Difference between revisions of "Team:Paris Saclay/Safety"

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<p>Students who were experimenting sometimes had to use dangerous chemical products. Extra precautions were taken to handle them :
 
<p>Students who were experimenting sometimes had to use dangerous chemical products. Extra precautions were taken to handle them :
  
[[File:T--Paris_Saclay--120916_tableau_safety_1.png|300px|thumb|right|Migration of pPS16_005(3.1) and pPS16_006(3.2)]]
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[[File:T--Paris_Saclay--120916_tableau_safety_1.png|300px|thumb|right]]
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<p>Contaminated waste was put in special trash, and packaged to be treated elsewhere in a safe manner.
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<p>Organisms and Biological parts used in experiments :
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[[File:T--Paris_Saclay--120916_tableau_safety_2.png|300px|thumb|right]]
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<p>Our project was designed to use two different strains of E. coli. These organisms are non-pathogenic chassis ranked in class 1. They do not induce any effects on humans and we could manipulate them safely without any special equipment in BLS 1 ( Biosafety Level 1) laboratory.
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<p>Biological parts:
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[[File:T--Paris_Saclay--120916_tableau_safety_3.png|300px|thumb|right]]
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<p>Biological parts we engineered were integrated in E.Coli. New activities of these engineered bacteria are not dangerous for human health. Especially dcas9 do not have nuclease activity. Besides RNA guide do not target human genes.
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<p>Since we generated genetically modified organisms, we had to make sure it was not spread in the environment. We put biological waste in special trashes which were heated at high temperature to kill microorganisms. Then it was treated as usual waste. Moreover dcas9 proteins were not integrated  into the genome of sexually reproducing organisms. By this way, we prevent new genes transfert to other organisms than E.Coli.
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<p>Our project in the future
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<p>Our project aims to develop a new molecular tool to bring closer DNA strands in bacterial cells. If we manage to achieve our project, this new biological tool could only be used by scientists interested in DNA conformation study.
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They will be able to target any DNA sequences by designing their own guide RNAs. In order to prevent physical injuries and genetically modified organisms spreading, they will have to take the same precautions we took during the internship listed above.
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<p>Conclusion:
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<p>To conclude our new tool will provide new possibilities in biology research. Scientists will be able to change DNA 3D organization and thus study links between DNA organization and cellular functions in bacteria. As our new tool will used only by scientists  it do not really pose new safety issues.
  
  

Revision as of 15:00, 12 September 2016

Introduction

Safety is a crucial issue in iGEM projects. As students imagine their own project, they have to make sure that their idea is not hazardous. Likewise, realization of the project in the lab is a second challenge for young students in terms of security. Working on living organisms and biological parts requires good laboratory practices in order to prevent spreading, contamination, or physical injuries.

A good laboratory practice:

To prevent disorder and accidents, the lab was divided in two parts : a wet laboratory for experiments and a dry laboratory for personal working. Students who were performing experiments were always wearing lab coats and kept experiment materials in the wet laboratory.

Chemical product handling :

Students who were experimenting sometimes had to use dangerous chemical products. Extra precautions were taken to handle them : [[File:T--Paris_Saclay--120916_tableau_safety_1.png|300px|thumb|right]]

Contaminated waste was put in special trash, and packaged to be treated elsewhere in a safe manner.

Organisms and Biological parts used in experiments : [[File:T--Paris_Saclay--120916_tableau_safety_2.png|300px|thumb|right]]

Our project was designed to use two different strains of E. coli. These organisms are non-pathogenic chassis ranked in class 1. They do not induce any effects on humans and we could manipulate them safely without any special equipment in BLS 1 ( Biosafety Level 1) laboratory.

Biological parts: [[File:T--Paris_Saclay--120916_tableau_safety_3.png|300px|thumb|right]]

Biological parts we engineered were integrated in E.Coli. New activities of these engineered bacteria are not dangerous for human health. Especially dcas9 do not have nuclease activity. Besides RNA guide do not target human genes.

Since we generated genetically modified organisms, we had to make sure it was not spread in the environment. We put biological waste in special trashes which were heated at high temperature to kill microorganisms. Then it was treated as usual waste. Moreover dcas9 proteins were not integrated into the genome of sexually reproducing organisms. By this way, we prevent new genes transfert to other organisms than E.Coli.

Our project in the future

Our project aims to develop a new molecular tool to bring closer DNA strands in bacterial cells. If we manage to achieve our project, this new biological tool could only be used by scientists interested in DNA conformation study. They will be able to target any DNA sequences by designing their own guide RNAs. In order to prevent physical injuries and genetically modified organisms spreading, they will have to take the same precautions we took during the internship listed above.

Conclusion:

To conclude our new tool will provide new possibilities in biology research. Scientists will be able to change DNA 3D organization and thus study links between DNA organization and cellular functions in bacteria. As our new tool will used only by scientists it do not really pose new safety issues.

On this page of your wiki, you should write about how you are addressing any safety issues in your project. The wiki is a place where you can go beyond the questions on the safety forms, and write about whatever safety topics are most interesting in your project. (You do not need to copy your safety forms onto this wiki page.)

Safe Project Design

Does your project include any safety features? Have you made certain decisions about the design to reduce risks? Write about them here! For example:

  • Choosing a non-pathogenic chassis
  • Choosing parts that will not harm humans / animals / plants
  • Substituting safer materials for dangerous materials in a proof-of-concept experiment
  • Including an "induced lethality" or "kill-switch" device
Safe Lab Work

What safety procedures do you use every day in the lab? Did you perform any unusual experiments, or face any unusual safety issues? Write about them here!

Safe Shipment

Did you face any safety problems in sending your DNA parts to the Registry? How did you solve those problems?