Team:DTU-Denmark/Kinetic Model

From 2013.igem.org

(Difference between revisions)
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We also need to know how much ammonia the water we want to treat will contain. The ammonia concentration in different types of waste water is given in [5] as 1 mg/l in aquatic cultures, 10 mg/l for municipal waste water and more than 100 mg/l for industrial waste water. So the concentrations we want to look at in our model are: 1 mg/l, 10 mg/l, 100 mg/l and 500 mg/l ammonia.
+
We also need to know how much ammonia the water we want to treat will contain.
 +
The ammonia concentration in different types of waste water is given in [7] as 1 mg/L
 +
in aquatic cultures, 10 mg/L for municipal waste water and more than 100 mg/L for
 +
industrial waste water. So the concentrations we want to look at in our model are: 1
 +
mg/L (58.72μM), 10 mg/L (587.2μM), 100 mg/L(5.872 mM) and 500 mg/L (29.358
 +
mM) ammonia.
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The modeling was done in MATLAB using the Systems Biology Toolbox [6] and the models equations are given below. Results are shown in Figures 1-2.
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The equations of the two models for Mutant 1 and Mutant 2 are:
[[File:DTU_mod_1f.png|350px|center]]
[[File:DTU_mod_1f.png|350px|center]]
 +
 +
The modeling was done in MATLAB using the Systems Biology Toolbox [8] and
 +
the scripts are uploaded in the section scripts below. Results are shown in Figures 1-2.
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[4] Y Ishihama, T Schmidt, J Rappsilber, M Mann, FU Hartl, MJ Kerner, and D Frishman. Protein abundance profiling of the escherichia coli cytosol. ''BMC genomics'', 9, 2008.
[4] Y Ishihama, T Schmidt, J Rappsilber, M Mann, FU Hartl, MJ Kerner, and D Frishman. Protein abundance profiling of the escherichia coli cytosol. ''BMC genomics'', 9, 2008.
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[5] T.C. Jorgensen and L.R. Weatherley. Ammonia removal from wastewater by ion exchange in the presence of organic contaminants. ''Water Research'', 37:723–1728, 2003.
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[5] AB Hooper, PC Maxwell, and KR Terry. Hydroxylamine oxidoreductase from
 +
nitrosomonas: Absorption spectra and content of heme and metal. ''Biochemistry'',
 +
17:2984–2989, 1978.
 +
 
 +
[6] S Gilch, O Meyer, and I Schmidt. A soluble form of ammonia monooxygenase in
 +
nitrosomonas europaea. ''Biological Chemistry'', 390(9):863–873, 2009.
 +
 
 +
 
 +
[7] T.C. Jorgensen and L.R. Weatherley. Ammonia removal from wastewater by ion exchange in the presence of organic contaminants. ''Water Research'', 37:723–1728, 2003.
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[6] Systems biology toolbox for matlab: A computational platform for research in systems biology. ''Bioinformatics'', 22(4):514–515, 2006.
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[8] Systems biology toolbox for matlab: A computational platform for research in systems biology. ''Bioinformatics'', 22(4):514–515, 2006.
{{:Team:DTU-Denmark/Templates/EndPage}}
{{:Team:DTU-Denmark/Templates/EndPage}}

Revision as of 09:26, 4 October 2013

Contents


Kinetic model of the Pathway

In order to determine the practicality of our solution, we are applying kinetic modeling to investigate how much nitrous oxide our transformants will produce in a given amount of time.

The reactions of the pathway we are trying to integrate in E. coli are:


1a.png

The iGEM team from Taipei in 2012 was using Nir and Nos in their project as well and did some kinetic modeling based on literature research. To describe product formation by the enzymes they used the Michaelis-Menten approach:

DTU mod 1b.png
DTU mod 1c.png


Some of the necessary parameters can be found in literature, they are listed in Table 1.


DTU mod 1d.png

It is necessary to know or estimate the enzyme concentration if kcat values are used. Based on a paper we found that gives typical protein concentrations in E. coli [4] we chose to use four different enzyme concentrations in our model: 100, 500, 1000 and 100 000 enzymes per cell corresponding to low, medium, high and very high concentrations of enzyme.

DTU mod 1e.png


To be consistent in units we converted the vmax value of AMO and HAO to a kcat value in the following way: In [5] the amount of HAO in cell extract is given as 2.6% so for our conversion we assume 2% of the protein mass corresponds to AMO and another 2% correspond to HAO, summing up to 4%. This leads to a value of 39.75μmol min−1 mg of enzyme−1 . The molecular weight of AMO is given in [6] as 283 kDa and the molecular weight of HAO is given in [5] as 189 kDa. Summing those numbers leads to a molecular weight of 472 kDa corresponding to 7.838 · 10−16 mg. With this number we convert the vmax to 3.116 · 10−14 μmol min−1 . Then using the Avogadro number we derive a kcat value of 18765 min−1.


We also need to know how much ammonia the water we want to treat will contain. The ammonia concentration in different types of waste water is given in [7] as 1 mg/L in aquatic cultures, 10 mg/L for municipal waste water and more than 100 mg/L for industrial waste water. So the concentrations we want to look at in our model are: 1 mg/L (58.72μM), 10 mg/L (587.2μM), 100 mg/L(5.872 mM) and 500 mg/L (29.358 mM) ammonia.

The equations of the two models for Mutant 1 and Mutant 2 are:

DTU mod 1f.png

The modeling was done in MATLAB using the Systems Biology Toolbox [8] and the scripts are uploaded in the section scripts below. Results are shown in Figures 1-2.


DTU-NO2 1mg ammonia.jpgDTU-NO2 10mg ammonia.jpgDTU-NO2 100mg ammonia.jpgDTU-NO2 500mg ammonia.jpg

Figure 1: Kinetic modeling of Mutant 1. Nitrite concentration over time based on kinetic parameters found in literature and for different enzyme and substrate (here NO2) concentrations.


DTU-fig2.png

Figure 2: Kinetic modeling of Mutant 2. Nitrous oxide concentration over time based on kinetic parameters found in literature and for different enzyme and substrate (here NO2) concentrations.

References

[1] WK Keener and DJ Arp. Kinetic studies of ammonia monooxygenase inhibition in Nitrosomonas europaea by hydrocarbons and halogenated hydrocarbons in an optimized whole-cell assay. Applied and Environmental Microbiology, 59(8): 2501–2510, 1993.

[2] Serena Rinaldo. Biology of the Nitrogen Cycle. Francesca Cutruzzola, 2007 (37-55).

[3] SW Snyder and TC Hollocher. Purification and some characteristics of nitrous oxide reductase from paracoccus denitrificans. Journal of Biological Chemistry, 262: 6515–6525, 1987.

[4] Y Ishihama, T Schmidt, J Rappsilber, M Mann, FU Hartl, MJ Kerner, and D Frishman. Protein abundance profiling of the escherichia coli cytosol. BMC genomics, 9, 2008.

[5] AB Hooper, PC Maxwell, and KR Terry. Hydroxylamine oxidoreductase from nitrosomonas: Absorption spectra and content of heme and metal. Biochemistry, 17:2984–2989, 1978.

[6] S Gilch, O Meyer, and I Schmidt. A soluble form of ammonia monooxygenase in nitrosomonas europaea. Biological Chemistry, 390(9):863–873, 2009.


[7] T.C. Jorgensen and L.R. Weatherley. Ammonia removal from wastewater by ion exchange in the presence of organic contaminants. Water Research, 37:723–1728, 2003.

[8] Systems biology toolbox for matlab: A computational platform for research in systems biology. Bioinformatics, 22(4):514–515, 2006.