Team:UNAM Genomics Mexico/Modeling/Heavy Metal AND

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'''Metal AND'''<br /><br />
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[[File:UNAM_GENOMICS_MEXICO_AND_bf_hm.png | center]]
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Repressors<br />
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'''Repressors'''<br />
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(Tabla de verdad  de TFS)  https://2012.igem.org/File:UGM_tv_mtf.png
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[[File:UGM tv mtf.png | center]]
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Inputs<br />
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'''Inputs'''<br />
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(Tabla verdad inputs)  https://2012.igem.org/File:UGM_tv_mi.png  
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[[File:UGM tv mi.png |center]]
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<h2>'''Kappa'''</h2><br />
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There is no metal catabolism, so metals just reach an equilibrium and non-toxic concentration within the cell through exporting it out of the cytosol, maintaining the concentration constant. This makes the behavior of a single burst or a continuous dose similar, because the metal levels in just one dose will be constant since metals won’t be degraded. <br />
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[[File:6000metales.png | 400px]] [[File:Single an conti.png | 400px]]
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Revision as of 07:15, 25 October 2012


UNAM-Genomics_Mexico


AND's Results


Metal AND


Our system consists of a hybrid promoter which contains binding sites for two transcription factors that act as repressors, CzrA and ArsR. In the presence of Met1, CzrA losses affinity for its binding site.

Similarly, if there is Met2 in the cell, ArsR also dissociates itself from its binding site. Taking into account these facts, unless Met1 and Met2 are present in the culture, we can say that the genes under this hybrid promoter will be repressed, just like a AND gate should function!

UNAM GENOMICS MEXICO AND bf hm.png

Repressors

UGM tv mtf.png

Inputs

UGM tv mi.png


Kappa



There is no metal catabolism, so metals just reach an equilibrium and non-toxic concentration within the cell through exporting it out of the cytosol, maintaining the concentration constant. This makes the behavior of a single burst or a continuous dose similar, because the metal levels in just one dose will be constant since metals won’t be degraded.


6000metales.png Single an conti.png