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Team:Calgary/Project/HumanPractices/Design
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TITLE=Preliminary Design Considerations| | TITLE=Preliminary Design Considerations| | ||
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| + | <img src="https://static.igem.org/mediawiki/2012/c/c3/UCalgary2012_FRED_and_OSCAR_Design.png" style="float: right; padding: 10px; width: 250px;"></img> | ||
| - | <h2> Bioreactor Design Considerations </h2> | + | <p>FRED and OSCAR have been tasked with jobs that require them to be outside of a laboratory environment. Our discussions with industry experts emphasized the need to design a system that minimized the chance of bacteria escaping into the environment. Despite our belief that due to the increased metabolic load FRED and OSCAR are undertaking they would not be able to outcompete any native bacteria, we took these concerns to heart when we designed our project. We have designed multiple layers of controls for each system, utilizing both biological and physical controls.</p> |
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| + | <h2>Physical: The first line of defense</h2> | ||
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| + | <p>The best way to prevent FRED and OSCAR from spreading into the environment is to make sure that they cannot get to it. As such both our bioreactor and biosensor prototypes involve isolating the bacteria in closed systems. In our <a href="https://2012.igem.org/Team:Calgary/Project/FRED/Prototype">biosensor</a> we seal the tubes with a one way valve with FRED trapped inside. The tailings sample is added through the one way valve and then when the testing is done the cap is twisted slightly to release bleach into the sealed system. After the bleach is added the tube is disposed of in a safe manner.</p> | ||
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| + | <p>OSCAR presents more of a challenge, as he needs to remain in one place for an extended period of time to perform his tasks. For this we have created a <a href="https://2012.igem.org/Team:Calgary/Project/OSCAR/Bioreactor">bioreactor</a> house for him. In this sealed system filtered air is bubbled in to keep oxygen levels optimal while a HEPA filter is used to screen air coming out. To extract any hydrocarbons from the reactor a belt skimmer is used that selectively picks up oil while leaving bacteria behind. When the oil is separated from the belt skimmer it is exposed to UV to kill any bacteria, and then is placed into a fractional distillator that heats to 400°C to separate the hydrocarbons from each other.</p> | ||
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| + | <h2>Biological: Preparing for the worst</h2> | ||
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| + | <p>Although industry experts felt a genetic safety mechanism was important, they felt that it needed to fit into a cost effective remediation solution. It was stressed that price is a paramount factor to favor adoption at industrial scales, and so an inexpensive system would have a greater likelihood of being implemented outside the laboratory. Experts were also more concerned about the spread of DNA over the death of our organisms. As such, we needed a system where we avoided lysis of our cells, so as to prevent possible uptake of DNA by other surrounding organisms in soil and water, something that has been criticized in previous iGEM systems.</p> | ||
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| + | <p>We settled on an <a href="https://2012.igem.org/Team:Calgary/Project/HumanPractices/Killswitch">inducible ribo-killswitch system</a>. Although inducible systems have been shown to have a tendency to mutate, rendering them ineffective and allowing possible escape, they are more cost effective than other strategies. An auxotrophic marker could have been used for example, where a deletion in the genome would make the organism dependent on an externally supplemented metabolite. Although a mutation restoring the metabolite would be sufficiently complex as to be rendered improbable, metabolic supplements are considerably more expensive than the glucose and metal ions that our systems require. As such, we used an inducible system, but took several approaches so as to mitigate the risk of mutation.</p><p> Firstly, we engineered redundancy into our system. By using two kill genes, both would have to be rendered inoperable for the kill switch mechanism to malfunction. Knudsen <i>et al.</i> (1995) proposed that active kill switches containing a single kill element were subject to a mutation rate of 10<sup>-6</sup> per cell per generation, but that a second kill gene under a common regulatory element reduces this value by two orders of magnitude. The mutation rate of a system with two kill genes under independent controls might approach 10<sup>-12</sup> (Knudsen et al 1995). Secondly, the kill switch mechanism is, of course, only a failsafe measure for controlling our organism's spread. The primary means of preventing its escape is through the multiple layers of mechanical security provided by our bioreactor and biosensor. Only when these measures fail will the kill switch be required to function. We felt that this system would also mitigate the concern that an auxotrophic control mechanism would kill the organism without degrading its genetic material, thereby raising the possibility of horizontal gene transfer to other organisms.</p> | ||
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| + | <p> The OSCAR component of our project aims to remediate toxins in the oil sands tailings ponds using synthetic bacteria. Despite our belief that the metabolic burden of this system on our bacteria would not allow them to outcompete any native organisms, as we detail in our interviews page, our dialogue with experts really emphasized the need to design such a system so as to minimize any escape of our bacteria regardless. As such, we designed a closed <a href=https://2012.igem.org/Team:Calgary/Project/FRED/Prototype>biosensor</a> and a closed <a href=https://2012.igem.org/Team:Calgary/Project/OSCAR/Bioreactor>bioreactor</a> which incorporated built-in structural <a href=https://2012.igem.org/Team:Calgary/Project/HumanPractices/Design> design</a> safety mechanisms. In order to implement one more level of control, which industry felt was needed, we wanted an additional genetic-based containment mechanism to kill our bacteria upon escape from our system, thereby lessening the possibility of OSCAR spreading beyond the bioreactor or horizontally transferring genes to other organisms. We implemented novel ribo-killswitch parts. These contain riboswitch regulatory elements and exo/endonuclease kill genes.</p> | ||
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| + | <h2>Design Challenges from Industry</h2> | ||
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| + | <p> As we wanted our system to eventually be implemented in our tailings pond remediation system, we had several design challenges to take into account. Our interviews with industry experts helped us make </html>'''informed design choices'''<html> so as to maximize the probability of our system actually being implemented one day.</p> | ||
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| + | <p>Although industry experts felt a genetic safety mechanism was important, they felt that that it needed to fit into a cost effective remediation solution. It was stressed that price is a paramount factor in permitting adoption at industrial scales, and so an inexpensive system would have a greater likelihood of being implemented outside the laboratory. Experts were also more concerned about the spread of DNA over the death of our organisms. As such, we needed a system where we avoided lysis of our cells, so as to prevent possible uptake of DNA by other surrounding organisms in soil and water, something that has been a critique of previous iGEM systems. | ||
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| + | <h2> Our Solution</h2> | ||
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| + | <p>With these considerations in mind, we settled on an inducible system riobo-killswitch system. Although inducible systems have been shown to have a tendency to mutate, rendering them ineffective and allowing possible escape, they are more cost effective than other strategies. An auxotrophic marker could have been used for example. Here, a deletion form the genome would make the organism dependent on an externally supplemented metabolite. Although a mutation restoring the metabolite would be sufficiently complex as to be rendered improbable, metabolic supplements are considerably more expensive than the glucose and metal ions that our system requires. As such, we used an inducible system, but took several approaches so as to mitigate the risk of mutation. Firstly, we engineered redundancy into our system. By using two kill genes, both would have to be rendered inoperable for the kill switch mechanism to malfunction. Knudsen et al. (1995) proposed that active kill switches containing a single kill element were subject to a mutation rate of 10<sup>-6</sup> per cell per generation, but that a second kill gene under a common regulatory element reduces this value by two orders of magnitude. The mutation rate of a system with two kill genes under independent control elements could be as low as 10<sup>-12</sup> (Knudsen et al 1995). Secondly, the kill switch mechanism is, of course, only a failsafe measure for controlling our organism's spread. The primary means of preventing its escape is through the multiple layers of mechanical security provided by our bioreactor and biosensor. Only when these measures fail will the kill switch be required to function. We felt that this system would also mitigate the concern that an auxotrophic control mechanism would kill the organism without degrading its genetic material, thereby making possible horizontal gene transfer to other organisms. </p> | ||
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| + | <p>As industry was more interested in the transfer of genetic material over the death of the organism and we already have structural safety measures, we feel this is an appropriate solution as it responds to industry concerns. As such, our final system is a collection of novel inducible ribo-killswitchs making use of unique regulatory elements and novel exo/endonucleaes.</p> | ||
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| + | <h2>Bioreactor Design Considerations</h2> | ||
<p>Over the summer, much thought was put into the design of our bioreactor in order to optimize functionality, expense, and safety. Although many of the details of our design cannot be worked out due to the time constraint of a four-month period, there are still lots of theoretical aspects that we were able to cover. | <p>Over the summer, much thought was put into the design of our bioreactor in order to optimize functionality, expense, and safety. Although many of the details of our design cannot be worked out due to the time constraint of a four-month period, there are still lots of theoretical aspects that we were able to cover. | ||
</p> | </p> | ||
| - | <p> | + | <p>The first aspect of our design was choosing what type of bioreactor system to use. For lab scale experiments and design, we chose to use a system that is closest to that of a batch system. This system requires all reactants to be added at time zero, with everything being removed at once when the remediation has come to completion. However, our design uses a belt skimmer to continually remove any products (hydrocarbons) formed either emulsified or found on the top layer. This way, we are able to reuse our culture and remove product until all the toxins are converted. We then remove everything in the tank and begin the process again. Our skimmed product goes through UV radiation in order to kill any bacteria that happen to be left in the product. |
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| + | In addition, our bioreactor bacteria will contain kill genes. When our bacteria are in a glucose-free environment (a.k.a. outside the tank) the bacteria are programmed to self-destruct. Since we have three different intermediate steps for remediation (desulphurization, denitrification, decarboxylation) we will need three tanks with the product from the previous tank acting as the reactant for the next tank in line. The product of the last tank will go through distillation to purify our desired alkane. Distillation will also assist in classifying the different hydrocarbons we formed and ensure bacteria do not escape into the environment. The produced hydrocarbons may have different carbon and hydrogen bonds, thus its boiling and condensation temperature will vary. If the bacteria removed by the belt skimmer were to somehow survive UV radiation and thrive in a glucose-free environment, it would be distilled along with the rest of the skimmed material. In distillation the bacteria would be heated to an extremely high temperature and would consequently die as a result. | ||
</p> | </p> | ||
| - | <p> | + | <p>To improve the growth and environment of our bacteria, we will keep our bioreactor at ideal growth temperature (if <i>E. coli</i>, 37 °C; if <i>Pseudomonas</i>, 30°C). In addition, we will have an agitator (turbine) and an air sparger supplying filtered air to help mix and oxygenate our solution. In order to help maintain these ideal conditions, our bioreactor will be a closed system with our belt skimmer contained inside the tank.</p> |
| - | + | ||
| + | <h2>Biosensor Design Considerations</h2>--> | ||
| + | </html> | ||
}} | }} | ||
Latest revision as of 23:36, 26 October 2012
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Preliminary Design Considerations
FRED and OSCAR have been tasked with jobs that require them to be outside of a laboratory environment. Our discussions with industry experts emphasized the need to design a system that minimized the chance of bacteria escaping into the environment. Despite our belief that due to the increased metabolic load FRED and OSCAR are undertaking they would not be able to outcompete any native bacteria, we took these concerns to heart when we designed our project. We have designed multiple layers of controls for each system, utilizing both biological and physical controls.
Physical: The first line of defense
The best way to prevent FRED and OSCAR from spreading into the environment is to make sure that they cannot get to it. As such both our bioreactor and biosensor prototypes involve isolating the bacteria in closed systems. In our biosensor we seal the tubes with a one way valve with FRED trapped inside. The tailings sample is added through the one way valve and then when the testing is done the cap is twisted slightly to release bleach into the sealed system. After the bleach is added the tube is disposed of in a safe manner.
OSCAR presents more of a challenge, as he needs to remain in one place for an extended period of time to perform his tasks. For this we have created a bioreactor house for him. In this sealed system filtered air is bubbled in to keep oxygen levels optimal while a HEPA filter is used to screen air coming out. To extract any hydrocarbons from the reactor a belt skimmer is used that selectively picks up oil while leaving bacteria behind. When the oil is separated from the belt skimmer it is exposed to UV to kill any bacteria, and then is placed into a fractional distillator that heats to 400°C to separate the hydrocarbons from each other.
Biological: Preparing for the worst
Although industry experts felt a genetic safety mechanism was important, they felt that it needed to fit into a cost effective remediation solution. It was stressed that price is a paramount factor to favor adoption at industrial scales, and so an inexpensive system would have a greater likelihood of being implemented outside the laboratory. Experts were also more concerned about the spread of DNA over the death of our organisms. As such, we needed a system where we avoided lysis of our cells, so as to prevent possible uptake of DNA by other surrounding organisms in soil and water, something that has been criticized in previous iGEM systems.
We settled on an inducible ribo-killswitch system. Although inducible systems have been shown to have a tendency to mutate, rendering them ineffective and allowing possible escape, they are more cost effective than other strategies. An auxotrophic marker could have been used for example, where a deletion in the genome would make the organism dependent on an externally supplemented metabolite. Although a mutation restoring the metabolite would be sufficiently complex as to be rendered improbable, metabolic supplements are considerably more expensive than the glucose and metal ions that our systems require. As such, we used an inducible system, but took several approaches so as to mitigate the risk of mutation.
Firstly, we engineered redundancy into our system. By using two kill genes, both would have to be rendered inoperable for the kill switch mechanism to malfunction. Knudsen et al. (1995) proposed that active kill switches containing a single kill element were subject to a mutation rate of 10-6 per cell per generation, but that a second kill gene under a common regulatory element reduces this value by two orders of magnitude. The mutation rate of a system with two kill genes under independent controls might approach 10-12 (Knudsen et al 1995). Secondly, the kill switch mechanism is, of course, only a failsafe measure for controlling our organism's spread. The primary means of preventing its escape is through the multiple layers of mechanical security provided by our bioreactor and biosensor. Only when these measures fail will the kill switch be required to function. We felt that this system would also mitigate the concern that an auxotrophic control mechanism would kill the organism without degrading its genetic material, thereby raising the possibility of horizontal gene transfer to other organisms.
