Team:Harvard/Parts

From 2008.igem.org

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(The Genetic Circuitry)
(The Genetic Circuitry)
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We were able to create three such inducible systems:
We were able to create three such inducible systems:
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[[Team:Harvard/GenProtocols| Notebook]]
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[[Team:Harvard/Parts/LacI| Lactose inducible system]]
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[[Harvard/Parts/LacI| Lactose inducible system]]
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[[Team:Harvard/Parts/Other| Tetracycline inducible system]]
[[Team:Harvard/Parts/Other| Tetracycline inducible system]]
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[http://2008.igem.org/Team:Harvard/Parts/Tempsenseci| Heat inducible system]
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[[Team:Harvard/Parts/Tempsenseci| Heat inducible system]]

Revision as of 02:45, 30 October 2008



Parts Submitted to Registry

You can find the complete list of parts we submitted to the registry here.

The Critical Gene: mtrB

Many genes are involved in S. oneidensis’s complex respiratory system (Heidelberg et al. 2002). We focused on mtrB, a 679-amino-acid-long outer membrane protein thought to be involved in the binding of metals and the localization of outer membrane cytochromes during reduction (Bretschger et al. 2007). It is unfortunately toxic in E. coli (Saffarini). Bretschger et al. recently characterized the role of mtrB in anaerobic respiration of S. oneidensis by looking at the effects of knock-out and complementation of mtrB on the electrical output of S. oneidensis. It was found that the strain which lacked mtrB produced less than 20% of the current generated by the wild type strain. In complemented strains, where mtrB is expressed constitutively under the control of the lacZ promoter in the knock-out strain, the phenotype was rescued with a similar amount of current being produced to that of the wild type (Bretschger et al. 2007). Not only does this experiment demonstrate the importance of mtrB in reduction in S. oneidensis, it also suggests a mechanism by which this electrical output could be controlled. Transforming plasmids containing mtrB under the control of an inducible promoter into mtrB knock out S. oneidensis, would conceivably create a strain of S. oneidensis which could increase its electrical output in response to the turning-on of the promoter controlling mtrB expression. The creation of a strain with an inducible electrical output could have important applications in biotechnology by creating a system which couples the ability of S. oneidensis to respond to a diverse array of stimuli with the speed and ubiquity of electricity.

The Genetic Circuitry

In order to control the expression of exogenous mtrB we sought to create several different inducible systems. As depicted below, these systems consist of a repressor under the control of a constitutive promoter (blue). In the default state, the repressor will bind to the downstream promoter (red), preventing RNA polymerase from attaching to the DNA strand to start transcription. Thus, in this state, mtrB is not expressed.

In the presence of an inducer, mtrB expression does occur. In this case, the inducer binds the repressor protein, preventing it from attaching to the DNA sequence of the promoter (green). RNA polymerase is therefore able to bind to the DNA at the promoter, allowing for expression of mtrB.

Induction results in mtrB expression


We were able to create three such inducible systems:

Lactose inducible system

Tetracycline inducible system

Heat inducible system