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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 ( | + | 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 (\(g_{csgA}\)). The remaining genes are placed on another plasmid (\(g_{csgCEFG}\)). |
− | The rate of transcription is | + | The rate of transcription is primarily governed by the plasmid copy number and promoter strength. |
− | + | $$g_{csgA} + RNA_{pol} \overset{K_{1}}{\rightarrow} g_{csgA} + RNA_{pol} + mRNA_{csgA}$$ | |
+ | $$g_{csgCEFG} + RNA_{pol} \overset{K_{1}}{\rightarrow} g_{csgCEFG} + RNA_{pol} + mRNA_{csgCEFG}$$ | ||
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</p> | </p> | ||
<h4>2.2 Translation<h4> | <h4>2.2 Translation<h4> |
Revision as of 15:46, 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 (\(g_{csgA}\)). The remaining genes are placed on another plasmid (\(g_{csgCEFG}\)). The rate of transcription is primarily governed by the plasmid copy number and promoter strength. $$g_{csgA} + RNA_{pol} \overset{K_{1}}{\rightarrow} g_{csgA} + RNA_{pol} + mRNA_{csgA}$$ $$g_{csgCEFG} + RNA_{pol} \overset{K_{1}}{\rightarrow} g_{csgCEFG} + RNA_{pol} + mRNA_{csgCEFG}$$