Difference between revisions of "Team:Harvard/Model"

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<h1>Pathway Model</h1>
 
<h1>Pathway Model</h1>
  
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<h3>1 Overview</h3>
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<p>Curli is the main proteinaceous component of the extracellular matrix naturally produced by *E. coli*. Although the main structural component is the self-assembling csgA monomer, there are a number of other proteins involved in its production and export. The curli production pathway can be broken down into two main modules: gene expression and translocation. The first, gene expression, is comprised of transcription and translation. Translocation can be further broken down into periplasmic export and extracellular secretion.</p>
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<h3>2 Gene Expression</h3>
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<h4>2.1 Transcription<h4>
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<p>
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The naturally occurring genes corresponding to curli are organized into csgBAC and csgDEFG operons. csgD is a regulatory protein, and thus is not applicable for the expression of foreign plasmids. Additionally, due to the additional protein domains fused to the csgA monomer, it is placed on a plasmid on its own (g<sub>csgA</sub>). The remaining genes are placed on another plasmid (g<sub>csgCEFG</sub>).
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The rate of transcription is mainly governed by the plasmid copy number and promoter strength.
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g<sub>csgA</sub> + RNA<sub>pol</sub> &rarr; g<sub>csgA</sub> + RNA<sub>pol</sub> + mRNA<sub>csgA</sub>
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$$g_{csgA}$$
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$\alpha$
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\[(Arab:AraC)\overset{K}{\rightarrow}mRNA\overset{\alpha}{\rightarrow}P\]
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</p>
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<h4>2.2 Translation<h4>
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<h3>3 Translocation</h3>
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<h4>3.1 Periplasmic export</h4>
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<h4>3.2 Extracellular secretion</h4>
 
</div>
 
</div>
  

Revision as of 15:40, 6 July 2017

Pathway Model

1 Overview

Curli is the main proteinaceous component of the extracellular matrix naturally produced by *E. coli*. Although the main structural component is the self-assembling csgA monomer, there are a number of other proteins involved in its production and export. The curli production pathway can be broken down into two main modules: gene expression and translocation. The first, gene expression, is comprised of transcription and translation. Translocation can be further broken down into periplasmic export and extracellular secretion.

2 Gene Expression

2.1 Transcription

The naturally occurring genes corresponding to curli are organized into csgBAC and csgDEFG operons. csgD is a regulatory protein, and thus is not applicable for the expression of foreign plasmids. Additionally, due to the additional protein domains fused to the csgA monomer, it is placed on a plasmid on its own (gcsgA). The remaining genes are placed on another plasmid (gcsgCEFG). The rate of transcription is mainly governed by the plasmid copy number and promoter strength. gcsgA + RNApol → gcsgA + RNApol + mRNAcsgA $$g_{csgA}$$ $\alpha$ \[(Arab:AraC)\overset{K}{\rightarrow}mRNA\overset{\alpha}{\rightarrow}P\]

2.2 Translation

3 Translocation

3.1 Periplasmic export

3.2 Extracellular secretion