Difference between revisions of "Part:BBa K2924034"
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− | After 2 days’ growth, samples of 20 OD units were taken and used for protein measurements and SDS PAGE. The <i>Synechocystis</i> cells were disrupted using glass beads to shred the cells in a Precellys® 24 homogeniser. The cell extract was centrifuged to obtain a pellet of insoluble protein and a supernatant of soluble protein, which were separated | + | After 2 days’ growth, samples of 20 OD units were taken and used for protein measurements and SDS PAGE. The <i>Synechocystis</i> cells were disrupted using glass beads to shred the cells in a Precellys® 24 homogeniser. The cell extract was centrifuged to obtain a pellet of insoluble protein and a supernatant of soluble protein, which were separated <html> <a href="dx.doi.org/10.17504/protocols.io.ps6dnhe">(protocol)</a> </html>. |
The samples were used for an SDS-PAGE. A-s1-casein is a protein of approx. 25.4 kDa size. | The samples were used for an SDS-PAGE. A-s1-casein is a protein of approx. 25.4 kDa size. | ||
Revision as of 13:40, 18 October 2019
Pcpc560 + α-s1-casein + T1/T7 Terminator
Strong constitutive cyanobacterial promoter Pcpc560 expressing a-s1-casein with the T1/T7 double terminator.
The promoter was cloned into the pSHDY plasmid. The pSHDY plasmid is an RSF1010-based, low-copy self-replicating vector derived from pVZ321 and has a broad host range, which can ensure the conjugation from E. coli to cyanobacteria and other microorganisms1. After testing the strength of the promoter with a fluorescent reporter mVenus, it was used to express a protein from cow’s milk, a-s1-casein in Synechocystis sp. PCC 6803.
Usage and Biology
The Synechocystis cells were grown in 30 ml BG11 medium at 150 rpm, 1% CO2 and 80 µmol photons per second and square meter (80 µE).
The empty vector control (EVC) grew faster than the cultures with the heterologous protein, suggesting strong expression leading to a metabolic burden. The cells expressing mVenus had a higher metabolic burden because the gene was codon-optimized for Synechocystis , while the a-s1-casein gene was codon-optimized for E. coli.
After 2 days’ growth, samples of 20 OD units were taken and used for protein measurements and SDS PAGE. The Synechocystis cells were disrupted using glass beads to shred the cells in a Precellys® 24 homogeniser. The cell extract was centrifuged to obtain a pellet of insoluble protein and a supernatant of soluble protein, which were separated (protocol) . The samples were used for an SDS-PAGE. A-s1-casein is a protein of approx. 25.4 kDa size.
A band was visible slightly under 25 kDa, which was not visible in the empty vector control. This band is very likely the a-s1-casein protein, which ran slightly lower than expected. It is visible to a smaller degree in the insoluble protein fraction as well.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 1204
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
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