MODELING meow
Modeling Introduction
Our modeling consists of the following three parts:
- To make the project applicable in real life, we designed a device with modified engineering bacteria inside, which can be placed in soil to attract and kill nematodes.
- Assuming there is a farmland, we took advantage of gas diffusion model and nematodes’ movement analogue simulation to find the best position where for the device to be placed in this hypothetical farmland.
- We established a database to broaden the scope of our applications, combined with our methods, to kill more different pests. We hope that the new environment-friendly method, based on principles of synthetic biology, could be shared with and improved by the researchers all over the world.
Design
Device 1.0
In order to enable our project to be applied in real environment, we designed and made Device 1.0. Because the productivity of attracting substance by E.coli is limited and the price of man-made attracting substance is quite high. We choose low-cost CO2 as our assistant attracting substance since it was demonstrated that carbon dioxide has a function of attracting nematodes.
Our device has four areas. The first area is carbon dioxide generating area. We produce CO2 by mixing limestone and diluted hydrochloric acid together, which is widely used in industry. The second area is E.coli culturing area. It includes a medium inside the device - to culture modified engineering bacteria. The third area is light controlling area, which includes a LED light. When it is turned on, red emission will activate the promoter and bacterial cells will express attracting substance; while the LED light is turned off, toxalbumin will be produced. The forth area is made up of a cuboid outer shell, which can support our device.
The figure above shows our product – Device 1.0. Meanwhile, we simulate our device in the lab to show our system is able to work under real-world conditions.
There are 8 steps to apply our device in farmland just as it is showed in the video above. And all the procedures below were conducted in a fume hood.
- Step 1. We gathered a box of soil from our farmland.
- Step 2. We applied culture medium onto slide glasses. Unfortunately, because of the limitation of our wet lab condition, we didn’t apply real engineering bacteria this time.
- Step 3. We gathered several small stones used as CaCO3 and put them into the test tube.
- Step 4. We added HCl into the separating funnel.
- Step 5. We opened the faucet of the separating funnel in order to let HCl flow into the test tube under the atmospheric pressure. Then small stones reacted with HCl to liberate CO2. We also demonstrated how to use red LED light in the video.
- Step 6. We put the device into the soil.
- Step 7. After 3 hours of incubation, we took out the device and removed the slide glasses.
- Step 8. Finally, we tested the results using a microscope. In the video, we showed the movement of a nematode that we separated from soil from Hebei Province, China.
Device 2.0
After discussion among team members about device 1.0, we found several deficiencies. First of all, the size of our device is so limited that the reaction substrate (limestone and diluted hydrochloric acid) is not enough to generate CO2 constantly. Replenishing the reaction substrate frequently will greatly increase the cost. Secondly, the space utilization percentage is low on the slide medium; as a result, the production of both attractant and toxalbumin is low. Lastly, LED tube is sizable and needed to be powered constantly, thus not suitable for farmland. In device 2.0, we improved device 1.0 in those three aspects mentioned above. Indeed, we need to further improve our device.
Firstly, we assume that modified engineering bacteria can produce ideal concentration of attractant and toxalbumin (the ideal concentration is in reasonable range). Then, considering the problem of space utilization rate and the fact that E.coli can only grow on the surface of the medium, we changed the medium’s shape to sphericity to reach the highest space utilization percentage. Meanwhile, our device has been shaped to sphericity too, and the LED light has been moved to the center so that the whole surface can get the radiation evenly. A design like this enable us to use mini LED light bulb, and use solar energy instead of electricity as our power resource. This change fulfill our aim to save money and energy, which is also more economical and enviromentally friendly.
We also made a video to show the inner structure of device 2.0.
As shown above, device 2.0 has two shells – outer shell and inner shell. There are tiny holes on the outer shell, which allow nematodes to enter the device. The holes are designed to block other soil organisms from entering. The red LED light can be supplied with the power from solar power pane, which will be put on the surface of the farmland. And we can achieve remote control by using radio technology.
Simulation Modeling in farmland
After we improved our device, we want to figure out how we can put our device into practice in farmland, and whether our device would be more efficient and economical than the methods used currently used in killing nematodes (crop-dusting mostly). In order to answer these two questions, especially the second one, we need to conduct a simulation of the movement of nematodes to determine the most suitable place in the farmland to place our device. Our modeling process is given below:
Modeling assumptions
- Nematodes can be attracted if the attraction concentration of limonene is higher than the lowest attractant concentration and then can move towards the direction of the highest odor concentration after attracted by the limonene smell.
- Engineering bacteria in our device are able to produce enough limonene as we need.
- The creeping speed of nematode is fixed as 290μm/ s.
- Nematodes move on a 2D plane. Because the movement range of nematodes is within 10cm and the distance between two devices is much longer than 10cm, we can ignore the depth.
- When the gas diffuses in space, the concentration is not affected by temperature, aerodynamics or other factors.
- The device emits gas continuously and the concentration is uniform in space. And after the gas diffusion, the attractant concentration will stabilize.
Explanation of symbols
Table 1. Explanation of symbols | |||
---|---|---|---|
Symbol | Meaning | Symbol | Meaning |
V | Nematodes’ movement velocity | T | Attraction time |
L | The longest distance between nematodes and the equipment | S | Distance between two devices |
C0 | The lowest concentration | C | The concentration of every device |
Data sources
Table 2. Data sources | ||
---|---|---|
Variable | Value | Symbol |
Nematodes’ movement velocity | 290 | Xu J X, Deng X. Biological modeling of complex chemotaxis behaviors for C. elegans under speed regulation—a dynamic neural networks approach[J]. Journal of computational neuroscience, 2013, 35(1): 19-37. |
Nematodes’ density | \(1.89 \times {10^6 m^3}\) | Junli Zhang. Distribution and identification of sweet potato, soybean and vegetables plant-parasitic nematodes species in Hebei Province[D][D]. ,2004. |
The lowest concentration | \(99.3 {g/m^3}\) | Qiuhong Niu. New mechanism of attracting and killing nematodes by Bacillus nematocida B16. ,2009. |
Diffusion coefficient of limonene | 2.46 | Limm W, Begley T H, Lickly T, et al. Diffusion of limonene in polyethylene[J]. Food additives and contaminants, 2006, 23(7): 738-746. |
Running Time of Attractant(Days) | Distance between Divices |
0.5 | 17.7137 |
1 | 35.4345 |
1.5 | 53.1518 |
2 | 70.8691 |
2.5 | 88.5863 |
3 | 106.3036 |
Considering that odorousness will be reduced with the increase of distance away from the device, we should only consider about the superposed odorousness at point F(considering four equipment now) to reach the lowest attractant concentration. Thus we obtain:
$$C_1 = C_0/4$$
C1 is the superposed odorousness diffused from the device, C0 is the lowest attractant concentration.
We get the 3-D gas diffusion model according to Fick Law, and then we simplify the question into 1-D situation according to isotropy.
According to the Fick’s Law, we get the 3-D gas diffusion model. Since the three dimension has no difference between each other, we simplify the question into 1-D situation according to isotropy.
A brief introduction to the Fick’s Law: It points out that during the process of unsteady diffusion, at a distance of x, the change rate of concentration to time is equal to the negative value of the change rate of diffusion flux to distance. Its mathematical expression is as follows:
$$\frac{\partial C_{A}}{\partial t} = D_{A}\frac{\partial ^2 C_{A}}{\partial x^2}$$
Boundary value condition is: C(t,0)==N
C(x,t) is the concentration at the distance of x from gas source in t, N0 is the concentration of gas source, D is the diffusion coefficient.
According to the model above, we obtain the gas diffusion model in 3D. And according to the principle of isotropy, we simplify the problem in 1D.
Then we obtain the solution
$$c(x,t) = \frac{C_{0}}{2}(1-erf\frac{x}{2\sqrt{Dt}})$$
Adding that
$$erf(x) = \frac{2}{\sqrt{\pi}}\int^{x}_{0}e^{-\lambda^{2}}d\lambda$$
Then we can obtain the arithmetic solution.
The explanations of simulation: In the video above, we built up a simulation model of the movement of nematode using the cellular automaton in MATLAB. It shows how nematode moves in a real farmland with the device. We built up a 301×301 matrix in MATLAB, in place of a 20m*20m piece of farmland. The proportion of virtual nematode and real nematode is 0.0084.
We assume that the nematode is distributed randomly at the beginning. The rules of the movement are as follows:
- The nematodes move towards 4 different directions: front, behind, right and left;
- Every time the nematode choose one of the 4 directions randomly and the probability of these 4 directions are the same;
- If the nematode move to the place where the gas concentration is lower than the previous position, then the nematode will move back to the previous position.
We did the different simulation experiments with one device in the farmland and two devices in the farmland separately.
Database
In order to apply our idea and method to kill more agricultural pests, we established a database, we hope to take a better use of the new environmental friendly method from the synthetic biology aspect and share it with researchers all over the world. Our database contains 3 daughter databases: attractant, pests and toxalbumins bases. We will update relevant information about the engineering bacteria we designed to kill the pests in our database. Currently, our database contains the biobrick we established in this project and the one established by team ZJU-CHINA.
All the users have the permission to edit and add new contents, and we welcome everyone to use and enrich our database!
Our link address is:
All the users have the permission to edit and add new contents, and we welcome everyone to use and enrich our database!