Team:Edinburgh/Results

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Revision as of 17:28, 29 October 2008

Results and current status as of 29 October 2008. We are hoping to obtain some last-minute results to present at the Jamboree.

Overview

Our results are promising but our dream of using bacteria to convert cellulose into starch and β-carotene is still unrealised. Fortunately, the work will be continued by two undergraduate students after Christmas.

Cellulolysis device

cenA (endoglucanase) and cex (exoglucanase): Biobricks made and ribosome binding site added; ready to test. Last minute result: possible CenA activity detected using chromogenic substrate, but needs to be repeated and confirmed: hope for more results in our poster and talk at the Jamboree!
bglX (beta glucosidase): Biobrick made and ribosome binding site added; ready to test.
P_cstA (promoter): Biobrick made and tested - successful.
- P_cstA promoter assay with xylE as repoter

Glycogenesis device

glgC and glgC16 (ADP-glucose pyrophosphorylase, responsible for rate limiting step in glycogenesis): Biobricks made and tested - successful.

Starch synthesis device

su1 and iso2 (isoamylases): Work in progress - pre-BioBrick constructs in pSB1A2 have been made using the BABEL protocol, but it is still necessary to remove internal EcoRI sites before fully compliant BioBricks will be ready to test. This work will be continued in an undergraduate honours project.

Lycopene generator

dxs+crtE+crtB+crtI+crtY: Work in progress - encountered problem at final step. Assembly of the three genes crtE, crtBand crtI together in one construct has failed so consistently and in so many unexpected ways that we are starting to wonder whether this combination is toxic to our host strain under the growth conditions used, though there seems no obvious reason to expect this. Further experiments are required.

Limonene synthase device

dxs+LIMS+appY: Biobrick made - still being tested (last test failed to detect limonene synthesis).

@@ Line 27: / Line 27: @@
 ==Lycopene generator ==
 [[Image:Edinburgh Map4 BCarotene.jpg|150px]]
-* '''''dxs+crtE+crtB+crtI+crtY''''': Work in progress - encountered problem at final step.
+* '''''dxs+crtE+crtB+crtI+crtY''''': Work in progress - encountered problem at final step. Assembly of the three genes ''crtE, crtB''and ''crtI'' together in one construct has failed so consistently and in so many unexpected ways that we are starting to wonder whether this combination is toxic to our host strain under the growth conditions used, though there seems no obvious reason to expect this. Further experiments are required.
 ==Limonene synthase device==