Team:KU Leuven/Project/Oscillator/wetlab

From 2013.igem.org

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     <p align="justify">The most elegant solution would be to design a promoter that would perfectly exhibit the characteristics of an OR gate. In the wetlab we started a slightly altered design, in which the goal of a asymmetric time delay is still achieved. For a further elaboration on that option we refer you to the design page. We do propose a potential implementation for a genuine OR gate. This would consist of a gene that has two promoters in front of it. There would then be production when either one of the transcription factors is present and the increase when both are present would be reduced. In the case of C this looks as follows:</p>
     <p align="justify">The most elegant solution would be to design a promoter that would perfectly exhibit the characteristics of an OR gate. In the wetlab we started a slightly altered design, in which the goal of a asymmetric time delay is still achieved. For a further elaboration on that option we refer you to the design page. We do propose a potential implementation for a genuine OR gate. This would consist of a gene that has two promoters in front of it. There would then be production when either one of the transcription factors is present and the increase when both are present would be reduced. In the case of C this looks as follows:</p>
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Revision as of 14:04, 27 October 2013

iGem

Secret garden

Congratulations! You've found our secret garden! Follow the instructions below and win a great prize at the World jamboree!


  • A video shows that two of our team members are having great fun at our favourite company. Do you know the name of the second member that appears in the video?
  • For one of our models we had to do very extensive computations. To prevent our own computers from overheating and to keep the temperature in our iGEM room at a normal level, we used a supercomputer. Which centre maintains this supercomputer? (Dutch abbreviation)
  • We organised a symposium with a debate, some seminars and 2 iGEM project presentations. An iGEM team came all the way from the Netherlands to present their project. What is the name of their city?

Now put all of these in this URL:https://2013.igem.org/Team:KU_Leuven/(firstname)(abbreviation)(city), (loose the brackets and put everything in lowercase) and follow the very last instruction to get your special jamboree prize!

tree ladybugcartoon


Design

Robust, colony-wide synchronisation

Modelling

Mathematical view on our oscillator

Wetlab

You are here!

A well-known problem associated with the use of insect repellents is habituation. After a while insects will get used to the smell of the repellent and they won’t react anymore. Therefore we decided to implement an oscillator in our project for the production of (E)-β-farnesene (EBF) and methyl salicylate. In this part we will explain the genetics of our oscillator. For more information on the theoretical system and our in silico design, we refer to our design page and oscillator modelling page. We propose an implementation of the oscillator design and during the summer we focused on creating specifically a feed forward loop incorporating a quorum sensing molecule, since this is the workhorse of the oscillator.

The model

We will shortly describe the functionality of the model as this is necessary to understand the resulting genetic network. Our proposed model is a network consisting of different transcription factors (TF), as is displayed in the figure. When there is a high level of TF A, this induces the production of both TF X and TF C, of which the latter will repress TF A and induce TF B. The production of TF C will not stop, even after TF A has disappeared below its threshold, since there is still TF X present that induces TF C. This effect creates an extended repression of TF A, in order to make sure the level of TF A drops sufficiently, so there is no production of TF X and TF C while the other halve of the system is active. This extended period in which TF C is present, also induces the production of TF B and the same story can be told for this halve. This means there are sequential peaks in the different components, which means this is an oscillating system.

Aphid colors

Figure 1 ǀ The oscillator model

As mentioned on the design page of the oscillator we chose to use two quorum sensing molecules and four other transcription factors. The hurdles appear to be the implementation of all the required interactions between those transcription factors. Our proposition accomplishes these interactions by simply using four inducing transcription factors (on top of the two quorum sensing molecules). This section discusses how these can be used to create the OR gates and the AND gates.

How to implement an OR gate

The most elegant solution would be to design a promoter that would perfectly exhibit the characteristics of an OR gate. In the wetlab we started a slightly altered design, in which the goal of a asymmetric time delay is still achieved. For a further elaboration on that option we refer you to the design page. We do propose a potential implementation for a genuine OR gate. This would consist of a gene that has two promoters in front of it. There would then be production when either one of the transcription factors is present and the increase when both are present would be reduced. In the case of C this looks as follows:


Oscillator genes

Figure 2 | The proposed implementation of the OR gate.

The genes of the oscillator

Since we want a colony-wide synchronization, TF A has to be a quorum-sensing molecule (as well as TF B). We chose for the autoinducer synthetase (BBa_C0076) that leads to the production of the quorum-sensing molecule 3OH,C14:1-HSL. Before this gene we placed a TetR repressible promoter (BBa_R0040), so the quorum-sensing molecule is only produced if there is no TetR present. Because this is a proof of concept, we want to be able to control the production of the quorum-sensing molecule. Therefore we placed the gene coding for TetR (BBa_P0340) behind a T7 promotor (BBa_I719005). When we put the construct in a Rosetta strain, we can control the activity of the T7 promotor. This strain has a chromosomal copy of the T7 RNA polymerase gene behind a lacUV5 promotor, which can be induced by IPTG. By adding IPTG, T7 RNA polymerase will be formed, which leads to the transcription of the TetR gene so no quorum-sensing molecules will be produced.

To be active, 3OH,C14:1-HSL has to form a complex with the CinR activator. This complex can bind the promotor BBa_R0078 and activate transcription. The gene for the CinR activator (BBa_C0077) is also placed under control of a TetR repressible promotor. So if no TetR is present, CinR and 3OH,C14:1-HSL are formed and they combine to activate the promotor BBa_C0078 which is placed before the gene coding for AraC (BBa_C0080; representing TF X) and before a gene for GFP (BBa_K082003; representing TF C). So the complex makes sure that TF X and TF C are formed. In the real model TF C would be the gene for EBF, but in our proof of concept model we use GFP, which allows us to easily detect if the system works.


Oscillator genes

Figure 2 | Genetic network of the oscillator.

Our control mechanism does not only consist of TetR, but we also inserted a gene in our model that codes for the autoinducer inactivation enzyme AiiA (BBa_C0060). This enzyme can hydrolyze the quorum-sensing molecule. The gene is also placed behind a T7 promotor. If IPTG is added, no quorum-sensing molecule and receptor are formed anymore and the remaining quorum-sensing molecules are degraded by AiiA.

AraC also leads to the transcription of the GFP-gene by binding to an AraC regulated promotor (BBa_R0080). This means that not only TF A leads to formation of TF C but TF X as well. We want to prove in the lab that if TF X also activates production of TF C, the cell will fluoresce for a longer period than if TF X is excluded from the network.

As you can see on figure 2, the proof of concept of the oscillator exists of a lot of different genes. We started with creating TF C, which in our case exists of the GFP gene coupled to a promoter and a terminator. We ligated the GFP-reporter gene (BBa_K082003) to a double terminator (BBa_B0015). These form the new intermediate brick BBa_K1060006. On figure 3 you can see the insert and backbone after digestion of this new brick. Afterwards we focused on TF A, which consists of the genes coding for the auto-inducer synthetase and a receptor that binds the quorum-sensing molecule. We coupled the cinI gene which codes for the autoinducer synthetase (BBa_C0076) to the double terminator (BBa_B0015). These form the new intermediate brick BBa_K1060007.

Digestion of our new brick BBa_K1060006

Figure 3 ǀ Digestion of our new brick BBa_K1060006