Team:Warsaw/Safety

From 2013.igem.org

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Here we present answers to questions from safety forms.
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Here we present answers to questions asked in safety forms.
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| BBa_K1093000
| BBa_K1093000
| PartsRegistry BBa_I746909
| PartsRegistry BBa_I746909
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| Aequorea victoria
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| ''Aequorea victoria''
| 1
| 1
| fluorescence
| fluorescence
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| BBa_K1093001
| BBa_K1093001
| PartsRegistry BBa_I746909
| PartsRegistry BBa_I746909
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| Aequorea victoria
+
| ''Aequorea victoria''
| 1
| 1
| fluorescence
| fluorescence
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| BBa_K1093002
| BBa_K1093002
| PartsRegistry BBa_I746909
| PartsRegistry BBa_I746909
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| Aequorea victoria
+
| ''Aequorea victoria''
| 1
| 1
| fluorescence
| fluorescence
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| BBa_K1093003
| BBa_K1093003
| PartsRegistry BBa_I746909
| PartsRegistry BBa_I746909
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| Aequorea victoria
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| ''Aequorea victoria''
| 1
| 1
| fluorescence
| fluorescence
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| BBa_K1093004
| BBa_K1093004
| PartsRegistry BBa_I746909
| PartsRegistry BBa_I746909
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| Aequorea victoria
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| ''Aequorea victoria''
| 1
| 1
| fluorescence
| fluorescence
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| BBa_K1093005
| BBa_K1093005
| PartsRegistry BBa_I746909
| PartsRegistry BBa_I746909
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| Aequorea victoria
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| ''Aequorea victoria''
| 1
| 1
| fluorescence
| fluorescence
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| BBa_K1093006
| BBa_K1093006
| PartsRegistry BBa_I746909
| PartsRegistry BBa_I746909
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| Aequorea victoria
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| ''Aequorea victoria''
| 1
| 1
| fluorescence
| fluorescence
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| BBa_K1093007
| BBa_K1093007
| oligo.pl (complementary oligonucleotides)
| oligo.pl (complementary oligonucleotides)
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| Aequorea victoria
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| ''Aequorea victoria''
| 1
| 1
| fluorescence
| fluorescence
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| BBa_K1093008
| BBa_K1093008
| oligo.pl (complementary oligonucleotides)
| oligo.pl (complementary oligonucleotides)
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| Aequorea victoria
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| ''Aequorea victoria''
| 1
| 1
| fluorescence
| fluorescence
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| BBa_K1093009
| BBa_K1093009
| Synthesized, GeneRay
| Synthesized, GeneRay
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| Aequorea victoria
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| ''Aequorea victoria''
| 1
| 1
| fluorescence
| fluorescence
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| BBa_K1093010
| BBa_K1093010
| Synthesized, GeneRay
| Synthesized, GeneRay
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| Aequorea victoria
+
| ''Aequorea victoria''
| 1
| 1
| fluorescence
| fluorescence
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| BBa_K1093011
| BBa_K1093011
| Synthesized, GeneRay
| Synthesized, GeneRay
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| Aequorea victoria
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| ''Aequorea victoria''
| 1
| 1
| fluorescence
| fluorescence
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| BBa_K1093012
| BBa_K1093012
| Synthesized, GeneRay
| Synthesized, GeneRay
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| Aequorea victoria
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| ''Aequorea victoria''
| 1
| 1
| fluorescence
| fluorescence
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| BBa_K1093013
| BBa_K1093013
| Synthesized, GeneRay
| Synthesized, GeneRay
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| Aequorea victoria, Homo sapiens
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| ''Aequorea victoria, Homo sapiens''
| 1
| 1
| fluorescence/gluthatione-dependent redox enzyme
| fluorescence/gluthatione-dependent redox enzyme
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| BBa_K1093013
| BBa_K1093013
| Synthesized, GeneRay
| Synthesized, GeneRay
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| Aequorea victoria, Escherichia coli
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| ''Aequorea victoria, Escherichia coli''
| 1
| 1
| fluorescence/ gluthatione-dependent redox enzyme
| fluorescence/ gluthatione-dependent redox enzyme
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| BBa_K1093014
| BBa_K1093014
| PartsRegistry BBa_E0040
| PartsRegistry BBa_E0040
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| Aequorea victoria
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| ''Aequorea victoria''
| 1
| 1
| fluorescence
| fluorescence
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| BBa_K1093015
| BBa_K1093015
| PartsRegistry BBa_E0040
| PartsRegistry BBa_E0040
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| Aequorea victoria
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| ''Aequorea victoria''
| 1
| 1
| fluorescence
| fluorescence
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| BBa_K1093016
| BBa_K1093016
| PartsRegistry BBa_J06505
| PartsRegistry BBa_J06505
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| Discosoma sp.
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| ''Discosoma sp.''
| 1
| 1
| fluorescence
| fluorescence
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| BBa_K1093017
| BBa_K1093017
| PartsRegistry BBa_J06505
| PartsRegistry BBa_J06505
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| Discosoma sp.
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| ''Discosoma sp.''
| 1
| 1
| fluorescence
| fluorescence
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| BBa_K1093018
| BBa_K1093018
| PartsRegistry BBa_E2050
| PartsRegistry BBa_E2050
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| Discosoma sp.
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| ''Discosoma sp.''
| 1
| 1
| fluorescence
| fluorescence
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| BBa_K1093019
| BBa_K1093019
| PartsRegistry BBa_E2050
| PartsRegistry BBa_E2050
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| Discosoma sp.
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| ''Discosoma sp.''
| 1
| 1
| fluorescence
| fluorescence
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| BBa_K1093020
| BBa_K1093020
| Synthesized, GeneRay
| Synthesized, GeneRay
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| Homo sapiens, Aequorea victoria
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| ''Homo sapiens, Aequorea victoria''
| 1
| 1
| oxygen transport
| oxygen transport
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| BBa_K1093021
| BBa_K1093021
| Synthesized, GeneRay
| Synthesized, GeneRay
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| Homo sapiens, Aequorea victoria
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| ''Homo sapiens, Aequorea victoria''
| 1
| 1
| oxygen transport
| oxygen transport
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| BBa_K1093022
| BBa_K1093022
| Synthesized, GeneRay
| Synthesized, GeneRay
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| Homo sapiens
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| ''Homo sapiens''
| 1
| 1
| oxygen transport
| oxygen transport
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| BBa_K1093023
| BBa_K1093023
| Synthesized, GeneRay
| Synthesized, GeneRay
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| Escherichia coli, bacteriophage T4
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| ''Escherichia coli'', bacteriophage T4
| 1
| 1
| lysis/cell division
| lysis/cell division
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| BBa_K1093024
| BBa_K1093024
| Synthesized, GeneRay
| Synthesized, GeneRay
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| Escherichia coli, bacteriophage T4, Vibrio fisheri
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| ''Escherichia coli'', bacteriophage T4, ''Vibrio fisheri''
| 1
| 1
| lysis/cell division/quorum sensing
| lysis/cell division/quorum sensing
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| BBa_K1093025
| BBa_K1093025
| Synthesized, GeneRay
| Synthesized, GeneRay
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| Escherichia coli
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| ''Escherichia coli''
| 1
| 1
| cell division
| cell division
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| BBa_K1093026
| BBa_K1093026
| Synthesized, GeneRay
| Synthesized, GeneRay
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| Homo sapiens
+
| ''Homo sapiens''
| 1
| 1
| transcription factor
| transcription factor
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| BBa_K1093027
| BBa_K1093027
| Synthesized, GeneRay
| Synthesized, GeneRay
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| Homo sapiens
+
| ''Homo sapiens''
| 1
| 1
| transcription factor
| transcription factor
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| BBa_K1093028
| BBa_K1093028
| Synthesized, GeneRay
| Synthesized, GeneRay
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| Homo sapiens
+
| ''Homo sapiens''
| 1
| 1
| transcription factor
| transcription factor
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| BBa_K1093029
| BBa_K1093029
| Synthesized, GeneRay
| Synthesized, GeneRay
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| Homo sapiens
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| ''Homo sapiens''
| 1
| 1
| oxygen transport
| oxygen transport
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'''a. Please provide a link to your institution biosafety guidelines.'''
'''a. Please provide a link to your institution biosafety guidelines.'''
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Our instituion does not have any specific biosafety guidelines. ?
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Our institution does not have any specific biosafety guidelines.It is using the ones present at the Faculty of  Biology or the one present in the Institute of Biochemistry and Biophysics.
'''b. Does your institution have an Institutional Biosafety Committee, or an equivalent group? If yes, have you discussed your project with them? Describe any concerns they raised with your project, and any changes you made to your project plan based on their review.'''
'''b. Does your institution have an Institutional Biosafety Committee, or an equivalent group? If yes, have you discussed your project with them? Describe any concerns they raised with your project, and any changes you made to your project plan based on their review.'''
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There is no group of this kind at our institution.
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There is no group of this kind at our institution.But our project has been discussed with many experienced researchers that know well biosafety and they didn't raise any concerns.
'''c. Does your country have national biosafety regulations or guidelines? If so, please provide a link to these regulations or guidelines if possible.'''
'''c. Does your country have national biosafety regulations or guidelines? If so, please provide a link to these regulations or guidelines if possible.'''
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'''4. How did you physically acquire the organism or part?'''
'''4. How did you physically acquire the organism or part?'''
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We’ve obtained the cell lines from Institute of Genetics and Biotechnology.
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We have obtained the cell lines from the Institute of Genetics and Biotechnology.
'''5. What potential safety/health risks to team members, other people at your institution, or the general public could arise from your use of this organism/part?'''
'''5. What potential safety/health risks to team members, other people at your institution, or the general public could arise from your use of this organism/part?'''
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None. Mammalian cells that we’re using are unharmful for people and environment.  
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None. Mammalian cells that we are using are not harmful for people and environment.  
'''6. What measures do you intend to take to ensure that your project is safe for team members, other people at your institution, and the general public?'''
'''6. What measures do you intend to take to ensure that your project is safe for team members, other people at your institution, and the general public?'''
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'''8. Why do you need to use this organism/part? Is there an organism/part from a less dangerous Risk Group that would accomplish the same purpose?'''
'''8. Why do you need to use this organism/part? Is there an organism/part from a less dangerous Risk Group that would accomplish the same purpose?'''
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We are using different cell lines to demonstrate cytotoxic effect of acrylamide. As our work with  
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We are using different cell lines to demonstrate cytotoxic effects of acrylamide. As our work with  
mammalian cells is absolutely safe, there is no need to search for another solutions.
mammalian cells is absolutely safe, there is no need to search for another solutions.
'''9. Is the organism/part listed under the Australia Group guidelines, or otherwise restricted for transport? If so, how will your team ship this part to iGEM and the Jamborees?'''
'''9. Is the organism/part listed under the Australia Group guidelines, or otherwise restricted for transport? If so, how will your team ship this part to iGEM and the Jamborees?'''
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We are not going to ship the cell lines to iGEM. We’ll only present the outcomes on the Jamborees.
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We are not going to ship the cell lines to iGEM. We will only present the outcomes on the Jamborees.
'''10. Please describe the BioSafety Level of the lab in which the team works, or description of safety features of lab (Refer to Basic Safety form, question 8. d.). If you are using organisms with a BSL level greater than you lab, please explain any additional safety precautions you are taking.'''
'''10. Please describe the BioSafety Level of the lab in which the team works, or description of safety features of lab (Refer to Basic Safety form, question 8. d.). If you are using organisms with a BSL level greater than you lab, please explain any additional safety precautions you are taking.'''
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* placing materials to be decontaminated outside the cell lab in a durable, leak proof containers
* placing materials to be decontaminated outside the cell lab in a durable, leak proof containers
* using disposable glassware  
* using disposable glassware  
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* carefull management of glassware, especially broken pipettes must be handled carefully
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* careful management of glassware, especially broken pipettes must be handled carefully
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Lysozyme/holin-based lysis device (BBa_K112808) has been described in detail. While it is highly efficient in releasing proteins into the medium (thus making it ideal for our hemoglobin-based sensor), its creators concluded it did not meet their expectations as a kill switch, since a fraction of bacterial population usually adapted and was selected for following the device induction. Our initial idea was to improve upon this design by adding MinC protein to the system (cell division inhibitor, initialy tested by Warsaw 2010 Team). This brute force approach can be summarised by a simple pictorial:
Lysozyme/holin-based lysis device (BBa_K112808) has been described in detail. While it is highly efficient in releasing proteins into the medium (thus making it ideal for our hemoglobin-based sensor), its creators concluded it did not meet their expectations as a kill switch, since a fraction of bacterial population usually adapted and was selected for following the device induction. Our initial idea was to improve upon this design by adding MinC protein to the system (cell division inhibitor, initialy tested by Warsaw 2010 Team). This brute force approach can be summarised by a simple pictorial:
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[[File:Kill direct.png|700px|thumb|left|alt=A|Kill switch - the simple version BBa_K1093023]]
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[[File:Kill direct.png|700px|thumb|center|alt=A|Kill switch - the simple version BBa_K1093023]]
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We soon began to consider alternative solutions. Wouldn't it be better to inhibit cell division before inducing the lysis (and thus applying strong selective pressure against the effective expression of lysis device)? After all, MinC doee not inhibit bacterial growth or DNA replication, but it does prevent division. Thus even a few copies of kill switch without deleterious mutations preserved within the long filamentous bacterium should be sufficient to cause cell death. This reasoning lead us to the following design:
We soon began to consider alternative solutions. Wouldn't it be better to inhibit cell division before inducing the lysis (and thus applying strong selective pressure against the effective expression of lysis device)? After all, MinC doee not inhibit bacterial growth or DNA replication, but it does prevent division. Thus even a few copies of kill switch without deleterious mutations preserved within the long filamentous bacterium should be sufficient to cause cell death. This reasoning lead us to the following design:
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[[File:Kill delayed.png|700px|thumb|center|alt=A|Kill switch - the version with delayed lysis BBa_K1093024]]
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[[File:Kill delayed.png|700px|thumb|left|alt=A|Kill switch - the version with delayed lysis BBa_K1093024]]
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This design applies LuxI/LuxR-based countdown device in order to separate the expression of MinC and lysis device. Eventually, we decided to test both approaches.  
This design applies LuxI/LuxR-based countdown device in order to separate the expression of MinC and lysis device. Eventually, we decided to test both approaches.  
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Due to their size, synthesis of complete constructs would not be practical, both financially and timewise. The sequence of the simpler version was divided into two subparts. The delayed version was divided into five smaller fragments. Despite this effort, we only received two fragments of our kill switch prior to wiki freeze.
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Due to their size, synthesis of complete construct would not be practical, both financially and timewise. The sequence of the simpler version was divided into two subparts. The delayed version was divided into five smaller fragments. Despite this effort, we only received two fragments of kill switch prior to wiki freeze.
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[[File:Warsaw_Kill_swich_1.png|thumb|left|alt=A|Kill switch 1 - kinetic differential equations]]
[[File:Warsaw_Kill_swich_1.png|thumb|left|alt=A|Kill switch 1 - kinetic differential equations]]
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[[File:Warsaw_Kill_swich_2.png|thumb|rigth|alt=A|Kill switch 2 - kinetic differential equations]]
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The behavior of any genetic circuit can be described using ordinary differential equations (ODE) formalism. In our case we decided to applied ODE due to its relative simplicity. In this approximation a genetic circuit is treat similarly to a set of simple chemical reactions.  
The behavior of any genetic circuit can be described using ordinary differential equations (ODE) formalism. In our case we decided to applied ODE due to its relative simplicity. In this approximation a genetic circuit is treat similarly to a set of simple chemical reactions.  
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The first kill switch is relatively simple. Because the expression of repressor protein (Repr) is regulated by a constitutive promoter (pRepr), when temperature is 30 C its concentration is constant, hence expression of MinC, lysis protein 1 (LD1) and lysis protein 2 (LD2) is negligible. However, if the temperature is raised to 42 C the repressor is rapidly inactivated, which results in elevated expression of MinC, lysis protein 1 and lysis protein 2 which leads to cell disruption.  
The first kill switch is relatively simple. Because the expression of repressor protein (Repr) is regulated by a constitutive promoter (pRepr), when temperature is 30 C its concentration is constant, hence expression of MinC, lysis protein 1 (LD1) and lysis protein 2 (LD2) is negligible. However, if the temperature is raised to 42 C the repressor is rapidly inactivated, which results in elevated expression of MinC, lysis protein 1 and lysis protein 2 which leads to cell disruption.  
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The second kill switch is more complicated since it contains the so called "countdown device" based on quorum sensing system. In this circuit LuxR and Repr are under a constitutive promoter. In normal temperature an inactive transcription factor LuxR is expressed. On the other hand, LuxI (which expression is controlled by the pR promoter, along with MinC) is an enzyme capable of converting S-adenosyl-cysteine (PreM) to an active mediator (M), which acts as transcription factor upon binding M. The activated LuxR binds to pL promoter and this leads to expression of both lysis protein.  
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[[File:Warsaw_Kill_swich_2.png|thumb|rigth|alt=A|Kill switch 2 - kinetic differential equations]]
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The second kill switch is more complicated since it contains so called "countdown device" based on quorum sensing system. In this circuit LuxR and Repr are under a constitutive promoter. In normal temperature an inactive transcription factor LuxR is expressed. On the other hand, LuxI (which expression is controlled by the pR promoter, along with MinC) is an enzyme capable of converting S-adenosyl-cysteine (PreM) to an active mediator (M), which acts as transcription factor upon binding M. The activated LuxR binds to pL promoter and this leads to expression of both lysis protein.  
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Latest revision as of 03:19, 5 October 2013

Safety

Contents


Here we present answers to questions asked in safety forms.


Part 1

Please describe the chassis organism(s) you will be using for this project. If you will be using more than one chassis organism, provide information on each of them:

Species Strain Risk group Risk group soruce link Disease risk to humans
E. coli DH5 1 www.absa.org/riskgroups/bacteriasearch.php?genus=&species=coli Yes. May cause irritation to skin, eyes, and respiratory tract, may affect kidneys.
E. coli BL21 1 www.absa.org/riskgroups/bacteriasearch.php?genus=&species=coli Yes. May cause irritation to skin, eyes, and respiratory tract, may affect kidneys.
E. coli TOP10 1 www.absa.org/riskgroups/bacteriasearch.php?genus=&species=coli Yes. May cause irritation to skin, eyes, and respiratory tract, may affect kidneys.

3. List and describe all new or modified coding regions you will be using in your project. (If you use parts from the 2013 iGEM Distribution without modifying them, you do not need to list those parts.)

Part number. Where did you get the physical DNA for this part (which lab, synthesis company, etc) What species does this part originally come from? What is the Risk Group of the species? What is the function of this part, in its parent species?
BBa_K1093000 PartsRegistry BBa_I746909 Aequorea victoria 1 fluorescence
BBa_K1093001 PartsRegistry BBa_I746909 Aequorea victoria 1 fluorescence
BBa_K1093002 PartsRegistry BBa_I746909 Aequorea victoria 1 fluorescence
BBa_K1093003 PartsRegistry BBa_I746909 Aequorea victoria 1 fluorescence
BBa_K1093004 PartsRegistry BBa_I746909 Aequorea victoria 1 fluorescence
BBa_K1093005 PartsRegistry BBa_I746909 Aequorea victoria 1 fluorescence
BBa_K1093006 PartsRegistry BBa_I746909 Aequorea victoria 1 fluorescence
BBa_K1093007 oligo.pl (complementary oligonucleotides) Aequorea victoria 1 fluorescence
BBa_K1093008 oligo.pl (complementary oligonucleotides) Aequorea victoria 1 fluorescence
BBa_K1093009 Synthesized, GeneRay Aequorea victoria 1 fluorescence
BBa_K1093010 Synthesized, GeneRay Aequorea victoria 1 fluorescence
BBa_K1093011 Synthesized, GeneRay Aequorea victoria 1 fluorescence
BBa_K1093012 Synthesized, GeneRay Aequorea victoria 1 fluorescence
BBa_K1093013 Synthesized, GeneRay Aequorea victoria, Homo sapiens 1 fluorescence/gluthatione-dependent redox enzyme
BBa_K1093013 Synthesized, GeneRay Aequorea victoria, Escherichia coli 1 fluorescence/ gluthatione-dependent redox enzyme
BBa_K1093014 PartsRegistry BBa_E0040 Aequorea victoria 1 fluorescence
BBa_K1093015 PartsRegistry BBa_E0040 Aequorea victoria 1 fluorescence
BBa_K1093016 PartsRegistry BBa_J06505 Discosoma sp. 1 fluorescence
BBa_K1093017 PartsRegistry BBa_J06505 Discosoma sp. 1 fluorescence
BBa_K1093018 PartsRegistry BBa_E2050 Discosoma sp. 1 fluorescence
BBa_K1093019 PartsRegistry BBa_E2050 Discosoma sp. 1 fluorescence
BBa_K1093020 Synthesized, GeneRay Homo sapiens, Aequorea victoria 1 oxygen transport
BBa_K1093021 Synthesized, GeneRay Homo sapiens, Aequorea victoria 1 oxygen transport
BBa_K1093022 Synthesized, GeneRay Homo sapiens 1 oxygen transport
BBa_K1093023 Synthesized, GeneRay Escherichia coli, bacteriophage T4 1 lysis/cell division
BBa_K1093024 Synthesized, GeneRay Escherichia coli, bacteriophage T4, Vibrio fisheri 1 lysis/cell division/quorum sensing
BBa_K1093025 Synthesized, GeneRay Escherichia coli 1 cell division
BBa_K1093026 Synthesized, GeneRay Homo sapiens 1 transcription factor
BBa_K1093027 Synthesized, GeneRay Homo sapiens 1 transcription factor
BBa_K1093028 Synthesized, GeneRay Homo sapiens 1 transcription factor
BBa_K1093029 Synthesized, GeneRay Homo sapiens 1 oxygen transport


4. Do the biological materials used in your lab work pose any of the following risks? Please describe.

a. Risks to the safety and health of team members or others working in the lab?

Laboratory strains of E. coli are not pathogenic, thus they do not pose threat for anyone in the lab.

b. Risks to the safety and health of the general public, if released by design or by accident?

None of the biological materials we are working with this year can pose threat to safety and health of genral public.

c. Risks to the environment, if released by design or by accident?

The only materials possibly hazardous to the environment we are working with are plasmids containing genes coding resistance for antibiotics such as ampicillin, chloramphenicol and kanamycin.

d. Risks to security through malicious misuse by individuals, groups, or countries?

There is no possibility of malicious misuse.

5. If your project moved from a small-scale lab study to become widely used as a commercial/industrial product, what new risks might arise? (Consider the different categories of risks that are listed in parts a-d of the previous question.) Also, what risks might arise if the knowledge you generate or the methods you develop became widely available? (Note: This is meant to be a somewhat open-ended discussion question.)

Our project is not meant for public use in open environment. If our acrylamide sensor became widely used as a commercial product its area of usage would still be laboratories and other closed facilities. None of the biological parts, methods and ideas we developed introduce novelties that can be directly misused and therefore pose a risk to anyone.

6. Does your project include any design features to address safety risks? (For example: kill switches, auxotrophic chassis, etc.) Note that including such features is not mandatory to participate in iGEM, but many groups choose to include them.

Our project includes a kill switch. It is based on two components: MinC protein (which inhibits cell division) and T4 bateriophage derived lysis device. MinC expression will be induced firstly, to reduce the odds of bacteria adapting via negative selection. Expression of the lysis device will be delayed with the application of LuXI/LuxR timer device.

7. What safety training have you received (or plan to receive in the future)? Provide a brief description, and a link to your institution’s safety training requirements, if available.

As all students of University of Warsaw we received standard training in area of hygienic and safe work with special emphasis on matters connected to our area of study.

8. Under what biosafety provisions will / do you work?

We are working accoriding to the guidelines for conducting work with GMO issued by Polish government.

a. Please provide a link to your institution biosafety guidelines.

Our institution does not have any specific biosafety guidelines.It is using the ones present at the Faculty of Biology or the one present in the Institute of Biochemistry and Biophysics.

b. Does your institution have an Institutional Biosafety Committee, or an equivalent group? If yes, have you discussed your project with them? Describe any concerns they raised with your project, and any changes you made to your project plan based on their review.

There is no group of this kind at our institution.But our project has been discussed with many experienced researchers that know well biosafety and they didn't raise any concerns.

c. Does your country have national biosafety regulations or guidelines? If so, please provide a link to these regulations or guidelines if possible.

Yes, we do have such regulations: http://isap.sejm.gov.pl/DetailsServlet?id=WDU20010760811.

d. According to the WHO Biosafety Manual, what is the BioSafety Level rating of your lab? (Check the summary table on page 3, and the fuller description that starts on page 9.) If your lab does not fit neatly into category 1, 2, 3, or 4, please describe its safety features [see 2013.igem.org/Safety for help].

1

e. What is the Risk Group of your chassis organism(s), as you stated in question 1? If it does not match the BSL rating of your laboratory, please explain what additional safety measures you are taking.

The risk group of organisms is 1.

Part 2

1. Organism name and strain name or number.

Following mammalian cell lines:

  • HEK 293
  • HeLa
  • 143 B
  • SH SY5Y

2. Organism Risk Group:

As mammalian cells are not classified as microorganisms, they are not included in the ABSA Risk Group list

3. If you are using this organism as a chassis, write "chassis". If you are using a genetic part from the organism, give the name of the part and a brief description of what it does and why you are using it.

None of the above. See paragraph 8.

4. How did you physically acquire the organism or part?

We have obtained the cell lines from the Institute of Genetics and Biotechnology.

5. What potential safety/health risks to team members, other people at your institution, or the general public could arise from your use of this organism/part?

None. Mammalian cells that we are using are not harmful for people and environment.

6. What measures do you intend to take to ensure that your project is safe for team members, other people at your institution, and the general public?

As our work in the cell lab is safe and unharmful to others there is no need to undertake additional safety measurements. What we will be working on in our project is to check the cytotoxity of acrylamide. Our aim is to show how acrylamide may affect different tissues reflected by the cell lines derived from these tissues. We would like to examine how different concentrations of acrylamide may influence the cells and draw a parallel to living organisms.

7. If you are using only a part from the organism, and you believe the part by itself is not dangerous, explain why you believe it is not dangerous.

Question not relevant.

8. Why do you need to use this organism/part? Is there an organism/part from a less dangerous Risk Group that would accomplish the same purpose?

We are using different cell lines to demonstrate cytotoxic effects of acrylamide. As our work with mammalian cells is absolutely safe, there is no need to search for another solutions.

9. Is the organism/part listed under the Australia Group guidelines, or otherwise restricted for transport? If so, how will your team ship this part to iGEM and the Jamborees?

We are not going to ship the cell lines to iGEM. We will only present the outcomes on the Jamborees.

10. Please describe the BioSafety Level of the lab in which the team works, or description of safety features of lab (Refer to Basic Safety form, question 8. d.). If you are using organisms with a BSL level greater than you lab, please explain any additional safety precautions you are taking.

In our cell lab we obey all of the safety rules provided. Our supervisor familiarized us with the safety rules that are as follows:

  • wearing aprons and gloves while working in the lab
  • not drinking or eating in the lab
  • decontamination of stocks, and other materials before disposal, using an effective method.
  • placing materials to be decontaminated outside the cell lab in a durable, leak proof containers
  • using disposable glassware
  • careful management of glassware, especially broken pipettes must be handled carefully


Part 3

Kill switches: description

Lysozyme/holin-based lysis device (BBa_K112808) has been described in detail. While it is highly efficient in releasing proteins into the medium (thus making it ideal for our hemoglobin-based sensor), its creators concluded it did not meet their expectations as a kill switch, since a fraction of bacterial population usually adapted and was selected for following the device induction. Our initial idea was to improve upon this design by adding MinC protein to the system (cell division inhibitor, initialy tested by Warsaw 2010 Team). This brute force approach can be summarised by a simple pictorial:

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Kill switch - the simple version BBa_K1093023

We soon began to consider alternative solutions. Wouldn't it be better to inhibit cell division before inducing the lysis (and thus applying strong selective pressure against the effective expression of lysis device)? After all, MinC doee not inhibit bacterial growth or DNA replication, but it does prevent division. Thus even a few copies of kill switch without deleterious mutations preserved within the long filamentous bacterium should be sufficient to cause cell death. This reasoning lead us to the following design:

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Kill switch - the version with delayed lysis BBa_K1093024

This design applies LuxI/LuxR-based countdown device in order to separate the expression of MinC and lysis device. Eventually, we decided to test both approaches.

Due to their size, synthesis of complete constructs would not be practical, both financially and timewise. The sequence of the simpler version was divided into two subparts. The delayed version was divided into five smaller fragments. Despite this effort, we only received two fragments of our kill switch prior to wiki freeze.


Mathematical model of the kill switches

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Kill switch 1 - kinetic differential equations
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Kill switch 2 - kinetic differential equations


The behavior of any genetic circuit can be described using ordinary differential equations (ODE) formalism. In our case we decided to applied ODE due to its relative simplicity. In this approximation a genetic circuit is treat similarly to a set of simple chemical reactions.

The first kill switch is relatively simple. Because the expression of repressor protein (Repr) is regulated by a constitutive promoter (pRepr), when temperature is 30 C its concentration is constant, hence expression of MinC, lysis protein 1 (LD1) and lysis protein 2 (LD2) is negligible. However, if the temperature is raised to 42 C the repressor is rapidly inactivated, which results in elevated expression of MinC, lysis protein 1 and lysis protein 2 which leads to cell disruption.

The second kill switch is more complicated since it contains the so called "countdown device" based on quorum sensing system. In this circuit LuxR and Repr are under a constitutive promoter. In normal temperature an inactive transcription factor LuxR is expressed. On the other hand, LuxI (which expression is controlled by the pR promoter, along with MinC) is an enzyme capable of converting S-adenosyl-cysteine (PreM) to an active mediator (M), which acts as transcription factor upon binding M. The activated LuxR binds to pL promoter and this leads to expression of both lysis protein.