Difference between revisions of "Part:BBa K2273037"
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A signal peptide ([https://parts.igem.org/Part:BBa_K2273023 AmyE SP]) was fused n-terminally to this construct to induce secretion. | A signal peptide ([https://parts.igem.org/Part:BBa_K2273023 AmyE SP]) was fused n-terminally to this construct to induce secretion. | ||
| − | [[File:Tag mCherry | + | [[File:Tag mCherry.png|thumb|centre|600px|'''Figure 1:''': Genetic constructs with mCherry. Depicted is a translational fusion construct downstream of the PxylA promotor, that was cloned in the multiple cloning site of the pBS2E<i><sub>PxylA</sub></i> vector. The constructs contain a signal peptide sequence, the gene coding for mCherry, n-terminally fused SpyTag and a his-tag.]] |
Revision as of 17:02, 1 November 2017
| Part Information | |
|---|---|
| RFC standard | RFC 25 |
| Fused Tag | BBa_K2273014: Spytag |
| Fluorescent Protein | BBa_K2273022: mCherry His-tagged |
| Submitted by | [http://2017.igem.org/Team:TU_Dresden TU Dresden] |
mCherry with N-Terminal SpyTag and C-Terminal His Tag
This composite part was used for evalutaion in the [http://2017.igem.org/Team:TU_Dresden/Project/Secretion secretion project] of 2017 TU_Dresden iGEM [http://2017.igem.org/Team:TU_Dresden team]. It codes for a fluorescent reporter protein (mCherry) and a functional tag (SpyTag), mediating covalent bonding with its tag partner (SpyCatcher). It is optimized for usage in Bacillus subtilis.
Design
A signal peptide (AmyE SP) was fused n-terminally to this construct to induce secretion.
Figure 1:: Genetic constructs with mCherry. Depicted is a translational fusion construct downstream of the PxylA promotor, that was cloned in the multiple cloning site of the pBS2EPxylA vector. The constructs contain a signal peptide sequence, the gene coding for mCherry, n-terminally fused SpyTag and a his-tag.
Application
The successful secretion could be proven with a fluorescence assay using the supernatants of B. subtilis (Figure 2). The functionality of the SpyTag/SpyCatcher was proven via SDS-PAGE, using the supernatants (Figure 3).
Figure 2:: Endpoint measurement of the fluorescence from supernatants carrying our constructs and the wild type. Expression of the single copy mCherry or sfGFP fusion SpyTag/SpyCather constructs (purple) was induced with 1% xylose and the supernatants were harvested after 16 h of incubation. Wild type supernatant is shown as a control (pink). Excitation wavelength for sfGFP was set to 480 nm and emission was recorded at 510 nm and for mCherry excitation wavelength was set to 585 nm and emission was recorded at 615 nm . The fluorescence was normalized by the optical density (OD600). Graph shows mean values and standard deviations of at least two biological and three technical replicates.
Figure 3: SDS gel with crude and purified supernatants. Expression of the multi copy mCherry constructs was induced with 1% Xylose and the supernatants were harvested after 16 h of incubation. The his-tagged proteins were purified with Ni-NTA agarose beads. Lane 1 was loaded with 3 µl of NEB´s “Color Prestained Protein Standard Broad Range” ladder. Crude (c) and purified (p) supernatant of wild-type (WT) are shown as a control in lane 2 and 3. Lane 4 and 5 contain the supernatant of B. subtilis producing mCherry-mini. SpyCatcher fusion protein (36,6 kDa). Lane 4 and 5 contain the supernatant of B. subtilis producing mCherry-SpyTag fusion protein (31,9 kDa). The crude supernatants of the two mCherry producing strains were combined, incubated for 4 h, purified and loaded onto lane 8 and 9. The fusion product of the mCherry constructs is visable in the crude and purified supernatant.