Team:Aberdeen Scotland/parameters

From 2009.igem.org

(Difference between revisions)
(Internal Dynamics Parameters)
(Internal Dynamics Parameters)
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<td>0.018</td>
<td>0.018</td>
<td>pops</td>
<td>pops</td>
 +
<td>1</td>
 +
</tr>
 +
 +
<tr>
 +
<td>K<sub>LacI</sub></td>
 +
<td>Dissociation constant for LacI to LacO </td>
 +
<td>700</td>
 +
<td>m</td>
 +
<td>see explanation</td>
 +
</tr>
 +
 +
<tr>
 +
<td>K<sub>LacI-IPTG</sub></td>
 +
<td>1200</td>
 +
<td>m</td>
 +
<td>see explanation</td>
 +
</tr>
 +
 +
<tr>
 +
<td>K<sub>TetR</sub></td>
 +
<td>7000</td>
 +
<td>m</td>
 +
<td>see explanation</td>
 +
</tr>
 +
 +
<tr>
 +
<td>K<sub>cI</sub></td>
 +
<td>7000</td>
 +
<td>m</td>
 +
<td>see explanation</td>
 +
</tr>
 +
 +
<tr>
 +
<td>K<sub>P</sub></td>
 +
<td>700</td>
 +
<td>m</td>
 +
<td>see explanation</td>
 +
</tr>
 +
 +
<tr>
 +
<td>n<sub>LacI</sub></td>
 +
<td>Hill coefficient </td>
 +
<td>2</td>
 +
<td></td>
 +
<td>1</td>
 +
</tr>
 +
 +
<tr>
 +
<td>n<sub>cI</sub></td>
 +
<td>Hill coefficient </td>
 +
<td>2</td>
 +
<td></td>
 +
<td>1</td>
 +
</tr>
 +
 +
<tr>
 +
<td>n<sub>TetR</sub></td>
 +
<td>Hill coefficient </td>
 +
<td>3</td>
 +
<td></td>
 +
<td>1</td>
 +
</tr>
 +
 +
<tr>
 +
<td>n<sub>P</sub></td>
 +
<td>Hill coefficient </td>
 +
<td>2</td>
 +
<td></td>
<td>1</td>
<td>1</td>
</tr>
</tr>

Revision as of 13:49, 13 August 2009

University of Aberdeen iGEM 2009

Internal Dynamics Parameters

When modeling any process, it is essential to use parameters which reflect reality, otherwise the model will not give accurate predictions. Thus we spend a considerable time researching, analysing and estimating parameters so that our model will reflect real life behaviour as accuratly as possible.

Parameter Description Value Unit Reference
Rate of production of HSL from LuxI 0.45 1 2
HSL Rate of diffusion of HSL in/out of the cell 0.4 1 2
IPTG Rate of diffusion of IPTG in/out of the cell 0.014 1 2
IPTG Rate of diffusion of IPTG in/out of the cell 0.014 1 2
pproduction Number of plasmids 10 medium plasmid number
platch Number of plasmids 10 medium plasmid number
plysis Number of plasmids 10 medium plasmid number
panti-lysis Number of plasmids 10 medium plasmid number
pQS Number of plasmids 10 medium plasmid number
max_production Maximal production rate of lux box promoter 0.44 pops 2
max_production Minimal production rate of lux box promoter 0.013 pops estimated
max_production Maximal production rate of latch promoter 0.28 pops 1
max_production Maximal production rate of lysis promoter 0.0426 pops 1
max_production Maximal production rate of anti-lysis promoter 0.0066 pops 1
max_production Maximal production rate of QS promoter 0.018 pops 1
KLacI Dissociation constant for LacI to LacO 700 m see explanation
KLacI-IPTG 1200 m see explanation
KTetR 7000 m see explanation
KcI 7000 m see explanation
KP 700 m see explanation
nLacI Hill coefficient 2 1
ncI Hill coefficient 2 1
nTetR Hill coefficient 3 1
nP Hill coefficient 2 1
X Degradation of X 0.00000802 2 1
Y Degradation of Y 0.00000802 1 4
λ-CI Degradation of lambda CI 0.002888 1 6
LacI Degradation of LacI 0.001155 1 8
TetR Degradation of TetR 0.00288811 1 10
Holin Degradation of Holin 0.0002 1 guessed; half-life of an hour
Endolysin Degradation of Endolysin 0.0002 1 guessed; half-life of an hour
Antiholin Degradation of Antiholin 0.0002 1 guessed; half-life of an hour
LuxI Degradation of LuxI 0.002888 1 tagged; half-life of 4 min
LuxR Degradation of LuxR 0.0002 1 0
HSL Degradation of HSL 0.00016667 1 0; value for AHL
Protein Translation rate of Protein 0.1 1 2
P Rate of formation of the HSL-LuxI complex 0.00010 1 2
-P Rate of dissociation of the HSL-LuxI complex 0.003 1 2


References

[1] Goryachev, A.B., D.J. Toh and T. Lee. “System analysis of a quorum sensing network: Design constraints imposed by the functional requirements, network topology and kinetic constant.” BioSystems 2006: 83, 178-187.

[2] Alon, Uri. “An Introduction to Systems Biology Design Principles of Biological Circiuts.” London: Chapman & Hall/CRC, 2007.

[3] Kepes, A., 1960, “Etudes cinetiques sur la galactoside-permease D'Escherichia coli. Biochim.” Biophys. Acta 40, 70-84.

[4] Canton, B. and Anna Labno. “Part: BBa_F2620.” BioBrick Registry. 13th August 2009. <http://partsregistry.org/Part:BBa_F2620>

[5] Andersen JB, Sternberg C, Poulsen LK, Bjorn SP, Givskov M, Molin S. “New Unstable Variants of Green Fluorescent Protein for Studies of Transient Gene Expression in Bacteria.” Appl Environ Microbiol. 1998 Jun; 64(6):2240-6.

[6] Elowitz MB, Leibler S.; “A synthetic oscillatory network of transcriptional regulators.” Nature 2000 Jan; 403(6767):335-8.;

[7] BCCS-Bristol 2008. “Modelling Parameters” iGEM wiki. 13th August 2009. <https://2008.igem.org/Team:BCCS-Bristol/Modeling-Parameters>

[8] Subhayu Basu; “A synthetic multicellular system for programmed pattern formation.” Nature April 2005: 434, 1130-1134

[9] KULeuven 2008. “Cell Death”iGEM wiki. 13th August 2009. <https://2008.igem.org/Team:KULeuven/Model/CellDeath>