Team:Aberdeen Scotland/parameters
From 2009.igem.org
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<td>Rate of formation of the HSL-LuxI complex</td> | <td>Rate of formation of the HSL-LuxI complex</td> | ||
<td>0.00010</td> | <td>0.00010</td> | ||
- | <td>1</td> | + | <td>1/ms</td> |
- | <td> | + | <td>[1]</td> |
</tr> | </tr> | ||
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<td>Rate of dissociation of the HSL-LuxI complex</td> | <td>Rate of dissociation of the HSL-LuxI complex</td> | ||
<td>0.003</td> | <td>0.003</td> | ||
- | <td>1</td> | + | <td>1/s</td> |
- | <td> | + | <td>[1]</td> |
</tr> | </tr> | ||
Revision as of 14:20, 13 August 2009
University of Aberdeen - Pico Plumber
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/s | [1] | |
HSL | Rate of diffusion of HSL in/out of the cell | 0.4 | 1/s | [1] |
IPTG | Rate of diffusion of IPTG in/out of the cell | 0.014 | 1/s | [3] |
pproduction | Number of plasmids | 10 | medium plasmid number; decided within the team | |
platch | Number of plasmids | 10 | medium plasmid number; decided within the team | |
plysis | Number of plasmids | 10 | medium plasmid number; decided within the team | |
panti-lysis | Number of plasmids | 10 | medium plasmid number; decided within the team | |
pQS | Number of plasmids | 10 | medium plasmid number; decided within the team | |
max_production | Maximal production rate of lux box promoter | 0.44 | pops | [1] |
min_production | Minimal production rate of lux box promoter | 0.013 | pops | estimated* |
latch | Maximal production rate of latch promoter | 0.28 | pops | nick |
lysis | Maximal production rate of lysis promoter | 0.0426 | pops | nick |
anti-lysis | Maximal production rate of anti-lysis promoter | 0.0066 | pops | nick |
QS | Maximal production rate of QS promoter | 0.018 | pops | nick |
KLacI | Dissociation constant for LacI to LacO | 700 | m | see explanation |
KLacI-IPTG | Dissociation constant for IPTG to LacI | 1200 | m | see explanation |
KTetR | Dissociation constant for TetR to TetO | 7000 | m | see explanation |
KcI | Dissociation constant for cI to operon | 7000 | m | see explanation |
KP | Dissociation constant for P to lux box | 700 | m | see explanation |
nLacI | Hill coefficient | 2 | [10] | |
ncI | Hill coefficient | 2 | [11] | |
nTetR | Hill coefficient | 3 | 1 | |
nP | Hill coefficient | 2 | [1] | |
mRNA | Degradation of mRNA | 0.00288 | 1/s | [2] |
X | Degradation of X | 0.00000802 | 1/s | [5] |
Y | Degradation of Y | 0.00000802 | 1/s | [5] |
λ-CI | Degradation of lambda CI | 0.002888 | 1/s | [5] |
LacI | Degradation of LacI | 0.001155 | 1/s | [8] |
TetR | Degradation of TetR | 0.00288811 | 1/s | tagged; half-life of 4 min |
Holin | Degradation of Holin | 0.0002 | 1/s | estmated; half-life of an hour |
Endolysin | Degradation of Endolysin | 0.0002 | 1/s | estimated; half-life of an hour |
Antiholin | Degradation of Antiholin | 0.0002 | 1/s | estimated; half-life of an hour |
LuxI | Degradation of LuxI | 0.002888 | 1/s | tagged; half-life of 4 min |
LuxR | Degradation of LuxR | 0.0002 | 1/s | [1] |
HSL | Degradation of HSL | 0.00016667 | 1 | [8]; value for AHL |
Protein | Translation rate of Protein | 0.1 | 1/s | [2] |
P | Rate of formation of the HSL-LuxI complex | 0.00010 | 1/ms | [1] |
-P | Rate of dissociation of the HSL-LuxI complex | 0.003 | 1/s | [1] |
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>
[10] ETHZ 2007. “Engineering” iGem wiki. 13th August 2009. <http://parts.mit.edu/igem07/index.php/ETHZ/Engineering>
[11] Bintu, Lacramioara, Terence Hwa. “Transcriptional regulation by the numbers: applications.” Current Opinion in Genetics & Development 2005, 15:125–135.