Team:Edinburgh/Data
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* Shown that INP (<partinfo>BBa_K523008</partinfo>, based on <partinfo>BBa_K265008</partinfo>) can be used to carry proteins to the cell membrane, by constructing <partinfo>BBa_K523013</partinfo>. | * Shown that INP (<partinfo>BBa_K523008</partinfo>, based on <partinfo>BBa_K265008</partinfo>) can be used to carry proteins to the cell membrane, by constructing <partinfo>BBa_K523013</partinfo>. | ||
- | * Made and tested a new β-glucosidase BioBrick, <partinfo>BBa_K523002</partinfo>. | + | * Made and tested a new β-glucosidase ''(bglX)'' BioBrick, <partinfo>BBa_K523002</partinfo>. |
- | * Made new versions of other cellulases, in a format compatible with | + | * Made ''bglX'' into a format compatible with our BioSandwich assembly protocol (<partinfo>BBa_K523004</partinfo>). |
+ | * Made new versions of other cellulases, in a format compatible with the BioSandwich protocol. | ||
==Phage Display System== | ==Phage Display System== |
Revision as of 22:37, 13 September 2011
Data Overview
This page provides an overview of the purely biological aspects of our feasibility study, and links to the relevant Parts Registry pages.
Contents |
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
Progress
We have:
- Shown that INP (<partinfo>BBa_K523008</partinfo>, based on <partinfo>BBa_K265008</partinfo>) can be used to carry proteins to the cell membrane, by constructing <partinfo>BBa_K523013</partinfo>.
- Made and tested a new β-glucosidase (bglX) BioBrick, <partinfo>BBa_K523002</partinfo>.
- Made bglX into a format compatible with our BioSandwich assembly protocol (<partinfo>BBa_K523004</partinfo>).
- Made new versions of other cellulases, in a format compatible with the BioSandwich protocol.
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
Progress
We have:
- Made and tested a new amylase (malS) BioBrick, <partinfo>BBa_K523001</partinfo>.
- Attempted to fuse it to the major coat protein pVIII.
Favourite BioBricks
(A complete list of parts made during the project is found at the dedicated Parts page.)
- <partinfo>BBa_K523000</partinfo>: 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. 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.
- <partinfo>BBa_K523006</partinfo>: 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.
- <partinfo>BBa_K523013</partinfo>: 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.
- <partinfo>BBa_K523014</partinfo>: 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.