            <li class="toclevel-1"><a href="#growth"><span class="tocnumber">3</span> <span class="toctext">Identification of bacterial growth parameters</span></a></li>
+            <li class="toclevel-1"><a href="#HSL"><span class="tocnumber">4</span> <span class="toctext">Estimation of the spontaneous degradation of HSL in M9 medium and in cultures at different pH values</span></a></li>
+            <li class="toclevel-1"><a href="#t9002"><span class="tocnumber">5</span> <span class="toctext">Characterization of BBa_T9002 biosensor</span></a></li>
+          </ul></td>
+      </tr>
+    </table>
+  </div>
+  <script>if (window.showTocToggle) { var tocShowText = "show"; var tocHideText = "hide"; showTocToggle(); } </script>
+  <br><em> NB: unless differently specified, all tests were performed in <a href='https://2011.igem.org/Team:UNIPV-Pavia/Protocols#MG1655Z1'><em>E. coli</em> MGZ1</a> in M9 supplemented medium at 37°C. For the cloning of the parts, <a href='https://2011.igem.org/Team:UNIPV-Pavia/Protocols#TOP10'><em>E. coli</em> TOP10</a> was used.
+<br><br>
+For more details on parts characterization, please visit the <a href='https://2011.igem.org/Team:UNIPV-Pavia/Parts/Characterized'>parts section</a>.  </em> <br>
+  <br>
+  <!-------------------------------->
+  <!-------------------------------->
+  <!-------------------------------->
+  <!-----------ASSEMBLY------------->
+  <!-------------------------------->
+  <!-------------------------------->
+  <!-------------------------------->
+  <a name='assembly'></a>
+  <h1>Parts assembly</h1>
+  All the parts have been cloned with success. The part name, plasmids and quality controls are reported in the <a href='https://2011.igem.org/Team:UNIPV-Pavia/Freezer'>Freezer section</a>.
+  <div align="right"><small><a href="#indice" title="">^top</a></small></div>
+  <!-------------------------------->
+  <!-------------------------------->
+  <!-------------------------------->
+  <!-------CHARACTERIZATION--------->
+  <!-------------------------------->
+  <!-------------------------------->
+  <!-------------------------------->
+  <a name='characterization'></a>
+  <h1>Characterization of basic modules</h1>
+  <!-------------------------------->
+  <!-------------------------------->
+  <!-------------------------------->
+  <!--------pTet and pLux----------->
+  <!-------------------------------->
+  <!-------------------------------->
+  <!-------------------------------->
+  <a name='promoters'></a>
+  <h2>Characterization of promoters pTet and pLux</h2>
+  <p align='justify'>
+  <p>Inducible promoters pLux and pTet were assembled upstream of mRFP coding sequences containing an RBS from the Community collection.</p>
+  <p>The assembled RBSs are:</p>
+  <br>
+  <div align='center'>
+    <table class='data'>
+      <tr>
+        <td class="row"><b>BioBrick code</b></td>
+        <td><b> Declared efficiency</b></td>
+      </tr>
+      <tr>
+        <td class="row">BBa_B0030 </td>
+        <td class="row"> 0,6</td>
+      </tr>
+      <tr>
+        <td class="row">BBa_B0031 </td>
+        <td class="row"> 0,07</td>
+      </tr>
+      <tr>
+        <td class="row">BBa_B0032 </td>
+        <td class="row"> 0,3</td>
+      </tr>
+      <tr>
+        <td class="row">BBa_B0034 </td>
+        <td class="row"> 1</td>
+      </tr>
+    </table>
+  </div>
+  <br>
+<div class="listcircle">
+  <div align="justify">
+  <p>The RBS variation has the purpose to stretch the induction curve, thus modulating the PoPs-OUT range of the inducible device.</p>
+  <p>The complex RBS-promoter acts as a whole regulatory element and determines the amount of translated protein.
+    RBSs have been reported to have an un-modular behavior, since the translational efficiency is not independent on the coding sequences, but variates as an effect of different mRNA structure stability [Salis et al., Nat Biotec, 2009]. It is not possible to separate the effects of the sole promoter and of the sole RBS on the total amount/activity of gene product (in this case study, mRFP).</p>
+  <p>For this reason, every combination 'Promoter+RBS' was studied as a different regulatory element. Regulatory elements were characterized using mRFP reporter protein for different RBSs in terms of Synthesis rate per Cell (<b>S<sub>cell</sub></b>) and <b>R.P.U.s</b> (Relative Promoter Units) as explained in <a href='https://2011.igem.org/Team:UNIPV-Pavia/Measurements'>measurements</a> section.</p>
+  </p>
+  <p>Operative parameters of the promoter are derived from the estimated Hill equations obtained by <em>nonlinear least squares</em> fitting (<em>lsqnonlin</em> Matlab routine) of the <a href='https://2011.igem.org/Team:UNIPV-Pavia/Project/Modelling#Equations_for_gene_networks'>Hill function</a> expressed in RPUs:</p>
+  <p></p>
+  <p>
+  <ol>
+    <ul>
+      <li><b> RPU<sub>max</sub></b> is equal to the &alpha; and represents the maximum promoter activity
+        </p>
+      </li>
+      <p>
+      <li><b> RPU<sub>min</sub></b> is equal to the &alpha; * &delta; represents the minimum promoter activity
+        </p>
+      </li>
+      <p>
+      <li> <b>Switch point</b> is computed as the abscissa of the inflection point of the Hill curve and it is representative of the position of linear region
+        </p>
+      </li>
+      <p>
+      <li> <b>Linearity boundaries</b> are determined as the intersection between the tangent line to the inflection point and the upper and lower horizontal boundaries of the Hill curve.
+      </li>
+      </p>
+    </ul>
+  </ol>
+  </p>
+  <div align="justify"> The estimated parameters for the Hill functions of pLux are summarized in the table below. For more details on parameter estimation, see the <a href='https://2011.igem.org/Team:UNIPV-Pavia/Project/Modelling#Ptet_&_Plux'>model section</a>. </div>
+  <table class='data' width='100%'>
+    <tr>
+      <td class="row"><b>RBS</b></td>
+      <td class="row"><b>&alpha;<sub>p<sub>Lux</sub></sub> [(AUr/min)/cell]</b></td>
+      <td class="row"><b>&delta;<sub>p<sub>Lux</sub></sub> [-]</b></td>
+      <td class="row"><b>&eta;<sub>p<sub>Lux</sub></sub> [-]</b></td>
+      <td class="row"><b>k<sub>p<sub>Lux</sub></sub> [ng/ml]</b></td>
+    </tr>
+    <tr>
+      <td class="row">BBa_B0030</td>
+      <td class="row">438 [10]</td>
+      <td class="row">0.05 [>100]</td>
+      <td class="row">2 [47]</td>
+      <td class="row">1.88 [27]</td>
+    </tr>
+    <tr>
+      <td class="row">BBa_B0031</td>
+      <td class="row">9.8 [7]</td>
+      <td class="row">0.11 [57]</td>
+      <td class="row">1.2 [29]</td>
+      <td class="row">1.5 [26]</td>
+    </tr>
+    <tr>
+      <td class="row">BBa_B0032</td>
+      <td class="row">206 [3]</td>
+      <td class="row">0 [>>100]</td>
+      <td class="row">1.36 [10]</td>
+      <td class="row">1.87 [9]</td>
+    </tr>
+    <tr>
+      <td class="row">BBa_B0034</td>
+      <td class="row">1105 [6]</td>
+      <td class="row">0.02 [>100]</td>
+      <td class="row">1.33 [19]</td>
+      <td class="row">2.34 [18]</td>
+    </tr>
+  </table>
+  <div align="center">Data are provided as average [CV%].</div>
+  <br>
+  <p>The operative parameters of pLux are summarized in the table below:</p>
 </div>
-<script>if (window.showTocToggle) { var tocShowText = "show"; var tocHideText = "hide"; showTocToggle(); } </script>
-<em>
-NB: unless differently specified, all tests were performed in <a href='https://2011.igem.org/Team:UNIPV-Pavia/Protocols#MG1655Z1'><em>E. coli</em> MGZ1</a> in M9 supplemented medium at 37°C. For the cloning of the parts, <a href='https://2011.igem.org/Team:UNIPV-Pavia/Protocols#TOP10'><em>E. coli</em> TOP10</a> was used.
-</em>
-<br>
-<br>
-<!-------------------------------->
-<!-------------------------------->
-<!-------------------------------->
-<!-----------ASSEMBLY------------->
-<!-------------------------------->
-<!-------------------------------->
-<!-------------------------------->
-<a name='assembly'></a><h1>Parts assembly</h1>
-All the parts have been cloned with success. The part name, plasmids and quality controls are reported in the <a href='https://2011.igem.org/Team:UNIPV-Pavia/Freezer'>Freezer section</a>.
-<div align="right"><small><a href="#indice" title="">^top</a></small></div>
-<!-------------------------------->
-<!-------------------------------->
-<!-------------------------------->
-<!-------CHARACTERIZATION--------->
-<!-------------------------------->
-<!-------------------------------->
-<!-------------------------------->
-<a name='characterization'></a><h1>Characterization of basic modules</h1>
-<!-------------------------------->
-<!-------------------------------->
-<!-------------------------------->
-<!--------pTet and pLux----------->
-<!-------------------------------->
-<!-------------------------------->
-<!-------------------------------->
-<a name='promoters'></a><h2>Characterization of promoters pTet and pLux</h2>
-<p align='justify'>
-<p>Inducible and constitutive promoters were assembled upstream of different coding sequences containing an  RBS from the Community collection.</p>
-<p>The assembled RBSs are:</p>
-<br>
-<div align='center'>
-<table class='data'>
-<tr><td class="row"><b>BioBrick code</b></td><td><b>   	Declared efficiency</b></td></tr>
-<tr><td class="row">BBa_B0030 </td><td class="row">		0,6</td></tr>
-<tr><td class="row">BBa_B0031 </td><td class="row">		0,07</td></tr>
-<tr><td class="row">BBa_B0032 </td><td class="row">		0,3</td></tr>
-<tr><td class="row">BBa_B0034 </td><td class="row">	1</td></tr>
-</table></div>
-<br>
-<div align="justify"><p>For an inducible device, the RBS variation has the purpose to stretch the induction curve, thus modulating its PoPs-OUT range.</p>
-<p>The complex RBS-promoter acts as a whole regulatory element and determines the amount of translated protein.
-RBSs have been reported to have an un-modular behavior, since the translational efficiency is not independent on the coding sequences, but variates as an effect of different mRNA structure stability [Salis et al., Nat Biotec, 2009]. It is not possible to separate the effects of the sole promoter and of the sole RBS on the total amount/activity of gene product (in this case study, mRFP).</p>
-<p>For this reason, every combination 'Promoter+RBS' was studied as a different regulatory element. Regulatory elements were characterized using mRFP reporter protein for different RBSs in terms of Synthesis rate per Cell (<b>S<sub>cell</sub></b>) and <b>R.P.U.s</b> (Relative Promoter Units) as explained in <a href='https://2011.igem.org/Team:UNIPV-Pavia/Measurements'>measurements</a> section.</p>
-</p>
-<p>Operative parameters of the promoter are derived from the estimated Hill equations obtained by <em>nonlinear least squares</em> fitting (<em>lsqnonlin</em> Matlab routine) of the <a href='https://2011.igem.org/Team:UNIPV-Pavia/Project/Modelling#Equations_for_gene_networks'>Hill function</a> expressed in RPUs:</p><p></p>
-<p><ol><ul><li><b>
-RPU<sub>max</sub></b> is equal to the &alpha; and represents the maximum promoter activity</p>
-</li><p><li><b>
-RPU<sub>min</sub></b> is equal to the &alpha; * &delta; represents the minimum promoter activity</p>
-</li><p><li>
-<b>Switch point</b> is computed as the abscissa of the inflection point of the Hill curve and it is representative of the position of linear region</p>
-</li>
-<p><li>
-<b>Linearity boundaries</b> are determined as the intersection between the tangent line to the inflection point and the upper and lower horizontal boundaries of the Hill curve.</div></li></p>
-</ul></ol>
-</p>
-<p align='justify'>
-The estimated parameters for the Hill functions of pLux are summarized in the table below. For more details on parameter estimation, see the <a href='https://2011.igem.org/Team:UNIPV-Pavia/Project/Modelling#Ptet_&_Plux'>model section</a>.
-</p>
-<table class='data' width='100%'>
-<tr>
-<td class="row"><b>RBS</b></td>
-<td class="row"><b>&alpha;<sub>p<sub>Lux</sub></sub> [(AUr/min)/cell]</b></td>
-<td class="row"><b>&delta;<sub>p<sub>Lux</sub></sub> [-]</b></td>
-<td class="row"><b>&eta;<sub>p<sub>Lux</sub></sub> [-]</b></td>
-<td class="row"><b>k<sub>p<sub>Lux</sub></sub> [ng/ml]</b></td>
-</tr>
-<tr><td class="row">BBa_B0030</td>
-<td class="row">438 [10]</td>
-<td class="row">0.05 [>100]</td>
-<td class="row">2 [47]</td>
-<td class="row">1.88 [27]</td>
-</tr>
-<tr><td class="row">BBa_B0031</td>
-<td class="row">9.8 [7]</td>
-<td class="row">0.11 [57]</td>
-<td class="row">1.2 [29]</td>
-<td class="row">1.5 [26]</td>
-</tr>
-<tr><td class="row">BBa_B0032</td>
-<td class="row">206 [3]</td>
-<td class="row">0 [>>100]</td>
-<td class="row">1.36 [10]</td>
-<td class="row">1.87 [9]</td>
-</tr>
-<tr><td class="row">BBa_B0034</td>
-<td class="row">1105 [6]</td>
-<td class="row">0.02 [>100]</td>
-<td class="row">1.33 [19]</td>
-<td class="row">2.34 [18]</td>
-</tr>
-</table>
-<div align="center">Data are provided as average [CV%].</div><br>
-<p>The operative parameters are summarized in the table below:</p></div>
 <table align='center' class='data' width='100%'>
-<tr>
+  <tr>
-<td class='row'><b>RBS</b></td>
+    <td class='row'><b>RBS</b></td>
-<td class='row'><b>RPU<sub>max</sub></b></td>
+    <td class='row'><b>RPU<sub>max</sub></b></td>
-<td class='row'><b>RPU<sub>min</sub></b></td>
+    <td class='row'><b>RPU<sub>min</sub></b></td>
-<td class='row'><b>Switch point [nM]</b></td>
+    <td class='row'><b>Switch point [nM]</b></td>
-<td class='row'><b>Linear boundaries [MIN; MAX] [nM]</b></td>
+    <td class='row'><b>Linear boundaries [MIN; MAX] [nM]</b></td>
-</tr>
+  </tr>
-<tr>
+  <tr>
-<td class='row'>B0030</td><td class='row'>4.28</td><td class='row'>0.20</td><td class='row'>1.08</td><td class='row'>[0.36; 3.27]</td>
+    <td class='row'>B0030</td>
-</tr>
+    <td class='row'>4.28</td>
-<tr>
+    <td class='row'>0.20</td>
-<td class='row'>B0031</td><td class='row'>4.93</td><td class='row'>0.55</td><td class='row'>0.25</td><td class='row'>[0.03; 2.30]</td>
+    <td class='row'>1.08</td>
-</tr>
+    <td class='row'>[0.36; 3.27]</td>
-<tr>
+  </tr>
-<td class='row'>B0032</td><td class='row'>9.49</td><td class='row'>0.02</td><td class='row'>0.47</td><td class='row'>[0.07; 3.07]</td>
+  <tr>
-</tr>
+    <td class='row'>B0031</td>
-<tr>
+    <td class='row'>4.93</td>
-<td class='row'>B0034</td><td class='row'>21.53</td><td class='row'>0.51</td><td class='row'>0.53</td><td class='row'>[0.08; 3.77]</td>
+    <td class='row'>0.55</td>
-</tr>
+    <td class='row'>0.25</td>
+    <td class='row'>[0.03; 2.30]</td>
+  </tr>
+  <tr>
+    <td class='row'>B0032</td>
+    <td class='row'>9.49</td>
+    <td class='row'>0.02</td>
+    <td class='row'>0.47</td>
+    <td class='row'>[0.07; 3.07]</td>
+  </tr>
+  <tr>
+    <td class='row'>B0034</td>
+    <td class='row'>21.53</td>
+    <td class='row'>0.51</td>
+    <td class='row'>0.53</td>
+    <td class='row'>[0.08; 3.77]</td>
+  </tr>
 </table>
+<table width='100%'>
+  <tr>
-<table width='100%'><tr><td width='50%'>
+    <td width='50%'><div style="text-align:justify">
-<div style="text-align:justify"><div class="thumbinner" width='100%'><a href="https://static.igem.org/mediawiki/2011/5/50/E17_RPU_80.jpg" class="image"><img alt="" src="https://static.igem.org/mediawiki/2011/5/50/E17_RPU_80.jpg" class="thumbimage" width="100%"></a></div></div>
+        <div class="thumbinner" width='100%'><a href="https://static.igem.org/mediawiki/2011/5/50/E17_RPU_80.jpg" class="image"><img alt="" src="https://static.igem.org/mediawiki/2011/5/50/E17_RPU_80.jpg" class="thumbimage" width="100%"></a></div>
-</td>
+      </div></td>
-<td width='50%'>
+    <td width='50%'><div style="text-align:justify">
-<div style="text-align:justify"><div class="thumbinner" width='100%'><a href="https://static.igem.org/mediawiki/2011/c/c4/E18_RPU_80.jpg" class="image"><img alt="" src="https://static.igem.org/mediawiki/2011/c/c4/E18_RPU_80.jpg" class="thumbimage" width="100%"></a></div></div>
+        <div class="thumbinner" width='100%'><a href="https://static.igem.org/mediawiki/2011/c/c4/E18_RPU_80.jpg" class="image"><img alt="" src="https://static.igem.org/mediawiki/2011/c/c4/E18_RPU_80.jpg" class="thumbimage" width="100%"></a></div>
-</td></tr>
+      </div></td>
-<tr><td width='50%'>
+  </tr>
-<div style="text-align:justify"><div class="thumbinner" width='100%'><a href="https://static.igem.org/mediawiki/2011/7/78/E19_RPU_80.jpg" class="image"><img alt="" src="https://static.igem.org/mediawiki/2011/7/78/E19_RPU_80.jpg" class="thumbimage" width="100%"></a></div></div>
+  <tr>
-</td>
+    <td width='50%'><div style="text-align:justify">
-<td width='50%'>
+        <div class="thumbinner" width='100%'><a href="https://static.igem.org/mediawiki/2011/7/78/E19_RPU_80.jpg" class="image"><img alt="" src="https://static.igem.org/mediawiki/2011/7/78/E19_RPU_80.jpg" class="thumbimage" width="100%"></a></div>
-<div style="text-align:justify"><div class="thumbinner" width='100%'><a href="https://static.igem.org/mediawiki/2011/5/55/E20_RPU_80.jpg" class="image"><img alt="" src="https://static.igem.org/mediawiki/2011/5/55/E20_RPU_80.jpg" class="thumbimage" width="100%"></a></div></div>
+      </div></td>
-</td></tr>
+    <td width='50%'><div style="text-align:justify">
+        <div class="thumbinner" width='100%'><a href="https://static.igem.org/mediawiki/2011/5/55/E20_RPU_80.jpg" class="image"><img alt="" src="https://static.igem.org/mediawiki/2011/5/55/E20_RPU_80.jpg" class="thumbimage" width="100%"></a></div>
+      </div></td>
+  </tr>
 </table>
 <p>The protocols for the characterization of p<sub>Tet</sub> promoter are reported in the <a href='https://2011.igem.org/Team:UNIPV-Pavia/Measurements#pTet_protocol'>p<sub>Tet</sub> measurement section</a>.</p>
-<p>
+<p> Here we have characterized its transcriptional strength as a function of aTc induction (ng/ml) for different RBSs. Three different induction curves were obtained and are reported in figure:</p>
-Here we have characterized its transcriptional strength as a function of aTc induction (ng/ul) for different RBSs. Three different induction curves were obtained and are reported in figure:</p></div>
-<center><a href="https://static.igem.org/mediawiki/2011/a/af/E32_RPU_80.jpg" class="image">
+<center>
-<img alt="" src="https://static.igem.org/mediawiki/2011/a/af/E32_RPU_80.jpg" class="thumbimage" width="50%"></a>
+  <a href="https://static.igem.org/mediawiki/2011/a/af/E32_RPU_80.jpg" class="image"> <img alt="" src="https://static.igem.org/mediawiki/2011/a/af/E32_RPU_80.jpg" class="thumbimage" width="50%"></a>
 </center>
 <table width='100%'>
-<tr><td width='50%'>
+  <tr>
-<div style="text-align:justify"><div class="thumbinner" width='100%'><a href="https://static.igem.org/mediawiki/2011/9/99/E34_RPU_80.jpg" class="image"><img alt="" src="https://static.igem.org/mediawiki/2011/9/99/E34_RPU_80.jpg" class="thumbimage" width="100%"></a></div></div>
+    <td width='50%'><div style="text-align:justify">
-</td>
+        <div class="thumbinner" width='100%'><a href="https://static.igem.org/mediawiki/2011/9/99/E34_RPU_80.jpg" class="image"><img alt="" src="https://static.igem.org/mediawiki/2011/9/99/E34_RPU_80.jpg" class="thumbimage" width="100%"></a></div>
-<td width='50%'>
+      </div></td>
-<div style="text-align:justify"><div class="thumbinner" width='100%'><a href="https://static.igem.org/mediawiki/2011/e/e4/E35_RPU_80.jpg" class="image"><img alt="" src="https://static.igem.org/mediawiki/2011/e/e4/E35_RPU_80.jpg" class="thumbimage" width="100%"></a></div></div>
+    <td width='50%'><div style="text-align:justify">
-</td></tr>
+        <div class="thumbinner" width='100%'><a href="https://static.igem.org/mediawiki/2011/e/e4/E35_RPU_80.jpg" class="image"><img alt="" src="https://static.igem.org/mediawiki/2011/e/e4/E35_RPU_80.jpg" class="thumbimage" width="100%"></a></div>
+      </div></td>
+  </tr>
 </table>
+<p align='justify'> The estimated parameters of the Hill curves described in the figures are summarized in the table below: </p>
-<p align='justify'>
-The estimated parameters of the Hill curves described in the figures are summarized in the table below:
-</p>
 <br>
 <table class='data' width='100%' title='parameter value'>
-<tr>
+  <tr>
-<td class="row"><b>RBS</b></td>
+    <td class="row"><b>RBS</b></td>
-<td class="row"><b>&alpha;<sub>p<sub>Tet</sub></sub> [(AUr/min)/cell]</b></td>
+    <td class="row"><b>&alpha;<sub>p<sub>Tet</sub></sub> [(AUr/min)/cell]</b></td>
-<td class="row"><b>&delta;<sub>p<sub>Tet</sub></sub> [-]</b></td>
+    <td class="row"><b>&delta;<sub>p<sub>Tet</sub></sub> [-]</b></td>
-<td class="row"><b>&eta;<sub>p<sub>Tet</sub></sub> [-]</b></td>
+    <td class="row"><b>&eta;<sub>p<sub>Tet</sub></sub> [-]</b></td>
-<td class="row"><b>k<sub>p<sub>Tet</sub></sub> [nM]</b></td>
+    <td class="row"><b>k<sub>p<sub>Tet</sub></sub> [nM]</b></td>
-</tr>
+  </tr>
-<tr><td class="row">BBa_B0030</td>
+  <tr>
-<td class="row">230.67 [3.7]</td>
+    <td class="row">BBa_B0030</td>
-<td class="row">0.028 [91.61]</td>
+    <td class="row">230.67 [3.7]</td>
-<td class="row">4.61 [23.73]</td>
+    <td class="row">0.028 [91.61]</td>
-<td class="row">8.75 [4.16]</td>
+    <td class="row">4.61 [23.73]</td>
-</tr>
+    <td class="row">8.75 [4.16]</td>
-<tr><td class="row">BBa_B0031</td>
+  </tr>
-<td class="row">ND</td>
+  <tr>
-<td class="row">ND</td>
+    <td class="row">BBa_B0031</td>
-<td class="row">ND</td>
+    <td class="row">ND</td>
-<td class="row">ND</td>
+    <td class="row">ND</td>
-</tr>
+    <td class="row">ND</td>
-<tr><td class="row">BBa_B0032</td>
+    <td class="row">ND</td>
-<td class="row">55.77 [12]</td>
+  </tr>
-<td class="row">1.53E-11 [>>100]</td>
+  <tr>
-<td class="row">4.98 [57.62]</td>
+    <td class="row">BBa_B0032</td>
-<td class="row">7.26 [14.98]</td>
+    <td class="row">55.77 [12]</td>
-</tr>
+    <td class="row">1.53E-11 [>>100]</td>
-<tr><td class="row">BBa_B0034</td>
+    <td class="row">4.98 [57.62]</td>
-<td class="row">120 [5.95]</td>
+    <td class="row">7.26 [14.98]</td>
-<td class="row">0.085 [40.6]</td>
+  </tr>
-<td class="row">24.85 [47.6]</td>
+  <tr>
-<td class="row">9 [5.43]</td>
+    <td class="row">BBa_B0034</td>
-</tr>
+    <td class="row">120 [5.95]</td>
+    <td class="row">0.085 [40.6]</td>
+    <td class="row">24.85 [47.6]</td>
+    <td class="row">9 [5.43]</td>
+  </tr>
 </table>
-Data are provided as average [CV%]
+<div align="center">Data are provided as average [CV%]</div> <br>
-<br><br>
+<br>
+<p align='justify'> The operative parameters are summarized in the table below: </p>
-<p align='justify'>
-The operative parameters are summarized in the table below:
-</p>
 <table align='center' class='data' width='100%'>
-<tr>
+  <tr>
-<td class='row'><b>RBS</b></td>
+    <td class='row'><b>RBS</b></td>
-<td class='row'><b>RPU<sub>max</sub></b></td>
+    <td class='row'><b>RPU<sub>max</sub></b></td>
-<td class='row'><b>RPU<sub>min</sub></b></td>
+    <td class='row'><b>RPU<sub>min</sub></b></td>
-<td class='row'><b>Switch point [ng/ml]</b></td>
+    <td class='row'><b>Switch point [ng/ml]</b></td>
-<td class='row'><b>Linear boundaries [MIN; MAX] [ng/ml]</b></td>
+    <td class='row'><b>Linear boundaries [MIN; MAX] [ng/ml]</b></td>
-</tr>
+  </tr>
-<tr>
+  <tr>
-<td class='row'>B0030</td><td class='row'>1.53</td><td class='row'>~0</td><td class='row'>7.95</td><td class='row'>[4.66;11.99]</td>
+    <td class='row'>B0030</td>
-</tr>
+    <td class='row'>1.53</td>
-<tr>
+    <td class='row'>~0</td>
-<td class='row'>B0031</td><td class='row'>ND</td><td class='row'>ND</td><td class='row'>ND</td><td class='row'>ND</td>
+    <td class='row'>7.95</td>
-</tr>
+    <td class='row'>[4.66;11.99]</td>
-<tr>
+  </tr>
-<td class='row'>B0032</td><td class='row'>3.16</td><td class='row'>~0</td><td class='row'>6.7</td><td class='row'>[4.45;10.05]</td>
+  <tr>
-</tr>
+    <td class='row'>B0031</td>
-<tr>
+    <td class='row'>ND</td>
-<td class='row'>B0034</td><td class='row'>2.73</td><td class='row'>0.23</td><td class='row'>8.96</td><td class='row'>[8.27;9.71]</td>
+    <td class='row'>ND</td>
-</tr>
+    <td class='row'>ND</td>
+    <td class='row'>ND</td>
+  </tr>
+  <tr>
+    <td class='row'>B0032</td>
+    <td class='row'>3.16</td>
+    <td class='row'>~0</td>
+    <td class='row'>6.7</td>
+    <td class='row'>[4.45;10.05]</td>
+  </tr>
+  <tr>
+    <td class='row'>B0034</td>
+    <td class='row'>2.73</td>
+    <td class='row'>0.23</td>
+    <td class='row'>8.96</td>
+    <td class='row'>[8.27;9.71]</td>
+  </tr>
 </table>
 <div align="right"><small><a href="#indice" title="">^top</a></small></div>
+<!-------------------------------->
+<!-------------------------------->
+<!-------------------------------->
+<!--------AiiA and LuxI----------->
+<!-------------------------------->
+<!-------------------------------->
+<!-------------------------------->
+<a name='enzymes'></a>
-<!-------------------------------->
+<h2>Characterization of enzymes AiiA and LuxI</h2>
-<!-------------------------------->
+<p align='justify'> LuxI has been characterized through the Biosensor BBa_T9002 (see <a href='https://2011.igem.org/Team:UNIPV-Pavia/Project/Modelling#introduction_to_T9002'>modelling section</a>) using the <a href='https://2011.igem.org/Team:UNIPV-Pavia/Parts/Characterized#pTetLuxI'>p<sub>Tet</sub>-RBSx-LuxI-TT</a> measurement systems. <br>
-<!-------------------------------->
+  The parameters V<sub>max</sub>, k<sub>M,LuxI</sub> and &alpha;<sub>RBSx</sub> were estimated with a simultaneous fitting of the data collected as described in <a href='https://2011.igem.org/Team:UNIPV-Pavia/Measurements#LuxI'>measurement section</a> for the four measurement parts <a href='https://2011.igem.org/Team:UNIPV-Pavia/Parts/Characterized#pTetLuxI'>p<sub>Tet</sub>-RBSx-LuxI-TT</a> assayed by <a href='https://2011.igem.org/Team:UNIPV-Pavia/Measurements#T9002'>BBa_T9002 biosensor</a> section.
-<!--------AiiA and LuxI----------->
+<div align="justify">
-<!-------------------------------->
+  <div class="thumbinner" style="width: 850px;"> <a href="https://static.igem.org/mediawiki/2011/4/40/Luxi_prod.jpg"> <img alt="" src="https://static.igem.org/mediawiki/2011/4/40/Luxi_prod.jpg" class="thumbimage" width="85%" height="50%"></a></div>
-<!-------------------------------->
+</div>
-<!-------------------------------->
+<div align="justify">
+  <p>The estimated parameters for the enzymatic activity of LuxI are reported in the table below:</p>
-<a name='enzymes'></a><h2>Characterization of enzymes AiiA and LuxI</h2>
+</div>
+<div align="center">
+  <table align="center" class='data'>
-<p align='justify'>
+    <tr>
+      <td class='row'><b>V<sub>max</sub></b></td>
-LuxI has been characterized through the Biosensor BBa_T9002 (see <a href='https://2011.igem.org/Team:UNIPV-Pavia/Project/Modelling#introduction_to_T9002'>modelling section</a>) using the <a href='https://2011.igem.org/Team:UNIPV-Pavia/Parts/Characterized#pTetLuxI'>p<sub>Tet</sub>-RBSx-LuxI-TT</a> measurement systems.
+      <td class='row'><b>k<sub>M,LuxI</sub></b></td>
+      <td class='row'><b>&alpha;<sub>B0030</sub></b></td>
+      <td class='row'><b>&alpha;<sub>B0031</sub></b></td>
+      <td class='row'><b>&alpha;<sub>B0032</sub></b></td>
+      <td class='row'><b>&alpha;<sub>B0034</sub></b></td>
+    </tr>
+    <tr>
+      <td class='row'>3.56*10<sup>-9</sup></td>
+      <td class='row'>6.87*10<sup>3</sup></td>
+      <td class='row'> 87 </td>
+      <td class='row'>8.5</td>
+      <td class='row'>ND</td>
+      <td class='row'> 252 </td>
+    </tr>
+  </table>
+</div>
 <br>
-The parameters V<sub>max</sub>, k<sub>M,LuxI</sub> and &alpha;<sub>RBSx</sub> were estimated with a simultaneous fitting of the data collected as described in <a href='https://2011.igem.org/Team:UNIPV-Pavia/Measurements#LuxI'>measurement section</a> for the four measurement parts <a href='https://2011.igem.org/Team:UNIPV-Pavia/Parts/Characterized#pTetLuxI'>p<sub>Tet</sub>-RBSx-LuxI-TT</a> assayed by <a href='https://2011.igem.org/Team:UNIPV-Pavia/Measurements#T9002'>BBa_T9002 biosensor</a> section.
-<div align="justify"><div class="thumbinner" style="width: 850px;">
-<a href="https://static.igem.org/mediawiki/2011/4/40/Luxi_prod.jpg">
-<img alt="" src="https://static.igem.org/mediawiki/2011/4/40/Luxi_prod.jpg" class="thumbimage" width="85%" height="50%"></a></div></div>
-<div align="justify"><p>The estimated parameters for the enzymatic activity of LuxI are reported in the table below:</p></div>
-<div align=center">
-<table align="center" class='data'>
-<tr>
-<td class='row'><b>V<sub>max</sub></b></td>
-<td class='row'><b>k<sub>M,LuxI</sub></b></td>
-<td class='row'><b>&alpha;<sub>B0030</sub></b></td>
-<td class='row'><b>&alpha;<sub>B0031</sub></b></td>
-<td class='row'><b>&alpha;<sub>B0032</sub></b></td>
-<td class='row'><b>&alpha;<sub>B0034</sub></b></td>
-</tr>
-<tr><td class='row'>3.56*10<sup>-9</sup></td>
-<td class='row'>6.87*10<sup>3</sup></td>
-<td class='row'> 87 </td>
-<td class='row'>8.5</td>
-<td class='row'>ND</td>
-<td class='row'> 252 </td>
-</tr></table>
-</div>
-<br>
 </p>
 </p>
+<p align='justify'> The provided parameters k<sub>M</sub> and V<sub>max</sub> represent the enzymatic activity of LuxI, described by our model. They must not be confused with the operative parameters of the Michaelis-Menten relation.
-<p align='justify'>
+  These synthetic parameters have a great importance, since they can be used in more complicated models in order to predict the behavior of complex circuits. </p>
-The provided parameters k<sub>M</sub> and V<sub>max</sub> represent the enzymatic activity of LuxI, described by our model. They must not be confused with the operative parameters of the Michaelis-Menten relation.
+<p align='justify'> The AiiA enzyme activity has been characterized under the regulation of p<sub>tet</sub> promoter, assaying its enzymatic activity. </p>
-These synthetic parameters have a great importance, since they can be used in more complicated models in order to predict the behavior of complex circuits.
+<p align='justify'> The parameters k<sub>cat</sub>, k<sub>M,AiiA</sub> and &alpha;<sub>RBSx</sub> would have been estimated with a simultaneous fitting of the data collected as described in <a href='https://2011.igem.org/Team:UNIPV-Pavia/Measurements#AiiA'>measurement section</a> for the four measurement parts <a href='https://2011.igem.org/Team:UNIPV-Pavia/Parts/Characterized#pTetAiiA'>p<sub>Tet</sub>-RBSx-AiiA-TT</a> assayed by <a href='https://2011.igem.org/Team:UNIPV-Pavia/Measurements#T9002'>BBa_T9002 biosensor</a> section.
-</p>
+  Unfortunately, their estimation revealed difficult.<br>
+  In the first experiments with the measurement system <a href="https://static.igem.org/mediawiki/2011/1/11/Pc_aiia.jpg">p<sub>Tet</sub>-RBSx-AiiA-TT</a> in LOW-COPY at pH=7 no degradation of HSL was observed. The collected data are shown in the figure below. HSL degradation is identical in the measurement system and in the negative control after 21 hours.
-<p align='justify'>
+<table width='100%'>
-The AiiA enzyme activity has been characterized under the regulation of p<sub>tet</sub> promoter, assaying its enzymatic activity.
+  <tr>
-</p>
+    <td width='50%'><div style="text-align:justify">
+        <div class="thumbinner" width='100%'> <a href="https://static.igem.org/mediawiki/2011/6/69/Aiia_LC_B0030.jpg"> <img alt="" src="https://static.igem.org/mediawiki/2011/6/69/Aiia_LC_B0030.jpg" class="thumbimage" width="100%"></a></div>
-<p align='justify'>
+      </div></td>
-The parameters k<sub>cat</sub>, k<sub>M,AiiA</sub> and &alpha;<sub>RBSx</sub> would have been estimated with a simultaneous fitting of the data collected as described in <a href='https://2011.igem.org/Team:UNIPV-Pavia/Measurements#AiiA'>measurement section</a> for the four measurement parts <a href='https://2011.igem.org/Team:UNIPV-Pavia/Parts/Characterized#pTetAiiA'>p<sub>Tet</sub>-RBSx-AiiA-TT</a> assayed by <a href='https://2011.igem.org/Team:UNIPV-Pavia/Measurements#T9002'>BBa_T9002 biosensor</a> section.
+    <td width='50%'><div style="text-align:justify">
-Unfortunately, their estimation revealed difficult.<br>
+        <div class="thumbinner" width='100%'> <a href="https://static.igem.org/mediawiki/2011/6/63/Aiia_LC_B0031.jpg"> <img alt="" src="https://static.igem.org/mediawiki/2011/6/63/Aiia_LC_B0031.jpg" class="thumbimage" width="100%"></a></div>
-In the first experiments with the measurement system <a href="https://static.igem.org/mediawiki/2011/1/11/Pc_aiia.jpg">p<sub>Tet</sub>-RBSx-AiiA-TT</a> in LOW-COPY at pH=7 no degradation of HSL was observed. The collected data are shown in the figure below. HSL degradation is identical in the measurement system and in the negative control after 21 hours.
+      </div></td>
+  </tr>
+  <tr>
-<table width='100%'><tr><td width='50%'>
+    <td width='50%'><div style="text-align:justify">
-<div style="text-align:justify"><div class="thumbinner" width='100%'>
+        <div class="thumbinner" width='100%'> <a href="https://static.igem.org/mediawiki/2011/f/f5/Aiia_LC_B0032.jpg"> <img alt="" src="https://static.igem.org/mediawiki/2011/f/f5/Aiia_LC_B0032.jpg" class="thumbimage" width="100%"></a></div>
-<a href="https://static.igem.org/mediawiki/2011/6/69/Aiia_LC_B0030.jpg">
+      </div></td>
-<img alt="" src="https://static.igem.org/mediawiki/2011/6/69/Aiia_LC_B0030.jpg" class="thumbimage" width="100%"></a></div></div>
+    <td width='50%'><div style="text-align:justify">
-</td>
+        <div class="thumbinner" width='100%'> <a href="https://static.igem.org/mediawiki/2011/8/8d/Aiia_LC_B0034.jpg"> <img alt="" src="https://static.igem.org/mediawiki/2011/8/8d/Aiia_LC_B0034.jpg" class="thumbimage" width="100%"></a></div>
-<td width='50%'>
+      </div></td>
-<div style="text-align:justify"><div class="thumbinner" width='100%'>
+  </tr>
-<a href="https://static.igem.org/mediawiki/2011/6/63/Aiia_LC_B0031.jpg">
-<img alt="" src="https://static.igem.org/mediawiki/2011/6/63/Aiia_LC_B0031.jpg" class="thumbimage" width="100%"></a></div></div>
-</td></tr>
-<tr><td width='50%'>
-<div style="text-align:justify"><div class="thumbinner" width='100%'>
-<a href="https://static.igem.org/mediawiki/2011/f/f5/Aiia_LC_B0032.jpg">
-<img alt="" src="https://static.igem.org/mediawiki/2011/f/f5/Aiia_LC_B0032.jpg" class="thumbimage" width="100%"></a></div></div>
-</td>
-<td width='50%'>
-<div style="text-align:justify"><div class="thumbinner" width='100%'>
-<a href="https://static.igem.org/mediawiki/2011/8/8d/Aiia_LC_B0034.jpg">
-<img alt="" src="https://static.igem.org/mediawiki/2011/8/8d/Aiia_LC_B0034.jpg" class="thumbimage" width="100%"></a></div></div>
-</td></tr>
 </table>
-<div align="justify">
-Experiments on these parts gave us the opportunity to characterize only the activity of the enzyme in <em>E. COLI</em> TOP10 in high copy number plasmid, providing only some information about the order of magnitude of the model parameters, which has been designed to work in <em>E. COLI</em> MGZ1 in low copy number plasmid.<div>
+Experiments on these parts gave us the opportunity to characterize only the activity of the enzyme in <em>E. COLI</em> TOP10 in high copy number plasmid, providing only some information about the order of magnitude of the model parameters, which has been designed to work in <em>E. COLI</em> MGZ1 in low copy number plasmid.
+  <div align="right"><small><a href="#indice" title="">^top</a></small></div>
-<div align="right"><small><a href="#indice" title="">^top</a></small></div>
+  <!-------------------------------->
+  <!-------------------------------->
+  <!-------------------------------->
-<!-------------------------------->
+  <!--------------RBS--------------->
-<!-------------------------------->
+  <!-------------------------------->
-<!-------------------------------->
+  <!-------------------------------->
-<!--------------RBS--------------->
+  <!-------------------------------->
-<!-------------------------------->
-<!-------------------------------->
+  <a name='rbs'></a>
-<!-------------------------------->
+  <h2>Characterization of the efficiency of RBSs from the community collection</h2>
+  RBSs were used for the fine tuning of CTRL+E. Different experimental conditions were assayed. <br>
-<a name='rbs'></a><h2>Characterization of the efficiency of RBSs from the community collection</h2>
+  <br>
+  Estimated efficiencies in pSB4C5 plasmid with -RBSx-mRFP-TT coding sequence under the control of the specified promoter: <br>
-RBSs were used for the fine tuning of CTRL+E. Different experimental conditions were assayed.
-<br><br>
-Estimated efficiencies in pSB4C5 plasmid with -RBSx-mRFP-TT coding sequence under the control of the specified promoter:
-<br><br>
-<div align="center"><table class='data' width='70%'><tr>
-<td class='row'><b>RBS</b></td>
-<td class='row'><b>eff<sub>p<sub>Lux</sub></sub></b></td>
-<td class='row'><b>eff<sub>p<sub>Tet</sub></sub></b></td>
-<td class='row'><b>eff<sub>J23101</sub></b></td>
-<td class='row'><b>Declared efficiency</b></td>
-</tr><tr>
-<td class='row'>B0030</td><td class='row'>0.40</td><td class='row'>1.6814</td><td class='row'>2.45</td><td class='row'>0,6</td>
-</tr><tr>
-<td class='row'>B0031</td><td class='row'>0.01</td><td class='row'>ND</td><td class='row'>0.04</td><td class='row'>0,07</td>
-</tr><tr>
-<td class='row'>B0032</td><td class='row'>0.19</td><td class='row'>0.4193</td><td class='row'>0.40</td><td class='row'>0,3</td>
-</tr><tr>
-<td class='row'>B0034</td><td class='row'>1</td><td class='row'>1</td><td class='row'>1</td><td class='row'>1</td>
-</tr></table></div>
-<br><br>
-Estimated efficiencies in pSB4C5 plasmid with pTet-RBSx-GeneX-TT, with GeneX=mRFP, AiiA or LuxI:
-<br><br>
-<div align="center"><table class='data' width='70%'><tr>
-<td class='row'><b>RBS</b></td>
-<td class='row'><b>eff<sub>mRFP</sub></b></td>
-<td class='row'><b>eff<sub>AiiA</sub></b></td>
-<td class='row'><b>eff<sub>LuxI</sub></b></td>
-<td class='row'><b>Declared efficiency</b></td>
-</tr><tr>
-<td class='row'>B0030</td><td class='row'>1.72</td><td class='row'>0.53</td><td class='row'>0.45</td><td class='row'>0,6</td>
-</tr><tr>
-<td class='row'>B0031</td><td class='row'>0.03</td><td class='row'>0.83</td><td class='row'>0.028</td><td class='row'>0,07</td>
-</tr><tr>
-<td class='row'>B0032</td><td class='row'>0.37</td><td class='row'>0.50</td><td class='row'>N.D.</td><td class='row'>0.3</td>
-</tr><tr>
-<td class='row'>B0034</td><td class='row'>1</td><td class='row'>1</td><td class='row'>1</td><td class='row'>1</td>
-</tr></table></div>
-<div align="right"><small><a href="#indice" title="">^top</a></small></div>
-<!-------------------------------->
-<!-------------------------------->
-<!-------------------------------->
-<!-----------growth--------------->
-<!-------------------------------->
-<!-------------------------------->
-<!-------------------------------->
-<a name='growth'></a><h2>Identification of bacterial growth parameters</h2>
-<div class="listcircle">
-<p align='justify'>
-The bacterial growth curve has been modelled as a logistic curve and is represented by the following equation:
-<br><br>
-dN/dt=N*&mu;*(N<sub>max</sub>-N)/N<sub>max</sub><br>
-N(0)=n<sub>0</sub>
-<br><br>
-where &mu; represents the growth rate of the cells (<em>E. coli</em> MGZ1 in M9 supplemented medium) and N<sub>max</sub> represents the maximum number of cells in the well. For a detailed description of the parameters, see <a href='https://2011.igem.org/Team:UNIPV-Pavia/Project/Modelling#Table_of_parameters'>modelling section</a>. For details on parameters identification, see <a href='https://2011.igem.org/Team:UNIPV-Pavia/Project/Modelling#N'>identification section.</a>
-The growth curves in all the performed experiments are measured in O.D.<sub>600</sub>. Since the <em>N</em> species in the model is expressed in <em>cell number</em>, a conversion factor has been estimated. The conversion factor <b>K<sub>O.D.toC.F.U.</sub></b> has been estimated as follows.
-<ol><ul>
-<li>Two cultures C1 and C2 (MGZ1 cells) were grown in 1ml M9 medium till saturation (ON liquid culture, 37°C, 220 rpm).</li>
-<li>Next morning, both C1 and C2 were diluted in M9 medium with a final volume of 1ml with the following dilution factors:
-<ul><li>1:1</li><li>1:10</li><li>1:100</li><li>1:1000</li>
-</ul> in fresh M9 medium. These cultures were grown for further 1 hour at 37°C, 220 rpm.
-</li>
-<li>After 1 hour, O.D.<sub>600</sub> was measured using TECAN microplate reader (don't forget to measure a M9 sample for blanking!)<br>
-<em>NB: from now on, cultures must be placed in ice to stop cell growth.</em></li>
-<li>At the same time, proper dilution of the cultures were plated on LB agar plates.<br>
-<em>NB: All the dilutions are performed moving 100 &mu;l of culture in previously ice-chilled 900 &mu;l fresch M9. 100 &mu;l of the final dilution are plated (It still represents a 1:10 dilution!)</em></li>
-<li>Plates were grown overnight and next morning C.F.U. were counted.</li>
-<li>C.F.U. values were corrected by the dilution factor and a linear regression (N vs O.D.<sub>600</sub>) was performed in order to evaluate the conversion factor <b>K<sub>O.D.toC.F.U.</sub></b>. </li>
-<li><b>K<sub>O.D.toC.F.U.</sub></b> was used as conversion factor to multiply the O.D.<sub>600</sub> value of saturation in the growth curves (~0,5). </li>
-</ul></ol>
-<p>The results are summarized in the table and in the figure below: </p>
-<center>
-  <table class='data'><tr><td class='row'><b>	Culture	</b></td><td class='row'><b>	O.D.<sub>600</sub> TECAN	</b></td><td class='row'><b>	O.D.<sub>600</sub> Spectrophotometer	</b></td><td class='row'><b>	C.F.U.	</b></td><td class='row'><b>	Dilution Factor (10^)	</b></td><td class='row'><b>	N	</b></td>	</tr>
-<tr><td class='row'>	C1	</td><td class='row'>	0,367950002	</td><td class='row'>	0,758004416	</td><td class='row'>	990	</td><td class='row'>	5	</td><td class='row'>	990000000	</td>	</tr>
-<tr><td class='row'>	C1	</td><td class='row'>	0,044649998	</td><td class='row'>	0,091982322	</td><td class='row'>	141	</td><td class='row'>	6	</td><td class='row'>	1410000000	</td>	</tr>
-<tr><td class='row'>	C1	</td><td class='row'>	0,004799999	</td><td class='row'>	0,009888356	</td><td class='row'>	136	</td><td class='row'>	5	</td><td class='row'>	136000000	</td>	</tr>
-<tr><td class='row'>	C1	</td><td class='row'>	0,000549998	</td><td class='row'>	0,001133037	</td><td class='row'>	20	</td><td class='row'>	6	</td><td class='row'>	200000000	</td>	</tr>
-<tr><td class='row'>	C2	</td><td class='row'>	0,54840003	</td><td class='row'>	1,129744917	</td><td class='row'>	165	</td><td class='row'>	4	</td><td class='row'>	16500000	</td>	</tr>
-<tr><td class='row'>	C2	</td><td class='row'>	0,058200002	</td><td class='row'>	0,119896339	</td><td class='row'>	23	</td><td class='row'>	5	</td><td class='row'>	23000000	</td>	</tr>
-<tr><td class='row'>	C2	</td><td class='row'>	0,008700002	</td><td class='row'>	0,017922652	</td><td class='row'>	251	</td><td class='row'>	3	</td><td class='row'>	2510000	</td>	</tr>
-<tr><td class='row'>	C2	</td><td class='row'>	0,000100002	</td><td class='row'>	0,000206011	</td><td class='row'>	24	</td><td class='row'>	4	</td><td class='row'>	2400000	</td>	</tr>
-</table></center><br>
-</p>
-<center>
-<img alt="" src="https://static.igem.org/mediawiki/2011/3/35/UNIPV_ODvsCFU.png" width="90%">
-</center>
-<p>The estimation of &mu; parameter was performed by determining the slope of the logarithmic curve of O.D.<sub>600</sub> in exponential phase. Exponential phase was determined by visual inspection as the linear phase of the logarithmic curve of O.D.<sub>600</sub>.
-  <br><br>
-  The estimated parameters are summarized in the table below:
    <br>
-</p>
+  <div align="center">
-<center>
+    <table class='data' width='70%'>
-   <table width='50%' class='data'><tr>
+      <tr>
-<td class='row'><b>N<sub>max</sub> [cell number]</b></td>
+        <td class='row'><b>RBS</b></td>
-<td class='row'><b>&mu; [min<sup>-1</sup>]</b></td>
+        <td class='row'><b>eff<sub>p<sub>Lux</sub></sub></b></td>
-</tr>
+        <td class='row'><b>eff<sub>p<sub>Tet</sub></sub></b></td>
-<tr><td class='row'>1*10<sup>9</sup></td>
+        <td class='row'><b>eff<sub>J23101</sub></b></td>
-<td class='row'>0.004925</td>
+        <td class='row'><b>Declared efficiency</b></td>
-</tr>
+      </tr>
-</table>
+      <tr>
-</center>
+        <td class='row'>B0030</td>
-<p>&nbsp;</p>
+        <td class='row'>0.40</td>
-<p>The reported value of &mu; corresponds to a doubling time of 142 minutes.
+        <td class='row'>1.6814</td>
+        <td class='row'>2.45</td>
+        <td class='row'>0,6</td>
+      </tr>
+      <tr>
+        <td class='row'>B0031</td>
+        <td class='row'>0.01</td>
+        <td class='row'>ND</td>
+        <td class='row'>0.04</td>
+        <td class='row'>0,07</td>
+      </tr>
+      <tr>
+        <td class='row'>B0032</td>
+        <td class='row'>0.19</td>
+        <td class='row'>0.4193</td>
+        <td class='row'>0.40</td>
+        <td class='row'>0,3</td>
+      </tr>
+      <tr>
+        <td class='row'>B0034</td>
+        <td class='row'>1</td>
+        <td class='row'>1</td>
+        <td class='row'>1</td>
+        <td class='row'>1</td>
+      </tr>
+    </table>
+   </div>
+  <br>
+  <br>
+  Estimated efficiencies in pSB4C5 plasmid with pTet-RBSx-GeneX-TT, with GeneX=mRFP, AiiA or LuxI: <br>
+  <br>
+  <div align="center">
+    <table class='data' width='70%'>
+      <tr>
+        <td class='row'><b>RBS</b></td>
+        <td class='row'><b>eff<sub>mRFP</sub></b></td>
+        <td class='row'><b>eff<sub>AiiA</sub></b></td>
+        <td class='row'><b>eff<sub>LuxI</sub></b></td>
+        <td class='row'><b>Declared efficiency</b></td>
+      </tr>
+      <tr>
+        <td class='row'>B0030</td>
+        <td class='row'>1.72</td>
+        <td class='row'>0.53</td>
+        <td class='row'>0.45</td>
+        <td class='row'>0,6</td>
+      </tr>
+      <tr>
+        <td class='row'>B0031</td>
+        <td class='row'>0.03</td>
+        <td class='row'>0.83</td>
+        <td class='row'>0.028</td>
+        <td class='row'>0,07</td>
+      </tr>
+      <tr>
+        <td class='row'>B0032</td>
+        <td class='row'>0.37</td>
+        <td class='row'>0.50</td>
+        <td class='row'>N.D.</td>
+        <td class='row'>0.3</td>
+      </tr>
+      <tr>
+        <td class='row'>B0034</td>
+        <td class='row'>1</td>
+        <td class='row'>1</td>
+        <td class='row'>1</td>
+        <td class='row'>1</td>
+      </tr>
+    </table>
+  </div>
+  <div align="right"><small><a href="#indice" title="">^top</a></small></div>
-</p>
+  <!-------------------------------->
-<div align="right"><small><a href="#indice" title="">^top</a></small></div>
+  <!-------------------------------->
+  <!-------------------------------->
+  <!-----------growth--------------->
+  <!-------------------------------->
+  <!-------------------------------->
+  <!-------------------------------->
+  <a name='growth'></a>
+  <h2>Identification of bacterial growth parameters</h2>
-<!-------------------------------->
-<!-------------------------------->
+    <p align='justify'> The bacterial growth curve has been modelled as a logistic curve and is represented by the following equation: <br>
-<!-------------------------------->
+      <div align="center"><br>
-<!--------------HSL--------------->
+      dN/dt=N*&mu;*(N<sub>max</sub>-N)/N<sub>max</sub><br>
-<!-------------------------------->
+      N(0)=n<sub>0</sub> <br></div>
-<!-------------------------------->
+      <br>
-<!-------------------------------->
+      where &mu; represents the growth rate of the cells (<em>E. coli</em> MGZ1 in M9 supplemented medium) and N<sub>max</sub> represents the maximum number of cells in the well. For a detailed description of the parameters, see <a href='https://2011.igem.org/Team:UNIPV-Pavia/Project/Modelling#Table_of_parameters'>modelling section</a>. For details on parameters identification, see <a href='https://2011.igem.org/Team:UNIPV-Pavia/Project/Modelling#N'>identification section.</a> The growth curves in all the performed experiments are measured in O.D.<sub>600</sub>. Since the <em>N</em> species in the model is expressed in <em>cell number</em>, a conversion factor has been estimated. The conversion factor <b>K<sub>O.D.toC.F.U.</sub></b> has been estimated as follows.
+    <ol>
+      <ul>
+        <li>Two cultures C1 and C2 (MGZ1 cells) were grown in 1ml M9 medium till saturation (ON liquid culture, 37°C, 220 rpm).</li>
+        <li>Next morning, both C1 and C2 were diluted in M9 medium with a final volume of 1ml with the following dilution factors:
+           <ul class="disc">
+            <li>1:1</li>
+            <li>1:10</li>
+            <li>1:100</li>
+            <li>1:1000</li>
+          </ul>
+          in fresh M9 medium. These cultures were grown for further 1 hour at 37°C, 220 rpm. </li>
+        <li>After 1 hour, O.D.<sub>600</sub> was measured using TECAN microplate reader (don't forget to measure a M9 sample for blanking!)<br>
+          <em>NB: from now on, cultures must be placed in ice to stop cell growth.</em></li>
+        <li>At the same time, proper dilution of the cultures were plated on LB agar plates.<br>
+          <em>NB: All the dilutions are performed moving 100 &mu;l of culture in previously ice-chilled 900 &mu;l fresch M9. 100 &mu;l of the final dilution are plated (It still represents a 1:10 dilution!)</em></li>
+        <li>Plates were grown overnight and next morning C.F.U. were counted.</li>
+        <li>C.F.U. values were corrected by the dilution factor and a linear regression (N vs O.D.<sub>600</sub>) was performed in order to evaluate the conversion factor <b>K<sub>O.D.toC.F.U.</sub></b>. </li>
+        <li><b>K<sub>O.D.toC.F.U.</sub></b> was used as conversion factor to multiply the O.D.<sub>600</sub> value of saturation in the growth curves (~0,5). </li>
+      </ul>
+    </ol>
+    <p>The results are summarized in the table and in the figure below: </p>
+    <center>
+      <table class='data'>
+        <tr>
+          <td class='row'><b> Culture </b></td>
+          <td class='row'><b> O.D.<sub>600</sub> TECAN </b></td>
+          <td class='row'><b> O.D.<sub>600</sub> Spectrophotometer </b></td>
+          <td class='row'><b> C.F.U. </b></td>
+          <td class='row'><b> Dilution Factor (10^) </b></td>
+          <td class='row'><b> N </b></td>
+        </tr>
+        <tr>
+          <td class='row'> C1 </td>
+          <td class='row'> 0,367950002 </td>
+          <td class='row'> 0,758004416 </td>
+          <td class='row'> 990 </td>
+          <td class='row'> 5 </td>
+          <td class='row'> 990000000 </td>
+        </tr>
+        <tr>
+          <td class='row'> C1 </td>
+          <td class='row'> 0,044649998 </td>
+          <td class='row'> 0,091982322 </td>
+          <td class='row'> 141 </td>
+          <td class='row'> 6 </td>
+          <td class='row'> 1410000000 </td>
+        </tr>
+        <tr>
+          <td class='row'> C1 </td>
+          <td class='row'> 0,004799999 </td>
+          <td class='row'> 0,009888356 </td>
+          <td class='row'> 136 </td>
+          <td class='row'> 5 </td>
+          <td class='row'> 136000000 </td>
+        </tr>
+        <tr>
+          <td class='row'> C1 </td>
+          <td class='row'> 0,000549998 </td>
+          <td class='row'> 0,001133037 </td>
+          <td class='row'> 20 </td>
+          <td class='row'> 6 </td>
+          <td class='row'> 200000000 </td>
+        </tr>
+        <tr>
+          <td class='row'> C2 </td>
+          <td class='row'> 0,54840003 </td>
+          <td class='row'> 1,129744917 </td>
+          <td class='row'> 165 </td>
+          <td class='row'> 4 </td>
+          <td class='row'> 16500000 </td>
+        </tr>
+        <tr>
+          <td class='row'> C2 </td>
+          <td class='row'> 0,058200002 </td>
+          <td class='row'> 0,119896339 </td>
+          <td class='row'> 23 </td>
+          <td class='row'> 5 </td>
+          <td class='row'> 23000000 </td>
+        </tr>
+        <tr>
+          <td class='row'> C2 </td>
+          <td class='row'> 0,008700002 </td>
+          <td class='row'> 0,017922652 </td>
+          <td class='row'> 251 </td>
+          <td class='row'> 3 </td>
+          <td class='row'> 2510000 </td>
+        </tr>
+        <tr>
+          <td class='row'> C2 </td>
+          <td class='row'> 0,000100002 </td>
+          <td class='row'> 0,000206011 </td>
+          <td class='row'> 24 </td>
+          <td class='row'> 4 </td>
+          <td class='row'> 2400000 </td>
+        </tr>
+      </table>
+    </center>
+    <br>
+    </p>
+    <center>
+      <a href="https://static.igem.org/mediawiki/2011/3/35/UNIPV_ODvsCFU.png"><img alt="" src="https://static.igem.org/mediawiki/2011/3/35/UNIPV_ODvsCFU.png" width="90%"> </a>
+    </center>
+    <p>The estimation of &mu; parameter was performed by determining the slope of the logarithmic curve of O.D.<sub>600</sub> in exponential phase. Exponential phase was determined by visual inspection as the linear phase of the logarithmic curve of O.D.<sub>600</sub>. <br>
+      <br>
+      The estimated parameters are summarized in the table below: <br>
+    </p>
+    <center>
+      <table width='50%' class='data'>
+        <tr>
+          <td class='row'><b>N<sub>max</sub> [cell number]</b></td>
+          <td class='row'><b>&mu; [min<sup>-1</sup>]</b></td>
+        </tr>
+        <tr>
+          <td class='row'>1*10<sup>9</sup></td>
+          <td class='row'>0.004925</td>
+        </tr>
+      </table>
+    </center>
+    <p>The reported value of &mu; corresponds to a doubling time of 142 minutes. </p>
+    <div align="right"><small><a href="#indice" title="">^top</a></small></div>
+    <!-------------------------------->
+    <!-------------------------------->
+    <!-------------------------------->
+    <!--------------HSL--------------->
+    <!-------------------------------->
+    <!-------------------------------->
+    <!-------------------------------->
+    <a name='HSL'></a>
+    <h2>Estimation of the spontaneous degradation of HSL in M9 medium and in cultures at different pH values</h2>
+    <p align='justify'> In order to estimate the spontaneous degradation rate of HSL in M9 medium and in a culture of MGZ1 cells as a function of pH, two simple tests have been performed.<br>
+      Two different M9 media were prepared, one with the nominal pH (7.0) and one with pH=6.0.<br>
+      These media, now named respectively M9<sub>pH 7</sub> and M9<sub>pH 6</sub>, were added with a known concentration of HSL (100 nM) and then incubated at 37°C, 220 rpm (NB: the media were not infected with any culture but the standard growth conditions were reproduced). The amount of HSL present in the medium was assayed through the BBa_T9002 biosensor at 4 time points: <br>
+    <ul>
+      <li>t=0 h;</li>
+      <li>t=1 h;</li>
+      <li>t=2 h;</li>
+      <li>t=4 h;</li>
+      <li>t=8 h;</li>
+    </ul>
+    <p>The obtained time series of HSL amounts were processed to evaluate the time constant governing the dynamic of HSL degradation, supposing an exponential decay. The results are reported in the table below: </p>
+    <center>
+      <table class='data'>
+        <tr>
+          <td class='row'></td>
+          <td class='row'><b>t<sub>1/2</sub><sup>*</sup> [h]</b></td>
+          <td class='row'><b>&gamma;<sub>HSL</sub><sup>**</sup> [h<sup>-1</sup>]</b></td>
+        </tr>
+        <tr>
+          <td class='row'><b>M9<sub>pH 6</sub></b></td>
+          <td class='row'>32 </td>
+          <td class='row'>0.022 </td>
+        </tr>
+        <tr>
+          <td class='row'><b>M9<sub>pH 7</sub></b></td>
+          <td class='row'>8 </td>
+          <td class='row'>0.087 </td>
+        </tr>
+      </table>
+    </center>
+    <p> The described experiment was repeated with a MGZ1 culture in order to evaluate the effect of culture on HSL stability. The estimated values are reported in the table below:</p>
+    <center>
+      <table class='data'>
+        <tr>
+          <td class='row'></td>
+          <td class='row'><b>t<sub>1/2</sub><sup>*</sup> [h]</b></td>
+          <td class='row'><b>&gamma;<sub>HSL</sub><sup>**</sup> [h<sup>-1</sup>]</b></td>
+        </tr>
+        <tr>
+          <td class='row'><b>Culture<sub>pH 6</sub></b></td>
+          <td class='row'>&#8734; </td>
+          <td class='row'>0 </td>
+        </tr>
+        <tr>
+          <td class='row'><b>Culture<sub>pH 7</sub></b></td>
+          <td class='row'>19 </td>
+          <td class='row'>0.037 </td>
+        </tr>
+      </table>
+    </center>
+    <p>It is evident from the reported data that the spontaneous degradation of HSL is negligible when CTRL+E is implemented in MGZ1 cells grown in M9 medium with pH=6.0 and pH=7.0.<br>
+      Thus in the simulations we set &gamma;<sub>HSL</sub>=0; </p>
+    </p>
+    <div align="right"><small><a href="#indice" title="">^top</a></small></div>
+    <!-------------------------------->
+    <!-------------------------------->
+    <!-------------------------------->
+    <!-------------t9002-------------->
+    <!-------------------------------->
+    <!-------------------------------->
+    <!-------------------------------->
+    <a name='t9002'></a>
+    <h2>Characterization of BBa_T9002 biosensor</h2>
+    <div align="justify">As described in the <a href="https://2011.igem.org/Team:UNIPV-Pavia/Project/Modelling#introduction_to_T9002">modelling section</a>, BioBrick <a href="http://partsregistry.org/Part:BBa_T9002">BBa_T9002</a> is an HSL biosensor, which provides a non linear relationship between HSL input and S<sub>cell</sub> output. More precisely, the characteristic sigmoidal curve requires synthetic parameters for its accurate identification. These are the minimum and maximum values, the swtich point (i.e., the curve inflection point), and the upper and lower boundaries of linearity. This biosensor revealed greatly reliable, providing measurement repeatability and minimal experimental noise. Referring to its activation formula, the calibration curve is shown below.<br></div>
+    <br>
+    <div style='text-align:center'>
+      <div class="thumbinner" style="width:100%;"> <a href="https://static.igem.org/mediawiki/2011/5/50/Activation_T9002.jpg"><img alt="" src="https://static.igem.org/mediawiki/2011/5/50/Activation_T9002.jpg" class="thumbimage"  width="47%" height="50%"></a></div>
+    </div>
+    <br>
+    <div style='text-align:center'>
+      <div class="thumbinner" style="width:100%;"> <a href="https://static.igem.org/mediawiki/2011/4/4e/T9002_activation.jpg"><img alt="" src="https://static.igem.org/mediawiki/2011/4/4e/T9002_activation.jpg" class="thumbimage"  width="100%"></a></div>
+    </div>
+    <center>
+      <table width='50%' class='data'>
+        <tr>
+          <td class='row'><b>Minimum [S<sub>cell</sub>]</b></td>
+          <td class='row'><b>Maximum [S<sub>cell</sub>]</b></td>
+          <td class='row'><b>Switch point [nM]</b></td>
+          <td class='row'><b>Lower boundary of linearity [nM]</b></td>
+          <td class='row'><b>Upper boundary of linearity [nM]</b></td>
+        </tr>
+        <tr>
+          <td class='row'>17.31</td>
+          <td class='row'>739.4</td>
+          <td class='row'>1.39</td>
+          <td class='row'>0.38</td>
+          <td class='row'>5.07</td>
+        </tr>
+      </table>
+    </center>
+    <br>
+    <br>
+    <div align="justify">In order to determine the threshold sensitivity of T9002 biosensor, experiments were performed with several HSL inductions minimally interspaced in the region of low detectability. Hypothesizing that the inducer is 1:20 diluted (as for all of our tests), the minimum detectable HSL concentration is 3 nM.</div>
+    <div align="right"><small><a href="#indice" title="">^top</a></small></div>
+<h1>Conclusions</h1>
-<a name='HSL'></a><h2>Estimation of the spontaneous degradation of HSL in M9 medium and in cultures at different pH values</h2>
 <p align='justify'>
-In order to estimate the spontaneous degradation rate of HSL in M9 medium and in a culture of MGZ1 cells as a function of pH, two simple tests have been performed.<br>
+To sum up the results of our project, we have characterized several basic parts and documented all of our experiments in the experience pages. All the data collected have been reported and synthetic parameters to describe the behavior of promoters, RBSs and genes have been provided. Such parameters can be used for the <em>in silico</em> simulation of mathematical models of complex circuits. <br>
-Two different M9 media were prepared, one with the nominal pH (7.0) and one with pH=6.0.<br>
+For what concerns CTRL+E, that is a proof of concept of the modular behavior of systems in synthetic biology, all the parameters of pTet, pLux and LuxI have been estimated. AiiA parameters revealed difficult to estimate.<br>
-These media, now named respectively M9<sub>pH 7</sub> and M9<sub>pH 6</sub>, were added with a known concentration of HSL (100 nM) and then incubated at 37°C, 220 rpm (NB: the media were not infected with any culture but the standard growth conditions were reproduced). The amount of HSL present in the medium was assayed through the BBa_T9002 biosensor at 4 time points: <br>
+Reasonable values for AiiA parameters have been derived from experiments in different contexts. These values were used to simulate the behavior of CTRL+E.<br>
-<ul>
-<li>t=0 h;</li>
-<li>t=1 h;</li>
-<li>t=2 h;</li>
-<li>t=4 h;</li>
-<li>t=8 h;</li>
-</ul>
-<p>The obtained time series of HSL amounts were processed to evaluate the time constant governing the dynamic of HSL degradation, supposing an exponential decay. The results are reported in the table below: </p>
-<center>
+Further experiments are necessary to evaluate the consistence of the derived parameters for AiiA. <br>
-<table class='data'>
+Once the most promising module combinations will be evaluated, a library of differently tuned controller will be built and characterized in order to assess the correspondence between the model predictions and the real data.
-<tr>
-<td class='row'>
-</td>
-<td class='row'>
-<b>t<sub>1/2</sub><sup>*</sup> [h]</b>
-</td><td class='row'>
-<b>&gamma;<sub>HSL</sub><sup>**</sup> [h<sup>-1</sup>]</b>
-</td>
-</tr>
-<tr><td class='row'><b>M9<sub>pH 6</sub></b>
-</td>
-<td class='row'>32
-</td>
-<td class='row'>0.022
-</td>
-</tr>
-<tr><td class='row'><b>M9<sub>pH 7</sub></b>
-</td>
-<td class='row'>8
-</td>
-<td class='row'>0.087
-</td>
-</tr>
-</table>
-</center>
-<p>
-  The described experiment was repeated with a MGZ1 culture in order to evaluate the effect of culture on HSL stability. The estimated values are reported in the table below:</p>
-<center>
-  <table class='data'>
-<tr>
-<td class='row'>
-</td>
-<td class='row'>
-<b>t<sub>1/2</sub><sup>*</sup> [h]</b>
-</td><td class='row'>
-<b>&gamma;<sub>HSL</sub><sup>**</sup> [h<sup>-1</sup>]</b>
-</td>
-</tr>
-<tr><td class='row'><b>Culture<sub>pH 6</sub></b>
-</td>
-<td class='row'>&#8734;
-</td>
-<td class='row'>0
-</td>
-</tr>
-<tr><td class='row'><b>Culture<sub>pH 7</sub></b>
-</td>
-<td class='row'>19
-</td>
-<td class='row'>0.037
-</td>
-</tr>
-</table>
-</center>
-<p>It is evident from the reported data that the spontaneous degradation of HSL is negligible when CTRL+E is implemented in MGZ1 cells grown in M9 medium with pH=6.0 and pH=7.0.<br>
-  Thus in the simulations we set &gamma;<sub>HSL</sub>=0;
-  </p>
 </p>
-<div align="right"><small><a href="#indice" title="">^top</a></small></div>
-<!-------------------------------->
-<!-------------------------------->
-<!-------------------------------->
-<!-------------t9002-------------->
-<!-------------------------------->
-<!-------------------------------->
-<!-------------------------------->
-<a name='t9002'></a><h2>Characterization of BBa_T9002 biosensor</h2>
+</html>
-As described in the <a href="https://2011.igem.org/Team:UNIPV-Pavia/Project/Modelling#introduction_to_T9002">modelling section</a>, BioBrick <a href="http://partsregistry.org/Part:BBa_T9002">BBa_T9002</a> is an HSL biosensor, which provides a non linear relationship between HSL input and S<sub>cell</sub> output. More precisely, the characteristic sigmoidal curve requires synthetic parameters for its accurate identification. These are the minimum and maximum values, the swtich point (i.e., the curve inflection point), and the upper and lower boundaries of linearity. This biosensor revealed greatly reliable, providing measurement repeatability and minimal experimental noise. Referring to its activation formula, the calibration curve is shown below.<br><br>
-<div style='text-align:center'><div class="thumbinner" style="width:100%;">
-<img alt="" src="https://static.igem.org/mediawiki/2011/5/50/Activation_T9002.jpg" class="thumbimage"  width="47%" height="50%"></a></div></div>
-<br>
-<div style='text-align:center'><div class="thumbinner" style="width:100%;">
-<img alt="" src="https://static.igem.org/mediawiki/2011/4/4e/T9002_activation.jpg" class="thumbimage"  width="100%"></a></div></div>
-<center>
-<table width='50%' class='data'><tr>
-<td class='row'><b>Minimum [S<sub>cell</sub>]</b></td>
-<td class='row'><b>Maximum [S<sub>cell</sub>]</b></td>
-<td class='row'><b>Switch point [nM]</b></td>
-<td class='row'><b>Lower boundary of linearity [nM]</b></td>
-<td class='row'><b>Upper boundary of linearity [nM]</b></td>
-</tr>
-<tr>
-<td class='row'>17.31</td>
-<td class='row'>739.4</td>
-<td class='row'>1.39</td>
-<td class='row'>0.38</td>
-<td class='row'>5.07</td>
-</tr>
-</table>
-</center>
-<br><br>
-In order to determine the threshold sensitivity of T9002 biosensor, experiments were performed with several HSL inductions minimally interspaced in the region of low detectability. Hypothesizing that the inducer is 1:20 diluted (as for all of our tests), the minimum detectable HSL concentration is 3 nM.
-<div align="right"><small><a href="#indice" title="">^top</a></small></div>
-</div>
-</div>
-<br><br>
-</html>
 {{end}}