Team:Edinburgh/Data

Data Overview

This page provides an overview of the purely biological aspects of our feasibility study, and links to the relevant Parts Registry pages.

Cell Surface Display System

(Further details are at the dedicated Cell Surface Display page.)

This system aims at achieving synergy between the enzymes by displaying them at high copy number on the cell's outer membrane. Ice Nucleation Protein is used as a carrier for display of the enzymes; it carries them to the outer membrane.

Schematic diagram

The completed system should contain:
  A promoter (BBa_K523000) controlling:
    an INP—Endoglucanase fusion (BBa_K523008 + BBa_K523011)
    an INP—β-glucosidase fusion (BBa_K523008 + BBa_K523004)
    an INP—Exoglucanase fusion (BBa_K523008 + BBa_K523009)

Ribosome Binding Sites are indicated as green ovals.

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

A test system to prove that BBa_K523008 can be used to carry proteins to the outer membrane uses a fusion of INP to Yellow Fluorescent Protein (YFP) instead.

Progress

We have:

• Shown that INP (BBa_K523008, based on BBa_K265008) can be used to carry proteins to the cell membrane, by constructing BBa_K523013.
• Made and tested a new β-glucosidase (bglX) BioBrick, BBa_K523002.
• Made bglX into a format compatible with our BioSandwich assembly protocol (BBa_K523004).
• Made new versions of other cellulases, in a format compatible with the BioSandwich protocol.
• Tested an old exoglucanase gene, BBa_K118022.
• Made fusions of INP to bglX (β-glucosidase) and cex (exoglucanase).

Phage Display System

(Further details are at the dedicated Phage Display page.)

This system aims at achieving synergy between the enzymes by displaying them on an M13 phage. The major coat protein pVIII is used as a carrier for display of the enzymes; it incorporates them into the phage.

Schematic diagram

The completed system should contain:
  A promoter (BBa_K523000) 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.

Progress

We have:

• Made and tested a new amylase (malS) BioBrick, BBa_K523001.
• Attempted to fuse it to the major coat protein pVIII.

BioSandwich

BioSandwich (RFC 81) is a new assembly protocol that we used.

Parts made using BioSandwich that we believe are correct (subject to final verification sequencing) include:

• BBa_K523013: PlacLacZ-INP-YFP
• BBa_K523019: PlacLacZ-INP-cex
• BBa_K523020: PlacLacZ-INP-bglX
• BBa_K523022: PlacLacZ-crtEIB

Favourite BioBricks

(A complete list of parts made during the project is found at the dedicated Parts page.)

BBa_K523000: Plac + lacZ; with 5' BglII site

Intended as a cloning vector (when present in pSB1C3), this part allows Blue/White selection of newly PCR'ed BioBricks. The PCR primers required are shorter than would be required using the standard method. It encodes LacZα; new BioBricks that have successfully replaced the part will be white on plates containing IPTG and Xgal. Parts created in this way will also be compatible with the BioSandwich assembly protocol. We proved this part worked by using it to create several other BioBricks.

BBa_K523006: Plac + malS

malS is a periplasmic E. coli amylase gene. It ought to be usable for a fusion to INP or pVIII. But to test its normal activity, we placed it under the control of the lac promoter in a high copy number plasmid. We found evidence of starch degrading activity.

BBa_K523013: Plac + INP-EYFP

A fusion of Ice Nucleation Protein and Enhanced Yellow Fluorescent Protein under the control of the Lac promoter. Fluoresces yellow under blue light. May be localised to the outer membrane.

BBa_K523014: Plac + bglX

bglX is a cryptic β-glucosidase gene from E. coli. It ought to be usable for a fusion to INP or pVIII. But to test its normal activity, we placed it under the control of the lac promoter in a high copy number plasmid. We found it to be capable of degrading the cellobiose analog, MUG.

Other BioBricks analysed

(More details of this are found at the dedicated Collaboration page. The information has also been added to the parts' "Experience" sections.)

[http://partsregistry.org/Part:BBa_K118022:Experience BBa_K118022]: C. fimi exoglucanase

At the same time as we tested bglX for activity, we also tested this old part's ability to degrade the cellobiose analog MUG (weak ability) and the cellulose analog MUC (strong ability).

[http://partsregistry.org/Part:BBa_K415151:Experience BBa_K415151]: p8-GR1

Supposed to encode a fusion of the pVIII protein to a GR1 zipper. It actually encodes part of the E. coli aminopeptidase N gene.

[http://partsregistry.org/Part:BBa_K392008:Experience BBa_K392008]: C. fimi β-glucosidase

We discovered that this part almost certainly starts its coding sequence at the second ATG present, not the first. This is highly relevant information for anyone trying to tune its expression via use of custom Ribosome Binding Sites.