Team:Tokyo-NoKoGen/Project/aggregation
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<h2>Introduction</h2> | <h2>Introduction</h2> | ||
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+ | In our EcoTanker, the goal is to collect objective substance automatically by using <i>E. coli</i>. However, to collect substance, we have to collect the cell at first. So we aimed to construct a device, which signals <i>E. coli</i> to self-aggregate and we focused on a protein, Antigen 43. This protein is derived from <i>E. coli</i>.<br> | ||
+ | Antigen 43 consists of two protein subunits, α and β, with apparent molecular masses of about 50 and 53 kDa. The β subunit is attached to the cell surface via interaction with the β subunit, which is an integral outer membrane component (Fig.1). Antigen 43 has the N-terminal signal peptide and it directs translocation across the cytoplasmic membrane to the periplasm via the general secretory pathway. Subsequently, the β domain forms a β barrel structure in the outer membrane through which the β domain gains access to the cell exterior [1]. | ||
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Revision as of 11:59, 27 October 2010
Aggregation
Introduction
In our EcoTanker, the goal is to collect objective substance automatically by using E. coli. However, to collect substance, we have to collect the cell at first. So we aimed to construct a device, which signals E. coli to self-aggregate and we focused on a protein, Antigen 43. This protein is derived from E. coli.
Antigen 43 consists of two protein subunits, α and β, with apparent molecular masses of about 50 and 53 kDa. The β subunit is attached to the cell surface via interaction with the β subunit, which is an integral outer membrane component (Fig.1). Antigen 43 has the N-terminal signal peptide and it directs translocation across the cytoplasmic membrane to the periplasm via the general secretory pathway. Subsequently, the β domain forms a β barrel structure in the outer membrane through which the β domain gains access to the cell exterior [1].
Antigen 43 consists of two protein subunits, α and β, with apparent molecular masses of about 50 and 53 kDa. The β subunit is attached to the cell surface via interaction with the β subunit, which is an integral outer membrane component (Fig.1). Antigen 43 has the N-terminal signal peptide and it directs translocation across the cytoplasmic membrane to the periplasm via the general secretory pathway. Subsequently, the β domain forms a β barrel structure in the outer membrane through which the β domain gains access to the cell exterior [1].