Team:Brown/Project/Overview
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====Compact and user-friendly==== | ====Compact and user-friendly==== | ||
- | The physical bio-sensor envisioned by our team would be hand-held, consisting of a small compartment of bacterial cells with electrical probes fixed in this compartment. The probes feed information to a simple circuit within the sensor which monitors changes in the current of the bacterial solution and outputs that change via a simple LED light signal (See the "Application" below for more details). This novel electrical reporting system would enable any person with little or no knowledge of the machinery of the bio-sensor to utilize it effectively. | + | The physical bio-sensor envisioned by our team would be hand-held, consisting of a small compartment of bacterial cells with electrical probes fixed in this compartment. The probes feed information to a simple circuit within the sensor which monitors changes in the current of the bacterial solution and outputs that change via a simple LED light signal (See the "Application" below for more details). This novel electrical reporting system would enable any person with little or no knowledge of the machinery of the bio-sensor to utilize it effectively. Additionally, in comparison to a physical detection system, in which the number and surface area of the probes are fixed and limited, with a biological system, there are billions of bacteria, each with the ability to sense. |
====Economically feasible==== | ====Economically feasible==== | ||
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- | [[Image:BrownPorta chem sensor.png|left|thumb| | + | [[Image:BrownPorta chem sensor.png|left|thumb|450px|The proposed biosensor]]</div></td> |
- | <td><div align="center">[[Image:Cyclic.jpg|left|thumb| | + | <td><div align="center">[[Image:Cyclic.jpg|left|thumb|390px|Current Water Contamination Machinery]]</div></td> |
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*Possible use in biofilms | *Possible use in biofilms | ||
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+ | =Overview Presentation= | ||
+ | Presented before the Faculty Advising Committee at Brown University, April 9 2008 | ||
+ | <html> | ||
+ | <div style="width:425px;text-align:left" id="__ss_695236"><a style="font:14px Helvetica,Arial,Sans-serif;display:block;margin:12px 0 3px 0;text-decoration:underline;" href="http://www.slideshare.net/neilparikh/brown-igem-toxipop-presentation-presentation?type=powerpoint" title="Brown iGEM Toxipop Presentation"></a><object style="margin:0px" width="425" height="355"><param name="movie" value="http://static.slideshare.net/swf/ssplayer2.swf?doc=resistance-4-updates-1225059052545214-8&rel=0&stripped_title=brown-igem-toxipop-presentation-presentation" /><param name="allowFullScreen" value="true"/><param name="allowScriptAccess" value="always"/><embed src="http://static.slideshare.net/swf/ssplayer2.swf?doc=resistance-4-updates-1225059052545214-8&rel=0&stripped_title=brown-igem-toxipop-presentation-presentation" type="application/x-shockwave-flash" allowscriptaccess="always" allowfullscreen="true" width="425" height="355"></embed></object></div></html> |
Latest revision as of 03:57, 30 October 2008
Project OverviewInspired by the need for a simple, inexpensive, and portable means of toxin detection, Brown University’s Team Toxipop wanted to create a biosensor that utilizes a novel method to detect the presence of a toxin in a solution of bacteria. After a great deal of brainstorming and research, our team finalized on a design for our project that interfaces both biological and electrical systems. Our design is primarily based on a list that our team compiled of ideal bio-sensor guidelines: Biological
Engineering
Minimal biological machineryOur biological construct consists of three interacting proteins under the control of a single promoter. Such a simple construct increases efficiency and minimizes sources of error in the system. Direct induction of system by inducer optimizes sensitivityThe triggering of the lysis gene cassette is directly influenced by inducer presence, creating a sensitive system that should maintain a constant gain. Versatile constructThe simplicity of our construct lends to its versatility. The promoter controlling the lysis cassette can easily be interchanged, optimizing our system's potential to detect several different types of toxins and other substances. For example, a mercury-induced, arsenic-induced, or lead-induced promoter, all of which have been introduced by iGEM teams in the past, could be placed in control of the lysis cassette, creating three separate and specific toxin detection systems. Compact and user-friendlyThe physical bio-sensor envisioned by our team would be hand-held, consisting of a small compartment of bacterial cells with electrical probes fixed in this compartment. The probes feed information to a simple circuit within the sensor which monitors changes in the current of the bacterial solution and outputs that change via a simple LED light signal (See the "Application" below for more details). This novel electrical reporting system would enable any person with little or no knowledge of the machinery of the bio-sensor to utilize it effectively. Additionally, in comparison to a physical detection system, in which the number and surface area of the probes are fixed and limited, with a biological system, there are billions of bacteria, each with the ability to sense. Economically feasibleE. coli bacteria, which provide the main machinery of the bio-sensor, are inexpensive to obtain, grow, and store. Additionally, after consultation with mechanical engineers, we discovered that the circuit required for our proposed system would be simple to create and inexpensive to produce, in the range of a few dollars.
ApplicationThe proposed prototype for Team Toxipop's biosensor is pictured on above on the left. It would be inexpensive to produce, portable, and user-friendly compared to a current water detection system, as pictured above on the right.
Other ApplicationsAfter some brainstorming, the team came up with some other possible applications for our electrical reporting system and our auto-lysis cassette:
The auto-lysis device could have several applications, some of which are listed below:
Overview PresentationPresented before the Faculty Advising Committee at Brown University, April 9 2008 |