Team:Tokyo Tech/Safety

From 2014.igem.org

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<li><a href="#">Experiment</a>
<li><a href="#">Experiment</a>
  <ul>
  <ul>
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        <li><a href="https://2014.igem.org/Team:Tokyo_Tech/Experiment/C4HSL-dependent_3oxoC12HSL_production" style="width:400px; margin-left:-135px;">C4HSL-dependent 3oxoC12HSL production</a></li>
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        <li><a href="https://2014.igem.org/Team:Tokyo_Tech/Experiment/Prhl_reporter_assay" style="width:400px; margin-left:-135px;">Prhl reporter assay </a></li>
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        <li><a href="https://2014.igem.org/Team:Tokyo_Tech/Experiment/3oxoC12HSL-dependent_C4HSL_production" style="width:400px; margin-left:-135px;">3oxoC12HSL-dependent C4HSL production</a></li>
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        <li><a href="https://2014.igem.org/Team:Tokyo_Tech/Experiment/C4HSL-dependent_3OC12HSL_production" style="width:400px; margin-left:-135px;">C4HSL-dependent 3OC12HSL production</a></li>
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        <li><a href="https://2014.igem.org/Team:Tokyo_Tech/Experiment/3OC12HSL-dependent_C4HSL_production" style="width:400px; margin-left:-135px;">3OC12HSL-dependent C4HSL production</a></li>
        <li><a href="https://2014.igem.org/Team:Tokyo_Tech/Experiment/Symbiosis_confirmation_by_co-culture" style="width:400px; margin-left:-135px;">Symbiosis confirmation by co-culture </a></li>
        <li><a href="https://2014.igem.org/Team:Tokyo_Tech/Experiment/Symbiosis_confirmation_by_co-culture" style="width:400px; margin-left:-135px;">Symbiosis confirmation by co-culture </a></li>
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        <li><a href="https://2014.igem.org/Team:Tokyo_Tech/Experiment/Prhl_reporter_assay" style="width:400px; margin-left:-135px;">Prhl reporter assay </a></li>
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        <li><a href="https://2014.igem.org/Team:Tokyo_Tech/Experiment/Transporter_assay" style="width:400px; margin-left:-135px;">Transporter assay</a></li>
 
 
  </ul>
  </ul>

Revision as of 09:54, 12 October 2014

Tokyo_Tech

Safety

Safety informations for our organisms
 
Safety Form
 
 
1.) Your Training
 
a.) Have your team members received any safety training yet?
- Yes,we have already received safety training.
 
b) Please briefly describe the topics that you learned about (or will learn about) in your safety training.
- Microbiological experiments (including recombinant DNA) Safety in Recombinant DNA Experiments
 
c) Please give a link to the laboratory safety training requirements of your institution (college, university, community lab, etc). Or, if you cannot give a link, briefly describe the requirements.
- SAFETY HANDBOOK wrote by Committee for Practice on management of Safety in Tokyo Institure Microbiological experiments (including recombinant DNA)
 
 
2.) Your Local Rules and Regulations
 
a) Who is responsible for biological safety at your institution? (You might have an Institutional Biosafety Committee, an Office of Environmental Health and Safety, a single Biosafety Officer, or some other arrangement.) Have you discussed your project with them? Describe any concerns they raised, and any changes you made in your project based on your discussion.
- Our institute has recombinant DNA committee
 
b) What are the biosafety guidelines of your institution? Please give a link to these guidelines, or briefly describe them if you cannot give a link.
- http://www.rpd.titech.ac.jp//rpdiv/somu/docs/idenshikumikaejikken_anzenkanrikisoku.pdf
 
c) In your country, what are the regulations that govern biosafety in research laboratories? Please give a link to these regulations, or briefly describe them if you cannot give a link.
- http://www.lifescience.mext.go.jp/bioethics/anzen.html
 
 
3.) The Organism and Parts that You Use
 
 

*Species: E. coli MG1655

 

*Risk Group: 1

*Risk Group Source: NIH Guidelines

*Disease risk to humans:No

*Part number/name: ppX

*Natural function of part: exopolyphosphatase

*How did you acquire it: made by PCR

*How will you use it?: exopolyphosphatase

 

*Species: E. coli MG1655

 

*Risk Group: 1

*Risk Group Source: NIH Guidelines

*Disease risk to humans:No

*Part number/name: phoU

*Natural function of part: regulation of the phosphate regulon

*How did you acquire it: made by PCR

*How will you use it?: regulation of the phosphate regulon

 

*Species: E. coli MG1655

 

*Risk Group: 1

*Risk Group Source: NIH Guidelines

*Disease risk to humans:No

*Part number/name: ydeD

*Natural function of part: transportation of cystein

*How did you acquire it: made by PCR

*How will you use it?: transportation of cystein

 

*Species: E. coli MG1655

 

*Risk Group: 1

*Risk Group Source: NIH Guidelines

*Disease risk to humans:No

*Part number/name: yfiK

*Natural function of part: transportation of cystein

*How did you acquire it: made by PCR

*How will you use it?: transportation of cystein

 

*Species: E. coli MG1655

 

*Risk Group: 1

*Risk Group Source: NIH Guidelines

*Disease risk to humans:No

*Part number/name: rpoS

*Natural function of part: regulation of transcription

*How did you acquire it: made by PCR

*How will you use it?: regulation of transcription, growth inhibition

 

*Species: E. coli MG1655

 

*Risk Group: 1

*Risk Group Source: NIH Guidelines

*Disease risk to humans:No

*Part number/name: crl

*Natural function of part: regulation of transcription, activagtor of rpoS

*How did you acquire it: made by PCR

*How will you use it?: regulation of transcription, activagtor of rpoS

 

*Species: Burkholderia glumae

 

*Risk Group: 2

*Risk Group Source: NIH Guidelines

*Disease risk to humans:No

*Part number/name: obcA

*Natural function of part: synthesis of oxalic acid

*How did you acquire it: Gene synthesis by IDT

*How will you use it?: synthesis of oxalic acid

 

*Species: E. coli MG1655

 

*Risk Group: 2

*Risk Group Source: NIH Guidelines

*Disease risk to humans:No

*Part number/name: obcB

*Natural function of part: synthesis of oxalic acid

*How did you acquire it: Gene synthesis by IDT

*How will you use it?: synthesis of oxalic acid

 
 
4.) Risks of Your Project Now
 
a) Risks to the safety and health of team members, or other people working in the lab:
- Without drinking large amount of sample, there is no risk.Such taking might cause irritation to skin,eyes,and respiratory tract.
 
b) Risks to the safety and health of the general public (if any biological materials escaped from your lab):
- Wihtout drinking large amount of sample, there is no risk.Such taking might cause irritation to skin,eyes,and respiratory tract.
 
c) Risks to the environment (from waste disposal, or from materials escaping from your lab):
- Production of AHL might perturbate communications in wild bacteria.
 
d) Risks to security through malicious mis-use by individuals, groups, or countries:
- Use of plant hormone in the opposite direction could disrupt growth of crops.Malicious usage of phage might pertubate intestinal flora.
 
e) What measures are you taking to reduce these risks? (For example: safe lab practices, choices of which organisms to use.)
- Do not eat,drink,smoke,prepare or store foods in laboratories.
     - Wear a lab-coat(white coat) while you are in a bio-lab.
     - Keep the lab tidy and clean.
     - Put labels on containers.
     - Practice disinfection,sterilization,and washing hands.
 
5.) Risks of Your Project in the Future
 
a) What new risks might arise from your project's growth? (Consider the categories of risk listed in parts a-d of the previous question: lab workers, the general public, the environment, and malicious mis-uses.) Also, what risks might arise if the knowledge you generate or the methods you develop became widely available?
- Excess produce of oxalic acid may cause urinary stone.(a)
     - We can farm any poisonous plants easily. (b)
     - Too many phosphate may cause contamination of environment.(c)
     - Diabetes patient may have danger if he or she intakes Cystein over 1500mg.(a)
 
b) Does your project currently include any design features to reduce risks? Or, if you did all the future work to make your project grow into a popular product, would you plan to design any new features to minimize risks? (For example: auxotrophic chassis, physical containment, etc.) Such features are not required for an iGEM project, but many teams choose to explore them.
- We have to consider potential risks in Bioremediation. When our project grow, limitation of solid use will be needed.