BME494 Project Group8: Difference between revisions

From OpenWetWare
Jump to navigationJump to search
Line 27: Line 27:
==ABSTRACT==
==ABSTRACT==
<!-- Below is the code for making a thumbnail image to embed in your text. See BME494_Wiki_Help for help with uploading images to OpenWetWare and using them on your page.-->
<!-- Below is the code for making a thumbnail image to embed in your text. See BME494_Wiki_Help for help with uploading images to OpenWetWare and using them on your page.-->
[[Image:BME494_placeholder|thumb|frame|left|Write a description of the image here]]  
[[Image:Ethanol-3d-balls 3-14-2012.png|thumb|180px|left|A ball-model of a ethanol molecule]]  


Our body has two enzymes that allow us to breakdown alcohol ADH (Ethanol – CH3CHO) and ALDH (CH3CHO -- CH3COOH). Our idea is to put these enzymes into Lactobacillus, a bacteria common in the intestinal track. Our modified bacteria can be put into yogurt and be administered by eating the yogurt. This will be more healthy then the drugs currently on the market for this purpose. Also these bacteria can stay in the gut for long periods of time increasing the treatment time.  
Our body has two enzymes that allow us to breakdown alcohol ADH (Ethanol – CH3CHO) and ALDH (CH3CHO -- CH3COOH). Our idea is to put these enzymes into Lactobacillus, a bacteria common in the intestinal track. Our modified bacteria can be put into yogurt and be administered by eating the yogurt. This will be more healthy then the drugs currently on the market for this purpose. Also these bacteria can stay in the gut for long periods of time increasing the treatment time. Our proof of concept will have a visual indicator to indicate how it is working, this is crucial for tuning. The first portion of our system is the control aspect and is a promoter that is repressed in the presence of ethanol and produces Green Florescent Protein (GFP). The second part of the system is induced in the presence of ethanol and produces the two proteins needed to break down ethanol and Red Florescent Protein (RFP), creating a visual indication of the production of the proteins.  


<!-- "<br>" is a line break. Line "returns" will not show up on a wiki page. You have to end lines of text with "<br>". I've added these to spread out the main sections -->
<!-- "<br>" is a line break. Line "returns" will not show up on a wiki page. You have to end lines of text with "<br>". I've added these to spread out the main sections -->

Revision as of 22:25, 14 March 2012

Home        People        Course Projects        Course Materials        Syllabus        Photos        Wiki Editing Help       

ABSTRACT

A ball-model of a ethanol molecule

Our body has two enzymes that allow us to breakdown alcohol ADH (Ethanol – CH3CHO) and ALDH (CH3CHO -- CH3COOH). Our idea is to put these enzymes into Lactobacillus, a bacteria common in the intestinal track. Our modified bacteria can be put into yogurt and be administered by eating the yogurt. This will be more healthy then the drugs currently on the market for this purpose. Also these bacteria can stay in the gut for long periods of time increasing the treatment time. Our proof of concept will have a visual indicator to indicate how it is working, this is crucial for tuning. The first portion of our system is the control aspect and is a promoter that is repressed in the presence of ethanol and produces Green Florescent Protein (GFP). The second part of the system is induced in the presence of ethanol and produces the two proteins needed to break down ethanol and Red Florescent Protein (RFP), creating a visual indication of the production of the proteins.






BACKGROUND

File:BME494 placeholder
Write a description of the image here

Alcohol, more specifically ethanol is the most abused drug in the United States [1]. There have been many ways that people have tried to help alcoholics with their problem, and one way is medical intervention. The theory behind our design is that if the alcohol is broken-down before it gets into the blood stream you can stop the person from getting drunk and stop the cycle of alcohol abuse.






PROOF OF CONCEPT DESIGN

  • New Natural Part: Why are you using this part? How did you find this part? What database/ resources did you use? What primers will you use to isolate it and turn it into a BioBrick?
  • Key Pre-existing Part: If you didn't need to use a new natural part, describe one important pre-existing BioBrick from the parts registry.org that you will use. Why are you using it? Describe how well-documented the part is. Do you trust it?


Assembly Scheme


File:BME494 placeholder







TESTING


Measurement



Expected Observations



Tuning Our System








HUMAN PRACTICES

OUR TEAM

Your Name
Your area of study/ academic program/ major, why you are taking BME494, and something interesting about yourself. You may add a link to your personal OWW page.


Your Name
Your area of study/ academic program/ major, why you are taking BME494, and something interesting about yourself. You may add a link to your personal OWW page.


Your Name
Your area of study/ academic program/ major, why you are taking BME494, and something interesting about yourself. You may add a link to your personal OWW page.


Your Name
Your area of study/ academic program/ major, why you are taking BME494, and something interesting about yourself. You may add a link to your personal OWW page.