Difference between revisions of "Part:BBa K3924044"
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<partinfo>BBa_K3924044 SequenceAndFeatures</partinfo> | <partinfo>BBa_K3924044 SequenceAndFeatures</partinfo> | ||
+ | ==Profile== | ||
+ | Name: mchIBX<br/> | ||
+ | Base Pairs:607bp<br/> | ||
+ | Origin: Escherichia coli, merge mchI,mchB, and mchX<br/> | ||
+ | Properties: A polycistron can express MchI, MchB and MchI. MchB is the precursor of microcin H47(MccH47).MchI is the immunity protein of MccH47.MchX's function is unsure, which might play a role in regulating the expression of mchB and mchI.<br/> | ||
+ | ==Usage and Biology== | ||
+ | The mchB, mchI and mchX are all from E.coli CA46. The mchB encodes MchB, which is the precursor of microcin H47(MccH47). The mchI encodes MchI, which is the immunity protein of MccH47.The mchx encodes MchX, whose's function is unsure<sup>[1]</sup>The polycistron is the basis of constructing a big plasmid which contains the whole MccH47 expressing system.<br/> | ||
+ | ==Design and Construction== | ||
+ | To construct the plasmid, we use endonuclease SpeI to cut RGP-mchI at 2bp after mchI open reading frame(ORF), then we used NEB Hifi DNA assembly to add RBS(ribosome binding site)-mchX between mchB and rrnB terminator.<br/> | ||
+ | [[Image: mchIBX.png|center|600px|thumb|'''Figure 1: The design of mchIBX''']] | ||
+ | ==Functional Verification== | ||
+ | We did western blotting(WB) to test whether the polycistron can express MchI and MchB successfully. Maybe because all of the them are small peptide, the bands can not be separated successfully in the WB result.<br/> | ||
+ | [[Image: Western Blotting.png|center|600px|thumb|'''Figure 3: The Western Blotting result''']] | ||
+ | |||
+ | ==Reference== | ||
+ | [1] Vassiliadis G, Destoumieux-Garzón D, Lombard C, Rebuffat S, Peduzzi J. Isolation and characterization of two members of the siderophore-microcin family, microcins M and H47. Antimicrobial Agents and Chemotherapy. 2010 Jan;54(1):288-297. DOI: 10.1128/aac.00744-09. PMID: 19884380; PMCID: PMC2798501. <br/> | ||
<!-- Uncomment this to enable Functional Parameter display | <!-- Uncomment this to enable Functional Parameter display |
Revision as of 09:38, 21 October 2021
mchI-mchB-mchX polycistrons with Ptac lacO promoter
mchI-mchB-mchX polycistrons with Ptac lacO promoter
Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Illegal EcoRI site found at 99
Illegal PstI site found at 310
Illegal PstI site found at 319 - 12INCOMPATIBLE WITH RFC[12]Illegal EcoRI site found at 99
Illegal PstI site found at 310
Illegal PstI site found at 319 - 21INCOMPATIBLE WITH RFC[21]Illegal EcoRI site found at 99
- 23INCOMPATIBLE WITH RFC[23]Illegal EcoRI site found at 99
Illegal PstI site found at 310
Illegal PstI site found at 319 - 25INCOMPATIBLE WITH RFC[25]Illegal EcoRI site found at 99
Illegal PstI site found at 310
Illegal PstI site found at 319 - 1000COMPATIBLE WITH RFC[1000]
Profile
Name: mchIBX
Base Pairs:607bp
Origin: Escherichia coli, merge mchI,mchB, and mchX
Properties: A polycistron can express MchI, MchB and MchI. MchB is the precursor of microcin H47(MccH47).MchI is the immunity protein of MccH47.MchX's function is unsure, which might play a role in regulating the expression of mchB and mchI.
Usage and Biology
The mchB, mchI and mchX are all from E.coli CA46. The mchB encodes MchB, which is the precursor of microcin H47(MccH47). The mchI encodes MchI, which is the immunity protein of MccH47.The mchx encodes MchX, whose's function is unsure[1]The polycistron is the basis of constructing a big plasmid which contains the whole MccH47 expressing system.
Design and Construction
To construct the plasmid, we use endonuclease SpeI to cut RGP-mchI at 2bp after mchI open reading frame(ORF), then we used NEB Hifi DNA assembly to add RBS(ribosome binding site)-mchX between mchB and rrnB terminator.
Functional Verification
We did western blotting(WB) to test whether the polycistron can express MchI and MchB successfully. Maybe because all of the them are small peptide, the bands can not be separated successfully in the WB result.
Reference
[1] Vassiliadis G, Destoumieux-Garzón D, Lombard C, Rebuffat S, Peduzzi J. Isolation and characterization of two members of the siderophore-microcin family, microcins M and H47. Antimicrobial Agents and Chemotherapy. 2010 Jan;54(1):288-297. DOI: 10.1128/aac.00744-09. PMID: 19884380; PMCID: PMC2798501.