Team:Edinburgh/Data

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Data Page

The iGEM rules require us to have simple illustrations of how our devices work and where the Parts function in the system; and links to the Registry for the parts/constructs for which we have produced data.

See the sample Data page.


Cell Surface Display System

The completed system should contain:
  A promoter (<partinfo>BBa_K523000</partinfo>) controlling:
    an INP—Endoglucanase fusion (<partinfo>BBa_K523008</partinfo> + <partinfo>BBa_K523011</partinfo>)
    an INP—β-glucosidase fusion (<partinfo>BBa_K523008</partinfo> + <partinfo>BBa_K523010</partinfo>)
    an INP—Exoglucanase fusion (<partinfo>BBa_K523008</partinfo> + <partinfo>BBa_K523009</partinfo>)

Ribosome Binding Sites are indicated as green ovals.

Cellulose degradation is shown at top. In reality, tens of thousands of enzymes will cover the outer membrane in random places.

A test system to prove that <partinfo>BBa_K523008</partinfo> can be used to carry proteins to the outer membrane uses a fusion of INP to Yellow Fluorescent Protein (YFP) or the E. coli amylase MalS instead.


Phage Display System

The completed system should contain:
  A promoter (<partinfo>BBa_K523000</partinfo>) controlling:
    an Endoglucanase—pVIII fusion
    a β-glucosidase—pVIII fusion
    an Exoglucanase—pVIII fusion

Ribosome Binding Sites are indicated as green ovals. "Signal" means a periplasmic signal sequence, directing the protein to the periplasm to be assembled into the phage.

A test system uses a fusion of pVIII to E. coli amylase MalS instead.