Difference between revisions of "Part:BBa K523014"
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(characterize by SDU-Denmark) | (characterize by SDU-Denmark) | ||
− | It was not possible to detect that ''E.coli'' can live on cellubiose in fluid media ethier. On the figure below, it is shown that this biobrick cannot make ''E.coli'' grow only on cellobiose. It is compared to another biobrick that has the ability to degrade cellobiose <partinfo>BBa_K2449004</partinfo> | + | It was not possible to detect that ''E.coli'' can live on cellubiose in fluid media ethier. On the figure below, it is shown that this biobrick cannot make ''E.coli'' grow only on cellobiose. It is compared to another biobrick that has the ability to degrade cellobiose cep94A/<partinfo>BBa_K2449004</partinfo> |
<center> | <center> |
Revision as of 09:37, 31 October 2017
Plac + LacZ + bglX
The E. coli periplasmic β-glucosidase gene bglX under the control of the lac promoter. The native ribosome binding site is present.
Usage and Biology
The BglX β-glucosidase is expected to be localised to the periplasm. It ought to be capable of breaking down cellobiose.
MUG/MUC experiment
We (Edinburgh 2011) conducted two assays, comparing the activity of this part (Plac-bglX) with that of the exoglucanase cex under the control of the lac promoter (BBa_K523016) on two different substrates:
- 4-methylumbelliferyl β- D- glucuronide (MUG, left photo). This substrate is a cellobiose analog.
- 4-methylumbelliferyl β- D- cellobioside (MUC, right photo). This substrate is larger and is more like a cellulose analog.
Both substrates produce a fluorescent product when cleaved. Our plates below show the results of placing cell lysate and cell debris on an MUG plate and an MUC plate. Present on both plates are:
- Left side of plate: lysate/debris from JM109 expressing this part, K523014
- Right side of plate: lysate/debris from JM109 expressing exoglucanase cex, BBa_K523016
- Bottom of plate: lysate/debris from JM109 cells
MUG assay. bglX on left, cex on right. | MUC assay. bglX on left, cex on right. |
As can be seen, bglX is capable of degrading MUG (the cellobiose analog) while exoglucanase displays much weaker activity. By contrast, exoglucanase is much better at degrading MUC.
Inability to grow on cellobiose
We tested the ability of E. coli with this part to grow on minimal media with cellobiose as the only carbon source. It could not. By contrast, it did grow if glucose was the carbon source, showing that it is fundamentally capable of growing on minimal media.
Cellobiose as the only carbon source. K523014 (bottom) fails to grow. | Glucose as the only carbon source. K523014 can grow. |
E.coli in fluid media
(characterize by SDU-Denmark)
It was not possible to detect that E.coli can live on cellubiose in fluid media ethier. On the figure below, it is shown that this biobrick cannot make E.coli grow only on cellobiose. It is compared to another biobrick that has the ability to degrade cellobiose cep94A/BBa_K2449004
Figure 3:Growth on cellubiose comparing BBa_523014/bglX to BBa_2449004/cep94A compared
Conclusion
This biobrick does not work as intended.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 607
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal AgeI site found at 2266
Illegal AgeI site found at 2488
Illegal AgeI site found at 2677 - 1000COMPATIBLE WITH RFC[1000]