"
Team:Braunschweig/Safety
From 2014.igem.org
| Line 90: | Line 90: | ||
} | } | ||
| + | table, th, td { | ||
| + | border: 1px solid black; | ||
| + | border-collapse: collapse; | ||
| + | } | ||
| + | th, td { | ||
| + | padding: 15px; | ||
| + | } | ||
</style> | </style> | ||
| Line 206: | Line 213: | ||
<p> | <p> | ||
In order to minimize the working risk as much as possible, the iGEM Team Braunschweig 2014 exclusively worked with non-pathogenic organisms classified as risk group S1. | In order to minimize the working risk as much as possible, the iGEM Team Braunschweig 2014 exclusively worked with non-pathogenic organisms classified as risk group S1. | ||
| - | |||
| - | |||
| - | |||
| - | |||
| - | |||
| - | |||
| - | |||
| - | |||
| - | |||
| - | |||
| - | |||
| - | |||
| - | |||
| - | |||
<table style="width:100%"> | <table style="width:100%"> | ||
| Line 232: | Line 225: | ||
<td>endA1 gyrA96(nalR) thi-1 recA1 relA1 lac glnV44 F'[ ::Tn10 proAB+ lacIq Δ(lacZ)M15 Amy CmR] hsdR17(rK- mK+)</td> | <td>endA1 gyrA96(nalR) thi-1 recA1 relA1 lac glnV44 F'[ ::Tn10 proAB+ lacIq Δ(lacZ)M15 Amy CmR] hsdR17(rK- mK+)</td> | ||
<td>S1</td> | <td>S1</td> | ||
| - | < | + | <td>Non-pathogenic, may cause irritation to skin, eyes and respiratory tract, may affect kidneys</td> |
</tr> | </tr> | ||
<tr> | <tr> | ||
| Line 238: | Line 231: | ||
<td>wildtype</td> | <td>wildtype</td> | ||
<td>S1</td> | <td>S1</td> | ||
| - | < | + | <td>Non-pathogenic, may cause irritation to skin, eyes and respiratory tract, may affect kidneys</td> |
</tr> | </tr> | ||
<tr> | <tr> | ||
| Line 244: | Line 237: | ||
<td>F– ompT gal dcm lon hsdSB(rB- mB-) λ(DE3 [lacI lacUV5-T7 gene 1 ind1 sam7 nin5]</td> | <td>F– ompT gal dcm lon hsdSB(rB- mB-) λ(DE3 [lacI lacUV5-T7 gene 1 ind1 sam7 nin5]</td> | ||
<td>S1</td> | <td>S1</td> | ||
| - | < | + | <td>Non-pathogenic, may cause irritation to skin, eyes and respiratory tract, may affect kidneys</td> |
</tr> | </tr> | ||
<tr> | <tr> | ||
| Line 250: | Line 243: | ||
<td>endA1 glnV44 thi-1 relA1 gyrA96 recA1 mcrB+ Δ(lac-proAB) e14- [F' traD36 proAB+ lacIq lacZΔM15] hsdR17(rK-mK+)</td> | <td>endA1 glnV44 thi-1 relA1 gyrA96 recA1 mcrB+ Δ(lac-proAB) e14- [F' traD36 proAB+ lacIq lacZΔM15] hsdR17(rK-mK+)</td> | ||
<td>S1</td> | <td>S1</td> | ||
| - | < | + | <td>Non-pathogenic, may cause irritation to skin, eyes and respiratory tract, may affect kidneys</td> |
</tr> | </tr> | ||
</table> | </table> | ||
Revision as of 15:13, 12 October 2014
Project Safety Concerns
The safety concerns of our project were a very important issue for this years iGEM Team of the Technische Universität Braunschweig. Because the use of an antibiotic resistance was necessary for selection of bacteria we included an ampicillin resistance gene in our final construct. Ampicillin is a standard antibiotic commonly used in everyday laboratory work. The methane monooxygenase (MMO) plasmid construct for our E. cowli was planned to be expressed via a promoter which is inducible by methane. Although there is a constitutive promoter in the construct first, cloning according to iGEM standard biobrick format allows an easy exchange of parts. Therefore, various variants are easily constructed out of the broad iGEM Registry in case safety concerns arise. Additionally, we prepared special alginate beads in which our E. cowli will be embedded. These special beads allow the diffusion of gases and offer necessary nutritions. Since E. cowli is not able to grow in the natural rumen fluid of the cow, the beads enable its growth, controlling its localisation at once. For further application we planned to include a kill switch system based on a light induced promoter. Usually the risk of bacteria passing the abomasum of a cow is very low. Nevertheless an additional light induced kill switch will disable E. cowli to live out of its provided rumen system decreasing the risk of an uncontrolled distribution.
Laboratory Safety Concerns
Bacterial Strains Used
In order to minimize the working risk as much as possible, the iGEM Team Braunschweig 2014 exclusively worked with non-pathogenic organisms classified as risk group S1.
| Strain | Genotype | Risk Group | Risk to Humans |
|---|---|---|---|
| E. coli XL1-Blue-MRF‘ | endA1 gyrA96(nalR) thi-1 recA1 relA1 lac glnV44 F'[ ::Tn10 proAB+ lacIq Δ(lacZ)M15 Amy CmR] hsdR17(rK- mK+) | S1 | Non-pathogenic, may cause irritation to skin, eyes and respiratory tract, may affect kidneys |
| Methylococcus capsulatus | wildtype | S1 | Non-pathogenic, may cause irritation to skin, eyes and respiratory tract, may affect kidneys |
| E. coliBL21 DE3 | F– ompT gal dcm lon hsdSB(rB- mB-) λ(DE3 [lacI lacUV5-T7 gene 1 ind1 sam7 nin5] | S1 | Non-pathogenic, may cause irritation to skin, eyes and respiratory tract, may affect kidneys |
| E. coliJM109 | endA1 glnV44 thi-1 relA1 gyrA96 recA1 mcrB+ Δ(lac-proAB) e14- [F' traD36 proAB+ lacIq lacZΔM15] hsdR17(rK-mK+) | S1 | Non-pathogenic, may cause irritation to skin, eyes and respiratory tract, may affect kidneys |
Safety equipment
The lab was standardly provided with safety equipment according to the S1 safety forms. Safety showers, eye showers, fire-extinguishers and a fire blanket were installed and easily accessible. Furthermore, lab coats, safety gloves and goggles were available at any time in the lab. Specially labelled areas were restricted to working with carcinogenic substances such as ethidium bromide.
Personal safety
Before starting any work in the lab every team member had to be given an instruction concerning health and safety. Additionally there was a tour of our own and adjacent labs with a supervisor. Instructions were given by a supervisor when using new equipment and techniques. Hazardous and carcinogenic chemicals and substances were avoided whenever possible. In case these chemicals could not be substituted, safety equipment such as special gloves were used. Furthermore, to prevent any risk, the team members worked exclusively in groups of at least two members.
Sterile Work
To keep our lab sterile, working spaces and necessary equipment were cleaned with 70 % ethanol. Ethanol is easily flammable and was therefore used carefully and only for small areas. To avoid contaminations of our cultures and for selection antibiotics were added to the used media with the note that they can cause health problems in large amounts. Furthermore, they can cause undesirable resistances in bacteria and thus were used only if necessary. Ethidium bromide was used for gel electrophoresis with special care because of its DNA-intercalating and cancerogenous properties. Use of UV light was necessary for visualization of DNA in agarose gels.
Bioethics
Bioethics was a very important topic for the team. Working with bacteria as chassis for recombinant protein production is common in science and generally accepted in society. Therefore, no bioethical questions were expected to arise in this matter. In case our project is turned into reality and cows are provided with our E. cowli strain we expect a lot of bioethical questions from the public. People are expected to react sceptically due to our planned use of recombinant organisms in animals intended for food production, which, in fact, is reasonable. The work on animals probably has to be handled in a more sensitive way than the work on other, simpler organisms such as bacteria. It has to be questioned whether the advantages for climate change resulting from the use of E. cowli can compensate the risk every recombinant organism brings up in the environment. Alternatively we planned to design a barn filter provided with a methane filter system based on E. cowli. This technologie would render it possible to decrease methane emission without providing animals directly with a recombinant organism. Therefore ethical problems are minimised as well.
Environmental Impacts
In case our project will be realized in cows, it is necessary to reconsider every possible risk recombinant organisms bring to nature and environment. Although there is no possible use of our project regarding national issues and although no toxins or pathogenic substances are expressed, it would be important to question as many risks as possible. Under these circumstances E. cowli will be justifiable due to the positive impact on the minimisation of climate change coming along with it. Additionally, construction of a kill switch is planned in order to avoid any possible risk in case E. cowli escapes into the environment. Furthermore, the application of E. cowli as a part of a barn filter system prevents every risk of its integration into the cow's rumen.
Working with Methane
Due to the fact that we had to use methane during the experiments with Methylococcus capsulatus and our transformed E. cowli various security aspects had to be considered. Since methane is a flammable gas which, when mixed with air in a certain ratio, is also explosive we took the following safety precautions: The setup was exclusively handled with the correct ratio of methane, air and carbon dioxide under a hood without power sockets or other potential sources of electrical sparks or fire. All experiments were conducted at methane-air-ratios under 5% (Lower Explosive or Flammable Limit LEL/LFL) and over 15% (Upper Explosive or Flammable Limit UEL/UFL) to eliminate the risk of a combustible atmosphere. Hence, we accepted suboptimal conditions for the purpose of safety concerns. Gas cylinders were stored according to the manufacturer’s instructions and closed completely when no experiment was running. Before using the respective gas for creating the needed ratio the system pressure of each cylinder was set to 1 bar. All equipment, including flow controllers, tubes and valves were screened for leak tightness regularly and their suitability for the used gas pressures.
Our Supporters
