Difference between revisions of "Part:BBa K4321005"
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<partinfo>BBa_K4321005 short</partinfo> | <partinfo>BBa_K4321005 short</partinfo> | ||
− | pCG004 is an E.coli - Bacillus subtilis shuttle plasmid that was created based off of the pHT01 plasmid. This plasmid contains | + | pCG004 is an E.coli - Bacillus subtilis shuttle plasmid that was created based off of the pHT01 plasmid. This plasmid contains serval features that can be used to selectively expressed desired genes inserted within this dropout region. The dropout region contains a green fluorescent protein (GFP) flanked by BsaI sites. Upstream of this region is the lacI sequence (encodes a lac repressor), and an overlapping lac operator (lacO) and pgrac promoter. |
+ | |||
+ | When IPTG is not present, the lac repressor (LacI) is expressed and bound to lacO. Due the to overlap between lacO and pGrac, downstream expression from Pgrac cannot occur due to promoter unavailability. This results in the repression of the downstream genes. When IPTG is present, it bind to LacI such that a conformational change occurs. This changes the shape of the lacO binding site in LacI and releases it from the lac operator. Since LacI is now removed, transcription factor now have access to Pgrac and the strong expression of the down stream genes can occur. | ||
− | |||
===Usage and Biology=== | ===Usage and Biology=== | ||
− | This plasmid can replicate in both E.coli and B.subtilis and can be used when B.subtilis is | + | This plasmid can replicate in both E.coli and B.subtilis and can be used when B.subtilis is chosen as the destination bacteria. If insertion is in the dropout site, expression of the desired genes will be under the control of a strong IPTG responsive promoter, Pgrac. |
− | + | ||
===Sequence and Features=== | ===Sequence and Features=== | ||
<partinfo>BBa_K4321005 SequenceAndFeatures</partinfo> | <partinfo>BBa_K4321005 SequenceAndFeatures</partinfo> |
Revision as of 21:38, 8 October 2022
E.coli to Bacillus subtilis shuttle plasmid (pCG004)
pCG004 is an E.coli - Bacillus subtilis shuttle plasmid that was created based off of the pHT01 plasmid. This plasmid contains serval features that can be used to selectively expressed desired genes inserted within this dropout region. The dropout region contains a green fluorescent protein (GFP) flanked by BsaI sites. Upstream of this region is the lacI sequence (encodes a lac repressor), and an overlapping lac operator (lacO) and pgrac promoter.
When IPTG is not present, the lac repressor (LacI) is expressed and bound to lacO. Due the to overlap between lacO and pGrac, downstream expression from Pgrac cannot occur due to promoter unavailability. This results in the repression of the downstream genes. When IPTG is present, it bind to LacI such that a conformational change occurs. This changes the shape of the lacO binding site in LacI and releases it from the lac operator. Since LacI is now removed, transcription factor now have access to Pgrac and the strong expression of the down stream genes can occur.
Usage and Biology
This plasmid can replicate in both E.coli and B.subtilis and can be used when B.subtilis is chosen as the destination bacteria. If insertion is in the dropout site, expression of the desired genes will be under the control of a strong IPTG responsive promoter, Pgrac.
Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Illegal prefix found in sequence at 9048
Illegal suffix found in sequence at 1
Illegal EcoRI site found at 3615
Illegal EcoRI site found at 6835 - 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 3615
Illegal EcoRI site found at 6835
Illegal EcoRI site found at 9048
Illegal NheI site found at 3451
Illegal SpeI site found at 2
Illegal PstI site found at 16
Illegal NotI site found at 9
Illegal NotI site found at 9054 - 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 3615
Illegal EcoRI site found at 6835
Illegal EcoRI site found at 9048
Illegal BglII site found at 361
Illegal BglII site found at 6306
Illegal XhoI site found at 365 - 23INCOMPATIBLE WITH RFC[23]Illegal prefix found in sequence at 9048
Illegal suffix found in sequence at 2
Illegal EcoRI site found at 3615
Illegal EcoRI site found at 6835 - 25INCOMPATIBLE WITH RFC[25]Illegal prefix found in sequence at 9048
Illegal EcoRI site found at 3615
Illegal EcoRI site found at 6835
Illegal XbaI site found at 9063
Illegal SpeI site found at 2
Illegal PstI site found at 16 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 6234
Illegal BsaI.rc site found at 5170
Illegal SapI.rc site found at 2338
Illegal SapI.rc site found at 7459
References
PCG004 (plasmid #87377). Addgene. (n.d.). Retrieved October 8, 2022, from https://www.addgene.org/87377/
Tran, D. T., Phan, T. T., Doan, T. T., Tran, T. L., Schumann, W., & Nguyen, H. D. (2020). Integrative expression vectors with Pgrac promoters for inducer-free overproduction of recombinant proteins in bacillus subtilis. Biotechnology Reports, 28. https://doi.org/10.1016/j.btre.2020.e00540